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Project Quality Manager Metallurgy

Ansök    Nov 20    Cleverex Bemanning AB    Kvalitetschef
Om tjänsten We are seeking for an experienced and driven Project Quality Manager within metallurgy to build a team in northern Sweden. In this role, you will have the opportunity to lead and develop quality work within AFRY's major projects in the mining and metallurgy industries. You will have both an operational and strategic role, working closely with clients and internal departments, while building and shaping your team in the region. You will play a k... Visa mer
Om tjänsten
We are seeking for an experienced and driven Project Quality Manager within metallurgy to build a team in northern Sweden. In this role, you will have the opportunity to lead and develop quality work within AFRY's major projects in the mining and metallurgy industries. You will have both an operational and strategic role, working closely with clients and internal departments, while building and shaping your team in the region. You will play a key role in ensuring that quality processes are implemented and continuously improved, while also supporting and developing junior colleagues.

AFRY is a leading European company in engineering, design, and advisory services, with over 19,000 specialists in infrastructure, industry, energy, and digitalization. Their inclusive culture fosters courageous leaders who support individual growth. Here, you’ll have the opportunity to grow while contributing to meaningful, long-term sustainable solutions for future generations.

This is a direct recruitment. This means that we, Cleverex Bemanning, are a recruitment partner to AFRY, and you will be employed directly by them.



Du erbjuds
• A leadership role where you will have the opportunity to build and shape the quality work in a growing region.
• The chance to be part of an innovative company with a strong focus on sustainability and long-term investments within metallurgy and mining industries.
• The opportunity to lead and recruit your own team and develop strong relationships with clients and contractors in the region.
• A dynamic position where you will combine both operational and strategic work while contributing to new EPC projects.

Arbetsuppgifter
You will have the opportunity to build and lead a quality-focused team in northern Sweden and establish a local office with a strong network in the industry. In this role, you will lead and oversee quality work within metallurgy projects, both on-site and across various processes. Additionally, you will perform and support quality analyses, root cause analyses, and collect and analyze data to improve processes. As the Project Quality Manager, you will work closely with the engineering manager, HSE team, and project managers to ensure project goals are met. Furthermore, you will:
• Support contractors and ensure that quality standards and safety regulations are followed throughout the project chain.
• Coordinate and conduct quality-related meetings, workshops, audits, and inspections with clients and suppliers.
• Recruit and develop team members, and act as a mentor for junior colleagues.

Din profil
• You hold a Master’s degree in Metallurgy, Mining, or a similar technical field. Experience from Bergs at KTH is an advantage.
• At least 5 years of experience in quality work, preferably within the metal or mining industries.
• You have leadership experience, both operational and strategic, and enjoy developing and supporting your team.
• You have experience working with quality standards such as ISO 9001 and have a good understanding of EPC contracts and related risks.
• You are fluent in English, and Swedish is an advantage.
• A driver's license is required, and you are willing to travel in northern Sweden, from Luleå to Sundsvall.
As a person, you are analytical, communicative, and capable of handling technical discussions and processes at a high level. You thrive in a leadership role and are eager to develop your team.


Övrigt
Start date: By agreement
Location: from Sundsvall and north
Scope: Full-time
The recruitment process is handled by Cleverex Bemanning, and we kindly ask that all inquiries regarding the position be directed to [email protected].

Does this sound like your next challenge? We look forward to receiving your application!


Om oss
At Cleverex Bemanning, we work to recruit and place the right employees with the right customers. Our main focus is on our clients, consultants, and candidates, and our goal is for you as a candidate to feel like you’ve found the perfect fit! Visa mindre

Kvalitetsansvarig till vår verksamhet i Luleå

Ansök    Okt 25    Als Scandinavia AB    Kvalitetschef
Kvalitetsansvarig till vår verksamhet Luleå ALS Scandinavia AB är ett företag inom ALS Group, ett av de största uppdragslaboratorierna för kemiska analyser i världen. I Norden är vi ca 420 anställda inom ALS med laboratorier i Sverige; Luleå, Stockholm, Landskrona, Danmark; Humlebæk, Odense samt i Oslo och Helsingfors. I Luleå finns ett av världens mest avancerade kommersiella laboratorium specialiserat på grundämnen och isotoper. Läs mer på www.alsgloba... Visa mer
Kvalitetsansvarig till vår verksamhet Luleå

ALS Scandinavia AB är ett företag inom ALS Group, ett av de största uppdragslaboratorierna för kemiska analyser i världen. I Norden är vi ca 420 anställda inom ALS med laboratorier i Sverige; Luleå, Stockholm, Landskrona, Danmark; Humlebæk, Odense samt i Oslo och Helsingfors.
I Luleå finns ett av världens mest avancerade kommersiella laboratorium specialiserat på grundämnen och isotoper.
Läs mer på www.alsglobal.se
Vill du bli en viktig del i vårt framgångsrika kvalitetsteam? Då kanske du är vår nästa medarbetare!
Om tjänsten
ALS Scandinavia AB är ett ackrediterat laboratorium, enligt ISO 17025, som erbjuder våra kunder korta leveranstider vilket innebär att arbetet ska utföras effektivt och med god kvalitet. ALS Scandinavia AB i Luleå är även certifierade av Läkemedelsverket för arbete enligt GMP (Good Manufacuring Practice) samt innehar ett ”Statement of GLP compliance” för analyser under ”Good Laboratory Practice”.
I rollen som kvalitetsansvarig har du ansvaret för att utveckla och driva kvalitetsarbetet inom Luleås laboratoriet med fokus på ISO 17025, men även att säkerställa att kvalitetsledningssystemt uppfyller kraven som ställs på genom GMP och GLP.
Dina huvudsakliga arbetsuppgifter kommer vara att:
Utveckla och samordna kvalitetsarbetet
Underhålla kvalitetssystemet och utveckla kvalitetsriktiga arbetssätt
Samordna tillsyn och förnyade bedömningar som utförs av Swedac, samt övrig kontakt med Swedac
Delta i det övergripande kvalitetsarbetet mellan de olika siterna inom ALS Scandinavia
Skriva, granska och godkänna kvalitetsstyrande dokument
Ansvara vid externa inspektioner, tillsyner och bedömningar av företaget
Ansvara för interna revisioner
Ansvara för att kvalitetssäkra valideringar inom ISO 17025
Leda, stödja och utbilda medarbetare i kvalitetsarbetet
Ansvara för att kvalitetssystemet uppfyller kraven i ISO 17025 samt GMP och GLP


Egenskaper
Vi söker dig som har naturvetenskaplig akademisk utbildning, gärna inom kemi eller teknisk kemi.
Du bör ha dokumenterad erfarenhet och gedigna kunskaper inom kvalitetssäkring, gärna ISO 17025 samt vana att hantera och driva förändringsarbete.
För att lyckas i rollen som kvalitetsansvarig är du resultatorienterad, analytisk och strukturerad. Arbetet innebär varierande frågeställningar, vilket innebär att du självständigt ska kunna planera och prioritera ditt arbete.
Du ska ha lätt för att samarbeta och vara lyhörd för din omgivning. Eftersom arbetet kräver interaktion med många olika personer krävs det att du är pedagogisk, kommunikativ och har god social förmåga.
Goda kunskaper i engelska och svenska, såväl skriftligt som verbalt, är ett krav.

ALS erbjuder
Vi erbjuder en spännande miljö med avancerad teknik och kompetens, möjlighet att påverka och utvecklas i ett internationellt företag med fokus på goda värderingar, ansvarstagande och viljan att lyckas.
Tjänsten avser en tillsvidareanställning på heltid med sex månaders provanställning.

Intresserad?
Skicka din ansökan innehållande CV och personligt brev till
[email protected] senast den 15 november 2024
Ange referens Kvalitetsansvarig Luleå i din ansökan.

För närmare upplysningar angående tjänsten kontakta
Kristina Svedenbjörk, Kvalitetschef
0920-28 99 58, [email protected]

Fackliga representanter,
Unionen: Jenny Lundmark, 0920-28 99 64, [email protected] Visa mindre

Kvalitetsansvarig till vår verksamhet i Luleå

Ansök    Jun 24    Als Scandinavia AB    Kvalitetschef
Kvalitetsansvarig till vår verksamhet Luleå ALS Scandinavia AB är ett företag inom ALS Group, ett av de största uppdragslaboratorierna för kemiska analyser i världen. I Norden är vi ca 420 anställda inom ALS med laboratorier i Sverige; Luleå, Stockholm, Landskrona, Danmark; Humlebæk, Odense samt i Oslo och Helsingfors. I Luleå finns ett av världens mest avancerade kommersiella laboratorium specialiserat på grundämnen och isotoper. Läs mer på www.alsgloba... Visa mer
Kvalitetsansvarig till vår verksamhet Luleå

ALS Scandinavia AB är ett företag inom ALS Group, ett av de största uppdragslaboratorierna för kemiska analyser i världen. I Norden är vi ca 420 anställda inom ALS med laboratorier i Sverige; Luleå, Stockholm, Landskrona, Danmark; Humlebæk, Odense samt i Oslo och Helsingfors.
I Luleå finns ett av världens mest avancerade kommersiella laboratorium specialiserat på grundämnen och isotoper.
Läs mer på www.alsglobal.se
Vill du bli en viktig del i vårt framgångsrika kvalitetsteam? Då kanske du är vår nästa medarbetare!
Om tjänsten
ALS Scandinavia AB är ett ackrediterat laboratorium, enligt ISO 17025, som erbjuder våra kunder korta leveranstider vilket innebär att arbetet ska utföras effektivt och med god kvalitet. ALS Scandinavia AB i Luleå är även certifierade av Läkemedelsverket för arbete enligt GMP (Good Manufacuring Practice) samt innehar ett ”Statement of GLP compliance” för analyser under ”Good Laboratory Practice”.
I rollen som kvalitetsansvarig har du ansvaret för att utveckla och driva kvalitetsarbetet inom Luleås laboratoriet med fokus på ISO 17025, men även att säkerställa att kvalitetsledningssystemt uppfyller kraven som ställs på genom GMP och GLP.
Dina huvudsakliga arbetsuppgifter kommer vara att:
Utveckla och samordna kvalitetsarbetet
Underhålla kvalitetssystemet och utveckla kvalitetsriktiga arbetssätt
Samordna tillsyn och förnyade bedömningar som utförs av Swedac, samt övrig kontakt med Swedac
Delta i det övergripande kvalitetsarbetet mellan de olika siterna inom ALS Scandinavia
Skriva, granska och godkänna kvalitetsstyrande dokument
Ansvara vid externa inspektioner, tillsyner och bedömningar av företaget
Ansvara för interna revisioner
Ansvara för att kvalitetssäkra valideringar inom ISO 17025
Leda, stödja och utbilda medarbetare i kvalitetsarbetet
Ansvara för att kvalitetssystemet uppfyller kraven i ISO 17025 samt GMP och GLP


Egenskaper
Vi söker dig som har naturvetenskaplig akademisk utbildning, gärna inom kemi eller teknisk kemi.
Du bör ha dokumenterad erfarenhet och gedigna kunskaper inom kvalitetssäkring, gärna ISO 17025 samt vana att hantera och driva förändringsarbete.
För att lyckas i rollen som kvalitetsansvarig är du resultatorienterad, analytisk och strukturerad. Arbetet innebär varierande frågeställningar, vilket innebär att du självständigt ska kunna planera och prioritera ditt arbete.
Du ska ha lätt för att samarbeta och vara lyhörd för din omgivning. Eftersom arbetet kräver interaktion med många olika personer krävs det att du är pedagogisk, kommunikativ och har god social förmåga.
Goda kunskaper i engelska och svenska, såväl skriftligt som verbalt, är ett krav.

ALS erbjuder
Vi erbjuder en spännande miljö med avancerad teknik och kompetens, möjlighet att påverka och utvecklas i ett internationellt företag med fokus på goda värderingar, ansvarstagande och viljan att lyckas.
Tjänsten avser en tillsvidareanställning på heltid med sex månaders provanställning.

Intresserad?
Skicka din ansökan innehållande CV och personligt brev till
[email protected] samt [email protected] senast den 12 augusti 2024
Ange referens Kvalitetsansvarig Luleå i din ansökan.

För närmare upplysningar angående tjänsten kontakta
Kristina Svedenbjörk, Kvalitetschef
0920-28 99 58, [email protected]

Fackliga representanter,
Unionen: Jenny Lundmark, 0920-28 99 64, [email protected] Visa mindre

SSAB - Senior Construction Manager

Ansök    Aug 26    SSAB Emea AB    Kvalitetschef
Becoming part of the SSAB family means joining a journey. A journey that we believe is essential for the sustainability of this planet. Steel has been one of the most important materials for developing our society and it will continue to be so. In the roofs over our heads, in the bridges connecting our cities and in the cars of tomorrow. At SSAB we are proud of our history and leadership in high-strength steel. But we are also aware that the production of ... Visa mer
Becoming part of the SSAB family means joining a journey. A journey that we believe is essential for the sustainability of this planet. Steel has been one of the most important materials for developing our society and it will continue to be so. In the roofs over our heads, in the bridges connecting our cities and in the cars of tomorrow. At SSAB we are proud of our history and leadership in high-strength steel. But we are also aware that the production of steel is one of the largest emitters of greenhouse gases in the world. That has to change. That is why we have developed the world’s ?rst fossil free steel production and has committed to becoming largely fossil-free by around 2030. As part of SSAB you will be instrumental in realizing this goal and push for the green transformation of the whole steel industry.
About the position
Your main responsibility is to oversee the successful completion of all construction management activities and deliverables, within the approved safety, schedule, cost & quality criteria for the TO project. This includes responsibility for detailed daily/ weekly construction work planning and execution of activities necessary to successfully construct the project's scope of facilities according to approved success metrics and best practice construction project management principles.
In addition to managing the construction for Transformation Office in Luleå project, you will also contribute to the development of SSABs ability to construct projects in a way that competes on a global scale. You will be seen as an expert in project construction management within your area and will develop your cross-functional team accordingly.
Main responsibilities
Responsible as part of SSAB´s owner team for onsite construction management during project execution.
Manage planning, coordination and follow up of on site construction and installation activities during project execution.
Organize and conduct site visits to inspect work, and ensure staff are following health and safety guidelines.
Oversee and follow up the logistical requirements of a project.
Together with Site Supervision crew, follow construction and installation works, report and follow up on claims or change orders.
Responsible for ensuring construction contractors’ compliance with project requirements.
Inspire and motivate the project team at site.
Regularly review of timings, budget, labor, risk and project plans.
Secure that that flow of material, equipment, vehicles, labor to the construction areas are secured.
Secure highest level of safety standards at the construction areas.
Ensuring the delivery of high-quality work within contract timescales.
Secure that information received from site is prepared timely and is including accurate information that can be used as basis for decision making.

About You
Proven track record and experience of on-site construction management of major projects.
Strong experience and leadership skill in setting targets, objectives, structure, and responsibilities for all supervised staff.
Capacity to coordinate internal/external staff during construction phase based on HSE requirements, schedule, scope, and budget.
Minimum 15 years industry experience, of which at least 12 years with hands-on project leadership experience in demanding industrial environment.
Fluent in in English.



Our offer
At SSAB we strive for a diverse and inclusive environment. We use our values – driven, true and ahead – in making everyday decisions, keeping the customer at the heart of what we do. This makes us all team players, each with the drive to improve. When joining SSAB you will become part of an organization of passionate problem solvers working together on important challenges. We will support your growth by providing a safe and friendly workplace that contributes to work-life balance. If you set out to achieve it, at SSAB you will have the possibility of broadening your skills and grow within your field or beyond.
We offer a wide range of appreciated benefits to our employees. Some examples of these are listed here:
Profit sharing
Life balance through reduction of working hours
Wellness grants
Background check may be a part of the recruitment process.
Got questions about this position?
Tommy Krohn, Director of Strategic Projects linkedin.com/in/tommy-krohn-3463854 [email protected]
Petra Fekete, Interim Talent Acquisition linkedin.com/in/petra-fekete-50038726 Partner [email protected]
We decline contacts from recruitment agencies and ad sellers regarding this advertisement.
Trade union information is provided by Akademikerföreningen, Unionen and Ledarna, phone +46 920 920 00.
Word from your future manager
"As a Construction Manager (CM) for this transformation project, I’m looking for a person that will be a clear leader for the site organization. You will motivate and ensure that the site team will reach the project objectives (and stay positive). You will also have an excellent understanding of ongoing site activities to ensure that the project stay in schedule and within the budget. Safety is very important for SSAB and as a CM you ensure that the persons at the site follow the safety regulations. You also act as a role-model to others when it comes to HSE. If you identify a problem at site, you swiftly solve the issue balancing cost, schedule and quality. As a CM you will be the contact at site for a lot of stakeholders (both internal / external) and your communication skills are excellent. As a manager I encourages open communication, while always trying to help each other to achieve the best result. Welcome to the team!"
SSAB is a Nordic and US-based steel company that builds a stronger, lighter and more sustainable world through value added steel products and services. Working with our partners, SSAB has developed SSAB Fossil-free™ steel and plans to reinvent the value chain from the mine to the end customer, largely eliminating carbon dioxide emissions from our own operations. SSAB Zero™, a largely carbon emission-free steel based on recycled steel, further strengthens SSAB’s leadership position and our comprehensive, sustainable offering independent of the raw material. SSAB has employees in over 50 countries and production facilities in Sweden, Finland and the US. SSAB is listed on Nasdaq Stockholm and has a secondary listing on Nasdaq Helsinki. Join us on our journey! www.ssab.com, Facebook, Instagram, LinkedIn, X and YouTube. Visa mindre

Project Quality Manager Metallurgy

Ansök    Okt 16    Cleverex Bemanning AB    Kvalitetschef
Om tjänsten We are seeking for an experienced and driven Project Quality Manager within metallurgy to build a team in northern Sweden. In this role, you will have the opportunity to lead and develop quality work within AFRY's major projects in the mining and metallurgy industries. You will have both an operational and strategic role, working closely with clients and internal departments, while building and shaping your team in the region. You will play a k... Visa mer
Om tjänsten
We are seeking for an experienced and driven Project Quality Manager within metallurgy to build a team in northern Sweden. In this role, you will have the opportunity to lead and develop quality work within AFRY's major projects in the mining and metallurgy industries. You will have both an operational and strategic role, working closely with clients and internal departments, while building and shaping your team in the region. You will play a key role in ensuring that quality processes are implemented and continuously improved, while also supporting and developing junior colleagues.

AFRY is a leading European company in engineering, design, and advisory services, with over 19,000 specialists in infrastructure, industry, energy, and digitalization. Their inclusive culture fosters courageous leaders who support individual growth. Here, you’ll have the opportunity to grow while contributing to meaningful, long-term sustainable solutions for future generations.

This is a direct recruitment. This means that we, Cleverex Bemanning, are a recruitment partner to AFRY, and you will be employed directly by them.



Du erbjuds
• A leadership role where you will have the opportunity to build and shape the quality work in a growing region.
• The chance to be part of an innovative company with a strong focus on sustainability and long-term investments within metallurgy and mining industries.
• The opportunity to lead and recruit your own team and develop strong relationships with clients and contractors in the region.
• A dynamic position where you will combine both operational and strategic work while contributing to new EPC projects.

Arbetsuppgifter
You will have the opportunity to build and lead a quality-focused team in northern Sweden and establish a local office with a strong network in the industry. In this role, you will lead and oversee quality work within metallurgy projects, both on-site and across various processes. Additionally, you will perform and support quality analyses, root cause analyses, and collect and analyze data to improve processes. As the Project Quality Manager, you will work closely with the engineering manager, HSE team, and project managers to ensure project goals are met. Furthermore, you will:
• Support contractors and ensure that quality standards and safety regulations are followed throughout the project chain.
• Coordinate and conduct quality-related meetings, workshops, audits, and inspections with clients and suppliers.
• Recruit and develop team members, and act as a mentor for junior colleagues.

Din profil
• You hold a Master’s degree in Metallurgy, Mining, or a similar technical field. Experience from Bergs at KTH is an advantage.
• At least 5 years of experience in quality work, preferably within the metal or mining industries.
• You have leadership experience, both operational and strategic, and enjoy developing and supporting your team.
• You have experience working with quality standards such as ISO 9001 and have a good understanding of EPC contracts and related risks.
• You are fluent in English, and Swedish is an advantage.
• A driver's license is required, and you are willing to travel in northern Sweden, from Luleå to Sundsvall.
As a person, you are analytical, communicative, and capable of handling technical discussions and processes at a high level. You thrive in a leadership role and are eager to develop your team.


Övrigt
Start date: By agreement
Location: from Sundsvall and north
Scope: Full-time
The recruitment process is handled by Cleverex Bemanning, and we kindly ask that all inquiries regarding the position be directed to [email protected].

Does this sound like your next challenge? We look forward to receiving your application!


Om oss
At Cleverex Bemanning, we work to recruit and place the right employees with the right customers. Our main focus is on our clients, consultants, and candidates, and our goal is for you as a candidate to feel like you’ve found the perfect fit! Visa mindre

Quality Manager

Ansök    Apr 5    Baxter Medical AB    Kvalitetschef
This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered signific... Visa mer
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
As a Quality Manager you ensure product quality through the implementation of various control and improvement opportunities and coordination of work within the area of Quality Management system, CAPA and Learning Management system. Support to Sr. QA Manager in ensuring that processes needed for the quality management system are established, implemented, and maintained. Ensure the promotion of awareness of regulatory and customer requirements throughout the organization.
Essential Duties and Responsibilities
Management and further development of the QMS Team
Intelligently deploy resources to meet daily business needs in a timely manner while evolving the work processes to become more proactive, efficient, and effective
Provide strategic direction and leadership to the team to ensure operations adhere to requirements of compliance and product quality
Define and coordinate tasks within the scope of the objective and task definition, as well as review and discuss work results
Plan and execute local Audit program
Control and track the products and processes quality and regulatory compliance through adequate performance metrics and plans.
Stop, if required, the delivery and/or the production of products in case of non-conformity.
Ensure that adequate records of data and results concerning tests and product controls are taken
Manages effective cross-function relationships and in particular work with concept, product and commercialization teams to ensure quality of product and process.
Drive data analysis of performance data to identify high priority issues relating to safety, regulatory compliance and customer satisfaction.
Coordination of resources within area of Quality Management system, CAPA and Learning Management system
Continuous improvements of processes within area of responsibility
Implementation of the company-specific quality policy and quality goals
Ensuring product conformity, reducing production deviations
Ensuring compliance with design and development activities
Communication of the quality principles to promote quality awareness in the company
Ensuring compliance with production and process controls
Ensuring product conformity, reducing production deviations
Ensuring compliance with acceptance and validation activities
Management of non-compliant products and investigation of problems with regards to product quality, as well as support for processing: Carry out root cause analyzes, introduce corrective measures to eliminate or reduce the identified causes.
Serve as primary point of contact for quality and regulatory issues related to manufacturing processes
Lead efforts to identify and execute initiatives to improve manufacturing process and product quality

EDUCATION, EXPERIENCE AND QUALIFICATIONS:
Proficient with Quality System Regulations, IS013485, Medical Device Regulation and ISO 13485 Quality System Standards.
Demonstrated ability to succeed in team environments and possesses effective interpersonal skills.
Demonstrated attention to detail, analytical decision-making, and problem-solving skills.
Proven ability to succeed in an environment of continuous improvement and to identify improvement opportunities.
Strong customer orientation and excellent written and verbal communication skills.
Ability to effectively navigate rapidly changing quality, regulatory and business environments and succeed in an environment of change.
Bachelor’s degree (minimum) in an Engineering field, preferable mechanical, electrical, or industrial engineering.
5+ years of experience in Quality Assurance or Regulatory Affairs in the Medical Device or Pharmaceutical industry.
Strong management and analytical skills
Strong process and continuous improvement skills
Supportive, positive attitude and approach to work
Good communication skills, both verbal and written
Able to work independently or as part of a team
Strategic skills, ability to holistic/global perspective
Additional training in Risk Management, Six Sigma, Lean Manufacturing and Statistical Methods is preferred.
Experience of an R&D and production site is a plus
Fluent in Swedish and English, other languages are beneficial Visa mindre

Quality Manager

Ansök    Mar 5    Baxter Medical AB    Kvalitetschef
This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered signific... Visa mer
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
As a Quality Manager you ensure product quality through the implementation of various control and improvement opportunities and coordination of work within the area of Quality Management system, CAPA and Learning Management system. Support to Sr. QA Manager in ensuring that processes needed for the quality management system are established, implemented, and maintained. Ensure the promotion of awareness of regulatory and customer requirements throughout the organization.
Essential Duties and Responsibilities
Management and further development of the QMS Team
Intelligently deploy resources to meet daily business needs in a timely manner while evolving the work processes to become more proactive, efficient, and effective
Provide strategic direction and leadership to the team to ensure operations adhere to requirements of compliance and product quality
Define and coordinate tasks within the scope of the objective and task definition, as well as review and discuss work results
Plan and execute local Audit program
Control and track the products and processes quality and regulatory compliance through adequate performance metrics and plans.
Stop, if required, the delivery and/or the production of products in case of non-conformity.
Ensure that adequate records of data and results concerning tests and product controls are taken
Manages effective cross-function relationships and in particular work with concept, product and commercialization teams to ensure quality of product and process.
Drive data analysis of performance data to identify high priority issues relating to safety, regulatory compliance and customer satisfaction.
Coordination of resources within area of Quality Management system, CAPA and Learning Management system
Continuous improvements of processes within area of responsibility
Implementation of the company-specific quality policy and quality goals
Ensuring product conformity, reducing production deviations
Ensuring compliance with design and development activities
Communication of the quality principles to promote quality awareness in the company
Ensuring compliance with production and process controls
Ensuring product conformity, reducing production deviations
Ensuring compliance with acceptance and validation activities
Management of non-compliant products and investigation of problems with regards to product quality, as well as support for processing: Carry out root cause analyzes, introduce corrective measures to eliminate or reduce the identified causes.
Serve as primary point of contact for quality and regulatory issues related to manufacturing processes
Lead efforts to identify and execute initiatives to improve manufacturing process and product quality

EDUCATION, EXPERIENCE AND QUALIFICATIONS:
Proficient with Quality System Regulations, IS013485, Medical Device Regulation and ISO 13485 Quality System Standards.
Demonstrated ability to succeed in team environments and possesses effective interpersonal skills.
Demonstrated attention to detail, analytical decision-making, and problem-solving skills.
Proven ability to succeed in an environment of continuous improvement and to identify improvement opportunities.
Strong customer orientation and excellent written and verbal communication skills.
Ability to effectively navigate rapidly changing quality, regulatory and business environments and succeed in an environment of change.
Bachelor’s degree (minimum) in an Engineering field, preferable mechanical, electrical, or industrial engineering.
5+ years of experience in Quality Assurance or Regulatory Affairs in the Medical Device or Pharmaceutical industry.
Strong management and analytical skills
Strong process and continuous improvement skills
Supportive, positive attitude and approach to work
Good communication skills, both verbal and written
Able to work independently or as part of a team
Strategic skills, ability to holistic/global perspective
Additional training in Risk Management, Six Sigma, Lean Manufacturing and Statistical Methods is preferred.
Experience of an R&D and production site is a plus
Fluent in Swedish and English, other languages are beneficial Visa mindre

Quality Manager

Ansök    Feb 2    Baxter Medical AB    Kvalitetschef
This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered signific... Visa mer
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
As a Quality Manager you ensure product quality through the implementation of various control and improvement opportunities and coordination of work within the area of Quality Management system, CAPA and Learning Management system. Support to Sr. QA Manager in ensuring that processes needed for the quality management system are established, implemented, and maintained. Ensure the promotion of awareness of regulatory and customer requirements throughout the organization.
Essential Duties and Responsibilities
Management and further development of the QMS Team
Intelligently deploy resources to meet daily business needs in a timely manner while evolving the work processes to become more proactive, efficient, and effective
Provide strategic direction and leadership to the team to ensure operations adhere to requirements of compliance and product quality
Define and coordinate tasks within the scope of the objective and task definition, as well as review and discuss work results
Plan and execute local Audit program
Control and track the products and processes quality and regulatory compliance through adequate performance metrics and plans.
Stop, if required, the delivery and/or the production of products in case of non-conformity.
Ensure that adequate records of data and results concerning tests and product controls are taken
Manages effective cross-function relationships and in particular work with concept, product and commercialization teams to ensure quality of product and process.
Drive data analysis of performance data to identify high priority issues relating to safety, regulatory compliance and customer satisfaction.
Coordination of resources within area of Quality Management system, CAPA and Learning Management system
Continuous improvements of processes within area of responsibility
Implementation of the company-specific quality policy and quality goals
Ensuring product conformity, reducing production deviations
Ensuring compliance with design and development activities
Communication of the quality principles to promote quality awareness in the company
Ensuring compliance with production and process controls
Ensuring product conformity, reducing production deviations
Ensuring compliance with acceptance and validation activities
Management of non-compliant products and investigation of problems with regards to product quality, as well as support for processing: Carry out root cause analyzes, introduce corrective measures to eliminate or reduce the identified causes.
Serve as primary point of contact for quality and regulatory issues related to manufacturing processes
Lead efforts to identify and execute initiatives to improve manufacturing process and product quality

EDUCATION, EXPERIENCE AND QUALIFICATIONS:
Proficient with Quality System Regulations, IS013485, Medical Device Regulation and ISO 13485 Quality System Standards.
Demonstrated ability to succeed in team environments and possesses effective interpersonal skills.
Demonstrated attention to detail, analytical decision-making, and problem-solving skills.
Proven ability to succeed in an environment of continuous improvement and to identify improvement opportunities.
Strong customer orientation and excellent written and verbal communication skills.
Ability to effectively navigate rapidly changing quality, regulatory and business environments and succeed in an environment of change.
Bachelor’s degree (minimum) in an Engineering field, preferable mechanical, electrical, or industrial engineering.
5+ years of experience in Quality Assurance or Regulatory Affairs in the Medical Device or Pharmaceutical industry.
Strong management and analytical skills
Strong process and continuous improvement skills
Supportive, positive attitude and approach to work
Good communication skills, both verbal and written
Able to work independently or as part of a team
Strategic skills, ability to holistic/global perspective
Additional training in Risk Management, Six Sigma, Lean Manufacturing and Statistical Methods is preferred.
Experience of an R&D and production site is a plus
Fluent in Swedish and English, other languages are beneficial Visa mindre

Resbar Kvalitetsingenjör QA/QC

Ansök    Nov 20    AFRY AB    Kvalitetschef
Företagsbeskrivning AFRY erbjuder tjänster inom teknik, design, digitalisering och rådgivning för att accelerera omställningen till ett mer hållbart samhälle. Vi är 19 000 hängivna experter inom industri, energi- och infrastruktur, som skapar värde för kommande generationer. AFRY har en global räckvidd med djupa rötter i Norden. Making Future Jobbeskrivning Vill du jobba med hela världen men samtidigt ha en trygg samhörighet i ett team med specia... Visa mer
Företagsbeskrivning


AFRY erbjuder tjänster inom teknik, design, digitalisering och rådgivning för att accelerera omställningen till ett mer hållbart samhälle.


Vi är 19 000 hängivna experter inom industri, energi- och infrastruktur, som skapar värde för kommande generationer. AFRY har en global räckvidd med djupa rötter i Norden.


Making Future


Jobbeskrivning


Vill du jobba med hela världen men samtidigt ha en trygg samhörighet i ett team med specialister där alla bidrar med värdefull kompetens, erfarenhet och glädje? Vårt marknadsområde Quality Engineering (QE) har lite drygt 30 medarbetare utspridda över landet och nu söker vi fler medarbetare. I vårt team är vi allt från nyexaminerade till seniora med en bred kompetens inom kvalitet, svets och material.
Som Kvalitetsingenjör, QA/QC, kommer du arbeta med kvalitetssäkring och kvalitetskontroll såväl internt som hos våra kunder. Du kommer att vara involverad i upphandling, konstruktion, tillverkning, installation och slutdokumentation i samband med mekaniska installationer, ombyggnationer och reparationer. Majoriteten av din tid kommer du spendera hos våra kunder och då vi både har kunder i Sverige och globalt innebär rollen en del tjänsteresor, både långa och korta. Till den här rollen söker vi dig som är resbar och kan tänka dig konsultuppdrag som innehåller veckopendling.


Kravspecifikation


Som person är du driven och ansvarstagande. Vi tror även att du är en god kommunikatör med god förmåga att rapportera och presentera kvalitetsrelaterade milstolpar. Du trivs med att samarbeta i grupp men även självständigt under eget ansvar.
Lämplig utbildning är civilingenjör alternativt högskoleingenjör med 3–5 års arbetslivserfarenhet av kvalitetsarbete inom läkemedels-, process-, gruv- eller energiindustrin.
Eftersom mycket av arbetet även kan vara mot internationella kunder, behärskar du både svenska och engelska i tal och skrift.


Ytterligare information


Är du intresserad av att jobba i ett teknikintresserat gäng med kunniga specialister, där vi lär av varandra och det ges goda möjligheter för utveckling? Då söker du dig till rätt team!
Quality Engineering erbjuder en mångfald bland kollegor med olika specialistområden, en bredd på uppdrag och en möjlighet att själv utvecklas åt det håll man vill! Läs mer om oss på Quality Engineering och våra spännande satsningar här: https://afry.com/sv/nyhetsrum/nyheter/afrys-quality-engineering-kanner-av-den-grona-omstallningen
AFRY är en arbetsplats med framåtanda och trygghet i form av kollektivavtal och personalförmåner för samtliga av våra medarbetare. Vår personalklubb arrangerar sociala aktiviteter på och utanför kontoret. Allt från skidresor, sjunga i kör till att spela brädspel – det finns något för alla.
Har du frågor gällande tjänsten, kontakta någon av de rekryterande cheferna på:
Fredrik Videll, [email protected]
Sami Paloaho, [email protected]
Har du frågor gällande rekryteringsprocessen, kontakta rekryterare Fanny Sjödell, [email protected]
Vi har ej möjlighet att ta emot ansökningar via e-post. Vi intervjuar löpande, så vänta inte med att söka tjänsten. Välkommen med din ansökan, senast den 10 december!
På AFRY driver vi förändring i allt vi gör. Vi anser att förändring sker när modiga idéer möts, när vi samarbetar, skapar innovation och omfamnar kreativa lösningar, det är så vi skapar framtiden. Vi söker konstant kvalificerade kandidater som vill ansluta sig till våra inkluderande team runt om i världen. Bli en del av oss och påskynda den gröna omställningen Visa mindre

Quality Manager

Ansök    Nov 28    Baxter Medical AB    Kvalitetschef
This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered signific... Visa mer
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
As a Quality Manager you ensure product quality through the implementation of various control and improvement opportunities and coordination of work within the area of Quality Management system, CAPA and Learning Management system. Support to Sr. QA Manager in ensuring that processes needed for the quality management system are established, implemented, and maintained. Ensure the promotion of awareness of regulatory and customer requirements throughout the organization.
Essential Duties and Responsibilities
Management and further development of the QMS Team
Intelligently deploy resources to meet daily business needs in a timely manner while evolving the work processes to become more proactive, efficient, and effective
Provide strategic direction and leadership to the team to ensure operations adhere to requirements of compliance and product quality
Define and coordinate tasks within the scope of the objective and task definition, as well as review and discuss work results
Plan and execute local Audit program
Control and track the products and processes quality and regulatory compliance through adequate performance metrics and plans.
Stop, if required, the delivery and/or the production of products in case of non-conformity.
Ensure that adequate records of data and results concerning tests and product controls are taken
Manages effective cross-function relationships and in particular work with concept, product and commercialization teams to ensure quality of product and process.
Drive data analysis of performance data to identify high priority issues relating to safety, regulatory compliance and customer satisfaction.
Coordination of resources within area of Quality Management system, CAPA and Learning Management system
Continuous improvements of processes within area of responsibility
Implementation of the company-specific quality policy and quality goals
Ensuring product conformity, reducing production deviations
Ensuring compliance with design and development activities
Communication of the quality principles to promote quality awareness in the company
Ensuring compliance with production and process controls
Ensuring product conformity, reducing production deviations
Ensuring compliance with acceptance and validation activities
Management of non-compliant products and investigation of problems with regards to product quality, as well as support for processing: Carry out root cause analyzes, introduce corrective measures to eliminate or reduce the identified causes.
Serve as primary point of contact for quality and regulatory issues related to manufacturing processes
Lead efforts to identify and execute initiatives to improve manufacturing process and product quality

EDUCATION, EXPERIENCE AND QUALIFICATIONS:
Proficient with Quality System Regulations, IS013485, Medical Device Regulation and ISO 13485 Quality System Standards.
Demonstrated ability to succeed in team environments and possesses effective interpersonal skills.
Demonstrated attention to detail, analytical decision-making, and problem-solving skills.
Proven ability to succeed in an environment of continuous improvement and to identify improvement opportunities.
Strong customer orientation and excellent written and verbal communication skills.
Ability to effectively navigate rapidly changing quality, regulatory and business environments and succeed in an environment of change.
Bachelor’s degree (minimum) in an Engineering field, preferable mechanical, electrical, or industrial engineering.
5+ years of experience in Quality Assurance or Regulatory Affairs in the Medical Device or Pharmaceutical industry.
Strong management and analytical skills
Strong process and continuous improvement skills
Supportive, positive attitude and approach to work
Good communication skills, both verbal and written
Able to work independently or as part of a team
Strategic skills, ability to holistic/global perspective
Additional training in Risk Management, Six Sigma, Lean Manufacturing and Statistical Methods is preferred.
Experience of an R&D and production site is a plus
Fluent in Swedish and English, other languages are beneficial Visa mindre

Quality Manager

Ansök    Okt 24    Baxter Medical AB    Kvalitetschef
This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered signific... Visa mer
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
As a Quality Manager you ensure product quality through the implementation of various control and improvement opportunities and coordination of work within the area of Quality Management system, CAPA and Learning Management system. Support to Sr. QA Manager in ensuring that processes needed for the quality management system are established, implemented, and maintained. Ensure the promotion of awareness of regulatory and customer requirements throughout the organization.
Essential Duties and Responsibilities
Management and further development of the QMS Team
Intelligently deploy resources to meet daily business needs in a timely manner while evolving the work processes to become more proactive, efficient, and effective
Provide strategic direction and leadership to the team to ensure operations adhere to requirements of compliance and product quality
Define and coordinate tasks within the scope of the objective and task definition, as well as review and discuss work results
Plan and execute local Audit program
Control and track the products and processes quality and regulatory compliance through adequate performance metrics and plans.
Stop, if required, the delivery and/or the production of products in case of non-conformity.
Ensure that adequate records of data and results concerning tests and product controls are taken
Manages effective cross-function relationships and in particular work with concept, product and commercialization teams to ensure quality of product and process.
Drive data analysis of performance data to identify high priority issues relating to safety, regulatory compliance and customer satisfaction.
Coordination of resources within area of Quality Management system, CAPA and Learning Management system
Continuous improvements of processes within area of responsibility
Implementation of the company-specific quality policy and quality goals
Ensuring product conformity, reducing production deviations
Ensuring compliance with design and development activities
Communication of the quality principles to promote quality awareness in the company
Ensuring compliance with production and process controls
Ensuring product conformity, reducing production deviations
Ensuring compliance with acceptance and validation activities
Management of non-compliant products and investigation of problems with regards to product quality, as well as support for processing: Carry out root cause analyzes, introduce corrective measures to eliminate or reduce the identified causes.
Serve as primary point of contact for quality and regulatory issues related to manufacturing processes
Lead efforts to identify and execute initiatives to improve manufacturing process and product quality

EDUCATION, EXPERIENCE AND QUALIFICATIONS:
Proficient with Quality System Regulations, IS013485, Medical Device Regulation and ISO 13485 Quality System Standards.
Demonstrated ability to succeed in team environments and possesses effective interpersonal skills.
Demonstrated attention to detail, analytical decision-making, and problem-solving skills.
Proven ability to succeed in an environment of continuous improvement and to identify improvement opportunities.
Strong customer orientation and excellent written and verbal communication skills.
Ability to effectively navigate rapidly changing quality, regulatory and business environments and succeed in an environment of change.
Bachelor’s degree (minimum) in an Engineering field, preferable mechanical, electrical, or industrial engineering.
5+ years of experience in Quality Assurance or Regulatory Affairs in the Medical Device or Pharmaceutical industry.
Strong management and analytical skills
Strong process and continuous improvement skills
Supportive, positive attitude and approach to work
Good communication skills, both verbal and written
Able to work independently or as part of a team
Strategic skills, ability to holistic/global perspective
Additional training in Risk Management, Six Sigma, Lean Manufacturing and Statistical Methods is preferred.
Experience of an R&D and production site is a plus
Fluent in Swedish and English, other languages are beneficial Visa mindre

Kvalitetschef vid Norrbottens Flygflottilj

Ansök    Jun 9    Försvarsmakten    Kvalitetschef
Kvalitetschefen är C F 21 företrädare med ansvar för bevakning av att tillämpliga regler och förfaranden inom det militära luftfartssystemet följs. I rollen deltar du även aktivt i F 21  ledningsarbete där du förväntas kunna leda projekt för att kvalitetssäkra och förbättra strukturer och metoder inom ditt kompetensområde. Huvudsakliga arbetsuppgifter Uppgifterna innebär bl.a. att: • Planera och genomföra revisioner av i syfte att bevaka att tillämpl... Visa mer
Kvalitetschefen är C F 21 företrädare med ansvar för bevakning av att tillämpliga regler och förfaranden inom det militära luftfartssystemet följs. I rollen deltar du även aktivt i F 21  ledningsarbete där du förväntas kunna leda projekt för att kvalitetssäkra och förbättra strukturer och metoder inom ditt kompetensområde.

Huvudsakliga arbetsuppgifter

Uppgifterna innebär bl.a. att:


• Planera och genomföra revisioner av i syfte att bevaka att tillämpliga regler och förfaranden inom det militära luftfartssystemet följs
• Samordna Flygsäkerhetsinspektörens och Transportstyrelsens tillsyner av militär respektive civil uftfart.
• Övergripande samordna utveckling och vidmakthållande av F 21 verksamhetsledningssystem.
• Bevaka att bestämmelser rörande militär luftfart omhändertas i lokala verksamhetsledande dokument.
• Bevaka att transportstyrelsens föreskrifter och andra bestämmelser kopplat till certifikat för civil luftfart omhändertas i lokala verksamhetsledande dokument.
• Rapportera hur verksamhetens system fungerar och säkra att beslut och resursallokering för ständig förbättring kommer till stånd.
• Stödja C F 21 och övriga chefer i kvalitets- och verksamhetsutvecklingsfrågor.
• Genomföra utbildning i frågor rörande militär luftfart inklusive utbildning av revisorer

 

Kvalifikationer


• Goda kunskaper om regler för militär luftfart
• Erfarenhet som revisionsledare
• FM revisorsutbildning eller annan likvärdig utbildning
• Akademisk examen eller annan relevant utbildning/erfarenhet som arbetsgivaren anser likvärdig


Meriterande


• Kvalitetschefsutbildning eller annan likvärdig utbildning
• Flerårig erfarenhet av regler för militär luftfart
• Fördjupningskurser inom kvalitetsområdet exempelvis Black-belt, Green-belt och Leanledarutbildning.
• Flerårig erfarenhet av kvalitetsarbete
• Goda kunskaper i emlia (MS Sharepoint)
• Utbildning och erfarenhet av arbete med verksamhetssäkerhet exempelvis Safety Management Systems (SMS).
• Erfarenhet av att leda större projekt och-/eller komplexa verksamheter
• Erfarenhet av arbete i statlig förvaltning

 

Personliga egenskaper

För tjänsten krävs att du är en självgående och handlingskraftig person, du är väl bevandrad inom kvalitetsområdet och kan definiera vad som är viktigt för verksamheten. Du har en utvecklad analytisk förmåga, är noggrann, kommunikativ och fungerar väl i samarbetet med andra. Inom ditt område är du trygg, du leder kvalitetsarbetet och säkerställer att framdrivning och rapportering sker korrekt och i tid.

Stor vikt kommer att läggas vid personlig lämplighet.



För att myndighetens uppdrag ska vara framgångsrikt förutsätts att alla medarbetare uppträder enligt den värdegrund som finns. Försvarsmaktens värdegrund slår vakt om alla människors lika värde, rättvisa och jämlikhet och främjar demokrati och mänskliga rättigheter (läs mer på www.forsvarsmakten.se).



Övrigt
Anställningsform: Tillsvidare
Sysselsättningsgrad: Heltid
Arbetsort: Luleå
Tillträdesdatum: Enligt överenskommelse


För upplysningar om befattningen kontakta:

C F 21 Carl-Fredrik Edström, 070-223 93 29


Fackliga företrädare:
OF F 21, OFR/S, SEKO, SACO – samtliga nås via F 21 växel 0920-23 40 00

Sista ansökningsdag 2022-06-26

Välkommen med din ansökan senast 2022-06-26. Din ansökan bör innehålla CV samt ansökningsbrev där du motiverar varför du är lämpad för denna befattning.


Ansökningar till denna befattning kommer endast tas emot via Försvarsmaktens webbplats.
--------------------------------------------------------
Information om Försvarsmakten och det rekryterande förbandet:

Norrbottens flygflottilj, F 21, är Sveriges nordligaste flygflottilj. Huvudbasen är i Luleå, med sidobaser i Jokkmokk och Vidsel.
F 21 övar kontinuerligt för att kunna leverera följande luftoperativa förmågor i såväl fred, kris som krig:

- Kontroll av luftrummet.
- Mark- och sjömålsbekämpning.
- Underrättelseinhämtning.
- Luftburen transport.
- Stöd till övriga stridskrafter, totalförsvaret och samhället i övrigt.

F 21 försvarar - tillsammans med övriga förband i Försvarsmakten - Sverige, landets intressen, vår frihet och rätt att leva som vi själva väljer.

Tillsammans med övriga flygvapnet bevakar och skyddar vi Sveriges luftrum dygnet runt, året runt.

I Försvarsmakten finns en stark värdegrund som bygger på öppenhet, resultat och ansvar. Professionell utveckling och personlig hälsa värdesätts och uppmuntras. Det finns goda förutsättningar för intern karriärrörlighet, friskvård samt bra balans mellan arbete och privatliv.

En anställning hos oss innebär placering i säkerhetsklass. Vanligtvis krävs svenskt medborgarskap.
Säkerhetsprövning med registerkontroll kommer att genomföras före anställning enligt 3 kap i säkerhetsskyddslagen. Med anställning följer en skyldighet att krigsplaceras. I anställningen ingår även en skyldighet att tjänstgöra utomlands. Innebörden av detta varierar beroende på typ av befattning.

Till ansökan om anställning ska CV och personligt brev bifogas. Om du går vidare i anställningsprocessen ska alltid vidimerade kopior av betyg och intyg uppvisas.

Samtal från externa rekryteringsföretag och säljare undanbedes. Visa mindre

Jämställdhetsintegrerings ansvarig projektledare

För Region Norrbotten söker vi nu en projektledare för jämställdhetsintegrerings arbete. Omfattning: 50-100% enligt ök från mitten av maj/början juni med ett år i taget med option om förlängning tre år. Distansarbete möjligt med vissa obligatoriska tillfällen att vara på plats i Luleå annars flexibelt och fritt enligt ök med regionen. Arbetsuppgifter: Uppdraget avser avtal på process- och kunskapsstöd inom jämställdhetsintegrering, jämställd budgetering... Visa mer
För Region Norrbotten söker vi nu en projektledare för jämställdhetsintegrerings arbete.
Omfattning:
50-100% enligt ök från mitten av maj/början juni med ett år i taget med option om förlängning tre år.
Distansarbete möjligt med vissa obligatoriska tillfällen att vara på plats i Luleå annars flexibelt och fritt enligt ök med regionen.
Arbetsuppgifter:
Uppdraget avser avtal på process- och kunskapsstöd inom jämställdhetsintegrering, jämställd budgetering och jämställdhetsanalyser. Uppdraget är för Region Norrbotten som processledare och kunskapsstöd inom området jämställdhetsintegering.
Uppdraget med jämställdhetsintegrering ligger placerat i regionstaben där en del av uppdraget går ut på att ge det stöd som efterfrågas. Ekonomi- och uppföljningsavdelningen ansvarar för stöd till ledning och verksamhet gällande strategisk planering och styrning, analys och uppföljning samt ekonomisk styrning, budgetering, redovisning och förvaltning
Jämställdhetsintegrera styrdokument – ex strategiska planen, regionstyrelsens plan, nämndsplaner, regionala utvecklingsstrategin, kompetensförsörjningsstrategin, kommunikationspolicyn samt stötta medarbetare i deras arbete med fortsätta jämställdhetsintegrera styrande dokument.
Stötta medarbetare i att identifiera ojämställdhetsproblem i organisationen – hur får våra patienter tillgång till vården – är det likvärdigt?
Ta fram ett lättillgängligt process- och kunskapsstöd exempelvis:
Tyddliggöra vad jämställdhetsintegrering innebär för varje aktör i styrkedjan, vad som förväntas av respektive aktör för att därmed öka förståelsen för hur jämställdhet främjar deras kärnverksamhet och därmed öka förutsättningarna för att arbetet genomförs.
Ta fram internt stödmaterial (handbok och mallar) för jämställdhetsanalyser
Utbilda oss som samordnare, avdelningen ekonomi och uppföljning, chefer och strateger
Stötta i arbetet med jämställdbudgetering
Utbilda i jämställdhet och jämställdhetsintegrering.
Processleda jämställd uppföljning och analys.
Samarbeta med regionstab och ekonomi- och uppföljningsavdelningen
Delta vid viktiga aktiviteter och möten.
Kommunicera iakttagelser, erfarenheter och kunskaper på ett pedagogiskt sätt som bidrar till ett gemensamt lärande
Stötta medarbetare i framtagandet av månads-, tertial- och årsrapporter för att säkerställa att jämställdhet genomsyrar rapporteringen.
Ge stöd vid jämställdhetsanalyser.
Ta fram två analysrapport, en med internt fokus och en med fokus på länet (dvs. externt)
Löpande avstämning med uppdragsgivare Region Norrbotten enligt överenskommelse.
Vid behov av arbetsplats kan leverantören nyttja Region Norrbottens lokaler i Luleå.
Konsulten förväntas jobba 50 till 100 procent under året, enligt ö.k.
Inför uppdragsstart kommer beställare och konsult att upprätta en årsarbetsplan för uppdraget.
Obligatoriska krav:
CV ska kunna styrkas med kursintyg, betyg och bevis på tidigare arbeten, tex skrivna rapporter. Det är viktigt att CV tydligt går att utläsa.
Erfarenhet av minst 2 liknande uppdrag
(kort beskrivning av syfte samt genomförandeplan)
Tillgänglighet under uppdragets genomförande
(möjlig arbetstid samt var arbetet genomförs)
Genomförandebeskrivning:
Möjlig arbetsomfattning för år 1.
Metod och arbetssätt, exempelvis möjlighet och behov av att finnas på plats i Luleå.
Utifrån erfarenhet av att jobba med jämställhetsintegrering som strategi ge förslag på upplägg och genomförande. Visa mindre

Senior Quality Manager

Ansök    Jan 10    Baxter Medical AB    Kvalitetschef
Now we are looking for a Senior Quality Manager in Luleå, Sweden. This is a great opportunity for you with a couple of years within QA wishing to grow into new responsibilities. This is where you as a Senior Quality Manager is the quality leader for Manufacturing Operations, the plant, and support facilities can be part of our important mission to save and sustain lives. This role provides leadership to all functions within the Luleå, Sweden Operation to e... Visa mer
Now we are looking for a Senior Quality Manager in Luleå, Sweden.
This is a great opportunity for you with a couple of years within QA wishing to grow into new responsibilities.
This is where you as a Senior Quality Manager is the quality leader for Manufacturing Operations, the plant, and support facilities can be part of our important mission to save and sustain lives. This role provides leadership to all functions within the Luleå, Sweden Operation to enable the organization to achieve Quality goals as well as aggressive growth objectives.
Essential Duties and Responsibilities
You will work as Quality Management Representative and PRRC (Person Responsible for Regulatory Compliance) for the manufacturing facilities, including hosting third party inspections and audits, and organizing and conducting periodic Management Reviews of the Quality System.
You will provide strategic direction and leadership to all functions and levels of the manufacturing organization to ensure operations adhere to the highest standards of compliance and product quality.
You will direct the implementation of corrective and preventive actions, ensuring timely and robust completion of actions to enterprise targets.
You will ensure product containment of manufacturing non-conformances, to include immediate correction activities as appropriate and determination of systemic corrective and preventive actions.
You will review complaint trending and drive actions to improve customer experience and lower complaints.
You will chair the local Corrective Action Board (CAB) and participate in the Corporate CAB.
You will be responsible for ensuring that the site participate effectively in monthly Product Performance Review meetings.
You will be responsible for product quality, including the transfer of product design to manufacturing facilities within the site.
You will oversee all aspects of supplier quality for the plants, including supplier selection, qualification, and control.
You will identify and mitigate gaps between Quality System requirements and all applicable regulations and corporate requirements.
You will be responsible for the quality of responses to FDA 483 observations, MOH observations, WL and other regulatory compliance correspondence from site and for ensuring completion of all GMP commitments to regulatory authorities (FDA, MOH’s, Notified Body, etc..) at sites.
You will lead, coach and train employees toward team concepts and foster an environment for empowered, high performance environment.

Qualifications
• Bachelor’s degree in a related medical, science or regulatory discipline required, engineering degree nice to have
• Knowledge and understanding of medical device regulations and standards, including but not limited to QSR, CMDR, Medical Device Directive
• ISO Quality System and other applicable industry requirements is required.
• 10+ years in the medical device industry or related GMP environment or equivalent.
• 5+ years of experience leading direct reports.
• Excellent verbal and written communication skills, including attention to detail; strong questioning and listening skills; and the ability to look beyond obvious answers in order to understand the impact on other areas is required.
• Exceptionally strong leadership and influencing skills.
• Must have the ability to make effective presentations to all levels of the organization.
• The proven ability to prioritize and manage multiple projects and meet deadlines is required.
• Must have the ability to work in both a collaborative (team) environment as well as perform independent work as required.
• Experience building a high performing team, managing performance of team members with varying levels of skill and experience, and mentoring high potential individuals to achieve greater impact on the organization.
• Strong appreciation of the impact of regulatory bodies on medical device product lifecycle is required.
• ASQ Certifications for Auditing and/or Quality Management is preferred
What we can offer
• A developing opportunity for you and a chance to work in a diverse and experienced team with a great mix of people. Joining Baxter means joining a team that you can truly learn from!
• Independent position with an opportunity to build your own strategy and make a real impact.
• A chance to further build your professional experience in the area of health care.
• Internal training tailored to business needs and career goals.
• Stability of employment in a recognizable and established company.
• You will gain excellent exposure and fantastic industry knowledge within the territory working for a global organization.
If you like the sound of the above role and if this role resonates with you, then we’d love to talk to you. Apply here as we would love to discuss it in more detail with you. Visa mindre

Quality Manager

Black Box is Hiring! QA Manager The Quality Assurance (QA) Manager plays an important role in Black Box's data center deployment program by monitoring all phases of the project to ensure that all external and internal requirements are met before our product reaches our customer. The goal of this position, is to assure the high quality of our operations and services leading to the long-term success of our business. Some of the key responsibilities includ... Visa mer
Black Box is Hiring! QA Manager

The Quality Assurance (QA) Manager plays an important role in Black Box's data center deployment program by monitoring all phases of the project to ensure that all external and internal requirements are met before our product reaches our customer. The goal of this position, is to assure the high quality of our operations and services leading to the long-term success of our business. Some of the key responsibilities include, developing a Quality Assurance Plan to support the program, executing Quality Control (QC), and the development and reporting of Key Performance Indicators (KPI).The ideal candidate will have an engineering background and enjoy providing end-to-end solutions to Infrastructure quality problems.

. Develop overall quality plan to support the data center rollout, including quality around technical delivery, logistics, inventory controls
. Develop and maintain Noncompliance Register
. Reviews requirements, specifications, and technical design documents to provide timely and meaningful feedback
. Creates detailed, comprehensive, and well-structured installation and test plans.
. Estimates, prioritizes, plans, and coordinates quality control and testing activities.
. Designs, develops, and executes QA scheduled reports (e.g. defects, installation deficiencies, project timelines and project level QA measurements)
. Identifies, records, and documents thoroughly and tracks deficiencies and corrective actions.
. Performs thorough review of all testing documentation.
. Monitors and inspects all operations that affect quality to align with industry and customer standards.
. Facilitates communications with internal and external teams to identify system requirements, failures, and process improvements.
. Monitors corrective action process results.
. Investigates the causes of non-conforming products and trains users to implement QC solutions.
. Tracks quality assurance metrics, such as defects, marginal results, and project specific KPI's.
. Stays up-to-date with new testing tools and test strategies.
. Maintains all testing documentation.
. Trains installers, where necessary, on testing methodologies.
. Assists Project Manager with reporting requirements.
. Develop Quality plans and run books.
. Oversee testing and installations
. Additional duties as assigned
. Proven work experience in Infrastructure deployment.
. Proven work experience in Infrastructure quality assurance.
. Strong knowledge of Project/Construction QA methodologies, tools, and processes.
. Experience in writing clear, concise and comprehensive test plans and test cases.
. Hands-on experience with QC implementation.
. Solid knowledge of testing and installation methodologies.
. Excellent MS Office and database skills.
. Excellent spoken and written communication as well as receptive listening skills.
. Superior collaboration and communication skills: team building, conflict resolution, stakeholder management and decision making.
. An innovator and disruptor in your specialist field

Qualifications:
. Bachelor's Degree preferred, or equivalent work experience.
. Minimum of 5 years of relevant experience.
Additional Ideal Qualifications:
. Experience working in a data center builds highly desirable
. Experience with fiber and copper performance testing highly desirable
. Certifications in QC is a strong advantage.
. RCDD and DCDC preferred
. Strong Knowledge of TIA and NEC Standards.
. Strong knowledge of BICSI and Data center installation standards.

Supervisory Responsibility:
. This position leads technical QA team but has no direct reports

Physical Environment/Working Conditions:

. Construction site environment- exposure to extreme heat or cold, loud noise, uneven ground
About Us:
Black Box is a leading technology solutions provider. Our mission is to accelerate our customers' business by valuing relationships with our team members, clients and stakeholders. By continuously growing our knowledge, we remain relevant in the market and are in a superior position to help customers design, deploy and manage their IT infrastructure. Through our values, such as innovation, ownership, transparency, respect and open-mindedness, we deliver high-value products and services through our global presence and 2,500+ team members in 24 countries and growing. Black Box is a wholly-owned subsidiary of AGC Networks.

Black Box is an equal opportunity employer. Black Box does not discriminate against individuals on the basis of race, color, marital status, sex, sexual orientation, religion, national origin, age, disability, veteran status, genetic information, or any other protected status, and endorses those policies and practices which seek to recruit, hire, train and promote the most qualified persons into available jobs. Visa mindre

Kvalitetsingenjör Team Leader

Ansök    Aug 12    Ponto AB    Kvalitetschef
Vi erbjuder tjänster inom bemanning och rekrytering. Med engagemang och lyhördhet hjälper vi företag och privatpersoner att hitta lösningar för att utvecklas. Kännetecknande för Ponto är vår kunskap om den lokala marknaden. För kunds räkning söker vi en gruppchef till kvalitetsavdelningen. För att lyckats i rollen behöver du i grunden ha en ingenjörsexamen, samt minst fem års erfarenhet av kvalitetsarbete inom tillverkande industri som kvalitetsingenjör... Visa mer
Vi erbjuder tjänster inom bemanning och rekrytering. Med engagemang och lyhördhet hjälper vi företag och privatpersoner att hitta lösningar för att utvecklas. Kännetecknande för Ponto är vår kunskap om den lokala marknaden.

För kunds räkning söker vi en gruppchef till kvalitetsavdelningen. För att lyckats i rollen behöver du i grunden ha en ingenjörsexamen, samt minst fem års erfarenhet av kvalitetsarbete inom tillverkande industri som kvalitetsingenjör eller motsvarande. 
 
Sista ansökningsdag: Tisdag 27 augusti 2019. Urval och intervjuer kommer att ske löpande. Tjänsten kan komma att bli tillsatt innan sista ansökningsdag, ansök därför så snart som möjligt.
 
För information: I denna rekrytering samarbetar vi med Ponto. Notera att du från start blir anställd av det aktuella företaget. Ponto hjälper endast till med rekryteringsprocessen. Vänligen kontakta mig rekryteringskonsult Ulrika Andersson ([email protected], 070-260 91 65) om du har frågor. Jag berättar gärna mer om tjänsten eller själva processen.



Krav:

Körkort:
* B (Personbil) Visa mindre