Kvalitetstekniker - Lediga jobb

Företagspresentation

Till vår kund Siemens Energy, en ledande global aktör inom energibranschen, söker vi nu en Kvalitetsingenjör – Interna Kvalificeringar för ett uppdrag på deras site i Finspång.

Företaget är tack vare högteknologisk och innovativ produktutveckling en etablerad partner inom energisektorn som levererar avancerade samt hållbara lösningar för marknadens nuvarande och framtida behov.

Du får genom det här uppdraget möjlighet att arbeta i en internationell och framåtsträvande miljö där utvecklingsmöjligheterna är många.

Det här är inledningsvis ett konsultuppdrag på 6 månader via Unik Resurs med mycket god möjlighet till förlängning.

Vi tillämpar löpande urval vilket innebär att uppdraget kan komma att tillsättas tidigare än sista ansökningsdatum.

Arbetsuppgifter och ansvarsområden

Som Kvalitetsingenjör ansvarar du för att leda och koordinera interna produkt- och processkvalificeringar (IPPQ) inom tillverkningen. Du driver kvalificeringsarbetet från start till mål och fungerar som en sammanhållande länk mellan flera olika delar av organisationen.

Arbetet sker i nära samarbete med ett tvärfunktionellt team bestående av bland annat konstruktion, produktionsteknik, planering, operatörer och inköpskvalitet.

Dina huvudsakliga arbetsuppgifter innebär bland annat att:

• Leda och koordinera interna produkt- och processkvalificeringar, IPPQ.
• Planera, strukturera och följa upp kvalificeringsaktiviteter från start till godkänt resultat.
• Samordna aktiviteter mellan olika funktioner inom organisationen.
• Säkerställa att kvalificeringar genomförs enligt gällande processer, kvalitetskrav och tidsplaner.
• Identifiera och driva åtgärder vid avvikelser eller risker.
• Bidra till utvecklingen av robusta och kvalitetssäkrade tillverkningsprocesser.
• Vara ett aktivt stöd till produktionen i kvalitetsrelaterade frågor.

Din profil

För att lyckas i rollen ser vi att du har erfarenhet från tillverkande industri och produktion samt är van vid att arbeta i en miljö där flera olika funktioner behöver samordnas.

Vi ser gärna att du har:

• Erfarenhet av kvalificeringar, PPQ, IPPQ eller motsvarande processtyrda projekt.
• Erfarenhet från tillverkande industri.
• Praktisk erfarenhet från produktion, vilket är ett krav för rollen.
• God förståelse för kvalitetssäkring och tillverkningsprocesser.
• Förmåga att leda och driva komplexa aktiviteter utan formellt personalansvar.
• Stark kommunikativ förmåga och lätt för att samarbeta med olika funktioner och kompetenser.
• Förmåga att strukturera, prioritera och följa upp aktiviteter mot uppsatta mål.

Personliga egenskaper

Som person är du driven, strukturerad och kommunikativ. Du trivs i en koordinerande roll där du får ta ansvar och driva arbetet framåt samtidigt som du skapar engagemang hos andra.

Du har lätt för att samarbeta med människor med olika kompetenser och är trygg i att ta initiativ, följa upp aktiviteter och säkerställa att arbetet når hela vägen i mål. Du har ett lösningsorienterat förhållningssätt och trivs nära produktionen där kvalitet, teknik och leverans går hand i hand.

Bli en del av Unik Resurs – Din karriär och utveckling är vår prioritet!

Vi värderar varje individs unika kompetens och engagemang. På Unik Resurs strävar vi efter att inte bara vara din arbetsgivare, utan en partner i din karriärsutveckling. Vi är ett team och genom regelbundna avstämningar jobbar vi tillsammans för att du både ska utvecklas och trivas i din roll som konsult.

Vårt erbjudande:

• Fast månadslön: Hos oss får du ekonomisk stabilitet med en konkurrenskraftig och pålitlig månadslön.
• Trygga anställningsvillkor: Vi följer kollektivavtal och erbjuder förmånliga försäkringar för din trygghet och välbefinnande.
• Personlig och professionell utveckling: Du kommer att ha kontinuerlig kontakt med din Konsultchef, som finns där för att ge både personlig support och professionell coachning.
• Unikt nätverk: Som en del av Unik Resurs är du aldrig ensam. Du blir en del av ett nätverk av professionella, där samarbete och stöd står i centrum.
• Kompetensutveckling genom Unik Academy: Vi investerar i din framtid genom kontinuerlig utbildning och utvecklingsmöjligheter via vår Unik Academy.

Ansök redan idag!

Passar du in på ovanstående profil, tveka inte att ansöka redan idag! Urval sker löpande vilket innebär att tjänsten kan komma att tillsättas innan sista ansökningsdatum.

Glöm inte att motivera så utförligt som möjligt varför just du är lämplig för denna tjänst och att uppdatera dina uppgifter i ditt CV.

Sök tjänsten genom att klicka på ansök och registrera dig i vår databas, detta för att följa riktlinjerna som gäller för GDPR.

För frågor gällande tjänsten eller rekryteringsprocessen vänligen kontakta ansvarigt rekryteringsteam;

Alexandra Linder

alexandra.linder@unikresurs.se

070 727 49 79

Unik Resurs

Välkommen till Unik Resurs!

Din rekryterings- & utvecklingspartner i med- & motgång

Hos oss är du alltid välkommen att kontakta ansvarig rekryterare om du har frågor eller funderingar kring ett annonserat uppdrag.

Om inte detta uppdrag passar dig är du välkommen att kontakta oss så kanske vi kan hitta ditt drömjobb tillsammans. Vi känner regionen och vet var du kan göra bäst nytta med din profil.

Lycka till!

#LI-Hybrid

Nanexa is now recruiting a Quality Assurance (QA) Manager. The position is full-time and based at our headquarters in Uppsala, and we are looking for a new colleague to join our growing organisation.

As a QA Manager at Nanexa, you will play a key role in building and shaping the quality function in a growing pharmaceutical company. This is not a traditional QA role in a large organisation – instead, you will be part of a small, highly skilled team where your contributions will have a direct and visible impact on how we work and grow. You will have the opportunity to develop, implement and continuously improve our Quality Management System while being actively involved in the full product lifecycle – from early development to manufacturing of clinical trial material. The role combines strategic responsibility with hands-on work and close collaboration across functions.

At Nanexa, you will not work in a silo. You will be involved across the organisation, working closely with colleagues in development, production and analytics, gaining a broad understanding of our technology, products and processes. As a company of approximately 15 employees, we offer an environment where each individual plays an important role, and where you will actively contribute to building something new.

The QA Manager will have a central role in the oversight of manufacturing and analytical activities from a quality perspective, covering the entire chain from development to clinical supply. You will report directly to the Head of Quality Assurance and be an important contributor to the continued development of the QA function and the company as a whole.

Your responsibilities will include:

- Develop, implement and continuously improve the Quality Management System in line with company growth and regulatory requirements

- Assess and approve batch-related documentation such as specifications, batch records, deviations and change requests

- Ensure that production and testing of clinical trial materials are conducted in accordance with applicable GMP requirements

- Review and approve SOPs, manage periodic reviews and support supplier qualification and re-evaluation

- Lead and participate in internal audits and audits of external service providers

- Represent QA in cross-functional project teams and contribute to project execution

- Provide guidance and support to the organisation in quality-related matters

- Perform internal training within GMP and quality systems

- Contribute to the strategic development of the QA function and quality processes

We are looking for a driven and quality-minded professional who enjoys working in a dynamic and developing environment.

Key qualifications include:

- MSc in Pharmacy, Biology, Chemistry, Engineering, or a related field

- Several years of experience within QA in a GMP-regulated pharmaceutical or biotech environment

- Experience in development and/or validation of manufacturing or analytical processes

- Experience in authoring and reviewing GxP-critical documentation, including SOPs, deviations, CAPAs and change controls

- Strong knowledge of Quality Systems and applicable GMP regulations

- Fluency in Swedish and English

As a person, you are proactive, structured and solution-oriented, with a strong sense of ownership and accountability. You thrive in a dynamic organisation where processes are still being developed, and where you have the opportunity to make a real impact. You are comfortable taking on multiple responsibilities and enjoy working both independently and in close collaboration with others.

At Nanexa, each employee contributes to the overall success of the company and you will have the opportunity to influence not only your own area of responsibility, but also the development of the company as a whole.

Nanexa is a Swedish pharmaceutical company developing long-acting injectable drugs based on our proprietary PharmaShell® technology. We operate at the intersection of material science and drug development, taking projects from early idea through development to proof-of-concept in clinical trials. In addition to our own pipeline, we collaborate with leading pharmaceutical companies to develop new products based on our technology. To learn more about Nanexa, please visit www.nanexa.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Job Scope

High level purpose of function.

A Quality Technician leads product and process quality compliance in production line. This role is responsible for confirming key quality attributes of intermediate products and processes as well as identifying and responding to non-conformity issues in production. In addition, this role is responsible for analysing test material, incoming parts, product intermediates and finalized products for Production using a range of instruments. This role will work closely with production staff and Quality Engineers. A Quality Technician is responsible for ensuring that production processes and products meet internal and customers’ quality specifications as well as defining problems, recommending solutions and follows-up on improvements.

Key Responsibilities

Overall areas of responsibilities and activities . Key responsibilities include (but are not limited to)  :

• Lead day-to-day quality assurance activities in production ensuring that production/product quality specifications are met.
• Ensure control checks are completed according to control plan in defined time.
• Ensure robust start of production and coordinated quality handover between shifts.
• Ensure 5S in control and measurement areas and participate in improving 5S methodology and actions together with production team.
• Ensure documentation and record of product and process quality data and utilize these to improve processes.
• Potential to operate various measurement equipment such as a Karl Fischer, measurement by ruler or micrometre, microscopes, perform testing with measuring instruments, perform basic data analysis, interpret data and report data/results as instructed.  
• Interpret data and report data/results on yearly, monthly, and daily basis.
• Understand and execute the testing plans for material, incoming parts, product intermediates and finalized products.  
• Help identify problems with test material, analysis methods, and instrumentation.  
• Organize test results in the expected template and/or LIMS system and maintain control charts.  
• Be able to troubleshoot instrument on basic and advance problems and utilizing the help of suppliers or experts for more major issues.  
• Act on deviations and ensure coordination with customer processes.
• Ensure imminent containment activities and decision making in case of non-conformities and quality issues.
• Mentor less experienced personnel on practical aspects of the analysis methods such as sample preparation and running instruments.  
• Maintain the instruments to a high standard.  
• Ensure conformity of cleanliness requirements in process.
• Conduct Layered Product audit according to schedule.
• Contribute to improvement actions in area of responsibility.
• Complete supplementary tasks as seen fit by management to effectively utilize time and resource for the benefit of the business.

Accountability/Authorization

• Budget responsibility: No
• Direct reports: No
• Work environment responsibility: No

All employees are accountable for complying with safety regulations and actively supporting a safe workplace.

Requirements

Educational background and previous experience required for the role

Qualifications and Experience

• Professional education (ideally in industry) is a plus.
• 2 years experience in manufacturing and 2 years experience in quality.
• Bachelor´s degree in a technical field is preferred but not required.
• Previous experience of quality control from automotive industry is preferred.  
• Familiar with Lean and Six Sigma concepts. 
• Familiar with SPC, FMEA, Quality troubleshooting tools and problem-solving methodology.

Specific skills & Knowledge

• Specific knowledge of quality management systems, e.g. ISO 9001, IATF16949, TQM is preferred.  
• Excellent English skills, both written and oral, are essential. Basic Swedish and other language skills are a plus. You should have good communication skills and be able to work in close collaboration with colleagues from many different teams.
• High work ethic, critical thinking, and strong problem-solving skills are a must.
• This role requires the ability to stand for extended periods and perform work in controlled environments, including clean-rooms and dry-rooms, while wearing appropriate PPE. The role also requires working shifts and working in multiple process areas, according to business needs.

Lyten Sweden is seeking experienced supplier quality engineer. In this role you will be responsible for leading supplier quality activities across Lyten’s global supply base—covering cathode active materials (CAM), graphite, copper foil, separator, electrolyte, and mechanical parts—to qualify, develop, and sustain a world-class supplier panel. Working within Lyten’s Supplier Onboarding Management (SOM) and Nonconformity Management (NCM) framework, the role spans the full lifecycle from Potential Supplier Assessment through Safe Launch exit and into ongoing performance management. Based at Lyten’s office in Västerås with frequent travel to the mass-production plant in Skellefteå and to global supplier sites. Reporting to the Senior Manager, Supplier Quality.

Key Responsibilities

• Lead supplier onboarding from nomination through Safe Launch exit: Potential Supplier Assessment (PSA), APQP gate reviews (G0–G5), PPAP/SPAR evaluation, and Run@Rate capacity verification

• Conduct VDA 6.3 process audits and IATF 16949 / ISO 9001 quality system audits at global supplier sites; manage all findings through to documented, verified closure

• Own the nonconformity lifecycle: classify incoming nonconformities (CC, SC, Standard), coordinate 24-hour IQC containment, drive 8D problem-solving, evaluate supplier 8D quality, and apply Controlled Shipping Levels (CSL1/CSL2/CSL3) where warranted

• Monitor and report supplier KPIs (PPM, Cpk/Ppk, OTD, audit score) through structured scorecards and periodic business reviews; escalate negative trends and initiate Supplier Improvement Plans (SIP) where required

• Review and approve supplier PPAP packages (PSW, PFMEA, Control Plans, MSA, capability studies) to Lyten’s acceptance criteria; issue Part Submission Warrants and maintain PPAP status through the SOM tracker

• Track Cost of Poor Quality (COPQ) in the NCR system and coordinate chargeback recovery with Purchasing

• Translate customer-specific requirements (CSRs) and Critical/Significant Characteristics (CC/SC) into supplier quality agreements and IQC acceptance criteria

• Assess and process supplier change requests and deviation requests (CR/DR; evaluate quality risk before any approval is granted
• Serve as the primary technical liaison between Lyten Production Quality, Procurement, and R&D for all supplier-facing quality topics

• Author and continuously improve SQE processes, work instructions, and templates

• Represent Lyten Quality in supplier technical reviews, cross-functional launch meetings, and external audit contexts as required

• Perform other tasks as assigned by the Senior Manager Supplier Quality

Requirements

Educational background and previous experience required for the role

• BSc or MSc degree in Chemistry, Materials Science, Chemical Engineering, Physics, or a related engineering discipline

Qualifications and Experience

• ISO 9001 Lead Auditor certification with a minimum of 5 years’ post-certification supplier auditing experience (mandatory)

• Minimum 5 years’ hands-on Supplier Quality Engineering experience in battery cell, automotive, aerospace, or related precision manufacturing industries

• Proficiency in AIAG core quality tools: APQP, PPAP, FMEA (AIAG-VDA), MSA, SPC, and 8D structured problem-solving

• VDA 6.3 Process Auditor (P2/P3) certification or equivalent process audit experience at battery or automotive suppliers; VDA 6.3 certification is a strong advantage

• Working knowledge of IATF 16949 requirements; IATF 16949 Lead Auditor certification is a plus

• Solid command of statistical quality methods: process capability (Cpk/Ppk), SPC control charts, and measurement system analysis (MSA/GR&R)

• Proven track record managing multiple concurrent supplier qualification programmes from nomination through Safe Launch exit and into volume production

Specific skills & Knowledge

• Excellent English written and oral communication skills

• Strong analytical mindset: able to distil supplier quality data into concise management reporting and actionable corrective-action direction

• Confident, methodical auditor: experienced at structured interviewing, objective finding documentation, and driving findings to verified closure

• Commercially aware: understands Cost of Poor Quality (COPQ) implications and drives systematic value recovery through the NCM process

• Highly organized; able to priorities effectively across a global, multi-commodity supplier base under competing deadlines without losing rigor

• Proactive and self-directed; comfortable working in a scale-up environment where processes are still being defined and refined

• Effective cross-cultural communicator; builds trust and drives action across diverse supplier organizations, internal functions, and seniority levels

• Prepared for frequent international travel, including to supplier sites in Europe and Asia and regular visits to Lyten’s production plant in Skellefteå

Lyten Sweden is seeking experienced supplier quality engineer. In this role you will be responsible for leading supplier quality activities across Lyten’s global supply base—covering cathode active materials (CAM), graphite, copper foil, separator, electrolyte, and mechanical parts—to qualify, develop, and sustain a world-class supplier panel. Working within Lyten’s Supplier Onboarding Management (SOM) and Nonconformity Management (NCM) framework, the role spans the full lifecycle from Potential Supplier Assessment through Safe Launch exit and into ongoing performance management. Based at Lyten’s office in Västerås with frequent travel to the mass-production plant in Skellefteå and to global supplier sites. Reporting to the Senior Manager, Supplier Quality.

Key Responsibilities

• Lead supplier onboarding from nomination through Safe Launch exit: Potential Supplier Assessment (PSA), APQP gate reviews (G0–G5), PPAP/SPAR evaluation, and Run@Rate capacity verification

• Conduct VDA 6.3 process audits and IATF 16949 / ISO 9001 quality system audits at global supplier sites; manage all findings through to documented, verified closure

• Own the nonconformity lifecycle: classify incoming nonconformities (CC, SC, Standard), coordinate 24-hour IQC containment, drive 8D problem-solving, evaluate supplier 8D quality, and apply Controlled Shipping Levels (CSL1/CSL2/CSL3) where warranted

• Monitor and report supplier KPIs (PPM, Cpk/Ppk, OTD, audit score) through structured scorecards and periodic business reviews; escalate negative trends and initiate Supplier Improvement Plans (SIP) where required

• Review and approve supplier PPAP packages (PSW, PFMEA, Control Plans, MSA, capability studies) to Lyten’s acceptance criteria; issue Part Submission Warrants and maintain PPAP status through the SOM tracker

• Track Cost of Poor Quality (COPQ) in the NCR system and coordinate chargeback recovery with Purchasing

• Translate customer-specific requirements (CSRs) and Critical/Significant Characteristics (CC/SC) into supplier quality agreements and IQC acceptance criteria

• Assess and process supplier change requests and deviation requests (CR/DR; evaluate quality risk before any approval is granted
• Serve as the primary technical liaison between Lyten Production Quality, Procurement, and R&D for all supplier-facing quality topics

• Author and continuously improve SQE processes, work instructions, and templates

• Represent Lyten Quality in supplier technical reviews, cross-functional launch meetings, and external audit contexts as required

• Perform other tasks as assigned by the Senior Manager Supplier Quality

Requirements

Educational background and previous experience required for the role

• BSc or MSc degree in Chemistry, Materials Science, Chemical Engineering, Physics, or a related engineering discipline

Qualifications and Experience

• ISO 9001 Lead Auditor certification with a minimum of 5 years’ post-certification supplier auditing experience (mandatory)

• Minimum 5 years’ hands-on Supplier Quality Engineering experience in battery cell, automotive, aerospace, or related precision manufacturing industries

• Proficiency in AIAG core quality tools: APQP, PPAP, FMEA (AIAG-VDA), MSA, SPC, and 8D structured problem-solving

• VDA 6.3 Process Auditor (P2/P3) certification or equivalent process audit experience at battery or automotive suppliers; VDA 6.3 certification is a strong advantage

• Working knowledge of IATF 16949 requirements; IATF 16949 Lead Auditor certification is a plus

• Solid command of statistical quality methods: process capability (Cpk/Ppk), SPC control charts, and measurement system analysis (MSA/GR&R)

• Proven track record managing multiple concurrent supplier qualification programmes from nomination through Safe Launch exit and into volume production

Specific skills & Knowledge

• Excellent English written and oral communication skills

• Strong analytical mindset: able to distil supplier quality data into concise management reporting and actionable corrective-action direction

• Confident, methodical auditor: experienced at structured interviewing, objective finding documentation, and driving findings to verified closure

• Commercially aware: understands Cost of Poor Quality (COPQ) implications and drives systematic value recovery through the NCM process

• Highly organized; able to priorities effectively across a global, multi-commodity supplier base under competing deadlines without losing rigor

• Proactive and self-directed; comfortable working in a scale-up environment where processes are still being defined and refined

• Effective cross-cultural communicator; builds trust and drives action across diverse supplier organizations, internal functions, and seniority levels

• Prepared for frequent international travel, including to supplier sites in Europe and Asia and regular visits to Lyten’s production plant in Skellefteå

Lyten Sweden is seeking experienced supplier quality engineer. In this role you will be responsible for leading supplier quality activities across Lyten’s global supply base—covering cathode active materials (CAM), graphite, copper foil, separator, electrolyte, and mechanical parts—to qualify, develop, and sustain a world-class supplier panel. Working within Lyten’s Supplier Onboarding Management (SOM) and Nonconformity Management (NCM) framework, the role spans the full lifecycle from Potential Supplier Assessment through Safe Launch exit and into ongoing performance management. Based at Lyten’s office in Västerås with frequent travel to the mass-production plant in Skellefteå and to global supplier sites. Reporting to the Senior Manager, Supplier Quality.

Key Responsibilities

• Lead supplier onboarding from nomination through Safe Launch exit: Potential Supplier Assessment (PSA), APQP gate reviews (G0–G5), PPAP/SPAR evaluation, and Run@Rate capacity verification

• Conduct VDA 6.3 process audits and IATF 16949 / ISO 9001 quality system audits at global supplier sites; manage all findings through to documented, verified closure

• Own the nonconformity lifecycle: classify incoming nonconformities (CC, SC, Standard), coordinate 24-hour IQC containment, drive 8D problem-solving, evaluate supplier 8D quality, and apply Controlled Shipping Levels (CSL1/CSL2/CSL3) where warranted

• Monitor and report supplier KPIs (PPM, Cpk/Ppk, OTD, audit score) through structured scorecards and periodic business reviews; escalate negative trends and initiate Supplier Improvement Plans (SIP) where required

• Review and approve supplier PPAP packages (PSW, PFMEA, Control Plans, MSA, capability studies) to Lyten’s acceptance criteria; issue Part Submission Warrants and maintain PPAP status through the SOM tracker

• Track Cost of Poor Quality (COPQ) in the NCR system and coordinate chargeback recovery with Purchasing

• Translate customer-specific requirements (CSRs) and Critical/Significant Characteristics (CC/SC) into supplier quality agreements and IQC acceptance criteria

• Assess and process supplier change requests and deviation requests (CR/DR; evaluate quality risk before any approval is granted
• Serve as the primary technical liaison between Lyten Production Quality, Procurement, and R&D for all supplier-facing quality topics

• Author and continuously improve SQE processes, work instructions, and templates

• Represent Lyten Quality in supplier technical reviews, cross-functional launch meetings, and external audit contexts as required

• Perform other tasks as assigned by the Senior Manager Supplier Quality

Requirements

Educational background and previous experience required for the role

• BSc or MSc degree in Chemistry, Materials Science, Chemical Engineering, Physics, or a related engineering discipline

Qualifications and Experience

• ISO 9001 Lead Auditor certification with a minimum of 5 years’ post-certification supplier auditing experience (mandatory)

• Minimum 5 years’ hands-on Supplier Quality Engineering experience in battery cell, automotive, aerospace, or related precision manufacturing industries

• Proficiency in AIAG core quality tools: APQP, PPAP, FMEA (AIAG-VDA), MSA, SPC, and 8D structured problem-solving

• VDA 6.3 Process Auditor (P2/P3) certification or equivalent process audit experience at battery or automotive suppliers; VDA 6.3 certification is a strong advantage

• Working knowledge of IATF 16949 requirements; IATF 16949 Lead Auditor certification is a plus

• Solid command of statistical quality methods: process capability (Cpk/Ppk), SPC control charts, and measurement system analysis (MSA/GR&R)

• Proven track record managing multiple concurrent supplier qualification programmes from nomination through Safe Launch exit and into volume production

Specific skills & Knowledge

• Excellent English written and oral communication skills

• Strong analytical mindset: able to distil supplier quality data into concise management reporting and actionable corrective-action direction

• Confident, methodical auditor: experienced at structured interviewing, objective finding documentation, and driving findings to verified closure

• Commercially aware: understands Cost of Poor Quality (COPQ) implications and drives systematic value recovery through the NCM process

• Highly organized; able to priorities effectively across a global, multi-commodity supplier base under competing deadlines without losing rigor

• Proactive and self-directed; comfortable working in a scale-up environment where processes are still being defined and refined

• Effective cross-cultural communicator; builds trust and drives action across diverse supplier organizations, internal functions, and seniority levels

• Prepared for frequent international travel, including to supplier sites in Europe and Asia and regular visits to Lyten’s production plant in Skellefteå

Lyten Sweden is seeking experienced supplier quality engineer. In this role you will be responsible for leading supplier quality activities across Lyten’s global supply base—covering cathode active materials (CAM), graphite, copper foil, separator, electrolyte, and mechanical parts—to qualify, develop, and sustain a world-class supplier panel. Working within Lyten’s Supplier Onboarding Management (SOM) and Nonconformity Management (NCM) framework, the role spans the full lifecycle from Potential Supplier Assessment through Safe Launch exit and into ongoing performance management. Based at Lyten’s office in Västerås with frequent travel to the mass-production plant in Skellefteå and to global supplier sites. Reporting to the Senior Manager, Supplier Quality.

Key Responsibilities

• Lead supplier onboarding from nomination through Safe Launch exit: Potential Supplier Assessment (PSA), APQP gate reviews (G0–G5), PPAP/SPAR evaluation, and Run@Rate capacity verification

• Conduct VDA 6.3 process audits and IATF 16949 / ISO 9001 quality system audits at global supplier sites; manage all findings through to documented, verified closure

• Own the nonconformity lifecycle: classify incoming nonconformities (CC, SC, Standard), coordinate 24-hour IQC containment, drive 8D problem-solving, evaluate supplier 8D quality, and apply Controlled Shipping Levels (CSL1/CSL2/CSL3) where warranted

• Monitor and report supplier KPIs (PPM, Cpk/Ppk, OTD, audit score) through structured scorecards and periodic business reviews; escalate negative trends and initiate Supplier Improvement Plans (SIP) where required

• Review and approve supplier PPAP packages (PSW, PFMEA, Control Plans, MSA, capability studies) to Lyten’s acceptance criteria; issue Part Submission Warrants and maintain PPAP status through the SOM tracker

• Track Cost of Poor Quality (COPQ) in the NCR system and coordinate chargeback recovery with Purchasing

• Translate customer-specific requirements (CSRs) and Critical/Significant Characteristics (CC/SC) into supplier quality agreements and IQC acceptance criteria

• Assess and process supplier change requests and deviation requests (CR/DR; evaluate quality risk before any approval is granted
• Serve as the primary technical liaison between Lyten Production Quality, Procurement, and R&D for all supplier-facing quality topics

• Author and continuously improve SQE processes, work instructions, and templates

• Represent Lyten Quality in supplier technical reviews, cross-functional launch meetings, and external audit contexts as required

• Perform other tasks as assigned by the Senior Manager Supplier Quality

Requirements

Educational background and previous experience required for the role

• BSc or MSc degree in Chemistry, Materials Science, Chemical Engineering, Physics, or a related engineering discipline

Qualifications and Experience

• ISO 9001 Lead Auditor certification with a minimum of 5 years’ post-certification supplier auditing experience (mandatory)

• Minimum 5 years’ hands-on Supplier Quality Engineering experience in battery cell, automotive, aerospace, or related precision manufacturing industries

• Proficiency in AIAG core quality tools: APQP, PPAP, FMEA (AIAG-VDA), MSA, SPC, and 8D structured problem-solving

• VDA 6.3 Process Auditor (P2/P3) certification or equivalent process audit experience at battery or automotive suppliers; VDA 6.3 certification is a strong advantage

• Working knowledge of IATF 16949 requirements; IATF 16949 Lead Auditor certification is a plus

• Solid command of statistical quality methods: process capability (Cpk/Ppk), SPC control charts, and measurement system analysis (MSA/GR&R)

• Proven track record managing multiple concurrent supplier qualification programmes from nomination through Safe Launch exit and into volume production

Specific skills & Knowledge

• Excellent English written and oral communication skills

• Strong analytical mindset: able to distil supplier quality data into concise management reporting and actionable corrective-action direction

• Confident, methodical auditor: experienced at structured interviewing, objective finding documentation, and driving findings to verified closure

• Commercially aware: understands Cost of Poor Quality (COPQ) implications and drives systematic value recovery through the NCM process

• Highly organized; able to priorities effectively across a global, multi-commodity supplier base under competing deadlines without losing rigor

• Proactive and self-directed; comfortable working in a scale-up environment where processes are still being defined and refined

• Effective cross-cultural communicator; builds trust and drives action across diverse supplier organizations, internal functions, and seniority levels

• Prepared for frequent international travel, including to supplier sites in Europe and Asia and regular visits to Lyten’s production plant in Skellefteå

Lyten Sweden is seeking experienced supplier quality engineer. In this role you will be responsible for leading supplier quality activities across Lyten’s global supply base—covering cathode active materials (CAM), graphite, copper foil, separator, electrolyte, and mechanical parts—to qualify, develop, and sustain a world-class supplier panel. Working within Lyten’s Supplier Onboarding Management (SOM) and Nonconformity Management (NCM) framework, the role spans the full lifecycle from Potential Supplier Assessment through Safe Launch exit and into ongoing performance management. Based at Lyten’s office in Västerås with frequent travel to the mass-production plant in Skellefteå and to global supplier sites. Reporting to the Senior Manager, Supplier Quality.

Key Responsibilities

• Lead supplier onboarding from nomination through Safe Launch exit: Potential Supplier Assessment (PSA), APQP gate reviews (G0–G5), PPAP/SPAR evaluation, and Run@Rate capacity verification

• Conduct VDA 6.3 process audits and IATF 16949 / ISO 9001 quality system audits at global supplier sites; manage all findings through to documented, verified closure

• Own the nonconformity lifecycle: classify incoming nonconformities (CC, SC, Standard), coordinate 24-hour IQC containment, drive 8D problem-solving, evaluate supplier 8D quality, and apply Controlled Shipping Levels (CSL1/CSL2/CSL3) where warranted

• Monitor and report supplier KPIs (PPM, Cpk/Ppk, OTD, audit score) through structured scorecards and periodic business reviews; escalate negative trends and initiate Supplier Improvement Plans (SIP) where required

• Review and approve supplier PPAP packages (PSW, PFMEA, Control Plans, MSA, capability studies) to Lyten’s acceptance criteria; issue Part Submission Warrants and maintain PPAP status through the SOM tracker

• Track Cost of Poor Quality (COPQ) in the NCR system and coordinate chargeback recovery with Purchasing

• Translate customer-specific requirements (CSRs) and Critical/Significant Characteristics (CC/SC) into supplier quality agreements and IQC acceptance criteria

• Assess and process supplier change requests and deviation requests (CR/DR; evaluate quality risk before any approval is granted
• Serve as the primary technical liaison between Lyten Production Quality, Procurement, and R&D for all supplier-facing quality topics

• Author and continuously improve SQE processes, work instructions, and templates

• Represent Lyten Quality in supplier technical reviews, cross-functional launch meetings, and external audit contexts as required

• Perform other tasks as assigned by the Senior Manager Supplier Quality

Requirements

Educational background and previous experience required for the role

• BSc or MSc degree in Chemistry, Materials Science, Chemical Engineering, Physics, or a related engineering discipline

Qualifications and Experience

• ISO 9001 Lead Auditor certification with a minimum of 5 years’ post-certification supplier auditing experience (mandatory)

• Minimum 5 years’ hands-on Supplier Quality Engineering experience in battery cell, automotive, aerospace, or related precision manufacturing industries

• Proficiency in AIAG core quality tools: APQP, PPAP, FMEA (AIAG-VDA), MSA, SPC, and 8D structured problem-solving

• VDA 6.3 Process Auditor (P2/P3) certification or equivalent process audit experience at battery or automotive suppliers; VDA 6.3 certification is a strong advantage

• Working knowledge of IATF 16949 requirements; IATF 16949 Lead Auditor certification is a plus

• Solid command of statistical quality methods: process capability (Cpk/Ppk), SPC control charts, and measurement system analysis (MSA/GR&R)

• Proven track record managing multiple concurrent supplier qualification programmes from nomination through Safe Launch exit and into volume production

Specific skills & Knowledge

• Excellent English written and oral communication skills

• Strong analytical mindset: able to distil supplier quality data into concise management reporting and actionable corrective-action direction

• Confident, methodical auditor: experienced at structured interviewing, objective finding documentation, and driving findings to verified closure

• Commercially aware: understands Cost of Poor Quality (COPQ) implications and drives systematic value recovery through the NCM process

• Highly organized; able to priorities effectively across a global, multi-commodity supplier base under competing deadlines without losing rigor

• Proactive and self-directed; comfortable working in a scale-up environment where processes are still being defined and refined

• Effective cross-cultural communicator; builds trust and drives action across diverse supplier organizations, internal functions, and seniority levels

• Prepared for frequent international travel, including to supplier sites in Europe and Asia and regular visits to Lyten’s production plant in Skellefteå

Lyten Sweden is seeking experienced supplier quality engineer. In this role you will be responsible for leading supplier quality activities across Lyten’s global supply base—covering cathode active materials (CAM), graphite, copper foil, separator, electrolyte, and mechanical parts—to qualify, develop, and sustain a world-class supplier panel. Working within Lyten’s Supplier Onboarding Management (SOM) and Nonconformity Management (NCM) framework, the role spans the full lifecycle from Potential Supplier Assessment through Safe Launch exit and into ongoing performance management. Based at Lyten’s office in Västerås with frequent travel to the mass-production plant in Skellefteå and to global supplier sites. Reporting to the Senior Manager, Supplier Quality.

Key Responsibilities

• Lead supplier onboarding from nomination through Safe Launch exit: Potential Supplier Assessment (PSA), APQP gate reviews (G0–G5), PPAP/SPAR evaluation, and Run@Rate capacity verification

• Conduct VDA 6.3 process audits and IATF 16949 / ISO 9001 quality system audits at global supplier sites; manage all findings through to documented, verified closure

• Own the nonconformity lifecycle: classify incoming nonconformities (CC, SC, Standard), coordinate 24-hour IQC containment, drive 8D problem-solving, evaluate supplier 8D quality, and apply Controlled Shipping Levels (CSL1/CSL2/CSL3) where warranted

• Monitor and report supplier KPIs (PPM, Cpk/Ppk, OTD, audit score) through structured scorecards and periodic business reviews; escalate negative trends and initiate Supplier Improvement Plans (SIP) where required

• Review and approve supplier PPAP packages (PSW, PFMEA, Control Plans, MSA, capability studies) to Lyten’s acceptance criteria; issue Part Submission Warrants and maintain PPAP status through the SOM tracker

• Track Cost of Poor Quality (COPQ) in the NCR system and coordinate chargeback recovery with Purchasing

• Translate customer-specific requirements (CSRs) and Critical/Significant Characteristics (CC/SC) into supplier quality agreements and IQC acceptance criteria

• Assess and process supplier change requests and deviation requests (CR/DR; evaluate quality risk before any approval is granted
• Serve as the primary technical liaison between Lyten Production Quality, Procurement, and R&D for all supplier-facing quality topics

• Author and continuously improve SQE processes, work instructions, and templates

• Represent Lyten Quality in supplier technical reviews, cross-functional launch meetings, and external audit contexts as required

• Perform other tasks as assigned by the Senior Manager Supplier Quality

Requirements

Educational background and previous experience required for the role

• BSc or MSc degree in Chemistry, Materials Science, Chemical Engineering, Physics, or a related engineering discipline

Qualifications and Experience

• ISO 9001 Lead Auditor certification with a minimum of 5 years’ post-certification supplier auditing experience (mandatory)

• Minimum 5 years’ hands-on Supplier Quality Engineering experience in battery cell, automotive, aerospace, or related precision manufacturing industries

• Proficiency in AIAG core quality tools: APQP, PPAP, FMEA (AIAG-VDA), MSA, SPC, and 8D structured problem-solving

• VDA 6.3 Process Auditor (P2/P3) certification or equivalent process audit experience at battery or automotive suppliers; VDA 6.3 certification is a strong advantage

• Working knowledge of IATF 16949 requirements; IATF 16949 Lead Auditor certification is a plus

• Solid command of statistical quality methods: process capability (Cpk/Ppk), SPC control charts, and measurement system analysis (MSA/GR&R)

• Proven track record managing multiple concurrent supplier qualification programmes from nomination through Safe Launch exit and into volume production

Specific skills & Knowledge

• Excellent English written and oral communication skills

• Strong analytical mindset: able to distil supplier quality data into concise management reporting and actionable corrective-action direction

• Confident, methodical auditor: experienced at structured interviewing, objective finding documentation, and driving findings to verified closure

• Commercially aware: understands Cost of Poor Quality (COPQ) implications and drives systematic value recovery through the NCM process

• Highly organized; able to priorities effectively across a global, multi-commodity supplier base under competing deadlines without losing rigor

• Proactive and self-directed; comfortable working in a scale-up environment where processes are still being defined and refined

• Effective cross-cultural communicator; builds trust and drives action across diverse supplier organizations, internal functions, and seniority levels

• Prepared for frequent international travel, including to supplier sites in Europe and Asia and regular visits to Lyten’s production plant in Skellefteå

Lyten Sweden is seeking experienced supplier quality engineer. In this role you will be responsible for leading supplier quality activities across Lyten’s global supply base—covering cathode active materials (CAM), graphite, copper foil, separator, electrolyte, and mechanical parts—to qualify, develop, and sustain a world-class supplier panel. Working within Lyten’s Supplier Onboarding Management (SOM) and Nonconformity Management (NCM) framework, the role spans the full lifecycle from Potential Supplier Assessment through Safe Launch exit and into ongoing performance management. Based at Lyten’s office in Västerås with frequent travel to the mass-production plant in Skellefteå and to global supplier sites. Reporting to the Senior Manager, Supplier Quality.

Key Responsibilities

• Lead supplier onboarding from nomination through Safe Launch exit: Potential Supplier Assessment (PSA), APQP gate reviews (G0–G5), PPAP/SPAR evaluation, and Run@Rate capacity verification

• Conduct VDA 6.3 process audits and IATF 16949 / ISO 9001 quality system audits at global supplier sites; manage all findings through to documented, verified closure

• Own the nonconformity lifecycle: classify incoming nonconformities (CC, SC, Standard), coordinate 24-hour IQC containment, drive 8D problem-solving, evaluate supplier 8D quality, and apply Controlled Shipping Levels (CSL1/CSL2/CSL3) where warranted

• Monitor and report supplier KPIs (PPM, Cpk/Ppk, OTD, audit score) through structured scorecards and periodic business reviews; escalate negative trends and initiate Supplier Improvement Plans (SIP) where required

• Review and approve supplier PPAP packages (PSW, PFMEA, Control Plans, MSA, capability studies) to Lyten’s acceptance criteria; issue Part Submission Warrants and maintain PPAP status through the SOM tracker

• Track Cost of Poor Quality (COPQ) in the NCR system and coordinate chargeback recovery with Purchasing

• Translate customer-specific requirements (CSRs) and Critical/Significant Characteristics (CC/SC) into supplier quality agreements and IQC acceptance criteria

• Assess and process supplier change requests and deviation requests (CR/DR; evaluate quality risk before any approval is granted
• Serve as the primary technical liaison between Lyten Production Quality, Procurement, and R&D for all supplier-facing quality topics

• Author and continuously improve SQE processes, work instructions, and templates

• Represent Lyten Quality in supplier technical reviews, cross-functional launch meetings, and external audit contexts as required

• Perform other tasks as assigned by the Senior Manager Supplier Quality

Requirements

Educational background and previous experience required for the role

• BSc or MSc degree in Chemistry, Materials Science, Chemical Engineering, Physics, or a related engineering discipline

Qualifications and Experience

• ISO 9001 Lead Auditor certification with a minimum of 5 years’ post-certification supplier auditing experience (mandatory)

• Minimum 5 years’ hands-on Supplier Quality Engineering experience in battery cell, automotive, aerospace, or related precision manufacturing industries

• Proficiency in AIAG core quality tools: APQP, PPAP, FMEA (AIAG-VDA), MSA, SPC, and 8D structured problem-solving

• VDA 6.3 Process Auditor (P2/P3) certification or equivalent process audit experience at battery or automotive suppliers; VDA 6.3 certification is a strong advantage

• Working knowledge of IATF 16949 requirements; IATF 16949 Lead Auditor certification is a plus

• Solid command of statistical quality methods: process capability (Cpk/Ppk), SPC control charts, and measurement system analysis (MSA/GR&R)

• Proven track record managing multiple concurrent supplier qualification programmes from nomination through Safe Launch exit and into volume production

Specific skills & Knowledge

• Excellent English written and oral communication skills

• Strong analytical mindset: able to distil supplier quality data into concise management reporting and actionable corrective-action direction

• Confident, methodical auditor: experienced at structured interviewing, objective finding documentation, and driving findings to verified closure

• Commercially aware: understands Cost of Poor Quality (COPQ) implications and drives systematic value recovery through the NCM process

• Highly organized; able to priorities effectively across a global, multi-commodity supplier base under competing deadlines without losing rigor

• Proactive and self-directed; comfortable working in a scale-up environment where processes are still being defined and refined

• Effective cross-cultural communicator; builds trust and drives action across diverse supplier organizations, internal functions, and seniority levels

• Prepared for frequent international travel, including to supplier sites in Europe and Asia and regular visits to Lyten’s production plant in Skellefteå