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Kenvue is currently recruiting for a: Supplier Quality Lead

What we do

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who We Are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to:

EMEA Supplier Quality Lead

Location: Europe/Middle East/Africa, Sweden, Skane, Helsingborg

Work Location: Fully Onsite

Role reports to: EMEA Supplier Quality Lead

Location: Helsingborg, Sweden

Travel %: up to 30%

What you will do

You will be responsible and accountable for the successful deployment, and implementation of the Supplier Quality Management (SQM) strategy and associated Kenvue quality standards, procedures, programs and initiatives that deliver quality/compliance, and value to Kenvue supply chain. Based on the Helsingborg site, you will actively partner with stakeholders, individuals and teams, and Direct Material (DM) suppliers to implement innovative solutions and continuous improvements with demonstrated and measurable business impact.

Key Responsibilities

• Own quality lifecycle management for Direct Material (DM) suppliers.
• Act as interface for the quality topics between the DM supplier and Kenvue.
• Ensure compliance with regulatory requirements and industry standards.
• Lead cross-functional teams to identify, develop and implement strategies to improve supplier reliability.
• Lead cross-functional supplier review governance meetings and supplier performance reviews with manufacturing sites.
• Establish close partnership with cross-functional team, Procurement, R&D, Raw Material Center, Global Packaging, Operations, to support Business growth and continuity, NPD, NPI & Cost improvement projects.
• Build strong partnership with Helsingborg Internal manufacturing site for leading investigation of the quality events, Supplier Event Notification (SEN), supporting material changes & participating in inspections/ audits
• Build strong partnership with key suppliers and coordinate continuous improvement process at the suppliers through KPI, Management Action Plan, and CAPA.
• Own the audit planning for the assigned supplier ensuring timely execution of the audits.
• Drive key programs and initiatives across Quality & Compliance.
• Use data driven insights and analytics to identify trends, patterns, and opportunities for improvement across different areas.
• Drive performance management and be accountable for metrics, scorecards, and processes.
• Elaborate and present data insights and recommendations clearly to both technical and non-technical audiences, including senior management.

What we are looking for

Required Qualifications

• Scientific bachelor’s degree (Pharmacy, Chemistry, Engineering or related field). Master preferred.
• 7-10 years of relevant business experience in pharma/cosmetic/ chemical/ food/ packaging component industry. Field experience in Quality control or Quality assurance is a plus.
• Excellent communication, interpersonal, and influencing skills.
• Must be able to work independently and with others.
• Ability to think creatively and strategically to support business results.
• Strong analytical and problem-solving skills.
• Knowledge of regulatory requirements and industry standards.
• Fluent English.
• Hands on experience with Quality Management System, GMP, Agency compliance expectations, and ISO 22716.
• Good understanding of the European regulatory guidelines for drug Products
• Detailed understanding and application of current Good Manufacturing Practices and Agency compliance expectations
• ​

Desired Qualifications

• Ability to lead, teach, and guide project teams in using tools, initiating change, and applying sound process improvement methodology.
• Ability to manage budgets and resources effectively.
• Prior Supplier Quality management experience is a plus.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Vi söker nu en Kvalitetsingenjör till Karlsborg, strax utanför Kalix i natursköna Norrbotten. Du kanske redan bor på orten eller funderar på att flytta till Kalix? Oavsett om du bor inom centralorten eller i någon av kommunens många levande byar får du här en unik närhet till allt från fritid, skärgård och skog, till människor, jobb och nöjen. Läs mer om Kalix här.

Som Kvalitetsingenjör kommer att tillhöra Verksamhetsutveckling och Kvalitet och rapportera till Simon Strömbäck. I denna roll får du en central position i att driva och utveckla förbättringsarbete för att optimera vår verksamhet. Du kommer att:

• Utveckla och implementera arbetssätt, metoder och processer i linje med Billeruds produktionssystem
• Ansvara för att säkra och utveckla ledningssystem inom kvalitet, energi, miljö och livsmedelssäkerhet
• Arbeta med interna och externa revisioner
• Bedöma kemikalier/emballagematerial ur produktsäkerhetsperspektiv
• Hantera kundfrågor
• Hålla sig a jour med aktuella lagstiftningar och implementera dessa
• Arbeta tvärfunktionellt och hantera kontakter såväl internt som externt

Tjänsten är en tillsvidareanställning på heltid och arbetstiden är förlagd till dagtid.

Vi sätter Safety First! Hos oss på Billerud ansvarar vi alla för att bidra till en säker arbetsmiljö. Läs mer om vårt Safety First initiativ här.

Kvalifikationer

För att lyckas i rollen som Kvalitetsingenjör tror vi att du har:

• Högskoleutbildning inom något av områdena: kemi, miljö, kvalitetsteknik eller motsvarande kompetens
• Flytande svenska och engelska, i tal och skrift

Meriterande om du har:

• Erfarenhet av ledningssystem, förbättringsarbete, revisionsteknik och produktsäkerhet

Personliga egenskaper

Vi lägger stor vikt vid din personlighet. Vi ser att du är strukturerad som kan hantera flera parallella uppgifter och har förmågan att självständigt driva aktiviteter enligt plan. Din förmåga att planera och prioritera är avgörande för att lyckas i rollen. Samtidigt är du noggrann och kvalitetsmedveten, vilket innebär att du ser detaljer men alltid har helheten i åtanke.

Du trivs med att samarbeta med olika funktioner och har lätt för att anpassa din kommunikation beroende på mottagare.

Våra värderingar är viktiga för oss och vi tror att du som söker känner igen dig i våra värdeord: Vi värnar om varandra och Vi håller vad vi lovar.

Kontakta oss

Vill du veta mer om tjänsten är du välkommen att kontakt Simon Strömbäck, Section Manager Operation Excellence & Quality, Tel: 0923-660 38 alt simon.stromback@billerud.com

Ansökningsinformation

Rekrytering sker löpande. Tveka inte att skicka in din ansökan redan idag.

Billerud är en jämställd arbetsgivare. Vi omfamnar mångfald och är engagerade i att skapa en inkluderande miljö för alla anställda och kandidater.

Varför oss?

• En möjlighet att bidra till en mer hållbar framtid
• Utvecklings- & karriärmöjligheter med många kollegor att lära av
• Balans mellan jobb och privatliv
• Prestationsbaserad bonus, tjänstepension och en rad olika förmåner enligt företagets policy.

Vår rekryteringsprocess innehåller intervjuer, rekryteringstester, referenstagning samt alkohol- & drogtest.

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

Kvalitetsteamet består idag av fyra kollegor och ansvarar för process- och kvalitetskontroll inom produktion och testföring vid utveckling av våra produkter. Vi stärker nu vårt kvalitetsfokus ytterligare och söker två kvalitetsingenjörer för att fortsatt möta vårt kund- och produktionsbehov.

Som kvalitetsingenjör är du den drivande kraften bakom stabila processer, hög kvalitet och kontinuerliga förbättringar. Du arbetar nära produktionen inom tvärfunktionella samarbeten och leder initiativ för att förbättra produktkvaliteten och förebygga fel. Du har ett nära samarbete med avdelningsteamen och ansvarar för att organisera och genomföra kompetenshöjande åtgärder inom hela organisationen.

• Delta i daglig styrning och rapportera kvalitetsstatus.

• Stödja operatörer med instruktioner, utbildning och daglig problemlösning.

• Driva implementering och förbättringsarbeten i linjen genom att utveckla processer, rutiner, instruktioner och arbetssätt

• Analysera kvalitetsutfall och eliminera kvalitetsbrister genom att driva avvikelsehantering, rotorsaksanalyser och korrigerande åtgärder

• Utifrån COPQ förbättra våra interna processer samt följa upp kvalitetsutfall i test- och produktionsdatabaser

• Implementera och följa upp kapabilliteter för våra processer i produktionen.

• Effektivisera produktkvalitet genom digitalisering

• Genomföra internrevisioner och följa upp åtgärder samt delta vid externa kundrevisioner inom området

• Implementering av kund- och gruppspecifikationer i linjen

• Följa processdata (SPC, waste, OEE) och initiera förbättringar.

Vi söker dig som trivs i en operativ roll där du dagligen är ute i verksamheten och säkerställer att våra produkter håller högsta standard. Du har ett genuint intresse för kvalitetsarbete och en stark övertygelse om ständig förbättring. Som person är du noggrann och ansvarsfull med ett pedagogiskt förhållningssätt. Du är drivande och lösningsorienterad samtidigt som du har god förmåga att planera, organisera och prioritera ditt arbete på ett effektivt sätt. Då vi verkar internationellt är det viktigt att du behärskar både svenska och engelska flytande i tal och skrift.

Vi ser också att du som söker har:

• En högskoleutbildning med inriktning mot industriell organisation, teknik, process, kemi eller motsvarande.

• Arbetslivserfarenhet inom produktkvalitet.

• Dokumenterad utbildning inom kvalitets- och förbättringsarbete, gärna inom Six Sigma metodiken.

• Kunskap i ISO9001, gärna även EN9100 eller andra branschspecifika standarder som exempelvis Automotive.

• Erfarenhet av metoder och processer som MSA, P-FMEA, PPAP, PRR, kontrollplaner och kapabilitetsstudier.

• Du har god vana av att arbeta i SharePoint och erfarenhet av att arbeta i verksamhetssystem.

Vi värdesätter erfarenhet av statistiska analyser och förmågan att hantera och analysera data. Utöver detta är Kunskap i 8D, SPC och grundläggande mätmetodik meriterande.

Diab är sedan över 70 år tillbaka världsledande inom utveckling, tillverkning och försäljning av högteknologiska kärnmaterial åt bland annat vindkraft, marin, industri, flygplanstillverkning och transportsektorn. På Diab i Laholm arbetar cirka 200 medarbetare med uppdrag som spänner från tillverkning av vårt material Divinycell, PVC-cellplast, till förädling av våra produkter. Vi stöttar våra kunder från ritningsstadie till färdig produkt genom kundspecifika produkter lösningar inom alla våra segment.

Vi erbjuder ett spännande, utmanande och utvecklande jobb på ett internationellt innovativt företag i Laholm. Här blir du en viktig del av ett team med branschledande kunskap och starkt engagemang för att göra våra kunders produkter mer konkurrenskraftiga och hållbara. Hos oss får du möjlighet att påverka, utveckla och bidra till framtidens kvalitetsarbete – samtidigt som du växer tillsammans med oss.

Vi söker två kvalitetsingenjörer, tjänsterna är tillsvidareanställningar motsvarande 100% med placering i Laholm. Dessa roller rapporterar direkt till Produktionsavdelningschef, vi söker en kvalitetsingenjör till vår Finishing avdelning och en kvalitetsingenjör till vår Kits-avdelning. Vill du veta mer om tjänsterna är du välkommen att kontakta Johan Hedlund, via mail: Johan.Hedlund@diabgroup.com

Du får inte vara astmatisk eller allergisk mot isocyanater eller epoxi.

Ansökan senast 2026-08-07. Urvalet sker löpande och annonsen kan därför komma att stängas innan sista ansökningsdag.

Vi ser fram emot din ansökan!

Kvalitetsteamet består idag av fyra kollegor och ansvarar för process- och kvalitetskontroll inom produktion och testföring vid utveckling av våra produkter. Vi stärker nu vårt kvalitetsfokus ytterligare och söker två kvalitetsingenjörer för att fortsatt möta vårt kund- och produktionsbehov.

Som kvalitetsingenjör är du den drivande kraften bakom stabila processer, hög kvalitet och kontinuerliga förbättringar. Du arbetar nära produktionen inom tvärfunktionella samarbeten och leder initiativ för att förbättra produktkvaliteten och förebygga fel. Du har ett nära samarbete med avdelningsteamen och ansvarar för att organisera och genomföra kompetenshöjande åtgärder inom hela organisationen.

• Delta i daglig styrning och rapportera kvalitetsstatus.

• Stödja operatörer med instruktioner, utbildning och daglig problemlösning.

• Driva implementering och förbättringsarbeten i linjen genom att utveckla processer, rutiner, instruktioner och arbetssätt

• Analysera kvalitetsutfall och eliminera kvalitetsbrister genom att driva avvikelsehantering, rotorsaksanalyser och korrigerande åtgärder

• Utifrån COPQ förbättra våra interna processer samt följa upp kvalitetsutfall i test- och produktionsdatabaser

• Implementera och följa upp kapabilliteter för våra processer i produktionen.

• Effektivisera produktkvalitet genom digitalisering

• Genomföra internrevisioner och följa upp åtgärder samt delta vid externa kundrevisioner inom området

• Implementering av kund- och gruppspecifikationer i linjen

• Följa processdata (SPC, waste, OEE) och initiera förbättringar.

Vi söker dig som trivs i en operativ roll där du dagligen är ute i verksamheten och säkerställer att våra produkter håller högsta standard. Du har ett genuint intresse för kvalitetsarbete och en stark övertygelse om ständig förbättring. Som person är du noggrann och ansvarsfull med ett pedagogiskt förhållningssätt. Du är drivande och lösningsorienterad samtidigt som du har god förmåga att planera, organisera och prioritera ditt arbete på ett effektivt sätt. Då vi verkar internationellt är det viktigt att du behärskar både svenska och engelska flytande i tal och skrift.

Vi ser också att du som söker har:

• En högskoleutbildning med inriktning mot industriell organisation, teknik, process, kemi eller motsvarande.

• Arbetslivserfarenhet inom produktkvalitet.

• Dokumenterad utbildning inom kvalitets- och förbättringsarbete, gärna inom Six Sigma metodiken.

• Kunskap i ISO9001, gärna även EN9100 eller andra branschspecifika standarder som exempelvis Automotive.

• Erfarenhet av metoder och processer som MSA, P-FMEA, PPAP, PRR, kontrollplaner och kapabilitetsstudier.

• Du har god vana av att arbeta i SharePoint och erfarenhet av att arbeta i verksamhetssystem.

Vi värdesätter erfarenhet av statistiska analyser och förmågan att hantera och analysera data. Utöver detta är Kunskap i 8D, SPC och grundläggande mätmetodik meriterande.

Diab är sedan över 70 år tillbaka världsledande inom utveckling, tillverkning och försäljning av högteknologiska kärnmaterial åt bland annat vindkraft, marin, industri, flygplanstillverkning och transportsektorn. På Diab i Laholm arbetar cirka 200 medarbetare med uppdrag som spänner från tillverkning av vårt material Divinycell, PVC-cellplast, till förädling av våra produkter. Vi stöttar våra kunder från ritningsstadie till färdig produkt genom kundspecifika produkter lösningar inom alla våra segment.

Vi erbjuder ett spännande, utmanande och utvecklande jobb på ett internationellt innovativt företag i Laholm. Här blir du en viktig del av ett team med branschledande kunskap och starkt engagemang för att göra våra kunders produkter mer konkurrenskraftiga och hållbara. Hos oss får du möjlighet att påverka, utveckla och bidra till framtidens kvalitetsarbete – samtidigt som du växer tillsammans med oss.

Vi söker två kvalitetsingenjörer, tjänsterna är tillsvidareanställningar motsvarande 100% med placering i Laholm. Dessa roller rapporterar direkt till Produktionsavdelningschef, vi söker en kvalitetsingenjör till vår Finishing avdelning och en kvalitetsingenjör till vår Kits-avdelning. Vill du veta mer om tjänsterna är du välkommen att kontakta Johan Hedlund, via mail: Johan.Hedlund@diabgroup.com

Du får inte vara astmatisk eller allergisk mot isocyanater eller epoxi.

Ansökan senast 2026-08-07. Urvalet sker löpande och annonsen kan därför komma att stängas innan sista ansökningsdag.

Vi ser fram emot din ansökan!