Summary of the role

Responsible for the development and administration of a Quality System compliant to FDA and ISO requirements, including the utilization of optimal, cost-effective lean manufacturing processes and methods for new and existing projects including inspection, test and label control operations.  Working with internal and external customers supports, quality and continuous improvement using appropriate tools, project leadership.

Tasks and Responsibilities

• Knowledgeable and adheres to TMS Quality Management System and its requirements.

• Supports internal and external audit program as necessary.
• Supports customer complaint (CC), Non-Conforming (NC) events and materials, and CAPAs per procedures.
  • Performs investigations, supports determination of the disposition of returned goods, determines re-inspection requirements, determines corrective and preventive actions (CAPA), issues complaint reports, supports completion of customer CAPAs, and approves to close. Looks for trends to determine actions to decrease number of NCs
  • Initiates and performs root cause analysis. Uses statistical and capability analysis to solve problems. Implements and verifies CAPAs
  • Performs trend analysis of CAPA, NCM, Complaint/Customer Feedback, Risk Management activities, Audits, etc. and presents periodic reports for management review.
• Authors and executes Quality Plans for Quality Management Systems and Organizational Objectives projects.
• Support TMS projects across sites from Quality perspective, as needed.
• Support Engineering, Manufacturing, NPD, and Inspection personnel in design, methods, tooling, validations, and other areas related to the control of product quality.
• Communicates with customers on complaints, process changes, clarification of specifications, completing customer documents, and other projects as needed
• Conducts studies including Gauge R&R’s to develop inspection methods and test equipment. Creates measurement system programs, when necessary.
• Establishes inspections and sampling procedures to ensure the control of quality at the most economical costs
• Creates, reviews and approves Equipment Qualifications, Process, Cleaning, and Software Validation, pFMEA and other documentation as necessary.
• Works closely with internal resources to establish processes and resolve issues
• Supports implementation of best practices through the application of effective quality engineering principals and procedures across functions.
• Drives best practices through the application of effective quality engineering principals and procedures across functions.

Education and Experience

Required:

• 4 year degree in quality, engineering or any related field
• 5+ years in a regulated manufacturing environment

• Knowledge and experience with GMP/ISO Standards: ISO 9000/9001, ISO 13485, and FDA 21CFR 820/11 (4/210/211 as applicable), EU/MDR.

Desired:

• Certified Six Sigma Yellow/Green

• ASQ Certified Quality Engineer and/or Auditor and/or equivalent
• Class I, II, and/or III Medical device manufacturing experience

Summary:

An EHS (Environment, Health, and Safety) Coordinator is responsible for planning, implementing, and overseeing an organization's comprehensive safety programs. They work to create a safe work environment, prevent injuries and accidents, and ensure compliance with legal and regulatory standards related to occupational health and safety, fostering a culture of employee well-being and environmental responsibility within the company.

Tasks and Responsibilities

• Implement and maintain ISO45001 (Occupational Health & Safety)
• Conduct Risk assessments and implement preventative measures to minimize workplace hazards.
• Lead the safety committee, conduct environmental and safety training and environmental and safety audits for Trelleborg Aerospace manufacturing sites.
• Evaluate practices, procedures, and facilities to ensure adherence to laws and regulations, developing and implementing relevant policies.
• Conduct training and presentations on health and safety matters and accident prevention to Trelleborg Aerospace manufacturing sites.
• Inspect equipment and machinery to identify potential safety hazards.
• Investigate accidents or incidents, determining causes, and handling worker's compensation claims.
• Prepare and presenting reports on accidents, violations, and trends in accident Statistics. Collect, analyze, and maintain Environmental and Safety Metrics. Includes monthly reporting.
• Conduct both internal and external safety audits to assess compliance and identify areas for improvement.
• Oversee waste management, environmental compliance, and emissions.
• Recommend solutions, improvement opportunities, and new prevention measures.
• Collaborate with other departments to develop and execute business contingency plans.
• Develop & maintain site layout & footprint of site including any in-facility restructuring as the business evolves in alignment with manufacturing operations, define required new machine specifications and coordinate logistics and rigging needs for installation to meet manufacturing demands and customer requirements.
• Manage and maintaining the Environmental Management System (EMS) and related certification, ensuring legislative compliance.
• Ensure compliance with all applicable environmental and safety regulations including hazardous waste management, air and water permitting, SARA, OSHA and applicable European standards.
• Ensure that wastes (hazardous and non-hazardous) are inspected and labeled, and ensure proper disposal procedures are being followed. Act as hazardous waste coordinator.
• Implement and achievement of ISO 14001 and secure certification (Operationally aligned today but not formally certified – in process).
• Corporate responsibility reporting, annual Blue Grading assessment of operations per corporate guidelines in relation to EH&S, local authority & Fire Department coordination/reporting, permit conformance, and coordinate of site security system.

Education and Experience

Required:

• Minimum of a Bachelor’s Degree in Environmental Health & Safety, Engineering or related technical field
• 8+ years of related experience in both facilities/maintenance and EH&S (Environmental, Health and Safety)
• 5+ years experience in a manufacturing environment
• 5+ years experience in a leadership role

Desired:

• Knowledge and experience with GMP/ISO Standards: ISO 9000/9001, ISO 13485, and FDA 21CFR 820/11 (4/210/211 as applicable)
• 3+ years in a maintenance leadership role
• Experience and/or understanding of blueprint reading, general mechanical skills. In addition experience with hydraulic, pneumatic, and electrically controlled and operated systems.

Competencies

• Aligned cooperation with operations management and engineering teams.
• Business and technical acumen a must.
• Ability to read, write, speak and understand the English language
• Ability to communicate clearly by conveying and receiving ideas, information and direction effectively
• Ability to demonstrate adequate job knowledge to deliver a world class performance
• Ability to challenge oneself to consistently meet all goals and deadlines
• Willingness to strive for excellence by producing work that is free of errors and mistakes
• Desire to delight both customers and coworkers by offering encouragement, fostering teamwork and addressing conflict appropriately
• Commitment to making improvements company wide
• Demonstrated competence using Microsoft Office
• Ability to use an MRP system as needed
• Ability to maintain a professional and respectful relationship with coworkers and company in a leadership capacity
• Able to provide compliance guidance based on knowledge of regulations, available relevant information, alternatives, and risk
• Problem solving; Ability to overcome obstacles
• Ability to manage cross-functional teams, coordinate outside vendor meetings
• Ability to influence for impact

Travel: 

• 30%

Compensation range: $105,000-$123,000 per annum

Benefits:

• 401(k) matching
• Dental insurance
• Disability insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Tuition reimbursement
• Vision insurance

Apply here!

As an EEO/Affirmative Action Employer all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status.

This position requires the use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR.  ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. Green Card Holder), Political Asylee or Refugee. 

All applicants must successfully complete a background check and drug screening as a condition of employment.

Do you want to experience new challenges and innovate the future of engineered polymer solutions? Accelerate your career with Trelleborg and start shaping industry from the inside.

Imagine working for one of the leading contract manufacturers in the world. Trelleborg Medical Solutions is located 30 miles from California’s pristine Central Coast. As a premier manufacturer for life-saving medical components, Trelleborg Medical Solutions is a forward-thinking company. We have been active in our lean manufacturing journey for many years and are advancing towards making our business a showcase of excellence in the medical industry.

Seize this rare opportunity to be part of a healthcare and medical business unit that has been in business for over 100 years, all while enjoying the benefits of living in one of California’s most desired locations!

As a valued Trelleborg team member, you will enjoy:

• Greater opportunity for impact;
• Competitive compensation;
• Outstanding benefits package: Health, Dental, Vision, STD, LTD, Life, 401k;
• Generous paid time off;
• Bonus potential

Quality Engineer

Trelleborg Medical Solutions is seeking a Quality Engineer to support the development, implementation, and maintenance of a Quality Management System compliant with FDA regulations and ISO standards. This role partners with cross-functional teams, customers, and suppliers to ensure product quality, regulatory compliance, and continuous improvement. The Quality Engineer will drive quality initiatives for new and existing products, utilizing Lean Manufacturing principles and quality tools to enhance manufacturing, inspection, testing, and labeling processes while supporting operational excellence and customer satisfaction.

Quality Engineer Expectations:

• Supports internal audit program as necessary.
• Supports customer complaint (CC) and RMA system per procedures. Performs investigations, supports determination of the disposition of returned goods, determines re-inspection requirements, determines corrective and preventive actions (CAPA), issues complaint reports, supports completion of customer CAPAs, and approves to close.  Looks for trends to determine actions to decrease number of CCs
• Maintains Non-Conforming (NC) system per procedures. Performs investigations, participates in MRB (Material Review Board) activities, supports determination of the disposition, determines re-inspection requirement, supports determination of corrections/corrective actions and approves to close. Looks for trends to decrease number of NCs and provide feedback to management
• Maintains corrective and preventive action (CAPA) system per procedures. Initiates and performs root cause analysis. Uses statistical and capability analysis to solve problems. Implements and verifies CAPAs
• Performs trend analysis of CAPA, NCM, Complaint/Customer Feedback, Risk Management activities, Audits, etc. and presents periodic reports for management review. Assesses Design and any associated activities for manufacturability.
• Adheres to the company’s Quality System (QS), writes and approves QS documents
• Authors and executes Quality Plans for Quality Management Systems and Organizational Objectives projects.
• Support Engineering, Manufacturing, and Inspection personnel in design, methods, tooling, validations, and other areas related to the control of product quality.

Required:

• 4 year degree in quality, engineering or any related field

Desired:

• 2+ years in a manufacturing environment in a technical support role
• ASQ Certified Quality Engineer
• Formal Six Sigma Yellow/ Green belt training
• Experience with ISO 13485 

Competencies:

• Ability to read, write, speak and understand the English language 
• Ability to communicate clearly by conveying and receiving ideas, information and direction effectively
• Ability to demonstrate adequate job knowledge to deliver a world class performance
• Ability to challenge oneself to consistently meet all goals and deadlines
• Willingness to strive for excellence by producing work that is free of errors and mistakes
• Desire to delight both customers and coworkers by offering encouragement, fostering teamwork and addressing conflict appropriately
• Commitment to making improvements company wide
• Demonstrated competence using Microsoft Office, Project, Access and JMP
• Comprehensive understanding of applicable Work Instructions, SOP’S, and ISO standards
• Working knowledge of statistical methods associated with six sigma and quality control.
• Able to perform math functions
• Effective project leader
• Experience with lean manufacturing principles and their implementation
• Good hand/eye coordination and depth perception
• Good manual dexterity
• Correctable normal reading distance vision

 Compensation package range: $90,000-$115,00 DOE

APPLY HERE

Trelleborg is looking to add a Quality Technician to our team!

The Quality Technician plays a critical role in ensuring that all incoming and outgoing materials meet established customer specifications, company standards, and regulatory requirements. This position is responsible for conducting thorough inspections, verifying product quality, and maintaining accurate documentation to support compliance and operational excellence. The ideal candidate is detail-oriented, reliable, and capable of working both independently and collaboratively in a fast-paced environment.

Tasks and Responsibilities:

• Perform inbound (receiving) inspections of materials and components.
• Perform in-process and final inspections to verify product conformance to specifications and quality standards.
• Perform outbound inspections and final release activities.
• Interpret blueprints, engineering drawings, specifications, and GD&T requirements.
• Utilize precision measurement and inspection equipment including calipers, micrometers, height gauges, optical comparators, and similar tools.
• Complete First Article Inspections (FAIs) and associated documentation, preferably using Net-Inspect/NetSpect.
• Acquire and maintain supporting documentation for orders.
• Other duties as assigned.

Education and Experience:

• High School Diploma or GED required.
• 2–3 years of experience in each of the following:
  • Quality inspection within an aerospace manufacturing environment or other regulated industry (e.g., medical device manufacturing).
  • GD&T (Geometric Dimensioning & Tolerancing).
  • Use of precision measurement and bench inspection tools, including calipers, micrometers, height gauges, optical comparators, and similar equipment.
  • Receiving, in-process, and final inspection activities.
  • First Article Inspections (FAIs), preferably using Net-Inspect/NetSpect.
• Ability to read and interpret blueprints and engineering drawings.

Highly Preferred:

• Associate's degree in a technical or related field.
• Experience operating Coordinate Measuring Machines (CMMs).
• Experience using vision inspection systems.

Competencies:

• Strong interpersonal and communication skills.
• Basic computer skills.
• Strong attention to detail and commitment to quality standards.
• Ability to read and interpret blueprints, engineering drawings, and specifications.
• Basic arithmetic skills.
• Time management skills, including meeting deadlines and supporting on-time delivery goals.
• Ability to successfully work independently.

Travel: 

• Local coverage
• Travel for offsite training when required, 5%

Compensation range: $29.00-37.00/hour

Benefits:

• 401(k) matching
• Dental insurance
• Disability insurance
• Employee assistance program
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Tuition reimbursement
• Vision insurance

Apply here!

As an EEO/Affirmative Action Employer all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status.

This position requires the use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR.  ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. Green Card Holder), Political Asylee or Refugee. 

All applicants must successfully complete a background check and drug screening as a condition of employment.

Trelleborg is looking to add a Quality Engineer to our team!

The Aerospace Quality Engineer supports AS9100-compliant quality activities for complex aerospace components and assemblies across commercial, defense, and space programs. This role ensures product conformity by translating customer, regulatory, and contractual requirements into effective inspection plans, manufacturing controls, supplier flow-downs, quality records, and audit-ready evidence. The Quality Engineer applies risk-based thinking, structured RCA/CAPA, AS9102 FAI/FAIR practices, MRB support, supplier quality follow-up, and data-driven improvement to prevent defects, reduce variation, protect product safety, and drive timely closure of customer, supplier, and production quality issues.

Tasks and Responsibilities:

• Ensure AS9100 QMS compliance by translating customer, regulatory, and aerospace requirements into inspection plans, manufacturing controls, supplier flow-downs, and quality records.
• Protect product safety and conformity by identifying quality risks, supporting production readiness, verifying special process controls, and ensuring requirements are met before delivery.
• Lead nonconformance, escape, complaint, and supplier-defect investigations; drive containment, root cause, corrective action, and preventive action through effective closure.
• Prepare, review, and submit AS9102 First Article Inspection Reports (FAIR/FAI) and supporting evidence to verify product and process conformance.
• Participate in MRB activities, disposition nonconforming material, and ensure risk-based containment, recovery, and customer/regulatory compliance.
• Perform and support internal, supplier, customer, and third-party audits; maintain audit readiness and objective evidence for AS9100 requirements.
• Evaluate and improve supplier quality performance through audits, scorecards, corrective action follow-up, and support for defect and delivery-risk reduction.
• Partner with engineering, manufacturing, inspection, program management, supply chain, customers, and suppliers to resolve quality issues and improve manufacturability, repeatability, and compliance.
• Maintain accurate quality documentation, certifications, inspection records, customer portal submissions, and status reporting for open quality actions.
• Use quality data, trend analysis, and continuous improvement methods to reduce variation, prevent recurrence, and improve process performance.

Education and Experience: 

• Bachelor's degree in a technical discipline required.
• 3+ years in quality engineering, manufacturing engineering, or process engineering in a regulated manufacturing environment.
• 2+ years hands-on with nonconformance management, root cause analysis, CAPA, MRB activities, and resolution of customer and supplier quality issues.
• Proficient in GD&T and reading engineering drawings, specifications, inspection plans, customer flow-down requirements, and manufacturing process documentation.
• Working knowledge of AS9100 and AS9102; FAIR preparation experience preferred
• Familiarity with PPAP, APQP, PFMEA, SPC, Lean/Six Sigma preferred

• Proficient in Microsoft Office Suite (Excel, Word, PowerPoint, Visio), experience with Minitab, ERP/MRP systems, customer portals, and electronic QMS platforms highly desirable.

• ISO 9001 / AS9100 internal/lead auditor experience a plus

Competencies: 

• AS9100/AS9102 quality mindset with sound judgment in regulated manufacturing environments.
• Product conformity focus, including drawings, GD&T, inspection plans, FAI/FAIR, certifications, and customer flow-downs.
• Risk-based nonconformance management, containment, MRB support, and customer-impact escalation.
• Disciplined RCA/CAPA execution using structured problem-solving methods (5-Why and 8D).
• Strong documentation discipline for traceability, audit evidence, quality records, and customer portal submissions.
• Data-driven improvement using Excel, Minitab, SPC, process capability, Pareto analysis, trends, and basic statistics.
• Effective collaboration with manufacturing, inspection, engineering, suppliers, customers, and cross-functional teams.
• Self-directed ownership, clear communication, and ability to manage production priorities to closure.

Travel: 

• The Quality Engineer may be required to travel throughout North America, Europe, and Asia.

The final compensation offered to the candidate may be based on geographical location, work experience and/or skill level. Additions to the compensation packing, including but not limited to paid time off, insurance benefits and 401(k) eligibility, will be outlined at the time of the job offer.

Application: 

Compensation range: $75,000-$105,000

401(k) matching
Dental insurance
Disability insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Tuition reimbursement
Vision insurance

Apply here!

As an EEO/Affirmative Action Employer all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status.

This position requires the use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR.  ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. Green Card Holder), Political Asylee or Refugee.

What you´ll do: 

Summary of the Role: 

Quality Engineers have the technical ability and expertise to solve complex problems. Problems can be either technical, with regards to product quality, or commercial, regarding processes. Both types of problems need specialized abilities to determine the root cause so that they can be resolved. Many quality functions, such as auditing or PPAP/FAIR need technical training and understanding of the applicable standards.

Tasks and Responsibilities: 

Summary of the Role: 

Quality Engineers have the technical ability and expertise to solve complex problems. Problems can be either technical, with regards to product quality, or commercial, regarding processes. Both types of problems need specialized abilities to determine the root cause so that they can be resolved. Many quality functions, such as auditing or PPAP/FAIR need technical training and understanding of the applicable standards. 

Tasks and Responsibilities:  

Do you approach new challenges with passion and take responsibility for your actions?

Be the change you want to see and start shaping industry from the inside.

About us

Trelleborg is a world leader in engineered polymer solutions for almost every industry in the world. And we are where we are because our talents brought us here.

At Trelleborg Marine & Infrastructure, we go beyond service, building lasting partnerships with engineers, contractors, and owners to deliver long-term solutions that make a real impact.

About the role

As the Quality Manager you will be responsible for defining, maintaining, and independently verifying product, process, and system quality across the organization. You will own the Quality Management System (QMS), ensure compliance with customer, regulatory, and internal requirements, and provide objective oversight of manufacturing activities. You will operate independently of production priorities and has authority over audits, nonconformance management, corrective actions, and product acceptance decision.

Your Responsibilities

• Own and maintain the Quality Management System (QMS) and related documentation
• Define quality standards, inspection criteria, control plans, and acceptance requirements
• Lead internal, external, customer, and regulatory audits
• Own the nonconformance, CAPA, and preventive action processes, including effectiveness verification
• Perform and validate root cause analysis for quality issues
• Oversee inspection, testing, and quality data analysis
• Manage supplier quality requirements, audits, and escalations
• Drive quality-focused continuous improvement initiatives
• Train employees on quality standards, procedures, and compliance expectations

What you bring

• Bachelor’s degree in Quality, Engineering, Manufacturing, or related discipline
• 5–10 years of experience in quality management within a manufacturing environment
• Experience with ISO or equivalent quality systems and customer audits
• Prior leadership or supervisory experience preferred.
• Chemistry or Chemical industry experience preferred.

Desired Competencies

• Quality management systems expertise
• Root cause analysis and problem-solving
• Audit leadership and regulatory knowledge
• Data analysis and risk-based thinking
• Clear, assertive communication
• Ability to operate independently and objectively

Traits we value

• High integrity and independence
• Detail-oriented and analytical
• Confident in escalation and decision-making
• Structured, methodical, and disciplined
• Collaborative while maintaining objectivity

Our Offer and Benefits

• A responsible and results-oriented task in an internationally active industrial company
• We provide an encouraging environment offering growth within the company while investing in your training/education
• Family and congenial working atmosphere with modern equipment
• Very attractive competitive compensation package
• Generous annual leave 

Application Process

Sound like the ideal environment for you?

Don't delay, apply now to shape your career at Trelleborg.

Trelleborg is an Equal Opportunity Employer, and we take pride in the diversity of our employees, valuing the special experience and expertise that people from different backgrounds bring to our business. The ability to develop ground-breaking technologies is one of our key assets and our people make it happen. 

We provide an encouraging environment which offers growth within the company while investing in employee training/education. Our facility is a close and friendly community which allows you to brainstorm your ideas with other colleagues.

We encourage applications from people of all nationalities, religions, genders, sexual identities, different ages and people with disabilities.

At Trelleborg our people are #shapingindustryfromtheinside

Die Trelleborg Sealing Solutions Switzerland AG ist ein führender Entwickler, Hersteller und Lieferant von Flüssigsilikonteilen für anspruchsvolle Anwendungen in der Medizintechnik, pharmazeutischen Industrie, Automobilindustrie und der Nahrungsmittel- und Getränkeindustrie. Wir sind zertifiziert nach ISO 9001, IATF 16949, ISO 13485 und ISO 14001 und zählen rund 140 Mitarbeitende. Unter anderem stellen wir 2-K-Formteile sowie Teile für die Medizinbranche im Reinraum her.

Wir suchen eine fachspezifisch qualifizierte Persönlichkeit im Bereich Qualitätssicherung, idealerweise mit fundierten Kenntnissen in ISO 13485 und/oder IATF 16949 sowie mehrjähriger Erfahrung in der industriellen Qualitätsarbeit – bevorzugt im Spritzgussumfeld.

Qualitätstechniker Technische Produktion (m/w/d)

Hauptaufgaben und Verantwortlichkeiten:

• Du bist einer der Qualitätstechniker für Prozessplanung, pFMEA und APQP – stets in Übereinstimmung mit den Anforderungen aus ISO 13485 und/oder IATF 16949.
• Du bist zentraler Ansprechpartner für interne und externe Kunden in allen qualitätsrelevanten Themen rund um die dir zugewiesenen Produkte.
• Du führst Erstbemusterungen nach normenkonformen Vorgaben durch und erstellst vollständige, nachvollziehbare Erstmusterprüfberichte.
• Du arbeitest an Validierungen gemäss Vorlagestufen und Kundenanforderungen und beherrschst die Validierungs‑Systematik (Prozessvalidierung, DQ, IQ, OQ, PQ) sowie – sofern zutreffend – die IATF‑Anforderungen (z. B. PPAP Level 3).
• Du führst Serienfreigaben durch und übernimmst die Serienüberwachung, um sicherzustellen, dass Produktion und Produkte jederzeit normkonform sind und sämtliche Kundenanforderungen erfüllen.
• Du verantwortest die 8D‑Reklamationsbearbeitung nach strukturiertem, normgerechtem Vorgehen.
• Du führst Fehleranalysen durch (z. B. Ishikawa, 5‑Why, DOE), leitest geeignete Massnahmen ab, stellst deren Umsetzung sicher und überprüfst deren Wirksamkeit (Effectiveness Check) – ein zentraler Bestandteil beider Normen.
• Du koordinierst Korrektur- und Vorbeugemassnahmen (CAPA) entsprechend den normativen Vorgaben.
• Du unterstützt den Leiter Qualität bei internen und externen Audits, einschliesslich Vorbereitung, Dokumentation und Nachverfolgung von CAPA‑Massnahmen.

Ihr Profil:

• Technische Grundausbildung, z. B. als Kunststofftechnologe, Werkzeugmacher, Mechaniker oder Feinmechaniker.
• Weiterbildung im Bereich Qualitätssicherung.
• Vertiefte Kenntnisse der gängigen QS‑Tools: FMEA, APQP/PQP, Statistik, 8D, CAPA, Fehleranalyse.
• Erfahrung in der Qualitätssicherung, idealerweise in der Massenproduktion und/oder im Spritzguss.
• Gute bis sehr gute Kenntnisse in ISO 13485 und/oder IATF 16949.
• Sehr gute Deutschkenntnisse sowie sichere Englischkenntnisse auf gutem Niveau.

Wir bieten:

• Ein abwechslungsreiches und verantwortungsvolles Aufgabenfeld
• Moderne Infrastruktur und ein erfahrenes, kompetentes Team
• Flache Hierarchien und kurze Entscheidungswege
• Hoher Gestaltungsspielraum und echte Eigenverantwortung
• Eine offene Unternehmenskultur mit Raum für eigene Ideen
• Eine gründliche, strukturierte und professionelle Einarbeitung

Bereit, Qualität neu zu definieren?
Dann freuen wir uns auf Ihre Bewerbung unter Angabe Ihrer frühestmöglichen Verfügbarkeit und Ihrer Gehaltsvorstellungen. 

Bei Fragen stehe ich Ihnen gerne zur Verfügung: Jennifer Lawrenz-Mancino, HR, Tel: +41 52 742 01 73

Summary of the Role: 

Quality Engineers have the technical ability and expertise to solve complex problems. Problems can be either technical, with regards to product quality, or commercial, regarding processes. Both types of problems need specialized abilities to determine the root cause so that they can be resolved. Many quality functions, such as auditing or PPAP/FAIR need technical training and understanding of the applicable standards.

Tasks and Responsibilities: 

• Partner with customers to understand their QA needs and provide solutions
• Complete customer complaints with customer and suppliers
• Complete plans for standard products and provide to customers and suppliers
• Lead and create internal and external trainings as subject matter expert
• Collaborate with cross-functional teams to ensure customer satisfaction
• Review FAIS from factory and send to customers
• Manage customer portals
• Perform and support internal AS9100 audits
• Partner with suppliers as needed to support inspection gaps
• Experience completing PPAP/FAI required

Education and Experience: 

• Bachelor’s degree in engineering or other technical discipline
• 3 years’ experience in an engineering role, preferably in a manufacturing role
• Master’s degree counts towards 2 years’ experience
• 2 years’ experience in quality including experience with complex surfaces and assemblies
• Knowledge of aerospace processes, such as AS9100
• Proficiency in Microsoft Word and PowerPoint

Competencies: 

• Strong analytical, decision making and problem-solving skills
• Strong mechanical and technical aptitude
• Ability to self-manage and successfully work without supervision
• Ability to handle and prioritize dynamic workload
• Strong oral and written communication skills
• Excellent organization skills
• Proven proficiency with presentations and public speaking

The final compensation offered to the candidate may be based on geographical location, work experience and/or skill level. Additions to the compensation packing, including but not limited to paid time off, insurance benefits and 401(k) eligibility, will be outlined at the time of the job offer.

Compensation range: $75,000-$105,000

401(k) matching
Dental insurance
Disability insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Tuition reimbursement
Vision insurance

Application: 

Apply here!

Last Application Date 8/8/2026

As an EEO/Affirmative Action Employer all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status.

This position requires the use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR.  ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. Green Card Holder), Political Asylee or Refugee.