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-$95,000

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 2/25/2026

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.

About the job

The Quality Manager plays a pivotal role in ensuring adherence to stringent quality standards and continuous improvement initiatives. Responsible for overseeing and implementing robust quality control processes, the Quality Manager is integral to maintaining the highest levels of product excellence and customer satisfaction.

Your Responsibilities

• Quality Control Oversight:
  • Implement and manage comprehensive quality control processes.
• Compliance Management:
  • Ensure adherence to industry regulations, certifications, and quality standards.
• Supplier Quality Management:
  • Collaborate with suppliers to establish and maintain rigorous quality standards.
• Quality Assurance Planning:
  • Develop and implement quality assurance plans, to guarantee reliability.
• Root Cause Analysis:
  • Investigate and identify root causes of quality issues, implementing corrective and preventive actions to eliminate recurring problems.
• Data Analysis and Reporting:
  • Utilize statistical methods and data analysis tools to track key quality metrics.
• Cross-functional Collaboration:
  • Collaborate with other departments to approach quality management and problem resolution.
• Risk Management:
  • Identify potential quality risks and develop strategies to mitigate them.
• Continuous Improvement:
  • Foster a culture of continuous improvement.
• Documentation and Record Keeping:
  • Maintain accurate and comprehensive records of quality activities.
• Auditing and Assessment:
  • Conduct regular internal audits to evaluate compliance with quality management systems and initiate corrective actions as needed.
• New Product Introduction (NPI):
  • Collaborate with product development teams to ensure that new products meet established quality standards.
• Quality Management System (QMS) Maintenance:
  • Oversee the development, implementation, and maintenance of a robust Quality Management System.
• Emergency Response Planning:
  • Develop and implement plans for responding to quality emergencies or recalls.
• Communication:
  • Effectively communicate quality objectives, expectations, and performance metrics to all levels of the organization.

Education and Experience

• Bachelor's degree in a relevant field such as engineering, quality management, industrial management, or a related discipline.
• Proven experience in quality management roles within a manufacturing environment.
• Demonstrated success in implementing and maintaining quality management systems.
• Certification in quality management systems, such as Certified Manager of Quality/Organizational Excellence (CMQ/OE) or similar, can be beneficial.

Competencies

• Strong leadership skills, with the ability to inspire and guide teams.
• Excellent problem-solving and analytical abilities to drive effective decisions.
• Solid knowledge of auditing, compliance, and health & safety regulations.
• Proven project management skills, delivering results on time and within scope.
• Strong customer focus, building trust and long-term relationships.
• Deep industry knowledge with a commitment to maintaining high ethical standards.
• A continuous improvement mindset, always seeking smarter and more efficient ways of working.

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

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

Job Role: To support the function of the quality department through the duties outlined below together with any other tasks as assigned by the Quality Manager.

Duties, responsibilities and authorities:

• Answer customer complaints through 8D report within the requested deadline
• Ensure that corrective actions in 8D reports are closed on time and reports updated and submitted accordingly
• Support departments with problem solving
• Ensure that revised copies of documentation are uploaded in QMS system such that integrity of QMS is maintained.
• Use equipment in quality lab in order to investigate parts (including customer returned samples)
• Checking of tool approvals and informing relevant BU of the results
• Carry out metrological confirmation of equipment as per schedule and procedures
• Provide part numbers as requested after going through quotation
• Review and confirmation of inspection plans
• Carry out MSAs as required
• Review new quotation requests in terms of quality requirements, including but not limited to dimensions and tolerances, surface quality, certificate requirements and other general requirements.
• Review and approval of drawings
• Recognise product safety/special characteristics on drawings and transfer information correctly
• Ensure department KPIs are met and propose actions to rectify negative results for continuous improvement where applicable.
• Ensure the promotion of customer focus throughout the organisation
• Support selection and implementation of appropriate preventive and corrective actions
• Has the authority to stop shipment or stop production (where applicable) to correct quality problems
• Inform relevant area management team immediately upon complaint notification to prevent possibility of further nonconforming product to be produced and/or shipped to the customer.
• Ensure that the Quality Management System (QMS) conforms to the requirements of IATF 16949:2016
• Report on the performance of the QMS and opportunities for improvement to management (particularly top management)
• Ensure that the integrity of the QMS is maintained when changes to the QMS are planned and implemented
• Implement improvements necessary to improve the systems following results of internal and external audits as necessary
  • Monitor implementation of IATF 16949:2016 across all departments within TSS Malta
  • Ensure all Environment, Health and Safety instructions are implemented
  • Ensure safety performance is adequately communicated
  • Participate in risk reduction plans
  • Use any customer portals such as: CAQ, process director etc.
  • Understanding customer requirements and liaising with relevant parties. This includes technical cleanliness for automotive parts.
  • Compliance with the requirements of the ISO 14001 Environmental Management System and ISO 45001 Occupational Health and Safety Management System.
  • Responsible for reporting any hazards / near misses / injuries immediately you’re aware of to the area management.
  • 
    

• Skills/Education:

  • Bachelor Degree in Engineering (Hons.) or equivalent.
  • Good use of Microsoft Office tools
  • Good understanding of statistics, ideally with a Six Sigma Green Belt or Black Belt training background.
  • Understanding of customer-specific requirements
  • Understanding of applicable core tools
  • Technical understanding of manufacturing process as applicable
  • Understanding of product requirements
  • Understanding how to operate equipment to test parts to check conformance to product requirement, as applicable.
  • Excellent verbal and written communication skills in English.
  • Able to work under own initiative.
  • Able to prioritize tasks as needed to meet deadlines.
  • Able to work with different teams and maintain good working relationships both external and internal customers.
  • Attentive to detail, logical, practical and proactive.

Workplace Culture: 

At Trelleborg Malta, we believe in creating a vibrant and inclusive workplace where your voice matters. You'll be recognized for your contributions and have plenty of opportunities for growth and development. Join us and be part of a team that supports and celebrates each other!

What we offer: 

• Trelleborg University: Enhance your skills by studying while you work!
• Career Development: Explore dynamic career paths and learn from our experienced employees.
• Comprehensive Health Coverage: Benefit from health insurance for you and your dependents.
• Flexible Working Hours: Customize your schedule to achieve work-life balance.
• Study Leave: Take advantage of study leave to further your education.
• Convenient Parking: Enjoy easy, hassle-free parking facilities.
• Social and Well-Being initiatives: Doctor on site, and frequent social activities

Trelleborg is an equal opportunity employer. Join us and experience a rewarding, balanced work environment!

Do you want to make a lasting difference for our customers and the environment? Start shaping industry from the inside.

Who are we?

Trelleborg’s Engineered Coated Fabrics operation is a world leader in engineered polymer solutions for almost every industry globally. We are where we are because our talents brought us here. By specializing in the polymer engineering that makes innovation and application possible, Trelleborg works closely with leading industry brands to accelerate their performance, drive their business forward—and along the way, shape the industry and progress that will benefit humankind in the exciting years ahead.  Our people are Shaping Industry from the Inside.

About the Job

The Quality Lab Technician supports the facility by performing testing on production and development samples to required test methods, organizing lab tasks, and monitoring workload and lab performance. Responsible for communicating in-process test results to production floor and alerting the operations team and shipping personnel to final inspection results outside of product specifications.  Responsibilities include working in a fast-paced production lab environment with operators, supervisors, production support staff, quality personnel, and development personnel while maintaining a professional and courteous environment.

Responsibilities

• Conform to all safety guidelines and procedures
• Perform physical testing on fabrics in accordance with ASTM, Federal, Military, AATCC, company, and/or customer test methods.
• Complete lab testing with little direct supervision and ensure completion of all required product testing in a timely manner and verify whiten enough testing has been completed per sample frequency.
• Enter test data into database and clearly communicate results to all required Trelleborg personnel.
• Maintain test equipment appropriately, performing periodic calibration checks as required
• Maintain lab records, including storage of records and sample retains, per procedure
• Interact with on-site customer source inspectors to uphold customer requirements in a professional, courteous manner.
• Check inventory of laboratory supplies ensuring supplies are ordered before supply runs out.
• Notify Supervisor of out of control, discrepancy or unexpected results in timely manner.
• Answer inquiries about test results and answer questions about specific factors that can influence test results.
• Perform routine laboratory maintenance tasks including organization and cleaning of work areas.

Qualifications

• High School Diploma or GED required; at least one-year technical, associate degree or equivalent manufacturing and lab experience
• Excellent written and verbal skills, as well as effective problem analysis and organizational skills
• Proficient in MS Office: (PowerPoint, Access, Excel) – SAP/AS400 experience, preferred
• General understanding of SAP or similar ERP systems is a plus

Successful candidates will have strengths in the following:

• Attention to Detail
• Self-starter, capable of working with minimum supervision
• Ability to multi-task
• Ability to perform at a high level under stress
• Integrity
• Establish and maintain interpersonal relationships
• Flexible, capable of adapting to changes within the department and/or process
• Excellent written and verbal communication skills
• Capable of working in a fast-paced environment
• Must be team-oriented
• Quick learner
• Dependable
• Capable of maintaining high standards

Benefits  

As a valued Trelleborg team member, you will enjoy: 

• Competitive salary 
• Generous benefits package: Health, Dental, Vision, STD, LTD, Life, 401k 
• Paid time off 
• Paid holidays 
• Employee assistance program 
• A rewarding career with greater opportunity for impact

Trelleborg is an equal opportunity employer! We celebrate diversity and are committed to creating an inclusive environment for all employees. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

At Trelleborg our people are #shapingindustryfromtheinside

Apply here!

Summary of the Role: 

Inspectors will verify the product coming in and the product going out determining if they meet customer requirements.

Tasks and Responsibilities: 

• Inbound Inspection
• Outbound inspection
• Acquire supporting documentation for orders
• Other duties as assigned

Education and Experience:

• Associates degree preferred, HS diploma or GED required.
• Minimum 1 year experience in Quality inspection required.
• Basic blueprint reading skills required

Competencies: 

• Strong interpersonal and communication skills.
• Basic computer skills
• Basic reading skills
• Basic arithmetic skills
• Time management skills including meeting deadlines for OTD.
• Ability to successfully work independently

Travel: 

• Local coverage
• Travel for off site training when required, 5%

Application: 

Last Application 2/9/2026

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.

Summary of the Role:

 As a Quality Control Manager, you will be responsible for overseeing and implementing quality assurance measures in the logistic process, ensuring adherence to industry standards and specifications. Your role will involve managing a team, conducting inspections, and implementing corrective actions to uphold and improve product quality in accordance with organizational objectives.

Tasks and Responsibilities: 

• Develop and Implement Quality Standards: Establish and maintain quality control standards and procedures.
• Inspection and Testing: Oversee the inspection and testing of materials, parts, or finished products.
• Quality Audits: Conduct regular quality audits to identify areas for improvement and ensure compliance.
• Team Management: Manage and lead a team providing guidance, training, and performance evaluations.
•  Process Improvement: Collaborate with production and engineering teams to identify and implement process  improvements that enhance quality and efficiency.
• Documentation and Record Keeping: Maintain accurate records of quality control activities, and corrective actions.
•  Root Cause Analysis: Investigate and analyze the root causes of quality issues, implementing corrective and preventive actions to address underlying problems.
• Continuous Monitoring: Implement systems for continuous monitoring of quality metrics and key performance indicators, providing regular reports.
• Training Programs: Develop and implement training programs for employees to ensure understanding and adherence to quality control standards and procedures.
• Regulatory Compliance: Ensure compliance with relevant industry standards, regulations, and certifications.
• Collaboration: Collaborate with cross-functional teams, to implement improvements.
• Data Analysis: Utilize statistical tools and data analysis to identify trends, patterns, and improvements.
• Quality Culture Promotion: Foster a culture of quality consciousness throughout the organization.
• Communication: Communicate quality objectives, issues, and improvements effectively to all relevant stakeholders.

Education and Experience: 

•  A bachelor's degree in a relevant field such as quality management, engineering, industrial management, or a related discipline is required.

 Experience:

• Quality Management Experience: At least 7 years of experience in quality management, quality control, or a related role within a manufacturing environment.
• Leadership Experience: Proven experience in leading and managing a quality control team.
• AS9100 Auditor Experience required

Skills and Competencies: 

• Quality Control Techniques
• Analytical Skills
• Communication skills
• Project Management
• Strategic thinking
• Decision-Making
• Customer Focus
• Ethical Conduct
• Team Collaboration
• Innovation
• Audit Skills

The financial 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: $100,000 - $145,000

401(k) matching

Dental Insurance 

Disability Insurance 

Employee Assistance Program 

Flexible Spending Account 

Health Insurance 

Life Insurance 

Paid time off 

Tuition Reimbursement 

Vision Insurance  

Application: 

Last Application Date 2/9/2026

Application:

Apply here!

Last Application Date 2/9/2026

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.

Make your mark on the future.

Accelerate your career with Trelleborg and start shaping industry from the inside.

Who are we?

Trelleborg Industrial Solutions (TIS) is a global leader in innovative polymer-based solutions for key industries and critical infrastructure. We are one of three Business Areas within the Trelleborg Group, with a total of about 6 200 employees around the world.

About the role

As the QHSE Manager you will be responsible for ensuring that the company’s quality, health, safety and environmental operations meet or exceed regulatory, customer, and organizational standards. This role develops and implements management systems, policies, and programs to maintain safe, efficient, and compliant business operations. You will lead continuous improvement initiatives, ensures adherence oversees risk mitigation, and fosters a culture of safety, quality, and environmental responsibility across the organisation.

Tasks & Responsibilities:

• Quality Management: Develop, implement, and maintain quality management systems to ensure products meet or exceed regulatory, customer, and company standards. Conduct regular audits, inspections, and quality assessments to drive continuous improvement.
• Health & Safety Oversight: Establish and enforce health and safety policies, procedures, and protocols to maintain a safe working environment. Conduct risk assessments, monitor workplace safety, and ensure compliance with occupational health and safety regulations.
• Environmental Compliance: Ensure business operations comply with environmental regulations, permits, and sustainability initiatives. Implement environmental management programs, including waste reduction, emissions control, and resource efficiency.
• Risk Assessment & Mitigation: Identify potential quality, safety, environmental, and facility risks, developing strategies to mitigate them. Implement corrective and preventive actions for incidents or non-conformities.
• Training & Awareness: Design and deliver QHSE and facilities-related training programs to promote awareness, safe practices, and regulatory compliance across the organization.
• Incident Management: Facilitate investigations into quality, safety, environmental, and facility incidents, documenting findings and implementing corrective measures to prevent recurrence.
• Regulatory Liaison: Maintain up-to-date knowledge of relevant regulations, standards, and industry best practices. Liaise with authorities and ensure timely reporting of compliance matters.
• Continuous Improvement: Drive initiatives to improve QHSE and facilities performance, integrating best practices, audits, and performance metrics to enhance operational excellence.
• Reporting & Documentation: Prepare and present QHSE reports, KPIs, and performance metrics to senior management. Maintain accurate records for audits, certifications, and regulatory compliance.
• Cross-Functional Collaboration: Work closely with operations, engineering, production, and other departments to ensure QHSE requirements are embedded in processes, projects, and facilities planning.
• Undertake any other reasonable duties or responsibilities as requested by the company, in line with the overall purpose of the role and the needs of the business.

Education & Experience:

• Bachelor's degree in a relevant field such as engineering, quality management, industrial management, or a related discipline.
• Proven experience in quality management roles within a manufacturing environment.
• Demonstrated success in implementing and maintaining quality management systems.

Why Join Us?

• Competitive salary and benefits.
• Flexible working options and generous annual leave.
• National and International travel and career development opportunities.
• A supportive team and cutting-edge technology.

Application Process

Sound like the ideal environment for you?

Don't delay, apply now to shape your career at Trelleborg. 
Send us your CV / application in an English format to grow your career!

Trelleborg is an equal opportunity employer! 

We celebrate diversity and are committed to creating an inclusive environment for all employees. 

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. 

Please contact us to request accommodation.

At Trelleborg our people are #ShapingIndustryfromtheInside 

Join Our Team at Trelleborg Medical Solutions!

Imagine working for one of the leading contract manufacturers in the world, nestled just 30 miles from California’s stunning Central Coast. At Trelleborg Medical Solutions, we are not just a premier manufacturer of life-saving medical components; we are a forward-thinking company committed to excellence and innovation. Our journey in lean manufacturing has been ongoing for years, and we are on the path to becoming a showcase of excellence in the medical industry. 

Seize this rare opportunity to be part of a medical solutions business with over 100 years of history, all while enjoying the benefits of living in one of California’s most desired locations!

Why join us?

As a valued Trelleborg team member, you will enjoy:

• Life Insurance
• Medical Insurance
• Vision Insurance
• Dental Insurance
• 401(k) plan
• Generous PTO plan
• 12 paid holidays

Position: Senior Quality Systems Specialist

Trelleborg Medical Solutions is currently accepting application for a Senior Quality Systems Specialist (QSS). The Senior QSS is focused on the maintenance of the Quality Management System (QMS) to ensure compliance with regulatory, quality, company policies and manufacturing requirements.

Key Responsibilities:

• Supports all aspects of the internal audit program, ISO notified body audits, customer audits and FDA inspections, including but not limited to:
  • Serve as an auditor for internal audits
  • Create and maintain internal audit schedule
  • Audit controlled document files in preparation for regulatory inspections and provides support during regulatory inspections and client audits
  • Initiate and execute audits, including developing and documenting the audit plan, leading the audit, generating the audit report, and tracking subsequent actions with the team
  • Provide support during external audits including scheduling, hosting, preparing audit responses
  • Work with subject matter experts to ensure audit record content is accurate, well documented, and meets the requirement of the process
• Develops metrics and performs trend analysis of key QS areas such internal and external audit findings, CAPAs, nonconforming material, training, deviations, etc. to identify areas for improvement. Escalates trends to an appropriate quality system such as CAPA or CI; presents analysis to management
• Supports maintenance of the CAPA program
  • Serves as CAPA Owner as needed, driving necessary investigation, correction, and corrective/preventive actions
  • Ensures all internal and external audit findings are entered into the CAPA system, assigned to the appropriate personnel, and are completed in accordance to the CAPA procedures, within specified time periods
  • Approve corrective action plans and verify effective and timely implementation of corrective actions for audit nonconformities
• Oversees completion and control of customer questionnaires and other customer-required documents
• Initiates, facilitates and/or manages projects to expand, change, enhance and improve the quality system, as assigned
• Supports and coordinates activities related to nonconforming material, complaint/customer feedback, deviations, RMA, and CAPA processes
• Provides quality system training for the organization as needed
• Manages review of documents to ensure ISO/FDA compliance of controlled documents lifecycle including annual review management
• Own or co-lead strategic quality initiatives, such as QMS harmonization, digital transformation, or audit program redesign.
• Communicate quality system changes effectively across the organization, ensuring understanding and adoption
• Own or support projects and associated activities to ensure ongoing compliance as related to QMS.
• Design and deliver targeted training programs based on audit findings, CAPAs trends, or regulatory updates.
• Mentor and train junior QS Specialists, auditors, and CAPA owners.
• Own complex CAPAs or systemic issues that require cross-departmental or cross-site coordination.
• Perform deep-dive trend analysis across multiple quality subsystems and present findings to senior leadership. Recommend strategic actions based on data insights (e.g., training needs, process changes, risk mitigation).
• Develop and implement enhancements to the QMS based on audit trends, CAPA effectiveness, and regulatory changes. 

Education and Experience:

Required:

• Minimum of 2 year degree in Quality, Regulatory, Manufacturing or related field; OR certificate in Regulatory Science or Medical Product Development plus 1 year of regulated industry work experience
• 3+ years of quality/regulatory experience in medical device or related industry
• 2+ year experience conducting investigations and root cause analysis for complex/advanced issues

Desired:

• 4 year degree in Quality, Regulatory, Manufacturing or related field
• ISO13485:2016 and/or ISO9001:2015 Auditor Certification
• Knowledge and experience with GMP/ISO Standards: ISO 9000/9001, ISO 13485, and FDA 21CFR 820/11 (4/210/211 as applicable)

 Salary: $70,000-$85,000 DOE

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.

Zur Verstärkung unseres Teams suchen wir am Standort Stein am Rhein zum nächstmöglichen Zeitpunkt einen

Quality Manager (m/w/d)

Ihre Mission:

Als Quality Manager sind Sie die treibende Kraft hinter der Sicherstellung und kontinuierlichen Weiterentwicklung unseres Qualitätsmanagementsystems (QMS). Sie fördern aktiv eine Unternehmenskultur der kontinuierlichen Verbesserung und Teamarbeit und agieren als zentrale Schnittstelle zwischen Geschäftsführung, operativen Bereichen und externen Stakeholdern. Mit Ihrer proaktiven Haltung treiben Sie Veränderungen und Qualitätsinitiativen voran und tragen massgeblich zur Einhaltung regulatorischer Anforderungen sowie zur Kundenzufriedenheit bei.

Hauptaufgaben und Verantwortlichkeiten:

• Strategische Verantwortung:

• Berichterstattung zur Leistung des QMS im Rahmen von Management-Review-Sitzungen

  Vorbereitung von Tagesordnungen und Protokollen für Management-Reviews

  Vertretung der Geschäftsführung bei internen und externen Audits

  • Qualitätsmanagement & Compliance:

• Sicherstellung, dass alle QMS-relevanten Prozesse etabliert, implementiert und aufrechterhalten werden

  Förderung des Bewusstseins für regulatorische und kundenspezifische Anforderungen im gesamten Unternehmen. Überwachung und Koordination von Kundenanforderungen, behördlichen Vorgaben und internen Audits

  • Operative Qualitätssicherung:

• Planung und Kontrolle von Programmen zur Sicherstellung der Produktqualität über alle Phasen hinweg (Einkauf, Produktion, Fertigwaren). Genehmigung und Pflege aller QS-Dokumente, inkl. QSM, SOPs und Arbeitsanweisungen. Verantwortung für Lieferantenbewertungen, Prüfungen, Reklamationsmanagement und CAPA-Prozesse

  • Systeme & Prozesse:

• Leitung des internen Auditprogramms inkl. Planung, Durchführung und Freigabe Betreuung des Kalibrierungssystems, Schulungsprogramms und Dokumentenkontrollsystems Unterstützung bei Validierungsaktivitäten und Genehmigungen

  • Kommunikation & Schulung:

• Durchführung von qualitätsrelevanten Schulungen für Mitarbeitende

  Pflege von Qualitätsvereinbarungen mit Kunden

Ihr Profil:

Abgeschlossenes Studium im Bereich Qualitätsmanagement, Ingenieurwesen, Naturwissenschaften oder vergleichbare Qualifikation. Mehrjährige Berufserfahrung im Qualitätswesen, idealerweise in einem regulierten Umfeld (z. B. MedTech, Pharma). Fundierte Kenntnisse in ISO 9001 und ISO 13485, CAPA, Auditmanagement und regulatorischen Anforderungen. Ausgeprägte Kommunikationsfähigkeit, Durchsetzungsstärke und Leadership-Kompetenz. Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift

Wir bieten:

• Eine verantwortungsvolle Schlüsselrolle mit hoher Sichtbarkeit im Unternehmen
• Gestaltungsspielraum für die Weiterentwicklung des QMS
• Kollegiales Arbeitsumfeld mit flachen Hierarchien
• Attraktive Vergütung und Weiterbildungsmöglichkeiten

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

About the Company

Pawling Engineered Products, LLC. is a leading global specialty rubber products manufacturer. We produce highly specialized and innovative elastomeric products designed to withstand the rigorous requirements of the world’s leading original equipment manufacturers, designers, engineers and new product developers. These customers rely on our inflatable and compression seals, gaskets, clamps and other specialty rubber products for a wide range of applications in dominant industries and emerging technologies. Located in Pawling, NY. We are proud to be a part of Trelleborg since October, 2022.

About the Role

Lead the Quality Team in direct support of manufacturing. Drive continuous improvement in product quality and compliance while partnering with production, and process engineering teams in achieving customer, cost and delivery objectives. Assess performance against and develop quality policies that help to ensure products meet a high standard of customer satisfaction and conform to global standards and regulatory requirements. Own and manage quality discrepancies related to process, product or customer feedback. May serve as liaison between the Pawling facility and various government agencies, customer contacts and External 3rd Party auditors.

Responsibilities

• Manage manufacturing quality resources and daily operations of the team.
• Manage systems, complaint resolution, and in-process & Final Quality Process.
• Ensure customer requirements as identified in quality and technical agreements are reviewed, align with organizational capabilities, and are satisfied within existing or new quality system procedures or work instructions.
• Ensure applicable regulations and standards are followed, inclusive of ISO9001, 21 CFR50 Appendix B, REACH and RoHS, and related ancillary standards.
• Coordinate and lead all regulatory inspections, customer and quality system audits.
• This position serves as contact with outside regulatory agencies when needed.
• Partner with operations and engineering to ensure processes are capable and able to yield products that meet customer and quality requirements.
• Review any changes to the Company’s Quality Policies, Procedures and Work Instructions to ensure they can effectively convey information and requirements and provide oversight to ensure they are communicated as appropriate.

Qualifications

Required:

• Bachelor’s degree in engineering (Mechanical, Electrical, Industrial or Chemical) or related field.
• Master’s degree preferred.
• 6 sigma black belt or other structured problem-solving coursework.
• In lieu of a bachelor’s degree, you must have Quality Management experience.

Desired:

• 8 years of experience in Quality Engineering or Continuous Improvement.
• 2 years of experience in a leadership or management role.
• Experience and ability to mentor and support others with Advance Quality Planning activities, including the development of potential Failure Mode Effects Analysis (FMEAs) Control Plans, Process Flow Diagrams, Production Part Approval (PPAP) documents.
• Experience and ability to mentor and support others with Measurement System Analysis (MSA), including in the use of inspection procedures, measuring equipment, blueprint reading, gage R&R studies, and statistical process control.
• Possesses theoretical knowledge and current practical experience in root cause analysis and preventive actions, knowledge of Lean Enterprise and six sigma methodology: proficient computer skills and ability to supply presentations.
• Proven experience in managing multiple continuous improvement projects.
• Rubber, silicone experience preferred.
• Experience in representing organizations in customer and agency audits.

Required Skills

• Strong leadership skills.
• Superior skills in planning, organizing and motivational skills are a must.
• Excellent written and verbal communication skills.
• Excellent interpersonal and presentation skills.
• Excellent math skills.

Benefits

• Medical, dental, vision, and disability benefits
• Healthcare and dependent care FSA and HSA programs
• Bonus/incentive opportunity
• Paid Time Off
• Paid Parental Leave
• Reward and recognition programs
• Training and development
• 401(k) retirement savings plan with company match
• Tuition reimbursement
• Company Paid Life Insurance: Employee / Spouse / Child
• Supplemental Disability and Life Plans available
• Employee Assistance Program (EAP)

Pay range and compensation package

$100,000 to $120,000 depending on experience

ITAR Statement

This position requires the use of information that 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. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c)

Apply here!