Quality

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!

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

Gehen Sie neue Herausforderungen mit Leidenschaft an und übernehmen Sie Verantwortung für Ihr Handeln?

Seien Sie der Wandel, den Sie sehen möchten, und gestalten Sie die Branche von innen heraus mit.

Wer sind wir?

Trelleborg Industrial Solutions (TIS) ist ein weltweit führender Anbieter innovativer polymerbasierter Lösungen für Schlüsselindustrien und kritische Infrastrukturen.

Wir sind einer von drei Geschäftsbereichen innerhalb der Trelleborg-Gruppe und beschäftigen weltweit ca. 6.200 Mitarbeiter.

Über die Stelle

Als Qualitätsingenieur (m/w/d) spielen Sie eine Schlüsselrolle bei der Sicherstellung der Lieferantenleistung, der Produktqualität und der Einhaltung internationaler Standards. Zu Ihren Aufgaben gehören die Qualifizierung und Entwicklung von Lieferanten, die Durchführung interner und externer Audits sowie die Verwaltung des integrierten Managementsystems gemäß der DIN Normen ISO 9001, 14001, 45001, 50001 und ISO/TS 22163. Sie überwachen Lieferantenbewertungen, Erstmusterfreigaben und Korrekturmaßnahmen und sorgen gleichzeitig für eine enge Zusammenarbeit zwischen den Abteilungen Einkauf, Entwicklung und Qualität.

In dieser Funktion wenden Sie Ihr technisches Fachwissen in mechanischen oder metallverarbeitenden Prozessen wie Gießen, Schmieden, Schweißen und Beschichten an, um eine kontinuierliche Verbesserung entlang der gesamten Lieferkette voranzutreiben. Sie überwachen Qualitätsziele anhand von Kennzahlen und Dashboards, tragen zu Produktentwicklungsaktivitäten wie FMEA und EMPB bei und stellen sicher, dass alle Prozesse die Compliance- und Leistungserwartungen erfüllen. Dies ist eine dynamische Position, die ausgeprägte analytische Fähigkeiten, eine proaktive Denkweise und die Bereitschaft zu ausgiebigen Reisen erfordert, um Lieferanten und interne Stakeholder zu unterstützen.

Ihre Aufgaben

• Qualifizierung und Weiterentwicklung von Lieferanten
• Lieferanten- und Prozessaudits
• Verantwortlich für die Durchführung und Planung der erforderlichen internen und externen Audits
• Verwaltung des integrierten Managementsystems einschließlich Dokumentenmanagement gemäß ISO 9001 / 14001 / 45001 / 50001 sowie ISO/TS 22163
• Verantwortung für die Aufrechterhaltung der Normkonformität des Systems und dessen Weiterentwicklung
• Erstbemusterung bei Lieferanten und deren Freigabe / Ablehnung
• Nachverfolgung von Beanstandungen und Korrekturmaßnahmen aufgrund von Audits oder anderen Abweichungen
• Erstellung von Audit-, Besuchs- und Kennzahlenberichten
• Bewertung von Lieferanten gemeinsam mit der Einkaufsabteilung
• Schnittstelle zwischen Einkaufs- und Qualitätsabteilung und dem Lieferanten
• Effiziente und effektive Anwendung von Qualitätstechniken
• Unterstützung bei der Kontrolle relevanter Qualitätsziele und Leistungskennzahlen; inkl. Verwaltung eines Qualitäts-Dashboards
• Mitwirkung am Produktentwicklungsprozess (z. B. FMEA, PLP, QPA, EMPB) in direkter Abstimmung mit Einkauf und Entwicklung.

Ausbildung und Erfahrung

• Technischer Hochschulabschluss oder abgeschlossene Berufsausbildung, mehrjährige Berufserfahrung und Qualifikationen im Qualitätsmanagement
• Umgang mit Lieferanten und Kunden
• Kenntnisse im Maschinenbau und/oder in der Metallverarbeitung
• Erfahrung und Kenntnisse in speziellen Verfahren (Gießen, Schmieden, Schweißen, Beschichten)
• Fähigkeit zum Lesen von Zeichnungen, gutes technisches Verständnis von Produkten und Prozessen
• Grundlagen der Betriebswirtschaft
• Fundierte Kenntnisse der Normen ISO 9001 / ISO 14001
• Kenntnisse der Normen IAFT 16949 oder ISO/TS 22163 sind von Vorteil
• Kenntnisse und Erfahrungen in der Planung, Durchführung und Bewertung von Audits und Erstmustern
• Bereitschaft zu umfangreichen Reisetätigkeiten ist Voraussetzung

Unser Angebot und Ihre Vorteile

• Eine verantwortungsvolle und ergebnisorientierte Aufgabe in einem international tätigen Industrieunternehmen
• Wir bieten ein motivierendes Umfeld, das Ihnen Wachstum innerhalb des Unternehmens ermöglicht, und investieren in Ihre Aus- und Weiterbildung
• Familiäre und angenehme Arbeitsatmosphäre mit moderner Ausstattung
• Attraktives, wettbewerbsfähiges Vergütungspaket
• 30 Tage Jahresurlaub

Bewerbungsverfahren

Klingt das nach dem idealen Umfeld für Sie?

Zögern Sie nicht und bewerben Sie sich jetzt, um Ihre Karriere bei Trelleborg zu gestalten. Bewerben Sie sich jetzt mit einer englischen Version Ihres Lebenslaufs.

Trelleborg ist ein Arbeitgeber, der Chancengleichheit fördert, und wir sind stolz auf die Vielfalt unserer Mitarbeiter. Wir schätzen die besonderen Erfahrungen und Fachkenntnisse, die Menschen mit unterschiedlichem Hintergrund in unser Unternehmen einbringen. Die Fähigkeit, bahnbrechende Technologien zu entwickeln, ist einer unserer wichtigsten Vorteile, und unsere Mitarbeiter machen dies möglich.

Wir bieten ein motivierendes Umfeld, das Wachstum innerhalb des Unternehmens ermöglicht und gleichzeitig in die Aus- und Weiterbildung unserer Mitarbeiter investiert.

Wir begrüßen Bewerbungen von Menschen aller Nationalitäten, Religionen, Geschlechter, sexuellen Identitäten, unterschiedlichen Alters und mit Behinderungen.

Bei Trelleborg gestalten unsere Mitarbeiter die Industrie von innen heraus (#shapingindustryfromtheinside).

About the job

As a Quality Engineer, you will play a key role in ensuring supplier performance, product quality, and compliance with international standards. Your responsibilities will include qualifying and developing suppliers, conducting internal and external audits, and managing the integrated management system across ISO 9001, 14001, 45001, 50001, and ISO/TS 22163 frameworks. You will oversee supplier evaluations, initial sample approvals, and corrective actions while maintaining strong collaboration between purchasing, development, and quality departments.

In this role, you’ll apply your technical expertise in mechanical or metalworking processes such as casting, forging, welding, and coating to drive continuous improvement across the supply chain. You’ll monitor quality targets through metrics and dashboards, contribute to product development activities like FMEA and EMPB, and ensure all processes meet compliance and performance expectations. This is a dynamic role that requires strong analytical ability, a proactive mindset, and willingness to travel extensively to support suppliers and internal stakeholders.

Your Responsibilities

• Qualification and further development of suppliers
• Supplier and process auditing
• Responsible for the implementation and scheduling of the necessary internal and external audits
• Management of the integrated management system including document management according to ISO 9001 / 14001 / 45001 / 50001, as well as ISO/TS 22163
• Responsible for maintaining the standard conformity of the system and its further development
• Initial sampling at suppliers and their approval / rejection
• Follow-up of complaints and corrective measures due to audits or other deviations
• Preparation of audit, visit and key figure reports
• Evaluating suppliers together with the purchasing department
• Interface between the purchasing and quality department and the supplier
• Efficient and effective use of quality techniques
• Support in the control of relevant quality targets and performance metrics; incl. management of a quality dashboard
• Participation in the product development process (e.g. FMEA, PLP, QPA, EMPB) in direct coordination with Purchasing and Development.

Education and Experience

• Technical university degree or completed vocational training, several years of professional experience and qualifications in quality management
• Dealing with suppliers and customers
• Knowledge of mechanical engineering and/or metalworking
• Experience and knowledge of special processes (casting, forging, welding, coating)
• Ability to read drawings, good technical understanding of products and processes
• Fundamentals of business administration
• In-depth knowledge of ISO 9001 / ISO 14001
• Knowledge of IAFT 16949 or ISO/TS 22163 is an advantage
• Knowledge and experience in planning, conducting, and evaluating audits and initial samples
• Willingness to travel extensively is a prerequisite

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
• 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 colleges.

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

At Trelleborg our people are #shapingindustryfromtheinside

Trelleborg Medical Solutions is seeking a Quality Engineer to join their team. 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.

Responsibilities:

• 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.
• 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.
• Participates in customer and ISO audits.

Qualifications:

Required:
• 4 year degree in quality, engineering or  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

As a valued team member with Trelleborg, you will enjoy:

Competitive compensation: Plus, bonus opportunities!
Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement, and more!
Clean work environment: Enjoy working in a very clean and climate-controlled environment every day!
Greater opportunity for impact: You will impact the production of life-saving devices.
Growth and advancement: Join a global company that loves to promote from within and allows for advancement.

Salary information:  $72-91k based on experience 

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%

Benefits include:

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

Application: 

Apply here!

Last Application Date 12/13/2025

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 colleges.

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

At Trelleborg our people are #shapingindustryfromtheinside

At Trelleborg Sealing Solutions, we are seeking a Quality Planner for Initial Sampling to join our dynamic team! This outstanding role places you at the forefront of ensuring our products meet world-class standards from the very first sample. If you demonstrate attention to detail and a dedication to quality, this is the perfect opportunity for you to excel in an ambitious and collaborative environment.

🎯 Your Responsibilities:

• Coordinate and clarify customer requirements, including contract review, in collaboration with Sales departments
• Govern quality-relevant requirements with producers to determine feasibility
• Build initial sample reports, requirement lists, and certificate templates according to customer requirements
• Accurately measure physical dimensions, weights, and other critical parameters using appropriate tools, such as optical measuring devices, calipers, micrometers, and scales
• Conduct visual inspections for defects or deviations to ensure initial product samples meet quality standards and customer requirements
• Ensure complete and accurate initial sample reporting for successful customer submission and approval

✅ What We’re Looking For:

• Technician or comparable vocational training
• Proven experience in manufacturing, lab work, or quality control is preferred
• Familiarity with initial sampling processes, such as PPAP and PPF
• Knowledge of quality assurance techniques
• Experience in various material measurement methods, with a preference for elastomers and plastics
• Knowledge in the area of elastomers and PTFE/PU is preferred
• Strong computer skills, including MS Office, CAQ systems, and ERP systems
• Proficient in English (spoken and written)

Our benefits for You:

• Modern multicultural work environment that fosters diversity and inclusion
• Several weeks of induction training to familiarize you with our company, contacts, and structures
• An exciting, multifaceted, and interdisciplinary field of activity that keeps you engaged
• Extensive product training to ensure you are well-equipped to succeed
• Flexible office hours with remote work opportunities for a better work-life balance

Why join Us?

• Opportunity to drive real impact in a fast-paced manufacturing environment
• To be a part of a new and innovative team
• Career growth and professional development opportunities
• Be part of a company that values continuous improvement and sustainability
• Food vouchers to enjoy lunch or dinner on us
• Multisport card for fitness, swimming, and wellness activities
• Performance-related bonuses (additional variable payment)
• Comprehensive health insurance coverage

Ready to take the next step in your career? Send us your CV in English and become a key player in crafting our production excellence! You will be contacted by our HR team in Germany.