Quality

Within Quality you define and specify activities, processes, or standards to fulfill the quality requirements for services, materials, components, or products.

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Jobbtitel
Plats
Ansök senast
Jobbtitel: Summer Quality Intern
On-site
Plats: USA - Fort Wayne, IN
Ansök senast: 2024-03-13

Summary of the Role:

Work with the AeroHub Quality team to inspect and plan for future project needs related to rubber, PTFE and plastic components for the Aerospace industry.

Tasks and Responsibilities: 

  • Perform basic inspection of products to ensure they are compliant to the print 
  • Draft quality plans for new projects
  • Other duties as assigned to support the business 

Education and Experience:

  • HS Diploma or GED required 
  • Actively pursuing an engineering degree 
  • Fluent in MS office 
  • Proficient with measuring devices (Caliper, Micrometer, Pi Tape) 

Competencies: 

  • Excellent oral and written skills
  • Ability to read and interpret drawings 
  • Attention to detail and quality conscientious 
  • Must be responsible, self-motivated and function well in a team environment 
  • Ability to work effectively to meet objectives 

Application: 

Apply Here 

Last Application Date 3/13/2024

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

Jobbtitel: Quality Inspector
On-site
Plats: USA - Chalfont, PA
Ansök senast: 2024-04-08

Tasks and Responsibilities:

  • Perform inspection of all incoming material and assist in final inspections using Military and Industrial standards
  • Perform mechanical inspection using micrometers, calipers, comparators and various other inspection tools.
  • Identify non-conformances of finished components through established inspection methods
  • Perform First Article inspections
  • Input inspection results into spreadsheets and databases
  • Enter data into MRP system (Purchase orders, sales orders)

Education and Experience:

  • High School Diploma or equivalent required.
  • Associates degree or higher a plus.
  • Ability to read and interpret mechanical drawings, industry specifications, and work instructions are required.
  • Experience with precision measurement or CNC equipment beneficial, (calipers, micrometers, CMM, etc.) strongly preferred.
  • Work experience in production or quality environment preferred.
  • Ability to lift and move up to 25 lbs occasionally

Competencies:

  • Ability to learn, understand, and effectively apply sampling plans
  • Excellent communication and interpersonal skills
  • Working knowledge of windows-based software programs (Excel, Word, etc.)
  • Attention to detail and quality conscious
  • Must be responsible, self-motivated, and function well in a team environment

Application: 

Apply Here 

Last Application Date 4/8/2024

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.

Jobbtitel: Quality Assurance Specialist
On-site
Plats: DNK - Helsingør
Ansök senast: 2024-03-15

Er du passioneret omkring kvalitetssikring? Har du lyst til at arbejde med interne audits, afvigelses- og reklamationsbehandling? Og besidder du stærke engelskkundskaber, kommunikationsevner og et positivt mindset? Så kunne du meget vel være vores nye kollega hos TSS Helsingør.

Plats: USA - Northborough, MA
Ansök senast: 2024-03-10

Summary of Role

Trelleborg Sealing Solutions Health & Medical Business Unit, located in Northborough MA, is looking for a Quality Manager to join our growing team! This position is responsible for the leadership and management of personnel and resources to ensure adherence and compliance to US H&M Trelleborg Quality Management System (QMS) processes and policies.

Tasks & Responsibilities

  • Reports on the performance of the Quality System (QS) for Management Review meetings and any need for improvement; prepares agenda and establishes records for Management Review meetings.
  • Plans, manages, and controls programs and procedures that maintain an acceptable level of product quality as established by various federal, state, customer, and company requirements, including quality of purchased material, in-process material, and finished goods. 
  • Provides leadership and guidance in implementing action for quality programs and for controlling quality costs.
  • Serves as Management Representative for the QS and represent the Company in all audits.
  • Ensures that processes needed for the QMS are established, implemented and maintained.
  • Ensures the promotion of awareness of regulatory and customer requirements throughout the organization.
  • Ensures establishment and maintenance of site regulatory registrations.
  • Supports, coordinates and oversees site customer-requested, external regulatory, and internal audits.
  • Provides oversight and ensure compliance of QS support elements for the site QMS: Internal audits, Training, Document Control, Supplier Quality Management, Complaint Management, CAPA, NC Management, and Calibration Systems
  • Reviews and approves of QS documents.
  • Maintains higher level quality system documents including Quality System Manual (QSM), Work Instructions (WI), Standard Operating Procedures (SOP) related to Quality.
  • Ensures that processes needed for the quality management system are established, implemented and maintained.
  • Manages the internal audit program including planning, scheduling, review and approval of audits.
  • Has responsibility for product quality issues (i.e., supplier evaluations and approvals, inspection, test and measurement, nonconforming product, etc.)
  • Supports Material Review Board (MRB) activities for nonconforming product.
  • Has responsibility for the Corrective and Preventive Action (CAPA) system, complaint handling system, training program, documentation control system, and quality records.
  • Supports validation activities and approvals, as needed.
  • Provides quality training for personnel as needed.
  • Maintains compliance to customer Quality Agreements, as required.
  • Other activities as assigned/needed

Education & Experience

  • 4-year degree in manufacturing or industrial engineering, quality assurance, regulatory affairs, science or related field
  • 5+ years of experience in Quality Assurance and/or Regulatory Affairs
  • Auditor certificate or equivalent experience
  • 3 years supervisory experience

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
  • Demonstrate senior leadership abilities with the capacity to accept responsibility and delegate authority.
  • Good managerial, analytical, organizational, and communication skills.
  • Math and computer literate.
  • Understanding of basic statistics.
  • Competent knowledge of equipment and manufacturing operations.
  • Thorough understanding of Validations (including equipment qualification (IQ/OQ), process validation, test method validation, computer systems and software validations, etc.); understanding of process capability.
  • Thorough understanding of medical device quality system standards, specifications, laws, and regulations, i.e., FDA Quality System Regulations (21 CFR Part 820) and Current Good Manufacturing Practices (21 CFR Part 210 & 211), ISO 13485, and other industrial standards as applicable.
  • Correctable normal reading distance vision.
  • Knowledge of product drawings, specifications as well as measuring and testing devices.
  • Comprehensive working knowledge of applicable corporate policies and quality system documentation.
  • Ability to maintain a professional and respectful relationship with coworkers and company.

Application

Last Application Date: March 9, 2024

Apply Here

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Plats: DEU - Lindau
Ansök senast: 2024-06-28

Zum nächstmöglichen Zeitpunkt suchen wir für unseren Standort in Lindau am Bodensee Sie als Leitung Qualitätssicherung / Leiter Qualität & Auditwesen (m/w/d).

Sie übernehmen eigenverantwortlich

  • Sorgt dafür, dass die ihm unterstellten Mitarbeiter optimal in Bezug auf ihre Fähigkeiten eingesetzt werden
  • Ist sowohl für die strategische Ausrichtung der Abteilung nach Gesichtspunkten der Wirtschaftlichkeit und Erfordernissen aus Betrieb und Kundensicht, als auch für eine reibungslose Zusammenarbeit aller internen und externen Schnittstellen verantwortlich
  • Erstellt Auswertungen und analysiert Verbesserungsmöglichkeiten betreffend aller Aktivitäten, die sich mit der Optimierung von Herstellprozessen, Ausbringung, Bestandsoptimierung und Ressourcennutzung beschäftigen
  • Stellt die periodische Erstellung des Management Reports und daraus sich ergebenden Maßnahmen sicher
  • Leitet interne und externe Auditierungsprozesse ein, was deren Planung und Durchführung betrifft, unter Berücksichtigung der Lieferanten- und Kundenvorgaben
  • Beachtet den effizienten Einsatz von Ressourcen und den Schutz der Umwelt im Bereich Arbeitsschutz / ISO 14001 gemäß der gesetzlichen Vorgaben & BG Richtlinien bei Audits 
  • Wirkt bei der Weiterentwicklung des Managementsystems (IMS) mit, um sicherzustellen, dass das Managementsystem bei geplanten Änderungen funktionsfähig bleibt

Dafür bringen Sie mit

  • Abgeschlossenes technisch-orientiertes Studium sowie Weiterbildung Qualitätsmanager und/oder Auditor
  • mehrjährige Berufserfahrung in einer Leitungsfunktion im Bereich Qualität in der Industrie sowie in QM/QS und entsprechende ISO-Zertifizierungen (EN9100, ISO9001, ISO14001, ISO50001)
  • Organisationsstärke, argumentative Durchsetzungskraft und ein Blick fürs Wesentliche
  • Wirtschaftliches und strategisches Denken und Handeln
  • Teamplayer mit einem hohen Maß an Kundenorientierung und Führungskompetenz
  • sehr gute Deutsch- und Englischkenntnisse

Wir bieten Ihnen

  • Ein abwechslungsreiches Aufgabengebiet in einem wachsenden Unternehmen
  • Flexible Arbeitszeit mit "mobile Work" Anteil
  • Corporate Benefits, 30 Tage Urlaub im Jahr + extra Urlaub durch Zukunftstage sowie eine attraktive Vergütung nach Tarifvertrag "Chemie West"
  • Leben und Arbeiten in einer der schönes Urlaubsregionen Deutschlands

Nehmen Sie Ihre Karriere jetzt in die Hand!

Wir freuen uns auf Ihre Bewerbung unter Angabe Ihrer frühestmöglichen Verfügbarkeit und Ihrer Gehaltsvorstellung.

Bei Fragen steht Ihnen das Recruiting Team sehr gerne zur Verfügung:

Robert Karsten, Personalreferent Tel: +49 172 1524884

#ShapingIndustryfromtheInside

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

Jobbtitel: Manager Quality Assurance
On-site
Plats: IND - Bangalore
Ansök senast: 2024-03-31

Are you a talent looking to build business skills, gain experience, and take on exciting challenges? Grow your career with Trelleborg and start shaping the industry from the inside.

About the Job

We are looking for Quality Manager with experience in handling customer complaints, providing quality planning for automotive & aerospace projects, and implementing quality systems, such as ISO, TS, AS, in SCM India.

Take advantage of this rare opportunity to partner with one of the leading seal manufacturers in the world! Leverage your  experience, grow in a role and enjoy the support and stability of an organization that has been in business for over 100 years.

About the Ideal Candidate

  • Bachelor degree in engineering as preferred.
  • Between 5 to 6 years of experience in Quality or engineering position in international manufacturing environment
  • Experience in automotive industry will be a plus.
  • Knowledge of Quality Standards such as ISO9000 is necessary, familiarity with TS
  • Handling supplier audits and onboarding.
  • Experience in Customer portal Management on Quality aspects

Scope of your role

  • Planning & Implementation of APQP Process across newly developed Parts.
  • Good communication skill in oral and written English.
  • Knowledge of CAQ.
  • Knowledge on quality systems, such as ISO, TS,AS, in SCM India
  • Preparing PPAP Documents
  • Handling 3rd party quality complains and process audit
  • Reviewing quality agreement with customers and suppliers, and process supplier audit based on TSS Quality Standard
  • Perform Internal process Audits, FIFO Audits, 5s Audits & Suppliers Audits

Application Process

Apply before March 15 for immediate consideration. We will reach out to you, to get more information about you, once you apply.

Ashwini Venkatesh,

You may reach out, on ashwini.venkatesh@trelleborg.com

Jobbtitel: Quality Engineer
On-site
Plats: USA - Aurora, OH
Ansök senast: 2024-03-01

Want to join a global organization and enhance your career? Trelleborg in Aurora, Ohio is seeking a Quality Engineer to join their dynamic team.

Jobbtitel: Quality Manager
On-site
Plats: USA - Menomonie, WI
Ansök senast: 2024-04-05

​​Imagine leveraging your Quality Mgmt experience while working for one of the leading contract manufacturers in the world. Seize this rare opportunity to be part of an exciting, Healthcare and Medical Business Unit with the support and stability of an organization that has been in business for over 100 years.

This position is responsible for the leadership and management of personnel and resources to ensure adherence and compliance to US H&M Trelleborg Quality Management System (QMS) processes and policies.​

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

  • Competitive compensation:
  • Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement, and more!
  • 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.

 

Education and Experience: 

Required:

  • 4 year degree in manufacturing or industrial engineering, quality assurance, regulatory affairs, science or related field
  • 5+ years of experience in Quality Assurance and/or Regulatory Affairs
  • Auditor certificate or equivalent experience
  • 3 years supervisory experience

Tasks and Responsibilities:

  • Reports on the performance of the Quality System (QS) for Management Review meetings and any need for improvement; prepares agenda and establishes records for Management Review meetings.  
  • Plans, manages, and controls programs and procedures that maintain an acceptable level of product quality as established by various federal, state, customer, and company requirements, including quality of purchased material, in-process material, and finished goods.   
  • Provides leadership and guidance in implementing action for quality programs and for controlling quality costs.  
  • Serves as Management Representative for the QS and represent the Company in all audits. 
  • Ensures that processes needed for the QMS are established, implemented and maintained. 
  • Ensures the promotion of awareness of regulatory and customer requirements throughout the organization. 
  • Ensures establishment and maintenance of site regulatory registrations. 
  • Support, coordinate and oversee site customer-requested, external regulatory, and internal audits. 
  • Provides oversight and ensure compliance of QS support elements for the site QMS: Internal audits, Training, Document Control, Supplier Quality Management, Complaint Management, CAPA, NC Management, and Calibration Systems 
  • Reviews and approves of all QS documents. 
  • Maintains higher level quality system documents including Quality System Manual (QSM), Work Instructions (WI), Standard Operating Procedures (SOP) related to Quality. 
  • Ensures that processes needed for the quality management system are established, implemented and maintained. 
  • Manages the internal audit program including planning, scheduling, review and approval of audits. 
  • Has responsibility for product quality issues (i.e., supplier evaluations and approvals, inspection, test and measurement, nonconforming product, etc.) 
  • Supports Material Review Board (MRB) activities for nonconforming product. 
  • Has responsibility for the Corrective and Preventive Action (CAPA) system, complaint handling system, training program, documentation control system, and quality records. 
  • Supports validation activities and approvals, as needed.  
  • Provides quality training for personnel as needed. 
  • Maintains Quality Agreements (as required) with customers. 

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   
  • Demonstrate senior leadership abilities with the capacity to accept responsibility and delegate authority. 
  • Good managerial, analytical, organizational, and communication skills. 
  • Math and computer literate. 
  • Understanding of basic statistics. 
  • Competent knowledge of equipment and manufacturing operations.  
  • Thorough understanding of Validations (including equipment qualification (IQ/OQ), process validation, test method validation, computer systems and software validations, etc.); understanding of process capability. 
  • Thorough understanding of medical device quality system standards, specifications, laws, and regulations, i.e., FDA Quality System Regulations (21 CFR Part 820) and Current Good Manufacturing Practices (21 CFR Part 210 & 211), ISO 13485, and other industrial standards as applicable. 
  • Correctable normal reading distance vision. 
  • Knowledge of product drawings, specifications as well as measuring and testing devices.  
  • Comprehensive working knowledge of applicable corporate policies and quality system documentation. 
  • Ability to maintain a professional and respectful relationship with coworkers and company. 

 

Apply here!

 

Plats: DEU - Lindau
Ansök senast: 2024-05-30

Zum nächstmöglichen Zeitpunkt suchen wir für unseren Standort in Lindau einen 

Mitarbeiter Qualitätssicherung (m/w/d) 

Sie unterstützen die Abteilung Qualität bei

  • Überwachung und Sicherstellung der Einhaltung der Qualitätsstandards in der Produktion
  • Aufgaben im Bereich Wareneingangskontrolle sowie Unterstützung bei Fertigungsüberprüfung
  • Sperren von Produkten im Wareneingang und in Produktion
  • Erstellen von Dokumentationen wie FAI, SID, Prüfberichte Stellungnahme
  • Reklamationsbearbeitung

Dafür bringen Sie mit

  • Berufserfahrung im Bereich Qualitätssicherung, wünschenswert sind Q-Scheine 
  • Ausgeprägtes Qualitätsbewusstsein
  • Sicherer Umgang mit MS Office
  • Erfahrung mit den spezifischen Materialnormen und Produkten
  • gute Deutsch-und Englischkenntnisse

Wir bieten Ihnen

  • Ein abwechslungsreiches Aufgabengebiet in einem wachsenden Unternehmen
  • Flexible Arbeitszeit mit "mobile Work" Anteil
  • Corporate Benefits, 30 Tage Urlaub im Jahr + extra Urlaub durch Zukunftstage sowie eine attraktive Vergütung nach Tarifvertrag "Chemie West"
  • Leben und Arbeiten in einer der schönes Urlaubsregionen Deutschlands

Nehmen Sie Ihre Karriere jetzt in die Hand!

Wir freuen uns auf Ihre Bewerbung unter Angabe Ihrer frühestmöglichen Verfügbarkeit und Ihrer Gehaltsvorstellung.

Bei Fragen steht Ihnen das Recruiting Team sehr gerne zur Verfügung:

Robert Karsten, Personalreferent Tel: +49 172 1524884

#ShapingIndustryfromtheInside

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

Jobbtitel: Quality Engineer
Plats: GBR - Cadley Hill
Ansök senast: 2024-02-29

Trelleborg Sealing Solutions Cadley Hill, is looking to appoint a Quality Engineer. This role will report to the Senior Quality Engineer and will work as part of the Quality Team. The successful person will be responsible for ensuring internal and external quality requirements are fully adhered to during all stages of the production process.  

Key Duties & Responsibilities

Support Company Requirements

  • All Quality Control and Quality Assurance activities are supported and continually reviewed in relation to improvements in efficiency and cost reduction.
  • Assist in maintaining accredited systems required by the business and its customers i.e. AS9100, ISO14001, Ensure compliance and adherence to all system requirements including AS9100, Health & Safety, Risk Assessments, COSHH, Environmental, ISO: 14001, and housekeeping.
  • Ensure that all goods manufactured and received by the Company comply with Customer drawings and specifications.
  • Compliance with continuous improvement of key measures i.e. quality, returns.
  • Support the production and engineering in all Quality related aspects of manufacturing and new product introduction and targets for rejects.
  • Carry out timely assessments of sub-contractors.
  • Support production, engineering, sales, suppliers, and Customers in the development of quality standards to fulfil both Company and Customer requirements.
  • Ensure that manufacturing and quality control specifications and procedures are readily available and adhered to.
  • Ensure timely reviews of procedural effectiveness are conducted, including recommendations for any necessary amendments.
  • Manage the internal calibration and audit schemes to the standards set out at the time.
  • Ensure compliance with applicable environmental legislation within the job holder’s responsibilities.

Support Employee Requirements

  • Educate and promote in all areas of quality control.
  • Ensure that personnel are fully conversant and compliant with the content and application of manufacturing and quality control specifications.
  • Appraisal performance of team members to develop and improve individuals.
  • Assist in the induction process regarding Quality related initiatives.
  • Advising all persons in other functions where influence on product quality can be affected by the knowledge of Quality Assurance and control concepts, methods, and procedures.

Performance Measures

  • Key facility/business measures and targets will be set and communicated as part of the business planning process, to include quality and productivity.
  • Undertake an appraisal as part of individual personal development.
  • Obtain and maintain associated Quality accreditations.
  • Assist in the reduction of customer returns.
  • Continually assess and further develop manufacturing standards documentation for Quality purpose.

Relationships

  • Support, communicate, influence, and control the quality standards in force at that time.
  • Assume the role of promoter and teacher to all personnel on quality related issues.
  • Close working relationships with relevant teams must be developed and maintained.
  • Inter departmental team working to ensure targets are met.
  • Ensure good working relationships are maintained with both customers and suppliers.

Knowledge / Experience

  • Ability to communicate and develop skills effectively at all levels within the business.
  • Experience of presenting to teams.
  • Experience of modern techniques/systems within Quality and methods of working.
  • Preferable knowledge and experience in the Aerospace industry.
  • Computer literate and familiar with relevant software packages including Quality related systems.
  • Holding Quality approved qualification/certification.

Personal Qualities

  • Good written, verbal, and organisational skills.
  • Team player.
  • Ability to interface at all levels of business.
  • Commitment, drive, determination, assertiveness, and adaptability.
  • Relevant Quality technical skills and ability.