Site Quality Source Technician
Johnson & Johnson Services, Inc
Tuttlingen, Germany
vor 10 Tg.

Job Description

Johnson & Johnson, through its operating companies, is the world's most comprehensive and broadly-based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets.

We strive to provide scientifically sound, high quality products and services to help heal, cure disease and improve the quality of lifeThe Site Quality Source Technician is responsible for the execution of the Product Release Certification and Monitoring program for JJMD (Johnson & Johnson Medical Devices) products manufactured by the Strategic Collaborator (SC).

He / she ensures that the SC has a clear understanding and the ability to execute against JJMD’s product release requirements.

Main Responsibilities & Duties : Executes the Lot Release Certification and Monitoring Program for JJMD products according to established procedures.

Training of SC personnel performing product release of JJMD sterile and non-sterile products as part of the Certification Program.

Perform certification, re-certification, and decertification of SC product release personnel.Monitor SC’s product release performance through the review of a sample of Device History Records (DHR) in accordance to approved sampling plans.

Develop work plans to meet certification and monitoring weekly requirements including any necessary adjustments based on production schedules, holidays, and sampling plan revisions.

Generate Nonconformance Reports (NCR) resulting from the product release monitoring process as per applicable approved procedures.

Partnerships with the SC on the timely resolution of product release monitoring related NCRs and any other discrepancies found during the DHR monitoring process.

Track lot release certification and monitoring data in order to measure program effectiveness and to identify trends. Report data analysis, including any negative trend, to his / her direct supervisor.

QualificationsBachelor s degree in Quality management or engineering preferred.3- 5 yearsof related experience.Strongcommunication skills, quality-

oriented mindset & team player.Independence,flexibility, attention to detail and service minded are required.Fluent inGerman and good English skills.

The well-being and development of our employees are central aspects of our company creed. Individuals who would like to fully realize their potential as part of our international, innovation-

driven corporate family and who aspire to have challenging work, will find that our company provides just the right conditions.

We consider intensive initial training, further education that is tailored to our employees' work and excellent opportunities for development -

both nationally and internationally - to be just as essential as a good work-life balance, attractive compensation and above-

average employee benefits. One aspect that distinguishes our company is the large number of measures we have to support our trainees and promote career development in ways that are also compatible with family life.

Primary LocationGermany-Baden Württemberg-Tuttlingen-OrganizationSynthes Tuttlingen (7131)Job FunctionQuality SystemsRequisition ID1905736819W

Johnson & Johnson, through its operating companies, is the world's most comprehensive and broadly-based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets.

We strive to provide scientifically sound, high quality products and services to help heal, cure disease and improve the quality of life

The Site Quality Source Technician is responsible for the execution of the Product Release Certification and Monitoring program for JJMD (Johnson & Johnson Medical Devices) products manufactured by the Strategic Collaborator (SC).

He / she ensures that the SC has a clear understanding and the ability to execute against JJMD’s product release requirements.

  • Executes the Lot Release Certification and Monitoring Program for JJMD products according to established procedures.
  • Training of SC personnel performing product release of JJMD sterile and non-sterile products as part of the Certification Program.
  • Perform certification, re-certification, and decertification of SC product release personnel.
  • Monitor SC’s product release performance through the review of a sample of Device History Records (DHR) in accordance to approved sampling plans.
  • Develop work plans to meet certification and monitoring weekly requirements including any necessary adjustments based on production schedules, holidays, and sampling plan revisions.
  • Generate Nonconformance Reports (NCR) resulting from the product release monitoring process as per applicable approved procedures.
  • Partnerships with the SC on the timely resolution of product release monitoring related NCRs and any other discrepancies found during the DHR monitoring process.

  • Track lot release certification and monitoring data in order to measure program effectiveness and to identify trends. Report data analysis, including any negative trend, to his / her direct supervisor.
  • Bachelor s degree in Quality management or engineering preferred.
  • 3- 5 yearsof related experience.
  • Strongcommunication skills, quality-oriented mindset & team player.
  • Independence,flexibility, attention to detail and service minded are required.
  • Fluent inGerman and good English skills.
  • The well-being and development of our employees are central aspects of our company creed. Individuals who would like to fully realize their potential as part of our international, innovation-

    driven corporate family and who aspire to have challenging work, will find that our company provides just the right conditions.

    We consider intensive initial training, further education that is tailored to our employees' work and excellent opportunities for development -

    both nationally and internationally - to be just as essential as a good work-life balance, attractive compensation and above-

    average employee benefits. One aspect that distinguishes our company is the large number of measures we have to support our trainees and promote career development in ways that are also compatible with family life.

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

    Equal Employment Opportunity PostersIf you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please complete the form below.

    If you’d like to view a copy of the company’s affirmative action plan, please complete this form.This site is governed solely by applicable U.

    S. laws and governmental regulations. Please see our Privacy Policy. Use of this site constitutes your consent to application of such laws and regulations and to our Privacy Policy.

    Your use of the information on this site is subject to the terms of our Legal Notice. You should view the News section and the most recent SEC Filings in the Investor section in order to receive the most current information made available by Johnson & Johnson Services, Inc.

    Contact Us with any questions or search this site for more information.

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