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Eurofins

Global lab testing and analytics network

Quality Assurance Specialist - Quality Assurance & Compliance

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeKonstanz, GermanyNo salary listedIn-person

About the Job

Requirements

  • Completed scientific or pharmaceutical vocational training or an equivalent qualification.
  • Professional experience in the pharmaceutical industry or a GMP-regulated environment is advantageous.
  • Knowledge and ideally practical experience implementing the requirements of a GMP-compliant quality management system.
  • Knowledge of handling quality-relevant processes such as deviations, CAPAs, and OOS/OOE events is advantageous.
  • Understanding of operational processes in a pharmaceutical or analytical laboratory environment is advantageous.
  • Ability to work independently, structurally, and to meet deadlines within the assigned area of responsibility.
  • Strong service and solution orientation, with a good understanding of priorities and efficient workflows.
  • Reliability, communication skills, and ability to work in a team.
  • Flexibility, commitment, and initiative.
  • Good written and spoken German and English skills.

Responsibilities

  • Support the maintenance, development, and optimization of the quality management system and help ensure GMP compliance.
  • Provide operational support to the laboratory area on quality-related and GMP-related matters.
  • Review quality-related documents, including equipment qualifications, internal changes, and other GMP-relevant documentation.
  • Participate in processing quality-relevant events, including deviations, OOS/OOE events, and CAPAs, within the assigned area of responsibility.
  • Track and verify measures and ensure timely follow-up.
  • Create, revise, and review documents and documentation templates within the assigned area of responsibility.
  • Take ownership of defined QA work packages and process them in a structured and timely manner.
  • Monitor quality-relevant processes, including the qualification status of equipment and facilities.
  • Advise site employees on quality assurance and GMP matters.
  • Provide timely support in clarifying quality-related questions between Quality Assurance and the laboratory.
  • Support efficient processing and prioritization of QA tasks based on operational requirements.
  • Work closely with colleagues in Quality Assurance, the broader quality function, and the laboratory.
  • Contribute to reliable QA coverage during operationally required times, particularly in the afternoon.
  • Actively contribute to the continuous improvement, standardization, and efficient design of QA processes and interfaces.
  • Support customer audits and regulatory inspections.
  • Support self-inspections.

Desired Qualifications

  • Professional experience in the pharmaceutical industry or a GMP-regulated environment.
  • Practical experience implementing GMP quality management system requirements.
  • Experience handling deviations, CAPAs, or OOS/OOE events.
  • Understanding of operational processes in a pharmaceutical or analytical laboratory environment.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size
10,001+
Company stage
IPO
Headquarters
Luxembourg
Founded
1987

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