Quality Assurance Associate (m/f/d) at cLEcta
04103 Leipzig, , Germany -
Full Time


Start Date

Immediate

Expiry Date

01 Oct, 25

Salary

0.0

Posted On

02 Jul, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Iso, Natural Sciences, Gmp, Communication Skills

Industry

Pharmaceuticals

Description

YOU WANT TO START A CAREER IN QUALITY ASSURANCE AND YOU ENJOY WORKING WITH METICULOUS CARE AND SEE BOTH POTENTIAL AND ADDED VALUE IN CONTINUOUS PROCESS IMPROVEMENT? THEN YOU’VE COME TO THE RIGHT PLACE!

As Quality Assurance Associate (m/f/d) you will expand our QA team and support us in all aspects of operational quality assurance in the manufacture of biotechnological products. You will work within our existing quality management system according to ISO 9001 and the guidelines of Good Manufacturing Practice (GMP) for pharmaceutical excipients and food hygiene standards.

YOUR SKILLS:

  • A degree in natural sciences (e.g. biotechnology, pharmacy or comparable)
  • At least 2 years of professional experience in quality assurance, ideally in pharmaceutical production (regulated environment)
  • Knowledge of ISO 9001 and Good Manufacturing Practice (GMP) is an advantage
  • Precise and goal-oriented way of working with a high level of initiativeStrong team player and excellent communication skills
  • Very good German and English language skills (both oral and written)
    Convinced? Then please apply by specifying your salary expectations and your desired stating date.

How To Apply:

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Responsibilities
  • You will support quality assurance processes in the production of biotechnological products.
  • You will assist in coordinating and documenting the processing of deviations and changes.
  • You will participate in coordinating preventive and corrective actions and monitoring their implementation.
  • You will create and review standard operating procedures.
  • You will provide support in processing customer complaints.
  • You will also be responsible for reviewing manufacturing, shipping, and testing specifications.
  • You will actively participate in continuous optimization processes and prepare quality audits as part of a team.
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