Pharmaceutical Quality Control (m/f/d) (Chemist)

BS Wutow GmbHFrankfurt am MainEURESpublished 07/01/2026
Machine translation — original language: German.Show original

Other job titles: Degree in Biology; Degree in Food Chemistry

Job Description: On behalf of our client, a leading global pharmaceutical company, we are looking for

you as:

QC Analytical Expert (gn) | Pharmaceutical Quality Control

Your tasks:

  • Ensuring the timely execution and GMP-compliant

documentation of quality testing of pharmaceutical active ingredients and

finished products in accordance with AMWHV, AMG and the valid marketing authorization documents

  • Implementation and support of laboratory-specific quality assurance systems,

including OOS/OOT management, Change Controls, Deviations and Failure

Investigations

  • Technical support during authority inspections and internal

quality audits by providing analytical expertise

  • Planning, coordination and evaluation of verification, validation and

transfer studies in compliance with internal and external guidelines

  • Monitoring and implementation of occupational safety as well as health and

environmental protection regulations (HSE) within your own area of responsibility

  • Participation in cross-functional project teams

Your profile:

  • You have a successfully completed degree in the natural sciences,

whether as a Chemist (m/f/d), Pharmacist (m/f/d), Biochemist (m/f/d) or

in a related field of study such as Biology (m/f/d) or Food Chemistry

(m/f/d)

  • In addition, you bring at least 3 years of professional experience in

pharmaceutical quality control

  • Sound GMP knowledge as well as familiarity with regulatory

requirements (AMWHV, AMG)

  • Structured, independent and proactive way of working with a

strong sense of responsibility

  • Quick comprehension and high commitment
  • Proficient use of MS Office
  • Good written and spoken English skills

Your benefits:

  • Flexible working hours with autonomy over working hours at 37.5 hours per week
  • Employment in an established, international pharmaceutical environment with high

quality standards

  • Classification according to AT L2-2 based on the Equal Pay model
  • Varied activity with project responsibility and

cross-departmental tasks

  • Opportunity to actively contribute your expert knowledge to authority inspections and audits

Additional information: Requirements for the applicant: Basic knowledge: Occupational safety, accident prevention, quality management, biochemistry, international pharmaceutical standards (e.g. GLP, GMP), manufacturing and control management (AMG)

Contact person

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