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Scientist imp in-process controls

Basel
Coopers Group GmbH
EUR 30’000 - EUR 80’000 pro Jahr
Inserat online seit: 14 Januar
Beschreibung

Talent Acquisition Consultant at Coopers Group AG - Life Science
Location: Basel

Contract end date: 30/09/2026

The Manufacturing Analytics team is responsible for process analytics during the production of chemically synthesized Active Pharmaceutical Ingredients (APIs). This includes reaction monitoring and analysis of isolated intermediates in strict compliance with cGMP, safety, and regulatory requirements .

We are looking for a motivated, hands‑on analytical specialist to actively contribute to a wide range of challenging and meaningful tasks within a GMP manufacturing environment.

Key Responsibilities

Provide technical guidance to laboratory colleagues on planning, execution, and completion of analytical tests for in‑process and intermediate analytics.

Ensure full compliance with cGMP, safety standards, and regulatory requirements in all analytical activities.

Review analytical methods and specifications transferred from Analytical Development .

Implement and establish new analytical methods into routine manufacturing analytics .

Create, review, and maintain high‑quality analytical documentation with a strong focus on data integrity and timelines .

Take ownership of deviations, non‑conformances, and investigations, ensuring timely and compliant processing.

Actively support quality assessments and root cause investigations.

Contribute to process optimization and continuous improvement, including the development of lean and efficient workflows.

Must Haves

Master’s degree in Natural Sciences or completed Chemical Laboratory Technician apprenticeship with extensive relevant professional experience (no PhD).

Advanced German (C1) and English skills (written and spoken).

Minimum 3 years of hands‑on experience with analytical techniques relevant to chemical manufacturing processes.

Strong expertise in physical‑chemical analytical methods, especially chromatography .

Solid knowledge of GMP principles and pharmaceutical regulatory requirements.

High awareness of data integrity, documentation quality, and compliance .

Seniority level: Associate

Employment type: Contract

Job function: Science

Industries: Pharmaceutical Manufacturing and Biotechnology Research

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