Scientist IMP In-Process Controls

Scientist IMP In-Process Controls (m / f / d)- : chemical manufacturing / cGMP / analytical techniques / Chromatography / English / German

Project : For our client based in Basel, we are looking for a Scientist IMP In-Process Controls (m / f / d)

Background :

The department is responsible for the process analytics during the manufacturing of chemically synthesized Active Pharmaceutical Ingredients (APIs). This includes reaction controls and the analysis of isolated intermediates, strictly adhering to cGMP, safety, and regulatory requirements. We are seeking motivated individuals to actively contribute to a variety of engaging tasks within our Manufacturing Analytics Team.

The Perfect Candidate : The ideal candidate is a hands-on analytical expert with a Master's degree and at least three years of experience mastering physical-chemical techniques like chromatography within a cGMP environment. They bridge the gap between development and production by seamlessly implementing new methods while ensuring rigorous data integrity, documentation accuracy, and proactive management of deviations. Fluency in both German and English is essential for this role, as the candidate must navigate a dynamic matrix organization to mentor colleagues and drive cross-functional process optimizations.

Tasks & Responsibilities :

• Provide essential guidance to laboratory colleagues on the planning, execution, and conclusion of analytical tests for in-process and intermediate analytics
• Ensure strict compliance with cGMP (current Good Manufacturing Practice), safety standards, and regulatory requirements across all analytical activities
• Thoroughly review analytical methods and specifications originating from the analytical development department
• Implement and establish new analytical methods from development into the production-accompanying control process
• Generate and meticulously check analytical documentation, maintaining a high focus on quality, data integrity, and meeting defined deadlines
• Take initiative and ownership in the timely processing and documentation of deviations and non-conformances
• Actively participate in crucial quality assessments and investigations to uphold product integrity
• Contribute to process optimization by assisting in the development and implementation of lean, efficient working processes

Must Haves :

Reference No. : 924665

Role : Scientist IMP In-Process Controls

Industry : Pharma

Location : Basel

Workload : 80 - 100%

Start : Asap

Duration : 6++ Months

Deadline : 13 / 01 / 2026

If this position has piqued your interest, please send us your complete resume. If this position does not quite match your profile and you would like to receive other positions directly, you can also send us your resume via this ad or to jobs[at]itcag[dot]com.

Contact us for more information about our company, our positions, or our attractive payroll-only program : +41 41 760 77 01.

About us :

ITech Consult is an ISO 9001 : 2015-certified Swiss company with offices in Germany and Ireland. ITech Consult specializes in placing h j4id10018616a j4it0102a j4iy26a