Jobdescription
For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Scientist IMP In-Process Controls.
General Information :
- Start date : ASAP
- Latest start date : 01.03.2026
- Planned duration : 30.09.2026 with the possibility of extension
- Contract : temporary contract via Randstad
- Workplace : Basel
- Workload : 80-100%
- Home Office : not possible
- Team : 8 People
- Department : Analytical Research & Development (MMDCA)
- Working Hours : Standard
About the job :
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 analyticsEnsure strict compliance with cGMP (current Good Manufacturing Practice), safety standards, and regulatory requirements across all analytical activitiesThoroughly review analytical methods and specifications originating from the analytical development departmentImplement and establish new analytical methods from development into the production-accompanying control processGenerate and meticulously check analytical documentation, maintaining a high focus on quality, data integrity, and meeting defined deadlinesTake initiative and ownership in the timely processing and documentation of deviations and non-conformancesActively participate in crucial quality assessments and investigations to uphold product integrityContribute to process optimization by assisting in the development and implementation of lean, efficient working processesMust Haves :
You hold a Master's degree or university degree in Natural Sciences, or have completed a Chemical Laboratory Technician apprenticeship with extensive, relevant professional experience. Please note candidates with a PhD degree are considered overqualified.Min. 3 year proven, hands-on experience with a variety of analytical techniques relevant to chemical manufacturing processes.Confident with physical chemical analytical techniques (Chromatography)Strong commitment to quality and a high level of awareness regarding data integrity and documentation accuracy.Sound knowledge of GMP principles (Good Manufacturing Practice) and regulatory requirements in the pharmaceutical industryTo perform effectively in this role, advanced German (C1) & English language skills are requiredAble to demonstrate excellent organizational skills and the ability to effectively manage and prioritize multiple tasks in a dynamic environmentProactive team player with a strong sense of responsibility and a high willingness to learn and adaptYou are capable of thriving in an agile matrix organization and successfully contributing to shared, cross-functional objectives.Sounds interesting? Apply Now! We look forward to receiving your application.