Scientific Associate

vor 1 Woche


Basel, Schweiz Datalynx AG Vollzeit

For our client, a well-known pharmaceutical company in Basel, we are looking for a Scientific Associate (M/F/d) in Pharmaceutical Analytics.

**Background**

This position plays a crucial role in supporting the development and quality assurance of pharmaceutical products through advanced analytical techniques. The role involves working within a regulated environment, ensuring compliance with industry standards such as GMP and GLP, while collaborating with cross-functional teams. It provides an opportunity to contribute to the advancement of innovative therapies by delivering reliable analytical results and maintaining high-quality standards.

**General Information***:

- Start date: ASAP
- Duration: 12 months
- Extension: Possible
- Workload: 100%
- Work location: Basel

**Tasks & Responsibilities***:
- Plan, organize, execute, and document scientific experiments for Drug Substances (DS) and Drug Products- Develop, validate, and transfer analytical methods as well as conduct stability and release testing- Ensure adherence to Good Documentation Practices (GDP) and Good Laboratory Practices (GLP) in all laboratory activities- Document and submit raw data in appropriate data systems (e.g., LIMS)- Evaluate and interpret results, including investigations of SST failures, OOX/deviations, and change controls- Responsible for assigned laboratory areas (e.g., management of chemicals, reagents, consumables, samples, and equipment)- Proactively communicate critical topics to management and relevant project team members- Ensure compliance with Key Quality Indicators (KQI) and Key Performance Indicators (KPI)- Actively contribute to achieving team and organizational goals- Work according to applicable SOPs, GMP, GLP, QM, HSE, and ISRM guidelines

**Must Haves***:
- Bachelor's or Master's degree in Life Sciences (e.g., analytical/organic chemistry, pharmacy, pharmaceutical development) or equivalent qualification- At least 3 years of relevant experience in a GMP environment- Strong understanding of regulatory and quality requirements- Solid scientific background and excellent communication and presentation skills- Experience in scientific/technical writing- Fluent in English (spoken and written)

**Contact**:
Jan Schmitz-Elsen
Team Lead Talent Acquisition
+41 79 425 10 45



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