Pre-clinical Manufacturing Senior Scientist
Pre-clinical Manufacturing Senior Scientist
Lonza
Basel, Switzerland
Key responsibilities:
- Lead pre-clinical parenteral drug product manufacturing campaigns for therapeutic modalities, including biologics, small molecules, peptides, oligonucleotides, (bio)conjugates, and viral vectors
- Manufacturing non-GMP drug product samples for supportive stability studies and preclinical use (e.g. GLP tox studies) applying aseptic working techniques
- Ensure the accurate maintenance and qualification of equipment, safety, and health protection following lab and safety instructions and all cGMP regulations
- Document data (Batch Record) following applicable lab procedures, current documentation practices and aligning with data integrity standards. Evaluate results and summarize in reports
- Collaborate with other teams within pharmaceutical development, analytical development, the DP manufacturing network, and QC and quality assurance
Key requirements:
- Degree in Chemistry, Biochemistry, Pharmaceutical Sciences or equivalent experience as lab technician or pharmaceutical technologist
- Experience as a research/technical assistant in the pharmaceutical or chemical industry (preferred in an aseptic environment related to parenteral or biological manufacturing or development)
- Experiences with High potent molecules and with qualification of new equipment is an asset
- Good documentation skills in creating Batch manufacturing documentation
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