\\n Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see .

Analytical Project Manager QC (f/m/d)

We are looking for an experienced Analytical Project Manager, who suits well our highly motivated and dynamic team by knowledge and character. We are seeking for someone who not only complements our team capabilities, but also provides additional input.

Your Tasks

• Working in interdisciplinary teams as responsible Analytical Project Manager for peptide and oligonucleotide NCE projects representing Analytical Operations in CMC sub-teams for assigned projects
• Lead and manage all analytical activities including but not limited to release, stability testing, characterization of the API, method development and validation, setting of specifications, know-how transfer
• Evaluate analytical results, draw relevant conclusions, and communicate effectively to the customer and across organizational interfaces
• Support trouble shooting within own and broader area of responsibility
• Lead the transfer of know-how or procedures to other departments, sites, or external partners and vice versa
• Assess and consolidate resource needs and timelines for projects
• Direct interaction with different internal departments on all sites and with our global customers
• Close collaboration with our Business Development group to align with customer needs

Your Profile

• University degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, any related field or equivalent technical education and industrial experience
• At least 5 years of experience working in analytical development or QC preferably with cGMP experience; ideally in peptide or oligonucleotide analysis
• Capable of interpreting and presenting complex analytical data and providing solutions with a hands-on mentality externally and internally
• Excellent communication and presentation skills
• Solid analytical knowledge and understanding of CMC development
• Sound scientific project management and matrix leadership skills
• Ability to manage multiple interfaces and tight timelines
• Knowledge of CMC requirements for regulatory filings, understanding of regulatory expectations
• Strong command of English and German (at least C1, both oral and written)
• Sound knowledge of MS Office incl. MS Project

We offer an exciting and challenging job in a dynamic and growing environment, which guarantees diversity and personal advancement. If this information draws your attention and if you enjoy working and communicating across disciplines, we look forward to receiving your complete dossier.

Interested? Please submit your complete application through our recruitment system.\\n \\n \\n \\n \\n \\n

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