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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland · Hybrid
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Basel, Basel-City, Switzerland · On-site
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Basel, Basel-City, Switzerland • On-site
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Lead and manage pharmaceutical development projects for drug entities within Development Bioanalytics across various pre-clinical phases. Ensure the successful delivery of work packages, including analytical testing results, reports, and compliance with ISO standards.
A PhD in Biochemistry, Biotechnology, Analytical Science, or a related Life Science subject is required. Candidates must have bio-pharmaceutical industry experience and proficiency in analytical methodologies and cGMP documentation.
The actual location of this job is in Basel Stücki, Switzerland.
For our successful Drug Product (DP) focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the (Associate) Principal Scientist Bioanalytics position.
An agile career and a dynamic work culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
Responsible for leading and managing pharmaceutical development projects of drug entities within Development Bioanalytics (DevBA) from various customers and in different pre-clinical development phases
Accountable for the successful delivery of work packages for assigned projects. This includes on-time close out/authorization and provision of required analytical testing results, documents and reports (e.g. establishment, pre-validation, non GMP batch release, non GMP stability), leading investigation in compliance with ISO standards
Accountable to independently and proactively address risks and resolve issues of deliverables on time for mitigation, including good communication to all stakeholders potentially affected
Represents DevBA in Lonza internal project meetings and customer meetings for complex topics as SME (Subject Matter Expert)
Supports the relevant stakeholder (e.g. APL) to maintain all relevant planning tools
PhD Degree in Biochemistry, Biotechnology, Analytical Science or related Life Science subject is required
Experience working within the Bio-Pharmaceutical industry as a research or technical assistance
Knowledgeable in several analytical methodologies, including mammalian cell culture, preparation of primary cells, ligand-binding assays (ELISA, SPR and CBA)
Good knowledge of cGMP documentation
Excellent communication skills, team player, flexible and able to manage complexity
Fluent in English is a must. Any other languages are a plus
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Making the Medicines of Tomorrow
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow. Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs. For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
Offices: Muenchensteinerstr. 38, Basel, 4002, CH · 8830 Biggs Ford Road, Walkersville, MD 21793, US · 35 Tuas South Ave 6, SG, 637377, SG · 228 Bath Road, Slough, Berkshire SL1 4DX, GB · Rottenstrasse 6, Visp, VS 3930 , CH
There are currently 44 open manufacturing positions in Basel, Switzerland listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Roche, Exyte Central Europe GmbH, Novartis, Lonza, Jet Aviation, among others. Browse the listings above to see every active employer.
Yes — 7 of the 44 open manufacturing positions offer remote or hybrid work (1 remote, 6 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
