[ref. d56768202] T2507 - Bioanalysis Scientist (Maternity Cover - temporary)

At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases. As a privately-owned Swiss biopharmaceutical company, we’re driven by science, but above all, by the people behind every treatment — the patients and their families.

Through our unique “development only” model, we bring forward promising therapies and transform them into treatments that can reach those who need them most, faster.

We are currently looking for a motivated and collaborative professional to join our Translational Medicine department based at our Headquarters in Lausanne, Switzerland as

Bioanalysis Scientist 100%

(Maternity Cover - temporary)

You will play a key role in advancing Debiopharm’s innovative therapeutics by shaping and executing bioanalytical strategies. Your work will directly support the progression of drug candidates through nonclinical and clinical development, in line with regulatory standards and internal R&D objectives.

• Contribute to the bioanalytical strategy defined in the Translational Medicine Development Plan for assigned programs.
• Support the generation of high-quality bioanalytical data to inform key development decisions.
• Design, plan, and manage bioanalytical studies for small molecules and biologics, including:

1. Method development, qualification, validation, transfer, and cross-validation
2. Nonclinical sample analysis for PK, toxicokinetics, and ADME (exploratory and regulatory)

• Lead bioanalytical phases of clinical studies:

1. Contribute to protocols, IBs, ICFs, lab manuals, SAPs, and CSRs
2. Implement and oversee sample analysis (PK, , biomarker, co-medication, etc.)
3. Ensure data transfer and documentation align with GCP/GCLP standards

• Oversee timelines and budgets for assigned activities
• Manage outsourcing to CROs or academic partners (RFP preparation, contract review, and budget negotiation…)
• Collaborate with Regulatory Affairs to prepare documentation (IND, IMPD, briefing books)
• Identify patentable innovations and work with Legal to support IP filings
• Support licensing activities through scientific evaluations and due diligence
• Contribute to publications, posters, oral presentations, and scientific communications

• PhD or equivalent in Life Sciences, Pharmaceutical Sciences, or Bioengineering, with experience in translational research (postdoc experience valued)
• Solid understanding of GCP, GCLP, GLP, ICH guidelines, and animal welfare standards (training available if needed)
• Strong analytical mindset and excellent data interpretation skills
• Effective communicator in both written and spoken English
• Collaborative team player with strong interpersonal skills
• Familiarity with project management is a plus
• Being part of a company where innovation, collaboration, and impact aren’t just values — they’re how we work every day
• Partner with teams across disciplines, at the forefront of oncology and anti-infective development
• An inclusive and respectful workplace — proud to be Equal-Pay certified
• Grow in a culture that values people, purpose, and performance
• A chance to grow, share, and shape the future of healthcare

What to Expect in the Recruitment Process:

If your application is selected, you’ll be invited to interviews with Talent Acquisition and the Hiring Manager via Teams, followed by a panel interview and reference checks. Communication is handled via Workable—check your spam folder for emails from *@outbound.workable.com.

Please contact our HR Department prior to submitting any profiles. We cannot accept unsolicited applications from agencies or recruiters.