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.

Your Mission.

• 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

More than a checklist of skills, we-re looking for someone who shares our commitment to science with purpose.

• 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.