Beschreibung
***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.*