T2507 - Bioanalysis Scientist (Maternity Cover - temporary)
T2507 - Bioanalysis Scientist (Maternity Cover - temporary)
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Salary Not Disclosed
1 Vacancy
Job Description
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 were 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 Debiopharms 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:
- Method development qualification validation transfer and cross-validation
- Nonclinical sample analysis for PK toxicokinetics and ADME (exploratory and regulatory)
- Lead bioanalytical phases of clinical studies:
- Contribute to protocols IBs ICFs lab manuals SAPs and CSRs
- Implement and oversee sample analysis (PK biomarker co-medication etc.)
- 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 were looking for someone who shares our commitment to science with purpose.
Requirements
- 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
Benefits
- Being part of a company where innovation collaboration and impact arent just values theyre 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 youll 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 Workablecheck your spam folder for emails from *@.
Please contact our HR Department prior to submitting any profiles. We cannot accept unsolicited applications from agencies or recruiters.
Employment Type
Temp
