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Lausanne, Waadt, Schweiz Debiopharm VollzeitAbout DebiopharmDebiopharm is a leading biopharmaceutical company dedicated to the development of innovative therapies for oncology and infectious diseases. Our mission is to improve patient outcomes and quality of life through the development of high-quality medicines.Job SummaryWe are seeking a highly skilled Senior Scientist to join our Pharmaceutical...
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Lausanne, Waadt, Schweiz Debiopharm VollzeitAbout DebiopharmDebiopharm International SA is a privately-owned Swiss biopharmaceutical company dedicated to research in oncology and infectious diseases. Our mission is to develop innovative therapies to improve patient outcomes and quality of life.Job SummaryWe are seeking a Senior Scientist, Analytical Development and Quality Control to join our...
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Lausanne, Waadt, Schweiz Debiopharm VollzeitAbout DebiopharmDebiopharm is a biopharmaceutical company based in Switzerland, dedicated to research in oncology and infectious diseases to improve patient outcomes and quality of life. Our main activities include drug development, manufacturing, and digital health investment. We aim to develop innovative therapies targeting high unmet medical needs, acting...
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Lausanne, Waadt, Schweiz Debiopharm VollzeitAbout DebiopharmDebiopharm is a biopharmaceutical company based in Switzerland, dedicated to research in oncology and infectious diseases to improve patient outcomes and quality of life. Our main activities include drug development, manufacturing, and digital health investment. We aim to develop innovative therapies targeting high unmet medical needs.Job...
Senior Materials Scientist
vor 2 Monaten
We are seeking an experienced Sr. Material Scientist to join our team at Michael Page Switzerland.
About the RoleAs a Sr. Material Scientist, you will be responsible for delivering high-quality particulate studies and extractables & leachables studies for our client, a leading manufacturer of medical devices in Switzerland.
Key Responsibilities- Deliver particulate studies as per USP 788, counting, sizing, and identifying.
- Deliver extractables & leachables studies as per ISO on new design Ceres Mod2DK with new tubing force and DK IT.
- Develop and implement test procedures and protocols.
- Manage and report on test results.
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
To be successful in this role, you will need:
- A Master's degree in Materials Science, Polymer Science, Biomedical Engineering, or a related field.
- At least 10 years of experience in a similar field.
- Well-founded knowledge and practical experience of relevant regulations (ISO13485, FDA 21 CFR Part 820).
We offer a long-term temporary project opportunity (11 months) with a reputable client in the medical device industry.