10 no experience required English-speaking jobs in Mendrisio

logging, metrics, tracing) Testing (unit and/or integration) Kubernetes Nice to have points: Working experience

validations for LAL testing, sterility testing, and bioburden testing Carry out sampling and analyses required ... Biotechnology, Pharmaceutical Chemistry and Technology (CTF), or related disciplines At least 5 years of experience

validations for LAL testing, sterility testing, and bioburden testingCarry out sampling and analyses required ... Biotechnology, Pharmaceutical Chemistry and Technology (CTF), or related disciplinesAt least 5 years of experience

At least 10 years of previous experience in regulatory affairs with a focus on the US projects (NDA, ... responsibilities Definition and execution of US regulatory strategies, providing strategic oversight and, if required

Previous experience with non-EU registrations is an advantage. ... Previous experience with finished pharmaceutical medicinal products is mandatory. ... Proven experience with EU registration procedures (MRP/DCP MAAs, variations, extensions, and renewals ... Minimum of 4–5 years of experience in Regulatory Affairs within the pharmaceutical industry focused on ... Applications limited to experience in medical devices, food supplements, cosmetics, or APIs will not

Previous experience with non‑EU registrations is an advantage. ... Previous experience with finished pharmaceutical medicinal products is mandatory. ... Proven experience with EU registration procedures (MRP/DCP MAAs, variations, extensions, and renewals ... Minimum of 4–5 years of experience in Regulatory Affairs within the pharmaceutical industry focused on ... Applications limited to experience in medical devices, food supplements, cosmetics, or APIs will not

Practical experience applying QbD principles and/or DoE in drug product development. ... Strong experience with late-stage development, scale-up and commercial product support. ... At least 10 years of post-degree work experience, including at least 5 years in Pharma R&D context.

Experience in small molecules and small peptides constitute a plus. ... Minimum of 10 years of experience in a similar role in the pharmaceutical industry. ... Proven experience in drafting and revising clinical sections of regulatory documents, clinical trials

At least 3 years of post-degree work experience, including at least 2 years in a Pharmaceutical Laboratory

Experience in small molecules and small peptides constitutes a plus. ... Minimum of 10 years of experience in a similar role in the pharmaceutical industry. ... Proven experience in drafting and revising clinical sections of regulatory documents, clinical trials