) for IT systems in Life Sciences, with a deep understanding of regulatory frameworks (GXP, GMP, GAMP 5, FDA 21 CFR Part 11, EU...
Job Description: We are looking for candidate over 5 years of experience with Veeva Vault QMS, demonstrating a strong understanding of quality management processes and a proven track record in support roles, handling technical issues and u...
Responsibilities: As a Regulatory Affairs Coordinator, you will be part of the compliance department supporting various teams Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation sy...
Responsibilities: Coordination and maintenance of CQV. Review of Protocols. Execution of approved protocols including generating/closure of all protocol deficiencies (deviation). Generation of maintenance plans within CMMS. Generation...