Responsibilities: Participate in the development of the CMC regulatory strategy for small molecules. These submissions include health authority briefing packages, IND/CTA, NDA, and MAA regulatory filings. Prepare and review CMC submissio...
Job Description: We are seeking a highly organized and adaptable professional to support our medical device development and quality operations. This role is ideal for a jack of all trades. someone who enjoys creating order, connecting cr...
Job Description: Our client, a leading Life Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring project work. Respons...
Responsibilities: Manage end-to-end delivery of data management services concurrently for single/multi-service projects with little-to-no guidance, ensuring quality deliverables on time and within budget to customer satisfaction. Provide...
Roles & Responsibilities: Develop new processes, assess and document new and existing processes of high-volume automated Injection Moulding. Implement and evaluate changes to existing processes designed to improve product quality, produc...
Roles & Responsibilities: Strong Experience with Test Method Validation and MSAs. Strong Risk Management Experience (Experience in Risk Documentation: Write, review, approve multiple quality records includes but not limited to: Design ...
Responsibilities: The Principal Regulatory Affairs is responsible for regulatory strategy development and execution for high-complexity diagnostics specifically Companion Diagnostics and digital pathology in the clinical oncology environm...