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CQV Documentation & IV Lead — Life Sciences

Job in New Bedford, Bristol County, Massachusetts, 02740, USA
Listing for: Project Delivery Partners Pte Ltd
Full Time position
Listed on 2026-11-01
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Regulatory Compliance Specialist, Quality Engineering
Salary/Wage Range or Industry Benchmark: 120000 - 150000 USD Yearly USD 120000.00 150000.00 YEAR
Job Description & How to Apply Below
A consultancy in life sciences is seeking a Document and IV Execution Lead to enhance CQ documentation processes. The successful candidate will implement and manage critical documentation using the Kneat platform. Responsibilities include leading a team, adhering to project milestones, and ensuring compliance with pharmaceutical regulations. Strong experience in Quality Assurance and team training is essential. English fluency and a Bachelor's degree in a related field are required.
We have an opening for a CQV Documentation & IV Lead — Life Sciences in MA, United States within Management & Operations. If your experience matches this role, we encourage you to apply. All applications are reviewed carefully by our team. The position is based in MA, United States. This opportunity is part of our work in Management & Operations.

The advertised compensation is 120..
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