CQV Documentation & IV Lead — Life Sciences

Project Delivery Partners Pte Ltd; Massachusetts; On-site; USD 120,000 - 150,000; Full time

Job summary

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.

Qualifications

• Minimum 10 years of experience in Quality Assurance (QA), Qualification and Validation.
• Strong knowledge of Installation Verification, Commissioning, and Validation.

Responsibilities

• Implement and support CQ related Documentation.
• Manage lifecycle CQ Documentation within the Kneat platform.
• Support recruitment and training of new team members.

Skills

Quality Assurance (QA)

Qualification and Validation

Team Leadership

Pharmaceutical Manufacturing

English fluency

Education

Bachelor's degree in a related field

Job description

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.