C
Cagents6mo ago
CQV Project Manager
SwitzerlandFull TimemidOperationsOtherProject ManagerProject & Program Management
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Quick Summary
Key Responsibilities
* Provide cGMP leadership and guidance to integrate and deliver CQV services for life sciences clients. * Manage mid-sized to large projects involving process equipment and clean utilities,
Requirements Summary
* Provide cGMP leadership and guidance to integrate and deliver CQV services for life sciences clients. * Manage mid-sized to large projects involving process equipment and clean utilities,
Technical Tools
OperationsOtherProject ManagerProject & Program Management
Project Manager – Switzerland / EU
Drive life-changing therapies to market while building your career as an owner.
At CAI, every employee is an owner. Since 1996, we’ve grown to 850+ professionals worldwide by living our values: integrity, teamwork, respect, and a relentless focus on doing what’s right for our clients and society.
As a Project Manager, you’ll lead mid- to large-scale life sciences projects, guiding commissioning, qualification, and validation (CQV) activities from design to delivery. You’ll collaborate with recognized subject-matter experts and play a critical role in ensuring safe, compliant, and efficient project execution.
What you’ll do:
* Provide cGMP leadership and guidance to integrate and deliver CQV services for life sciences clients.
* Manage mid-sized to large projects involving process equipment and clean utilities, including start-up and commissioning.
* Lead design reviews, equipment installation, and site acceptance activities.
* Write, review, and approve CQV documents in compliance with 21 CFR standards. Documents may include SOPs, impact assessments, risk assessments, specifications (URS/FRS/DDS), FATs, SATs, IQ/OQ/PQs, validation protocols, and commissioning test plans.
* Support onsite and offsite activities such as FATs, SATs, system walkdowns, and execution phases.
* Manage all aspects of C&Q, including change controls, contractor and vendor coordination, document control, and punch list management.
* Allocate project resources efficiently and track progress to ensure deliverables meet schedules.
What we’re looking for
Must have:
* BS or MS in a relevant science or engineering field, or equivalent.
* 8+ years of commissioning, qualification, validation, and compliance experience in life sciences or regulated industries.
* Strong technical knowledge of EU and global regulatory requirements and proficiency in cGMP standards.
* Experience managing CQV deliverables across one or multiple projects.
* Skilled in planning and tracking project activities and schedules.
* Strong interpersonal skills to form relationships with internal teams and external clients.
* Excellent problem-solving, communication, and customer-focused skills.
* Familiarity with life science manufacturing processes, including biotech, aseptic fill/finish, OSD, or gene therapy.
* Flexibility to travel domestically and internationally as required.
Nice to have:
* Experience with complex or multi-site project coordination.
* Prior experience leading international project teams.
What’s in it for you
* Employee ownership: your success drives collective success.
* Career investment: professional training, certifications, and development opportunities built into your role.
* Global exposure: collaborate on projects across Switzerland and beyond.
* Collaborative culture: team-first environment where successes are celebrated together.
Are you CAI Ready?
Join us and become a key player in delivering the future of advanced medicine!
#LI-JD1
Listing Details
- Posted
- October 2, 2025
- First seen
- March 26, 2026
- Last seen
- April 24, 2026
Posting Health
- Days active
- 29
- Repost count
- 0
- Trust Level
- 23%
- Scored at
- April 24, 2026
Signal breakdown
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External application · ~5 min on Cagents's site
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CQV Project Manager