Pharma Validation Engineer: CQV & Field Verification
CAI
Bridgewater (MA)
On-site
USD 72,800 - 80,100
Full time
14 days+
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Benefits offered by this job
Comprehensive Health Insurance
24 days Paid Time Off
15% Company Contribution (US Only)
Company paid Life Insurance
Company paid Long Term Disability
Job summary
A professional services company is seeking a Validation Engineer in Bridgewater, Massachusetts. This role focuses on technical responsibilities including developing documentation for CQV activities and executing protocols. Candidates should have a Bachelor’s degree in science or engineering with 2–4 years of experience in a regulated industry. Full-time position with competitive compensation and benefits.
Qualifications
2–4 years of experience in commissioning and qualification in a regulated industry.
Familiarity with pharmaceutical manufacturing processes.
Preferred experience in utilities and equipment startup.
Responsibilities
Develop documentation for CQV activities.
Write and execute protocols for technical responsibilities.
Manage small teams in document development.
Skills
Documentation skills
Project management
Technical writing
Troubleshooting
Education
Bachelor’s degree in science or engineering
Tools
ISPE Baseline Guide 5
Job description
A professional services company is seeking a Validation Engineer in Bridgewater, Massachusetts. This role focuses on technical responsibilities including developing documentation for CQV activities and executing protocols. Candidates should have a Bachelor’s degree in science or engineering with 2–4 years of experience in a regulated industry. Full-time position with competitive compensation and benefits.