What are the responsibilities and job description for the Computer Systems Validation (CSV) Supervisor position at AL Solutions?
🔍 Computer Systems Validation (CSV) Supervisor | Portsmouth, NH
I'm currently supporting a global life sciences organisation looking to add an experienced Computer Systems Validation professional to their growing Quality team.
This is an excellent opportunity for someone with a strong background in CSV within a cGMP-regulated environment who enjoys leading validation activities, driving compliance initiatives, and partnering with cross-functional teams on critical projects.
Key areas of focus:
- Computer Systems Validation lifecycle ownership
- Change Controls, Deviations & CAPAs
- 21 CFR Part 11 & GAMP compliance
- Gap Assessments & Remediation Planning
- Quality Systems & Regulatory Compliance
- Analytical & Manufacturing Computerised Systems
We're looking to speak with professionals who have:
• 3 years of Computer Systems Validation experience
• Experience working within pharmaceutical, biotech, or medical device environments
• Strong knowledge of cGMP regulations, 21 CFR Part 11 and GAMP guidelines
• The ability to work independently while collaborating across Quality, Engineering and Manufacturing functions
Relocation assistance available
If you're interested in learning more, or know someone who could be a fit, please get in touch for a confidential conversation.
#CSV #ComputerSystemsValidation #Validation #QualityAssurance #PharmaJobs #BiotechJobs #LifeSciences #GMP #GAMP5 #QualitySystems #Hiring #NewHampshire