CSV Associate role at Pharmaron, UK
Pharmaron is hiring a detail-oriented Computer System Validation (CSV) Associate in Hoddesdon. Join our team to support GMP informatics platforms and laboratory software while building your career in life sciences jobs.
Job Details:
- Job Title: Computer System Validation (CSV) Associate
- Location: Hoddesdon, Hertfordshire
- Support R&D and QC laboratories as System Admin on 20+ systems
- Back-up System Admin for Agilent OpenLab CDS and Revvity Signals (E3) ELN
- Assist in validation activities for COTS systems
- Draft and maintain validation documentation (IA, URS, FS, IQ, OQ, PQ, QP, TRM, QSR, etc.)
- Conduct GMP Risk & Impact Assessments and Data Integrity Risk Assessments
- Manage user accounts, system changes, upgrades, deviations, and investigations
- Participate in internal audits and external inspections
About Pharmaron :
Pharmaron is a fast-growing, innovative company offering contract research services to leading pharmaceutical companies. Based in Hoddesdon, our campus features state-of-the-art GMP facilities for API development, oral solid dose manufacture, formulation development, and process chemistry. Pharmaron fosters a collaborative, team-focused environment, providing excellent opportunities for life sciences jobs growth and professional development.
Educational Requirements for CSV Associate role:
- Bachelor’s or Master’s degree in Life Sciences, Computer Science, or related fields
- 0–2 years of experience in IT or CSV support in pharmaceutical or similar industries
- Understanding of SDLC, QMS, GMP, ALCOA+, and Data Integrity principles
Key Responsibilities for CSV Associate role:
- Support R&D and QC laboratories as System Admin on multiple systems
- Assist as back-up System Admin on Agilent OpenLab CDS and Revvity Signals (E3) ELN
- Support validation activities and draft related documentation
- Perform GMP Risk & Impact Assessments and Data Integrity Risk Assessments
- Collaborate with IT and QA to manage system changes and investigations
- Conduct periodic system reviews and decommissioning activities
- Provide technical support for validated systems and participate in audits
- Act as liaison between business users and IT for system-related issues
Skills Required for CSV Associate role:
- Knowledge of laboratory systems, instruments, and associated software
- Familiarity with IT systems (Client-Server environment, Windows, LAN/WAN, data backup/restore)
- Some coding experience (e.g., Python) is desirable
- Strong attention to detail, communication, and teamwork skills
Benefits of the Role:
- Competitive salary and comprehensive employee benefits
- Exposure to cutting-edge GMP laboratory systems and software
- Opportunities for growth, training, and professional development
- Supportive, collaborative team environment
- Work on impactful life sciences projects at Pharmaron
