Jobs in Coventry, United Kingdom
Computer System Validation Consultant
Rephine Limited
Remote Residential Conveyancer – 75% Fees, Flexible
FDR Law Limited
Residential Conveyancer – Self-Employed Consultant
FDR Law Limited
Residential Conveyancer – Self-Employed Consultant
FDR Law Limited
Discover more opportunities than anywhere else. Find more jobs nowRemote Freelance Statistician & Python AI Tutor
Mindrift
Statistician with Python - Freelance AI Trainer
Mindrift
Connect with headhunters to apply for similar jobsRemote ML Engineer — AI Data Trainer (Sequencing Logs)
Alignerr Corp.
Machine Learning Engineer - AI Data Trainer
Alignerr Corp.
Onboarding & Monitoring Analyst (6-Month) Remote
InvestEngine Limited
Onboarding and Transaction Monitoring Analyst (6-Month Fixed-Term Contract)
InvestEngine Limited
Volunteer Digital Content Creator for Digital Inclusion
Wavemaker
EdTech Co-Founder / CEO (100 % remote) (m/f/d)
TAFFin.Tech
EdTech Founder & CEO — 100% Remote, Scale to €100M
TAFFin.Tech
Field Service Engineer – UK Hospitals (Midlands, SW & Wales)
Getinge Group
Freelance Book Ghostwriter – Fiction & Nonfiction
Reedsy Limited
Field Service Engineer - Midlands, South West and Wales
Getinge Group
Computer System Validation Consultant
Job summary
A leading consultancy in Life Sciences is seeking a remote CSV Consultant (L2) based in the UK. This role involves providing senior-level support to pharmaceutical clients, ensuring compliance with GMP and GxP standards. Ideal candidates should have over 5 years of validation and CSV project experience, excellent communication skills, and a degree in Life Sciences or Engineering. The position offers competitive compensation, flexible hours, and opportunities for professional growth in a dynamic team.
Benefits
Qualifications
- 5+ years in validation and CSV projects in a regulated environment.
- Strong understanding of GMP, GxP, and regulatory standards.
- Experience in consulting or client-facing roles is a plus.
Responsibilities
- Lead and execute CSV and validation activities.
- Ensure compliance with GMP, GxP, and Data Integrity.
- Act as the main client contact for validation topics.
- Review and approve validation documentation.
- Guide and mentor junior consultants.
- Work with clients in a consultancy environment.
- Manage project timelines and deliverables.
Skills
Education
Tools
At Rephine, we set the standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, and China, we support Pharmaceutical, Biotech, and Medical Device supply chains globally.
We are looking for a Consultant (L2) – CSV to join our team remotely from the UK. This role is ideal for professionals with experience in validation and CSV projects who want to provide senior-level support to pharmaceutical clients, acting as a trusted consultant and technical reference.
Provide senior-level support to pharmaceutical clients in CSV, validation, and potentially other GMP-related projects, ensuring compliance and delivering high-quality consultancy services.
- Lead and execute CSV and validation activities (planning, risk assessments, IQ/OQ/PQ, reporting).
- Ensure compliance with GMP, GxP, and Data Integrity requirements.
- Act as the main client contact for validation topics.
- Review and approve validation documentation.
- Provide guidance and mentoring to junior consultants.
- Collaborate with client stakeholders in a consultancy environment.
- Manage project timelines and deliverables to meet client expectations.
- 5+ years in validation and CSV projects in the pharmaceutical or regulated environment.
- Strong understanding of GMP, GxP, and regulatory expectations (EU GMP Annex 11, FDA 21 CFR Part 11, GAMP5).
- Consulting or client-facing experience is a strong plus.
- University degree in Life Sciences, Engineering, or similar.
- Excellent communication and interpersonal skills.
- Proactive, structured, and solution-oriented mindset.
- Ability to work independently in remote project setups.
- Comfortable working in multidisciplinary, multicultural teams.
- Experience leading and participating in CSV projects across systems like ERPs, eDMS, eQMS, LIMS, SCADA, EBRs, and pharmacovigilance systems.
- Ability to assess system compliance with global regulatory standards.
- Excited to work with clients on critical projects from a remote location in the UK.
- Comfortable managing technical, regulatory, and client-facing responsibilities.
- Eager to learn and grow in a role exposing you to diverse systems and industries.
- Competitive Compensation: Salary reflects your experience, plus additional benefits.
- Work-Life Balance: Remote work, flexible hours, shorter Fridays.
- Global Exposure: Multicultural team across multiple countries.
- Dynamic Environment: Young, enthusiastic team where your ideas are valued.
- Opportunities for Growth: Career development, leadership opportunities, and continuous learning.
- Drive Digital Transformation: Work on projects using the latest technologies to optimize quality processes.
For over 20 years, Rephine has helped leading Life Sciences companies improve manufacturing quality processes. Join us to grow your career and make an impact in a fast-evolving, global company.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.