At a Glance
- Tasks: Lead and execute validation activities for pharmaceutical clients, ensuring compliance and quality.
- Company: Join Rephine, a global leader in Life Sciences quality assurance.
- Benefits: Competitive salary, remote work, flexible hours, and career development opportunities.
- Other info: Collaborate with a multicultural team and drive digital transformation in the industry.
- Why this job: Make a real impact on critical projects while working remotely with a dynamic team.
- Qualifications: 5+ years in validation projects and strong understanding of GMP and GxP.
The predicted salary is between 36000 - 60000 £ per year.
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.
Role Purpose
Provide senior-level support to pharmaceutical clients in CSV, validation, and potentially other GMP-related projects, ensuring compliance and delivering high-quality consultancy services.
Key Responsibilities
- 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.
Experience & Background
- 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.
Soft Skills
- 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.
What You Bring
- 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.
- Fluent in English.
Why This Role is for You
- 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.
Why Choose Rephine
- 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.
Applications must be in English.
Computer System Validation Consultant in Brighton employer: Rephine
Rephine is an exceptional employer for those seeking a meaningful career in the Life Sciences sector, offering remote work flexibility from the UK. With a strong emphasis on work-life balance, competitive compensation, and a dynamic, multicultural team, employees are encouraged to share their ideas and grow through continuous learning and leadership opportunities. Join us to make a significant impact while working on innovative projects that drive digital transformation in quality assurance and compliance.
StudySmarter Expert Advice🤫
We think this is how you could land Computer System Validation Consultant in Brighton
✨Tip Number 1
Network like a pro! Reach out to your connections in the life sciences field and let them know you're on the lookout for opportunities. You never know who might have a lead or can refer you to someone at Rephine.
✨Tip Number 2
Prepare for those interviews! Brush up on your knowledge of GMP, GxP, and CSV processes. Be ready to discuss your past experiences and how they relate to the role at Rephine. Confidence is key!
✨Tip Number 3
Showcase your soft skills! Communication and teamwork are crucial in consultancy roles. Think of examples where you've successfully collaborated with clients or mentored others, and be ready to share them.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're genuinely interested in joining the Rephine team.
We think you need these skills to ace Computer System Validation Consultant in Brighton
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of a CSV Consultant. Highlight your experience in validation and compliance, and don’t forget to mention any specific systems you've worked with that are relevant to the job.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about the role and how your background makes you a perfect fit for Rephine. Be sure to mention your understanding of GMP and GxP requirements.
Showcase Your Soft Skills:In addition to your technical skills, we want to see your soft skills too! Highlight your communication abilities and your proactive approach to problem-solving, as these are key in a consultancy environment.
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and get you on our radar quickly!
How to prepare for a job interview at Rephine
✨Know Your CSV Inside Out
Make sure you brush up on your knowledge of Computer System Validation (CSV) and related regulations like EU GMP Annex 11 and FDA 21 CFR Part 11. Be ready to discuss specific projects you've worked on, showcasing your experience in leading validation activities and ensuring compliance.
✨Showcase Your Consulting Skills
Since this role involves client-facing responsibilities, prepare examples that highlight your consulting experience. Think about times when you acted as a trusted advisor or provided guidance to clients, and be ready to explain how you managed project timelines and deliverables.
✨Communicate Clearly and Confidently
Excellent communication is key in this role. Practice articulating your thoughts clearly and confidently, especially when discussing complex topics like risk assessments and validation documentation. Remember, the interviewers will be looking for your ability to convey technical information effectively.
✨Demonstrate Your Proactive Mindset
Be prepared to discuss how you approach problem-solving in a structured and solution-oriented way. Share examples of how you've taken initiative in past projects, whether it was mentoring junior consultants or collaborating with multidisciplinary teams to achieve project goals.
