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For Companies At a Glance
- Tasks: Lead process validation for cutting-edge cell and gene therapy manufacturing.
- Company: Join a pioneering biopharma company focused on curative treatments.
- Benefits: 12-month contract with opportunities for career growth and development.
- Why this job: Be part of an exciting project that makes a real difference in healthcare.
- Qualifications: Experience in process validation and familiarity with regulatory requirements.
- Other info: Dynamic team environment with a focus on innovation and collaboration.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Are you a Process Validation Specialist professional with experience in Cell & Gene therapy? Are you looking to take the next step in your career and be part of an exciting new project? Then the position of process validation specialist is exactly what you’re looking for.
This is your chance to work for a company that is a pioneer in gene and cell therapy focussing on long-term curative treatments. With vast investment being made into the organisation and new build projects on the horizon this is the ideal time to join the team and establish yourself as a key team member.
Led by an experienced executive team, this is a fantastic opportunity to work for a high-profile Biopharma client.
Responsibilities
- Lead and execute process validation activities for cell and gene therapy manufacturing processes.
- Develop and author process validation documentation.
- Conduct ancillary validation studies (e.g., hold time validation, mixing studies, sterile filter validation).
- Ensure compliance with regulatory requirements for process validation and PPQ.
- Collaborate with cross-functional teams to support process characterization and control strategy development.
Desirable Experience
- Proven track record in process validation and process performance qualification (PPQ) within GMP manufacturing environments.
- Hands-on experience authoring validation documentation.
- Familiarity with regulatory requirements for process validation.
- Experience conducting ancillary validation studies.
- Prior exposure to cell & gene therapy or biologics preferred; small molecule experience acceptable.
Process Validation Specialist in England employer: QCS Staffing
Contact Detail:
QCS Staffing Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Process Validation Specialist in England
✨Tip Number 1
Network like a pro! Reach out to professionals in the cell and gene therapy field on LinkedIn. Join relevant groups and engage in discussions to get your name out there and show your passion for process validation.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge. Be ready to discuss your hands-on experience with process validation and any specific projects you've worked on. We want to see your expertise shine!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds.
✨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 our exciting projects in the biopharma sector.
We think you need these skills to ace Process Validation Specialist in England
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in process validation and cell & gene therapy. We want to see how your skills match the job description, so don’t be shy about showcasing relevant projects or achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re excited about this role and how your background makes you a perfect fit. We love seeing genuine enthusiasm, so let your personality come through!
Showcase Your Documentation Skills: Since the role involves authoring validation documentation, make sure to mention any relevant experience you have in this area. We’re looking for someone who can hit the ground running, so highlight those hands-on skills!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to keep track of your application and ensures you get all the latest updates. Plus, we love seeing applications come in through our own platform!
How to prepare for a job interview at QCS Staffing
✨Know Your Stuff
Make sure you brush up on your knowledge of process validation, especially in the context of cell and gene therapy. Familiarise yourself with the latest regulatory requirements and be ready to discuss how your experience aligns with the responsibilities outlined in the job description.
✨Showcase Your Experience
Prepare specific examples from your past roles that demonstrate your hands-on experience with process validation documentation and ancillary validation studies. Use the STAR method (Situation, Task, Action, Result) to structure your answers and make them impactful.
✨Collaborate Like a Pro
Since the role involves working with cross-functional teams, think of instances where you've successfully collaborated with others. Be ready to share how you contributed to team goals and how you can bring that collaborative spirit to their organisation.
✨Ask Smart Questions
At the end of the interview, don’t forget to ask insightful questions about the company’s projects and future plans in cell and gene therapy. This shows your genuine interest in the role and helps you gauge if it’s the right fit for you.
