At a Glance
- Tasks: Support facility expansion projects by planning and executing validation activities.
- Company: Leading pharmaceutical organisation focused on innovation and quality.
- Benefits: Competitive salary, dynamic work environment, and opportunities for professional growth.
- Other info: Join a diverse team committed to inclusion and excellence.
- Why this job: Make a real impact in the pharmaceutical industry with cutting-edge projects.
- Qualifications: Experience in validation within pharma or biotech, strong collaboration skills.
The predicted salary is between 30000 - 40000 £ per year.
Join Our Team as a Quality Validation Specialist – Projects (FTC). Are you an experienced quality professional with a passion for advancing pharmaceutical manufacturing processes? We’re seeking a highly motivated Quality Validation Specialist to support pivotal facility expansion projects within a leading organization. This is a fixed-term contract opportunity designed to make a tangible impact on cutting-edge initiatives in a dynamic, regulated environment. If you thrive in fast-paced settings, possess strong validation expertise, and are eager to contribute to critical projects, we want to hear from you!
In this role, you will play a key part in supporting expansion efforts by planning, executing, and overseeing validation activities for new and upgraded facilities and systems. Your expertise will ensure that all qualification and validation documentation meets GMP, GDP, Annex 15, and GAMP 5 standards. You’ll collaborate closely with engineering teams, reviewing and approving validation protocols, risk assessments, commissioning reports, and traceability matrices. The position offers an exciting opportunity to work on projects involving storage solutions, cold chain logistics, and new packaging lines for auto-injectors and vials, all within a highly regulated pharmaceutical environment.
Key Skills And Qualifications
- Proven experience in qualification and validation activities within pharma or biotech sectors.
- Strong knowledge of facility and utility systems, including HVAC, compressed air, environmental monitoring, and temperature-controlled storage.
- Solid understanding of GMP, GDP, Annex 15, and GAMP 5 compliance standards.
- Ability to draft, review, and approve validation documentation such as IQ/OQ/PQ protocols and validation reports.
- Excellent collaboration skills to work effectively with engineering and cross-functional teams.
- Well-versed in risk assessments and validation traceability.
- HVAC expertise is essential; prior experience with validation of HVAC systems is non-negotiable.
- Computer system validation experience is desirable but not mandatory.
Nice To Have Skills
- Prior involvement in computer system validation projects.
- Experience supporting facility expansions or similar capital projects.
- Knowledge of cold chain logistics and storage solutions.
Preferred Education And Experience
- Bachelor’s degree or higher in Science, Engineering, Pharmacy, or related field.
- Several years of validation experience in a regulated pharmaceutical environment, with a focus on facility and utility systems.
If you’re a dedicated validation professional ready to make a meaningful contribution to groundbreaking projects, don’t miss this chance to join a forward-thinking organization. Take the next step in your career and apply now to become a vital part of this exciting expansion!
QUALITY VALIDATION SPECIALIST – PROJECTS (FTC) employer: Planet Pharma
Join a leading organisation in Hertfordshire as a Quality Validation Specialist and be part of a dynamic team dedicated to advancing pharmaceutical manufacturing processes. With a strong emphasis on employee growth, collaboration, and a commitment to diversity and inclusion, this role offers the chance to work on cutting-edge projects in a highly regulated environment. Enjoy a supportive work culture that values your expertise and provides opportunities for meaningful contributions to pivotal facility expansion initiatives.
StudySmarter Expert Advice🤫
We think this is how you could land QUALITY VALIDATION SPECIALIST – PROJECTS (FTC)
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the hunt for a Quality Validation Specialist role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your validation knowledge. Be ready to discuss your experience with GMP, GDP, and GAMP 5 compliance standards. We want to see you shine when it comes to showcasing your expertise!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for the latest openings and make sure to tailor your application to highlight how your skills match the job description.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in leaving a positive impression. It shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.
We think you need these skills to ace QUALITY VALIDATION SPECIALIST – PROJECTS (FTC)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in quality validation and compliance. We want to see how your skills align with the role, so don’t be shy about showcasing your expertise in GMP, GDP, and other standards!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality validation in the pharmaceutical sector and how you can contribute to our exciting projects. Keep it engaging and personal!
Showcase Your Collaboration Skills:Since this role involves working closely with engineering teams, make sure to highlight any past experiences where you’ve successfully collaborated on projects. We love seeing teamwork in action!
Apply Through Our Website:We encourage you to apply directly through our website for a smoother application process. It’s the best way to ensure your application gets the attention it deserves, so don’t miss out!
How to prepare for a job interview at Planet Pharma
✨Know Your Validation Standards
Make sure you brush up on GMP, GDP, Annex 15, and GAMP 5 standards before your interview. Being able to discuss these in detail will show that you’re not just familiar with the requirements but can also apply them practically in a regulated environment.
✨Showcase Your Collaboration Skills
Since this role involves working closely with engineering teams, be prepared to share examples of how you've successfully collaborated on past projects. Highlighting your teamwork skills will demonstrate that you can effectively contribute to cross-functional initiatives.
✨Prepare for Technical Questions
Expect questions about your experience with HVAC systems and validation documentation like IQ/OQ/PQ protocols. Brush up on your technical knowledge and be ready to discuss specific challenges you’ve faced and how you overcame them.
✨Express Your Passion for Quality
Let your enthusiasm for quality validation shine through during the interview. Share why you’re passionate about advancing pharmaceutical manufacturing processes and how you see yourself making a tangible impact in this role.
