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For Companies At a Glance
- Tasks: Lead method validation activities and optimise analytical methods for product testing.
- Company: Established pharmaceutical manufacturer with a strong R&D focus.
- Benefits: Competitive salary, bonus, and opportunities for professional growth.
- Why this job: Join a growing company and make a real impact in the life sciences industry.
- Qualifications: BSc in chemistry or related field, with expertise in method validation.
- Other info: Supportive culture with collaborative teams and career development opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Join a business on an impressive trajectory of growth. Great routes forward for progression.
About Our Client
Our client is an established Pharmaceutical Manufacturer with an impressive on-site R&D facility.
Job Description
- Manage and execute method validation activities in alignment with regulatory requirements.
- Develop and optimise analytical methods for product testing.
- Prepare, review, and approve validation protocols and reports.
- Collaborate with cross-functional teams to support product development and quality control.
- Ensure compliance with GMP, GLP, and other relevant guidelines.
- Provide technical guidance and training to team members.
- Maintain accurate records of validation activities and findings.
- Identify and implement process improvements to enhance efficiency and accuracy.
The Successful Applicant
- BSc or higher in chemistry, biochemistry, or a related field.
- Proven expertise in method validation within the life sciences industry.
- Knowledge of GMP, GLP, and regulatory compliance requirements.
- Experience in analytical techniques such as HPLC, GC, or spectroscopy.
What’s on Offer
- Competitive Salary + Bonus
- Permanent position based in Leeds.
- Opportunities for professional growth and development.
- Supportive and collaborative company culture.
Analytical Method Validation Lead employer: Michael Page (UK)
Contact Detail:
Michael Page (UK) Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Analytical Method Validation Lead
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge and understanding of GMP and GLP guidelines. We recommend practising common interview questions related to method validation and analytical techniques to boost your confidence.
✨Tip Number 3
Showcase your skills! Bring along examples of your previous work, like validation protocols or reports, to demonstrate your expertise. We want to see how you’ve contributed to process improvements in your past roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Analytical Method Validation Lead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the job description. Highlight your expertise in method validation and analytical techniques like HPLC or GC, as these are key for us.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're the perfect fit for the Analytical Method Validation Lead role. Share specific examples of your past work in method validation and how you’ve contributed to compliance with GMP and GLP.
Showcase Your Team Spirit: Since collaboration is crucial for us, mention any experience working with cross-functional teams. We love candidates who can demonstrate their ability to support product development and quality control.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!
How to prepare for a job interview at Michael Page (UK)
✨Know Your Stuff
Make sure you brush up on your knowledge of analytical methods, especially HPLC, GC, and spectroscopy. Be ready to discuss your previous experiences with method validation and how they align with the regulatory requirements mentioned in the job description.
✨Showcase Your Team Spirit
Since collaboration is key in this role, think of examples where you've worked with cross-functional teams. Highlight how you contributed to product development and quality control, and be prepared to discuss how you can bring that collaborative spirit to their team.
✨Be Compliance Savvy
Familiarise yourself with GMP, GLP, and other relevant guidelines. During the interview, demonstrate your understanding of these regulations and how you've ensured compliance in your past roles. This will show that you're not just technically skilled but also aware of the industry's standards.
✨Process Improvement Mindset
Think about times when you've identified and implemented process improvements in your previous positions. Be ready to share specific examples that highlight your ability to enhance efficiency and accuracy in method validation activities.
