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- Tasks: Ensure compliance and quality standards for innovative OTC sunscreen products.
- Company: Join a leading science-led organisation in skincare innovation.
- Benefits: Enjoy 25 days holiday, flexible working, and private medical insurance.
- Why this job: Make a real impact in the skincare industry with your expertise.
- Qualifications: Degree in chemistry or related field; experience in regulated environments required.
- Other info: Dynamic team environment with opportunities for growth and development.
The predicted salary is between 40000 - 60000 £ per year.
An opportunity to work for a leading science-led organisation at the heart of skincare innovation and development. The business has backing from one of the leading cosmetics businesses in the industry.
Currently looking for a Senior Analytical and Compliance Scientist/specialist to join the team and contribute to the high-quality standards and global compliance of OTC sunscreen products. Reporting to the Head of Quality Compliance and working very closely with our R&D team, you will ensure all our OTC testing and documentation comply with all necessary regulatory and customer requirements.
Your Role Will Include:
- Preparing, reviewing, and maintaining OTC regulatory documentation (stability protocols, reports, specifications).
- Perform and oversee HPLC analyses, including method development, validation, and troubleshooting.
- Support process validation activities in alignment with GMP requirements.
- Draft, review, and update SOPs, quality manuals, and related GMP documentation.
- Ensure audit readiness through training, documentation control, and CAPA follow-up.
- Collaborate with cross-functional teams (R&D, QC, Manufacturing) to ensure product compliance throughout the lifecycle.
- Contribute to stability studies and interpret analytical data for regulatory submissions.
Requirements:
- Bachelor’s or master’s degree in chemistry, Pharmaceutical Sciences, or a related discipline.
- Proven experience in an OTC, pharmaceutical, or related regulated environment.
- Hands-on expertise in HPLC and analytical method development/validation.
- Strong knowledge of GMP, ICH, and FDA/TGA guidelines.
- Experience authoring and reviewing stability protocols, reports, and validation documentation.
- Excellent attention to detail, organisational, and documentation skills.
- Ability to train colleagues on SOPs and support internal/external audits.
The role comes with some of the perks include:
- 25 days holiday + bank holidays
- Flexible & Hybrid working
- Private Medical Insurance + Mental Health support
- Employee Assistance Program (EAP)
- Annual Performance Bonus
- Long Service Awards
- 75% discount + Annual Product Allowance
- Flexible Career opportunities
- Up-skilling support + regular Lunch & Learns
- 2 Volunteering days per year
- Matched Charitable Giving Scheme
You MUST have the full right to work in the UK and also be able to commute to site 3x a week.
Senior Analytical and Compliance Specialist in Milton Keynes employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Analytical and Compliance Specialist in Milton Keynes
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend relevant events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their compliance standards and be ready to discuss how your experience aligns with their needs. Show them you’re not just another candidate, but someone who truly gets their mission.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to HPLC and regulatory compliance. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your achievements.
✨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 Senior Analytical and Compliance Specialist in Milton Keynes
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Analytical and Compliance Specialist role. Highlight your experience with HPLC, regulatory documentation, and any relevant compliance work. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about skincare innovation and how your background fits with our mission. Keep it concise but engaging – we love a good story!
Showcase Your Attention to Detail: In this role, attention to detail is key. When you submit your application, double-check for any typos or formatting issues. We appreciate candidates who take the time to ensure everything is perfect!
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’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Regulations
Make sure you brush up on GMP, ICH, and FDA/TGA guidelines before the interview. Being able to discuss these regulations confidently will show that you’re not just familiar with them, but that you can apply them in real-world scenarios.
✨Showcase Your Analytical Skills
Prepare to talk about your hands-on experience with HPLC and analytical method development. Bring specific examples of challenges you've faced and how you overcame them, as this will demonstrate your problem-solving abilities and technical expertise.
✨Collaboration is Key
Since the role involves working closely with R&D and other teams, think of examples where you’ve successfully collaborated across departments. Highlighting your teamwork skills will show that you can contribute positively to their cross-functional environment.
✨Attention to Detail Matters
Be ready to discuss how you ensure accuracy in your work, especially when preparing regulatory documentation. Mention any systems or processes you use to maintain high standards, as this will reflect your commitment to quality compliance.
