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- Tasks: Lead analytical teams and ensure compliance with GMP and regulatory standards.
- Company: Join Pharmaron, a global leader in life sciences and drug development.
- Benefits: Professional growth opportunities in a vibrant, supportive environment.
- Why this job: Make a real impact on high-value projects and global partnerships.
- Qualifications: 10+ years of experience in Analytical Chemistry or Quality Control required.
- Other info: Dynamic workplace with a commitment to scientific excellence and integrity.
The predicted salary is between 72000 - 108000 £ per year.
Pharmaron is a global CRO helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 23 sites in the UK, US and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
We are now seeking a highly experienced and forward-thinking Head of Analytical Quality Control to lead our Analytical QC operations at our Cramlington site. This is a key leadership position driving scientific excellence, operational performance, regulatory compliance and team development within our Analytical QC organisation.
At Pharmaron we offer:
- A vibrant, fast-growing business working at the forefront of the life sciences sector
- Excellent opportunities for professional development within a rapidly expanding global organisation
- A collaborative, supportive team environment where high standards and scientific excellence are celebrated
- The chance to make a direct impact on high-value CMC programmes and global client partnerships
Key roles and responsibilities:
- Lead multiple analytical teams and enable delivery of complex, multi-disciplinary projects
- Ensure Analytical QC operations comply with GMP, regulatory requirements and Pharmaron procedures
- Manage resources, forecast capacity and address constraints to meet project timelines
- Oversee laboratory investigations, ensuring thorough, timely and compliant execution
- Maintain governance of QMS documentation including deviations, CAPAs and change controls, ensuring on-time closure
- Develop and review departmental metrics, monitor trends and implement CAPAs where required
- Act as point of escalation for complex technical or operational issues
- Provide regular updates to senior management on technical matters, resource status and departmental performance
- Shape scientific strategy, drive innovation and introduce new analytical technologies
- Independently author or oversee high-quality technical reports, publications and presentations
- Lead Analytical QC support during client audits and regulatory inspections (e.g. MHRA, FDA)
- Collaborate cross-functionally to harmonise processes and support business activities including proposals and client visits
- Manage forecasting, procurement, installation, qualification and maintenance of analytical instrumentation
- Provide leadership, coaching, performance management and development for the Analytical QC team
Requirements:
- 10+ years (PhD) or 15+ years (MSc/BSc) of relevant industry experience
- Extensive leadership experience within Analytical Chemistry or Quality Control in a GMP environment
- Strong background in analytical sciences applied to API development, with deep understanding of core and advanced analytical techniques
- Proven experience managing multi-disciplinary scientific teams, including coaching, performance management and capability development
- Demonstrated ability to operate strategically, manage complex projects and make sound scientific and operational decisions
- Strong understanding of GMP, GLP and ICH guidelines with experience supporting audits and regulatory inspections
- Excellent communication and stakeholder-management skills, with the ability to influence across functions and at senior levels
- Highly organised, able to prioritise effectively and drive delivery in a fast-paced environment
- Proactive, resilient and solution-focused leader with strong attention to detail and commitment to quality
- Strong interpersonal skills, collaborative mindset and ability to build a positive team culture
- High level of integrity, professionalism and respect for confidentiality
Our Cramlington site has an established history of cGMP manufacturing services for an array of Active Pharmaceutical Ingredients (API), ranging from pilot scale to commercial metric ton scale. The site operates from small scale in the laboratory through to large manufacturing scale. It also offers chemistry and analytical development service.
Head of Analytical Quality Control in Cramlington employer: Pharmaron
Contact Detail:
Pharmaron Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Head of Analytical Quality Control in Cramlington
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can land you that dream job.
✨Tip Number 2
Prepare for interviews by researching the company inside out. Understand their values, recent projects, and challenges they face. This way, when you walk into that interview, you’ll be able to show how you can contribute to their success, making you a standout candidate.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. We can’t stress enough how being well-prepared can help you articulate your experience and skills effectively during the real deal.
✨Tip Number 4
Don’t forget to follow up after interviews! A simple thank-you email can go a long way in keeping you top of mind. Plus, it shows your enthusiasm for the role and appreciation for the opportunity, which is always a good look.
We think you need these skills to ace Head of Analytical Quality Control in Cramlington
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Head of Analytical Quality Control role. Highlight your leadership experience and any relevant projects you've managed in the past. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills can contribute to our team at Pharmaron. Keep it engaging and personal, so we get a sense of who you are.
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples that demonstrate your impact in previous roles, especially in analytical chemistry or quality control. We love seeing results!
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 ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Pharmaron
✨Know Your Analytical Chemistry Inside Out
Make sure you brush up on your analytical chemistry knowledge, especially the core and advanced techniques relevant to API development. Be prepared to discuss how you've applied these in a GMP environment and how they relate to the role at Pharmaron.
✨Showcase Your Leadership Skills
As a Head of Analytical Quality Control, you'll need to demonstrate your leadership experience. Prepare examples of how you've managed multi-disciplinary teams, coached individuals, and driven performance improvements in previous roles.
✨Understand Regulatory Compliance
Familiarise yourself with GMP, GLP, and ICH guidelines, as well as your experience with audits and regulatory inspections. Be ready to discuss specific instances where you've ensured compliance and how you handled any challenges that arose.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to manage complex projects. Think of scenarios where you've had to make sound scientific decisions under pressure, and be ready to explain your thought process and outcomes.