At a Glance
- Tasks: Lead the transfer and optimisation of pharmaceutical manufacturing processes to enhance patient care.
- Company: Proclinical, a forward-thinking company revolutionising medicine through innovative practices.
- Benefits: Competitive salary, global collaboration, and opportunities for professional growth.
- Other info: Dynamic role with travel opportunities and a commitment to continuous improvement.
- Why this job: Make a real impact in healthcare while working with cutting-edge technologies and global teams.
- Qualifications: Degree in Life Sciences or related field; experience in pharmaceutical manufacturing and technical transfers.
The predicted salary is between 70000 - 90000 £ per year.
Looking to uncover insights that could revolutionise the future of medicine and drive breakthroughs in patient care? Proclinical is seeking an MSAT Associate Director to oversee the successful transfer and optimisation of pharmaceutical manufacturing processes. In this role, you will leverage your scientific expertise to ensure compliance with GxP regulations, manage technical transfers between sites, and drive continuous improvement initiatives. You will work closely with internal teams and external partners to maintain product quality, resolve manufacturing challenges, and support portfolio growth. This position involves global collaboration and occasional travel to manufacturing sites. Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities
- Ensure adherence to GxP regulations and standard operating procedures.
- Lead technical transfers of manufacturing processes, providing critical expertise and direction.
- Establish and track KPIs, budgets, and timelines for process transfers and improvements.
- Represent technical expertise in cross-functional projects, including supply chain, regulatory, and commercial activities.
- Provide scientific advice to procurement and regulatory teams, addressing batch failures, recalls, and variations.
- Conduct technical reviews and due diligence for potential acquisitions and divestments.
- Collaborate with manufacturing sites to optimise processes and resolve compliance or quality issues.
- Review and approve technical documentation, including certificates of analysis, stability data, and risk assessments.
- Manage quality records such as change control requests and deviations.
- Propose and implement technical and business improvements to enhance practices and systems.
Key Skills and Requirements
- Degree in Life Sciences, Pharmacy, Pharmaceutical Sciences, or Chemistry.
- Proven experience in site-to-site technical transfers and pharmaceutical manufacturing processes.
- Familiarity with small molecule formats, including sterile products, capsules, creams, gels, ointments, and solid dose.
- Knowledge of Quality Management Systems, including change control and deviation management.
- Experience in operational budget management and strategic alignment.
- Proficiency in project management tools, templates, and methodologies.
- Strong problem-solving skills and ability to adapt to high-speed changes.
- Excellent organisational, communication, and time management skills.
- Demonstrated leadership and collaboration abilities across global teams.
- Commitment to continuous improvement and ethical standards.
If you are having difficulty in applying or if you have any questions, please contact Ed Little at . If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
MSAT Associate Director in England employer: Proclinical Staffing
Proclinical Staffing is an excellent employer, offering a dynamic work environment in Barnard Castle where innovation meets quality. Employees benefit from a strong focus on professional development, with opportunities for growth within the quality control team, while enjoying a collaborative culture that prioritises adherence to GMP standards and excellence in microbiological testing.
StudySmarter Expert Advice🤫
We think this is how you could land MSAT Associate Director in England
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Show them you’re not just another candidate; you’re genuinely interested in how you can contribute to their mission of revolutionising patient care.
✨Tip Number 3
Practice your pitch! Be ready to explain how your experience with GxP regulations and technical transfers makes you the ideal fit for the MSAT Associate Director role. Confidence is key, so rehearse until it feels natural.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, you can easily track your application status and get updates directly from us.
We think you need these skills to ace MSAT Associate Director in England
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the MSAT Associate Director role. Highlight your expertise in pharmaceutical manufacturing processes and any relevant GxP compliance experience. We want to see how you can bring value to our team!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you're passionate about revolutionising patient care and how your background aligns with our mission. Be sure to mention specific achievements that demonstrate your leadership and problem-solving skills.
Showcase Your Technical Expertise:In your application, don’t shy away from showcasing your technical knowledge. Discuss your experience with site-to-site technical transfers and any familiarity with small molecule formats. We love seeing candidates who can dive deep into the nitty-gritty of pharmaceutical processes!
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of being noticed. It’s straightforward and ensures your application gets to the right people. Plus, if you have any questions, feel free to reach out to Ed Little for assistance!
How to prepare for a job interview at Proclinical Staffing
✨Know Your GxP Regulations
Make sure you brush up on GxP regulations before the interview. Being able to discuss how you've ensured compliance in past roles will show that you understand the importance of these standards in pharmaceutical manufacturing.
✨Showcase Your Technical Transfer Experience
Prepare specific examples of your experience with site-to-site technical transfers. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and expertise in managing complex processes.
✨Demonstrate Leadership and Collaboration
Think of instances where you've led cross-functional teams or collaborated with external partners. Be ready to share how you fostered teamwork and drove projects forward, as this role requires strong leadership and collaboration abilities.
✨Prepare for Questions on Continuous Improvement
Expect questions about how you've implemented continuous improvement initiatives in your previous roles. Have a few examples ready that illustrate your commitment to enhancing practices and systems, as this aligns perfectly with the responsibilities of the position.
