MSAT Associate Director

MSAT Associate Director

Full-Time 36000 - 60000 £ / year (est.) No home office possible
Proclinical Staffing

At a Glance

  • Tasks: Lead the transfer and optimisation of pharmaceutical manufacturing processes to enhance patient care.
  • Company: Proclinical, a leading life sciences recruiter with a global reach.
  • Benefits: Competitive salary, opportunities for global collaboration, and career advancement.
  • Why this job: Make a real impact in medicine while working with cutting-edge technologies and diverse teams.
  • Qualifications: Degree in Life Sciences or related field and experience in pharmaceutical manufacturing.
  • Other info: Dynamic role with a commitment to continuous improvement and ethical standards.

The predicted salary is between 36000 - 60000 £ 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.

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 e.little@proclinical.com. 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 employer: Proclinical Staffing

Proclinical is an exceptional employer that fosters a collaborative and innovative work culture, empowering employees to drive meaningful advancements in patient care. With a strong commitment to professional development, employees have access to global opportunities and resources that enhance their skills and career growth. Located in a vibrant area, Proclinical offers a dynamic environment where scientific expertise is valued, and every team member plays a crucial role in shaping the future of medicine.
Proclinical Staffing

Contact Detail:

Proclinical Staffing Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land MSAT Associate Director

✨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; demonstrate your passion for their mission and how your expertise can drive breakthroughs in 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 noticed. Plus, if you have any questions, reach out to us – we’re here to help you land that dream job!

We think you need these skills to ace MSAT Associate Director

GxP Compliance
Technical Transfer Management
KPI Tracking
Pharmaceutical Manufacturing Processes
Quality Management Systems
Budget Management
Project Management
Problem-Solving Skills
Organisational Skills
Communication Skills
Leadership Abilities
Collaboration Skills
Continuous Improvement
Scientific Expertise

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the MSAT Associate Director role. Highlight your experience with GxP regulations and technical transfers, as these are key for us. Use specific examples that showcase your expertise in pharmaceutical manufacturing processes.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about revolutionising patient care and how your background aligns with our mission at StudySmarter. Keep it concise but impactful!

Showcase Your Problem-Solving Skills: In your application, don’t forget to mention instances where you've tackled challenges in manufacturing or compliance. We love seeing candidates who can adapt and drive continuous improvement initiatives, so share those stories!

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 quickly. Plus, we’re here to help if you have any questions!

How to prepare for a job interview at Proclinical Staffing

✨Know Your GxP Regulations

Make sure you brush up on Good Practice (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.

✨Be Ready to Discuss KPIs and Budgets

Since you'll be responsible for establishing and tracking KPIs and budgets, come prepared to talk about your experience in these areas. Think of metrics you've used in the past and how they contributed to successful project outcomes.

✨Emphasise Collaboration Skills

This role involves working closely with various teams, so be ready to share examples of how you've successfully collaborated in cross-functional projects. Highlight your communication skills and ability to lead teams towards common goals.

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