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For Companies At a Glance
- Tasks: Support pharmaceutical manufacturing processes and collaborate with teams to optimise production.
- Company: Join Proclinical, a leading biotech innovating in life sciences globally.
- Benefits: Enjoy opportunities for global collaboration and occasional travel to CMOs.
- Why this job: Be part of a dynamic team driving innovation in vital medicine production.
- Qualifications: Degree in Life Sciences or related field; experience in pharmaceutical manufacturing preferred.
- Other info: Project management certification is a plus; strong communication skills are essential.
The predicted salary is between 36000 - 60000 £ per year.
Job Description
Join a trailblazing biotech on the cutting edge of science and technology.
Proclinical is seeking an MSAT Scientist to join a dynamic team in Surrey, UK. In this role, you will leverage your scientific expertise to support the technical transfer of pharmaceutical manufacturing processes. This includes working with Contract Manufacturing Organizations (CMOs) to optimize production, address quality challenges, and ensure the continuous supply of vital medicines. You will play a key role in improving manufacturing efficiency, supporting product growth, and contributing to regulatory submissions.
This position offers a global scope, with opportunities for collaboration across cross-functional teams and occasional travel to CMOs. If you are passionate about driving innovation in pharmaceutical manufacturing and thrive in a collaborative environment, this role is for you.
Responsibilities:
- Support the initiation, planning, and execution of site-to-site manufacturing process transfers by managing technical documentation, data collection, and internal communication.
- Collaborate with senior team members to compile technical data for regulatory submissions related to new site registrations.
- Represent the MSAT department in cross-functional project meetings, providing technical insights alongside Supply Chain, Regulatory, and Commercial teams.
- Prepare and organize technical documentation for internal and external manufacturing sites, ensuring clear communication of technical requirements.
- Assist in creating purchase orders (POs) and tracking project budgets, including CAPEX and CoGs, to ensure alignment with approved cost estimates.
- Address technical and quality-related issues by coordinating with internal experts and external partners, such as CMOs and CROs.
- Review and organize technical documents, including product quality reports, certificates of analysis, stability reports, and batch records, ensuring compliance with product registrations.
- Support technical due diligence activities for potential product acquisitions by gathering background information and documentation.
- Maintain accurate and up-to-date documentation in shared systems, adhering to internal procedures for file storage and data handling.
- Raise and track Change Control Requests (CCRs) and ensure compliance with SOPs and in-house procedures.
Key Skills and Requirements:
- Familiarity with small molecule formats such as steriles, capsules, creams, gels, ointments, and solid dose.
- Degree in Life Sciences, Pharmacy, Pharmaceutical Sciences, or Chemistry.
- Demonstrated experience in site technical transfers, including exposure to pharmaceutical manufacturing, QC testing, and packaging.
- Proven ability to manage and execute projects successfully, including site tech transfers.
- Global experience in manufacturing, registering, and distributing pharmaceuticals.
- Project management certification (e.g., Prince2, PMP) is advantageous.
- Strong organizational and time management skills with attention to detail.
- Excellent written and verbal communication skills.
- Ability to work collaboratively in a team environment and adapt to high-speed changes.
- Problem-solving mindset with the ability to assimilate data from diverse scientific areas.
- Commitment to integrity, ethical standards, and accountability.
If you are having difficulty in applying or if you have any questions, please contact Ingrid Aymes at i.aymes@proclinical.com
Apply Now:
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.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.proclinical.com/privacy-policy
MSAT Scientist - small molecules employer: Proclinical Staffing
Contact Detail:
Proclinical Staffing Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land MSAT Scientist - small molecules
✨Tip Number 1
Familiarise yourself with the specific small molecule formats mentioned in the job description, such as steriles and capsules. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the role.
✨Tip Number 2
Network with professionals in the biotech and pharmaceutical manufacturing sectors. Attend industry conferences or webinars to connect with potential colleagues and learn more about current trends and challenges in MSAT.
✨Tip Number 3
Prepare to discuss your project management experience in detail, especially any relevant certifications like Prince2 or PMP. Be ready to provide examples of how you've successfully managed technical transfers or similar projects.
✨Tip Number 4
Research Proclinical and their recent projects or collaborations. Understanding their mission and values will allow you to tailor your conversation during interviews and show that you're aligned with their goals.
We think you need these skills to ace MSAT Scientist - small molecules
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the MSAT Scientist position. Understand the key responsibilities and required skills, such as familiarity with small molecule formats and experience in site technical transfers.
Tailor Your CV: Customise your CV to highlight relevant experience and skills that align with the job requirements. Emphasise your background in pharmaceutical manufacturing, project management, and any specific technical expertise related to small molecules.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for pharmaceutical manufacturing and your ability to work collaboratively. Mention specific examples of past experiences where you successfully managed technical transfers or addressed quality challenges.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A well-presented application reflects your attention to detail, which is crucial for the role.
How to prepare for a job interview at Proclinical Staffing
✨Know Your Small Molecules
Make sure you brush up on your knowledge of small molecule formats like steriles, capsules, and creams. Being able to discuss these in detail will show your expertise and passion for the role.
✨Highlight Your Project Management Skills
Since project management is key in this role, be prepared to share specific examples of how you've successfully managed site technical transfers or similar projects. Mention any relevant certifications like Prince2 or PMP.
✨Prepare for Technical Questions
Expect to answer questions related to pharmaceutical manufacturing processes and quality control. Review common challenges faced in these areas and think about how you would address them.
✨Showcase Your Collaborative Spirit
This position requires working with cross-functional teams, so be ready to discuss your experience collaborating with different departments. Share examples that demonstrate your ability to communicate effectively and work as part of a team.
