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- Tasks: Join our MSAT team to manage and optimise bioprocesses in pharmaceutical manufacturing.
- Company: Work with a leading global healthcare company dedicated to innovation and quality.
- Benefits: Enjoy flexi-time, private healthcare, enhanced pension, and a bonus scheme.
- Why this job: This role offers a chance to impact healthcare while developing your skills in a dynamic environment.
- Qualifications: Degree in a scientific field and experience in GMP manufacturing or process development required.
- Other info: Ideal for those ready to take on new challenges in a fast-paced setting.
The predicted salary is between 36000 - 60000 £ per year.
SRG are excited to be working with a global name in the healthcare industry to help them find a Bioprocess Engineer/Specialist within their Manufacturing, Science & Technology (MSAT) team. This is a great opportunity for someone with strong GMP pharmaceutical manufacturing or process development experience who is ready for a new challenge. This role offers flexi-time and excellent benefits such as private healthcare, enhanced pension and bonus scheme.
The Role:
- Prepare GMP batch records for use in manufacturing processes
- Review, approve, and issue manufacturing documentation
- Determine scale up criteria from development to manufacturing scale
- Generate process mass balances and flow diagrams
- Identify, design and define large scale manufacturing equipment
- Define materials for use in a GMP manufacturing environment
- Generate quality documentation for raw materials and equipment
- Work within the QMS and carry out investigations where required
- Implement CAPAs and change controls
- Project manage all aspects of the introduction of processes to manufacturing
- Evaluate process materials for suitability for use in manufacturing
Requirements:
- Degree in a relevant scientific or technical discipline and/or relevant industry experience
- Proven GMP pharmaceutical manufacturing or process development experience and technical knowledge and ability
- Experience of managing projects
- Prior experience of process scale up and technical transfer
- Good leadership and organisational skills
- Experience writing GMP batch records and documentation
- Ability to work in a fast paced environment
MSAT Bioprocess Specialist employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land MSAT Bioprocess Specialist
✨Tip Number 1
Network with professionals in the bioprocessing and pharmaceutical manufacturing sectors. Attend industry conferences, webinars, or local meetups to connect with people who work in MSAT roles. This can help you gain insights into the company culture and potentially get a referral.
✨Tip Number 2
Familiarise yourself with the latest trends and technologies in GMP manufacturing and process development. Being knowledgeable about current practices will not only boost your confidence but also impress interviewers with your commitment to staying updated in the field.
✨Tip Number 3
Prepare to discuss specific projects where you've successfully managed process scale-up or technical transfers. Use the STAR method (Situation, Task, Action, Result) to structure your responses, showcasing your leadership and organisational skills effectively.
✨Tip Number 4
Research the company’s values and recent developments in their MSAT team. Tailoring your conversation during interviews to align with their goals and demonstrating how your experience can contribute to their success will make you a standout candidate.
We think you need these skills to ace MSAT Bioprocess Specialist
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the key responsibilities and requirements for the MSAT Bioprocess Specialist position. Tailor your application to highlight your relevant experience in GMP pharmaceutical manufacturing and process development.
Highlight Relevant Experience: In your CV and cover letter, emphasise your proven experience in GMP environments, project management, and any specific achievements related to process scale-up and technical transfer. Use quantifiable examples where possible.
Craft a Strong Cover Letter: Write a compelling cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role and the company. Mention how your skills align with the company's goals and values.
Proofread Your Application: Before submitting, thoroughly proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in a GMP environment.
How to prepare for a job interview at SRG
✨Know Your GMP Fundamentals
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be prepared to discuss how you've applied these principles in your previous roles, especially in relation to batch records and documentation.
✨Showcase Your Project Management Skills
Since project management is a key part of the role, think of specific examples where you've successfully managed projects. Highlight your organisational skills and how you ensured timely delivery while maintaining quality standards.
✨Prepare for Technical Questions
Expect technical questions related to process scale-up and equipment design. Review your past experiences and be ready to explain your thought process when determining scale-up criteria or generating process mass balances.
✨Demonstrate Leadership Qualities
Even if you're not applying for a managerial position, showcasing your leadership skills can set you apart. Share instances where you've led a team or taken initiative in problem-solving, particularly in a fast-paced environment.
