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- Tasks: Lead the transfer of innovative drug processes from development to manufacturing.
- Company: Join Piramal Group, a leader in biopharmaceutical solutions.
- Benefits: Enjoy competitive pay, career growth, and a diverse work environment.
- Why this job: Make a real difference in healthcare by working on cutting-edge bioprocesses.
- Qualifications: BSc in Science or Engineering and experience in GMP biologics required.
- Other info: Collaborative team culture with opportunities for professional development.
The predicted salary is between 36000 - 60000 £ per year.
Responsible for the technology transfer of both new and repeat Antibody Drug Conjugate (ADC) processes from Process Development to Manufacturing in compliance with Good Manufacturing Practices (GMP), including generation of all required process and technical documentation. Work compliantly within Piramal Quality Management System (QMS) to ensure processes meet company and regulatory requirements. Lead and manage implementation of improvement actions identified through CAPA actions and end of campaign lessons learned.
Key Roles/Responsibilities:
- Prepare GMP batch records for use in GMP 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 Piramal quality system to initiate, manage and evaluate requests for change.
- Perform investigations, close CAPA’s and deviations.
- Project manage all aspects of the introduction of processes to manufacturing.
- Perform risk assessments in alignment with ICH 9Q.
- Evaluate process materials for suitability for use in manufacturing.
Qualifications:
- Preferably BSc (Hons) in Science or Engineering discipline (or equivalent) required.
- Proven GMP Biologics manufacturing or process development experience.
- Strong planning and organization skills to influence and gain support from key stakeholders that collaborate to deliver technical transfer projects.
- Process scale-up, transfer and manufacturing support.
- A proven track record to meet project deadlines.
- Ability to communicate with vast cross sections of people at all levels of the business.
- Evaluation of materials for process suitability.
- Writing GMP batch records.
- Commercialization of biological medicines and process validation.
- Experience of process improvement and process mapping.
- Definition, sourcing, and validation of large-scale process equipment.
MSAT Bioprocess Engineer in Larbert employer: Piramal Group
Contact Detail:
Piramal Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land MSAT Bioprocess Engineer in Larbert
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at Piramal. A friendly chat can open doors and give you insights that job descriptions just can't.
✨Tip Number 2
Prepare for interviews by diving deep into the specifics of the MSAT role. Brush up on GMP practices and be ready to discuss your experience with process development and scale-up. Show us you know your stuff!
✨Tip Number 3
Don’t just apply; engage! When you submit your application through our website, follow up with a quick email to express your enthusiasm. It shows initiative and keeps you on our radar.
✨Tip Number 4
Be ready to showcase your problem-solving skills. Think of examples where you've tackled challenges in process improvement or project management. We love candidates who can think on their feet!
We think you need these skills to ace MSAT Bioprocess Engineer in Larbert
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience with GMP and bioprocess engineering. We want to see how your skills align with the MSAT role, so don’t hold back on showcasing relevant projects!
Showcase Your Attention to Detail: Given the nature of the job, it’s crucial to demonstrate your high level of attention to detail. Use specific examples from your past work where you’ve successfully managed documentation or compliance tasks.
Highlight Teamwork Skills: We’re all about collaboration here at Piramal. Make sure to mention any experiences where you’ve worked effectively in a team, especially in cross-functional settings. It’ll show us you can communicate well with various stakeholders.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Piramal Group
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practices (GMP) before your interview. Understand how they apply to the bioprocessing field, especially in relation to Antibody Drug Conjugates (ADCs). Being able to discuss specific examples of how you've adhered to GMP in past roles will show you're a strong candidate.
✨Prepare for Technical Questions
Expect to be asked about process scale-up and the generation of batch records. Review your previous experiences with these processes and be ready to explain your approach to generating process mass balances and flow diagrams. This will demonstrate your technical expertise and problem-solving skills.
✨Showcase Your Teamwork Skills
Since this role requires strong collaboration with various stakeholders, think of examples where you've successfully worked in a team. Be prepared to discuss how you influenced others and gained support for technical transfer projects. Highlighting your ability to communicate effectively will set you apart.
✨Demonstrate Your Attention to Detail
In bioprocess engineering, attention to detail is crucial. Prepare to discuss instances where your meticulousness led to successful outcomes, whether it was in writing GMP documentation or conducting risk assessments. This will reassure the interviewers that you can handle the precision required in this role.
