Advanced Bioprocessing Scientist

Drive cutting-edge sterile manufacturing and transform lives with next-gen gene therapies.

R&D Partners is seeking an Advanced Bioprocessing Scientist to join a leading pharmaceutical company in the UK. This role focuses on advanced manufacturing and continuous improvement activities for the production of sterile gene therapy products in compliance with current Good Manufacturing Practice (cGMP).

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Perform manufacturing activities across multiple unit operations, adhering to GMP instructions and best practices.
• Drive personal development and coach/train Bioprocessing Scientists in line with the Training Plan.
• Identify, report, and investigate issues, as well as coach others on investigations.
• Collaborate on and deliver continuous improvements to enhance safety, quality, and workflow within the manufacturing area.
• Operate effectively within a cleanroom environment to maintain low bioburden and aseptic operations.
• Monitor the manufacturing facility to ensure compliance and safety.
• Perform sanitization of manufacturing materials and facilities.
• Ensure materials used in manufacturing are correct, clean, and ready for production according to the agreed schedule.

Key Performance Indicators:

• Safe working practices for self and team.
• Compliance with GMP requirements, including Data Integrity.
• Excellent cleanroom behavior.
• Timely closure of GMP commitments, issues, BMRs, CAPAs, and change controls.
• Adherence to the manufacturing schedule.

Key Competencies:

• Aseptic Processing: Operates to avoid cross-contamination and ensures sterile processing.
• Problem Solving: Identifies and resolves issues efficiently, analyzes information, and develops alternative solutions.
• Motivation: Sets and achieves challenging goals, demonstrates persistence, and measures self against standards of excellence.
• Planning & Organizing: Prioritizes tasks, uses time efficiently, and plans for additional resources.
• Professionalism: Treats others with respect, reacts well under pressure, and follows through on commitments.
• Quality Management: Promotes quality improvements and ensures accuracy and thoroughness.
• Communication Skills: Demonstrates strong oral and written communication skills, including clear presentation and effective documentation.

Requirements:

• University degree in Science or Engineering.
• Experience in pharmaceutical product manufacturing, with a preference for biologics and aseptic manufacturing.
• Strong awareness of GMP and demonstrated competency in multiple areas of bioprocessing.
• Proven ability to manage quality events and ensure compliance with GxP standards.

For more information, please contact Timi Asseez.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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