• Support investigations relating to material supply and manufacturing readiness activities.
• Manage and coordinate change controls associated with manufacturing materials and processes.
• Support qualification activities for manufacturing single-use consumables and components.
• Evaluate opportunities for shelf-life extensions and material optimisation initiatives.
• Collaborate with Manufacturing, Quality, Validation, Engineering, Supply Chain, and Technical Operations teams.
• Liaise with suppliers and internal stakeholders to gather information required for investigations and change controls.
• Support troubleshooting and resolution of operational issues impacting manufacturing activities.
• Present findings and recommendations to cross-functional review boards.
• Ensure all activities are completed in accordance with GMP, GDP, Quality, and EHS requirements.
• Generate and maintain accurate documentation and records.
• Participate in continuous improvement projects and operational excellence initiatives.
• Support training and knowledge sharing within the team.

• Level 8 qualification in Biotechnology, Biochemistry, Microbiology, Engineering, Pharmaceutical Science, or a related discipline.
• Strong communication and interpersonal skills.
• Excellent attention to detail and organisational ability.
• Ability to manage multiple priorities in a fast-paced environment.
• Strong problem-solving mindset and willingness to learn.
• Ability to work effectively within cross-functional teams.

• Experience working in a GMP-regulated pharmaceutical, biotechnology or life sciences environment.
• Exposure to manufacturing support, process support, quality systems, validation, technical operations, or supply chain activities.
• Experience with change controls, deviations, CAPAs, or investigations.
• Knowledge of SAP, TrackWise, electronic documentation systems, or similar business systems.
• Lean Six Sigma or other problem-solving methodologies.
• Project experience within a regulated industry.

What you need to do now

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