Lead the planning, preparation, and execution of pilot-scale batches for downstream processes, ensuring delivery to agreed timelines and customer outcomes.
Drive the technical transfer of new and existing processes from internal and external customers using structured, compliant approaches.
Work closely with Process Development, R&D, MSAT, and New Product Introduction (NPI) teams to resolve technical and operational challenges before and during batch execution.
Prepare and review high-quality process documentation, including batch process descriptions, datasheets, and transfer documentation, suitable for scale-up to cGMP manufacturing.
Proactively identify, assess, and manage technical and operational risks, escalating appropriately where support is required.
Analyse batch data using structured approaches, identify trends, and contribute to process summary reports and continuous improvement initiatives.
Support a culture of safety, quality, and continuous improvement, contributing to EHS initiatives, productivity improvements, and yield optimization.
What we are looking for:
Recognised scientific and technical expertise in downstream processing within a pilot plant or manufacturing-related environment.
Strong ability to lead routine and non-routine unit operations independently, using a structured and compliant approach.
Proven experience in preparing technical documentation, reports, protocols, and SOPs to a high standard.
Demonstrated problem-solving capability, with strong attention to technical detail and a continuous improvement mindset.
Effective communication and collaboration skills, with the ability to build strong working relationships across scientific and operational teams.
A proactive, self-motivated approach, with the ability to manage multiple priorities and deliver results with minimal supervision.
A Bachelor’s degree (BSc or BEng) in Biological Sciences, Biochemical Engineering, or a related discipline, or equivalent transferable experience.
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