Summary: The role of Technical Expert in the Biopharmaceutical industry involves defining and selecting drug product manufacturing processes for clinical manufacture, designing lab studies, and collaborating with various stakeholders. This position is a 12-month contract based in the Berkshire area, focusing on injectable drug product manufacturing processes. The successful candidate will contribute to the timely manufacture of stability and clinical drug product batches.

Key Responsibilities:

• Define and select drug product manufacturing processes and parameters for clinical manufacture.
• Design and execute lab studies related to drug product development activities, capturing and analysing data.
• Cooperate with a wide range of internal and external stakeholders, including contract manufacturing organisations, as part of a project team.
• Provide support to ensure timely manufacture of stability and clinical drug product batches.

Key Skills:

• Relevant degree in a scientific discipline.
• Proven industry experience in liquid drug product development and/or manufacturing within the pharmaceutical industry.
• A working knowledge and practical experience with cGMP manufacturing under aseptic conditions.

Salary (Rate): undetermined

City: undetermined

Country: United Kingdom

Working Arrangements: undetermined

IR35 Status: undetermined

Seniority Level: undetermined

Industry: Other