Bioprocess Associate

• Support operations team to consistently deliver on specific Key Performance Indicators (KPIs), e.g. Environmental Health and Safety (EHS) metrics, Production Plan, Overall Equipment Effectiveness (OEE), compliance and team training.
• Execute commercial manufacturing processes according to established work instructions and
• Standard Operating Procedures (SOPs).
• Ensures that all assigned task related to manufacturing documentation support is in accordance with good manufacturing practices.
• Routinely talk about any safety issues you are concerned about.
• Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
• Generate SOPs/ Work Instructions (WIs) to ensure compliance with regulatory standards.
• Maintain/ support a high standard of safety/ Good Manufacturing Practice (GMP) compliance at all times.
• Determine solutions by referencing relevant past experiences as part of problem solving activities.
• Get actively involved by participating in inspections, GEMBA’s and Go-See’s.
• Act as a team member on process deviation reviews and Gemba walkdowns.
• Mentor new members of staff in specific plant activities.
• Be prepared to answer auditor questions during site walkdowns.
• Engage in implementing innovative solutions that drive a high performance organisational culture that accommodates rapid growth and highly dynamic expectations ensuring attainment of site operational and development goals.

• Level 7 qualification in a science or engineering discipline, or level 6 with a minimum of 3+ years’ experience in a GMP Manufacturing environment.
• Experience of Upstream/ Downstream Processing.
• Start-up experience in a large-scale commercial drug substance facility, or similar.
• A proven ability to work with automated systems such as Manufacturing Execution System (MES), Systems Applications and Products (SAP), Delta V etc.

Life Science Recruitment