Bio-Process Associate

We are seeking an Upstream Bioprocess Associate to support commercial manufacturing and the commissioning and qualification of process equipment within a large-scale biopharmaceutical facility.

Reporting to the Shift Lead, this position requires shift work as the site operates 24/7.

Key Responsibilities

• Execute manufacturing processes and operate production equipment in accordance with GMP, SOPs and approved work instructions.
• Prepare and update operating procedures and manufacturing documentation.
• Use process automation, manufacturing execution and data monitoring systems to support operations.
• Support batch record and exception report reviews with Quality Assurance.
• Contribute to investigations, troubleshooting and process improvements.
• Collaborate with Manufacturing, Engineering, Qualification, Automation and Validation teams to support equipment qualification and operational readiness.
• Promote safe working practices, continuous improvement and operational excellence.

Requirements

• Minimum Level 6 qualification in Science or Engineering, or relevant experience in a similar regulated industry.
• At least three years' experience in a large-scale biopharmaceutical manufacturing facility.
• Experience with process control, manufacturing execution and data acquisition systems.
• Strong understanding of GMP and controlled manufacturing documentation.
• Good problem-solving, communication and teamwork skills.
• Ability to work independently, meet scheduled timelines and collaborate across functions.
• Availability to work shifts in a 24/7 manufacturing environment.