Posted: 12 June
The role
Responsible for installation, maintenance, troubleshooting, and optimization of biologics manufacturing equipment in a GMP-regulated environment. Supports equipment reliability, process improvements, validation activities, and operational efficiency initiatives. Please note this for an initial 12-month subcontracting role.
Key Responsibilities
Provide day-to-day technical support for manufacturing equipment.
Troubleshoot equipment and process issues to minimize downtime.
Develop and maintain operational procedures and training materials.
Lead technical investigations and continuous improvement initiatives.
Support validation protocol development and execution.
Collaborate across functions to support lean manufacturing objectives.
Develop expertise in aseptic filling and lyophilization systems.
Required Qualifications
Bachelor’s degree in Engineering or related discipline, or equivalent experience.
Experience in biologics or pharmaceutical manufacturing environments.
Familiarity with GMP requirements and regulated operations.
Preferred Qualifications
Experience with aseptic filling and lyophilization processes.
Strong problem-solving, communication, and collaboration skills.
Fast-paced manufacturing environment focused on operational excellence, compliance, and continuous improvement.
For a confidential discussion and more information on the role, please contact Kevin Griffin (021) 2427108
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