Job Description
As a Bioprocess Associate, you will be responsible for working with the wider Manufacturing teams to support the production of biological products at the Dundalk facility.
This role will be responsible for procedures and processes associated with the manufacture of commercial large-scale Drug Substance.
Key Responsibilities
* Maintain a safety-oriented culture and cGMP compliant work environment.
* Assist in Facility and Equipment start-up and Validation activities.
* Provide input on equipment installation, start-up, operation, and troubleshooting.
* Support the delivery of production output targets and quality levels on schedule.
* Carry out all production operations in the assigned area as directed by SOPs and Manufacturing Batch Records.
* Perform initial troubleshooting of issues identified during routine operations.
* Take part in investigations and optimization of processes using scientific, engineering, and lean principles.
* Train and mentor colleagues in SOPs, process execution, and equipment operation.
About You
The ideal candidate for this position will have:
* A Certificate, Diploma, Degree, or equivalent qualification in Science, Engineering, or a related field.
* 0-3 years experience in biopharmaceutical or pharmaceutical cGMP manufacturing.
* Thorough knowledge of current Good Manufacturing Practices (cGMP).
* Knowledge of biotech manufacturing processes and their translation into documentation.
* Technical knowledge of bioprocessing/biotechnology and Upstream and/or Downstream biologics processes.
What We Offer
* Bonus scheme
* Education Assistance
* Laptop
* Life Assurance
* Pension Scheme
* Healthcare