Bioprocess Associate
- Dublin
- Contract
- Full-time
- Collaborate with the manufacturing operations group, project design team, CQV team, and Automation/CSV representatives to implement project design and validation for the facility.
- Create operating procedures and other relevant documentation for large scale manufacturing.
- Execute commercial manufacturing processes according to established work instructions.
- Adhere to Good Manufacturing Practices and Standard Operating Procedures.
- Participate in investigations and process optimisations using scientific, engineering, and lean principles.
- Operate production equipment within the assigned functional area.
- Use process automation systems (Delta V, Syncade Interactions, OSI/Pi Historian) and supporting business systems (SAP, Trackwise, Maximo).
- Review batch and exception reports in conjunction with Quality representatives and provide input to investigations and QA audit activities.
- Support a culture of continuous improvement and operational excellence through ownership of process, equipment, and safe working practices.
- Minimum Level 6 qualification in Engineering or Science, or relevant experience in a regulated industry (cGMP, ISO, or cleanroom strongly preferred).
- 1 to 3+ years of experience in a large scale biopharmaceutical manufacturing facility preferred.
- Experience with Delta V and MES is an advantage.
- Ability to work independently and as part of a team.
- Strong problem solving skills with the ability to meet scheduled timelines.
- Excellent communication skills and proven ability to collaborate in cross functional environments.