Bioprocess Engineer

Headcount Solutions is sourcing Bioprocess Associates to support our multinational client’s biologics manufacturing facility in Dublin. These roles will support the ongoing manufacturing operations within the facility, as well as commissioning and qualification activities for the process equipment where required.

• Working with the manufacturing operations group, project design team, the CQV team, and the Automation/CSV reps to facilitate the implementation of the project design and validation of the manufacturing facility.
• Creation of operating procedures and other relevant documentation for large scale manufacturing.
• Execution of commercial manufacturing processes according to established work instructions.
• Adhere to Good Manufacturing Practices and Standard Operating Procedures.
• Participation in investigations and optimisations of processes using scientific, engineering and lean principles.
• Effectively use process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.).
• Assist with reviewing batch and exception reports for each manufacturing lot in conjunction with Quality representative and provide input to related investigations and QA audit activities.
• Engages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and safe work environment.

• Ideally possess 2+ years’ working experience in a large-scale biopharmaceutical manufacturing facility
• Experience with Delta V and MES would be considered an advantage.
• The successful candidates must demonstrate problem solving ability and to adhere to scheduled timelines.
• Excellent communication skills and the ability to work in a cross functional collaborative environment are required

• The successful candidates will ideally possess a minimum of Level 6 qualification in an Engineering/Science related discipline; however, relevant experience in a similar regulated industry will also be considered (e.g. cGMP, ISO or similar cleanroom industry experience strongly preferred)