BioProcess Associate

BioProcess Associate - Dublin - 12 Months

One of the top 10 best companies to work in Ireland is looking for a BioProcess Associate for their large-scale new facility in Dublin. Is this you?

An exciting project offers lots of opportunities to learn new technology and develop current skills within a fast-paced €1 billion project. This fantastic client provides the opportunity to work within a large-scale environment with cutting-edge technology.

Responsibilities include:

1. Execution of commercial manufacturing processes according to established work instructions.
2. Creation of operating procedures & other relevant documentation for large scale manufacturing.
3. Operating production equipment within the assigned functional area.
4. Adhering to Good Manufacturing Practices and Standard Operating Procedures.
5. Taking part in investigations and optimisation of processes using scientific, engineering, and lean principles.
6. Proficient use of process automation systems (i.e., Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e., SAP, Trackwise, Maximo, etc.).
7. Assisting with the review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representatives and providing input to related investigations and QA audit activities.
8. Working with the manufacturing operations group, the project design team, the CQV team, & the Automation/Computer Systems Validation teams to facilitate the implementation of the project design, validation, and operation of the MPCC manufacturing facility.
9. Engaging in and supporting a culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment, and a safe working environment.

Key requirements include:

1. The successful candidate 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).
2. Working experience in a large-scale biopharmaceutical manufacturing facility would be a distinct advantage.
3. Experience with Delta V and MES or similar control and data acquisition systems would be desirable.
4. The candidate must demonstrate an ability to work independently and also as part of a team.
5. A successful candidate will have a demonstrated problem-solving ability and the ability to adhere to scheduled timelines.
6. Excellent communication skills and the ability to work in a cross-functional, collaborative, and fast-paced environment are essential.

If this role is of interest, please apply now

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