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Downstream Bioprocess Associate

Job description

12 months contract
Location - Dublin 15.

Force recruitment have partnered with one of the top biopharmaceuticals who are on a look out for a downstream bioprocess associate role.

*** We are not providing sponsorships for this role, candidates need to hold EU passports or stamp 4 to apply****

Key Duties and Responsibilities:

  • Working with the manufacturing operations group, project design team, the CQV team, & the Automation/CSV reps to facilitate the implementation of the project design and validation of the MPCC manufacturing facility.

  • Creation of operating procedures & other relevant documentation for large scale manufacturing

  • Execution of commercial manufacturing processes according to established work instructions.

  • Adheres to Good Manufacturing Practices and Standard Operating Procedures.

  • Takes part in investigations and optimisations of processes using scientific, engineering and lean principles

  • Operates all production equipment within the assigned functional area

  • Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.).

  • Assists 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.

Qualifications, Knowledge and Skills Required:

  • 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)

  • Ideally possess 1-3+ years’ working experience in a large-scale biopharmaceutical manufacturing facility

  • Experience with Delta V and MES would be considered an advantage.

  • The successful candidate must demonstrate an ability to work independently and also as part of a team.

  • The successful candidate 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.

Due to the nature of the manufacturing role, shift work will be required for 24/7 mode of operations.