Bristol Myers Squibb Manufacturing Bioprocess Associate in Mulhuddart, Ireland

Title: Manufacturing Bioprocess Associate

Location: EU-IE-Dublin-Mulhuddart

Job Number: 1702567

Manufacturing Bioprocess Associate

Bristol-Myers Squibb is currently building a new state of the art large-scale biologics manufacturing facility in Cruiserath, Dublin 15, approximately $1 billion investment. Once completed, the new facility will significantly increase Bristol-Myers Squibb’s biologics manufacturing capacity and play a central role in its global manufacturing network.

BMS Cruiserath Biologics is seeking to recruit permanent Upstream & Downstream Bioprocess Associates within the Manufacturing Operations group. Reporting to the shift lead, the role will involve commissioning and qualification of the process equipment and then supporting the ongoing manufacturing operation of the facility.

Responsibilities will include (but not limited to):

  • 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 LSCC 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:

Qualifications and Experience required:

The successful candidate must possess:

  • a Bachelor in Engineering/ Science related subject.

  • at least 2 years’ work experience in biopharmaceutical manufacturing.

  • 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.

Job: Mfrg Ops/Process Dev