Bioprocess Associate

PE Global (UK); Dublin; On-site; EUR 40,000 - 60,000; Full time

Job summary

PE Global (UK) is currently seeking a Bioprocess professional for a 12-month contract with a leading Biotech client in Dublin. This role requires overseeing the manufacturing operations group and developing documentation for large scale production.

The ideal candidate must have a Level 6 qualification in Engineering/Science and 1-3+ years of experience in biopharmaceutical manufacturing. Proficiency with Delta V and MES is advantageous. Note: Visa sponsorship is not available.

Qualifications

• Minimum of Level 6 qualification in Engineering/Science or relevant experience in a regulated industry.
• 1-3+ years working experience in a large-scale biopharmaceutical manufacturing facility.
• Experience with Delta V and MES is an advantage.

Responsibilities

• Facilitate implementation of project design and validation of the manufacturing facility.
• Create operating procedures for large scale manufacturing.
• Execute commercial manufacturing processes according to established work instructions.

Skills

Problem solving ability

Excellent communication skills

Ability to work independently and as part of a team

Education

Level 6 qualification in Engineering/Science

Tools

Delta V

SAP

Trackwise

Maximo

Job description

PE Global is currently recruiting for a Bioprocess for a leading multi-national Biotech client based in Dublin West. This is an initial 12-month contract position working on a 4 cycle 12-hour shift pattern as part of the Downstream Manufacturing operation.

Role

• 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.

Requirements

• 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.

Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland.