Our client a biopharmaceutical company is seeking to recruit a Downstream Manufacturing Bioprocess Associate for their Manufacturing Operations group to work on shift with a competitive uplift. This would be based in their best in class manufacturing facility in West Dublin. If you're interested in getting hands on experience with a global organization and learning from some of the very best in the industry please reach out today.
Role Summary:
Reporting to the Senior Manager, Downstream Manufacturing Shift Lead. It will support the ongoing manufacturing operations within the facility, as well as commissioning and qualification activities for the process equipment where required.
Main 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 optimizations 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.
Experience & Qualifications:
• 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.
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