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 and Experience required:

• The successful candidate must possess a Bachelor in Engineering/ Science related subject.
• The successful candidate must possess at least 1 years' work experience in biopharmaceutical manufacturing.
• 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.
• The successful candidate will be hired on a temporary 12 month contract.