Specialist, Upstream Manufacturing (Upstream Bioprocess Associate)

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BMS Cruiserath Biologics is seeking to recruit Specialist, Upstream Manufacturing (Upstream Bioprocess Associate) within the Manufacturing Operations group. Reporting to the shift lead, the role will involve in supporting the ongoing manufacturing operation of the facility and assist in the introduction of New Products into the facility. The Bioprocess Associate is a key contributor of the BMS team to add biologics manufacturing capacity to the BMS network in Cruiserath and help deliver lifesaving products to patients around the world.  Due to the nature of the manufacturing role, shift work will be required 24/7 mode of operations. Responsibilities will include (but not limited to): Working with the manufacturing operations and other departments to group to ensure successful implementation of New products into MPCC 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.

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 A minimum of 1-2 years’ large-scale experience in a biopharmaceutical manufacturing facility. 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. Why you should apply You will help patients in their fight against serious diseases You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees. You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance,  life assurance and on-site gym #LI-Onsite If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work