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Specialist, Downstream Manufacturing ( Downstream Bioprocess Associate)

Details of the offer

The Role BMS Cruiserath Biologics isseekingto recruit a permanent Specialist, Downstream Manufacturing within the Manufacturing Operations group. Reporting to the Senior Manager, Downstream Manufacturing Shift Lead, the Specialist, Downstream Manufacturing will support the ongoing manufacturing operations within the facility, as well as commissioning and qualification activities for the process equipment. This is a 24/7 shift role. Key DutiesAndResponsibilities Working with the manufacturing operations group, project design team, the CQV team, & the Automation/CSV reps tofacilitatethe 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,engineeringand lean principles Operatesall production equipment within the assigned functional area Effectively uses process automation systems (i.e. Delta V andSyncadeInteractions, OSI/Pi Historian) and some supporting business systems (i.e. SAP.Infinity, Maximo etc.). Assistswith 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,equipmentand safe work environment. Qualifications ,Knowledge And Skills Required 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) Min 1-2years working experience in a large-scale biopharmaceutical manufacturing facility Experience with Delta V and MES would be considered an advantage. The successful candidate mustdemonstratean ability to work independentlyand alsoas part of a team. The successful candidate mustdemonstrateproblem solving ability and to adhere to scheduled timelines. Excellent communication skills and the ability to work in a cross functional collaborative environment arerequired. Due to the nature of the manufacturing role, shift work will berequired for 24/7 mode of operations. 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. Youll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, life assurance and on-site gym Skills: Downstream experience Buffer chromatography column packing


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