The RoleMy client is seeking to recruit a Contingent Worker for the position of BioProcess Associate Upstream Manufacturing within the Manufacturing Operations group.
Reporting to the Senior Manager, Upstream Manufacturing Shift Lead, this role will support the ongoing manufacturing operations within the facility, as well as commissioning and qualification activities for the process equipment.This is a shift role.Key Duties and Responsibilities:Execution of commercial manufacturing processes according to established work instructionsCreation of operating procedures & other relevant documentation for large scale manufacturingOperating production equipment within the assigned functional areaAdhering to Good Manufacturing Practices and Standard Operating ProceduresTaking part in investigations and optimisation of processes using scientific, engineering and lean principlesProficient use of process automation systems (i.e.
Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e.
SAP.
Trackwise, Maximo etc.
)Assisting with review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative and provide input to related investigations and QA audit activitiesWorking with the manufacturing operations group, the project design team, the CQV team, & the Automation/Computer Systems Validation teams to facilitate the implementation of the project design, validation and operation of the MPCC manufacturing facilityEngages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and a safe working environmentQualifications, 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)Working experience in a large-scale biopharmaceutical manufacturing facility would be a distinct advantageExperience with Delta V and MES or similar control and data acquisition systems would be desirableThe candidate must demonstrate an ability to work independently and also as part of a team.A successful candidate will have a demonstrated problem-solving ability and the ability to adhere to scheduled timelinesExcellent communication skills and the ability to work in a cross-functional, collaborative and fast-paced environment are essential