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Job Description
Responsibilities:
MEDS document administrator: to coordinate the timely update and approval of standard operating procedures
To liaise with the Learning & Development team to plan instructor-led training for the production teams
Maintain critical training records and activities for the teams, to include (but not limited to) eye test examinations and gowning qualifications
To liaise with the Supply Chain and Warehousing team to ensure inventory checks are planned and executed according to the schedule
In conjunction with the production teams, ensure that all preventative maintenance activities are appropriately recorded in our production schedules
Review status of corrective work order requests and ensure timely closure by the responsible team member
Review open purchase order requests and liaise with owner to ensure timely closure or update
Raise ad-hoc purchase requisitions for the IPT as needed
Scheduling of safety walkthroughs, housekeeping and GEMBA walks
Review and communication of other KPI’s relevant to production operation
Other administrative support to production management as required
Input into projects and improvement initiatives as required
Skills Required:
Effective communicator; able to communicate clearly across multiple disciplines (verbally and in written form)
Highly organised and able to prioritise
High level of Microsoft Office proficiency
Experience of working in a GMP environment
Closing date for applications: 3rd December 2024
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
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