To manufacture and pack Medical Devices to a high-quality standard in line with customer specification. To support the Production Supervisor in all aspects of safety, quality, costs, delivery, and people in line with business key performance metrics and business objectives.
This role will report directly to the Production Supervisor.
What the role involves:
- To have a proactive approach to safety by highlighting any observations or concerns.
- Ensure you and the team are always working in a safe manner.
- Ensure high standards of quality are achieved in line with Medical Device Standards ISO13485.
- Ensure products and information is in line with customer specification.
- Work to highest levels of Good Manufacturing Practice (GMP) across the manufacturing facility.
- Ensure batch documentation and associated documents are complete to a high standard of Good Document Practice (GDP)
- To work to achieve an hourly performance based on standard times.
- To work with the team to keep waste to a minimum escalating to the Production Supervisor when waste is increasing.
- Participate in achieving the production plan to achieve the highest levels of customer satisfaction (On Time in Full – OTIF)
- To actively work to achieve a targeted Operational Equipment Effectiveness (OEE).
- To attend your place of work prepared and on time, reporting any absence to the Production Supervisor prior to shift start.
- To develop your skills to enable flexibility within the team.
- To attend and actively participate in a pre-shift meeting.
- To effectively Manufacture product according to specification, continually working to identify opportunities to reduce waste and lower costs within the business.
- The job holder has no budget setting or spending responsibilities.
- The jobholder will be required to ensure product quality once trained and competent to do so, escalating to the appropriate person any matters of concern. Liaising closely with other members of the facility.
- The job holder has day to day interaction with Operations, Stores, Quality and Engineering departments.
- The job holder has no day-to-day supervisory responsibilities.
What we're looking for:
- Previous experience in manufacturing environment.
- Understanding of Health and Safety procedures.
- Understanding of Good Manufacturing Practice (GMP).
- The ability to accurately follow instructions.
- The ability to read and follow standard procedures.
- Ability to work well within a team.
- Ability to train to run multiple processes.
- Ability to be flexible with working hours to meet business demands
Shift pattern Monday - Friday 6am-2pm / 2pm-10pm alternative weeks
