
SPN Production Team Lead
4 weeks ago
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embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. For more information, visitembecta.comor follow our social channels onLinkedIn,Facebook,InstagramandX.
Why join us?
A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program – which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components – is designed to support the varying needs of our diverse and global employees.
SPN Production Team Leader
- Reporting to the SPN Value Stream Leader, the SPN Production Team Lead role is responsible for coordinating production activities across Safety Pen Needle operations in addition to being a critical partner with relevant stakeholders including PQS Operators, Technicians, Process Engineering and QA Personnel
- Coordinate and lead the shift SPN team to meet SQDCP goals.
- Champion safety within the cell and promote a positive safety culture within the team.
- Work as part of a team to ensure optimum flow of units through the production process.
- Ensure compliance with Work Instructions, SOP's and GMP requirements at all times.
- Identify opportunities to improve work processes and methods as part of site CI/ Op Ex program.
- Assist in drawing up and communicating production schedule plans – liaise with buyer / planners and moulding suppliers as required.
- Monitor hour-by-hour performance across the assembly cell and support the team to improve performance where required and escalating where appropriate.
- Champion the NOE Quality process within the cell and ensure the team are raising NOEs for defective / suspected defective materials and support the material investigation to conclusion.
- Review documents in the device history records to ensure accuracy and timely completion.
- Work in conjunction with the Shift Manager and Training Team to develop team cross skilling capabilities.
- Liaise with the Quality department as required . Manage any sampling of lots and document as appropriate.
- Manage levels of WIP and take appropriate decisions with relevant personnel to
- Monitor raw material inventory and take action to address where required.
- Support the shift teams in managing work order accuracy to 100%
- Ensure production area is compliant with required quality standards
- As required, be involved in project planning and future developments.
- Perform other duties as assigned by management
- Second-level qualification coupled with appropriate experience
- Training in Good Manufacturing Practices
- Relevant Further Education – eg: Supervisory/Production management or Quality
- Minimum of 3 years' experience in a regulated manufacturing environment
- Leadership/Coordination experience in a production operation
- Lean Manufacturing
- Excellent documentation skills and attention to detail
- The ability to follow tasks through to completion
- Knowledge of Standard Operating Procedures.
- Excellent interpersonal and communication skills
- The ability to work as part of a team and on your own initiative
- Good PC skills
- Proactive – someone who anticipates potential problems and is a step ahead.
- Seniority levelMid-Senior level
- Employment typeFull-time
- Job functionManagement and Manufacturing
- IndustriesMedical Device
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