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Manufacturing Team Lead - Medical Device - Tilton, NH - Tilton New Hampshire
Company: Michael Page Location: Tilton, New Hampshire
Posted On: 05/03/2024
In this Manufacturing Team Lead role you will be responsible for overseeing production operations within the medical device manufacturing sector. The successful candidate will lead a team of dedicated engineers to ensure the efficient and timely production of high-quality medical devices while adhering to strict regulatory requirements. Client Details My client is a global CMO in the Medical Equipment Manufacturing industry. From concept to commercialization, my client offers end-to-end capabilities to help bring their customers' medical technology solutions to life. Description The Manufacturing Team Lead will report directly into the Engineering Manager and be responsible for: - Lead, motivate, and develop a team of approximately six (five manufacturing engineers and one technician).
- Collaborate with cross-functional teams including engineering, quality assurance, and supply chain to drive continuous improvement initiatives.
- Monitor production processes and implement corrective actions to address deviations and optimize efficiency.
- Plan, develop and execute process and test method validation (IQ/OQ/PQ).
- Ensure compliance with regulatory standards such as ISO 9001, ISO 13485, and FDA regulations.
- Drive initiatives to reduce waste, improve productivity, and enhance overall operational efficiency.
- Maintain accurate production records, documentation, and reports as required by regulatory authorities.
- Provide regular performance feedback, coaching, and training to team members to foster a culture of continuous learning and development. Apply today for immediate consideration! Profile
- Bachelors Degree in Engineering (Masters in Engineering or MBA is a plus)
- 5-7+ years of experience in a contract manufacturing industry (Medical Device preferred)
- Knowledge of continuous improvement, lean and six sigma tools (greenbelt preferred)
- Working knowledge of ISO 9001, ISO 13485 and FDA regulations
- Strong communication skills and ability to work in cross-collaborative teams
- Ability to prioritize tasks, solve problems, and make sound decisions in a fast-paced environment
- Demonstrated ability to lead and develop a diverse team of professionals Job Offer
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