Manager, Production - CR (Shift A)
Position Overview
Direct and coordinate activities concerned with production of the company product(s) utilizing knowledge of product technology, production methods and procedures, and managing resources appropriately. Job duties:
- Plan, direct, and coordinate manufacturing operations, establishing priorities to ensure adherence to the production schedule.
- Review and analyze operational metrics to identify causes of nonconformity with product specifications.
- Promote world-class manufacturing practices on the production floor.
- Facilitate continuous improvement initiatives in collaboration with cross-functional teams. Ensure all production training is current, and that required documentation is maintained.
- Partner with managers and leadership to promote employee engagement, boost morale, and strengthen team dynamics.
- Set clear expectations, provide regular feedback, and conduct performance evaluations to support continuous improvement.
- Oversee daily operations by providing direction and support to production supervisors and their teams across assigned shifts.
- Monitor raw material inventory level and manage production WIP/Orders.
- Develop and implement plans to improve production efficiency.
- Oversee the production process, ensuring that it runs smoothly and according to schedule.
- Drive operational efficiency and achieving the organizational objectives.
- Monitor production costs and implement cost savings strategies.
- Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
- Perform additional duties as required.
- Bachelor's degree in a technical Engineering field, Business Administration, or related field of study.
- A minimum of seven (7) years of professional experience in medical device environment or similar field.
- A minimum of three (3) years of experience in a management capacity, overseeing teams, resources, and operational initiatives.
- Strong knowledge of industry regulations, quality standards (e.g., ISO 13485, FDA, etc.), and best practices.
- Strong knowledge of lean manufacturing principles.
- Strong written and verbal communication and interpersonal skills.
- Written and verbal English proficiency (B2 – C1).
- Excellent organizational skills.
- Proficient computer skills including MS Word, Excel, PowerPoint, Outlook, and Teams.
- Master’s degree in engineering or related field of study.
- Knowledge of regulatory guidelines, medical and biomedical development, and production equipment.
- Working knowledge of product planning and production control tools.
- Proven ability to lead, influence, and motivate associates at all levels of the organization, from frontline staff to senior leadership.
- Strong data analysis and structured problem-solving skills, with the ability to interpret complex information, identify root causes, and develop effective data-driven solutions.