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Value Stream Supervisor – 1st Shift

Job Category: Production
Job Type: Full Time
Job Location: Memphis
Country: US

Elos Medtech, a leading development and production partner for medical technology companies worldwide. At our locations in Sweden, Denmark, Switzerland, Germany, China, and the USA, Elos runs operations in four business areas – Dental, Orthopedics, Advanced Surgical and Precision. Elos Medtech has extensive expertise and specializes in development and design, along with contract manufacturing of medical devices, such as implants and instruments.

We are always aware of the millions of patients we can help worldwide and are committed to meeting and exceeding our customers’ high expectations. The company, headquartered in Gothenburg, Sweden, employs more than 1,500 people worldwide. In a globally growing healthcare market, we are looking for a full-time Value Stream Supervisor to strengthen our team in Memphis, TN.

The Value Stream Supervisor (1st Shift) leads a production value stream to achieve excellence in safety, quality, delivery, and cost in a medical device manufacturing environment. This role is responsible for developing team members, driving continuous improvement, and fostering a culture rooted in the core values of passion, trustworthiness, results-orientation, and togetherness. The supervisor will model leadership behaviors to engage people, lead by example, set direction, and foster inclusion.

Key Responsibilities:

  • Health & Safety Compliance: Promote and enforce safe working practices to maintain a secure work environment for all team members
  • Lead by Example: Demonstrate professionalism, integrity, accountability, and a strong work ethic in all interactions. Set the tone for team culture and performance
  • Engage and Empower Team Members: Motivate and support team members to perform at their best. Provide coaching, feedback, and development opportunities to foster growth and retention
  • Set Direction and Drive Results: Clearly communicate goals and expectations. Monitor performance metrics, allocate resources efficiently, and guide the team toward achieving operational and strategic objectives
  • Foster Inclusion and Collaboration: Create a respectful, inclusive work environment where diverse perspectives are welcomed and valued. Encourage open communication and teamwork
  • Oversee Time Keeping and Attendance Tracking: Ensure timely and accurate reporting in accordance with company policy
  • Ensure Operational Excellence: Oversee daily operations to ensure productivity, quality, and compliance with company standards, policies, and medical device regulatory requirements
  • Problem Solving and Decision Making: Identify issues, analyze root causes, and implement effective solutions in a timely manner
  • Performance Management: Conduct regular check-ins, evaluations, and performance reviews. Address performance issues constructively and in alignment with company practices

TRAINING

  • Participate in onboarding and leadership training programs as required
  • Ensure all team members receive proper job-specific training, including safety, quality, and standard work procedures
  • Maintain up-to-date training records for all employees in the value stream
  • Support and coach cross-training efforts to increase workforce flexibility and minimize production interruptions
  • Promote a continuous learning environment by identifying skill gaps and recommending development opportunities
  • Conduct regular refreshers and re-certifications to maintain compliance with regulatory and company standards

REQUIREMENTS:

EDUCATION:

  • High school diploma or equivalent required
  • Associate degree in manufacturing, business, engineering, or a related field preferred
  • Bachelor’s degree is a plus

EXPERIENCE:

  • 3-5 years of experience in manufacturing or production operations, preferably in medical device or regulated industries
  • Minimum of 2 years in a leadership or supervisory role, ideally within a value stream or lean manufacturing environment
  • Experience with FDA QSR, ISO 13485, GMP and validation processes preferred

SKILLS:

  • Strong leadership and team-building skills
  • Excellent written and verbal communication
  • Problem-solving and decision-making ability under pressure
  • Proficient in interpreting production metrics and KPIs
  • Must maintain good attendance and punctuality
  • Demonstrated ability to lead, engage, and develop diverse teams
  • Excellent organizational and time management skills
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook, Teams, etc.)
  • Strong organizational and multitasking abilities
  • Ability to maintain discretion and handle confidential information professionally

DRESS CODE:

Supervisors are expected to set the standard for appearance and safety compliance

  • Clothing must be clean, professional, and suitable for a manufacturing environment

PHYSICAL DEMANDS:

  • Ability to stand and move within a manufacturing environment for extended periods of time
  • Must be able to occasionally lift and/or move up to 40 lbs.
  • Ability to wear Personal Protective Equipment as required
  • Visual acuity to inspect parts, read documents, computer screens, etc.

WORKING CONDITIONS:

  • Work is performed primarily in a manufacturing environment, including production floor, assembly areas, and clean rooms
  • Exposure to noise, odors, moving mechanical parts, and varying temperatures depending on the season
  • Frequent interaction with machinery, tools, and production materials
  • Monday – Friday with weekend work as needed

    REPORTING STRUCTURE:
  • This position will report to the Operations Manager

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Elos Medtech
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