Production Supervisor

Bracco Medical Technologies; Eden Prairie (MN); On-site; USD 75,000 - 81,000; Full time

Benefits offered by this job

Paid Time Off

401(k) plan

Medical, dental, vision insurance

Tuition reimbursement

Job summary

Bracco Medical Technologies in Eden Prairie, MN, seeks a Supervisor of Production to oversee the assembly of regulated medical devices. You will manage daily production, ensure on-time output within budget, and maintain adherence to GMP and quality systems.

The role emphasizes building a capable team, guiding performance, coordinating planning, and driving continuous improvements in manufacturing processes while ensuring accurate documentation and regulatory compliance.

Qualifications

• 2-year Associates degree or equivalent plus 5 years in electronics manufacturing.
• 2+ years supervisory or lead experience in manufacturing.
• Strong written and verbal communication skills.
• Ability to build relationships with staff and management.
• Proficient with ERP systems and MS Office.

Responsibilities

• Supervise daily assembly activities of production staff.
• Develop and coach production team members.
• Coordinate production planning and ensure inventory targets.
• Ensure GMP compliance and document control.
• Implement process improvements and lead audits.

Skills

Supervisory experience

Electronics manufacturing

MS Office

ERP systems

Communication skills

Organizational skills

Problem solving

Education

Associates degree

BS in Manufacturing Engineering

Tools

MS Office Suite

ERP software

Job description

Why Join Bracco Medical Technologies?

We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way. Each member of the Bracco Medical Technologies team has the power to make a difference......every day!

The Supervisor, Production is responsible for overseeing the assembly and production of the company's highly regulated medical devices. This role ensures that all production activities are completed efficiently, on schedule, within budget, and in compliance with quality and customer requirements.

The Supervisor ensures adherence to Good Manufacturing Practices (GMP) and established Quality Systems through effective process management, documentation control, and metric-driven performance oversight. Regular communication and updates to team members are essential to maintain alignment, support daily operations, and ensure successful execution of production plans.

Primary Duties & Responsibilities:

Supervision and Employee Development

• Supervise the daily activities of Assemblers and employees in the assembly of Medical Devices.
• Recruit, select and retain a high-performance Production team
• Balance the assembly lines and test area in relation to availability of staff and demands of daily production schedule
• Set and communicate performance expectations and hold team members accountable for achieving expectations and completing assignments
• Promote and manage employee development and foster employee growth of employees within the production group through:
  • Full-cycle Performance management
  • Skills development
  • Ongoing performance feedback and timely performance appraisal
  • Recognition and motivational techniques/tools to drive high levels of employee satisfaction.
• Manage conflict by dealing effectively with others in an antagonistic situation; use appropriate interpersonal styles and methods to reduce tension and conflict between two or more people
• Oversee and/or conduct training of new or existing employees and facilitates the assimilation of new members and changes.

Production Planning and Inventory

• Execute and offer input to the weekly, quarterly, and yearly production planning activities to maintain output to required inventory levels and customer demand.
• Monitor usage of materials to ensure efficiency of operations. Communicate with planning and procurement on priorities. Perform timely transactions online utilizing ERP/MRP system including Production Orders and the creation of NCMR's

Quality and Continuous Improvement

• Work closely with the manufacturing engineering and sustaining engineering groups to lead updates and improvements to manufacturing processes. Help develop, update, and maintain procedures and documentation to assure compliance to Quality System and Regulations.
• Maintain process records and metrics data gathering and reporting. Monitor quality of production output products by reviewing routers and test records.
• Initiate and execute change orders and updates to work instructions to ensure continuance of production.
• Develop and recommend improvements to facilities, equipment, or procedures that improve safety, quality, and efficiency.
• Implement existing production and business processes; make adjustments and recommendations as necessary to produce products within specifications.

Audit and Compliance Responsibility

• Work within the company's quality policy, established business practices and SOP's (Standard Operating Procedures) to ensure the operations environment is organized, compliant, and maintained.
• Accompany auditors as required.
• Recommend and implement action plans to correct deviations noted during audits.

Qualifications (Knowledge, Skills & Abilities):

Minimum

• 2-year Associates degree or, in lieu of degree, High School Diploma or equivalent plus five (5) years experience in an electronics manufacturing environment.
• 2+ years demonstrated supervisory or leadership (i.e. production lead) experience in a manufacturing environment
• Effective oral and written communication skills
• Demonstrated organizational and administrative skills.
• Demonstrated ability to build strong working relationships with direct reports, peers, and senior management across the organization
• Demonstrated problem-solving skills
• Moderate level of computer experience including MS Office Suite and familiarity with ERP systems
• Ability to prioritize and handle multiple tasks.

Preferred:

• BS in Manufacturing Engineering or Operations Management
• 5 yrs experience as a leader in a regulated environment
• Demonstrated ability to perform job duties of all subordinate positions
• Demonstrated expertise in a variety of process technologies and manufacturing environments
• Experience leading lean manufacturing and other process improvements in a regulated environment.

Compensation & Total Rewards:

• Estimated starting salary: $75k - 81k
• *Estimated starting salary is intended to reflect the salary Bracco Medical Technologies reasonably expects to pay for the position. The provided range is based on salary and market data and may vary based on an employee's eligibility for geographic differential pay in high-cost-of-labor markets.

Total Rewards:

• Paid Time Off, Company Holidays & Paid Family Leave - We provide PTO and Company Holidays to help you recharge, relax and do what's important to you, when it's important to you. Our 100% paid family leave options for parents, grandparents and eligible family members provide support for growing families as well.
• Achieve - Beyond competitive compensation, we offer options to help you plan for a financially secure future, including an annual incentive plan and 401k savings plan contributions.
• Live well - We offer comprehensive benefit options to help protect you along the way, including medical, dental, vision, and life insurance, employer HSA contributions, employee assistance program, short-term disability, etc.
• Evolve - Through structured on-the-job learning, workshops, seminars, and our tuition reimbursement program, you'll find many opportunities to grow, personally and professionally.
• Choose -You won't find "stuffy" here whether your position requires a hybrid or in-the-office working arrangement. That means business casual for your attire and flexibility in your schedule, wherever possible.

Bracco Medical Technologies is an Affidative Action/Equal Opportunity Employer. Bracco Medical Technologies desires priority referrals of protected veterans for all openings.