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Plastic Injection Molding Manager

Job in Clinton Charter Township, Clinton Township, Macomb County, Michigan, 48035, USA
Listing for: TriMas Corporation
Full Time position
Listed on 2026-10-18
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Manufacturing Engineer, Production Manager, Quality Engineering
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below
Location: Clinton Charter Township

Plastic Injection Molding Manager

Company:
Omega Plastics Inc

Primary

Location:

24401 Capital Blvd, Clinton Township, MI 48036 USA

Workplace Type:
On-site

Employment Type:

Salaried | Full-Time

Function:
Manufacturing Production / Distribution

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

Main

Duties & Responsibilities

Position Summary: Owns the manufacturing
client experience from the time the project is introduced to the manufacturing
floor through final part or assembly shipment. Responsible for providing input
to mold design to ensure successful sampling and production. Responsible for
the overall success and development of Omega's manufacturing operations team;
this includes all resources utilized to develop repeatable processes, molded
parts, and assemblies in a compliant, safe, productive, and profitable
environment. Provides the strategic development and evolution of medical device
manufacturing including development of volume production and assembly
processes. Responsible for the profitability, quality, and timeliness of the manufacturing
operations. This is accomplished through approximately 70% of daily
on-the-floor interaction.

Top accountabilities (no more than
3):
  • On-time delivery of product
  • Product quality/Compliance (Cost
    of Waste + Scrap)
  • Gross margin performance of molding
    department
Authority
  • Stop any activity that is considered in violation of company, regulatory or safety requirements
  • Identify capital equipment needed to Plant Manager for approval
  • Initiate training within approved budget and matrix requirements
  • Initiate hiring/counseling/dismissal process with HR for both direct and indirect reports
  • Direct and set hours for shift supervisors, process techs & engineers, mold setters, and warehouses lead to meet the schedule requirements
  • Initiate a problem-solving process at the press
Specific Responsibilities
  • Uphold and communicate the
    purpose, principles, and vision of the company.
  • Safety and cleanliness of
    manufacturing work environment (compliant with state & federal
    requirements)
  • Responsible for implementing the
    daily schedule, communicate unresolvable issues to Program Managers
  • Ensure shift leads are hitting
    cycle times, reporting properly on good product, scrap and non-conforming product
  • Direct Process Techs and Engineers for new samplings, technical consulting, problem resolution and schedule
  • Escalate immediately to the Plant Manager on jobs that are not going to meet the committed daily schedule
  • Responsible for training and leadership development of direct reports - includes staffing, recommendations, effective and timely training along with mid-year and annual reviews
  • Initiate and complete required
    controlled documentation improvements to Work Order Instructions and/or Process improvements
  • Responsible for direct report's
    compliance for all batch history records for medical molding and assembly operations
  • Direct daily team meetings to
    ensure alignment of schedule priorities and issue resolution
  • Ensure that appropriate systems
    and structures are in place to produce, package and release acceptable medical device products in accordance with GMP, GDP, FDA and client requirements
  • Coordinate with the Quality Manager and Quality Assurance Teams to ensure quality levels of product meet expectations
  • Provide Engineering support of
    new projects (processes, protocols, work instructions etc.)
  • Ensure Departmental compliance to
    QMS
  • Train team on lean, 5s, and
    appropriate best-in-class manufacturing processes that adhere to FDA regulations and
  • ISO
    13485 requirements to cultivate an environment of continuous improvement
  • Optimize cycle time and efficiencies through the addition of cobots, automation and end-of-arm tooling.
  • Other specified duties as
    required by the Plant Manager

This position is onsite 5 days a week at our Clinton Township facility

About Us

Tri Mas Life Sciences is a global provider of precision injection-molded components and assemblies for the medical device, diagnostic, pharmaceutical and surgical markets. The company serves key industries, including medical, packaging, industrial and consumer goods, and through our trusted brands, we deliver innovative, high-quality solutions that support our customers from prototype to full-scale production.

Our work enables life-saving technologies and products that improve people's lives, and we take pride in being part of that purpose every day.

Why Join Tri Mas Life Sciences?

At Tri Mas Life Sciences, we believe our success begins with our people. We are committed to creating an environment where every…

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