Program Manager

Program Manager

Company: Omega Plastics Inc

Primary Location: 24401 Capital Blvd, Clinton Township, MI 48036 USA

Employment Type: Salaried Full-Time

Function: Manufacturing Production / Distribution

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

Main Duties & Responsibilities

Position Summary:

This position provides

overall Program Management responsibility for assigned major projects

contributing to top-line business growth. This includes leading initiatives

involving a Contract Design Manufacturer (CDM) for medical devices and tooling,

ensuring seamless collaboration and execution of design, development, and

manufacturing processes. Additional responsibilities include managing product

changes, cost savings, and capacity expansion initiatives. The role requires

strong leadership in working with cross-functional teams to navigate roadblocks

and ensure project success. A demonstrated ability to influence across

functional areas and coordinate both external and internal resources is essential,

along with a proven track record of successfully leading and delivering large,

complex projects. The successful candidate will exemplify best-in-class program

management practices.

Essential Duties &

Responsibilities:

Apply

fundamental, sound program management techniques and workflow processes

when executing assigned projects, particularly those involving a CDM for

medical devices and tooling.

Develop and

maintain project plans using MS Project and WBS structures, clearly

outlining objectives, timelines, and risks, while adapting to evolving

project requirements.

Oversee

communication planning, project risk assessment, and change management

strategies, ensuring alignment with both internal stakeholders and

external manufacturing partners.

Facilitate

effective team and client meetings, fostering strong relationships with

CDM partners to drive project milestones and quality outcomes.

Resolve and/or

escalate issues in a timely fashion, particularly those impacting design

transfer, regulatory compliance, and production timelines.

Communicate

effectively with project teams to identify needs and evaluate alternative

business solutions.

Ensure

compliance with FDA regulations and ISO 13485 standards for medical device

manufacturing, maintaining proper documentation of project activities.

Aid in the

development and implementation of Program Management guidelines and

processes, incorporating best practices for working with external

manufacturers.

Support

training events on execution processes to improve internal capabilities in

managing CDM relationships.

Act as a

subject matter expert (SME) for program management, particularly in the

integration of contract manufacturing partners into development pipelines.

Periodic travel

may be required to visit CDM facilities, suppliers, and stakeholders. To view our benefits, please visit: trimasbenefits.com

Qualifications

Bachelor's degree in business,

engineering, medical technology, or a related discipline.

Minimum 5+ years' experience as a

project manager delivering medium to large, complex technical projects,

preferably in medical devices, contract manufacturing, or regulated

industries.

Experience managing CDM

relationships with a focus on product development, tooling, and

commercialization.

Strong verbal, written, and

interpersonal skills, with the ability to build trust and foster

collaboration across teams.

Proven track record of successfully

executing complex projects on time and within budget, with a focus on

medical devices and precision tooling.

Advanced proficiency in Microsoft

Office, MS Project, and project visualization tools, with the ability to

generate graphs, presentations, and reports.