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.
