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.

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.