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Full Time Manager Medical Device Jobs (NOW HIRING)

Freudenberg

Program Manager - Medical Device

Beverly, MA

$120K - $140K/yr

... Medical Device or related industry. * 6+years' experience in Project/Program Management in a manufacturing environment, with advanced experience of leading work within a project plan framework ...

Prismatik

Project Manager - Medical Device

Irvine, CA · On-site

$81K - $115K/yr

Minimum three (3) years of experience in project management; medical device industry experience, a plus. * Demonstrated knowledge of International Organization for Standardization (ISO) and Food and ...

PrideStaff

Assembly Tech - Medical Device

San Clemente, CA · On-site

$21 - $22/hr

We're hiring a Medical Device Assembler / Assembly Technician for a full-time, temp-to-hire opportunity. This position is ideal for candidates with experience in medical device assembly, electronics ...

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Full Time Manager Medical Device information

What is the difference between Full Time Manager Medical Device vs Medical Device Quality Assurance Specialist?

AspectFull Time Manager Medical DeviceMedical Device Quality Assurance Specialist
CredentialsTypically requires a Bachelor's or Master's in Engineering, Life Sciences, or related field; certifications like RAC or ISO auditor are commonUsually holds a Bachelor's in Life Sciences, Engineering, or Quality Assurance; certifications such as CQE or ISO auditor are often preferred
Work EnvironmentLeads teams, manages projects, and oversees compliance in manufacturing or R&D settingsFocuses on quality systems, audits, and compliance activities within manufacturing or quality departments
Employer & Industry UsageUsed by medical device companies for leadership roles overseeing product development and complianceCommonly employed in quality departments to ensure product safety and regulatory adherence

The Full Time Manager Medical Device typically holds leadership responsibilities, managing teams and projects, while the Medical Device Quality Assurance Specialist focuses on quality compliance and audits. Both roles require relevant certifications and work within the same industry environment, but their core functions differ in scope and focus.

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Full Time Manager Medical Device jobs near you

Program Manager - Medical Device

Sterling Engineering Inc.

Chicago, IL • On-site

$70/hr

Full-time

Posted 4 days ago

Job description

Program Manager – Medical Device

Location: Chicago, IL – Ravenswood/Montrose area
Pay: Up to $70/hr
Potential Direct Hire: Yes — target $120K–$140K+, depending on background

Position Overview
A leading medical device manufacturer specializing in drug delivery devices is seeking a Program Manager to lead and coordinate product development programs from initial quotation through design freeze and process validation. This role will serve as a key customer interface while leading cross-functional teams to ensure projects meet quality, cost, timing, and risk objectives.
Medical device experience is a MUST.

Key Responsibilities
  • Lead and manage internal and external customers as the primary program contact.
  • Coordinate cross-functional teams throughout medical device development.
  • Develop and manage program plans, budgets, timelines, and expenses.
  • Identify program risks and drive action plans to keep projects on track.
  • Manage multiple programs simultaneously.
  • Present program status and updates during governance meetings.
  • Coordinate with Finance to track program costs and budgets.
  • Participate in technical decisions and supplier selection.
  • Lead multidisciplinary teams across multiple locations.
Must Have
  • Medical device industry experience — REQUIRED
  • Bachelor’s degree in Engineering, Science, or related field.
  • 3–5+ years of Program Management experience.
  • Experience leading multidisciplinary project teams.
  • Strong customer-facing experience.
  • Excellent leadership, communication, and organizational skills.
Highly Preferred
  • Experience with high-volume manufacturing, injection molding, and automation.
  • Medical device or combination product development experience.
  • Familiarity with FDA 21 CFR 820, ISO 13485, and ISO 62366.
  • Experience managing programs across multiple sites.


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.