Medical Murray
Job Description
Job Description
Join Us as a Product Manager – Lead, Innovate, and Deliver Excellence We are seeking an experienced
Product Manager
to oversee the full manufacturing lifecycle of a key medical device. In this critical role, you’ll serve as the bridge between product management, operations, quality, regulatory, and engineering — ensuring products are manufactured efficiently, meet FDA and ISO standards, and consistently deliver on quality, safety, and reliability. If you thrive on turning complex challenges into streamlined solutions, and you want your work to have a direct impact on patient care and product success, this is your opportunity. What You’ll Do
Oversee the
full production lifecycle
for assigned medical device products, aligning production, quality, regulatory, and delivery goals.
Serve as the
primary liaison
across project management, manufacturing, quality, regulatory, and engineering teams.
Ensure compliance with
FDA (21 CFR Part 820) ,
ISO 13485 , and other applicable regulations.
Lead production readiness for
new product introductions (NPI) , including documentation, tooling, training, and process optimization.
Monitor production metrics (yield, throughput, quality, delivery) and drive improvements.
Manage engineering change orders (ECOs) and maintain accurate production documentation (DMRs, BOMs, work instructions).
Drive continuous improvement initiatives for cost, manufacturability, and quality.
Collaborate with Supply Chain to ensure material readiness and resolve supply constraints.
Participate in internal and external audits as needed.
What We’re Looking For
Bachelor’s degree in Engineering, Life Sciences, Operations, or related field (or equivalent experience).
3+ years
in medical device manufacturing, product management, or operations within regulated environments.
Strong knowledge of
FDA QSR
and
ISO 13485
requirements.
Proven success leading cross-functional teams from development through production.
Supervisory experience in manufacturing.
Strong analytical, organizational, and problem-solving skills.
Proficiency in Microsoft Office 365; ERP/MRP knowledge is a plus.
Experience with Lean, Six Sigma, or other process improvement methods preferred.
Why You’ll Love It Here
Be a key player in
life-changing medical device production .
Collaborate with an exceptional cross-functional team.
Competitive pay, comprehensive benefits, and professional growth opportunities.
A culture committed to
quality, innovation, and compliance .
Ready to take ownership of a product’s journey from production floor to patient impact? Apply now and help us set the standard for manufacturing excellence in the medical device industry.
Job Description
Join Us as a Product Manager – Lead, Innovate, and Deliver Excellence We are seeking an experienced
Product Manager
to oversee the full manufacturing lifecycle of a key medical device. In this critical role, you’ll serve as the bridge between product management, operations, quality, regulatory, and engineering — ensuring products are manufactured efficiently, meet FDA and ISO standards, and consistently deliver on quality, safety, and reliability. If you thrive on turning complex challenges into streamlined solutions, and you want your work to have a direct impact on patient care and product success, this is your opportunity. What You’ll Do
Oversee the
full production lifecycle
for assigned medical device products, aligning production, quality, regulatory, and delivery goals.
Serve as the
primary liaison
across project management, manufacturing, quality, regulatory, and engineering teams.
Ensure compliance with
FDA (21 CFR Part 820) ,
ISO 13485 , and other applicable regulations.
Lead production readiness for
new product introductions (NPI) , including documentation, tooling, training, and process optimization.
Monitor production metrics (yield, throughput, quality, delivery) and drive improvements.
Manage engineering change orders (ECOs) and maintain accurate production documentation (DMRs, BOMs, work instructions).
Drive continuous improvement initiatives for cost, manufacturability, and quality.
Collaborate with Supply Chain to ensure material readiness and resolve supply constraints.
Participate in internal and external audits as needed.
What We’re Looking For
Bachelor’s degree in Engineering, Life Sciences, Operations, or related field (or equivalent experience).
3+ years
in medical device manufacturing, product management, or operations within regulated environments.
Strong knowledge of
FDA QSR
and
ISO 13485
requirements.
Proven success leading cross-functional teams from development through production.
Supervisory experience in manufacturing.
Strong analytical, organizational, and problem-solving skills.
Proficiency in Microsoft Office 365; ERP/MRP knowledge is a plus.
Experience with Lean, Six Sigma, or other process improvement methods preferred.
Why You’ll Love It Here
Be a key player in
life-changing medical device production .
Collaborate with an exceptional cross-functional team.
Competitive pay, comprehensive benefits, and professional growth opportunities.
A culture committed to
quality, innovation, and compliance .
Ready to take ownership of a product’s journey from production floor to patient impact? Apply now and help us set the standard for manufacturing excellence in the medical device industry.