Project Manager
Guaynabo, PR · On-site
IEM is looking for a Full Time - Project Manager to join our team. The role is responsible for ... medical condition, genetic information, pregnancy (including childbirth and related medical ...
Guaynabo, PR · On-site
IEM is looking for a Full Time - Project Manager to join our team. The role is responsible for ... medical condition, genetic information, pregnancy (including childbirth and related medical ...
Guaynabo, PR · On-site
IEM is looking for a Full Time - Project Manager to join our team. The role is responsible for ... medical condition, genetic information, pregnancy (including childbirth and related medical ...
Anasco, PR · On-site
Food and Drug Administration regulations, ISO 9001, ISO 13485, EU MDR, the Canadian Medical Device ... Software and systems: ERP systems (e.g., SAP), CRM platforms, statistical analysis tools, project ...
Anasco, PR · On-site
Food and Drug Administration regulations, ISO 9001, ISO 13485, EU MDR, the Canadian Medical Device ... Software and systems: ERP systems (e.g., SAP), CRM platforms, statistical analysis tools, project ...
Food and Drug Administration regulations, ISO 9001, ISO 13485, EU MDR, the Canadian Medical Device ... Software and systems: ERP systems (e.g., SAP), CRM platforms, statistical analysis tools, project ...
Food and Drug Administration regulations, ISO 9001, ISO 13485, EU MDR, the Canadian Medical Device ... Software and systems: ERP systems (e.g., SAP), CRM platforms, statistical analysis tools, project ...
Juncos, PR · On-site
$96K - $125K/yr
... medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San ... Lead and manage packaging projects, including design, development, testing, and implementation.
Juncos, PR · On-site
$96K - $125K/yr
... medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San ... Lead and manage packaging projects, including design, development, testing, and implementation.
PR · On-site
... and Medical Devices industries in the following areas: Laboratory, Compliance, Computer ... Project Manager - Liquid Manufacturing & Filling Operations Position Summary We are seeking an ...
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PR · On-site
... and Medical Devices industries in the following areas: Laboratory, Compliance, Computer ... Project Manager - Liquid Manufacturing & Filling Operations Position Summary We are seeking an ...
PR · On-site
... Management, Business Administration, or a related field. * Minimum 3 years of experience in project scheduling or project controls in a regulated industry (pharmaceutical, biotech, medical device, or ...
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PR · On-site
... Management, Business Administration, or a related field. * Minimum 3 years of experience in project scheduling or project controls in a regulated industry (pharmaceutical, biotech, medical device, or ...
Capital Projects & Continuous Improvement * Lead or support equipment upgrades, automation, and ... Master's Degree + 3 years of experience in med device industry OR * Ph.D. + no experience Required
Capital Projects & Continuous Improvement * Lead or support equipment upgrades, automation, and ... Master's Degree + 3 years of experience in med device industry OR * Ph.D. + no experience Required
The Project Coordinator collaborates with cross-functional teams to monitor timelines, manage ... management processes, and supplier coordination workflows. * Experience in medical device ...
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The Project Coordinator collaborates with cross-functional teams to monitor timelines, manage ... management processes, and supplier coordination workflows. * Experience in medical device ...
Capital Projects & Continuous Improvement * Lead or support equipment upgrades, automation, and ... Master's Degree + 3 years of experience in med device industry OR * Ph.D. + no experience Required
Capital Projects & Continuous Improvement * Lead or support equipment upgrades, automation, and ... Master's Degree + 3 years of experience in med device industry OR * Ph.D. + no experience Required
Juncos, PR · On-site
$101K - $139K/yr
Pharmaceutical or Medical Device manufacturing environments. * Packaging equipment and ... Collaborate with Project Managers to ensure projects are completed on schedule, within budget, and ...
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Juncos, PR · On-site
$101K - $139K/yr
Pharmaceutical or Medical Device manufacturing environments. * Packaging equipment and ... Collaborate with Project Managers to ensure projects are completed on schedule, within budget, and ...
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
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... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
Punta Santiago, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
Punta Santiago, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
Punta Santiago, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
Punta Santiago, PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
Quick apply
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
Quick apply
PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
PR · On-site
... Medical Device industries in the areas of Laboratory, Compliance, Computer Systems, Engineering, Project Management, Validation, and related technical services. We are seeking a talented and ...
Quick apply
PR · On-site
... Medical Device industries in the areas of Laboratory, Compliance, Computer Systems, Engineering, Project Management, Validation, and related technical services. We are seeking a talented and ...
PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
Quick apply
PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
Quick apply
PR · On-site
... biotechnology, medical device, or other FDA-regulated industries. * Experience supporting ... Familiarity with technical documentation, change management, engineering coordination, and project ...
PR · On-site
... Medical Device industries in the areas of Laboratory, Compliance, Computer Systems, Engineering, Project Management, Validation, and related technical services. We are seeking a talented and ...
Quick apply
PR · On-site
... Medical Device industries in the areas of Laboratory, Compliance, Computer Systems, Engineering, Project Management, Validation, and related technical services. We are seeking a talented and ...
PR · On-site
... Medical Device industries in the areas of Laboratory, Compliance, Computer Systems, Engineering, Project Management, Validation, and related technical services. We are seeking a talented and ...
Quick apply
PR · On-site
... Medical Device industries in the areas of Laboratory, Compliance, Computer Systems, Engineering, Project Management, Validation, and related technical services. We are seeking a talented and ...
| Aspect | Seasonal Medical Device Project Manager | Medical Device Quality Assurance Specialist |
|---|---|---|
| Credentials | Project management certification (PMP), relevant industry experience | ISO 13485 training, quality assurance certifications |
| Work Environment | Project teams, manufacturing sites, regulatory agencies | Quality departments, laboratories, compliance offices |
| Employer & Industry Usage | Medical device companies during peak seasons or product launches | Manufacturers ensuring product quality and regulatory compliance |
| Search & Comparison Intent | Understanding project management roles in medical device industry | Quality assurance roles and compliance responsibilities |
The Seasonal Medical Device Project Manager focuses on managing projects during specific seasons or product launches, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Assurance Specialist concentrates on maintaining product quality, compliance with regulations, and conducting audits. Both roles require industry-specific certifications and work within the medical device manufacturing environment, but their core responsibilities differ significantly.

Full-time
Retirement, PTO
This job post has expired today. Applications are no longer accepted.
IEM is looking for a Full Time - Project Manager to join our team. The role is responsible for managing the execution of complex projects, ensuring alignment with program goals, regulatory compliance, and timely delivery. This includes coordinating cross-functional teams and external stakeholders, overseeing budgets and documentation, and ensuring adherence to federal requirements such as HUD CDBG-DR, NEPA, and Davis-Bacon. The position also supports risk management, audit readiness, and fosters a collaborative work environment focused on accountability, technical excellence, and service to the community.
Primary Location:
Travel Requirements:
Essential Functions:
Minimum Qualifications:
Preferred Qualifications:
Additional Information:
Benefits and more:
Equal Employment Opportunity: All IEM employment decisions, including recruiting, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination of employment, if necessary, are made without regard to an individual's race, color, religion, creed, sex (including sexual orientation, gender identity, and gender expression), national origin, ancestry, age, physical or mental disability, medical condition, genetic information, pregnancy (including childbirth and related medical conditions), marital status, military or veteran status, citizenship or immigration status, or any other characteristic protected under applicable law.
Reasonable Accommodation: IEM is committed to providing reasonable workplace accommodation for individuals with disabilities. If you require assistance or reasonable accommodation during any part of the application or employment process, please email IEMhumanresources@iem.com with specific details about the requested accommodation. All accommodation requests are reviewed case-by-case in compliance with applicable law.
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Business management consulting
1,001 - 5,000 Employees
Morrisville, NC, US
1985