PR · On-site
... or medical device industry. * Experience managing or supporting capital projects valued under $1.0 MM. * Bilingual (English & Spanish). * Problem-solving and root cause analysis. * Shift:
PR · On-site
... or medical device industry. * Experience managing or supporting capital projects valued under $1.0 MM. * Bilingual (English & Spanish). * Problem-solving and root cause analysis. * Shift:
Arecibo, PR · On-site
$90 - $130/hr
Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Experience supporting Capital Projects, Automation ...
Arecibo, PR · On-site
$90 - $130/hr
Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Experience supporting Capital Projects, Automation ...
Bachelor's degree in Engineering or related field * 5+ years of Project Management experience in pharmaceutical, biotech, medical device, or GMP-regulated industries * Strong experience managing ...
Bachelor's degree in Engineering or related field * 5+ years of Project Management experience in pharmaceutical, biotech, medical device, or GMP-regulated industries * Strong experience managing ...
PR · On-site
Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Experience supporting Capital Projects, Automation ...
Quick apply
PR · On-site
Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Experience supporting Capital Projects, Automation ...
PR · On-site
Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Experience supporting Capital Projects, Automation ...
Quick apply
PR · On-site
Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Experience supporting Capital Projects, Automation ...
PR · On-site
Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Experience supporting Capital Projects, Automation ...
Quick apply
PR · On-site
Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments. * Experience supporting Capital Projects, Automation ...
Manati, PR · On-site
For Project Management services in Capital Projects. WHAT MAKES YOU A FIT: The Technical Part ... Medical Device, and Manufacturing industry clients with top-notch quality talent. We're FITS! Are ...
Manati, PR · On-site
For Project Management services in Capital Projects. WHAT MAKES YOU A FIT: The Technical Part ... Medical Device, and Manufacturing industry clients with top-notch quality talent. We're FITS! Are ...
Cidra, PR · On-site
For Project Manager services in the Capital Projects area. WHAT MAKES YOU A FIT: The Technical Part ... Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are ...
Cidra, PR · On-site
For Project Manager services in the Capital Projects area. WHAT MAKES YOU A FIT: The Technical Part ... Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are ...
Cayey, PR · On-site
Project Management life cycle and skills. * Project Schedules and Cost Estimates * Support ... Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are ...
Cayey, PR · On-site
Project Management life cycle and skills. * Project Schedules and Cost Estimates * Support ... Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are ...
PR · On-site
For Project Management services in the Capital Projects area. WHAT MAKES YOU A FIT: The Technical ... Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are ...
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Quick apply
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Quick apply
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Quick apply
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Punta Santiago, PR · On-site
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Punta Santiago, PR · On-site
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Quick apply
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
Quick apply
Minimum of 8 years of experience managing capital projects within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries. * Demonstrated experience supporting manufacturing ...
PR · On-site
The incumbent will manage multiple well-defined projects and assignments, while supporting larger ... Experience in regulated industries such as pharmaceutical, biotechnology, or medical device ...
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PR · On-site
The incumbent will manage multiple well-defined projects and assignments, while supporting larger ... Experience in regulated industries such as pharmaceutical, biotechnology, or medical device ...
PR · On-site
The incumbent will manage multiple well-defined projects and assignments, while supporting larger ... Experience in regulated industries such as pharmaceutical, biotechnology, or medical device ...
PR · On-site
The incumbent will manage multiple well-defined projects and assignments, while supporting larger ... Experience in regulated industries such as pharmaceutical, biotechnology, or medical device ...
Gurabo, PR · On-site
The Senior Project Manager / Site Lead serves as JLL's primary project delivery leader for the ... Experience in pharmaceutical, medical device, biotechnology, GMP, FDA-regulated, life sciences, or ...
Gurabo, PR · On-site
The Senior Project Manager / Site Lead serves as JLL's primary project delivery leader for the ... Experience in pharmaceutical, medical device, biotechnology, GMP, FDA-regulated, life sciences, or ...
| 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.

Contractor
Posted 13 days ago