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Project Manager Latam Jobs in Raleigh, NC (NOW HIRING)

Project Manager Latam information

See Raleigh, NC salary details

$37.4K

$99.8K

$157.5K

How much do project manager latam jobs pay per year?

As of Aug 25, 2026, the average yearly pay for project manager latam in Raleigh, NC is $99,815.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,300.00 and $119,600.00 per year, depending on experience, location, and employer.

What is the difference between Project Manager Latam vs Project Coordinator Latam?

AspectProject Manager LatamProject Coordinator Latam
CertificationsPMP, CAPM, Agile certificationsPMI-ACP, CAPM, basic project management courses
Work EnvironmentLeads projects, manages teams, responsible for deliverySupports project tasks, coordinates activities, assists managers
Employer & Industry UsageUsed across industries like construction, IT, manufacturingCommon in similar industries, supporting project teams

The Project Manager Latam typically holds more advanced certifications and is responsible for leading projects and teams. In contrast, the Project Coordinator Latam supports project activities and assists the project manager. Both roles are essential in project execution, but the project manager has greater leadership and decision-making responsibilities.

What are popular job titles related to Project Manager Latam jobs in Raleigh, NC?

For Project Manager Latam jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Project Manager Latam jobs in Raleigh, NC look for?

The top searched job categories for Project Manager Latam jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Project Manager Latam jobs?

Cities near Raleigh, NC with the most Project Manager Latam job openings:

Senior Regulatory Affairs Specialist

Bioventus LLC

Durham, NC • On-site

$90 - $120/hr

Other

Re-posted 15 days ago


Job description

Position

Senior Regulatory Affairs Specialist – Durham, NC – Bioventus LLC.

Responsibilities
  • Author and submit regulatory applications (510(k), PMA supplements, and technical documentation) to obtain product clearance and approvals for new products and maintain existing registrations globally.
  • Author and maintain Technical Files compliant with MDD 93/42/EEC and EU MDR 2017/745.
  • Communicate with regulatory agencies regarding product submissions, changes (manufacturing, design, new development), and to represent regulatory affairs during internal and external audits.
  • Review protocols, reports, and marketing literature for scientific validity and regulatory compliance, providing scientific judgment to guide cross‑functional teams.
  • Perform regulatory assessments for design, manufacturing, and labeling changes to ensure compliance with applicable regulations and standards where the product is registered.
  • Research requirements, set priorities, and maintain project schedules; provide guidance and oversight to team members on regulatory compliance matters.
Qualifications
  • Master’s degree or foreign equivalent in Regulatory Affairs, Pharmaceutical Sciences, or a related field, plus a minimum of 3 years of experience in a regulatory affairs or related role within the medical and/or diagnostic device industry.
  • 3+ years of experience with regulatory assessment of engineering/design change execution; guiding cross‑functional teams; and preparing submission documents.
  • Regulatory registrations in at least three of the following agencies or regions: FDA, EMEA, Canada, LATAM, Japan, Australia.
  • Experience with product changes and submissions compliant with Medical Device Regulation (MDR) and EU Medical Device Directive (MDD).
  • Project management experience and proficiency in preparing and reviewing documentation regarding product changes.
Work Arrangement
  • Hybrid model: 3 days in office and 2 days remote within commuting distance.
  • National travel required approximately 25% of the time.
EEO Statement

Bioventus is committed to fostering an inclusive and diverse community. Qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion, or sexual orientation. All individuals, regardless of personal characteristics, are encouraged to apply.

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