Project Manager – Regulatory Affairs

About the Company

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

Position: Project Manager Regulatory Affairs
Location: Washington
Duration: Long Term

Job Overview

We are seeking a Project Manager Regulatory Affairs with 8+ years of global regulatory experience. The ideal candidate will have strong experience in global product registrations, regulatory submissions, dossier management, and LATAM regulatory activities, preferably with INVIMA.

Key Responsibilities

Lead global product registrations, re-registrations, renewals, and lifecycle activities.
Manage regulatory submissions across international markets.
Compile, review, and maintain regulatory dossiers and submission documents.
Coordinate variations, renewals, amendments, and regulatory compliance activities.
Manage regulatory deficiencies, agency queries, and affiliate requests.
Maintain accurate and submission-ready regulatory documentation.
Support regulatory remediation, gap closure, and registration recovery activities.
Work with R&D, Quality, Supply Chain, Manufacturing, Marketing, Legal, and global affiliates.
Track project timelines, milestones, risks, and launch readiness.
Maintain regulatory databases, submission trackers, and document management systems.
Provide regular project updates to stakeholders.
Act as the regulatory project contact for global stakeholders, affiliates, and regulatory agencies.

Required Qualifications

Bachelor's degree in Pharmacy, Life Sciences, Chemistry, Biotechnology, Regulatory Affairs, or a related field.
8+ years of Regulatory Affairs experience.
Strong experience with global product registrations, re-registrations, and renewals.
Experience with regulatory dossier compilation and submission management.
Experience managing multiple regulatory projects and timelines.
LATAM regulatory experience is preferred.
INVIMA experience is highly preferred.
Experience with regulatory remediation, gap closure, registration recovery, or market continuity programs.
Strong knowledge of regulatory documentation and quality compliance requirements.
Experience with regulatory databases and document management systems.
Strong project management, stakeholder management, communication, and problem-solving skills.

How to Apply

Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.