Project Manager

🕒 May 19

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Pharmavise Corporation

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2013

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.

📋 Description

• Lead and manage cross-functional projects within pharmaceutical, biotechnology, and/or medical device environments • Develop and maintain project plans, timelines, budgets, risk registers, and status reports • Coordinate project activities across Quality, Regulatory, Engineering, Validation, Manufacturing, Clinical, and Supply Chain teams • Facilitate stakeholder meetings and communicate project updates to client leadership and internal teams • Identify project risks, issues, and mitigation strategies to ensure successful project execution • Support project governance, resource planning, prioritization, and execution activities • Ensure projects align with applicable GxP, FDA, ISO, and industry compliance requirements • Drive accountability, action item tracking, and project deliverables across multiple stakeholders • Support continuous improvement and operational excellence initiatives • Maintain strong client relationships and represent Pharmavise professionally in client-facing environments.

🎯 Requirements

• Bachelor’s degree in Engineering, Life Sciences, Business, Healthcare, or related field • 5+ years of Project Management experience within the life sciences industry • Experience supporting pharmaceutical, biotechnology, and/or medical device organizations • Strong understanding of GxP-regulated environments • Demonstrated experience managing cross-functional teams, timelines, budgets, and project deliverables • Excellent communication, stakeholder management, and organizational skills • Ability to work independently in fast-paced client environments • Proficiency with project management and collaboration tools such as Microsoft Project, Smartsheet, Jira, SharePoint, or similar platforms • Preferred PMP certification or equivalent project management certification • Experience within consulting or professional services environments • Experience supporting Fortune 500 life sciences companies • Knowledge of FDA, ISO 13485, 21 CFR Part 11, ICH, GMP, GLP, or GCP requirements • Experience leading global or multi-site projects.

🏖️ Benefits

• Remote work options