Project Manager

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee and direct cross-functional projects within the pharmaceutical, biotechnology, and/or medical device sectors.

• Create and manage project plans, schedules, budgets, risk assessments, and progress reports.

• Coordinate project operations across Quality, Regulatory, Engineering, Validation, Manufacturing, Clinical, and Supply Chain teams.

• Organize stakeholder meetings and relay project updates to client leadership and internal teams.

• Recognize project risks, challenges, and mitigation strategies to guarantee successful project delivery.

• Assist with project governance, resource allocation, prioritization, and execution tasks.

• Ensure projects comply with relevant GxP, FDA, ISO, and industry standards.

• Promote accountability, track action items, and manage project deliverables across various stakeholders.

• Contribute to continuous improvement and operational excellence initiatives.

• Foster strong client relationships and represent Pharmavise with professionalism in client interactions.

⛳️ Requirements

• Bachelor's degree in Engineering, Life Sciences, Business, Healthcare, or a related discipline.

• Over 5 years of Project Management experience in the life sciences sector.

• Background in supporting pharmaceutical, biotechnology, and/or medical device companies.

• Strong grasp of GxP-regulated environments.

• Proven experience in managing cross-functional teams, timelines, budgets, and project outcomes.

• Exceptional communication, stakeholder management, and organizational abilities.

• Capacity to work autonomously in dynamic client settings.

• Proficiency in project management and collaboration tools like Microsoft Project, Smartsheet, Jira, SharePoint, or equivalent platforms.

• PMP certification or another equivalent project management certification is preferred.

• Experience in consulting or professional services environments.

• Background in supporting Fortune 500 life sciences organizations.

• Familiarity with FDA, ISO 13485, 21 CFR Part 11, ICH, GMP, GLP, or GCP regulations.

• Experience leading global or multi-site projects.

🏝️ Benefits

• Options for remote work.