Pharmavise Corporation is seeking experienced Project Managers with backgrounds in life sciences consulting and regulated GxP environments to support current and future client initiatives. The role involves leading cross-functional projects within pharmaceutical, biotechnology, and medical device organizations, focusing on quality remediation, regulatory compliance, and operational improvement initiatives.
Responsibilities:
- 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
- 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