Project Manager

This is a remote position.Pharmavise is seeking experienced Project Managers with backgrounds in life sciences consulting and regulated GxP environments to support current and future client initiatives. This is a pipeline/talent pool opportunity intended to identify professionals who can lead cross-functional projects within pharmaceutical, biotechnology, and medical device organizations.Projects may include quality remediation, manufacturing operations, validation, engineering, digital transformation, clinical operations, regulatory compliance, product development, PMO support, inspection readiness, system implementations, and operational improvement initiatives.The ideal candidate is highly organized, collaborative, client-facing, and experienced managing complex projects in FDA-regulated environments.Key ResponsibilitiesLead and manage cross-functional projects within pharmaceutical, biotechnology, and/or medical device environmentsDevelop and maintain project plans, timelines, budgets, risk registers, and status reportsCoordinate project activities across Quality, Regulatory, Engineering, Validation, Manufacturing, Clinical, and Supply Chain teamsFacilitate stakeholder meetings and communicate project updates to client leadership and internal teamsIdentify project risks, issues, and mitigation strategies to ensure successful project executionSupport project governance, resource planning, prioritization, and execution activitiesEnsure projects align with applicable GxP, FDA, ISO, and industry compliance requirementsDrive accountability, action item tracking, and project deliverables across multiple stakeholdersSupport continuous improvement and operational excellence initiativesMaintain strong client relationships and represent Pharmavise professionally in client-facing environmentsPreferred Project BackgroundsWe are interested in Project Managers with experience supporting initiatives such as:FDA remediation and inspection readinessCAPA and Quality Systems projectsManufacturing site expansions or tech transfersCommissioning, Qualification, and Validation (CQV)Computer System Validation (CSV) / CSA projectsProduct development and design control initiativesClinical operations and trial managementERP, QMS, MES, LIMS, or digital transformation implementationsPMO and enterprise transformation programsSupplier quality and operational excellence projectsQualificationsRequiredBachelor’s degree in Engineering, Life Sciences, Business, Healthcare, or related field5+ years of Project Management experience within the life sciences industryExperience supporting pharmaceutical, biotechnology, and/or medical device organizationsStrong understanding of GxP-regulated environmentsDemonstrated experience managing cross-functional teams, timelines, budgets, and project deliverablesExcellent communication, stakeholder management, and organizational skillsAbility to work independently in fast-paced client environmentsProficiency with project management and collaboration tools such as Microsoft Project, Smartsheet, Jira, SharePoint, or similar platformsPreferredPMP certification or equivalent project management certificationExperience within consulting or professional services environmentsExperience supporting Fortune 500 life sciences companiesKnowledge of FDA, ISO 13485, 21 CFR Part 11, ICH, GMP, GLP, or GCP requirementsExperience leading global or multi-site projects Originally posted on Himalayas