Senior Project Manager

Validation and Engineering Group, Inc

$100K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering
  • Experience in direct process/manufacturing areas
  • Fully bilingual (English/Spanish) with strong communication skills
  • Strong project management experience in regulated environments (pharmaceutical/biotechnology/life sciences)
  • Ability to manage complex projects and multiple priorities independently
  • Proficient with Smartsheet for project management tasks
  • Experience working with ALM and SAP

Responsibilities

  • Lead project planning, execution, tracking, and closeout activities
  • Develop and maintain project schedules, action logs, dashboards, and progress reports
  • Coordinate cross-functional team activities and ensure alignment on priorities
  • Track project milestones, deliverables, risks, and action items
  • Facilitate project meetings and resolve open items promptly
  • Provide project status updates to stakeholders and leadership
  • Manage project documentation and maintain accurate records

Benefits

  • Collaborative work environment
  • Opportunity to drive impactful projects within a highly regulated field
  • Professional development support
  • Exposure to complex project dynamics in the pharmaceutical industry
  • Possibility of flexible working hours based on project needs
Full Job Description
  • Senior Project Manager

Description:

We are seeking an experienced Project Manager to support project execution within a regulated pharmaceutical environment. The ideal candidate will have demonstrated success managing complex projects, coordinating cross-functional teams, driving schedules and deliverables, and providing clear visibility to project status, risks, and priorities.

The Project Manager will be expected to take ownership of project planning and execution, proactively manage competing priorities, and maintain strong communication across technical and business stakeholders.

Responsibilities:
  • Lead project planning, execution, tracking, and closeout activities.
  • Develop and maintain integrated project schedules, action logs, dashboards, and progress reports.
  • Coordinate activities across cross-functional teams and ensure alignment on priorities, responsibilities, and deadlines.
  • Track project milestones, deliverables, dependencies, risks, issues, and action items.
  • Facilitate project meetings and drive timely resolution of open items.
  • Provide clear and concise project status updates to key stakeholders and leadership.
  • Manage project documentation and maintain accurate records within applicable systems.
  • Support resource planning, forecasting, change management, and project controls activities.
  • Identify schedule or execution risks early and develop appropriate mitigation and recovery plans.
  • Coordinate with internal teams, vendors, contractors, and other project stakeholders as required.
  • Ensure project activities are executed in accordance with applicable procedures and expectations within a regulated environment.

Qualifications:
  • Bachelor's Degree in Engineering.
  • Experience in direct process / manufacturing areas.
  • Must be fully bilingual (English / Spanish) with strong written and verbal communication skills.
  • Strong project management experience, preferably supporting pharmaceutical, biotechnology, life sciences, or another regulated environment.
  • Demonstrated ability to independently manage complex projects and multiple priorities.
  • Strong proficiency with Smartsheet for project scheduling, tracking, dashboards, and reporting.
  • Experience working with ALM and SAP.
  • Strong organizational, analytical, communication, and stakeholder-management skills.
  • Ability to drive accountability and follow through on commitments across cross-functional teams.
  • Strong written and verbal communication skills
  • Available to work extended hours, possibility of weekends and holidays.

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