Life Sciences Project Manager – Inspection Readiness

PSC Biotech; North Carolina; On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical, Dental, and Vision - PSC pays

401(k) and 401(k) matching

PTO, Sick Time, and Paid Holidays

Education Assistance

Pet Insurance

Fitness Perks and Discounted Rates

Financial Perks and Discounts

Job summary

PSC Biotech is seeking an experienced Project Manager to support cross-functional readiness initiatives in a regulated Life Sciences setting. You will coordinate action plans, track milestones, manage risks, and provide governance for assigned initiatives.

The role requires 3-7 years of PM experience in Life Sciences, strong scheduling and communication skills, and collaboration with Quality, Manufacturing, Engineering, and Validation teams to drive timely execution and readiness outcomes.

Qualifications

• Bachelor's or advanced degree in engineering or life sciences.
• 3-7 years of project management experience in regulated Life Sciences.
• Experience coordinating complex cross-functional projects with multiple stakeholders.

Responsibilities

• Coordinate action plans, tracking milestones, and managing risks for readiness initiatives.
• Facilitate action planning meetings and align stakeholders on priorities and timelines.
• Monitor schedules, milestones, and due dates to ensure timely completion of activities.
• Identify and elevate project risks and roadblocks impacting readiness objectives.
• Track corrective actions and ownership, maintaining visibility through reports and dashboards.
• Support inspection readiness activities through documentation management and evidence collection.
• Communicate project status updates and KPIs to leadership.

Skills

Project management

Cross-functional collaboration

Communication

Education

Bachelor's or Advanced degree in engineering or life sciences

Job description

PSC Biotech is seeking an experienced Project Manager to support cross-functional readiness initiatives in a regulated Life Sciences setting. You will coordinate action plans, track milestones, manage risks, and provide governance for assigned initiatives.

The role requires 3-7 years of PM experience in Life Sciences, strong scheduling and communication skills, and collaboration with Quality, Manufacturing, Engineering, and Validation teams to drive timely execution and readiness outcomes.