Associate Project Manager

We have an opportunity for an Associate Project Manager to join our team. In this role, you will lead and facilitate projects across Product Development, Technical Services, and business continuity programs. You will manage project plans, budgets, and timelines to ensure successful completion. You will collaborate with cross-functional teams and external partners to achieve project goals while maintaining compliance with industry standards.

Responsibilities

Lead and facilitate projects across Product Development (NCE, generics, early-phase feasibility), Technical Services, commercial support, transfers, and business continuity programs; Develop and manage comprehensive project plans to ensure milestones, timelines, and budgets are achieved; Identify and remove roadblocks while leading meetings that drive progress and successful project completion; Oversee and manage capital budgets to ensure project funding is properly allocated, utilized, and closed according to plan; Select and coordinate effective cross-functional teams to support project objectives; Communicate project status and requirements with customers, cross-site project managers, suppliers, vendors, and contractors to ensure alignment and seamless execution; Ensure all project activities comply with current cGMP, EHS, and financial industry standards; Additional duties as assigned

Requirements

Bachelor's degree required in Engineering or Physical Sciences, including, but not limited to, Chemistry, Biology, Chemical, Mechanical, Electrical, or Civil Engineering, or Pharmacy; 1+ years of project management experience or other experience that demonstrates successful team leadership and project completion required; Working knowledge of project management principles and concepts in a cGMP environment; Ability to work effectively under pressure to meet deadlines; Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance; Be accessible to manufacturing floor and office staff and to use required office equipment; Specific vision requirements include reading of written documents and frequent use of computer monitor

Nice to have

3+ years of experience in FDA regulated industry; pharmaceutical CDMO industry experience preferred

Benefits

Competitive Paid Time Off plus 8 paid holidays; Medical, dental, and vision benefits effective day one of employment; Tuition Reimbursement; Employee Resource Groups focusing on Diversity and Inclusion; Environmentally friendly, community engagement green initiatives including regular participation in Beach Clean-up; Defined career path and annual performance review and feedback process with potential for career growth; WellHub program to promote overall physical and mental wellness; Perkspot discounts from approximately 900+ merchants