The Role
The Director of Project Management leads and coordinates drug development projects, ensuring timely delivery while managing client relationships and cross-functional teams.
Summary Generated by Built In
The Director of Project Management coordinates all projects related to client programs spanning across pre-formulation, formulation development, analytical development, cGMP manufacturing and stability studies for drug product development from preclinical to commercial. The Director of Project Management serves as the leader of the project management platform driving continuous improvement, by providing strategic direction, setting clear expectations and employing performance metrics to track delivery against client expectations. This role is accountable for managing our client programs internally and directly engaging with our clients throughout the life of the program. This position requires a scientific background with global expertise in current Good Manufacturing Processes (GMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), a comprehensive understanding of the drug development lifecycle and of clinical and commercial pharmaceutical manufacturing. The CDMO environment is fast-paced and requires an elevated level of multi-tasking skills that is essential to the success of this position.
ESSENTIAL DUTIES & RESPONSIBILITIES
- Provides operational leadership for customer projects in drug development and manufacturing
- Actively engages in and supports new business development opportunities
- Ensures timely and effective communication with business partners and leadership teams
- Manages a team of PMs who are directly assigned as the primary liaison for specific client programs
- Prepares meeting agendas, manages, and leads meetings, tracks action items via meeting minutes, and coordinates team activities through use of project management tools
- Develops a communication plan that will ensure alignment amongst the project team, client, internal subject matter experts, and all stakeholders
- Fosters a positive client experience and relationship, by providing industry leading customer service
- Establishes and manages project scope and work plans
- Ensures collaboration with appropriate team members across different functions for driving business decisions and client communication
- Manages changes in scope of projects through change orders
- Works closely with extended team to ensure project deliverables meet customer expectations and timelines
- Manages multiple client projects ensuring on-time, within-budget delivery.
- Accountable for hosting client visits to site. Ensures that all personnel involved with these activities on site are fully briefed regarding the nature of the visit, the customer, and their business interests
KNOWLEDGE, SKILLS, & ABILITIES
- A bachelor’s degree in science or engineering required; master’s degree and/or PMP preferred.
- Experience (10+ years) managing cross-functional teams or projects in a CDMO or pharmaceutical development or manufacturing setting
- Knowledge of project management techniques and tools
- Excellent leadership, written and verbal communication skills and ability to influence others
- Excellent negotiation and facilitation skills, with strong customer-service focus
- Strong aptitude for technical comprehension enabling rapid learning in a highly regulated environment
- Ability to lead multi-disciplinary project teams
- Strong understanding of pharmaceutical product development and manufacturing
- Strong knowledge of FDA regulation/ICH guidelines, U.S. drug development process and project management practices.
- Proficiency in Microsoft Office programs including Word, Excel, MS Project, and MS Teams
- Proficiency with ERP, CRM, and Quality Management Systems
PHYSICAL REQUIREMENTS
- Prolonged periods sitting at a desk and working on a computer.
- Must be able to lift up to 15 pounds at times.
August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.
Skills Required
- Bachelor's degree in science or engineering
- Master's degree and/or PMP
- 10+ years managing cross-functional teams or projects in a CDMO or pharmaceutical setting
- Knowledge of project management techniques and tools
- Excellent leadership and communication skills
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The Company
What We Do
August Bioservices is a Contract Development and Manufacturing Organization (CDMO) headquartered in Nashville, Tennessee. August Bio offers a full range of pharmaceutical contract development and manufacturing services to pharmaceutical and biotech clients. We focus on sterile injectables, topicals, highly-complex formulations, poorly soluble & highly viscous compounds, Uncommon container sizes & fill volumes and offer aseptic and non-aseptic terminally sterilized filling of vials (liquid and lyophilized), syringes and flexible IV bags.
