Manager of Project Management (Fishers)

Manager of Project Management WHO?: INCOG are seeking a Manager of Project Management (PM), who is an experienced leader with strong management capabilities, strategic thinking, and exceptional people development skills. They will report to the Director of PM and serve as a peer to the PMO Manager, leading a team of Associate PMs, PMs, and Senior PMs in delivering excellence across aseptic manufacturing, technology transfers, and new product launches. Are you passionate about developing high-performing teams while ensuring projects are delivered on time, within budget, and to the highest quality standards? Do you have the leadership skills to inspire and guide project management professionals in a fast-paced biopharmaceutical environment? If so, we want to meet you! WHAT?: Lead, mentor, and develop a team of Associate Project Managers, Project Managers, and Senior Project Managers, providing guidance, feedback, and career development opportunities to build a high-performing organization. Coordinate the portfolio team’s management of complex projects across entire Client’s portfolio of molecules, ensuring alignment with strategic objectives and customer requirements. Spearhead Project Portfolio Governance activities, including Operational Steering Committee logistics, agendas and facilitation as well as consolidated portfolio performance metrics and summary reporting as needed. Conduct regular performance reviews, set clear expectations and goals, and implement development plans for direct reports while fostering a culture of continuous improvement and accountability. Optimize resource allocation across the PM team, balancing workloads and ensuring appropriate skill sets are matched to project requirements and customer needs. Interface with senior leadership, cross-functional teams, and customers on significant project matters, providing regular updates on team performance, project status, and escalating issues as appropriate. Ensure consistent application of formal project management processes and tools across the team, working closely with the Project Management Leadership team to implement best practices and drive standardization. Support customer-facing activities including project reviews, business meetings, and issue resolution, maintaining strong relationships while ensuring customer satisfaction and retention. Collaborate with Project Management and Supply Chain Leadership on strategic initiatives, capacity planning, and organizational development to support business growth and operational excellence. Identify, assess, and manage significant risks across the project portfolio, developing mitigation strategies and ensuring proactive communication with stakeholders. Participate in recruitment and hiring activities to build and expand the PM team, identifying top talent and ensuring cultural fit with INCOG's values. Work closely with Manufacturing, Quality, Engineering, Technical Services, Supply Chain, and Business Development to ensure seamless project execution and delivery. YOU: Ideally, candidates will have a Bachelor’s degree in Business Administration, Project Management, or a related field, as well as the following: 8+ years of biotech/pharmaceutical experience with progressive project management responsibilities. 5+ years of experience in injectable drug product development and manufacturing, with deep understanding of aseptic manufacturing processes, technology transfers, and regulatory requirements. Proven track record of successfully leading and developing formal or informal teams or mentoring project management professionals, with demonstrated ability to drive performance and foster professional growth. Advanced knowledge of project management principles, methodologies, and tools applicable to the biopharmaceutical environment, with experience managing large-scale, complex projects. Proven ability to build and maintain strong customer relationships, with experience in customer-facing roles and managing escalated issues. PMP/PgMP certification or ability and willingness to obtain certification (Preferred). Previous experience in contract development and manufacturing organization (CDMO) environment (Preferred). Familiarity with FDA, EMA, and other regulatory requirements for sterile injectable products (Preferred). Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself… Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.