Job Summary:
Hologic, Inc. is a leading medical technology company dedicated to advancing women’s health and well-being. They are seeking a Sr Program Manager for their Diagnostics division who will manage new assay development and engineering projects, leading cross-functional teams to ensure successful project delivery.
Responsibilities:
• Act as an independent leader of complex instrument systems and platforms programs, technically challenging product development projects, and diverse product sustaining initiatives involving cross-functional teams.
• Establish project objectives and work plans including schedule, budgets, and resource requirements.
• Delegate assignments to functional area team members and track key project activities to successful completion. Report project status to divisional leadership.
• Lead, coach, guide, and mentor a team of highly motivated, high performing PMO team members.
• Responsible for the management of large international, cross-functional, business critical programs
• Exert influence within a highly matrixed organization
• Apply expertise to influence the future strategy of the PMO function and implement best practices
• Utilize expertise to proactively identify and resolve product and project risks
• Drive for program success while ensuring consistency and alignment across all product development projects by overcoming constraints, problems, and issues
• Exceed customer expectations, while maximizing value to Hologic and maintaining GMP FDA/ISO compliance
Qualifications:
Required:
• BS Degree in Science or Engineering required.
• Minimum of 8 - 10 years’ experience in Program Management leading large, cross functional development programs, with demonstrated experience leading diverse sustainability projects such as product improvements, reliability, regulatory, custom, regional, product lifecycle, and others.
• Expert in Program Management/Leadership.
• Advanced knowledge and deep understanding of stage-gate Product Development process.
• Expert in Product Development including Design Control procedures.
• Expert in management of project risks.
• Expert communication and interpersonal skills.
• Advanced talent management and development skills.
• Experience with ISO and FDA quality systems regulations and medical design and development cycles.
Preferred:
• MS, M.B.A or equivalent degree preferred.
• PMP Certification preferred.
• Experience within Diagnostics marketplace preferred; Molecular Diagnostics experience is a plus.
Company:
We’re an innovative medical technology company whose purpose is to enable healthier lives everywhere, every day. Founded in 1985, the company is headquartered in Marlborough, USA, with a team of 5001-10000 employees. The company is currently Late Stage.