- Act as an independent leader of complex assay development programs, technically challenging product development projects, and diverse product sustaining initiatives involving cross-functional teams
- Establish project objectives and work plans including schedule, budgets, scope, resource requirements and communicate proposals to leadership
- Exert influence within a highly matrixed organization
- 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
- Expert at project scheduling using MS Project, including dependencies and critical path determination and optimization
- Demonstrated leadership including ability to identify key issues, motivate and empower others to address them in a way which builds morale, generates ownership and commitment
- Self-starter with superior problem-solving, analytical and organizational skills and a track record for high performance and superior delivery
- Sound grasp of the key business drivers and considerations in the biotech and/or life science industries and recommends best practices to improve products, processes, or services
- Advanced knowledge 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
- Strong communication and interpersonal skills
- Excellent interviewing and influencing skills
- Experience with ISO and FDA quality systems regulations and medical design and development cycles
- BS Degree in Science or Engineering required. MS, M.B.A or equivalent degree preferred
- PMP Certification preferred
- Minimum of 10 years' experience in Program Management leading large, cross functional development programs that have delivered commercially successful products which exceed customer and commercial expectations
- Experience running programs that included assay development and validation
- Experience within Diagnostics marketplace preferred; Molecular Diagnostics experience is a plus
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Sr Program Manager, PMO - San Diego, United States - Hologic
Description
Sr Program Manager, PMO
San Diego, CA, United States
Hologic is seeking a Sr. Manager, PMO who will be dedicated to program management of new assay development and instrumentation/engineering project and programs.
Essential Duties and Responsibilities
The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
Qualifications
Education
Experience
The annualized base salary range for this role is $144,000 to $175,400 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.
Agency and Third Party Recruiter Notice
Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.