Project Manager, Medical Device - Hologic
Newark, DE
About the Job
Project Manager, Medical Device
Newark, DE, United States
Hologic is seeking a Project Manager to join our Breast and Skeletal Health Research and Development team.
In this pivotal role, you will oversee our project core teams, ensuring flawless interfaces and interdependencies between functions while holding the team accountable for their deliverables. Your leadership will be key in setting clear project objectives, establishing measurable goals, and creating project scorecards that keep everyone on track.You will have the exciting challenge of crafting and executing project strategies, translating them into cross-functional integrated schedules, and actively monitoring progress to ensure we meet our targets. Your ability to drive projects forward and collaborate effectively with a dedicated team will be crucial to our success.
Join us and take the lead in driving projects that shape the future of healthcare. Apply today and join us at our Innovation Center in Newark, DE !
What To Expect
+ Manage New Program Introduction (NPI) from charter through to commercialization into the marketplace.
+ Provide required support for efficient PI execution.
+ Oversee the project core team, ensure flawless interfaces and interdependencies between the functions, hold the team accountable to their deliverables.
+ Establish program objectives including measurable goals and program scorecards.
+ Author the Product Development Plan and ensure other functional planning documents are completed and up to date.
+ Establish program execution strategies and translate into cross functional integrated schedules; actively monitor.
+ Responsible for risks, risk mitigations and risk management activities, ensure effective mitigations in place; monitor risks throughout the program; transfers documentation.
+ Utilize Design Control phase/ gate process to execute the program. Adhere to the IDI business process and all applicable QMS process.
+ Facilitate phase gate exit readiness reviews and stage design reviews; demonstrate proper phase gate criteria for exit during gate reviews.
+ Coordinate Program Core Team meeting as needed, especially when key program impact decisions are necessary.
+ Prepare and present program status, provide escalation communications as needed.
+ Responsible for the turnover of the project to manufacturing operations including providing complete project documentation.
+ Responsible for monitoring and providing regular communication and updates on success factors such as progress, schedule, budget, project risks and resource or needs gaps.
What We Expect
+ Ability to adapt communication style to suit different audiences.
+ Create precise, accurate technical documentation and presentations and ability to facilitate group discussions.
+ Ability to coordinate cross-functional projects, people, and teams.
+ Thorough working knowledge of product development, project management, project risk identification and management, design control procedures.
+ Skilled in Microsoft Office, Microsoft Project, PPM tools, such as Smartsheet, Planview, reporting dashboards, etc.
+ Strong technical aptitude, analytical, business management and strategic thinking skills.
+ Self-starter with a strong proactive work ethic, well-organized and detail-oriented.
+ PMP Certification is beneficial.
+ Experience with ISO and FDA quality systems regulations and medical device design and development cycles is beneficial.
+ Prior experience in new product development is beneficial.
Education
+ Preferred Minimum Non-Technical Degree: College Degree 5-8 Years
+ Preferred Minimum Technical/Advanced Degree: Technical Bachelor’s Degree 2-5 Years with Technical Bachelor’s Degree, 1-3 Years with Master’s Degree, 0-1 Years with PhD
So why join Hologic?
We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and annual bonus scheme, one of our talent partners can discuss this in more detail with you.
If you have the right skills and experience and want to join our team, apply today. We can’t wait to hear from you!
The annualized base salary range for this role is $94,000 - $146,900 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.
LI-#DS1
Newark, DE, United States
Hologic is seeking a Project Manager to join our Breast and Skeletal Health Research and Development team.
In this pivotal role, you will oversee our project core teams, ensuring flawless interfaces and interdependencies between functions while holding the team accountable for their deliverables. Your leadership will be key in setting clear project objectives, establishing measurable goals, and creating project scorecards that keep everyone on track.You will have the exciting challenge of crafting and executing project strategies, translating them into cross-functional integrated schedules, and actively monitoring progress to ensure we meet our targets. Your ability to drive projects forward and collaborate effectively with a dedicated team will be crucial to our success.
Join us and take the lead in driving projects that shape the future of healthcare. Apply today and join us at our Innovation Center in Newark, DE !
What To Expect
+ Manage New Program Introduction (NPI) from charter through to commercialization into the marketplace.
+ Provide required support for efficient PI execution.
+ Oversee the project core team, ensure flawless interfaces and interdependencies between the functions, hold the team accountable to their deliverables.
+ Establish program objectives including measurable goals and program scorecards.
+ Author the Product Development Plan and ensure other functional planning documents are completed and up to date.
+ Establish program execution strategies and translate into cross functional integrated schedules; actively monitor.
+ Responsible for risks, risk mitigations and risk management activities, ensure effective mitigations in place; monitor risks throughout the program; transfers documentation.
+ Utilize Design Control phase/ gate process to execute the program. Adhere to the IDI business process and all applicable QMS process.
+ Facilitate phase gate exit readiness reviews and stage design reviews; demonstrate proper phase gate criteria for exit during gate reviews.
+ Coordinate Program Core Team meeting as needed, especially when key program impact decisions are necessary.
+ Prepare and present program status, provide escalation communications as needed.
+ Responsible for the turnover of the project to manufacturing operations including providing complete project documentation.
+ Responsible for monitoring and providing regular communication and updates on success factors such as progress, schedule, budget, project risks and resource or needs gaps.
What We Expect
+ Ability to adapt communication style to suit different audiences.
+ Create precise, accurate technical documentation and presentations and ability to facilitate group discussions.
+ Ability to coordinate cross-functional projects, people, and teams.
+ Thorough working knowledge of product development, project management, project risk identification and management, design control procedures.
+ Skilled in Microsoft Office, Microsoft Project, PPM tools, such as Smartsheet, Planview, reporting dashboards, etc.
+ Strong technical aptitude, analytical, business management and strategic thinking skills.
+ Self-starter with a strong proactive work ethic, well-organized and detail-oriented.
+ PMP Certification is beneficial.
+ Experience with ISO and FDA quality systems regulations and medical device design and development cycles is beneficial.
+ Prior experience in new product development is beneficial.
Education
+ Preferred Minimum Non-Technical Degree: College Degree 5-8 Years
+ Preferred Minimum Technical/Advanced Degree: Technical Bachelor’s Degree 2-5 Years with Technical Bachelor’s Degree, 1-3 Years with Master’s Degree, 0-1 Years with PhD
So why join Hologic?
We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and annual bonus scheme, one of our talent partners can discuss this in more detail with you.
If you have the right skills and experience and want to join our team, apply today. We can’t wait to hear from you!
The annualized base salary range for this role is $94,000 - $146,900 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.
LI-#DS1
Source : Hologic