Centre Program Manager providing strategic and operational leadership for the Centre for Energy and Mineral Processing. Fostering partnerships and research funding in clean energy and mineral processing.
About the role
- Senior Program Manager leading product initiatives for drug delivery devices in global technical operations at Johnson & Johnson. Partnering with cross-functional teams to drive successful projects and operational excellence.
Responsibilities
- The Senior Program Manager, Global Technical Operations serves as an expert within the technology community and leads program and/or portfolio initiatives for the organization.
- This role acts as the voice of supply chain during new product introduction for drug delivery devices.
- Applies analytics and reporting on an array of projects and creates data driven solutions for internal and external partners.
- Drives effective business decisions and communicates insights on organizational progress.
- Partnering with R&D, Quality, Commercial and Supply Chain teams to establish and implement the most effective strategy for the product manufacturing process.
- Working closely with manufacturing site during process introduction and scale-up phases.
- Step in as technical lead of strategic and NPI programs.
- Build strong functional teams, providing depth of knowledge and feedback and coaching to team members.
- Follow defined processes & procedures related to new product development and life cycle management to ensure compliance and meet business deliverables.
- Identify gaps in existing processes and drive improvement activities to close them.
- Define team's budget and support program/projects budget build.
Requirements
- Minimum of Bachelor’s degree and/or equivalent University degree required; focused degree in Engineering or Science related field preferred.
- Advanced degree or MBA preferred
- A minimum of ten (10) years of relevant professional work experience
- Demonstrated experience in managing complex, multi-functional projects with a focus on innovation and operational excellence.
- Strong knowledge of the medical devices industry, including regulatory requirements and industry trends.
- Project Management experience
- People management/leadership experience.
- Ability to develop program scope, develop people, manage technology, embrace financial goals and use customer-focused decision making.
- Change management, project management, the ability to work effectively and drive alignment in a global environment through strong communication and empowerment.
- Strong communication and management influence skills.
- Experience leading cross-functional teams.
- Experience leading medical device New Product Development teams.
- Experience in building business strategies and driving strategy implementation.
- Medical Device, Pharmaceutical and/or Biologics experience or other regulated industry preferred
- Combination Product experience
- Six Sigma/Process Excellence and/or Project Management/PMP/FPX certification
Benefits
- Vacation –120 hours per calendar year
- Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
- Holiday pay, including Floating Holidays –13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
Job title
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Experience level
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Degree requirement
Tech skills
Location requirements
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