Sr. R&D Program Manager

Posted 19 Hours Ago
Be an Early Applicant
3 Locations
126K-252K Annually
7+ Years Experience
Healthtech
The Role
The Sr. R&D Program Manager at Abbott in Alameda, California leads cross-functional teams in developing and executing strategies for new product development and commercialization. They manage programs ensuring milestones and deliverables are met, and report progress and recommendations to senior leadership. Responsibilities also include establishing program design history file, identifying risks, and improving business performance.
Summary Generated by Built In

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

The Opportunity
Our location in Alameda, California has an opportunity for a Sr. R&D Program Manager. This position manages programs of small to medium scope, or a significant subsection of a large program. Sr. Managers manage larger programs. Leads cross-functional teams to develop and execute strategies for new product development and successful commercialization. Manages matrixed resources to ensure programs meet their agreed upon milestones and deliverables. Represents the program to the organization, reports core team progress, program recommendations, risks, and resolutions of issues to senior leadership. 

What you will work on:

• Lead core teams towards program objectives.

• Communicates with all levels of the organization, from operators on the floor to the President in order to represent the objectives, risks, and needs for the program.

• Lead activities across numerous functions to meet the objectives of a given program including scope, budget, and schedule.

• Establish and maintain the program and product Design History File.

• In partnership with the Program Director and fellow core team members, • Develop comprehensive program plans, which identify objectives, strategy, risks/risk mitigation, budget, effort estimates and schedule for new product development.

• Identifies opportunities for improving overall business performance of the program.

• Develops plans with core members to eliminate and/or mitigate risk. If risks cannot be mitigated within the core team, determines appropriate means to communicate and elevate issues to appropriate individuals within the organization.

• In partnership with the Director, identifies opportunities for improving overall performance of the program.

• Work closely with functional core team leaders and mentor when necessary.

• Maintains a safe and professional work environment.

• Complies with worldwide medical device regulations including U.S. FDA, company policies and Good Manufacturing Practices.

• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Required Qualifications:

  • Bachelors Degree in Engineering or Science equivalent
  • 8+ years of experience required for progressively responsible experience in engineering or related technical discipline. (years of experience vary depending on Grade level)

Preferred Qualifications:

  • Ability to work in a matrixed and geographically diverse business environment. Strong leadership skills, including the ability to set goals and provide constructive feedback respectfully to build positive relationships and improve business results. Ability to work effectively within a team in a fast-paced changing environment. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multi-tasks, prioritizes and meets deadlines in timely manner. Strong organizational, planning, and follow-up skills and ability to hold others accountable.
  • Preferred- 3 years’ experience directly managing technical staff. Extensive medical device industry experience.
  • Program/Project Management certifications.
  • Experience working in a broader enterprise/cross division business unit model.
  • Ability to travel approximately 20% of the time, including internationally.

Apply Now 

  • * Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
  • Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

The base pay for this position is

$125,700.00 – $251,500.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Product Development

DIVISION:ADC Diabetes Care

LOCATION:United States > Alameda : 1360-1380 South Loop Road

ADDITIONAL LOCATIONS:United States > Milpitas : 1820 McCarthy Blvd

WORK SHIFT:Standard

TRAVEL:Yes, 20 % of the Time

MEDICAL SURVEILLANCE:Not Applicable

SIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

The Company
Abbot Park, IL
97,838 Employees
On-site Workplace

What We Do

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.

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