29 Jul
Sr Program Manager (Program Management, Project Management, Product Development, Certified PMP, Global Team Management, Design Controls 21 CFR 820.30, Medical Device Industry, Regulated Environment) in San Diego, CA
California, San diego , 92101 San diego USA

Vacancy expired!

Sr Program Manager (Program Management, Project Management, Product Development, Certified PMP, Global Team Management, Design Controls 21 CFR 820.30, Medical Device Industry, Regulated Environment) in San Diego, CA12+ years of experience Position: Sr Program Manager (Program Management, Project Management, Product Development, Certified PMP, Global Team Management, Design Controls 21 CFR 820.30, Medical Device Industry, Regulated Environment) Location: San Diego, CADuration: Full-Time ONSITE position (no contracts, no remote) Salary: Excellent Compensation with benefits + 401KSKILLS: Program Management, Project Management, Product Development, Certified PMP, Global Team Management, Design Controls 21 CFR 820.30, Regulated Environment, Medical Devices

DESCRIPTION:-
  • Experience in a Medical Device Manufacturing Industry is important for this role.
For one of our highly reputed clients, we have an immediate need for a Sr Program Manager to be based in San Diego, CA.The Senior Program Manager will lead the program to:
  • Reduce portfolio complexity across the business, improving business performance and growth
  • Reduce and optimize component complexity across the business, reducing risk and improving quality and product supply reliability.
We are recruiting for a highly driven Senior Program Manager with a passion for product development and a proven track record of successfully creating program execution strategies and delivering solutions that meet the customer requirements. The successful candidate has a unique opportunity to join a high-caliber PMO team responsible for the Design and Development of high growth businesses within corporate Delivery Solutions.

Reporting to the Director of Program Management, the Sr Program Manager is responsible for:
  • Managing a portfolio optimization program consisting of multiple projects.
  • Working within the constraints of budget, schedule, and scope, while managing risk, and ensuring adherence to established processes and methodologies.
  • Provides leadership and day-to-day direction to 2 program managers.
This position is highly visible across the organization. This position will serve as an excellent developmental opportunity and will provide the selected candidate the chance to drive this strategic initiative, add value to internal stakeholders and our customers and to partner closely with senior leaders.We strive to provide each individual with opportunities to develop skills, gain and share knowledge, understand and deliver what our customers want and build a rewarding and fulfilling career.

Responsibilities:
  • Drive the development of new medical device development programs through project completion within timeline, quality and budgetary limits
  • Lead and integrate cross-functional teams and manage deliverables and decision making in a matrix organization
  • Lead, manage and direct the development and execution of integrated project plans relevant to the deliverables and ensure alignment across relevant functions and a smooth transition among pipeline stages
  • Manage multiple projects across several departments while influencing project decisions in coordination with Marketing, Medical Affairs, R&D, Clinical, Regulatory Affairs, Quality, Manufacturing and Logistics
  • Identify and implement solutions to improve tracking, planning and collaboration
  • Ability to gain cooperation of others and effectively facilitates cross-functional meetings and discussions
  • Ensure effective, accurate and timely communication across functional areas and matrix
  • Serve as a primary point of contact for management regarding progress and goals
  • Work with the functional leaders to identify and resolve any team and individual performance issues
  • Bring a broadened business perspective to each project through an understanding of the inner-workings of Marketing, Quality, R&D, Finance, Regulatory, Manufacturing, Clinical, Medical Affairs, and Operations

Minimum Qualifications:
  • A minimum of a Bachelor's degree
  • A minimum of 5-7 years of Project Management experience
  • A minimum of 12+ years related work experience in product development.
  • Demonstrated success in several large Project/Program Management roles including Development and Deployment
  • Experience leading large global programs with distributed teams and leadership
  • Excellent interpersonal, communication, presentation and influencing skills
  • Ability and willingness to travel occasionally.

Preferred Qualifications:
  • PMP Certification
  • High volume device and/or drug development and project management within the medical device/pharmaceutical industry, or reasonable combination of the two
  • Strong familiarity with the integration of requirements and deliverables associated with Design Controls (

    21CFR820.30) into the product development process
  • Experience with short release cycles
  • Experience managing ambiguity and providing clarity for teams
  • Experience working in a highly

    government-regulated environment (

    FDA, MDR).
  • Must have led a cross-functional project team through regulatory submission and product commercialization
  • Demonstrated learning agility of new subject matter
  • Demonstrated application of product development and project management best practices on recent programs
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