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ATL Technology · 4 months ago

Global Program Manager

Full-time

Hybrid

Senior Level

7+ years exp

ATL Technology is a company focused on bringing medical devices to market through innovative engineering solutions. They are seeking a Global Program Manager to oversee program cost and schedule performance, manage risks, and ensure effective communication across global teams during the development of new products.

ElectronicsManufacturing

Responsibilities

Responsible for program cost and schedule for engineering development programs from prototype to full qualification. This will include defining the high-level strategy with the Business Unit Leaders (BUL)

Develop, manage and maintain a detailed deliverable based project schedule in conjunction with the site-level project managers to ensure work products are delivered as planned and that cross-site dependencies are flagged and monitored within a specific program. Will define work product expectations for each site within a program, and any resource needs and inter-site dependencies

Participate in program reviews with internal leadership, customers (as needed), and be able to communicate program status, needs and dependencies concisely and effectively

Establish communication and reporting mechanisms for efficient global communications and accountability

Participate in proposal preparation, developing estimates and soliciting and reviewing inputs from cross-functional teams

Develop, manage and maintain a risk and opportunity register in conjunction; responsible for soliciting, understanding, validating and reviewing risks with cross-functional teams

Travel up to 25% of time (Both domestic and international)

Able to work a flexible schedule as global programs, at times, will require early morning or evening meetings with international project teams

Performs other duties and responsibilities as assigned

Qualification

Program managementOperations managementISO 13485FDA QSR 820PMP certificationInternational collaborationCommunicationCross-functional leadership

Required

A Bachelor's degree with at least ten (10) years of prior relevant experience OR an Advanced degree with seven (7) years of relevant experience

Strong level of knowledge in program management or operations management in medical device manufacturing

Experience with ISO 13485 and FDA QSR 820 and the impacts to product design, project schedules and documentation requirements

Experience leading cross-functional teams on large, complex programs with concurrent design and production build activities

Experience collaborating with international project teams on global projects

Ability to effectively influence and lead others in a matrix organization by proactively reviewing program progress and course-correcting teams, driving issues to closure

Excellent communication skills