R&D Program Manager
Location: Southington
Posted on: June 23, 2025
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Job Description:
Position Summary The Program Manager for Infusion Consumables
R&D department for the Vascular Access, Sharps safety and Pain
Management business units. The Program Manager is responsible for
leading projects, with the support of an established Core Team and
Program Managers, through the medical device product life cycle of
development, qualification, manufacturing, and commercial release
process. Essential Duties & Responsibilities Provide Program and
Technical leadership for device development. Develop, maintain, and
document development plans through product development cycle. Drive
accountability in the position and within the cross functional
team. Identify resources needs, costs, program schedule, key
milestones, scope, and report the progress to the established plan.
Lead teams to process improvements to enable effective decisions
and outcomes. Comply with design control process and meet Quality
Management System requirements. Manage program budget: functional
expenses, capital requests, and forecasts. Prepare and report
program technical performance to different levels of organization
including senior leadership. Communicate with external partners to
meet program goals. Education and Experience Bachelor's degree in
in Engineering, Biological Sciences, Business or related fields
from an accredited college or university is required 10 years of
experience in product development leading multi-site global
programs Experience in the medical device or other regulated
industry with equivalent design controls High volume injection
molding experience is preferred. PMP Certification Agile Certified
Practitioner (ACP) a Plus Knowledge, Skills & Qualifications
Demonstrated experience in leading and managing cross-functional
multi-site teams to achieve program objectives in a matrix
organization. Ability to lead direct and indirect team members and
enabling them to grow. Experience in functional areas: High Volume
Medical device consumables Development, Quality, Medical,
Commercial, Manufacturing Operations, Procurement, and Regulatory
is preferred. Ability to evaluate and escalate changes that
significantly impact the scope, timeline, or business goals or the
program. Familiar with FDA and MDR regulatory submissions and
activities that lead to successful outcomes. Show history of
influencing technical teams, driving efficient decision making, and
leading team through complex problem solving. Use of metrics as
indicators of potential roadblocks, risks, and issues which could
block successful achievement of the program goals. Self-directed
with good interpersonal and communication skills to break down
complex issues and process into clear actions. Advanced knowledge
and hands-on experience with MS Office and MS Project. Nesco
Resource and affiliates (Lehigh G.I.T Inc, and Callos Resource,
LLC) is an equal employment opportunity employer and does not
discriminate on the basis of race, color, religion, sex, sexual
orientation, gender identity, national origin, disability, age, or
veteran status, or any other legally protected characteristics with
respect to employment opportunities.
Keywords: , New England , R&D Program Manager, Science, Research & Development , Southington, Northeast
