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Global Project Manager – Oral Care
Kentwood, MI, US
Scientific
Bachelors Degree
Full Time, Temporary
$60-70/hr
Manager (Manager/Supervisor)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Kentwood, MI, US
$60-70/hr
Manager (Manager/Supervisor)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Kentwood, Michigan
Kelly® Science & Clinical is seeking a Global Project Manager – Oral Care for a 6-month minimum contract position (with possibility to go longer) at one of our premier clients in the Kentwood, Michigan area. If you’re passionate about bringing innovation to market by coordinating global, cross-functional product development projects, trust The Experts at Hiring Experts.
Salary/Pay Rate/Compensation: $60–$70 per hour
Overview
This company is focused on advancing its innovation pipeline through product development and disciplined Stage Gate decisions.
In this role, you’ll work with the Global Oral Care category team and cross-functional partners in R&D, Regulatory, Medical Affairs, Supply Chain, etc. to coordinate new product development projects from planning through launch. You’ll keep timelines, tasks, meetings, and Stage Gate documentation on track while helping teams across the U.S., Europe, and Asia stay aligned. This is an opportunity to contribute to a broad portfolio of projects while supporting product innovation for the Oral Care business.
Schedule
Hybrid schedule with 3 days onsite and 2 days remote each week. The preferred schedule is 8:00 a.m.–5:00 p.m. Eastern Time, with flexibility; work hours are generally between 7:00 a.m. and 6:00 p.m. ET, for approximately eight hours per day. Travel is not required. This person would remotely with international teams as well and maybe occasional early morning or late evening calls.
Responsibilities
- Manage multiple Oral Care new product development projects, coordinating project plans, tasks, milestones, dependencies, and deliverables from initiation through launch.
- Build and maintain project timelines, monitor progress, follow up on actions, and identify critical-path risks or schedule impacts early.
- Coordinate cross-functional partners across R&D, Regulatory, Medical Affairs, Supply Chain, and category teams; schedule meetings and document actions, decisions, and next steps.
- Prepare and maintain Stage Gate documentation and project status updates to support reviews, project visibility, and timely decisions.
- Identify blockers, risks, and changes; communicate impacts, escalate issues when needed, and work with stakeholders to develop mitigation plans across global teams and time zones.
Qualifications
- Bachelor’s degree required; MBA preferred as well as PMP certification highly desirable.
- At least 8-10 + years of project management experience, with a track record of coordinating complex, cross-functional projects and multiple workstreams.
- Experience managing project schedules, deliverables, risks, meetings, and stakeholder follow-up; product development or NPD experience is an asset.
- Familiarity with Stage Gate processes and documentation; experience working with global or matrixed teams is preferred.
- Strong organization, communication, meeting facilitation, and collaboration skills, including the ability to work across functions and time zones. PMP certification or equivalent advanced project-management training is a plus, not required.
For more information or to be considered, send resumes to Tierra.Barbour@kellyscientific.com or call 804-991-0745
10443062
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Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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