Project Coordinator - III (Combination Products)Join a Global Leader in Workforce Solutions – Net2Source Inc. Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+.
Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place.
Right Price.Title: Project Coordinator - III (Combination Products) Onsite Position: Foster City - 5 days/week - Local Candidates Duration: 12 months contractThe Device Engineering team is seeking a qualified individual to support drug device combination products throughout the commercial lifecycle. This individual will be responsible for the management of combination product change records. Additional responsibilities include post market surveillance reports, risk management file maintenance, and general project management across the combination product portfolio.Job ResponsibilitiesCoordinate and manage combination product change control records –Initiate, route, and close change records for product and manufacturing process changes.Initiate, route, and close change records for the design and development of drug device combination products, including the creation and management of design control documentation.Manage implementation of changes at multiple manufacturing sites and change record closures.Coordinate post-market surveillance reports and risk management file updates –Collate surveillance information into yearly reports.Generate annual risk summaries and update risk management files.Support complaint investigations and documentation.Act as a central hub between cross-functional teams to ensure supply continuity.Knowledge & SkillsExceptional organizational and time management skills.Understanding of change controls in a regulated industry.Experience with project management.Working knowledge of relevant US, EU, and international medical device and pharmaceutical regulations.Experience with Veeva Vault.Ability to work with team members, vendors, suppliers, and contract manufacturers to coordinate changes.Education & Experience3 – 5 years relevant experience in related field and a BS or BA.Experience with medical device development and/or pharmaceutical operations (cGMP environment) required.Why Work With Us? We believe in more than just jobs—we build careers.
At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter. Our Commitment to Inclusion & Equity Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.Awards & RecognitionAmerica's Most Honored Businesses (Top 10%)Fastest-Growing Staffing Firm by Staffing Industry AnalystsINC 5000 List for Eight Consecutive YearsTop 100 by Dallas Business JournalSpirit of Alliance Award by Agile1