Project Coordinator - IT - III*
Verdi, CA
Date Posted:01-Jun-2026
Work Type:On-Site
Job Number:486567
Job Description
Job Title: Project Coordinator - IT - III
Location: Foster City, CA 94404 (Mostly Remote, with 10% travel)
Duration: 12 Months
The Device Engineering team at this company 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 Responsibilities
Coordinate and manage combination product change control records –
Act as a central hub between cross-functional teams to ensure supply continuity.
Knowledge & Skills
Education & Experience
Location: Foster City, CA 94404 (Mostly Remote, with 10% travel)
Duration: 12 Months
The Device Engineering team at this company 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 Responsibilities
Coordinate 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.
- Collate surveillance information into yearly reports.
- Generate annual risk summaries and update risk management files.
Act as a central hub between cross-functional teams to ensure supply continuity.
Knowledge & Skills
- Exceptional 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 & Experience
- 3 – 5 years relevant experience in related field and a BS or BA.
- Experience with medical device development and / or pharmaceutical operations (cGMP environment) required.
Applicant Notices & Disclaimers
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At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position's starting pay is: $102.18/hr.