Onsite Position: Foster City - 5 days/week - Local Candidates
Bill Rate: ***/hr***
The Device Engineering team at *** 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
o Initiate, route, and close change records for product and manufacturing process changes.
o 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.
o Manage implementation of changes at multiple manufacturing sites and change record closures.
Coordinate post-market surveillance reports and risk management file updates
o Collate surveillance information into yearly reports.
o 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 & 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.
EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.
Numbers & Facts
Location
Foster City, CA
Salary
$70–$80 Per Hour
Skills
Biotech and Pharmaceuticalunmatched
Change Controlunmatched
Change Managementunmatched
Contract Managementunmatched
Contract Manufacturingunmatched
Cross-Functionalunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Document Managementunmatched
Documentationunmatched
Drug Developmentunmatched
Drug Productsunmatched
File Maintenanceunmatched
Manufacturingunmatched
Manufacturing/Industrial Processesunmatched
Medical Equipmentunmatched
Product Controlunmatched
Product Managementunmatched
Project/Program Coordinationunmatched
Project/Program Managementunmatched
Regulationsunmatched
Riskunmatched
Risk Managementunmatched
Surveillanceunmatched
Time Managementunmatched
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