| Job alert | Jobs 1 - 10 of 784 |
Ex-FDA Investigators and Reviewers
Pharmatech Associates
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San Francisco, CA
... Posted Feb 29, 2024 Pharmatech Associates is seeking former FDA investigators and reviewers to provide consultation and remediation services to our pharmaceutical, biologics and medical device clients. The nature of our projects varies from client ... - May 02
MATERIAL SPECIALIST
Avinger, Inc
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Redwood City, CA, 94063
... Practices, and FDA regulations Ensure that all internal policies are followed Understand the job specific quality system procedures and processes as defined in the Training Matrix and adhere to the requirements listed in those documents. ... - May 01
CMC Quality Control Manager
GQR
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South San Francisco, CA, 94083
... Ensure all QC activities comply with regulatory requirements, including those of the FDA, EMA, and other relevant agencies. Support the development and validation of analytical methods used for QC testing. Implement and maintain quality systems to ... - Apr 19
Document Control Specialist
Digital Prospectors
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Redwood City, CA, 94063
... Knowledge of Quality Assurance principles (i.e., ISO 9001, ISO 13485, and FDA cGMP regulations) is preferred. POST-OFFER BACKGROUND CHECK IS REQUIRED. Digital Prospectors is an Equal Opportunity Employer and all qualified applicants will receive ... - May 03
Document Control Specialist
Digital Prospectors
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Redwood City, CA, 94063
... Knowledge of Quality Assurance principles (i.e., ISO 9001, ISO 13485, and FDA cGMP regulations) is preferred. POST-OFFER BACKGROUND CHECK IS REQUIRED. Digital Prospectors is an Equal Opportunity Employer and all qualified applicants will receive ... - May 03
Software Engineering Manager (C++)
HealthCare Recruiters International
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Belmont, CA, 94002
Hands-on Software Engineering Manager (C++) Our client is a well-funded, recently FDA-cleared Surgical Robotics startup located in the San Francisco Bay Area. This hands-on Software Engineering Manager will play a key role in the development of ... - Apr 26
Quality Engineer I/II
Medical Instrument Development Laboratories, Inc.
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San Leandro, CA, 94579
... Support company goals and objectives, policies and procedures, FDA Quality System Regulation-21 CFR, part 820, EU MDD/MDR and applicable global standards and regulations. Performs other duties as assigned by Supervisor. REQUIRED EXPERIENCE: ... - Apr 26
RA Specialist II
DivIHN Integration
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Alameda, CA, 94502
... Knowledge of APAC country regulations, such as TGA, NMPA, PMDA, MFDS, HSA, TFDA, FDA, MOH, etc. Knowledge of Agile, SharePoint, MS Office, and other software to increase work efficiency. Ability to manage time and projects. Strict to work 40hrs per ... - May 02
Technical Writer -Valgenesis
IT solutions Inc
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Foster City, CA
... Work closely with other validation team members to ensure system impact is assessed and mitigation strategy is in place for multiple sites using the Valgenesis application Demonstrates Strong knowledge of current Good Manufacturing Practice (FDA, EU ... - Apr 27
Clinical System Lead
Intelliswift Software
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South San Francisco, CA, 94080
... in leading the implementation of clinical systems, such as IxRS/IRT, ePRO and eCOA Working knowledge of Good Clinical Practices and FDA regulations governing clinical trial execution Detail-oriented and able to manage many projects simultaneously. ... - Apr 23