Roy Domingo
Quality Systems Training Manager, Audit Management, Risk Management, Supply Chain Management, Document Management, QMS Management
- Role
- Quality Assurance Specialist at Bionova Scientific
- Location
- Sunnyvale, CA, US
- LinkedIn followers
- 500 followers
About Roy Domingo
Results-driven Quality Management Systems Manager with extensive experience in risk management and mitigation, supplier management, audits, document control, customer compliant, post market surveillance, and training strategies within the pharmaceutical, medical device, and biotechnology regulated industries. Expertise in developing training programs to enhance quality standards and compliance, conducting internal audits, and driving continuous improvement initiatives. Proven ability to manage document control processes, ensuring accuracy and accessibility of key regulatory documents. Proven leader by managing direct reports to enlist maximum effort to achieve department and company goals. Committed to fostering a culture of quality and safety through effective training and communication.I am committed to developing teams through effective training and communication, and I thrive in cross-functional collaborations that lead to process optimization and risk mitigation. My focus on performance metrics and data-driven decision-making empowers organizations to stay ahead of regulatory challenges.If you would like to connect, please feel free to reach out!
Experience
Quality Assurance Specialist
Nov 2025 — Present
Education
University of California, Davis
Human Development, Minor in Asian American Studies
Skills
- Technology Transfer
- Iso 13485
- Assay Development
- Compliance
- Technical Training
- Life Sciences
- Lifesciences
- Purification
- Chromatography
- Polymerase Chain Reaction (Pcr)
- Quality System
- Quality Systems
- V&V
- Manufacturing
- Molecular Biology
- 21 Cfr Part 11
- Capa
- Gxp
- Discrepancy Investigations
- Hplc
- Internal Audit
- U.s. Food and Drug Administration (Fda)
- Quality Control
- Gmp
- Healthcare
- Sop
- Fda
- Biotechnology
- Corrective and Preventive Action (Capa)
- Fermentation
- Validation
- Pcr
- Tech Support
- Laboratory Information Management System (Lims)
- Laboratory
- Verification and Validation (V&V)
- Biopharmaceuticals
- Glp
- Quality Assurance
- Standard Operating Procedure (Sop)
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