- Abbott (Santa Clara, CA)
- …the product. + Maintain quality documentation in accordance with SOPs, WIs and GMP (CFRs). + Resolve quality -related issues in a timely manner. + Perform ... of employees, customers, contractors, and vendors. + Knowledge of Quality Systems, FDA regulations, ISO 13485 and applicable worldwide regulatory requirements. +… more
- Abbott (Sylmar, CA)
- …experience and demonstrated use of Quality tools/methodologies. + Detailed knowledge of FDA , GMP , ISO 13485, and ISO 14971. + Solid communication and ... OF ROLE** This position is responsible for developing and maintaining quality engineering methodologies and providing electrical development quality engineering… more
- Abbott (Alameda, CA)
- …medicines. Our 114,000 colleagues serve people in more than 160 countries. **Specialist Quality Assurance** **Working at Abbott** At Abbott, you can do work that ... and scientists. **The Opportunity** The primary function of the Quality Specialist is to assist in maintaining the ...(SOPs) and relevant regulatory (cGMP, ISO) regulations. + Reviews GMP related documentation for compliance such as batch records… more
- Kelly Services (Sacramento, CA)
- …Pharmaceutical or GMP -regulated environment. + Knowledge of cGMPs, Production Processes, Quality Systems, and FDA regulations + Proficiency in handling of ... ** Quality Management System (QMS) Lead** Kelly(R) Science &...role, you'll be responsible for managing and maintaining the Quality Management System (QMS), coordinating audits, analyzing quality… more
- Astrix Technology (Rancho Dominguez, CA)
- …Audits and assist with any documentation-related tasks during audits + Ensure adherence to GMP , Food Safety, Food Defense, and Food Quality regulations + Monitor ... in a food manufacturing environment + Familiarity with food safety programs and policies ( FDA , USDA, AIB, HACCP, GMP , Allergen Programs) + Knowledge of labeling… more
- Fortive Corporation (Irvine, CA)
- …and increase productivity. Ensure all designs and projects are compliant with GMP , FDA , ISO 13485, and applicable regulatory requirements. **Required ... components, and equipment used in our sterilization products and GMP -regulated manufacturing environment. This individual will support new product introduction,… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …discipline is preferred. + Minimum of 2 years of related experience in a pharmaceutical, GMP , or FDA regulated environment is required. + Equivalency: In lieu of ... to improve production methods, equipment performance, facility layout, and quality of product. Maintain a quality presence...of 4 years of related experience in a pharmaceutical, GMP , or FDA regulated environment. + Requires… more
- The Clorox Company (Pleasanton, CA)
- …activities at CROs. Experience working in a regulated lab environment such as GLP, GMP , and with EPA/ FDA submissions. + Strategic thinking and ability to ... to leveraging the latest technology to bring consumers the high- quality , innovative products they expect and deserve. **In this...goods (eg, personal care, food, water) with knowledge of GLP/ GMP , EPA/ FDA compliance, CRO oversight, and method… more
- Astrix Technology (San Bernardino, CA)
- …the food industry. + In-depth knowledge of food safety programs and compliance ( FDA , USDA, HACCP, GMP , Allergen Programs). + Understanding of labeling ... Rate High: 23 + Added - 12/08/2025 Apply for Job We are seeking a ** Quality Lead** to support our production processes by maintaining a strong presence on the… more
- Gilead Sciences, Inc. (Oceanside, CA)
- …Define and execute a comprehensive audit strategy aligned with global regulatory expectations ( FDA , EMA, MHRA, PMDA, PIC/S) and Kite's quality objectives. Ensure ... Oversight:** Oversee the planning, execution, and reporting of audits across all GMP subsystems, including Quality Systems, Production, Facilities & Equipment,… more