- ThermoFisher Scientific (San Francisco, CA)
- …lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, ... biological products etc.), Will work with hazardous/toxic materials **Job Description** **Title: Quality Control Scientist III - Cell and Gene Therapy** As part of… more
- Abbott (Sylmar, CA)
- …Our 114,000 colleagues serve people in more than 160 countries. **Job Title** **Software Quality Engineer II** **Working at Abbott** At Abbott, you can do work that ... Opportunity** Our location in **Sylmar, CA** currently has an opportunity for an **Software Quality Engineer** . **This is a fully onsite role** . This position is… more
- Abbott (Pleasanton, CA)
- …experience and demonstrated use of Quality tools/methodologies + Detailed knowledge of FDA , GMP , ISO 13485, and ISO 14971 + Solid communication and ... their lives. We are seeking an experienced, high caliber Senior Supplier Development Quality Engineer to be responsible to act as the site interface to suppliers.… more
- Kelly Services (Sacramento, CA)
- …pharmaceutical products. This includes ensuring compliance with cGMP regulations, internal quality standards, and applicable regulatory requirements (eg, FDA , ... or biotechnology industry is essential. + Knowledge of cGMPs, Production Processes, Quality Systems, and FDA regulations + Knowledge of current Good… more
- Abbott (Pleasanton, CA)
- …experience and demonstrated use of Quality tools/methodologies + Detailed knowledge of FDA , GMP , ISO 13485, and ISO 14971 + Project management and leadership ... to the development, maintenance and improvement of division supplier development quality program policies, procedures and forms. + May provide coaching, and… more
- Envista Holdings Corporation (Pomona, CA)
- …evaluate the current process and process changes. + Maintains a working knowledge of FDA GMP , ISO 13485 standards and other applicable standards. + Documents ... + Experience with statistical software (Minitab, JMP, etc.) + Certified Quality Engineer preferred. + FDA Quality System Regulation Part 820 and ISO 13485… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …best self. Become a **maker of possible** with us. **Job Overview** BD is seeking a Quality Assurance Engineer II to join our team. In this role, you will play a ... crucial part in ensuring the quality and compliance of our products and processes. You...records to comply with ISO 13485, ISO 9001, and FDA regulations. + Provide input to the Calibration and… more
- AbbVie (Pleasanton, CA)
- …chemical, electrical), or other technical discipline. Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing ... GD&T + performing daily assigned tasks in compliance with FDA 's Quality System Regulation (QSR), ISO 13485,...to medical device development life cycles, manufacturing processes & GMP ; & + working in a cross-functional team, in… more
- Catalent Pharma Solutions (San Diego, CA)
- ** Quality Control Chemist I** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... services that include analytical development, pre-formulation testing, formulation development, GMP (Good Manufacturing Practices) manufacturing and stability storage and… more
- Adecco US, Inc. (Los Angeles, CA)
- **Job Summary** We are seeking a ** Quality Assurance Specialist** to ensure our products and operations comply with all applicable US federal, state, and local ... with our global headquarters, overseeing product compliance, import documentation, product quality -related customer claims (VOC), and regulatory audits. You will be… more