- Medtronic (Northridge, CA)
- …with biological evaluation report (BER). + Liaise with internal ( manufacturing , regulatory, quality, product development, supplier quality, post market surveillance, ... of ISO 10993 and global medical device regulations (eg, EU MDR, FDA , REACH, Prop 65). + Experience with biocompatibility assessments, toxicological risk evaluation,… more
- University of Pennsylvania (Philadelphia, PA)
- …meetings and will be expected to adhere to all University of Pennsylvania, FDA , and GCP guidelines. The CRC-B/C will be responsible for accurate data collection ... of dealing with and handling the investigational product with the manufacturing /research lab, according to protocol. Oversee study preparation and sample processing,… more
- Danaher Corporation (Miami, FL)
- …It would be a plus if you also possess previous experience in: + FDA regulated environment warehousing or Manufacturing + Order fulfillment in a (Medical ... filing and storage coordination with "Iron Mountain" This position reports to the Materials Manager and is part of the Materials and Planning Dept located in Miami… more
- Medtronic (Lafayette, CO)
- …are conducted in compliance with Medtronic's QMS, ISO13485, EU-MDR and the FDA Quality System Regulations. * Lead cross-functional teams to develop product risk ... partially finished or finished materials product. + Collaborates with engineering and manufacturing functions to ensure quality standards are in place. + Devises and… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …Ltd. employs over 10,000 people in more than 60 countries, including twelve manufacturing facilities, five R&D centers, and front-ends in the US, EU, India, and ... pharmaceutical company. POSITION SUMMARY: Under the direction of the Senior Manager , Quality Compliance, the Quality Compliance Specialist is responsible for… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …of Quality, including Regulatory Affairs, Information Technology, Service, Repair, Manufacturing , Commercial teams and business leaders across all global regions. ... understanding and working knowledge of appropriate global regulations and standards including FDA Quality System Regulations and ISO 13485:2016 + Strength in people… more
- Astrix Technology (Pomona, CA)
- **QA Inspector- Cosmetics (2nd & 3rd)** Manufacturing Pomona, CA, CA, US Pay Rate Low: 20 | Pay Rate High: 25 + Added - 11/08/2025 Apply for Job _Our client, a ... personal care products comply with industry regulations and standards, such as FDA guidelines, and work towards continuous improvement in meeting these requirements.… more
- Astrix Technology (Pomona, CA)
- **QA Inspector (Multiple Openings)** Manufacturing Pomona, CA, US Pay Rate Low: 20 | Pay Rate High: 24 + Added - 20/05/2025 Apply for Job _Our client, a growing ... personal care products comply with industry regulations and standards, such as FDA guidelines, and work towards continuous improvement in meeting these requirements.… more
- US Foods (Rosemont, IL)
- …and regulatory programs and initiatives. + Other duties as assigned by manager . **Relationships:** + **Internal:** Close collaboration with US Foods' food safety and ... stakeholders. **Minimum Qualifications:** + Minimum 2 years of experience in manufacturing and/or food safety/quality knowledge. + Intermediate proficiency in Office… more
- Pilgrim's (Greeley, CO)
- …Systems and Recipe Development (eg, SAP). + Good understanding of USDA and/or FDA guidelines with occasional support from manager . + Proficient in Microsoft ... 0-2 years of relevant experience + Experience working in food manufacturing facility, operations, or continuous improvement strongly preferred. + Strong… more