- Caris Life Sciences (Phoenix, AZ)
- …Caris is where your impact begins.** **Position Summary** The CAPA / Quality Events Analyst primarily responsible for ensuring the integrity and ... effectiveness of Caris Life Sciences' CAPA and Quality Events programs....robust CAPA governance, effective Quality Event triage, and end-to-end documentation control. The Analyst… more
- Caris Life Sciences (Phoenix, AZ)
- …where your impact begins.** **Position Summary** The CAPA & Complaints Analyst provides day-to-day quality oversight for Corrective and Preventive Actions ( ... evening or weekend hours during audits, regulatory inspections, or critical quality events . **Conditions of Employment:** Individual must successfully complete… more
- Takeda Pharmaceuticals (Brooklyn Park, MN)
- …drug substance, and stability. + Oversee and author quality system events (ie, laboratory investigations, deviations, CAPA 's and change controls). + ... my knowledge. **Job Description** **About the role:** As a Quality Control Analyst II, you will build...laboratory investigations, basic complexity low and medium risk deviations, CAPA 's, and change controls of moderate scope within the… more
- Takeda Pharmaceuticals (Brooklyn Park, MN)
- …substance, and stability. You will own and author quality system events (ie, laboratory investigations, deviations, CAPA 's and change controls). This shift ... my knowledge. **Job Description** **About the role:** As a Quality Control Analyst , you will execute and...laboratory investigations, basic complexity low and medium risk deviations, CAPA 's, and change controls of moderate scope within the… more
- Astrix Technology (New Brunswick, NJ)
- …Conduct root cause analyses as part of laboratory investigations and assist in closing quality events . + Support regulatory and internal audits as needed. + ... **QC Analyst II** Laboratory Middlesex County, NJ, US Pay...and stability programs. + Ensure compliance with cGMP regulations, quality systems, and applicable ICH/regulatory guidelines. + Participate in… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …and maintain certified investigator training requirements. Perform investigation of the quality events assigned using root cause analysis tools, maintain ... Senior Microbiology Analyst Department: Microbiology Location: Monroe, NC START YOUR...(EM) in compliance with cGMP, USP, FDA, and internal quality standards. This position is in a fast-paced, FDA… more
- Curia (Albany, NY)
- …+ Perform CSV risk assessments Quality Management + Own CSV change records, CAPAs and Quality events for the CSV projects + Act as CSV reviewer on any CSV ... to save lives. The CSV Systems Engineer will be responsible for supporting Quality Management Systems and Computer System Validation efforts. This role will provide… more