- United Therapeutics (Eden Prairie, MN)
- …Disposition: Disposition raw materials, starting materials, and intermediates + Deviations & CAPA : Work with Manufacturing to investigate and resolve product ... with liver and kidney disease. How you'll contribute The Quality Assurance Specialist II ensures that all intermediates and products manufactured at the Miromatrix… more
- Boehringer Ingelheim (St. Joseph, MO)
- …and approval of CAPAs associated with the focus area. + Trains employees on Deviation / CAPA . + Grants system access to employees as appropriate. + Conducts ... **Description** The Principal Specialist of Quality Operations provides real-time Quality Assurance...facility or utility investigations. This role identifies and implements CAPA to prevent recurrence and drive toward Right First-Time… more
- Randstad US (Cambridge, MA)
- …Compliance Specialist is also responsible for owning and driving manufacturing compliance improvement through deviation resolution, applied root cause ... job summary: Exciting new opportunity for an experienced Compliance Specialist who will work closely within the Manufacturing... investigations and at times manage the implementation of CAPA . + Own manufacturing related change controls.… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- …complaints; preparing annual product reviews; tracking, trending and follow-up of the CAPA programs. Interacts directly with the manufacturing personnel and is ... of process controls in all applicable areas of the manufacturing operation. The Senior QA Specialist will...assessment are adequate, and recommend corrective actions to prevent deviation recurrence; ensure on time closure. + May author… more
- Bristol Myers Squibb (Bowdre, IL)
- …and Good Manufacturing Practices (GDP and GMP). Finally, the QC Specialist Incoming is supporting activities related to the Pharmacopeia compendial review for ... and in their personal lives. Read more: careers.bms.com/working-with-us . The QC Specialist Incoming is part of the Sample Management & Incoming testing Packaging… more
- Bristol Myers Squibb (Summit, NJ)
- …incredible. The ** Specialist , Senior Technical Writer** will collaborate with internal Manufacturing partners, such as but not limited to MS&T ( Manufacturing ... System (QMS) with the applicable information. The Senior Associate will lead Manufacturing No Impact Deviations. The Senior Associate will support the … more
- Gilead Sciences, Inc. (Foster City, CA)
- …monitoring data (as required), and associated documentation, including any deviation and investigation reports related to lot release of Clinical/Commercial ... + Lead or coordinate investigations and corrective and preventive action ( CAPA ) recommendations + Interface directly with contract manufacturers and alliance… more
- Novo Nordisk (Clayton, NC)
- …of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable ... treatments. At IFP, you'll join a global network of manufacturing professionals who are passionate about what they do....complex DVs, CRs, (SOPs), trend & report data for CAPA , Quality Management Reviews (QMRs) & Annual Product Review… more
- Charles River Laboratories (Memphis, TN)
- QA Release Specialist III Req ID #: 221971 Location: Memphis, TN, US, 38118Memphis, TN, US, 38118 For 75 years, Charles River employees have worked together to ... that you can feel passionate about. **Job Summary** The QA Release Specialist III is responsible for performing various Quality Assurance activities related to… more
- SpaceX (Redmond, WA)
- Supplier Quality Specialist , Aviation (Starlink) at SpaceX Redmond, WA SpaceX was founded under the belief that a future where humanity is out exploring the stars is ... with the ultimate goal of enabling human life on Mars. SUPPLIER QUALITY SPECIALIST , AVIATION (STARLINK) Starlink demands a new type of supply chain. We require… more
- Actalent (Brownsburg, IN)
- …Sample Prep, Clean Room, radiopharmaceutical, nuclear medicine, isolator, sterile environment, sterile manufacturing + CAPA , Deviation , SOP Review, Document ... grow within their new state-of-the-art facility for commercial-scale, sterile manufacturing of therapeutic radiopharmaceuticals. The Sterility Assurance Specialist… more
- Teva Pharmaceuticals (Salt Lake City, UT)
- …departmental Standard Operating Procedures as needed. + Responsible for effectively addressing CAPA and deviation resolutions as needed. + Responsible for ... Lead Documentation Specialist - SLC East Date: Apr 22, 2024...manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP's), Standard Operating Procedures (SOP's) and Batch… more
- Cambridge Isotope Laboratories, Inc. (Tewksbury, MA)
- …or reviewing related data + Prepare summary or trend reports + Write deviation , CAPA reports, including root cause analysis and implementing appropriate ... Inc. (CIL) is searching for a Quality Control Documentation Specialist based onsite in our Andover, MA facility. CIL...molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the… more
- Boehringer Ingelheim (St. Joseph, MO)
- …relating to these areas. The scope of support includes every stage of manufacturing in BIVI, including product received from 3rd Party contract manufacturing ... changes occur. + Creates new documents (SOPs/Forms/templates)as needed. + Deviations/ CAPA : + Initiates deviations in Quality electronic systems when non-conformances… more
- Charles River Laboratories (Memphis, TN)
- QC Specialist 1 Microbiology Req ID #: 222397 Location: Memphis, TN, US, 38118Memphis, TN, US, 38118 For 75 years, Charles River employees have worked together to ... a career that you can feel passionate about. **Job Summary** The QC Specialist I for the QC Microbiology Department will be responsible for reviewing laboratory… more
- Gilead Sciences, Inc. (Frederick, MD)
- …KLIMS related documentation (ie SOPs, SPCs, WRKs, URSs). + Assist with deviation , investigation, impact assessments, CAPA and change control activities. + ... job. **Job Description** As a KITE Laboratory Information Management System (KLIMS) Specialist in the Quality Control (QC) Technical Services group, this role will… more
- Gilead Sciences, Inc. (Foster City, CA)
- …industry practices, and standards. + Experience with Quality Systems processes ( Deviation , CAPA , Change Control, Audit, etc.) + Demonstrates familiarity ... Gilead and help create possible, together. **Job Description** _Quality Systems Specialist III_ , Metrics and Management Review Job Responsibilities + Responsible… more
- Cambridge Isotope Laboratories, Inc. (Tewksbury, MA)
- …Contributor to various QA Quality Program functions when needed (eg Deviation , CAPA , Supplier Management, Customer Complaints, biennial review, internal/external ... (CIL) has an outstanding opportunity for a Quality Assurance Specialist I to join the team responsible for the...molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the… more
- Boehringer Ingelheim (Athens, GA)
- …relating to these areas.The scope of support includes every stage of manufacturing in BIAH, including product received from 3rd Party contract manufacturing ... items as assigned. + Revises existing procedures as changes occur. + Deviations/ CAPA : + Initiates deviations in Quality electronic systems when non-conformances are… more
- Actalent (Foster City, CA)
- …across the clinical and commercial supply chains. * Reviews manufacturing records, environmental monitoring, and quality control data for in-process ... serve as a lead/coordinator of investigations and corrective and preventive action ( CAPA ) recommendations related to manufactured products. * May assist with cGMP… more