- Grifols (Texarkana, TX)
- …Clinical Laboratory Improvement Amendments (CLIA), and Current Good Manufacturing Practice ( cGMP ). * Accountable for donor selection, plasma collection and all ... Clinical Laboratory Improvement Amendments (CLIA), and Current Good Manufacturing Practice ( cGMP ). * Directs through the management team and with Training and… more
- Grifols (Salem, OR)
- …Laboratory Improvement Amendments (CLIA), and Current Good Manufacturing Practice ( cGMP ). Accountable for donor selection, plasma collection and all manufacturing ... Clinical Laboratory Improvement Amendments (CLIA), and Current Good Manufacturing Practice ( cGMP ). Directs through the management team and with Training and Quality… more
- Grifols (Cranston, RI)
- …related documentation. Ensures that job and center annual training (ie Advanced cGMP , Blood Borne Pathogen, and others as required) is completed, documented, and ... equivalent. Typically requires 2 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. Depending on the… more
- Grifols (San Diego, CA)
- …Operating Procedure (SOP) Manual, current State and Federal guidelines, OSHA, CLIA, CGMP , all internal company procedures and personal education and experience. . ... Ensures Donor and Staff confidentiality. . Responsible for donor awareness to potential hazards to include administering donor consent form. . Provides Donor education regarding general health assessment completed and provides counseling regarding unacceptable… more
- University of Southern California (Los Angeles, CA)
- cGMP Associate Director Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... a highly motivated individual to join the USC/CHLA Cell Therapy program and cGMP Facility. The successful candidate will work on the process development and… more
- University of Southern California (Los Angeles, CA)
- …cGMP Process Development SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... internal/external users in the university's current Good Manufacturing Practices ( cGMP ) facility. The Process Development Specialist is responsible for developing… more
- University of Southern California (Los Angeles, CA)
- …cGMP Microbiological TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... Medicine is seeking a specialized microbiological technician to support the cGMP facility and associated laboratories. The technician will execute microbiological… more
- University of Southern California (Los Angeles, CA)
- cGMP Senior Quality Control (QC) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Senior- cGMP ... it is. The Senior QC Specialist at the USC/CHLA cGMP Facility will lead advanced quality control activities to...GDPs). Extensitve experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work as an… more
- Sumitomo Pharma (Morrisville, NC)
- …and experienced individual for the position of Sr Manufacturing Associate, cGMP Manufacturing role. The Sr Manufacturing Associate will support facility start-up ... A minimum of 3+ years of experience in a cGMP manufacturing environment along with a degree in science...related discipline OR a minimum of 5+ years of cGMP manufacturing experience with a high school diploma is… more
- Danaher Corporation (Coralville, IA)
- …safeguard and improve human health. This position is part of the Quality Control cGMP located in Coralville, IA and will be indicate whether position is on-site. At ... you will have the opportunity to: + The Manager, cGMP Quality Control supervises the internal and external Quality...DNA for therapeutic use. + Support, maintain, and execute cGMP production facility analytical methods for testing of nucleic… more
- Danaher Corporation (Coralville, IA)
- …Our work is complex and cutting-edge, and our team members are curious, creative thinkers who understand that good data drives smart decisions. At IDT, we realize ... that although science may be uniform, people are unique. We promote a culture where engaged people are motivated and have opportunities to achieve their full potential, as part of one global team.IDT is one of 10 Life Sciences companies of Danaher. Together,… more
- Honeywell (Buffalo, NY)
- Join Honeywell as a Sr Quality Assurance expert for the Buffalo cGMP manufacturing team. Ensure that appropriate cGMP Quality Systems are in place through review ... operating procedures impacting the safety, identity, strength, quality or purity of the cGMP products manufactured at the site. Conduct routine audits of 3rd party… more
- Gilead Sciences, Inc. (Frederick, MD)
- …on-the-floor operations of our commercial cell therapy manufacturing facility in a cGMP environment including developing a team, and providing the necessary training ... operations of commercial cell therapy manufacturing facility in a cGMP environment + Develop a team, Provide leadership, guidance,...guidance, and necessary training to staff in alignment with cGMP requirements. + Generate SOPs, MPRs, and SPRs for… more
- Catalent Pharma Solutions (Harmans, MD)
- …healthier lives. Catalent's Harmans/BWI, MD facility is a FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies. The campus features two ... and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse. The… more
- Boehringer Ingelheim (Fremont, CA)
- …recognizing and reporting process and equipment anomalies. + Documents work according to cGMP and cGDP. + Adheres to established regulations and follows cGMP ... + Two (2) or more years of experience in cGMP regulated industry. + Ability to concentrate on detail...instructions and document work in a written format applying cGMP standards. + Ability to work as part of… more
- Boehringer Ingelheim (Fremont, CA)
- …recognizing and reporting process and equipment anomalies. + Documents work according to cGMP and cGDP. + Adheres to established regulations and follows cGMP ... + Four (4) or more years of experience in cGMP regulated industry. + Ability to concentrate on detail...instructions and document work in a written format applying cGMP standards. + Ability to work as part of… more
- Takeda Pharmaceuticals (Social Circle, GA)
- …are met while maintaining compliance with current Good Manufacturing Practices ( cGMP ), environmental health and safety (EHS) guidelines and any other regulations ... you will contribute:** + Oversee floor operations of our cGMP warehouse. + Oversee cycle count process to ensure...to consistently execute all processes with strict compliance to cGMP 's and EHS regulations. + Develop and implement key… more
- Fujifilm (College Station, TX)
- …II functions within a team based organization to actively address complex cGMP manufacturing issues. The individual is responsible for analyzing process technologies ... a CMO environment. **External US** **_Essential Functions:_** + Applies scientific and cGMP manufacturing expertise to address issues in the technology transfer and… more
- Stanford University (Stanford, CA)
- …therapy manufacturing consistent with principles of current Good Manufacturing Practice ( cGMP ) and aligned with the clinical trial investigational phase for treating ... CAR T cell therapies. + Train on biomanufacturing and cGMP procedures. + Plan and perform components of process...trials. + Perform upstream and downstream components of assigned cGMP projects. + Identify, document and report operating excursions… more
- Cardinal Health (Fort Lauderdale, FL)
- …quality functions at the PET manufacturing site, such as: + Handles cGMP documentation review related to product release, facilities and equipment, material ... the site manufactures products to meet the requirements of 21 CFR 212 ( cGMP ). + Handles and ensures quality of documentation (control, retention, and archival) to… more
