- Aequor (Thousand Oaks, CA)
- …is possible remote role Summary: Under general direction, functions as the Specialist Quality Control working at the Corporate QC Center. Description: Job Details: ... data. Additional responsibilities include providing and communicating results, maintaining global process trackers, develop project plan, support Business Continuity… more
- Merck & Co. (Durham, NC)
- …Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation . Our company is expanding its global recombinant human ... in process automation in a GMP environment.Experience programming Emerson DeltaV. Computer system validation and systems life-cycle development methodology… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Nordisk's life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well ... connected and functional Work with PM to conduct system testing and validation to ensure proper operation Programming and Configuration Assist with contractors to… more
- Kedrion Biopharma (Melville, NY)
- …agency requirements, internal company standards and current industry practices. The focus of the Computer Validation Specialist role is to identify or create ... hematology, immunology, neurology, and transfusion medicine. **JOB SUMMARY** The Computer System Validation Specialist at...relevant to 21 CFR part 11 compliance requirements and Global Computer System Validation and… more
- BioBridge Global (San Antonio, TX)
- _BioBridge Global is a San Antonio-based nonprofit, that integrates donor-to-patient services to enable the future of biotherapeutic solutions, including blood, ... of_ _cell and cell-based biologics and clinical trials support._ _We at BioBridge Global have been committed to saving and enhancing lives through the healing power… more
- Regeneron Pharmaceuticals (Cambridge, MA)
- We are seeking a highly skilled, self-motivated **Senior Validation Specialist - CSV** to ensure compliance of computerized systems with regulatory requirements ... 11, GAMP 5, and Annex 11. **As a Senior Validation Specialist , a typical day might include:**... validation documentation and explanations and communicates company's computer validation policies. + Generating, reviewing, editing,… more
- Catalent Pharma Solutions (Harmans, MD)
- **Lead Specialist , QA Validation & Engineering** Catalent Pharma Solutions is looking to hire a **Lead Specialist , QA Validation & Engineering** to ... will house 8 CGMP manufacturing suites and cold storage warehousing. The **Lead Specialist , QA - Validation & Quality Engineering** is responsible for providing… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- **Senior Cleaning Validation Specialist ** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) ... your most difficult development and manufacturing challenges The **Senior Cleaning Validation Specialist ** position involves creating cleaning cycle development… more
- Fujifilm (College Station, TX)
- …of Computer cGMP regulations and practices pertaining to computer validation principles, manufacturing processes, quality systems, engineering design ... **Position Overview** The QA Specialist III, QA Validation , will be...in Pharmaceutical or other regulated Industry. + Experience with qualification/ computer validation experience. + Experience with qualification/… more
- Envista Holdings Corporation (Madison, WI)
- **Job Description:** **Position Summary:** The ** Validation Specialist ** is primarily responsible for developing and executing validation protocols for new ... process issues. **Essential Duties and Responsibilities:** + Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and systems, including… more
- Astellas Pharma (Sanford, NC)
- ** Specialist , QA Validation ** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to ... For more information, please visit our website: www.astellasgenetherapies.com. **The Role** The Specialist , QA Validation will be primarily responsible for the… more
- Novo Nordisk (Clayton, NC)
- …which we will still be proud of 20 years from now. FF Expansions has a global approach, where you will be working with multiple sites and cultures across the world. ... us make what matters. The Position Primary responsibility is to provide/lead validation services required for the successful delivery of highly automated warehouse… more
- Mentor Technical Group (Juncos, PR)
- …MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South ... America. Job Summary: We are seeking a meticulous and experienced Validation Engineer specializing in Serialization to join our team. The ideal candidate will be… more
- Bank of America (New York, NY)
- CFO Valuation Specialist - Global Markets and International Finance New York, New York **Job Description:** At Bank of America, we are guided by a common purpose ... issues. Job expectations include partnering with model developers and validation teams, implementing new models, challenging price testing methodologies, and… more
- Abbott (Lake Forest, IL)
- …working mothers, female executives, and scientists. **The Opportunity** This position **Software Validation and Cybersecurity Specialist ** works out of our Lake ... attacks to blood disorders to infectious diseases and cancers. **Software Validation and Cybersecurity Specialist ** **Key Responsibilities also include:** +… more
- VTI Life Sciences (San Diego, CA)
- …of the biggest companies in the Life Sciences industry. We are looking for a Computer System Validation (CSV) Specialist to be responsible for ensuring that ... teamwork, creative talent, enthusiasm and diligence. As one of the leading global Commissioning, Qualification and Validation Services organizations, VTI is… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- …role supporting GxP systems required. + Pharmaceutical and/or life sciences experience including Computer System Validation , 21 CFR Part 11 and general GxP ... **Quality Specialist , Data Integrity & GxP Systems Compliance** **Position...Systems Compliance** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission… more
- Capgemini (Chicago, IL)
- …teams. *Ensure GxP compliance, data integrity, and adherence to client's CSV ( Computer System Validation ) procedures. Collaborate with QA, Manufacturing, IT, and ... **Title:** **POMSnet MES Specialist ** **Location: Chicago IL** **Duration: Full Time** **Job...GAMP 5, 21 CFR Part 11, Annex 11, and validation lifecycle. *Familiarity with ISA-95, ISA-88 models, and Pharma… more
- Amazon (Herndon, VA)
- …ACS/MEP Lifecycle drawing sets. You will provide support for this content through our Global Library as well as preforming on-site validation as needed. You ... Description We have an immediate opening for a Building Information Modeling Specialist in the Herndon, VA area This position requires that the candidate selected be… more
- Alight (Newton, IN)
- …Strada Global Page (http://www.stradaglobal.com) **QA & Compliance, Test Automation Specialist ** QA & Compliance, Test Automation Specialist will be ... rewards package, continuing education and training, and tremendous potential with a growing global organization, Strada is the perfect place to put your passion to… more
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