- Astellas Pharma (Sanford, NC)
- **QC Specialist III LIMS and Operational Support** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every ... more information, please visit our website: www.astellasgenetherapies.com. **The Role:** The QC Specialist III LIMS and Operational Support will be responsible… more
- Fujifilm (College Station, TX)
- **Position Overview** The QA Specialist III , QA Compliance, will be responsible for the review and approval of commissioning/qualification/Compliance protocols, ... and final reports and discrepancies for Quality Assurance. The QA Compliance Specialist III , QA Compliance, will handle all associated responsibilities in… more
- Curia (Albany, NY)
- QUALITY ASSURANCE SPECIALIST III (Analytical Labs) in Albany, NY CURIA provides global contract research and manufacturing services to the pharmaceutical ... are seeking a highly skilled and experienced Quality Assurance Specialist III (Analytical Labs) to join our...minimum of 5 years GxP experience in an FDA-regulated pharmaceutical environment (USA). + Must have a minimum of… more
- ThermoFisher Scientific (Greenville, NC)
- …lab coat, ear plugs etc.), Standing for full shift **Job Description** **Quality Specialist III , Quality on the Floor (12-hour Nights)** Greenville, NC **Work ... with previous experience in Quality Assurance or Quality control or Operations/ Manufacturing + Previous experience in pharmaceutical industry; preferably aseptic… more
- ThermoFisher Scientific (Greenville, NC)
- …Thermo Fisher Scientific Inc., we offer an outstanding opportunity for a Supply Chain Specialist III in our dynamic and innovative OSD organization. Located in ... + 5 years of experience in supply chain management, particularly within the manufacturing sector. Experience in a pharmaceutical or GMP environment highly… more
- ThermoFisher Scientific (Cincinnati, OH)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **PPI Business Systems Specialist III ** Join Thermo Fisher Scientific and contribute ... using various methodologies, tools and systems: lean, six sigma, pull manufacturing , total productive maintenance, waste reduction, Lean Leadership, Value Stream… more
- Novo Nordisk (Bloomington, IN)
- …in manufacturing , utility and/or packaging systems, preferably in the pharmaceutical or medical device field required + Demonstrated expertise in Regulations & ... 6 weeks paid family medical leave * Free access to Novo Nordisk-marketed pharmaceutical products * Tuition Assistance * Life & Disability Insurance * Employee… more
- ThermoFisher Scientific (Cincinnati, OH)
- …all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety Guidelines. + Maintains the ... of validated experience in GMP, GDP compliance and regulatory within the pharmaceutical industry. **Experience:** + 3+ years in Pharmaceutical Industry… more
- ThermoFisher Scientific (Cincinnati, OH)
- …Material and Finished Product Specifications (MLPs) for Commercial Operations and Pharmaceutical Development Services groups. Works closely with Business and Project ... all raw materials. + Evaluate the regulatory and current Good Manufacturing Practices (cGMP) impact of proposed materialsfor qualification of alternate/new… more
- ThermoFisher Scientific (Lenexa, KS)
- …through research, development and delivery of life-changing therapies. As a Senior Specialist (Scientist III ) within our Microbiology Division you'll be working ... to make the world healthier, cleaner and safer. **Job Title:** Scientist III (Senior Specialist , Quality Control Organisms) Join Thermo Fisher Scientific… more
- Quality Consulting Group (Juncos, PR)
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: + Performs analyses,… more
- Bayer (Berkeley, CA)
- …Cell Therapy Cell Culture- Berkeley, CA** **PURPOSE** This Production Specialist III is responsible for clinical manufacturing novel cell therapy drug ... integrity, regulatory requirements (FDA, EMA, etc.), and cGMP requirements for pharmaceutical manufacturing ; + Understands all equipment functionality such that… more
- West Pharmaceutical Services (Exton, PA)
- …Possesses technical leadership skills, as well as demonstrated understanding of pharmaceutical and/or medical device operations (eg, manufacturing , process ... Sr. Specialist , Regulatory Project Management (Evergreen Posting) Requisition ID:...(Medical Device Regulation), and Master Files (DMF/MAF) associated with pharmaceutical partner's NDAs (New Drug Applications), ANDAs (abbreviated new… more
- Fujifilm (Santa Ana, CA)
- **Position Overview** We are hiring a Clinical Affairs Specialist . The Clinical Affairs Specialist will be responsible for assisting in the development and ... devices and in vitro diagnostic devices. In addition, the Clinical Affairs Specialist will assist in performing annual activities associated with Post Market… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Sr. Current Good Manufacturing Practices (cGMP) Specialist is responsible for adherence to Standard Operating Procedures (SOPs) and ... preferred **WORK EXPERIENCE** + Five years of biotechnology or pharmaceutical industry experience with exposure to cGMP manufacturing...on the phase of the project (GLP, Phase I, PhaseII/ III etc.) + Ability to mentor and coach department… more
- Abbott (Pleasanton, CA)
- …and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Heart Failure Division on-site in Pleasanton, CA. As ... an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Current Good Manufacturing Practice (cGMP) Specialist position is responsible for adherence to Standard Operating Procedures (SOPs) and ... + Three years of experience in the biotechnology or pharmaceutical industry with exposure to cGMP manufacturing ...on the phase of the project (GLP, Phase I, PhaseII/ III etc.) **SUPPLEMENTAL REQUIREMENTS** **WORK ATTIRE** + Uniform No… more
- Amazon (Sunnyvale, CA)
- …of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to build best in class products. The ideal ... and regulatory and quality system procedures. * Provides regulatory assessment for manufacturing , design changes and product risk assessment. * Reviews and advises… more
- Abbott (Plymouth, MN)
- …**The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist ** to join our team on-site in Plymouth, MN. In this role, ... approving requests for product release. + Conducts reviews of product and manufacturing changes for compliance with applicable commercial and clinical regulations. +… more
- ThermoFisher Scientific (Cincinnati, OH)
- …safer. We are currently seeking a dedicated and daring Quality Specialist III -Supervisor Batch Disposition to join our world-class manufacturing team in the ... of more than five years in Quality Assurance, Quality Control, Operations/ Manufacturing , or other pharmaceutical experience in regulated environments is… more