- Merck & Co. (Rahway, NJ)
- …Process Research & Development, in Rahway, New Jersey is seeking a Senior Specialist to expand our capabilities to design and engineer proteins with novel functions. ... data analysis, for example using Python or R. - - We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QC Specialist , Lab Services - I, II, III as part of the Quality team based in ... Raritan, NJ. Role Overview The QC Specialist , Lab Services, is responsible for sample management. The...and retain management. Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and… more
- Dexian - DISYS (Bothell, WA)
- …SQL server also a plus.Experience with cell therapy or other biopharmaceutical manufacturing .Other highly regulated industries will be considered.Flexibility to ... The MES Recipe Engineer and Validation Specialist role will deliver electronic batch record (EBR)...record (EBR) configuration and validation in the Emerson Syncade Manufacturing Execution System (MES). This role will support new… more
- On-Board Companies (Bothell, WA)
- …SQL server also a plus.* Experience with cell therapy or other biopharmaceutical manufacturing . Other highly regulated industries will be considered.* ... Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits… more
- VTI Life Sciences (San Diego, CA)
- VTI Life Sciences (VTI) seeks a Talent Acquisition Specialist with GMP Pharmaceutical Commissioning, Qualification and Validation (CQV), and Automation recruiting ... experience. As a VTI Talent Acquisition Specialist , you will assist with our recruitment process, including competitive high-volume job searches. The position will… more
- Kelly Services (Juncos, PR)
- …Hiring Experts. **Salary: $38.00 per/hour** **Overview** This client is Global Biopharmaceutical company whose mission is to discover, develop and deliver innovative ... this role you'll be responsible for supporting the execution of manufacturing /quality systems such as non-conformances, process validation, procedures, training, and… more
- Parker Hannifin Corporation (Oxnard, CA)
- …the biopharmaceutical industry. Technical aptitude and experience in biopharmaceutical process development, manufacturing , validation and automation. Versed ... System Sales Specialist Location : OXNARD, CA, United States Job...Engineers and Territory Sales Managers, as well as Engineering, Manufacturing and Customer Service personnel. Additional activities may include… more
- Gilead Sciences, Inc. (Frederick, MD)
- …work. Kite is seeking a highly motivated individual to join us as a QC Specialist in our new commercial cell therapy production center located in Frederick, MD. You ... or Manager and provide Quality Control support of commercial manufacturing of final drug product. You will also perform...+ Bachelor's Degree and 2+ years' experience in a biotech/ biopharmaceutical setting OR + AA Degree and 4+ years'… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- …microbiology assay validation, sterilization and related documentation in support of biopharmaceutical manufacturing and testing. + Provide quality support of ... We are currently looking to fill a QA Microbiology Specialist (Drug Substance) position. This position is responsible for leading and being a team member for… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** **Quality Systems Specialist II - Document Management** Gilead Sciences, Inc. is a research-based ... biopharmaceutical company founded in 1987. Together we deliver life-saving...Global Quality Systems and Compliance organization, the Quality Systems Specialist II- Document Management will be responsible for partnering… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** **Quality Systems Specialist II** **- GxP Training** Gilead Sciences, Inc. is a research-based ... biopharmaceutical company founded in 1987. Together we deliver life-saving...Global Quality Systems and Compliance organization, the Quality Systems Specialist II - GxP Training will be responsible for… more
- Randstad US (Cambridge, MA)
- …job details job summary: Exciting new opportunity for an experienced Compliance Specialist who will work closely within the Manufacturing Compliance group ... Specialist is also responsible for owning and driving manufacturing compliance improvement through deviation resolution, applied root cause analysis and… more
- Charles River Laboratories (Memphis, TN)
- Quality Systems Specialist III Req ID #: 222127 Location: Memphis, TN, US, 38118Memphis, TN, US, 38118 For 75 years, Charles River employees have worked together to ... you can feel passionate about. **Job Summary** Quality Systems Specialist III will report to the manger in the...projects in the quality organization + Have understanding of manufacturing processes and quality systems elements + Communicate with… more
- Randstad US (Burlington, MA)
- …occupations + referenceAB_4506772 job details Our client, a large company in the biopharmaceutical industry, is seeking a Specialist /Senior Specialist to ... quality assurance specialist - gmp. + burlington , massachusetts +...support Quality On The Floor (OTF) oversight of manufacturing activities and facilities. This position will be based… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …+ Minimum 2 years of related technical and/or regulatory experience in biopharmaceutical industry. **_Sr. Regulatory Affairs Specialist I_** + Bachelor's degree ... requirements and company timelines. **Primary responsibilities for the Regulatory Affairs Specialist role:** + Manages dossier compilation for projects or assigned… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …+ Minimum 2 years of related technical and/or regulatory experience in biopharmaceutical industry. **_Sr. Regulatory Affairs Specialist I_** + Bachelor's degree ... and other duties as needed. **Primary responsibilities for the Regulatory Affairs Specialist role:** + Manages dossier compilation for product license renewals and… more
- Sartorius (San Francisco, CA)
- In the Field Application Specialist - Bioreactor role, you will be responsible for offering product expertise, application knowledge and technical support along each ... customers for application development work, initial startups and training. The Field Application Specialist position is based out of the home office which is to be… more
- ThermoFisher Scientific (Waltham, MA)
- …technical skills are required to discuss and support chromatography resins for biopharmaceutical process development and manufacturing groups. Ability to develop ... Affinity resins and columns) into process development and clinical/commercial manufacturing groups within biopharma accounts. Maintain the present customer base… more
- Editas Medicine (Cambridge, MA)
- …management, and maintenance at the Editas Waltham and Editas Devens GMP manufacturing facilities. Key Responsibilities: As the Senior Specialist , you will ... highly motivated and experienced quality professional to support internal GMP manufacturing operations. This position will be responsible for Quality Operations… more
- Charles River Laboratories (Memphis, TN)
- …based document management systems in clinical and commercial pharmaceutical/ biopharmaceutical manufacturing + Excellent working knowledge and experience ... Training Specialist Lead Req ID #: 222126 Location: Memphis,...experience in training + Strong knowledge in current Good Manufacturing Practices + Experience in managing paper based and… more
