- Cipla (Fall River, MA)
- Job Title : Quality Assurance Operation Specialist FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General: 8:30AM - 5:00PM ... : Quality Assurance Manager Salary Range: $72,800 - $93,600 Purpose: The QA operation specialist (MDI) position is an individual contributor role and a member of the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality Operations team based in Raritan, New Jersey. ... Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...oversight of all aspects of the cell therapy clinical manufacturing process.Support manufacturing activities for cGMP compliance… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Manufacturing , Warehouse and Logistics experience in the biotech/biopharma industry . Cell/Gene Therapy cGMP manufacturing experience preferred.Fundamental ... in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Specialist as part of the Technical Operations team based in Raritan, NJ.Role… more
- Merck & Co. (Durham, NC)
- …If so, then this is the opportunity for you! Description The Specialist , Manufacturing Automation, is responsible for Building Automation System (BAS), ... cold storage, and utility systems for the Digital Manufacturing Operations (DMO) team located at the Durham, NC...two (2) years of experience in a production regulated industry Minimum of two (2) years of experience in… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Validation Specialist III as part of the Quality team based in Raritan, NJ.Role OverviewThe ... QA Validation Specialist role is an exempt level position with responsibilities...systems, computer systems, and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist II as part of the Technical Operations team based in Raritan, NJ. ... support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be responsible in handling...attract and retain top talent in a highly competitive industry , we offer a best-in-class benefits package that supports… more
- Cipla (Fall River, MA)
- Job Title IT Specialist Organization Name InvaGen Pharmaceuticals, Inc Location 927 Currant Rd., Employment Type (Hourly/ Full Time) Exempt/Professional Salary Range ... Systems Support including Systems Implementation, Validation, Administration etc., for Manufacturing , Packaging, Warehouse, Quality etc., IT project coordinator role… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Investigations Specialist II as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QC Investigations Specialist is an exempt level position with responsibilities for...support of the QC testing laboratories related to the manufacturing of cell therapy products for clinical trials and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Support Specialist as part of the Technical Operations team based in Raritan, NJ. ... Role OverviewThe Operations Support Specialist will be part of the Technical Operations team...policies, quality systems, and cGMP requirements.Build strong partnerships with Manufacturing , Warehouse, Engineering, and Quality, and work as part… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality team based in Raritan, NJ.Role OverviewThe QA ... Change Control Specialist II role is an exempt level position with...over the change control process within a cell therapy manufacturing facility to support both clinical and commercial requirements… more
- Aequor (Framingham, MA)
- …minimum 6 years of Quality/Operations experience in a biotech/pharmaceutical cGMP manufacturing environment within an FDA-regulated industry , proficiency in ... Shift: 1st Work Schedule: Mon-Fri 800-430The Third Party Management Specialist will oversee Third Party Quality operations for the MA BioCampus, ensuring excellence… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Specialist , Lab Services, II/III as part of the Quality team based in Raritan, ... NJ. Role OverviewThe QC Specialist , Lab Services is responsible for sample management. The...sample and retain managementKnowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and… more
- Cipla (Fall River, MA)
- …ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating ... include but are not limited to the following: Review of batch manufacturing /packaging records. Release of raw materials, packaging materials and finished products… more
- Merck & Co. (Rahway, NJ)
- …current with all environmental regulations and as they apply to our industry . Identify the environmental requirements.-Works with company center of excellence for ... and organizational skills required.Demonstrated performance in a highly regulated industry with strict standards adherence and compliance initiatives.Good root cause… more
- Merck & Co. (Rahway, NJ)
- …processes. Previous experience in communications technology, life sciences, pharma industry , or clinical operations domain. Required Skills Asset Management, ... daily in-person attendance is required for, field-based positions; facility-based, manufacturing -based, or research-based positions where the work to be performed… more
- Merck & Co. (Omaha, NE)
- …License a plus.Minimum of five (5) years logistics experience in the pharmaceutical industry of which a minimum of 2 years functional expertise with international ... daily in-person attendance is required for, field-based positions; facility-based, manufacturing -based, or research-based positions where the work to be performed… more
- Cipla (Reid, WI)
- Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM ... (may vary based on business needs) Reports To : Department Head - Manufacturing Salary Range: $72,800 - $93,600 Job Overview Invagen Pharmaceuticals is searching for… more
- ValSource, Inc. (Durham, NC)
- Validation Specialist / Validation Engineer / CQV Engineer ValSource is currently looking to identify experienced and technically skilled leaders in Commissioning, ... projects with clients our clients in the pharmaceutical and biotech manufacturing industries throughout our Southeast Region (greater Raleigh/Durham area) and each… more
- Merck & Co. (Rahway, NJ)
- …to the information that they need.- Providing mentoring, coaching, and oversight to Specialist and Senior Specialist project managers working on common projects. ... in project management or a related role required; in a pharmaceutical/biotech industry preferredPreferred Experience and Skills:- Advanced degree (eg, MPH, MS, MBA,… more
- Merck & Co. (North Wales, PA)
- …and any adherence PSP that may be developed. Recognized as a specialist in patient experience and support program design, providing advanced functional guidance ... across our company as needed. Maintains awareness of competitor strategies and industry trends to inform and enhance patient experience initiatives. Shapes the… more
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