- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Support Specialist , Sun-Wed 2nd Shift as part of the Technical Operations team based ... in Raritan, NJ. Role OverviewThe Operations Support Specialist will be part of the Technical Operations team...support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be performed within a… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking 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 for providing quality oversight over the validation and qualification… more
- Aequor (Thousand Oaks, CA)
- …functions that enable the B20 plant to add value to the network: Manufacturing, Process Development , Supply Chain, Quality, and Facilities & Engineering. A high ... work alongside other innovative, driven professionals in this meaningful role. Role: Specialist Manufacturing, New Product Introduction Let's do this! At we strive… more
- Merck & Co. (Durham, NC)
- …Support, Project Management, Regulatory Compliance, Teamwork, Training and Development -Preferred Skills:Leadership, Materials Management, Process ImprovementsJob ... continue to be one of the world's biggest investors in Research & Development .We are seeking individuals with strong scientific and technical skills to contribute to… more
- University of Southern California (Los Angeles, CA)
- … (PD) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - Process - Development --PD-- ... cell and gene therapies and other biological products for internal/external users. The Process Development (PD) Specialist is responsible for developing… more
- Houston Methodist (Houston, TX)
- …production or quality control. + Collaborates with cross-functional teams including research, process development , quality assurance and quality control. + Works ... At Houston Methodist, the Sr. Current Good Manufacturing Practices ( cGMP ) Specialist is responsible for adherence to...the department, this position will actively contribute to the development of policies and procedures for the delivery of… more
- University of Southern California (Los Angeles, CA)
- …QC liaison to actively participate in cross-functional meetings with Manufacturing, Process Development , and Quality Assurance to ensure seamless coordination ... cGMP Senior Quality Control (QC) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP -Senior-Quality-Control--QC-- Specialist \_REQ20165200/apply) Keck School of Medicine Los… more
- Boehringer Ingelheim (St. Joseph, MO)
- …an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development , and delivery of our products to our patients and customers. Our ... programs reflect Boehringer Ingelheim's high regard for our employees. The Principal Specialist , CSVC oversees all aspects of computer system and computer system and… more
- Fujifilm (College Station, TX)
- …**_Summary:_** FUJIFILM Biotechnologies in Texas is seeking a Senior eQMS Specialist to support the configuration, implementation, analysis, and maintenance of the ... Quality Management Systems (eQMS). This role ensures system compliance with cGMP and regulatory requirements while optimizing eQMS functionality and efficiency. The… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …manufacturers or business partners. * Leading a sub-team in continuous process improvements, system/equipment implementation and/or strategy development . * ... We are currently looking to fill an External Manufacturing Specialist position. The External Manufacturing Specialist oversees all aspects of contract… more
- Abeona (Cleveland, OH)
- …Report to management as needed. + Work with the Manufacturing, Quality Control, Assay Development , and Process Development departments as a production area ... document management ensuring procedural and regulatory compliance throughout the manufacturing process . The Senior Specialist I, Quality Assurance will report… more
- Catalent Pharma Solutions (Harmans, MD)
- …and a warehouse. The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage ... **Lead Specialist , QA Validation & Engineering** Catalent Pharma Solutions...Harmans, MD Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to… more
- Merck (Durham, NC)
- …active ingredient, finished product, and laboratory testing for the BCG vaccine. The Specialist , Quality Control participates in a team of analysts in the ... development , validation, and routine testing for the BCG Product....Product. The position will focus on environmental monitoring, aseptic process simulation and support testing readiness in preparation for… more
- Adecco US, Inc. (Swiftwater, PA)
- …characterization, take lead in high throughput gene synthesis and plasmid production, process automation and protocol development , improvement of quality and ... Healthcare & Life Sciences is hiring a contract Project Specialist for our Pharmaceutical partner in Swiftwater, PA. The.... Investigate and correct safety standard deviations . Support cGMP compliance and participate in new team member training… more
- Kelly Services (Warwick, RI)
- …environment for Manager Level + A minimum of 5 years working in a cGMP regulated environment for Sr Specialist Level + Experience supporting quality oversight ... **Sr. Specialist , External Quality Small Molecules (Remote)** **Manager or...and complaints, including review and approval of non-conformances and development of robust CAPA plans. Provide support to the… more
- PACIV (San Juan, PR)
- …its Puerto Rico office. Job Description: The Computerized System Validation (CSV) Specialist /Engineer will be responsible for development and execution of ... Industry, mainly Bio-Pharma and/or Medical Devices. The resource will be responsible for development and execution of CSV deliverables, as per System Development … more
- Abeona (Cleveland, OH)
- …retention for select SOPs. + Work with the Manufacturing, Quality Control, Assay Development , and Process Development departments as a production area ... and document management ensuring procedural and regulatory compliance throughout the manufacturing process . The Specialist II, Quality Assurance will report to… more
- Kelly Services (Winston Salem, NC)
- …with incoming material qualification testing and lot release evaluations. + Support process development , validation activities, and data collection for ... **Manufacturing Specialist III - Cell Processing** **Location: Winston Salem...processing techniques, procedures, and regulatory compliance. + Drive continuous process improvement, incident investigations, and deviation resolutions. + Ensure… more
- Bristol Myers Squibb (Indianapolis, IN)
- …**Summary** Located at our Indianapolis, IN facility, The Quality Training Specialist will be responsible for supporting the training management processes related ... of and adherence to the quality procedures. Additionally, the Quality Training Specialist will become a subject matter expert (SME) in management related to… more
- Actalent (Durham, NC)
- …within the organization. Responsibilities + Assist in the development of cGMP operating procedures related to process , computer systems, and equipment ... Quality Specialist - Validation Job Description The Quality ...- Validation ensures adherence to current Good Manufacturing Practices ( cGMP ) and FDA Quality Systems throughout the evaluation, review,… more
