- COOLSOFT (Jackson, MS)
- Quality Assurance Technical Documentation User Acceptance Testing SCRUM Agile Analy Requirement id 155873 Job title Analyst Job location in Jackson, MS ... Skills required Project Management Experience, Workflow Analysis, Quality Assurance , Technical Documentation User Acceptance Open Date 07-Nov-2025 Close… more
- Merck & Co. (Durham, NC)
- Job DescriptionWe're looking for a Director of Quality Assurance to lead quality across the full value chain for a late-stage ophthalmic program. In this ... manufacturing excellence from development through commercialization. You'll partner across Quality , Regulatory, Technical , and Supply Chain teams-coaching,… more
- Insmed Incorporated (NJ)
- …degree (MS, PhD, PharmD) strongly preferred.Minimum of 15 years of relevant Quality Assurance experience in the biopharmaceutical industry, including at least ... strategic levels.Experience supporting regulatory submissions (eg, IND, IMPD, BLA/MAA) with high- quality documentation and Quality strategy input.Highly… more
- AUROBINDO (Dayton, OH)
- …family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In ... and equipment maintenance and lifecycle management.This role ensures that all technical manuals, maintenance records, and engineering change documentation are… more
- Twist BioScience (South San Francisco, CA)
- …compliance with QMS procedures and regulatory requirements.Prepare and maintain quality documentation , including risk management reports, corrective action ... to address identified hazards and prevent recurrence of non-conformities.Provide technical support to the R&D team on quality...You'll Bring to the Team Bachelor's degree in Engineering, Quality Assurance , or a related field.5+ years… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance , manufacturing compliance, clinical quality , or cell ... promise of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Quality Systems Lead as part of the Quality team based in Raritan,… more
- Cipla (Fall River, MA)
- Job Title : Quality Assurance (QMS) Production Lead FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General: 8:30AM - ... To : QA Manager Purpose: The purpose of the Quality Assurance Production Lead (QMS) is to...assurance in a cGMP pharmaceutical manufacturing operation environment. Technical Knowledge and Computer Systems Skills Understanding of machines… more
- Cipla (Hauppauge, NY)
- …8:30AM - 5:00PM (may vary based on business needs) Reports To : Quality Assurance Manager Purpose: This position requires a strong analytical chemistry/lab ... this position include but are not limited to the following: Scope : The Analytical Quality Assurance (AQA) associate I position is an team contributor role and… more
- Cipla (Central Islip, NY)
- …position include but are not limited to the following: Scope : The Analytical Quality Assurance (AQA) associate III position is an team or individual contributor ... role and reports to the Supervisor Analytical Quality Assurance for InvaGen Pharmaceuticals, Inc., a Cipla subsidiary located at Hauppauge, NY . The job duties… more
- 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 ... (may vary based on business needs) Reports To : Quality Assurance Manager Salary Range: $72,800 -...communication skills verbally, written, and interpersonally. Must possess strong documentation and technical writing skills, and able… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance , manufacturing compliance, clinical quality , or cell ... be responsible for reviewing and approving qualification protocols, reports, risk assessments, technical studies, and any associated documentation in support of… more
- Cipla (Central Islip, NY)
- …The QA Validation Associate role is responsible for providing Quality Assurance support for receiving/ releases GMP documentation of bulk drug substances ... Batch Disposition team, within the quality department and with quality counterparts including Manufacturing Operations, Technical Support, Supply Chain and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the candidate has experience working in a cGMP manufacturing facility, preferably in quality assurance , manufacturing compliance, clinical quality , or cell ... team setting with quality counterparts that include Manufacturing Operations, Quality Control, and Operations Technical Support.RequirementsA minimum of a… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …experience in an aseptic manufacturing facility, preferably in quality assurance , manufacturing compliance, clinical quality , technical operations or ... site personnel to provide guidance and determine immediate path forward for manufacturing quality issues.Review of all documentation , in accordance with Good … more
- Cipla (Hauppauge, NY)
- …and analyze all data, write final reports and obtain approvals. Review technical documentation such as batch records, SOPs, calibration records, preventive ... such as testing, calibration, scale-up, engineering and validation studies, and assurance that the necessary project documentation is complete, accurate… more
- Merck & Co. (North Wales, PA)
- …collaborate closely with various stakeholders, including Analytical Development, External Capabilities, Quality Assurance , Technical Operations, and CMC ... compliance audits, inspection activities, and investigation/CAPAs.-- Author and review technical documents. Complete assigned work within established project timelines.… more
- Cipla (Fall River, MA)
- …implement procedure as per Current Good Manufacturing Practices (cGMP) guidelines by Quality Assurance (QA). Check and monitor for cleanliness, maintenance, ... is preferred. Minimum of two to three (2-3) years' experience in quality assurance in a cGMP pharmaceutical manufacturing operation environment. … more
- Aequor (Northborough, MA)
- …these functions, Packaging interacts with and receives support from the Quality Assurance , Materials Management, Facilities Engineering, Validation, Metrology ... and Manufacturing Technical Support groups. In addition, Packaging interacts with outside.../ GED required2-10 years working in Packaging and Good Documentation Practices Environment.Demonstrated basic math skills and communication skills.Basic… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in an aseptic manufacturing facility, preferably cell therapy, testing facility, quality assurance , or manufacturing complianceKnowledge of cGMP regulations and ... other departments or outside contractors/vendors to complete tasksSupports and/or owns technical and quality investigations, CAPAs and correctionsDevelops and… more
- AUROBINDO (Durham, NC)
- …family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In ... and SOP ManagementAuthor and revise SOPs related to investigations and quality control.Ensure documentation is complete, accurate, and compliant with regulatory… more
