- Cipla (Hauppauge, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates. Job Title : QA Validation FLSA Classification : Professional, Exempt Work Location : Unit 1, Hauppauge, NY ... vary based on business needs) Reports To : QA Validation Manager Salary Range: $68,000 - $74,600 Purpose: The...all data, write final reports and obtain approvals. Review technical documentation such as batch records, SOPs, calibration records,… more
- Stellantis (Auburn Hills, MI)
- …government regulations. Perform and review DVP&R (Design Verification Plan and Report) before validation and define test protocols and test tools if needed. ... deliver solutions that meet program goals. Report vehicle issues discovered during validation to appropriate issue management tracking systems. Lead and… more
- Merck & Co. (Durham, NC)
- …growing pharmaceutical manufacturer? If so, then this is the opportunity for you!The Lead Tech, Engineering is a member of the Engineering team providing ... technical support within a capital project start-up in Durham,...Maintenance (PM) plans as requested. Responsible for SAP transactions, validation testing support, supporting root cause investigations and change… more
- ValSource, Inc. (Rahway, NJ)
- …other regulatory requirements. ResponsibilitiesOn-Site Project Management: Interface with clients, lead teams of validation professionals, and provide subject ... Performance Qualification (PQ). Troubleshoot and resolve issues that arise during validation activities, providing technical expertise and guidance. Ensure all… more
- Stellantis (Auburn Hills, MI)
- …will recommend Power Electronics strategies and technologies to meet future global requirements, Lead technical problem solving to find technical solutions ... Essential Duties and Responsibilities: Technical Responsibility: Contribute to the Global Technical Area (GTA) strategy and lead in the capability growth of… more
- Cipla (Fall River, MA)
- …to meet GMP by performing surprise checks Prepare and review the qualification, validation and other documents to maintain GMP Participate in the internal and ... production plan due to volatile demand. Overcome by rescheduling of plans More lead time for approval of regulatory documents by internal and external stakeholder… more
- Cipla (Fall River, MA)
- …Quality Team. The QA operation specialist (MDI) monitors and ensures validation and qualification of facility, utilities, equipment's, processes and ensure product ... deviation investigation and CAPAs. Review and approval of manufacturing/engineering validation and qualification documents. Provide daily/weekly updates to shop… more
- Bayer (IN)
- …You are proficient in the application of a broad set of analytical and technical tools within a single BAYER technical discipline (Mechanical, QA, ... emphasis on Risk Reduction testing (RRT) and Verification and Validation (V&V) testing; Possess the technical skills...and works to identify breadth of tasks. May take lead role in selected technical activities; Demonstrate… more
- Twist BioScience (South San Francisco, CA)
- …complex NGS workflows, with a focus on maximizing data quality and experimental efficiency. Lead NGS Tools Evaluation & Optimization: Design and execute rigorous ... biology and NGS workflows to generate high-quality data, provide critical technical insights, and drive scientific communication through publications and … more
- Eisai, Inc (Baltimore, MD)
- …regions. It also includes resource planning, budgeting, vendor management, and technical oversight to support the objectives of Global Regulatory Operations. The ... as the primary liaison between R&D functions, acting as the submission lead for designated global applications (eg, INDs, NDAs, MAAs, supplements, amendments, and… more
