1541 GMP Documentation Specialist 2
Position Summary:The QA Specialist III is responsible for reviewing and approving GMP documentation supporting site operations, including Manufacturing, Validation, Manufacturing Execution Systems (MES), Quality Control, equipment and instrumentation, maintenance validation, and computer and analytical systems.This position serves as a Quality Assurance subject matter expert for documentation review and supports customer-specific […]
1563 QC Analyst 3
JOB DESCRIPTION:The Quality Control Analyst will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities.Applies job skills and company’s policies and procedures to complete a variety of tasks of increased scope.Works on assignments that are semi-routine […]
1532 QC Analyst 3
Job Summary:The QC Analyst IV is a member of the Quality Control department responsible for supporting production of in-process and final product drug lots and for performing quality testing for ongoing customer stability studies.This role delivers timely, high-quality results to meet manufacturing needs, applies company policies and procedures to a […]
1463 GMP QA Compliance Specialist
Job Summary:The QA Specialist – QA Compliance supports and maintains the site Quality Management System (QMS) by ensuring local procedures align with the company’s Group Quality Standards and applicable GMP regulations.The role leads structured gap assessments, identifies and drives remediation activities, coordinates implementation of required changes, and partners with Global […]
1076 GMP Validation Specialist – Equipment and Cleaning
JOB DESCRIPTION:Equipment Validation and Cleaning Validation.Provide Subject Matter Expert support to Quality Control, Manufacturing and other departments for the design, operation and troubleshooting of equipment.Drive/own the validation plans and execution of equipment changes and process improvements.Execution of Installation Qualifications/Operational Qualifications and drafting Performance Qualifications as required.Perform Equipment Validation activities to […]