Executive-qa (Ahmedabad)

Work Schedule Standard Mon-Fri Environmental Conditions Adherence to all Good Manufacturing Practices GMP Safety Standards Office At Thermo Fisher Scientific Inc we are seeking an ambitious and dedicated QA qualified for the position of band 3 direct labour This role is pivotal in our mission to maintain world-class quality standards and ensure flawless operations Join us and be part of a team that is determined to make a difference Responsibilities Manage material receiving destruction in-process quality assurance IPQA and return activities Perform and conduct quality checks IPQA at decided intervals during packaging production Maintain the Archival Area in strict accordance with GMP guidelines Ensure accurate reconciliation of forms to demonstrate compliance and readiness during regulatory inspections Coordinate Clintrack printing jobs and line clearance Conduct EPO pre and post reviews to maintain the quality and conformity of our operations Requirements Proven experience 2-4 years in quality assurance within the pharmaceutical industry Outstanding attention to detail and strict adherence to GMP guidelines Ability to successfully implement quality checks and manage archival areas Strong skills in conducting regulatory inspections and form reconciliations Competence in managing Clintrack printing jobs and line clearance Ability to perform EPO pre and post reviews effectively This role offers an outstanding opportunity to contribute to a company that values integrity innovation and involvement We are looking for someone who can bring their proven expertise to our exceptionally ambitious team and help us achieve flawless results Work Schedule Standard Mon-Fri Environmental Conditions Adherence to all Good Manufacturing Practices GMP Safety Standards Office At Thermo Fisher Scientific Inc we are seeking an ambitious and dedicated QA qualified for the position of band 3 direct labour This role is pivotal in our mission to maintain world-class quality standards and ensure flawless operations Join us and be part of a team that is determined to make a difference Responsibilities Manage material receiving destruction in-process quality assurance IPQA and return activities Perform and conduct quality checks IPQA at decided intervals during packaging production Maintain the Archival Area in strict accordance with GMP guidelines Ensure accurate reconciliation of forms to demonstrate compliance and readiness during regulatory inspections Coordinate Clintrack printing jobs and line clearance Conduct EPO pre and post reviews to maintain the quality and conformity of our operations Requirements Proven experience 2-4 years in quality assurance within the pharmaceutical industry Outstanding attention to detail and strict adherence to GMP guidelines Ability to successfully implement quality checks and manage archival areas Strong skills in conducting regulatory inspections and form reconciliations Competence in managing Clintrack printing jobs and line clearance Ability to perform EPO pre and post reviews effectively This role offers an outstanding opportunity to contribute to a company that values integrity innovation and involvement We are looking for someone who can bring their proven expertise to our exceptionally ambitious team and help us achieve flawless results