QA Jobs at Amneal Careers | Officer QA Validation job role Openings in Hyderabad | Apply now
Looking for QA Jobs in the pharma industry? Explore exciting opportunities with Amneal Careers through this Officer, QA Validation role in Hyderabad, Telangana, designed for B.Pharmacy graduates and quality assurance professionals aiming to build a strong career in GMP, validation, and pharmaceutical quality systems.
- Job Title: Officer, QA Validation
- Location: Hyderabad, Telangana, India
- Job Identification: 7206
About the Company
Amneal is a global pharmaceutical company with manufacturing operations in Hyderabad, Telangana, India. Through QA Jobs at Amneal Careers, the organization focuses on maintaining high standards of quality assurance, GMP compliance, and validation across manufacturing, utilities, and quality systems.
Key Responsibilities
- Responsible for routine monitoring of Manufacturing Areas.
- Responsible for the routine GMP Inspection & review of Quality Records of other departments.
- To monitor and ensure the compliance level of the organization is as per the current GMP requirements
- Good Documentation recording, and updation.
- Responsible for review of URS, DQ, and vendor/supplier documents related to qualification.
- Responsible for the preparation of the Validation protocol and report.
- Responsible for execution and review of qualification / Re-Qualification and Validation activity of Equipment / System / Facility and Plant Utilities.
- Responsible for the adequacy of execution of validations being carried out at prescribed procedures.
- Responsible for the assurance of calibrations before performing qualifications.
- Responsible to co-ordinate with cross-functional department personnel for respective Qualification / Validation / Re-qualification activity for timely completion of activities.
- Responsible for the preparation of the Standard Operating Procedures of the Quality Assurance Department.
- Responsible for checking production shop floor compliance.
- Responsible for the preparation and review of the VMP.
- Responsible for the preparation, review, execution, data, and compilation of validation-related documents.
- Responsible for handling failures during qualification by using QMS tools.
- Responsible for the preparation, review, and execution of risk assessment activities related to Equipment / Process / Facility / System.
- Viable monitoring in the clean area of manufacturing and warehouse as per the defined schedule.
- Responsible for personnel monitoring.
- Responsible for participating in qualification, requalification, and area qualification activities.
- Calibration certification review and approval.
Qualifications
- B. Pharmacy
