Posted:11 hours ago|
Platform:
Work from Office
Full Time
Dear All,
Greetings from Aizant Drug Research Solutions!!We are looking for a motivated professional with strong expertise in Cleaning Validation (QA Formulations) to join our Quality Assurance team. The ideal candidate should have hands-on experience in planning, executing, and documenting cleaning validation activities as per regulatory requirements.Experience: 3-5 YearsLocation: Hyderabad(Dulapally)Department: Quality Assurance(Formulations)Key Responsibilities:-Preparation and review of Cleaning Validation protocols, reports, and risk assessments.-Execution and monitoring of Cleaning Validation studies as per cGMP guidelines.-Identification of worst-case products and development of cleaning validation strategies.-Preparation and review of SOPs related to cleaning and validation activities.-Review of analytical method suitability for cleaning validation.-Handling deviations, CAPA, and change controls related to cleaning validation.-Coordination with cross-functional teams (Production, QC, Regulatory, etc.) for smooth execution.-Ensuring compliance with international regulatory requirements (USFDA, EMA, MHRA, WHO, etc.).-Sound knowledge of cGMP, regulatory guidelines, and risk-based approach to cleaning validation.-Strong documentation and review skills.
Note: Immediate Joiners are more preferred
Aizant
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