An AI agent that applies to roles like this on employers' own sites. 25 applications free, no card needed.
Posted over 15 days ago, so the role may have closed. Confirm on the employer's page when you apply, or see similar jobs.
Job Description
Role & responsibilities
Preparation of Site Master File, Validation Master Plan and execution as per Plan, Preparation of Quality Manual & approved by QA Head, to prepare the standard operating procedures for conformance with good manufacturing practices & good laboratory practices. To take active part in conduction of an internal audit to ensure compliance to good manufacturing practices & other regulatory requirement, to review the market complaints.To review the product recall, To participate in validation of processing equipment, cleaning equipment, process & cleaning procedures are done on timely basis, to carry out the documentation in compliance with good manufacturing practices, provide the required documents to regulatory department.
Skills
Laboratory SkillsQuality ManualVMPQuality AssuranceSMFManualAssuranceQualityIf a job posting appears fraudulent, asks for payment, contains misleading information, or violates our guidelines, please report it immediately. Our team will review it promptly, Jobaaj does not charge any fee from the applicants.
About Company
Similar Jobs
View allNew Risk Management & Compliance roles in Ankleshwar.
One email a day. Unsubscribe any time.

