Job Description

Job involves QC/QA functions in a Pharma industry, Testing and Analysis of various Raw Materials, Finished Drugs , etc. Job requires coordination with production, Stores, and Full knowledge of documentation as per cGMP. experience in similar industry maintaining cGMP conditions, and proper records maintenance essential. Knowledge of Instrumental analysis on GC, HPLC required and essential. Must have good English, cGMP knowledge, and full computer skills.

Responsibilities and Duties

Job requires knowledge of functions of Quality Assurance in pharmaceutical manufacturing to strictly make sure plant is following GMP as per regulated market. Over-viewing finished product analysis data and releasing finished product. Performing all tasks required by QA such as making BMR's, SOP's, Change control system, Deviations, Market complaints, Annual review reports, Validations, Qualifications, Vendor Audits, Training, Preparing other Documentation for example Site Master File & Validation Master Plan, QMS Implementation etc. Candidate will also be responsible for facing Regulatory Audits from customers and authorities from regulated markets and be able to effectively communicate with them in English.
Job Types: Full-time, Permanent

Pay: ₹14,913.17 - ₹37,741.60 per month

Work Location: In person