Rahul Namdev Email & Phone Number

Ahmedabad, Gujarat, India

Preparation and review of QA and other departments related SOPs.Preparation of Qualification protocol & reports of equipment and instruments, and to ensure the execution of qualification activity.Preparation of Validation Master Plan.Preparation of Site Master File and Quality Manual.Responsible for documentation, effective implementation and proper closing of Quality Management System (QMS) activities such as deviation, change control, incident.Responsible to ensure that the training of individuals of all departments are conducted in timely manner.Responsible to ensure all the vendor of starting materials such as raw materials, packing materials etc. is qualified to meet the cGMP norms.

Dehradun, Uttarakhand, India

Handling of Change Control, Incident & Deviation.Impact assessment of Change control.To investigate the root cause of the Incident.Evaluation of root cause for the reported Incident.Suggesting CAPA for the Incident & Deviation.Preparation of seasonal trend for QMS activity.

Baddi, Himachal Pradesh, India

Preparation of Qualification and re-qualification protocol & reports of equipment and instruments, and to ensure the execution of qualification activity as per protocol.Preparation and execution of Process validation protocol and report.Monitoring of the process validation activity.Sampling at different manufacturing stage during the process validation.Compilation of the process validation report.

Baddi, Himachal Pradesh, India

Preparation of Qualification and re-qualification protocol & reports of equipment and instruments, and to ensure the execution of qualification activity as per protocol.Preparation and execution of Process validation protocol and report.Monitoring of the process validation activity.Sampling at different manufacturing stage during the process validation.Compilation of the process validation report.

Bhopal, Madhya Pradesh, India

Docuemnts control management like prepration, issunace, retrieval. handling IPQA activity, line clearance, inprocess verification, controll sample handling. FG inspection as per AQL. Documentation of market complaint, to assist in the investigation to be carried out against Market Complaints, appropriate CAPA and Closure of the compliant.Timely response to the complaint.Implementation of "cGMP" systems:To ensure for cGMP followed by all personnel’s.

Bachelor Of Pharmacy - Bpharm, Pharmacy, First Division

High School

Intermediate

Bachelor, Pharmacy