$0 - $0 /
Location
Type
Status
Open
Gurgaon, Haryana


Qualifications:

B. Sc. (Chemistry as main subject)/ M. Sc. (Chemistry)/B. Pharma /M. Pharma

Professional Experience:

Experience should be 2-3 yrs in pharmaceutical industry

Personality Traits:

Adaptive
Disciplined and enthusiastic
Able to work under pressure
Willing to learn and sharing ideas
Ability to work as a team

Specific Job Requirements:

Allocation of BMR (Batch Manufacturing Record) & BPR (Batch Packing Record)
Review of BMR/BPR & SOP
Review of Q.C. Reports
In process checking of production & packing department
Work as an IPQA Chemist on shop floor
Be actively involved in both internal & external audit
Dispensing of RM and PM
Preparation of BMR and BPR
Collection and Review of Control Sample
Collection of stability Sample
Preparation of Export Pack list
Verifying standard operating procedures (SOPs)
Coordinating with regulatory affairs (RA) and analytical laboratory teams to arrange required documents for timely submission of documents
Preparing all the documents with proper follow-up and record, store and archive documents.
Review the work of the department during routine monitoring and informing the supervisor for necessary improvements in the identified areas
Actively participate in laboratory investigations and incidents as well as ensuring proper compliance.
Maintain and ensure safety all times at workplace
Gurgaon, Haryana Qualifications: B. Sc. (Chemistry as main subject)/ M. Sc. (Chemistry)/B. Pharma /M. Pharma Professional Experience: Experience should be 2-3 yrs in pharmaceutical industry Personality Traits: Adaptive Disciplined and enthusiastic Able to work under pressure Willing to learn and sharing ideas Ability to work as a team Specific Job Requirements: Allocation of BMR (Batch Manufacturing Record) & BPR (Batch Packing Record) Review of BMR/BPR & SOP Review of Q.C. Reports In process checking of production & packing department Work as an IPQA Chemist on shop floor Be actively involved in both internal & external audit Dispensing of RM and PM Preparation of BMR and BPR Collection and Review of Control Sample Collection of stability Sample Preparation of Export Pack list Verifying standard operating procedures (SOPs) Coordinating with regulatory affairs (RA) and analytical laboratory teams to arrange required documents for timely submission of documents Preparing all the documents with proper follow-up and record, store and archive documents. Review the work of the department during routine monitoring and informing the supervisor for necessary improvements in the identified areas Actively participate in laboratory investigations and incidents as well as ensuring proper compliance. Maintain and ensure safety all times at workplace
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