Job for Assistant Chemist / QA Officer at NS Pharma

NS Pharma is a specialty pharmaceutical company that addresses critical needs for niche markets by developing and manufacturing a portfolio of high value semi-solid and liquid products. NS Pharma offers an assortment of prescription products that enhance healthcare conditions as well as non-prescription products that treat a range of all segments of life.

Post : Asst Chemist / QA Officer

No of Post : 03

Job Description :
1. Candidate will be responsible for Quality Assurance Documentation Activity in API.
1. Review the documents such as Specifications, LDR, Tech pack received from R&D, AR&D, etc. so that the same can be shared with authorities and customers.
2. Prepare SOPs required for R&D activity. Maintaining the calibration schedule of the R & D equipments and monitoring the calibration status.
3. Review the process change proposals and provide guidance on change proposals.
4. Ensuring that the raw materials used in the manufacturing are qualified and all data including the vendor qualification, route of synthesis, declarations etc are available.
5. Ensure that all R&D and analytical development data is recorded by the R&D scientists in laboratory notebooks and is reviewed for accuracy and traceability. This data should be recorded as per the requirements of GMP and should be securely stored / archived for future reference.
6. Ensure that a system is in place for document control and that procedures are in place for performing the activities, operating and calibrating the equipment and training the personnel.
7. Prepare in-house expert reports/Quality overall summary (QOS).
8. Conduct internal audits properly.
9. Review of BMR received from Plant. Inspect quality till the exhibit batch stage. Carry out proper documentations in labs as well as plants. Document all the procedures.
10. Responsible for overall quality of organization.

Candidate Profile
1. Candidate should be B.Sc. / M.Sc. / B.Pharma / M.Pharm 6-10 years experience in QA Documentation API related activity.
2. Candidate will be responsible for review the documents such as Specifications, LDR, Tech pack received from R&D, AR&D, etc. so that the same can be shared with authorities and customers.
3. Candidate will be responsible for prepare SOPs required for R&D activity. Maintaining the calibration schedule of the R & D equipments and monitoring the calibration status.

Additional Information
Experience : 6-10 years
Qualification : B.Sc. / M.Sc. / B. Pharma / M. Pharm
Location : Greater Noida
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : QA & QC
End Date : 30th March, 2022