Job Description

Must be good in documentation

Office hours 9-6(Sunday off)

Sarthak Biotech Pvt Ltd

is a pharmaceutical, herbal, and nutraceutical product manufacturing company based in India. We are dedicated to producing high-quality products that meet regulatory requirements and adhere to the highest standards of quality and efficacy.

Role Description -

This is a full-time on-site role for a QC documentation at Sarthak Biotech Pvt Ltd in Karnal. The role involves

Review and verify calculations and analytical records received from analyst as per specified procedure. Identify and report abnormalities/ deviations to the immediate supervisor/ appropriate authority in a timely manner. 100% adherence to cGMP and cGLP practices. Review of analytical documents, procedures, column logbooks, calibration records, qualification records, reagent solution preparations, control samples records, investigation reports, protocols, analyst qualification records, raw data pertaining to complaint responses, stability reports and audit trails.

Qualifications/Experience Requirements:

Any graduate. Preferred B.Sc/M.Sc Chemistry. Preference will be given to

Female Candidates

also FRESHERS CAN APPLY
Job Types: Full-time, Permanent

Pay: ?9,000.00 - ?15,000.00 per month

Benefits:

Paid sick time Paid time off Provident Fund
Ability to commute/relocate:

Karnal, Haryana: Reliably commute or planning to relocate before starting work (Required)
Work Location: In person