Qc Documentation

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.
- Responsible for the investigation of Out of Specifications, Out of Trends, deviations, laboratory occurrences and incidents as per specified procedures.
- 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**:

- FRESHERS CAN APPLY

**Job Types**: Full-time, Permanent

Pay: ₹9,000.00 - ₹10,000.00 per month

**Benefits**:

- Paid sick time
- Paid time off
- Provident Fund

Schedule:

- Day shift
- Morning shift

Supplemental Pay:

- Performance bonus
- Yearly bonus

Ability to commute/relocate:

- Industrial area, Karnal - 132001, Haryana: Reliably commute or planning to relocate before starting work (required)