Quality Control Analyst

  • icon job experience 3 - 6 Years
  • icon job opening 03 Openings
  • icon salary 2.5-5.0 Lac/Yr
  • icon job location Hyderabad
  • Face-to-Face interview Face-to-Face interview
Key Skills

Pharma Quality Control HPLC Quality Analysis Empower Software Method Development Pharma Quality Walk in

Job Description

1. To ensure compliance with Good laboratory practices and Good manufacturing practices.

2. Should be follow laboratory safety personal protective equipments while handling analysis.

3. Based on work allocation analysis should be perform and same day document completion.

4. All the analysis of raw materials, in-process, intermediate, stability, Recovery solvents, R&D

samples and finished product HPLC and GC analysis as per procedure.

5. All working standards HPLC and GC related analysis planned as per schedule date.

6. Working standard should be use by ensuring validity of standard within the period.

7. Chemist should be ensuring before using the instrument status and calibration of instrument

and earlier analysis results should be ensure.

8. Chemist should be ensure before starting analysis availability of standards, chemicals and

glasswares etc.,

9. Analyst should follow good laboratory practices laid down in the quality control laboratory.

10. Analyst should follow after completion of chromatography analysis ensure the results and

discard the solutions if results within the specification.

11. Analyst once started the sequence set of sample loading same day next day need to process

yesterday samples then only go for new work.

12. Analyst should process the samples contemporaneously if any abnormal results observed

inform immediately senior supervisor/reviewer/designee then only next decision to be taken.

13. Analyst is responsible for analysis and documentation and sample disposition.

14. Analyst is responsible for laboratory cleaning, instrument cleaning and maintenance in good

condition.

15. Results are reported as per rounding of the SOP.

16. Equipments calibration shall be performed as per internal calibration master schedule.

17. After usage of the working standards and reference standards it shall be kept in designated

place.

18. Monitoring the daily room temperature and its recording as per procedure.
  • Experience

    3 - 6 Years

  • No. of Openings

    03

  • Education

    B.Pharma, B.Sc, M.Pharma, M.Sc

  • Role

    Quality Control Analyst

  • Industry Type

    Manufacturing / Production / Quality

  • Gender

    Male

  • Job Country

    India

  • Type of Job

    Full Time

  • Work Location Type

    Work from Office

About Kreative Organics Private Limited

Kreative Organics Private Limited is a manufacturer of Active Pharmaceutical Ingredients (APIs) for the world market. Kreative started operations in 1990.
Kreative was established by Dr. S. Krishnamohan. Dr. Krishnamohan was formerly with TIFR, BARC, Caltech and NASA. He is a scientist of international repute and runs Kreative with professionalism and a focus on innovation.
Read More...
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