Executive

From 2 to 7 year(s) of experience
₹ Not Disclosed by Recruiter

Job Description

1. Needs to follow GLP compliance at right first time.

2. Ready to work in all the shifts and needs to complete the assigned work along with proper documentation

in time.

3. Work allotment for analysts on Raw material, packing materials, Bulk, finished, stability samples and get

it done.

4. Review the Raw material, packing materials, Bulk, finished, stability samples, calibration and other

documents.

5. Daily temperature and humidity recording for the stability chambers and prints to be taken on daily basis.

6. Maintenance of list of standards, list of chemicals and analytical columns required for all the Raw

material, packing materials, Bulk, finished, stability samples

7. Needs to follow the external testing laboratory for timely completion of analysis, needs to review the

reports on immediately for compliance.

8. Responsible for initiation of change control, deviation, OOS, CAPA and other QMS elements.

9. Maintenance of control samples and its periodic evaluation.

10. Monitor the temperature and Relative Humidity in the Instrumental room, Stability Chamber, and Control

Sample room, ensure the records are updated.

11. Responsible for monitor, storage and maintenance of volumetric solutions, reagents and indicators.

12. Maintenance of stability chambers, stability samples, Stability Schedules, Stability reports.

13. Analysis of raw Materials, cleaning validation, cleaning verification, intermediates, bulk, finished,

stability samples and others as required.

14. Perform the daily calibration of the balance, pH meters and other instruments and ensure the records are

updated.

15. Maintenance of control samples and its periodic evaluation.

16. Monitor the temperature and relative Humidity in the instrumental room, stability chamber, and control

sample room, ensure the records are updated.

17. Preparation of specification, standard testing procedures, analytical protocols and reports.

18. Review of certificate of analysis, bulk, finished, stability samples and others documents.

19. Maintenance of working and reference standards, calibration standards and calibration schedule.

20. Follow approved standard operating procedures, specifications and other standard test procedures of the

Desired Candidate Profile

PHARMACEUTICAL MANUFACTURING (OSD)



Role:QA / QC Executive

Salary: Not Disclosed by Recruiter

Industry:Pharmaceutical & Life Sciences

Functional AreaQuality Assurance

Role CategoryProduction & Manufacturing

Employment Type:Full Time, Permanent

Education

UG:B.Sc in Bio-Chemistry, Microbiology, Chemistry,B.Pharma in Any Specialization

PG:MS/M.Sc(Science) in Any Specialization,M.Pharma in Any Specialization

Company Profile

LINUX LIFE SCIENCES PRIVATE LIMITED

About Company

Incorporated In 2007, Linux Laboratories is an emerging global pharmaceutical company with Corporate office in, Chennai, India. Linux Laboratories is the Tenth largest speciality generic NEURO - PSYCHIATRIC & DERMA pharmaceutical company. We provide high-quality, affordable medicines trusted by healthcare professionals and patients all over India. Our success and growth is attributed to over 500 strong multi-cultural workforces from all over the nation. Our team has taken Linux laboratories to the heights that it has scaled and working to take it further up on its higher growth trajectory. We value our People as invaluable asset. The Culturally diverse workforce is one of our biggest strengths. The rich experience they bring, across varied skill-sets and backgrounds are instrumental.

Company Info
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Contact Company:LINUX LIFE SCIENCES PRIVATE LIMITED

Address:NO 492, NA, VIDUTHALAI NAGAR EXTENSION,KOVILAMBAKKAM, PALLAVARAM THORAIP,CHENNAI, Chennai, Tamilnadu, India