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Vacancy for Ph.D or M.Pharm, MSc in Quality Control at VBPL


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Vacancy for Ph.D or M.Pharm, MSc in Quality Control at VBPL

VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.

Post : Sr Manager or Asst General Manager

Department : Quality Control
No of Vacancies : 5

Qualification :  M.Sc, M.Pharma or Ph.D
Experience : 16 to 18 years
Budget : 18 to 20 Lpa

Job Description
1. Responsible for the overall activities of Quality control (QC) department in support of both biotech and pharma products.
2. Accountable for the preparation and approval of SOP’S for all QC test procedures, including method validation. Evaluates the current test procedures & methodologies and updates them as per the changing requirements & regulations.
3. Qualification and Handling of Working standards and its maintenance.
4. Preparation and execution of study protocols.
5. Responsible for timely release of quality control documents with accuracy
6. Handling of customer complaints & preparing Corrective Action Report.
7. Handling of joint analysis and preparation of joint analysis report
8. To check, investigate and review out of specification results data.
9. Initiation and handling of incidents and deviation.
10. To ensure & approval of the qualification documents for the new instruments received in the laboratory.

11. To monitor data integrity and laboratory compliance in the quality control department
12. Initiation and handling of change control as per requirement.
13. To ensure the safety compliance in quality control department.
14. Preparation of validated Excel sheets protocols, reports.
15. Execution validation of Excels sheets as per protocols.
16. To be responsible for Laboratory Quality management system and internal Audit.
17. To strategize and plan continual improvement in all laboratory activities as per GMP and GLP requirements.
18. To participate and documentation of the Internal and External audits and response to the audits to ensure compliance.
19.Coordinating with QA & RA departments for documentation to fulfill the audit requirements.
20. To train new personnel related to Quality control.

Job Location : Hyderabad

Interested candidates can share with the below mentioned mail-Id.

Last Date : 10th September, 2023

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