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

VBPL, headquartered in Hyderabad, is a prominent global contender in the Biopharma field. With over 15 years of operational prowess, we stand as an ISO 13485:2012 and WHO-GMP certified company. Our reach extends to the USA, where we maintain strategic offices.

At the core of our success lie two fundamental pillars: an inventive and perpetually driven research team, coupled with an unwavering commitment from our manufacturing unit to deliver excellence in every product. Quality remains our foremost priority, and it’s this dedication that sets us apart.

Post:

Senior Manager or Assistant General Manager

Department:

Quality Control

Number of Vacancies:

5

Qualification:

M.Sc, M.Pharma, or Ph.D

Experience Required at VBPL:

16 to 18 years

Budget: 18 to 20 Lpa

Job Description:

1. Overall QC Leadership: Oversee Quality Control (QC) activities for biotech and pharma products.
2. SOP Development: Prepare and approve SOPs for QC test procedures, including method validation. Update procedures to meet changing requirements and regulations.
3. Working Standards: Qualify and manage working standards, ensuring maintenance.
4. Study Protocols: Develop and execute study protocols.
5. Document Release: Ensure accurate and timely release of QC documents.
6. Customer Complaints: Handle customer complaints, prepare Corrective Action Reports.
7. Joint Analysis: Manage joint analysis and prepare joint analysis reports.
8. OOS Investigation: Review out-of-specification results, conduct investigations.
9. Incidents and Deviations: Initiate and manage incidents and deviations.
10. Instrument Qualification: Approve qualification documents for new lab instruments.
11. Data Integrity: Monitor data integrity and lab compliance.
12. Change Control: Initiate and handle change control as needed.
13. Safety Compliance: Ensure safety compliance in the QC department.
14. Excel Sheet Validation: Prepare and validate Excel sheets, protocols, and reports.
15. Continual Improvement: Strategize and plan lab activity improvements as per GMP and GLP.
16. Quality Management System: Manage Laboratory Quality Management System and internal audits.
17. Compliance Strategy: Plan continual improvement aligned with GMP and GLP.
18. Audit Participation: Participate in internal and external audits, ensure compliance.
19. QA & RA Collaboration: Coordinate with QA & RA for audit documentation.
20. Personnel Training: Train new QC personnel.

Job Location: Hyderabad

Interested candidates can share their profiles at: raghu@virchowbiotech.com

Last Date: September 10th, 2023