Sun Pharma, a globally recognized leader in the
pharmaceutical industry, is inviting qualified professionals to attend a
walk-in interview for the Quality Assurance Incharge position at its Palasbari
formulation plant in Assam. This prestigious role presents an opportunity to
work with one of the world's top generic pharmaceutical companies and No. 1 in
India, known for its innovation and excellence in healthcare.
Company Overview
Sun Pharma has established itself as a major player in the
pharmaceutical sector since its inception in 1983. With a strong presence in
over 100 countries, the company operates more than 40 manufacturing facilities
across six continents. Sun Pharma is committed to innovation, employing nearly
2,000 scientists across its research centers in India, Israel, and the United
States.
Quality Assurance Incharge Position
Role Details
- Department:
Quality Assurance Incharge
- Qualifications:
M.Pharm or B.Pharma in Pharmacy
- Experience:
3-8 years
- Salary:
Not disclosed
- Openings:
20 positions available
- Job
Location: Sun Pharma Formulation Plant, Palasbari, Assam
Responsibilities
The Quality Assurance Incharge role entails a broad range of
responsibilities aimed at ensuring product quality and compliance with industry
standards:
- Market
Complaint Handling: Overseeing the resolution of market complaints on
site.
- Deviation
Management: Managing and addressing deviations on site effectively.
- CAPA
and Global CAPA Management: Implementing corrective and preventive
actions and ensuring their effectiveness.
- Mock
Recall and Market Recall: Coordinating the execution of mock recalls
and market recalls.
- Audit
Response Tracking: Reviewing and tracking audit responses to maintain
compliance.
- Quality
Alert Management: Raising, reviewing, and tracking quality alerts to
address potential issues.
- Timely
Closure of QMS Documents: Ensuring that Quality Management System
(QMS) documents are closed in a timely manner.
- IPQA
Activities: Performing in-process quality assurance activities.
- Process
and Cleaning Validation: Executing validation protocols for processes
and cleaning activities.
- Review
of BMRs and BPRs: Reviewing batch manufacturing records and batch
processing records.
- Product
and Recipe Approval: Handling product and recipe approvals, as well as
sample posting in SAP HANA systems.
- Hold
Time Study Protocol: Preparing, executing, and sampling hold time
study protocols.
- Process
Validation Protocol and Report: Preparing and reviewing process
validation protocols and reports.
- Annual
Product Quality Review: Preparation and review of the annual product
quality review.
Walk-In Interview Details
- Date:
21st April 2024
- Time:
9:30 AM – 5:00 PM
- Venue:
Eco Paradise Resort, Rangpo, NH 10, Mining, Sikkim 737132
- Contact:
Akash Gogoi at 8473959757
Application Process
Candidates can submit their resumes via email to
[email protected]. For additional inquiries, you may contact Akash
Gogoi at the provided phone number.
Conclusion
This opportunity with Sun Pharma offers a chance for quality
assurance professionals to join a renowned company in the pharmaceutical
industry. Those seeking to advance their careers and contribute to cutting-edge
pharmaceutical research and development are encouraged to attend the walk-in
interview and seize this opportunity.