VerGo Pharma Research Labs Hiring IPQA Department
- Exciting IPQA Job Openings for B Pharm/M.Pharm Graduates at VerGo Pharma Research Labs – Verna, Goa
- Why Choose a Career in IPQA at VerGo Pharma?
- Key Responsibilities in IPQA Roles
- Shop Floor Monitoring and GMP Compliance
- Batch Record Review
- APQR Compilation
- Eligibility Criteria
- Educational Qualifications
- Experience Required
- Location and Work Environment
- How to Apply
- Job Summary Table
B Pharm/M.Pharm IPQA Jobs in Goa – Vacancies at VerGo Pharma Research Labs
Apply for IPQA jobs at VerGo Pharma in Goa. Openings for B Pharm/M.Pharm graduates with up to 3 years’ experience in solid dosage and APQR.
Exciting IPQA Job Openings for B Pharm/M.Pharm Graduates at VerGo Pharma Research Labs – Verna, Goa
VerGo Pharma Research Labs Pvt. Ltd., a reputed CDMO (Contract Development and Manufacturing Organization) based in Verna, Goa, is inviting applications for the IPQA (In-Process Quality Assurance) department. If you’re a recent graduate or an early-career professional with experience in pharmaceutical quality processes, this is a prime opportunity to work with a company known for its scientific excellence and regulatory compliance.
Why Choose a Career in IPQA at VerGo Pharma?
VerGo Pharma Research Labs stands out as a trusted name in the CDMO industry, offering robust career opportunities across research and quality domains. The IPQA department plays a crucial role in ensuring product integrity and compliance across manufacturing processes.
This position provides practical exposure to:
- Solid dosage forms (tablets, capsules, etc.)
- Shop floor monitoring for quality compliance
- Executed batch record review
- Annual Product Quality Review (APQR) compilation
Working in this environment allows professionals to deepen their understanding of cGMP guidelines, documentation standards, and regulatory expectations from agencies like the USFDA, EU-GMP, and WHO.
Key Responsibilities in IPQA Roles
Shop Floor Monitoring and GMP Compliance
- Real-time monitoring of manufacturing and packaging activities
- Ensuring adherence to SOPs and cGMP regulations
- Documentation of deviations and supporting CAPA implementation
Batch Record Review
- Review of executed batch production records (BPR) and batch packaging records (BPR)
- Cross-checking entries for accuracy and completeness
APQR Compilation
- Supporting Annual Product Quality Review activities
- Compiling trend data for critical parameters
- Highlighting improvements and gaps in manufacturing trends
Eligibility Criteria
Educational Qualifications
- Bachelor of Pharmacy (B Pharm)
- Master of Pharmacy (M.Pharm)
Courses under these degrees include:
- Pharmaceutical Chemistry
- Pharmacology
- Pharmaceutics
- Pharmaceutical Analysis
- Pharmaceutical Quality Assurance
- Industrial Pharmacy
- Clinical Research (M.Pharm)
- Regulatory Affairs (M.Pharm specialization)
Experience Required
- 0 to 3 years in IPQA-related roles
- Prior exposure to shop floor monitoring, BMR/BPR review, and APQR is preferred
Location and Work Environment
Location: VerGo Pharma Research Labs Pvt Ltd, Verna Industrial Estate, Goa
The facility is equipped with state-of-the-art infrastructure for formulation development, analytical services, and GMP manufacturing. Employees benefit from a compliance-driven, learning-focused environment.
How to Apply
Candidates meeting the eligibility criteria can send their updated CVs to:
Email: trupti.prabhudessai@vergolabs.com
Subject Line: “Application for IPQA Position – VerGo Pharma Goa”
Ensure that your resume highlights:
- Educational background
- Relevant experience (if any)
- Projects or internships in QA/IPQA
Job Summary Table
| Company Name | VerGo Pharma Research Labs Pvt. Ltd. |
|---|---|
| Current Vacancies | IPQA Department |
| Required Education | B Pharm / M.Pharm |
| Experience Required | 0 to 3 Years |
| Location | Verna, Goa |
To apply for this job email your details to trupti.prabhudessai@vergolabs.com
