Tagoor Laboratories, a rapidly growing pharmaceutical company specializing in APIs, Intermediates, KSMs, and IP management, is currently hiring experienced Quality Assurance (QA) professionals for its Rajahmundry facility. This opportunity is ideal for candidates with strong knowledge of GMP documentation, quality systems, regulatory compliance, and audit management in the API pharmaceutical industry.

Job Details

Position: Sr. Executive / Executive – Quality Assurance (QA)
Company: Tagoor Laboratories
Location: Rajahmundry, Andhra Pradesh
Experience: 5–6 Years in API Pharma Industry
Qualification: B.Pharm / M.Pharm / M.Sc Chemistry

Key Responsibilities

• Review and approve GMP documents, SOPs, BMR/BPR, protocols, and reports.
• Handle deviations, OOS (Out of Specification), OOT (Out of Trend), CAPA, change controls, and investigations.
• Ensure compliance with cGMP, USFDA, WHO, and ICH guidelines.
• Perform line clearance, batch review, and QA shop-floor activities.
• Support internal, customer, and regulatory audits.
• Drive quality system improvements and compliance initiatives.

Required Skills

• Strong understanding of Quality Management Systems (QMS).
• Experience in deviation handling and root cause investigations.
• Knowledge of regulatory requirements and GMP practices.
• Documentation review and approval expertise.
• Audit preparation and compliance management skills.

Why Join Tagoor Laboratories?

Tagoor Laboratories offers a dynamic work environment focused on operational excellence, innovation, and regulatory compliance. Employees get opportunities to work with advanced quality systems and contribute to maintaining global pharmaceutical standards.

How to Apply?

Interested candidates can send their updated resume to:

Email: career@tagoor.com

Technical FAQs

1. What is the role of QA in an API pharmaceutical company?

QA ensures that all manufacturing, documentation, and quality systems comply with GMP requirements and regulatory standards to maintain product quality and patient safety.

2. What is the difference between OOS and OOT?

OOS (Out of Specification) occurs when a test result falls outside predefined specifications, while OOT (Out of Trend) refers to results that are within specifications but show unusual variation from historical trends.

3. What is CAPA in pharmaceutical quality systems?

CAPA stands for Corrective and Preventive Action. It is a systematic process used to investigate quality issues, identify root causes, implement corrective measures, and prevent recurrence.

4. Why is batch record review important in QA?

Batch record review ensures that all manufacturing and testing activities were performed according to approved procedures and regulatory requirements before product release.

5. What regulatory guidelines should a QA professional be familiar with?

QA professionals should have knowledge of cGMP, USFDA, WHO-GMP, ICH Guidelines, Data Integrity requirements, Change Control, Deviations, and Audit Management to ensure regulatory compliance.