Looking for high-paying pharma jobs in India? Tagoor Laboratories is hiring experienced professionals for the DQA department. Apply now for roles with 2–10 years of experience. Email your CV to career@tagoor.com.
🚨 Hiring Alert | DQA Job Openings at Tagoor Laboratories Pvt. Ltd. | 2025
Are you a quality-driven pharmaceutical professional seeking a high-paying and growth-oriented role? Here’s your chance to join one of India’s most trusted and innovation-led pharma companies — Tagoor Laboratories Pvt. Ltd. We are currently hiring experienced professionals for our DQA (Document Quality Assurance) department.
Whether you’re currently employed or looking to transition into a better opportunity, we invite candidates with 2 to 10 years of experience to apply for dynamic roles at our growing organization.
🏢 About Tagoor Laboratories Pvt. Ltd.
Tagoor Laboratories is a well-established name in India’s pharmaceutical manufacturing landscape, known for its excellence in Active Pharmaceutical Ingredients (APIs), intermediates, and custom synthesis. We are committed to the highest standards of GMP compliance, regulatory quality, and innovation in drug development.
Our operations are focused on delivering quality pharmaceutical products to both domestic and international markets, aligned with USFDA, EDQM, and WHO-GMP standards. Our DQA department plays a pivotal role in ensuring documentation accuracy, regulatory compliance, and audit readiness.
💼 Open Position: DQA Department
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Designation: DQA Executive / Sr. Executive / Manager
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Department: Document Quality Assurance (DQA)
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Experience: 2 to 10 years in pharmaceutical QA documentation
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Location: Hyderabad / Visakhapatnam (depending on unit assignment)
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Industry: Pharmaceuticals / API Manufacturing / Bulk Drugs
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Email to Apply: 📩 career@tagoor.com
📝 Job Responsibilities:
✔️ Manage GMP documentation as per regulatory requirements
✔️ Review Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs)
✔️ Ensure timely completion and archival of documents
✔️ Coordinate with Quality Control (QC), Quality Assurance (QA), and Regulatory Affairs
✔️ Maintain compliance with ICH Q10, FDA, WHO, and ISO guidelines
✔️ Prepare for regulatory audits and customer inspections
✔️ Lead documentation initiatives to support change control, deviation, CAPA, and SOP writing.
🎯 Key Skills Required:
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In-depth knowledge of GMP documentation standards
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Familiarity with regulatory filings such as DMF, ANDA, CTD
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Experience in change control, deviation handling, CAPA
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Excellent communication and organizational skills
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Proficiency in MS Office, LIMS, SAP (preferred).
🎓 Qualification:
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B.Pharm / M.Pharm / B.Sc / M.Sc in Life Sciences / Chemistry / Pharmaceutical Sciences
💰 Salary & Benefits:
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Attractive salary packages based on experience and skillset
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Opportunities for internal career growth
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Exposure to global regulatory environments
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Performance incentives, learning modules, and on-the-job training.
📈 Why Join Tagoor Laboratories?
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💊 Work with a leading pharma manufacturer in India
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🧬 Exposure to cutting-edge API production and documentation processes
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🚀 Fast-track your career in DQA, QA, QC, Regulatory Affairs
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🌐 Work environment compliant with USFDA, WHO-GMP, and EDQM.
📬 How to Apply:
Interested and eligible candidates are requested to send their updated resumes with the subject line:
“Application for DQA – [Years of Experience] – [Current Location]”
To: career@tagoor.com
📄 Documents to Include:
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Updated Resume
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Educational Certificates (B.Pharm, M.Pharm, B.Sc, M.Sc)
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Experience Certificates
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Last 3 Months Salary Slips
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Aadhar Card Copy
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Recent Passport Size Photo.
