Apply now for the QA QMS position at Aurobindo Pharma – Unit 7 (Formulations) in Jadcherla, Telangana. We are hiring professionals with 2–5 years of experience in pharmaceutical quality systems. Only formulation background eligible.
🚨 Hiring Alert: QA QMS Role at Aurobindo Pharma – Unit 7 (Formulations)
Are you an experienced Quality Assurance (QA) professional specializing in Quality Management Systems (QMS) within the pharmaceutical formulations sector? Here’s your opportunity to join Aurobindo Pharma, one of India’s leading pharmaceutical manufacturers, at their advanced Unit 7 facility located in Jadcherla, Mahabubnagar, Telangana.
We are currently hiring QA QMS professionals with 2 to 5 years of hands-on experience in formulation-based manufacturing environments.
🧪 About Aurobindo Pharma
Aurobindo Pharma Limited is a globally trusted name in pharmaceuticals, recognized for its robust pipeline of high-quality generic and branded drugs. With multiple USFDA-approved facilities, state-of-the-art R&D centers, and a presence in over 150 countries, Aurobindo has carved a strong position in the global formulations market.
Unit 7 (Formulations), located in Jadcherla SEZ, is a premier manufacturing unit focusing on the production of solid oral dosage forms compliant with global regulatory standards such as USFDA, EU-GMP, and WHO-GMP.
📌 Job Details: QA QMS (Formulations)
Role: QA Officer/Sr. Officer – QMS
Department: Quality Assurance
Experience Required: 2 to 5 years
Employment Type: Full-Time
Work Mode: On-Site
Location: Aurobindo Pharma Unit 7, Jadcherla, Mahabubnagar, Telangana
✅ Key Responsibilities
As a QA QMS professional at Aurobindo Unit 7, your responsibilities will include:
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Change Control Handling: Initiating, reviewing, and closing change controls in compliance with regulatory and organizational SOPs.
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CAPA (Corrective and Preventive Action) Management: Performing root cause analysis, implementing corrective actions, tracking CAPA effectiveness, and ensuring timely closure.
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Deviation Management: Supporting investigation of deviations and preparing associated documentation for audits and regulatory submission.
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Documentation Review: Reviewing QMS-related documentation including SOPs, master documents, validation protocols, and audit trails.
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Audit Readiness: Supporting regulatory inspections, customer audits, and internal quality audits.
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Compliance Support: Ensuring that all QMS processes adhere to USFDA, EU-GMP, and WHO-GMP guidelines.
🎯 Required Candidate Profile
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Education: B. Pharma or M. Pharma (mandatory)
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Experience: 2–5 years exclusively in formulations QMS (solid oral dosage is preferred)
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Hands-on Knowledge:
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Change Control lifecycle management
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CAPA lifecycle management and effectiveness checks
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Good understanding of pharmaceutical manufacturing and quality systems
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Skill Set:
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Familiarity with TrackWise or similar QMS software is a plus
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Excellent documentation, organizational, and communication skills
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Important:
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Candidates must have experience in formulations
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QC or QMS experience from QC background is not eligible
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Profiles from API or injectable backgrounds will not be considered
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🏭 About Unit 7 – Aurobindo Pharma
Unit 7 is Aurobindo’s flagship formulations manufacturing unit, housing high-capacity production lines and world-class quality labs. Designed for regulatory compliance with stringent international norms, Unit 7 supports manufacturing for US, EU, and other regulated markets.
Key Features:
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EU-GMP certified
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Equipped with modern automation
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Fully integrated QMS and LIMS
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Dedicated to oral solids production
Working at Unit 7 means joining a high-performing team that contributes directly to the global supply of life-saving medications.
🌍 Why Join Aurobindo Pharma?
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Be part of a Fortune India 500 company with a global footprint
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Work in a regulated, high-compliance environment
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Get access to continuous learning and upskilling
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Grow your career in a well-structured QA ecosystem
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Attractive salary, benefits, and job security in a reputed organization
🕒 Walk-In Alternative
Though this isn’t a walk-in interview, interested and eligible candidates can apply by email with the subject line: “Application for QA QMS – Formulations”
📧 How to Apply
Step 1: Prepare Your Resume
Ensure your resume highlights:
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Your formulation experience in QA QMS
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Specific change control and CAPA tasks handled
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Tools and systems used (e.g., TrackWise)
Step 2: Send Your Resume
📩 Email: HRSEZ@aurobindo.com
📝 Subject: Application for QA QMS – Formulations
Selected candidates will be contacted directly by the HR team for further rounds.
📍 Job Location: Jadcherla, Mahabubnagar
Located approximately 80 kilometers from Hyderabad, Jadcherla is an industrial hub in Telangana known for its SEZ infrastructure and connectivity. Aurobindo’s Unit 7 is easily accessible via NH44 and has all facilities to support employee comfort and safety.
If you’re passionate about quality assurance in pharmaceutical formulations and ready to join a team that’s delivering global impact, Aurobindo Pharma’s QA QMS role at Unit 7 might be the perfect fit for you.
This is your chance to work in a world-class manufacturing unit, tackle real compliance challenges, and grow in a culture of operational excellence.
📩 Apply today — and take your QA career to the next level with Aurobindo Pharma.
