Join Dr. Reddy’s Laboratories as Engineering QMS at our Visakhapatnam Injectable site. We’re looking for professionals with 5–9 years of pharma experience, preferably in injectables. Apply now and grow with one of India’s leading pharmaceutical companies.
🚀 Exciting Career Opportunity at Dr. Reddy’s Laboratories – Engineering QMS at Injectable Site, Visakhapatnam
Are you an experienced pharmaceutical professional with a passion for quality and compliance? Do you have a strong background in Quality Management Systems (QMS), particularly within the injectable drug manufacturing domain? If so, this is your chance to join Dr. Reddy’s Laboratories, a globally respected name in the pharmaceutical industry.
We are currently seeking an Engineering QMS professional for our Injectable manufacturing site located in Visakhapatnam, Andhra Pradesh. This opportunity is ideal for individuals with 5–9 years of relevant experience, who thrive in a regulated environment and are committed to maintaining the highest standards in pharmaceutical manufacturing.
🔍 About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories Ltd. is a leading global pharmaceutical company based in India, committed to providing affordable and innovative medicines for healthier lives. With a robust portfolio across branded and generic pharmaceuticals, biologics, and active pharmaceutical ingredients (APIs), we operate across markets including India, the USA, Europe, and other global regions.
Our Injectable manufacturing facility in Visakhapatnam is one of the most advanced of its kind, supporting the production of sterile formulations for regulated markets including the US, EU, and emerging economies.
🛠️ Position Details
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Role: Engineering QMS
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Department: Quality Management Systems (QMS)
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Work Location: Dr. Reddy’s Injectable Manufacturing Facility, Visakhapatnam, Andhra Pradesh
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Experience Required: 5 to 9 years
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Qualification: B.Pharma / M.Pharma / B.Tech / M.Sc
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Industry: Pharmaceuticals / Biotech / Life Sciences
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Job Type: Full-Time, On-Site
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Preferred Background: Injectable manufacturing experience
📌 Key Responsibilities
As an Engineering QMS team member, you will be instrumental in ensuring that all engineering activities align with pharmaceutical quality standards and regulatory requirements. Your role will involve cross-functional collaboration and active participation in quality systems management. Key responsibilities include:
✅ Investigation & CAPA Management
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Lead investigations into deviations, OOS (Out of Specification) results, and other incidents within the engineering and production processes.
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Identify root causes using structured methods such as Fishbone, 5 Whys, and FMEA.
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Develop and implement Corrective Actions and Preventive Actions (CAPA) to mitigate reoccurrence.
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Ensure timely closure of investigation reports and CAPAs in line with regulatory timelines.
✅ Regulatory Compliance & Audits
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Support internal and external audits by regulatory authorities (USFDA, EU-GMP, MHRA, etc.).
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Provide documentation, responses, and justifications related to QMS activities.
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Assist in maintaining readiness for inspections by regulatory bodies at all times.
✅ Deviation Management
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Review deviation logs, classify criticality levels, and ensure appropriate actions are initiated.
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Coordinate with production, quality, and engineering teams to resolve deviations efficiently.
✅ Document Review & Control
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Review and approve Standard Operating Procedures (SOPs), investigation reports, and validation documentation.
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Ensure documentation meets GxP, GLP, and cGMP guidelines.
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Drive continuous improvement of documentation quality.
✅ Cross-Functional Support
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Work closely with engineering, production, quality assurance, and validation teams to ensure integrated QMS.
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Offer guidance during qualification and validation of equipment, facilities, and processes.
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Implement and maintain quality metrics and Key Performance Indicators (KPIs).
✅ Risk Management
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Identify quality risks in engineering and propose mitigation strategies.
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Conduct periodic risk assessments to ensure systems remain within compliance boundaries.
🎓 Candidate Profile – Who Should Apply?
We are looking for candidates who are not only technically proficient but also embody the values of integrity, quality, and innovation. Ideal applicants will possess:
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Educational Background: Bachelor’s or Master’s degree in Pharmacy, Technology, or Science.
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Experience: 5–9 years in pharmaceutical manufacturing, preferably in injectable/sterile dosage forms.
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Regulatory Understanding: Strong knowledge of USFDA, EU-GMP, WHO-GMP, and PIC/S guidelines.
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Key Skills:
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Excellent written and verbal communication
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Team collaboration and leadership
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Detail-oriented with strong analytical skills
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Proven problem-solving abilities in QMS scenarios
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🌍 Why Join Dr. Reddy’s?
At Dr. Reddy’s, we go beyond just a job — we offer a career full of possibilities. Here’s what sets us apart:
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Global Presence: Work with a multinational team and contribute to medicines distributed worldwide.
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Innovation-Driven Culture: Be part of a company known for R&D, innovation, and quality excellence.
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Career Growth: Multiple learning and development programs, leadership training, and internal mobility options.
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Employee Wellbeing: A strong focus on work-life balance, employee safety, and holistic growth.
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Purpose-Led Mission: “Good Health Can’t Wait” is more than a slogan; it’s our shared commitment.
📬 How to Apply
If you meet the above criteria and are ready to take the next step in your career with a global leader in pharmaceuticals, send your updated resume to: dhineshtejaummadisetti01@drreddys.com
Subject Line: “Application for Engineering QMS – Injectable Site”
📣 Don’t Miss This Opportunity!
This is your chance to join an elite pharmaceutical team, influence global healthcare outcomes, and grow in an environment that encourages continuous learning and innovation. If you’re a qualified professional passionate about QMS and injectable pharma manufacturing, apply now to be part of the Dr. Reddy’s Laboratories success story.
