Granules India Hiring Manager – QMS OSD Production | 8–12 Yrs Exp | Hyderabad

Granules India is hiring for Manager – QMS (OSD Production) in Hyderabad. Ideal candidates have 8–12 years of experience in handling QMS in OSD manufacturing. Apply now if you’re an expert in cGMP, deviations, CAPA, and regulatory compliance.

🌟 Granules India Hiring Manager – QMS OSD Production | Work Location: Gagillapur, Hyderabad

Granules India Limited, a leading pharmaceutical manufacturer known for its high-quality generic formulations and APIs, is seeking dynamic and experienced professionals for the Manager – QMS Production (OSD) position at its Gagillapur, Hyderabad facility.

If you have a solid background in OSD manufacturing, are driven by quality excellence, and possess in-depth experience with QMS, this could be your next career move.

📌 Job Overview

• Job Title: QMS Lead – OSD Production (Assistant Manager / Deputy Manager / Manager)

• Department: Production – Quality Management Systems (QMS)

• Work Location: Gagillapur, Hyderabad

• Experience Required: 8 to 12 Years (Only in OSD Production QMS)

• Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc

🎯 Key Responsibilities

The QMS Manager will play a critical role in ensuring compliance, documentation accuracy, and continuous quality improvement within the OSD (Oral Solid Dosage) production lines. Below are the detailed responsibilities:

🔹 Quality Management System (QMS) Implementation

• Lead the implementation and management of QMS in OSD production areas, including compression, coating, and capsule filling.

• Develop and maintain standard operating procedures (SOPs) aligned with global regulatory expectations.

🔹 Deviation & Investigation Management

• Manage and oversee the lifecycle of deviations, CAPAs, change controls, and risk assessments.

• Investigate quality events and ensure timely and thorough closure with proper documentation.

🔹 Compliance & Documentation

• Ensure compliance with cGMP, GDP, and regulatory requirements including USFDA, MHRA, WHO, and more.

• Review and ensure accuracy of BMRs (Batch Manufacturing Records) and BPRs (Batch Packing Records).

• Drive Good Documentation Practices (GDP) across the production unit.

🔹 Cross-Functional Collaboration

• Coordinate closely with QA, QC, and regulatory affairs to maintain audit readiness.

• Act as a point-of-contact for internal audits and regulatory inspections.

🔹 Training & Development

• Provide structured GMP training to production teams.

• Build awareness about quality practices and regulatory changes through regular workshops.

🔹 Continuous Improvement

• Initiate and support lean manufacturing practices and continuous improvement programs.

• Evaluate process inefficiencies and implement corrective strategies for optimization.

👨‍🔬 Ideal Candidate Profile

To succeed in this role, the candidate should demonstrate:

• Experience: 8–12 years in OSD QMS (Mandatory).

• Educational Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc.

• Technical Skills: Strong knowledge of cGMP, FDA 21 CFR Part 11, and ICH Q10 quality systems.

• Audit Readiness: Exposure to regulatory audits including USFDA, MHRA, WHO-GMP, TGA, ANVISA, etc.

• Soft Skills: Strong analytical thinking, leadership, attention to detail, and team management abilities.

🧠 Why Join Granules India?

Granules India is not just another pharma company. Here’s why you should consider applying:

💼 Reputable Employer

Granules India is a globally integrated pharmaceutical company with a strong product portfolio in key therapeutic segments. It operates across multiple continents and is known for its robust compliance, state-of-the-art infrastructure, and employee-centric culture.

🚀 Career Growth

Working at Granules means getting exposed to world-class systems, international regulatory inspections, and cross-functional projects. It’s a perfect workplace for professionals aiming for career elevation in pharmaceutical quality systems.

🤝 Collaborative Culture

With an inclusive and transparent environment, Granules fosters innovation and encourages employees to participate in decision-making processes and process improvement strategies.

📄 Application Process

Interested and eligible candidates are encouraged to send their updated CVs directly to: 📧 Khaleel.md@granulesindia.com

Please ensure your application includes:

• Updated Resume

• Summary of QMS projects handled

• Previous employment details and achievements

• Notice Period and Current CTC details

📝 Additional Tips for Applicants

To enhance your chances of selection:

• Be prepared with case studies or examples of deviation handling or CAPA effectiveness.

• Familiarize yourself with current regulatory changes in the OSD manufacturing domain.

• Ensure your resume highlights QMS-specific achievements and regulatory exposure.

🔍 Commonly Asked Interview Questions for QMS Roles

Here are some questions you might expect:

1. How do you manage CAPA effectiveness monitoring?

2. Describe a situation where you resolved a recurring deviation.

3. What documentation systems have you worked on (TrackWise, MasterControl, etc.)?

4. How do you ensure audit preparedness in a manufacturing setup?

5. Describe your approach to risk assessment and mitigation in production.

📣 Spread the Word

If you know someone who matches this profile and is looking for a great opportunity, share this post. It could make a difference in someone’s career journey!

🔗 Connect with Granules India – Where Quality Meets Innovation

At Granules India, you’ll be part of a team that pushes boundaries, embraces innovation, and ensures excellence in everything it does. This opening for QMS Lead – OSD Production is your chance to contribute to global health through pharmaceutical excellence.