Apply for QA Officer/Sr. Officer – IPQA roles at RRG Biotech, Hyderabad. 2–4 years of experience in injectable DPI manufacturing required. Attractive salary, growth in regulatory QA.
🧪 RRG Biotech Job Openings – QA Officer/Sr. Officer – IPQA Roles in Hyderabad (2–4 Yrs Experience in Injectable DPI)
Are you looking to elevate your pharmaceutical career in quality assurance? Join RRG Biotech Pvt. Ltd., a rapidly growing biotech company in India, as a QA Officer/Sr. Officer – IPQA at our state-of-the-art Hyderabad facility. If you have 2–4 years of hands-on experience in injectable manufacturing, especially Dry Powder Inhalers (DPIs), this role offers a high-impact opportunity in a regulated, GMP-compliant environment.
🧬 About RRG Biotech Pvt. Ltd.
RRG Biotech is a biopharmaceutical innovator specializing in:
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Injectables
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Dry Powder Inhalers (DPI)
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Sterile Formulations
As part of the OPi Group, the company is driven by quality, innovation, and regulatory excellence. RRG Biotech’s facilities are aligned with USFDA and EMA standards, ensuring global competitiveness in the healthcare sector.
🔗 Explore More: RRG Biotech Careers
🧾 Job Overview
| Detail | Information |
|---|---|
| Position | Officer/Sr. Officer – Quality Assurance (IPQA) |
| Department | Quality Assurance |
| Location | Hyderabad, Telangana |
| Work Mode | Onsite, Cleanroom Setting |
| Experience | 2–4 years with injectable/DPI experience |
| Salary Range | ₹3–5 Lakhs per annum (as per industry standards) |
🛠️ Key Responsibilities
As a QA IPQA Officer at RRG Biotech, your day-to-day responsibilities will include:
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In-process Quality Assurance: Overseeing DPI manufacturing activities including dispensing, compounding, filling, sealing, and packing.
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Line Clearance: Preventing cross-contamination and ensuring readiness before batch production.
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Documentation Review: Reviewing BMRs, BPRs, and SOPs for compliance and accuracy.
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Environmental Monitoring: Observing cleanroom parameters—temperature, humidity, pressure differentials (magnehelic gauge).
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Sampling and Analysis: Performing batch sampling, assisting in QC and sterility assurance.
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Deviation Handling: Managing CAPA, change control, and deviations per QMS protocols.
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Audit Preparation: Supporting USFDA, WHO-GMP, EMA, and MHRA audits, and ensuring inspection readiness.
🎓 Required Qualifications
| Criteria | Requirement |
|---|---|
| Education | B.Sc. (Biotechnology, Chemistry) / B.Pharm |
| Experience | 2–4 years in QA-IPQA roles in injectables/DPI |
| Certifications | GMP/GLP/QMS certifications preferred |
| Regulatory Exposure | Experience with USFDA/EMA audit environments |
| Skills | SOP writing, BMR/BPR handling, cGMP compliance |
| Tools Familiarity | Proficiency with cleanroom instruments & documentation |
🌟 Must-Have Skills
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Hands-on with Dry Powder Inhaler (DPI) production lifecycle.
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Competence in sterility monitoring, sampling, and QC interface.
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Strong understanding of Good Manufacturing Practices (GMP).
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Documentation control and audit trail management.
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High attention to detail, proactive problem-solving, and team collaboration.
💼 Why Join RRG Biotech?
✅ Global Compliance Focus
Work in a facility built for international regulatory approvals—exposure to USFDA and EMA requirements.
✅ Career Acceleration
Gain hands-on experience in DPI production, a cutting-edge formulation technology in respiratory medicine.
✅ GMP-Certified Environment
Engage with the latest biopharma technologies in a cleanroom setting under top-tier quality systems.
✅ Stability + Growth
Join a company with a consistent product pipeline and a reputation for quality assurance excellence.
💰 Salary & Benefits
| Component | Details |
|---|---|
| Annual Salary | ₹3–5 LPA (based on experience & qualifications) |
| Work Hours | Full-time, onsite with standard shifts |
| Learning Opportunities | On-job training for QMS tools and DPI documentation |
| Incentives | Performance-based bonuses, audit success rewards |
📨 How to Apply
📅 Application Deadline: June 30, 2025
✅ WhatsApp CV: +91-88996-92416
📧 Email: careers@rrgbiotech.com
📌 Subject Line: “IPQA Officer Application – June 2025”
💡 Application Tips
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Clearly mention your experience in injectable or DPI manufacturing on your CV.
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Highlight any exposure to regulatory audits (USFDA, EMA, etc.).
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Include BMR/BPR review responsibilities and QMS experience.
🏢 Work Environment at RRG Biotech
| Feature | Details |
|---|---|
| Location | Hyderabad, Telangana |
| Facility Type | GMP-certified, cleanroom compliant |
| Team Culture | Quality-focused, collaborative, regulatory-driven |
| Technologies Used | DPI manufacturing lines, digital documentation tools |
🌍 Equal Opportunity Employer
RRG Biotech is committed to fostering an inclusive and diverse work environment. We encourage applicants from all backgrounds and ensure equal opportunity across roles.
🚀 Take the Next Step in Your QA Career
If you’re an experienced QA professional with a focus on injectables and DPIs, this is your opportunity to join an emerging leader in Indian biopharmaceutical manufacturing.
📅 Apply before June 30, 2025
📍 Location: Hyderabad
🔗 Learn more about the company
🎯 Drive quality, ensure compliance, and deliver better healthcare with RRG Biotech.
