Description:
Explore a career at Hetero Labs as a Quality Control Analyst. Work in a dynamic environment focused on global healthcare impact, innovation, and strict GMP compliance.
✍️ Full 1000-Word Blog Post
Hetero Labs is Hiring Quality Control Analysts – Join the Hyderabad OSD Facility Today!
If you’re a pharmaceutical professional with an eye for detail and a passion for quality, this opportunity from Hetero Labs Limited could be your ideal next step. One of India’s premier pharmaceutical manufacturers, Hetero is currently recruiting Quality Control Analysts for its Oral Solid Dosage (OSD) formulation plant in Jadcherla, located just outside Hyderabad.
🌐 About Hetero Labs Limited
Hetero Labs is globally recognized as a leading manufacturer of generic drugs and active pharmaceutical ingredients (APIs). The company is especially renowned for being the world’s largest producer of anti-retroviral drugs used in the treatment of HIV/AIDS. With a global footprint and a commitment to affordability and quality, Hetero plays a key role in delivering life-saving medications across more than 125 countries.
Their manufacturing units uphold the highest international standards, and the Hyderabad OSD facility is no exception—offering employees access to cutting-edge infrastructure, training, and growth opportunities.
🧪 Job Role: Quality Control Analyst – OSD Formulation Unit
This hiring drive is focused on the Quality Control Department at Hetero’s Jadcherla unit, where several positions are open across levels such as Officer, Junior Executive, and Executive.
📍 Job Location:
Jadcherla, Hyderabad (Approx. 80 km from city center)
📄 Education Requirements:
- B.Pharmacy / M.Pharmacy
- B.Sc / M.Sc (Chemistry, Biotechnology, or related disciplines)
📆 Experience:
- 2 to 6 years in pharmaceutical QC roles preferred
- Freshers with strong academic records may also be considered
🔧 Key Responsibilities
Joining Hetero as a QC Analyst means you’ll be responsible for a wide range of essential tasks that uphold the company’s GMP (Good Manufacturing Practice) standards and contribute to product quality. Responsibilities include:
1️⃣ Analytical Testing
You will conduct various tests using HPLC, Dissolution Testers, Karl Fischer Titration, and other instrumentation to verify raw materials, in-process samples, and finished formulations.
2️⃣ Data Analysis & Reporting
Analyzing test results, identifying discrepancies, and preparing detailed documentation to ensure accurate reporting.
3️⃣ Compliance with GMP & Regulatory Protocols
Ensuring each analysis complies with regulatory norms such as WHO, USFDA, and EU guidelines.
4️⃣ Instrument Calibration & Maintenance
Collaborating with engineering or calibration teams to maintain accurate performance of analytical tools.
5️⃣ Method Validation Support
Participating in method validation, method transfer, and related documentation reviews.
💡 Ideal Candidate Profile
The right candidate will not only have technical knowledge but also possess analytical thinking, problem-solving skills, and a commitment to data integrity.
✅ Skills Required:
- Strong command of HPLC, Dissolution testing, KF titration
- Experience with software like Empower or similar chromatography systems
- Good documentation and data handling skills
- Understanding of GMP, GLP, and ICH guidelines
- Ability to handle multiple batches and testing protocols under deadlines
💼 What You Get in Return
🧑🔬 Professional Growth
Hetero Labs invests in its people through structured training, career pathways, and the opportunity to participate in international audits and regulatory inspections.
💰 Competitive Compensation
Salaries are aligned with industry benchmarks and include performance bonuses, medical benefits, and employee insurance schemes.
🌍 Purpose-Driven Work
At Hetero, you’re not just doing a job—you’re helping deliver affordable healthcare across the world. Your work directly contributes to making critical medicines accessible.
🏆 Global Reputation
With international operations and over 25+ approved facilities worldwide, you’re joining an employer recognized by WHO, USFDA, EUGMP, and PMDA.
✉️ How to Apply
If you’re interested and meet the qualifications, apply by sending your resume to:
📩 sonali.n@hetero.com
Subject Line: Application for QC Analyst
For any questions, you may call: +91 9100408534
📌 Additional Tips for Applicants
When applying, ensure your resume highlights:
- Specific analytical techniques you’re proficient in
- Hands-on experience with Empower software
- Batch testing and regulatory submissions you’ve contributed to
- Training, certifications, or audits you’ve participated in
🏭 Hetero’s Jadcherla Facility – What to Expect?
- Modern infrastructure: Fully equipped labs with automated instrumentation
- Healthy work-life balance: Structured shift hours and time-off policies
- Collaborative teams: A culture of mentorship, teamwork, and shared goals
- Innovation-driven approach: Exposure to stability studies, method development, and continuous improvement programs
🗓️ Don’t Miss Out
This is a prime opportunity for science graduates and pharmaceutical professionals seeking meaningful, well-paid, and impactful roles. With multiple positions available, now is the best time to take the next big step in your pharma career with Hetero Labs.
🌟 Final Takeaway
The Quality Control Analyst role at Hetero Labs is ideal for candidates who are looking to work at the forefront of pharmaceutical manufacturing and ensure that life-saving drugs meet global quality standards. If you’re committed to precision, integrity, and continuous learning, Hetero is the right place for you.
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