Join Aurobindo Pharma as a Quality Control Analyst in Naidupeta, Andhra Pradesh. We are hiring candidates with 2–5 years of OSD experience and hands-on skills in HPLC, LCMS, GCMS. Apply now!

📢 Aurobindo Pharma is Hiring: Quality Control Analyst – OSD | Naidupeta, Andhra Pradesh

Are you a skilled Quality Control professional with a passion for pharmaceutical excellence? Aurobindo Pharma, a global pharmaceutical leader, is actively hiring Quality Control Analysts for its APL Healthcare Unit IV located in Naidupeta, Tirupati District, Andhra Pradesh – 524421.

This is a fantastic opportunity for professionals with 2 to 5 years of experience in Oral Solid Dosage (OSD) forms and hands-on exposure to advanced analytical techniques including HPLC, LCMS, GCMS, and GC.

🧪 Department: Quality Control (QC)

We are expanding our Quality Control department and looking for highly motivated professionals to join our team as Analysts in:

• Finished Products (FP)

• In-Process (IP)

• Good Laboratory Practices (GLP)

• Raw Materials (RM)

As a QC Analyst, you will play a critical role in ensuring the safety, efficacy, and quality of our pharmaceutical products. This role is best suited for professionals who are analytical, detail-oriented, and committed to maintaining world-class quality standards.

✅ Who Should Apply?

We’re seeking candidates who meet the following qualifications and criteria:

🎓 Educational Qualifications:

• M.Sc. in Chemistry or related disciplines

• B. Pharma (Bachelor of Pharmacy)

✨ Experience Required:

• 2 to 5 years of relevant experience in a pharmaceutical Quality Control (QC) environment

• Must have exposure in OSD (Oral Solid Dosage) only

• Experience working in regulated environments with GLP/GMP standards

🔬 Technical Skills Must Include:

• HPLC (High Performance Liquid Chromatography)

• LCMS (Liquid Chromatography Mass Spectrometry)

• GCMS (Gas Chromatography Mass Spectrometry)

• GC (Gas Chromatography)

Candidates with immediate availability will be given preference.

🏢 Job Location:

📍 APL Healthcare Unit IV
Naidupeta, Tirupati District
Andhra Pradesh – 524421

This is a strategic manufacturing location for Aurobindo Pharma. The facility is equipped with advanced technology and follows the highest standards in pharmaceutical manufacturing and quality assurance.

🔍 Key Responsibilities:

As a Quality Control Analyst, your responsibilities will include but are not limited to:

• Performing analysis of raw materials, in-process materials, and finished products

• Ensuring compliance with GLP, GMP, and regulatory guidelines

• Conducting stability studies, method validation, and routine testing

• Operating and maintaining analytical instruments like HPLC, GCMS, LCMS, and GC

• Interpreting and documenting results with accuracy and attention to detail

• Supporting audits and regulatory inspections

• Collaborating with production, R&D, and QA teams to ensure product quality

• Reporting deviations and supporting root cause analysis

💼 Why Join Aurobindo Pharma?

Aurobindo Pharma is one of India’s leading pharmaceutical companies with a global presence in over 150 countries. We are known for our commitment to innovation, quality, and affordability. By joining our team, you get access to:

• 🌍 Global Work Environment

• 📈 Strong Career Growth Opportunities

• 🧪 Cutting-Edge Technology in QC Labs

• 💼 Job Security and Competitive Salary

• 🧠 Continuous Learning and Training

• 🤝 A collaborative team culture that values integrity and excellence

📋 Preferred Candidate Profile:

🚀 Immediate Joinees – Get Fast-Tracked!

If you’re available to join immediately, you will be prioritized for interviews and selection. We are currently streamlining the onboarding process for immediate hires to help fill critical roles swiftly.

📨 How to Apply?

Interested and eligible candidates are encouraged to share their updated resume at the below email address:

📧 Email: naidupetahr@aurobindo.com

Subject Line: Application for QC Analyst – Naidupeta

Make sure your resume includes the following:

• Educational qualifications

• Years of relevant experience

• Tools/instruments you are proficient with

• Current CTC and expected CTC

• Notice period or availability for joining

💡 Tips to Strengthen Your Application:

• Highlight specific QC responsibilities in previous roles

• Mention your OSD experience clearly

• Emphasize hands-on experience with HPLC, LCMS, GCMS

• Include details of audits you’ve participated in (if applicable)

• Attach certifications related to GLP, GMP, or instrumentation (if available)

📞 Contact & Queries:

For additional queries or clarifications, feel free to reach out via the same email. Our recruitment team is actively reviewing applications and will reach out to shortlisted candidates promptly.

🌟 Join a World-Class Pharma Leader – Aurobindo Awaits You!

Aurobindo Pharma has built a reputation as one of the most reliable names in pharmaceutical manufacturing and exports. If you’re a Quality Control Analyst looking for a stable, rewarding, and high-growth career in OSD formulation, this is your chance. Be part of our journey to deliver quality healthcare to millions across the globe. Apply now and take your career to the next level.