Career Opportunity: QC-Analytical Scientist at Ciro Pharma Private Limited

Job Summary

Ciro Pharma Private Limited is seeking a highly skilled and motivated QC-Analytical Scientist to join our team in Karakapatia, Hyderabad. We are looking for an experienced professional with 3–6 years of expertise in analytical method validation and testing for sterile and oncology products. This role offers the chance to work in a state-of-the-art facility dedicated to high-quality pharmaceutical manufacturing for global regulatory markets.

About the Company

Ciro Pharma Private Limited is a premier pharmaceutical formulation company specializing in the development and manufacturing of anti-cancer oncology drugs. Our commitment to excellence drives us to produce a wide range of dosage forms, including tablets, capsules, injections, and complex lyophilized products.

We take pride in our robust infrastructure and our global footprint, as we manage the direct marketing of our pharmaceutical products worldwide. Our Unit 1 facility is a specialized, state-of-the-art center for Soft Gel capsule manufacturing. Equipped with industry-leading technology and precision-controlled drying rooms, our facility ensures that every product meets the highest standards of safety, stability, and efficacy. As we continue to expand our reach in the international regulatory market, we are looking for talent that shares our dedication to quality and precision.

The Role: QC-Analytical Scientist

As a Quality Control Analytical Scientist, you will play a pivotal role in ensuring that our oncology and sterile products meet stringent international regulatory requirements. You will be responsible for the accuracy, reliability, and validation of analytical processes within our laboratory.

Key Responsibilities

• Analytical Method Validation: Lead and execute the validation of analytical methods to ensure regulatory compliance and process robustness.
• Quality Testing: Conduct thorough In-Process (IP), Finished Product (FP), and Stability testing to guarantee product integrity throughout the manufacturing lifecycle.
• Instrumental Analysis: Operate, calibrate, and troubleshoot advanced analytical instrumentation, including HPLC, GC, and Dissolution apparatus.
• Specialized Analysis: Apply deep technical knowledge to the testing of sterile and oncology-based pharmaceutical products, adhering to strict safety protocols.
• Documentation: Maintain precise, cGMP-compliant documentation for all analytical findings and laboratory activities.

Required Qualifications

• Experience: 3 to 6 years of proven experience in a pharmaceutical Quality Control environment.
• Technical Proficiency: Hands-on experience with HPLC, GC, and dissolution testing is mandatory.
• Domain Knowledge: Familiarity with analytical method validation and testing protocols for sterile and oncology products is highly preferred.
• Education: A degree in Pharmacy, Chemistry, or a related field (M.Sc./B.Pharm/M.Pharm).

Why Join Ciro Pharma?

• Cutting-Edge Environment: Work with state-of-the-art analytical equipment in a modern facility.
• Professional Growth: Gain deep exposure to the complex requirements of the global oncology drug market.
• Impact: Contribute to the manufacturing of life-saving medications that reach patients worldwide.

How to Apply

If you meet the above requirements and are passionate about pharmaceutical quality, we would like to hear from you.

• Application Process: Please send your updated Curriculum Vitae (CV) to our recruitment team at [email protected].
• Subject Line: Please mention “Application for QC-Analytical Scientist” in your email subject line.
• Work Location: The position is based at our facility in Karakapatia, Hyderabad.

Ciro Pharma Private Limited is an equal opportunity employer. We value technical expertise and a commitment to quality in all our team members.