Natco Pharma, a leading Indian multinational pharmaceutical company headquartered in Hyderabad, is renowned for manufacturing a wide range of pharmaceutical products, including finished dosage formulations, active pharmaceutical ingredients (APIs), and crop health science products. With a strong presence in both domestic and international markets, Natco Pharma has established itself as a trusted name in the pharmaceutical industry. The company is now conducting a walk-in interview for various roles in the Production, Quality Control (QC), and Quality Assurance (QA) departments.

Job Responsibilities:

1. Production (Granulation, Compression, Coating & Packing):
   • Operators and supervisors will be responsible for overseeing and managing the production processes.
   • Ensuring the manufacturing of high-quality pharmaceutical products by following standard operating procedures (SOPs).
   • Maintaining equipment, monitoring production lines, and ensuring the safety and quality standards are met.
2. Quality Control (QC) – Handling HPLC, UPLC & Dissolution:
   • QC Chemists/Officers will perform routine analytical tests and handle laboratory equipment like HPLC (High-Performance Liquid Chromatography), UPLC (Ultra-Performance Liquid Chromatography), and Dissolution apparatus.
   • Ensuring the raw materials and finished products meet the required quality standards.
3. Quality Assurance (QA) – IPQA & APQR:
   • QA officers will be responsible for conducting in-process quality assurance (IPQA) and assisting in the preparation of annual product quality reviews (APQR).
   • Ensuring compliance with all regulatory standards and maintaining the documentation required for audits and inspections.
4. Micro QA & AQA:
   • Handling microbiological testing and ensuring the pharmaceutical products meet microbiological standards.
   • Overseeing the AQA (Analytical Quality Assurance) and providing technical support for testing and validation procedures.
5. CSV & Cleaning Validation:
   • Ensuring compliance with computer system validation (CSV) requirements and maintaining cleanroom conditions.
   • Responsible for the validation of cleaning processes and ensuring that all cleaning and sanitation procedures are followed.
6. Audit Trail and Document Review:
   • Executing audits and ensuring compliance with regulatory requirements for the review of audit trails and documentation systems.

Qualifications:

• Production: I.T.I / Diploma / B. Sc / B. Pharm / M. Pharm
• Quality Control: M.Sc / B. Pharm / M. Pharm with 2-6 years of relevant experience
• Quality Assurance: B. Pharm / M. Pharm for IPQA & APQR; M. Sc / B. Pharm / M. Pharm / B. Tech for CSV & Cleaning Validation with experience ranging from 2 to 8 years depending on the role.

Skills Required:

• Knowledge and experience with production processes, quality control techniques, and assurance standards.
• Familiarity with pharmaceutical regulations and guidelines, especially OSD (Oral Solid Dosage) formulations and regulatory exposure.
• Strong analytical skills, attention to detail, and ability to work in a fast-paced environment.
• Experience with laboratory equipment such as HPLC, UPLC, and Dissolution apparatus.
• Good communication skills, team-oriented approach, and problem-solving abilities.

How to Apply: Interested candidates are invited to attend the walk-in interview at the following location:

• Date: 01st February 2025
• Venue: Natco House, Road No 2, Sanjara Hills, Hyderabad – 34

Important Notes:

• Candidates must have OSD formulation experience with regulatory exposure.
• Only those willing to work at the Vizag location should attend the interview.
• Preferably male candidates and immediate joiners are encouraged to apply.