Website:
malladi.co.in
Job details:
Company Description Malladi Drugs and Pharmaceuticals Limited is one of India’s most tradition-conscious and ethically driven pharmaceutical companies. Founded in 1980 by late Mr. M. L. N. Sastry, a pioneering microbiologist with deep expertise in fermentation technology, the company has built a strong reputation in the global market. Malladi is a leading manufacturer of Active Pharmaceutical Ingredients (APIs) in the cough and cold segment and holds a dominant presence in other therapeutic areas. These include anti-histamines, anti-convulsants, anti-depressants, and anxiolytics (CNS), offering a diverse portfolio for international pharmaceutical partners. The organization emphasizes quality, innovation, and integrity, providing a professional environment for individuals seeking meaningful careers in pharmaceuticals.
Role Description The Quality Control Executive is a full-time, on-site role based at the Ranipet facility. This role is responsible for performing routine and non-routine testing of raw materials, in-process samples, intermediates, and finished products in accordance with established quality standards and regulatory requirements. Day-to-day activities include operating and maintaining laboratory instruments, performing calibrations, documenting test results accurately, and investigating any out-of-specification or atypical results. The Quality Control Executive collaborates with Quality Assurance and Production teams to support batch release, change controls, and continuous improvement initiatives. The role also involves adhering to safety protocols, participating in internal audits, and contributing to the development and review of standard operating procedures (SOPs).
Qualifications
- Knowledge on handling instrument like HPLC,GC,UV,
- Candidates should possess strong Analytical Skills for interpreting test data, identifying trends, and supporting investigations.
- Candidates should possess Quality Control and Quality Assurance skills to ensure compliance with internal standards and regulatory guidelines.
- Candidates should possess Laboratory Skills, including handling of equipment, sample preparation, and good documentation practices.
- Candidates should possess Calibration skills to perform and verify instrument calibration and maintain accurate calibration records.
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biochemistry, or a related scientific discipline.
- Knowledge of cGMP, GLP, and regulatory requirements relevant to pharmaceutical manufacturing.
- Attention to detail, strong organizational skills, and ability to work effectively in cross-functional teams.
- Prior experience in pharmaceutical quality control or related laboratory environment is preferred.
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