QA Trainee

Company Description Malladi Drugs & Pharmaceuticals Pvt. Ltd. is a pharmaceutical company focused on the development and manufacture of high-quality drug products. The organization emphasizes strict compliance with regulatory standards and robust quality systems across its operations. Team members collaborate in a structured environment that values precision, safety, and continuous improvement. The company offers opportunities for learning, professional growth, and exposure to modern pharmaceutical manufacturing practices.
Role Description The QA Trainee will support the Quality Assurance team in monitoring and maintaining quality standards within the manufacturing facility. Day-to-day responsibilities include assisting in documentation review, supporting batch record verification, helping in deviation and change control processes, and participating in internal quality checks. The role also involves learning and applying relevant quality guidelines, supporting audits, and coordinating with production and quality control teams to resolve quality-related issues. This is a full-time, on-site role based in Chittoor, requiring active participation in daily plant operations and adherence to safety and compliance protocols.
Qualifications
Candidates should possess skills in Quality Assurance and Quality Control to support product and process verification activities.
Candidates should possess skills in Quality Management to assist in implementing and maintaining quality systems and procedures.
Candidates should possess knowledge of Good Manufacturing Practice (GMP) to ensure compliance with regulatory and industry standards.
Candidates should possess skills in Quality Auditing to support internal audits and preparation for external inspections.
Relevant education such as a degree or diploma in Pharmacy, Chemistry, Biotechnology, or a related field.
Strong attention to detail, documentation skills, and ability to follow standard operating procedures.
Willingness to learn, collaborate in cross-functional teams, and work in an on-site pharmaceutical manufacturing environment.
Basic computer skills and familiarity with MS Office for documentation and reporting.

Work arrangement
No