Quality Control Assistant

Company Description PANCHSHEEL ORGANICS LIMITED is a public listed, WHO-compliant and GMP-certified manufacturer and exporter based in India, with a corporate office in Mumbai. The company produces a wide range of APIs, intermediates, nutraceuticals, vitamins, hormones, steroids, finished formulations for human and veterinary use, and agri-biotech products such as bio fertilizers, bio stimulants, and growth promoters. Its portfolio also includes aquaculture solutions and dehydrated culture media, serving diverse segments of the life sciences and agriculture sectors. With more than three decades of experience, Panchsheel is promoted by the Turakhia Bros group, a well-established player in pharmaceutical trading and export-import. The organization offers career opportunities in a regulated, growth-oriented environment focused on quality and innovation.
Role Description The Quality Control Assistant is a full-time, on-site role based in Indore. The role involves conducting routine sampling, testing, and analysis of raw materials, intermediates, and finished products in accordance with established quality control procedures and regulatory standards. Responsibilities include operating laboratory instruments, documenting test results accurately, maintaining records, and supporting investigations of out-of-specification results. The Quality Control Assistant will work closely with Quality Assurance and production teams to ensure compliance with GMP, internal SOPs, and safety protocols. Additional duties may include assisting in method validation, calibration of equipment, and participation in internal audits and continuous improvement activities.
Qualifications

• Strong Quality Control and Quality Assurance skills, with understanding of GMP and regulatory requirements.
• Solid Analytical Skills, including data interpretation and problem-solving in a laboratory or manufacturing environment.
• Proficient Laboratory Skills, including handling of chemicals, use of analytical instruments, and adherence to safety standards.
• Effective Communication skills for clear documentation, reporting of results, and collaboration with cross-functional teams.
• Diploma or bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related scientific discipline.
• Basic knowledge of pharmaceuticals, nutraceuticals, or related products; prior QC experience in a GMP facility is an advantage.
• Ability to follow SOPs meticulously, manage time efficiently, and work with attention to detail in a regulated environment.
• Familiarity with MS Office and laboratory documentation systems; willingness to work in shifts if required.