TEAM LEAD/ASSOCIATE MANAGER-COMPLIANCE QA (BADDI)Himalaya Wellness Companyfull-timeRequired skillscomplianceinterpersonal skillsspecificationAbout the role Himalaya Wellness Company Website: himalayawellness.in Job details: Brief RequirementsShould have worked on the shop floor and have sound process knowledge in manufacturing Semisolid, Solid oral, Liquids, powder dosage forms, cosmetics and nutraceuticals.Should have thorough understanding of GMP guidelines and regulations applicable to Pharma, Personal Care, Cosmetics and food products.Should have Quality compliance auditing experience in Pharmaceutical industry.Role ExpectationsShould be able to Audit / verify compliance at contract manufacturing locations with vast process understating of Pharma, Cosmetics & Food products.Should be able to review & perform critical Investigations on his / her own. Should be ready to travel extensively. Excellent communication, documentation, and interpersonal skills. Ability to manage audits independently and handle multiple priorities. ISO certified auditor is an added advange.ResponsibilityResponsible for conducting external audits to ensure compliance with cGMP, regulatory guidelines, SOPs, and quality standards at the contract manufacturing locations. The role ensures that processes, systems, and documentation meet the requirements of regulatory authorities and company policies.To ensure audits of CMLs, Vendors, external laboratories, are carried out and compliance is verified. Prepare and submit audit reports to the Head QA and ensure compliance against the observations.Responsible to visit contract manufacturing locations regularly and to ensure risks are mitigated which may leading to non-conformances & product failures.To ensure product failures, market complaints, non-conformances are investigated thoroughly and compliance is maintained.Responsible to ensure CAPA system and CAPA effectiveness is achieved.Ensure effective & timely escalations of critical findings with management and to address the issues.Understanding and Review of Batch manufacturing & packing records.To ensure effective Quality Management systems like Change controls, Deviations, Out of Specification, Market complaints, Training, etc. are followed.Coordination with CML, Vendors, External laboratories, R&D, Production & other concern personnel in meeting compliance activities. Click on Apply to know more. This page is fully interactive when JavaScript is enabled. Please enable JavaScript to apply or browse related roles.