We are seeking an experienced Assistant QA – Documentation and Artwork Approval professional for our pharmaceutical manufacturing company. The role involves ensuring that all packaging materials, documentation, and related quality processes comply with current regulatory standards. Key Responsibilities: Artwork & Labeling Approvals: Review and approve all packaging artwork, including labels, cartons, inserts, and other printed materials, ensuring compliance with regulatory and company standards. Proofread artwork thoroughly to ensure accuracy of product information, regulatory text, and design elements. Collaborate with cross-functional teams such as Production and Marketing to manage and streamline the artwork approval process. Maintain detailed and traceable records of all artwork versions, approvals, and revisions. Coordinate with external vendors and printing agencies for artwork and label finalization. Documentation & Quality Systems: Review and control quality-related documents such as batch manufacturing records (BMR), batch packaging records (BPR), standard operating procedures (SOPs), and specifications. Ensure timely issuance, archival, and retrieval of controlled documents. Assist in change control, deviation, and CAPA documentation processes. Support the preparation, review, and submission of regulatory documents related to product packaging and labeling. Compliance and Audit Support Ensure that artwork, labeling, and documentation processes comply with cGMP, GLP, and relevant regulatory guidelines. Support internal and external audits by preparing, organizing, and presenting QA documentation as required. Contribute to continuous improvement initiatives within the QA department to enhance compliance and operational efficiency. Qualifications & Experience: Bachelor’s degree in Pharmacy. 1–3 years of experience in Quality Assurance in a pharmaceutical manufacturing company. Hands-on experience with artwork/label approval processes will be preferred. Familiarity with cGMP, GLP, and regulatory documentation practices. Strong attention to detail, accuracy, and organizational skills. Excellent communication and coordination abilities with cross-functional teams. Job Types: Full-time, Permanent Pay: ₹12,000.00 - ₹18,000.00 per month Work Location: In person
We are seeking an experienced Assistant QA – Documentation and Artwork Approval professional for our pharmaceutical manufacturing company. The role involves ensuring that all packaging materials, documentation, and related quality processes comply with current regulatory standards. Key Responsibilities: Artwork & Labeling Approvals: Review and approve all packaging artwork, including labels, cartons, inserts, and other printed materials, ensuring compliance with regulatory and company standards. Proofread artwork thoroughly to ensure accuracy of product information, regulatory text, and design elements. Collaborate with cross-functional teams such as Production and Marketing to manage and streamline the artwork approval process. Maintain detailed and traceable records of all artwork versions, approvals, and revisions. Coordinate with external vendors and printing agencies for artwork and label finalization. Documentation & Quality Systems: Review and control quality-related documents such as batch manufacturing records (BMR), batch packaging records (BPR), standard operating procedures (SOPs), and specifications. Ensure timely issuance, archival, and retrieval of controlled documents. Assist in change control, deviation, and CAPA documentation processes. Support the preparation, review, and submission of regulatory documents related to product packaging and labeling. Compliance and Audit Support Ensure that artwork, labeling, and documentation processes comply with cGMP, GLP, and relevant regulatory guidelines. Support internal and external audits by preparing, organizing, and presenting QA documentation as required. Contribute to continuous improvement initiatives within the QA department to enhance compliance and operational efficiency. Qualifications & Experience: Bachelor’s degree in Pharmacy. 1–3 years of experience in Quality Assurance in a pharmaceutical manufacturing company. Hands-on experience with artwork/label approval processes will be preferred. Familiarity with cGMP, GLP, and regulatory documentation practices. Strong attention to detail, accuracy, and organizational skills. Excellent communication and coordination abilities with cross-functional teams. Job Types: Full-time, Permanent Pay: ₹12,000.00 - ₹18,000.00 per month Work Location: In person