(Apply Now) Assistant Qa Chemist

6 days ago

Karnal HR IN Magnus Biotech Private Limited Full time

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

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