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Responsible for executing packaging processes, investigating non-conformance issues, reviewing manufacturing records, and maintaining inventory. Also serves as shift in charge for packaging line.
Conduct comprehensive Nitrosamine studies for Endo India ensuring product safety and regulatory compliance. Review study data, manage quality management system, support regulatory inspections, and coordinate with sites for method validation work.
Independently organizes and performs quality audits for Endo’s Branded Pharmaceuticals. Leads Pre-Approval Mock Inspections, assesses gaps in quality systems, and evaluates metrics for continuous improvement. Has extensive experience in over 10 audit areas. Manages auditing metrics program, audit activities, quality evaluations, and contributes to annual audit plans. Supports EQA department functions by leading programs, policies, audits, and providing guidance for compliance and improvement.
Perform routine line clearance, batch record review, in process sampling, in process checks, media fill, cleaning validation, and batch packing activities at Endo. Commitment to diversity, equity, and inclusion promoted within the company.
The Quality Associate Specialist performs routine collection of environmental and utility monitoring samples, reviews records for accuracy, determines product acceptability for release, ensures Quality events are closed before release, identifies errors, and participates in on-floor activities during manufacturing. Compliance with regulatory requirements and safety procedures is essential.
The Associate Trainee-ADL will support analytical development activities by performing engineering batch analysis of samples and maintaining lab equipment. This role requires an M.Sc. or M. Pharm degree. The company values diversity, equity, and inclusion within its team.
Review of the Analytical Documents and handling of QMS related activities.
The Associate Trainee - ADL will support analytical development activities, perform batch analysis of samples, handle lab equipment, and ensure compliance with cGMP and GLP.
The Manager, Global Quality & Compliance at Endo is responsible for developing global policies to ensure compliance practices, supporting a quality and compliance focused culture, evaluating metrics for continuous improvement, and ensuring compliance with emerging quality regulations. This role requires a B.A./B.S. Degree in Science or related field or 7 years of experience in pharmaceutical/quality operations.
Analytical support role for impurity and nitrosamines synthesis and qualification in Chemistry. Responsible for method development, routine support, and compliance in the laboratory setting.
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