In this role, you will be responsible for managing the internal site auditing program in conformance with Merck Policies, Guidelines, and Procedures. May participate in auditing of external sites and other Merck sites.
Performing Incoming Inspection, In-process audits and inspection, and final product inspection in conformance with drawings, Engineering Change Order, workmanship standards and Client policies and procedures.
Perform all aspects of routine, initial and follow-up audits, including internal quality systems audits and external audits to support the gxp compliance and inspection readiness of argos gxp systems, as well as the supplier qualification and management program.
In this role, you will collaborate with IT partners to educate about of the scope of data governance, the value of data quality, and available resources for implementing solutions in accordance with data quality standards.
Responsible for conducting routine and non-routine analysis of raw materials, in process, and finished formulations according to standard test methods. Test methods include gel electrophoresis, spectrophotometry, immunophenotyping, and northern blot analysis.
In this role, the selected candidate will ensure that testing activities allow the application to meet business requirements and systems goals, fulfill end-user requirements, and identify existing or potential issues.
In this role, the selected candidate will participate in validation of data migration and must have good hands on experience with SQL queries; QA analyst will also help in automation, load, performance and stress testing.
The quality analyst is responsible for quality review of operations transactions. He/she will represent operations in various external and internal audits. He/she will maintain and further develop deep knowledge of industry requirements and operation processes and effectively share that knowledge with others. He/she will observe and communicate opportunities for quality and production improvement within the department.