The Quality Engineer will act as a liaison between the customer and the organization in all matters related to quality with respective customers; this position will also ensure that processes and systems are in place that meets the needs of the customer and the business.
The Quality Engineer will drive the quality assurance activities in the manufacturing plant.
The Quality Engineer will work closely with all functional groups within the plant to design and implement quality assurance programs and procedures.
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.
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.
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, 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.
The Quality Engineer Outage Services will support the Quality System needs of the Outage Services Division and provide a resource for developing and implementing good Quality practices while supporting the Divisions overall business objectives.
In this entry-level role, under close supervision, you will assist with the review and approval of Purchase Requisitions, Purchase Orders, design drawings, design specifications and instruction/procedures for Manufacturing, Test and Inspection activities to assure compliance with Quality System requirements.
In this role, the selected candidate will partner with clients to fully understand business philosophy and IT Strategy; recommend process improvements to increase efficiency and reliability in ETL development.
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.
This role is accountable for administering the process control, inspection methods and supplier management and stability program elements of the Quality System to ensure regulatory compliance and robust process design for medical product consumables and reagents.
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.