Associate Quality Control Chemist, Senior (Data Review)

The businesses of Merck KGaA, Darmstadt, Germany•Sheboygan Falls, WI

6h•$25 - $39

About The Position

In this role responsibilities may include but are not limited to: Evaluate stock suitability and secondary analytical data in strict accordance with Quality Management System (QMS) guidelines. Ensure the precision of all data entries within the Enterprise Resource Planning (ERP) software and process management databases. Interpret complex scientific data, including titration, spectroscopy, and chromatography, while performing standard stoichiometry and unit conversions. Execute intermediate analytical troubleshooting and support general quality review functions to maintain operational standards. Identify opportunities for quality enhancement and document deviations for management review to ensure regulatory compliance. Contribute to the document management program by creating, reviewing, and updating Standard Operating Procedures (SOPs) based on expertise. Coordinate with management and cross-functional departments to uphold customer-focused excellence and support audit requirements. Manage and prioritize daily responsibilities to remain in alignment with established departmental goals and timelines.

Requirements

Bachelor’s Degree in Chemistry, Biology, or other Life Science Discipline.
High School Diploma or GED and 4+ years of quality experience.

Nice To Haves

Experience working independently.
Strong oral and written communication skills.
Experience with Microsoft Office Suite and SAP ERP systems.
Experience in data review and analysis.

Responsibilities

Evaluate stock suitability and secondary analytical data in strict accordance with Quality Management System (QMS) guidelines.
Ensure the precision of all data entries within the Enterprise Resource Planning (ERP) software and process management databases.
Interpret complex scientific data, including titration, spectroscopy, and chromatography, while performing standard stoichiometry and unit conversions.
Execute intermediate analytical troubleshooting and support general quality review functions to maintain operational standards.
Identify opportunities for quality enhancement and document deviations for management review to ensure regulatory compliance.
Contribute to the document management program by creating, reviewing, and updating Standard Operating Procedures (SOPs) based on expertise.
Coordinate with management and cross-functional departments to uphold customer-focused excellence and support audit requirements.
Manage and prioritize daily responsibilities to remain in alignment with established departmental goals and timelines.