Associate Quality Control Chemist, Senior (Data Review) Mid Shift

The businesses of Merck KGaA, Darmstadt, Germany•Milwaukee, WI

47d•$25 - $39•Onsite

About The Position

This role involves performing routine assignments using existing procedures or working autonomously within established procedures and practices that require knowledge of concepts and procedures within a job discipline or specialized technical expertise within an analytical/scientific method or operational process. The shift for this position is 10 am-6 pm, Monday-Friday. The role requires reviewing stock suitability and secondary analytical data in accordance with the Quality Management System (QMS), product specifications, established data libraries, and applicable guidelines. It also involves verifying ERP, sample-tracking, and metric-system entries; processing and routing samples and analytical data accurately; and maintaining complete, compliant records. The chemist will interpret analytical results, including titration, spectroscopy, and chromatography; perform stoichiometry, unit conversions, and intermediate-level troubleshooting. Responsibilities include preparing controlled documents such as Certificates of Analysis, product specifications, and investigation records. The role also entails conducting and supporting out-of-specification investigations, deviations, change requests, audits, and resolving master-data or product issues. Additionally, the chemist will create, review, and update SOPs, complete required training, train new hires, and collaborate cross-functionally on procedures and operations. The position also involves identifying, coordinating, and implementing department-level quality, process, and safety improvements in partnership with management, and communicating operational status, risks, and deviations. The role supports internal teams, customers, site visitors, and audits while prioritizing safe, timely work aligned with department and site objectives.

Requirements

Bachelor’s degree in Chemistry, or Other Life/Physical Science disciplines
2+ years laboratory, or quality review experience

Nice To Haves

Knowledge in chemistry, math, and general science
Some graduate coursework preferred
Ability to function in a team environment
Good customer service and communications skills, oral and written
Basic understanding analytical tools and equipment
Safe chemical handling practice
Compute chemical calculations and conversions
Ability to adapt, self-motivate, and critically think
Organization and time management skills
Database software management skills
Skilled in making decisions and attention to detail
Microsoft Office, Power Point, Excel, Word etc.
Basic understanding of Data Integrity
Basic understanding of Good Documentation Practices

Responsibilities

Review stock suitability and secondary analytical data in accordance with the Quality Management System (QMS), product specifications, established data libraries, and applicable guidelines.
Verify ERP, sample-tracking, and metric-system entries; process and route samples and analytical data accurately and maintain complete, compliant records.
Interpret analytical results, including titration, spectroscopy, and chromatography; perform stoichiometry, unit conversions, and intermediate-level troubleshooting.
Prepare controlled documents, including Certificates of Analysis, product specifications, investigation records, and other quality documentation.
Conduct and support out-of-specification investigations, deviations, change requests, audits, and resolution of master-data or product issues.
Create, review, and update SOPs; complete required training; train new hires and collaborate cross-functionally on procedures and operations.
Identify, coordinate, and implement department-level quality, process, and safety improvements in partnership with management.
Communicate operational status, risks, and deviations; support internal teams, customers, site visitors, and audits while prioritizing safe, timely work aligned with department and site objectives.