Interpretation Chemist – US, Germany

NAMSA

Interpretation Chemist analyzing data and performing calculations for medical device testing. Collaborating on studies and ensuring compliance in quality systems and documentation.

Posted 7/2/2026full-timeSt. Paul • Minnesota • 🇺🇸 United StatesMid-LevelSenior💰 $60,000 - $70,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in data analysis, method development, and compliance with GLP/GMP standards, while effectively managing project timelines and maintaining quality systems. Proficient in LC-MS, HPLC, and GC-MS techniques, with strong communication skills in both German and English.

Highest-signal resume keywords

Data AnalysisMethod DevelopmentGLP/GMP ComplianceLC-MS InstrumentationFluent in German and English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data InterpretationFeasibility TestingQuality Control (QC)HPLCGC-MSUPLC-MSSOP DevelopmentRoot Cause AnalysisFinal Report SigningDocument Improvement

Soft Skills

Strong Communication SkillsTeam PlayerOrganizational TalentHigh InitiativeStructured Working Style

Tools & Technologies

LC-MSHPLCGC-MSUPLC-MSQuality Systems

Industry Keywords

DIN EN ISO/IEC 17025Medical DevicesGLP Environment

About the role

Key responsibilities & impact

Independently analyze data, perform calculations, and interpret test/control results according to written instructions.
May assist in the interpretation of Feasibility testing, Method Development, and/ or Method Verifications
Works with management to ensure large studies are completed on or before the due date.
Maintain ancillary records.
May trend and evaluate QC data as appropriate.
Develop and maintain LC-MS compound library and database.
May assist with SOP, purchase specification, protocol, and work instruction creation and revisions.
Participate in the improvement of documents, test systems, quality systems, and workflow.
Responsible for review of paperwork for appropriateness and accuracy and taking all concerns to management as required.
Review work of other colleagues for scientific soundness and GLP/GMP and SOP compliance.
Helps ensure department compliance to site goals and objectives (i.e. financial, OPD, report revision).
May be responsible for final report signing.
In the event of test failure, may lead failure investigations identifying root cause and corrective/preventive actions.
May be responsible for client contact with regards to unexpected testing results, project updates, and deliverables.
Assist with Client Audits as needed.
Other duties as assigned.

Requirements

What you’ll need

Degree in Chemistry or a related scientific field, ideally with 3 years of professional experience
Alternatively, technical training in chemistry with at least 3 years of professional experience
Experience in a GLP environment as well as with DIN EN ISO/IEC 17025 in the field of medical devices is desirable
Experience handling HPLC and GC-MS instruments is an advantage
Experience in processing or interpreting UPLC-MS results is beneficial
High level of initiative and sense of responsibility
Strong hands-on mentality
Team player with strong communication skills
Organizational talent with a structured working style
Fluent in German and English, both written and spoken.

Benefits

Comp & perks

A challenging and varied role in a globally expanding company
A highly professional team and an international working environment
Attractive, performance-based compensation
Flexible working hours and home office options
Employer contribution to company pension scheme
Monthly fuel allowance for private car use
Electric vehicle charging station
Regular team events
Company restaurant with outdoor terrace