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NAMSA

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

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
Data InterpretationFeasibility TestingQuality Control (QC)HPLCGC-MSUPLC-MSSOP DevelopmentRoot Cause AnalysisFinal Report SigningDocument Improvement
Soft Skills
Strong Communication SkillsTeam PlayerOrganizational TalentHigh InitiativeStructured Working Style