Stability & Standards Analytical Chemist — QC

CordenPharma International

Boulder (CO)

In loco

USD 78.000 - 96.000

Tempo pieno

6 giorni fa
Candidati tra i primi

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Vantaggi offerti da questo lavoro

401(k) matching
Health insurance PPO/HSA
Tuition reimbursement
Paid parental leave
Wellness program
Vision insurance

Descrizione del lavoro

Corden Pharma Colorado in Boulder, CO is seeking an intermediate-level Standards and Stability Analytical Chemist to join the Quality Team. The role supports the Stability Program, coordinating study initiation, packaging, labeling, analytical testing, and data compilation to ensure cGMP-compliant stability data for R&D, QC, manufacturing and external clients.

The position involves routine and non-routine testing, instrument troubleshooting (uPLC/HPLC, GC, FTIR, UV/Vis), SAP/LIMS data entry, and

Competenze

  • Bachelor's Degree from a 4-year college or university; 2 years of related experience and/or training; or equivalent combination of education and experience.
  • Ability to read, write and communicate clearly; ability to work independently.
  • Experience with analytical techniques such as HPLC/UPLC, GC, FTIR, UV/Vis.

Mansioni

  • Support 24/7 stability monitoring and testing; weekends and/or nights may be required.
  • Run routine and non-routine stability tests and standard characterization/qualification testing.
  • Perform equipment calibration, titrant standardization, and stability chamber monitoring.
  • Identify and troubleshoot instruments; communicate problems and solutions; perform basic investigations.
  • Maintain lab cleanliness and safety per cGMP and regulatory policies; manage waste properly.

Conoscenze

Analytical chemistry
HPLC/UPLC
GMP knowledge
Troubleshooting
Laboratory data review

Formazione

Bachelor's degree

Strumenti

SAP
LIMS
Titration equipment

Descrizione del lavoro

Corden Pharma Colorado in Boulder, CO is seeking an intermediate-level Standards and Stability Analytical Chemist to join the Quality Team. The role supports the Stability Program, coordinating study initiation, packaging, labeling, analytical testing, and data compilation to ensure cGMP-compliant stability data for R&D, QC, manufacturing and external clients.

The position involves routine and non-routine testing, instrument troubleshooting (uPLC/HPLC, GC, FTIR, UV/Vis), SAP/LIMS data entry, and

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