Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Corden Pharma - A Full-Service CDMO

Standards and Stability Analytical Chemist

Corden Pharma - A Full-Service CDMO

. Perform analytical tasks to qualify standards and ensure reference materials are available for cGMP analytical testing .

Posted 10/28/2026full-timeBoulder • Colorado • United StatesJuniorMid-Level💰 $78,000 - $95,500 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in analytical chemistry and cGMP standards, with strong capabilities in conducting stability studies, troubleshooting analytical instruments, and maintaining laboratory compliance. Proficient in data management using SAP and LIMS, alongside effective communication and documentation skills.

Highest-signal resume keywords
Analytical ChemistryCGMP StandardsStability StudiesSAP and LIMS ManagementTroubleshooting Analytical Instruments

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Analytical TestingEquipment CalibrationTitrant StandardizationData CompilationRoutine Analytical Chemistry CalculationsFTIR InterpretationHPLC OperationUPLC OperationGC OperationUV Spectroscopy
Soft Skills
Attention to DetailGood Communication SkillsProblem-SolvingAbility to Work IndependentlyTeam Collaboration
Industry Keywords
Quality ControlResearch and DevelopmentStability ProgramGood Documentation PracticesChemical Hygiene

About the role

Key responsibilities & impact
  • Perform analytical tasks to qualify standards and ensure reference materials are available for cGMP analytical testing
  • Support Research and Development, Quality Control, Manufacturing, and external clients
  • Support the Stability Program, including study initiation, pull scheduling, packaging, labeling, analytical testing, and data compilation
  • Run routine and non-routine tests on samples, including stability studies and standard characterization/qualification testing
  • Perform equipment calibration, titrant standardization, stability chamber monitoring, and preventative maintenance
  • Troubleshoot analytical instruments and techniques in the QC laboratory
  • Identify and communicate problems and solutions related to processes, procedures, and materials
  • Investigate anomalous test results and take corrective action
  • Maintain laboratory cleanliness and organization in accordance with safety, regulatory, chemical hygiene, and cGMP policies
  • Maintain daily records in SAP and LIMS, update material statuses, and initiate incident reports
  • Manage hazardous and non-hazardous waste
  • Participate in Quality, R&D, and cross-functional team meetings
  • Package stability samples and standard materials using appropriate verified materials
  • Author technical documents, including Standards and Stability Program protocols and reports
  • Perform critical and time-sensitive testing, including high-potency materials and difficult methods
  • Support laboratory investigations and assist in determining root cause
  • Conduct thorough data review according to good documentation practices
  • Work independently without frequent supervisory oversight

Requirements

What you’ll need
  • Bachelor's Degree (BA) 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 and comprehend simple instructions, short correspondence, and memos
  • Ability to write simple correspondence
  • Ability to effectively present information in one-on-one and small group situations
  • Ability to execute routine analytical chemistry calculations, including concentration, percentage, ppm, and RSD calculations
  • Ability to interpret analytical testing information from FTIR, HPLC, UPLC, GC, UV, and titrations
  • Ability to conduct out-of-specification investigations when required
  • Ability to solve practical problems under strict cGMP standards
  • Analytical skills and knowledge of general or organic chemistry
  • Good communication skills and computer skills
  • Attention to detail
  • Ability to occasionally lift and/or move up to 50 pounds
  • Willingness to work weekends and/or nights for 24/7 stability monitoring/testing

Benefits

Comp & perks
  • 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
  • Accident Plan
  • Critical Illness Insurance
  • Dental Insurance
  • Disability Insurance
  • Employee Assistance Program
  • Flexible Spending Account
  • Health Insurance PPO/HSA
  • Hospital Indemnity Plan
  • ID Theft Protection
  • Life Insurance
  • Paid Paternal Leave
  • Tuition Reimbursement
  • Wellness Program
  • Vacation – Three Weeks 1st Year
  • Vision Insurance