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Corden Pharma - A Full-Service CDMO

Senior IPC QC Analyst

Corden Pharma - A Full-Service CDMO

. Run routine and advanced analyses on non-routine samples .

Posted 10/10/2026full-timeBoulder • Colorado • United StatesSenior💰 $33 - $43 per hourWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in advanced analytical techniques and quality control processes within a GMP-compliant laboratory environment. Proficient in laboratory software, SOP development, and statistical data analysis while ensuring adherence to safety and regulatory standards.

Highest-signal resume keywords
GMP ExperienceAdvanced Analytical Data AnalysisSOP Development and RevisionLaboratory Software ProficiencyProblem-Solving Skills

ATS Keywords

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Applicant Tracking System Keywords

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

Hard Skills
Analytical TechniquesStatistical Process ControlEquipment CalibrationTitrant StandardizationQC Instrument TroubleshootingData AnalysisChemical HygieneNon-Routine MethodsMechanical AptitudeRecord Keeping in SAP and LIMS
Soft Skills
Effective CommunicationTeam LeadershipProblem-SolvingOrganizational SkillsTraining and Mentoring
Tools & Technologies
SAPLIMSLaboratory EquipmentStatistical SoftwareWord Processing SoftwareSpreadsheet ApplicationsDatabase Applications
Industry Keywords
CGMPQuality ControlFDAGLPICH Q7QSHE PrinciplesChemical Hygiene PoliciesQuality Management System

About the role

Key responsibilities & impact
  • Run routine and advanced analyses on non-routine samples
  • Work with Process Chemists and QC Chemists to resolve problems and train new technicians
  • Perform equipment calibration, titrant standardization, and standard validation
  • Identify and correct QC laboratory instrument problems
  • Identify and communicate process, procedure, and material problems and solutions to QC Chemists
  • Research and take corrective action on anomalous test results
  • Maintain laboratory cleanliness and organization under safety, regulatory, and chemical hygiene policies
  • Troubleshoot QC laboratory instrumentation and methods
  • Perform daily record keeping in SAP and LIMS
  • Print labels, review certificates of analysis, and approve final product
  • Gather and compile data for statistical process control and perform LIMS modifications
  • Peer review analytical data
  • Manage hazardous and non-hazardous waste generation and accumulation
  • Attend QC team meetings and develop team skills
  • Act as shift lead in the absence of management
  • Write and revise SOPs and methods as directed
  • Support cGMP-compliant pharmaceutical manufacturing under the Corden Pharma Colorado Quality Management System

Requirements

What you’ll need
  • Bachelor's Degree from a 4-year college or university in a related science area and 5 years of GMP experience in a Quality Lab; or 5 years of related experience in a Quality environment; or equivalent combination of education and experience
  • Ability to read and interpret safety rules, operating and maintenance instructions, and procedure manuals
  • Ability to write routine reports and correspondence
  • Ability to speak effectively before groups of customers or employees
  • Ability to work with probability, statistical inference, geometry, trigonometry, fractions, percentages, ratios, and proportions
  • Ability to solve practical problems and interpret written, oral, diagram, or schedule instructions
  • Highly developed analytical skills and knowledge of general or organic chemistry
  • Specialized skills on non-routine methods
  • Mechanical aptitude with lab equipment
  • Advanced analytical data analysis and error detection
  • Demonstrated problem-solving skills
  • Commitment to QSHE Principles
  • Ability to write and revise SOPs and methods as directed
  • Advanced understanding of laboratory software
  • Ability to work 12-hour rotating shifts, nights or days, weekends, and holidays
  • Strong computer skills including word processing, spreadsheets, email, and database applications
  • Ability to occasionally lift and/or move up to 25 pounds
  • Must comply with safety, regulatory, chemical hygiene, GLP, GMP, FDA, ICH Q7, and applicable global regulatory requirements

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 Parental Leave
  • Tuition Reimbursement
  • Wellness Program
  • Vacation — Three Weeks 1st Year
  • Vision Insurance