FREE ACCESS
5,000–10,000 jobs/day
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.

Senior IPC QC Analyst
Corden Pharma - A Full-Service CDMO. Run routine and advanced analyses on non-routine samples .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
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
Tailor your resumeApplicant 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