Senior IPC QC Analyst — Lead Analytical Lab Excellence

Corden Pharma Boulder, Inc.; Boulder (CO); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

401(k) matching

Health Insurance PPO/HSA

Vacation 3 weeks

Tuition Reimbursement

Paid Parental Leave

Job summary

Corden Pharma Colorado is seeking a skilled Quality Laboratory professional to support GMP-compliant testing, data integrity, and documentation across QC processes. You will calibrate instruments, review CA certificates, and generate data for statistical control while maintaining strict safety and lab housekeeping standards.

The role emphasizes collaboration with Process Chemists and QC teams, training junior staff, and ensuring cGMP adherence within a 12-hour rotating shift environment at CPC.

Qualifications

• Bachelor's Degree in a related science field and GMP experience in a Quality Lab.
• 5 years of GMP experience in a Quality Lab or equivalent.
• Ability to read, write and interpret documents; communicate effectively.

Responsibilities

• Run routine and advanced analysis on samples with QC and Process Chemists collaboration.
• Perform equipment calibration, titrant standardization, and validation as required.
• Maintain cleanliness and organization of lab following GLP and GMP; ensure safety compliance.
• Record keeping on SAP and LIMS; review certificates of analysis and approve final product.
• Generate data for SPC and modify LIMS as needed; peer review analytical data.
• Manage hazardous and non-hazardous waste according to procedures.
• Participate in QC Team meetings and contribute to team skills development.
• Take ownership to achieve organizational goals.

Skills

Attention to detail

Troubleshooting

Communication skills

Education

Bachelor's Degree in a related science

Tools

SAP

LIMS

Job description

Corden Pharma Colorado is seeking a skilled Quality Laboratory professional to support GMP-compliant testing, data integrity, and documentation across QC processes. You will calibrate instruments, review CA certificates, and generate data for statistical control while maintaining strict safety and lab housekeeping standards.

The role emphasizes collaboration with Process Chemists and QC teams, training junior staff, and ensuring cGMP adherence within a 12-hour rotating shift environment at CPC.