QC Analyst — GMP Lab Precision & Career Growth

Corden Pharma - A Full-Service CDMO; Boulder (CO); On-site; USD 55,000 - 76,000; Full time

Benefits offered by this job

401(k) matching

Health Insurance

Paid Time Off

Tuition Reimbursement

Wellness Program

Job summary

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in APIs, excipients, drug products (DPs), and packaging. We seek a detail‑oriented technician to perform essential QC lab duties and support senior staff in a GMP setting.

The role involves running samples, calibrating equipment, documenting results in SAP/LIMS, and adhering to safety standards. Training will cover all procedures; overtime and 12‑hour shifts may apply.

Qualifications

• Bachelor's Degree or 1 year related experience recommended; GMP and lab equipment experience preferred.
• Knowledge of GMPs, GLPs, and general laboratory practices.
• Ability to read safety rules, operating instructions, and procedures.

Responsibilities

• Run routine samples of raw materials, intermediates, and final products.
• Calibrate equipment, standardize titrants, and perform standard validation.
• Identify and correct instrument issues in QC lab; communicate solutions.
• Maintain lab cleanliness and follow safety and chemical hygiene policies.
• Record daily SAP and LIMS data; manage status changes and incident reports.
• Generate and manage waste in accordance with regulations.
• Attend QC Team meetings and support skill development.

Skills

Math & reading skills

Chemistry knowledge

Lab equipment aptitude

QC support

Basic test methods

Communication & computer skills

QEH&S commitment

Attention to detail

12-hour shifts experience

Education

Bachelor's Degree (BA)

Job description

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in APIs, excipients, drug products (DPs), and packaging. We seek a detail‑oriented technician to perform essential QC lab duties and support senior staff in a GMP setting.

The role involves running samples, calibrating equipment, documenting results in SAP/LIMS, and adhering to safety standards. Training will cover all procedures; overtime and 12‑hour shifts may apply.