QC Analyst I: Start in Pharmaceutical Quality Lab

Colorcon, Inc.; Indianapolis (IN); On-site; USD 52,000 - 64,000; Full time

Benefits offered by this job

Bonus program

Medical plans

Dental Insurance

Vision Coverage

Wellness programs

Employee Assistance Programs (EAP)

CSR Groups

Parental Leave

Tuition Reimbursement

401(k) Matching

Paid Time Off

Paid Holidays

Job summary

Colorcon, Inc. is seeking a Quality Control (QC) Analyst I for our Indianapolis, Indiana facility. The role involves determining quality of raw materials, intermediates and finished products using analytical methods within the QC laboratory.

Responsibilities include performing chemical assays, maintaining Lab operations, calibration, and timely reporting while ensuring cGMP compliance and proper documentation under the supervision of the Quality Manager.

Qualifications

• Bachelor’s degree in a physical science is preferred.
• Minimum of three years in a QC analytical lab (without a bachelor’s degree).
• Familiarity with USP/NF procedures and cGMPs preferred.

Responsibilities

• Analyze raw materials, intermediates and finished products using physical, chemical and instrumental techniques per established procedures.
• Maintain lab inventory and calibrate equipment as needed.
• Submit accurate analytical reports and communicate OOS results promptly.

Skills

Analytical chemistry

Instrumental analysis

Data compilation

cGMPs knowledge

Technical writing

Communication skills

Education

Bachelor’s degree in physical science

Tools

Analytical instruments

Job description

Colorcon, Inc. is seeking a Quality Control (QC) Analyst I for our Indianapolis, Indiana facility. The role involves determining quality of raw materials, intermediates and finished products using analytical methods within the QC laboratory.

Responsibilities include performing chemical assays, maintaining Lab operations, calibration, and timely reporting while ensuring cGMP compliance and proper documentation under the supervision of the Quality Manager.