Pharma QC Chemist — Analytical Lab (cGMP)

ANI Pharmaceuticals, Inc.; Minnesota; Hybrid; USD 48,000 - 52,000; Full time

Benefits offered by this job

Health Insurance

Life Insurance

Disability Insurance

Retirement Savings Plans

Paid Leave & Holidays

Job summary

ANI Pharmaceuticals, Inc. is seeking a Quality Control Chemist to independently perform laboratory procedures, apply analytical knowledge, and mentor entry-level analysts in a regulated pharmaceutical environment.

The role focuses on testing, data integrity, equipment maintenance, and cGMP tasks, with opportunities to contribute to reports and SOP updates while upholding safety and quality standards.

Qualifications

• Bachelor's degree in Chemistry or closely related field.
• 2-5 years experience in an analytical chemistry lab in a Pharmaceutical or similarly regulated environment.
• Ability to work independently.
• Demonstrated expertise of Laboratory cGMPs.
• Follow written procedures and perform technical writing.

Responsibilities

• 50%: Perform laboratory testing on material and product samples; prepare standards and samples per procedures; operate equipment and collect data.
• 25%: Review data collected under approved test methods; assess data integrity and document findings.
• 10%: Calibrate, preventive maintenance, and repair on assigned equipment; update procedures.
• 10%: Perform cGMP tasks such as monitor expiry dates, audit documentation, and logbooks; prepare revisions.
• 5%: Perform other duties as assigned.

Skills

Communication

Integrity

Safety

Teamwork

Data Affinity

Project Management

Quality Standards

Technical Writing

Independence

cGMP Knowledge

Education

Bachelor's in Chemistry

Postgraduate education in Chemistry/Pharmacy

Job description

ANI Pharmaceuticals, Inc. is seeking a Quality Control Chemist to independently perform laboratory procedures, apply analytical knowledge, and mentor entry-level analysts in a regulated pharmaceutical environment.

The role focuses on testing, data integrity, equipment maintenance, and cGMP tasks, with opportunities to contribute to reports and SOP updates while upholding safety and quality standards.