Quality Associate — Pharmaceutical Manufacturing, 2nd Shift

Job overview

The Quality Associate — Pharmaceutical Manufacturing, 2nd Shift role is onsite in Seymour, IN; compensation is based on experience and no numeric amount is specified. The shift runs from 3:00 p.m. to 11:30 p.m. Codis manufactures pharmaceutical, nutraceutical, food, and over-the-counter products. The associate helps ensure products meet quality, safety, and regulatory standards by conducting and documenting testing, reviewing manufacturing records, and following standard operating procedures and applicable regulations.

What you'll do

• Perform incoming, in-process, and finished product testing
• conduct line, start-up, and cleaning checks
• review batch records
• report discrepancies
• conduct water sampling and environmental monitoring
• perform laboratory testing
• prepare certificates
• manage reagents and retention samples
• administer stability testing
• coordinate instrument calibration
• monitor storage temperatures
• participate in audits and investigations
• recommend corrective and preventive actions as needed.

What we're looking for

Skills & competencies

quality associate

pharmaceutical manufacturing

quality assurance

laboratory testing

gmp

fda compliance

seymour in

codis

2nd shift

3:00 p.m.–11:30 p.m.

paid time off

401(k) match

Work arrangement

• Weekend coverage required

Benefits & perks

• Paid time off from day one, health, dental, vision, and life insurance, 401(k) match with immediate vesting, 10 paid holidays, and growth opportunities.

Why this role

The posting identifies the role as second shift, 3:00 p.m.–11:30 p.m.; pay is based on experience.

About the employer

Codis is hiring for this role. Industry: Pharmaceutical Preparation Manufacturing. Sector: 32.