GMP API Production Technician

MilliporeSigma; Verona (WI); On-site; USD 34,000 - 56,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Retirement Contributions

Other perquisites

Job summary

MilliporeSigma is seeking a Pharmaceutical Manufacturing Technician to support GMP-compliant production of active pharmaceutical ingredients (APIs) in a lab-based environment. You will perform equipment setup, cleaning, verification tasks, and maintain safety and quality in the manufacturing area.

The role requires adherence to 21 CFR parts 210 & 211, 820 and ISO 14001/45001 standards. Shift is Monday–Thursday, 6:30pm–7:00am, with collaborative, cross-functional teamwork across shifts.

Qualifications

• High School Diploma or GED required.
• 2+ years of pharmaceutical manufacturing, chemical manufacturing, or analytical lab experience preferred.
• Read and understand written protocols.
• Basic computer literacy (Word, PowerPoint, Email) and problem solving skills.

Responsibilities

• Ensure safety and cleanliness in production areas and handle potent compounds.
• Update batch records and operating procedures as required.
• Serve as primary/secondary operator for cGMP production of APIs and intermediates.
• Operate production equipment during production, cleaning, and maintenance.
• Communicate production status via shift pass-off tools and systems.
• Address safety and process issues identified during inspections and audits.
• Support multi‑shift manufacturing and departmental duties as directed.

Skills

Read/write protocols

Basic computer literacy

Problem solving

Attention to detail

Team collaboration

Education

High School Diploma or GED

Job description

MilliporeSigma is seeking a Pharmaceutical Manufacturing Technician to support GMP-compliant production of active pharmaceutical ingredients (APIs) in a lab-based environment. You will perform equipment setup, cleaning, verification tasks, and maintain safety and quality in the manufacturing area.

The role requires adherence to 21 CFR parts 210 & 211, 820 and ISO 14001/45001 standards. Shift is Monday–Thursday, 6:30pm–7:00am, with collaborative, cross-functional teamwork across shifts.