GMP API Manufacturing Technician — Night Shift

MilliporeSigma

Verona (WI)

On-site

USD 34,000 - 56,000

Full time

Just now
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Benefits offered by this job

Health insurance
Paid time off
Retirement contributions
Other perquisites

Job summary

MilliporeSigma is seeking a Pharmaceutical Manufacturing Technician for a night-shift role focusing on the safe, compliant production of active pharmaceutical ingredients (APIs) in a GMP environment. You will help with equipment setup, cleaning, batch records, and routine verification tasks to ensure product quality.

The role demands meticulous adherence to procedures, strong attention to detail, and the ability to work across shifts in a collaborative manufacturing setting.

Qualifications

  • High School Diploma or GED required.
  • 2+ years of pharmaceutical or chemical manufacturing, or analytical lab experience.

Responsibilities

  • Adhere to GMP requirements per 21 CFR parts 210 & 211, 820, ICH Q7, and ISO standards.
  • Perform and assist in cGMP manufacturing of APIs and intermediates.
  • Maintain safety and quality in the production environment.
  • Operate and clean production equipment; support and verify batch records.
  • Communicate production status using shift pass-off tools and systems.
  • Address safety and process issues identified during inspections and audits.

Skills

Read protocols
Basic computer literacy
Communication skills
Mathematical basics
Multitasking

Education

High School Diploma or GED

Tools

Microsoft Word
PowerPoint
Email

Job description

MilliporeSigma is seeking a Pharmaceutical Manufacturing Technician for a night-shift role focusing on the safe, compliant production of active pharmaceutical ingredients (APIs) in a GMP environment. You will help with equipment setup, cleaning, batch records, and routine verification tasks to ensure product quality.

The role demands meticulous adherence to procedures, strong attention to detail, and the ability to work across shifts in a collaborative manufacturing setting.

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