Pharmaceutical Manufacturing Technician Weekend Overnight Shift

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 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

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role

Employee is responsible to adhere to the GMP requirements defined within 21 CFR parts 210 & 211, 820, ICH Q7, Safety standards set under ISO 14001 & 45001. This position primarily involves the safe and efficient manufacturing of active pharmaceutical ingredients (API’s) according to current Good Manufacturing Practice (cGMP) requirements. The role of Pharmaceutical Manufacturing Technician is a lab-based role primarily focused on supporting and executing activities in the manufacturing environment, including but not limited to: equipment cleaning and setup, verification tasks during GMP manufacturing, maintaining the safety and quality of the manufacturing environment, and other production tasks as directed.

The shift for this position is: Thursday-Sunday 6:30pm-7:00am, then Friday-Sunday 6:30pm-7:00am.

• Ensure safety and cleanliness in production areas, focusing on potent compound handling techniques.
• Utilize and update various written procedures, including batch records and operating procedures.
• Serve as a primary or secondary operator for cGMP production of APIs and intermediates.
• Operate production equipment effectively during production, cleaning, and maintenance.
• Communicate production status clearly using shift pass-off tools and computer systems.
• Address safety and process issues identified during inspections and audits promptly.
• Participate in a collaborative, multi-shift manufacturing environment and support departmental responsibilities as directed by leadership.

Physical Attributes

• Stand for long periods of time, lift and move up to 50 pounds with the assistance of equipment or teammates as necessary.
• Utilize proper personal protective equipment (PPE), including respiratory protection, lab coats, and full-body protection.
• Work with highly potent/hazardous materials and understanding chemical hazards
• Work in Class 1 / Div 2 areas and near moving mechanical parts.
• Operate hand tools, calculators, and weighing/measuring devices.

Who You Are

Minimum Qualifications:

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

Preferred Qualifications

• Read and understand written protocols.
• Basic computer literacy (Microsoft Word, PowerPoint, Email, etc.) and strong problem-solving skills
• Effective oral and written communication skills.
• Basic mathematical skills.
• High degree of motivation and self-starter attitude.
• Ability to multi-task while paying close attention to detail.

Pay Range for this position: $25.00-$41.00 per hour

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job‑related factors. Position may be eligible for sales or performance‑based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.

For more information click here.

RSREMD

What we offer:

We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!