Pharmaceutical Manufacturing Technician Weekend Overnight Shift

Merck Group; Town of Grand Rapids (WI); On-site; USD 34,000 - 56,000; Full time

Benefits offered by this job

Health insurance

Paid time off (PTO)

Retirement contributions

Other perquisites

Job summary

MilliporeSigma in the United States is seeking a Pharmaceutical Manufacturing Technician to support GMP production of active pharmaceutical ingredients (APIs) and intermediates in a lab-based setting. The role emphasizes safe handling of potent materials, adherence to 21 CFR and ISO standards, and collaboration across shifts to maintain quality and efficiency.

Primary duties include equipment setup, cleaning, task verification, and accurate documentation of batch records, with a Thursday-Sunday

Qualifications

• Experience in GMP environments.
• Knowledge of batch records and standard operating procedures.
• Ability to work in a multi-shift manufacturing environment.

Responsibilities

• Ensure safety and cleanliness in production areas, focusing on potent compound handling techniques.
• Utilize and update batch records and operating procedures.
• Serve as primary/secondary operator for cGMP production of APIs and intermediates.
• Operate production equipment during production, cleaning, and maintenance.
• Communicate production status using shift pass-off tools and computer systems.
• Address safety and process issues identified during inspections and audits.
• Participate in a multi-shift environment and support department tasks.

Skills

Pharmaceutical manufacturing

Chemical manufacturing

Analytical laboratory experience

Education

High School Diploma or GED

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.

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.

• Health insurance
• Paid time off (PTO)
• Retirement contributions
• Other perquisites

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!