Pharmaceutical Manufacturing Technician D Shift
About The Position
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. D shift is Thursday-Sunday 6:30pm-7:00am, then Friday-Sunday 6:30pm-7:00am.
Requirements
- High School Diploma or GED.
- 2+ years of pharmaceutical manufacturing, chemical manufacturing, or analytical lab experienc.
Nice To Haves
- 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.
Responsibilities
- 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.
Benefits
- Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
