Associate Production Scientist - B 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. 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 Associate Production Scientist is a lab-based role primarily focused on supporting and executing activities in the manufacturing environment, including but not limited to: executing existing production procedures, updating supporting documents, maintaining the safety and quality of the manufacturing process, and other production tasks as directed. B shift is Thursday – Sunday 6:30am – 7:00pm, then Friday – Sunday 6:30am – 7:00pm. Demonstrate proper lab safety practices and comply with FDA, OSHA, EPA, DNR, DOT, and other regulatory guidelines. Operate as a primary operator in multiple cGMP production areas, including Kilo Labs, and train secondary operators to achieve primary status. Draft preliminary reports on deviations from procedures, identifying potential contributing factors. Utilize and update written procedures, including operation and batch records, with assistance from supervisors. Mentor new employees through technical and on-the-job training, fostering a collaborative team environment. Maintain safety and cleanliness in production areas, focusing on potent compound handling techniques and proper PPE usage. Communicate production status effectively using shift pass-off tools and computer systems, while addressing safety and process issues promptly. Take ownership of departmental responsibilities, providing support through additional tasks as directed by leadership. Physical Attributes: Working with highly potent / hazardous materials. Standing for long periods of time. Lifting and moving up to 50 pounds with the assistance of equipment or teammates. Utilize proper personal protective equipment (PPE), including respiratory protection, lab coats, and full body protection. Operate hand tools, calculators, and weighing/measuring devices. Work in Class 1/Div 2 areas and near moving mechanical parts. 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! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Requirements
- Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or other Life Science discipline.
- 1+ years of regulated pharmaceutical or chemical production manufacturing experience in an academic or professional setting.
Nice To Haves
- Ability to read and understand written protocols.
- Basic computer literacy (Microsoft Office and Outlook tools, Electronic Document Management Systems, etc.).
- Effective oral and written communication skills.
- Basic mathematical skills.
- Possess a high degree of motivation and self-starter attitude.
- Ability to multi-task while paying close attention to detail.
Responsibilities
- 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.
- Safe and efficient manufacturing of active pharmaceutical ingredients (API’s) according to current Good Manufacturing Practice (cGMP) requirements.
- Executing existing production procedures
- Updating supporting documents
- Maintaining the safety and quality of the manufacturing process
- Other production tasks as directed.
- Demonstrate proper lab safety practices and comply with FDA, OSHA, EPA, DNR, DOT, and other regulatory guidelines.
- Operate as a primary operator in multiple cGMP production areas, including Kilo Labs, and train secondary operators to achieve primary status.
- Draft preliminary reports on deviations from procedures, identifying potential contributing factors.
- Utilize and update written procedures, including operation and batch records, with assistance from supervisors.
- Mentor new employees through technical and on-the-job training, fostering a collaborative team environment.
- Maintain safety and cleanliness in production areas, focusing on potent compound handling techniques and proper PPE usage.
- Communicate production status effectively using shift pass-off tools and computer systems, while addressing safety and process issues promptly.
- Take ownership of departmental responsibilities, providing support through additional tasks 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
