Associate Manufacturing Supervisor

SAFC•Verona, WI

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. Employee will 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 Manufacturing Supervisor is primarily focused on ensuring manufacturing staff execute required production operations to support the end users and patients of the compounds produced at MilliporeSigma. These responsibilities include but are not limited to executing existing production procedures, updating supporting documents, and maintaining the safety and quality of the manufacturing environment.

Requirements

Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or related Life Science discipline
2+ years of work experience in chemical or pharmaceutical manufacturing
Stand for long periods of time
Lift and move up to 50 pounds with the assistance of equipment or teammates as necessary

Nice To Haves

Leadership skills/previous leadership position
Ability to read and understand written protocols
Ability to demonstrate leadership skills and lead by example
Strong computer literacy (Microsoft Office and Outlook tools, Electronic Document Management Systems, etc.)
Effective oral and written communication skills
Mechanical and technical aptitude
Able to operate hand tools, calculators, and weighing / measuring devices
Strong mathematical skills
Possess a high degree of internal motivation
Ability to multi-task while paying close attention to detail

Responsibilities

Supervise, train, and motivate staff; lead shifts to meet deadlines, enforce expectations, and take corrective actions when necessary
Maintain safe, clean work environments and model ethical, professional behavior as a representative for customers and vendors
Ensure cGMP documentation accuracy, interpret in-process data, and provide secondary data review during off-shifts
Oversee and assist in API and intermediate manufacturing, serving as a primary operator and ensuring effective equipment operation and troubleshooting
Apply strong knowledge of MilliporeSigma procedures, synthetic/process chemistry, and EDMS system to support production activities
Author, review, and train staff on batch records, SOPs, and other written procedures while ensuring compliance with FDA, OSHA, EPA, DOT, and other regulations
Coordinate project flow, scale-up, and tech transfer between departments, providing status updates and generating cost models for quotes
Conduct employee training, performance reviews, recruitment, and cross-training to build effective teams within the production department
Identify production gaps, drive continuous improvement initiatives, and remain available for emergency support