cGMP Manufacturing Supervisor - Night Shift

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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:

At MilliporeSigma, as the cGMP Manufacturing Supervisor – Night Shift at our 3300 South Second Ave / Cherokee site, will manage production personnel in the manufacture of products and many support functions outside of manufacturing. Job duties include:

• 12 hour night shift (7:00pm - 7:30am) shifts with a 20% shift differential
• Oversee the manufacturing of Active Pharmaceutical Ingredients (API’s) regulated by the Food and Drug Administration and other regulatory bodies.
• This position will have direct reporting structures for scientists engaged in supporting the manufacturing operations, production coordinator, and manufacturing training program.
• Provide guidance Monday – Friday for scientists engaged in production readiness, including batch record review, equipment procurement, material transfer, training oversight and employee scheduling.
• This position will be overseeing a manufacturing training team currently consisting of people on rotating shifts (Day and Night Shift).
• This position will oversee a manufacturing coordination team consisting of people working Monday-Friday. Team responsibility includes material transfers from warehouse, material returns, and material consumptions.
• This position will have the primary purpose of ensuring goods receipts are performed in a timely manner after manufacturing campaign is complete.
• Lead a team of production scientists and operators in the scale-up, technology transfer, and execution of cGMP manufacturing.
• Develop employees’ knowledge and skills to improve performance and expand abilities as well as to coordinate the group’s efforts to assist meeting the departmental, company, and customer’s objectives.
• Adhere to protocols consistent with, and established according to, current Good Manufacturing Practices.
• Collaboration is important. Work cross-functionally with Project Management, MSAT, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance.
• Interact with our customers’ project management, technical and quality teams.
• Maintain departmental goals and objectives in a safe manner and in compliance with all applicable federal, state, and company regulations (OSHA, EPA, FDA, EMA etc.).
• Responsible for the management of capital for equipment and facility improvements, including balancing the departmental budget. A primary responsibility will be the creation of purchasing Process Orders.
• Support department efforts toward Process Improvement and company goals.
• Revise and approve procedures, batch records, and other documentation to ensure compliance with cGMP guidelines.
• Ensure employees remain current with all department and site training requirements.
• Assist and/or Lead root cause investigations and implement effective corrective and preventative actions related to manufacturing deviations.
• Provide leadership and support of safety initiatives within production operations to ensure compliance with OSHA requirements.
• Ensure tasks are done in accordance with approved site procedures, batch records and protocols.

Who You Are

Minimum Qualifications:

• Bachelor’s Degree in Chemistry, Biology, Biochemistry, Chemical Engineering, or other Life Science disciplines.
• 4+ years of manufacturing experience in a cGMP setting.
• 1+ years of Management, Supervisory, or Lead experience.

Preferred Qualifications:

• 3+ years of Management, Supervisory, or Lead experience in GxP environment.
• Customer interfacing audit experience.
• Knowledge of Six Sigma concepts/Lean Manufacturing or process improvement.
• Familiarity with large scale cGMP process equipment, tangential flow, and chromatography automation.
• Strong Microsoft Office experience for Manufacturing/Operating procedure writing, technical report generation, product tracking and trending data analysis and Operational Excellence reports.
• Strong interpersonal skills and conflict resolution experience
• Advanced written and verbal communication skills.

RSREMD

Pay Range for this position: $88,800 - $152,300 a year.

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

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!