Manufacturing Supervisor Weekend Day Shift Job Birmingham area,Alabama USA,Manufacturing / Production

Work Location:

Madison, Wisconsin

Shift:

Department: LS-SC-UYWMC Madison Manufacturing

Hiring Manager:
Ben Simoni

This information is for internals only. Please do not share outside of the organization.

Your Role:

The Manufacturing Supervisor position primarily involves the safe and efficient manufacturing of active pharmaceutical ingredients (API’s) according to current Good Manufacturing Practice (cGMP) requirements.

This position is for B shift. (Thursday – Sunday 6:30am – 7:00pm, then Friday – Sunday 6:30am – 7:00pm)

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 Millipore Sigma 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

Physical Attributes:

Stand for long periods of time.
Lift and move up to 50 pounds with the assistance of equipment or teammates as necessary.
Operate hand tools, calculators, and weighing / measuring devices

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 se responsibilities include but are not limited to executing existing production procedures, updating supporting documents, and maintaining the safety and quality of the manufacturing environment.

Who

You Are

Minimum Qualifications:

Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering or other Life Science discipline.
2+ years of work experience in chemical or pharmaceutical manufacturing.
2+ years of manager/supervisor experience

Preferred Qualifications:

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
Strong mathematical skills
Possess a high degree of internal motivation
Ability to multi-task while paying close attention to detail

Pay Range for this position: $85,000-$136,800.

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…