Supervisor, Formulation Manufacturing

Work Schedule

12 hr shift/nights

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Thermo Fisher Scientific is currently seeking a Front of Week Night Supervisor, Formulation Manufacturing for the Compression Manufacturing Area in Cincinnati, OH.

Front of Week Shift: Monday-Wednesday 6:00pm-6:30am

Responsibilities:

• Coordinates and completes the production schedule for Commercial Manufacturing.
• Supervises, directs and lead employees of 10+ employees
• Coordinates all company policies with respect to GMPs, validation, quality, safety, health, attendance, and environment.
• With QA, makes quality decisions regarding batches in each manufacturing area.
• Tracks departmental metrics and facilitates improvement efforts.
• Develops employees and coordinates training on new equipment.
• Improves quality of processes as well as identify safety and efficiency improvements.

• Requirements:
• High School Diploma/GED required
• Bachelor of Science in appropriate engineering discipline (ex: Chemical, Mechanical, Biomedical), preferred.
• 3 to 5 years previous related experience in engineering, pharmaceutical manufacturing, and process equipment
• Previous Leadership experience required.
• Previous experience in a Supervisor role, preferred.
• Manufacturing equipment knowledge and process preferred.
• Broad-based background in pharmaceutical manufacturing with a combination of experience and skills in one or more of the following areas: product/ process development, production support, engineering, validation or quality assurance.
• Strong written and verbal communications as well as project management skills are essential as the position requires interaction and collaboration with the scientific staff, internal and external customers, schedulers, project managers and production technicians.

• Desired Qualifications:
• Good working knowledge and understanding of GMPs related to dry products manufacturing.
• Ability to motivate, influence and develop team members.
• Ability to solve problems and make decisions independently.
• Proactively drives quality improvements to achieve department safety, quality, and productivity goals.
• Models effective and constructive communication and interactions with technical departments both orally and in writing; maintain acceptable proficiency in technical and non-technical (e.g. interpersonal) skills.

Equivalent combinations of education, training, and meaningful work experience may be considered.

Relocation assistance is NOT provided

Must be legally authorized to work in the United States without sponsorship, now or in the future.

Must be able to pass a comprehensive background check, which includes a drug screening.