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Supervisor, Formulation Manufacturing at Thermo Fisher Scientific
Thermo Fisher Scientific
Cincinnati, OH
Manufacturing
Posted 0 days ago
Job Description
Work Schedule12 hr shift/nightsEnvironmental ConditionsAble 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.)Job DescriptionJob DescriptionThermo Fisher Scientificis currently seeking aFront of Week Night Supervisor Formulation Manufacturingfor the PDS/Condo Manufacturing Area in Cincinnati OH.Front of Week Shift: Monday-Wednesday 6:00pm-6:30amResponsibilities:Coordinates and completes the production schedule for Commercial Manufacturing.Supervises directs and lead employees of 10 employeesCoordinates 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 requiredBachelor of Science in appropriate engineering discipline (ex: Chemical Mechanical Biomedical) preferred.3 to 5 years previous related experience in engineering pharmaceutical manufacturing and process equipmentPrevious 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 providedMust 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.Required Experience:Manager Key Skills Lean Manufacturing,Six Sigma,Continuous Improvement,FDA Regulations,Lean,Packaging,Production Planning,cGMP,Cell Culture,Leadership Experience,Supervising Experience,Manufacturing Employment Type : Full-Time Experience: years Vacancy: 1
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