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Supervisor, Formulation Manufacturing

Thermo Fisher Scientific

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Supervisor, Formulation Manufacturing

full-timePosted: Jan 12, 2026

Job Description

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.)

Job Description

Job Description

Thermo Fisher Scientific is currently seeking a Front of Week Night Supervisor, Formulation Manufacturing for the PDS/Condo 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. 

Locations

  • Cincinnati, Ohio, United States of America

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • GMP complianceintermediate
  • Leadership and team supervisionintermediate
  • Process improvementintermediate
  • Project managementintermediate
  • Strong written and verbal communicationintermediate

Required Qualifications

  • High School Diploma/GED required (experience)
  • Bachelor of Science in engineering (Chemical, Mechanical, Biomedical) preferred (experience)
  • 3-5 years related experience in engineering/pharmaceutical manufacturing (experience)
  • Previous leadership experience required (experience)
  • Supervisor experience preferred (experience)

Responsibilities

  • Coordinates and completes production schedule
  • Supervises 10+ employees
  • Coordinates company policies on GMPs, validation, quality, safety
  • Makes quality decisions with QA
  • Tracks metrics and facilitates improvements
  • Develops employees and coordinates training
  • Improves processes for quality, safety, efficiency

Benefits

  • general: No relocation assistance

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Thermo Fisher Scientific logo

Supervisor, Formulation Manufacturing

Thermo Fisher Scientific

Other Jobs

Supervisor, Formulation Manufacturing

full-timePosted: Jan 12, 2026

Job Description

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.)

Job Description

Job Description

Thermo Fisher Scientific is currently seeking a Front of Week Night Supervisor, Formulation Manufacturing for the PDS/Condo 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. 

Locations

  • Cincinnati, Ohio, United States of America

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • GMP complianceintermediate
  • Leadership and team supervisionintermediate
  • Process improvementintermediate
  • Project managementintermediate
  • Strong written and verbal communicationintermediate

Required Qualifications

  • High School Diploma/GED required (experience)
  • Bachelor of Science in engineering (Chemical, Mechanical, Biomedical) preferred (experience)
  • 3-5 years related experience in engineering/pharmaceutical manufacturing (experience)
  • Previous leadership experience required (experience)
  • Supervisor experience preferred (experience)

Responsibilities

  • Coordinates and completes production schedule
  • Supervises 10+ employees
  • Coordinates company policies on GMPs, validation, quality, safety
  • Makes quality decisions with QA
  • Tracks metrics and facilitates improvements
  • Develops employees and coordinates training
  • Improves processes for quality, safety, efficiency

Benefits

  • general: No relocation assistance

Target Your Resume for "Supervisor, Formulation Manufacturing" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Supervisor, Formulation Manufacturing. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Supervisor, Formulation Manufacturing" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Supervisor, Formulation Manufacturing @ Thermo Fisher Scientific.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.