ThermoFisher Scientific
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, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift
Job Description Lead Operator, Manufacturing Operations
Thermo Fisher Scientific’s oral solid dose (OSD) site in Cincinnati, Ohio, supported by over 800 employees, offers various drug development and commercial manufacturing services. These services include controlled and sustained release solid oral dosage forms, osmotic release dosage forms (laser drilling), liquid fill hard capsules, controlled substances manufacturing, and abuse-deterrent dosage forms.
Discover Impactful Work
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Every day, our colleagues bring our Mission to life—enabling our customers to make the world healthier, cleaner, and safer. In this role, you’ll support critical manufacturing operations that contribute to protecting the environment, ensuring food safety, and advancing life‑saving therapies.
Position Summary Join our manufacturing team as a Lead Operator, where you will play a critical role in leading daily production activities while mentoring and developing team members. You will ensure consistent execution of manufacturing processes, uphold the highest standards of safety and quality, and drive continuous improvement initiatives. This role offers the opportunity to work with advanced manufacturing technologies while supporting operational excellence in a regulated environment.
Shift Monday-Wednesday 6:00pm-6:30am
A Day in the Life You will:
Lead and coordinate daily manufacturing operations to ensure production goals are met safely, efficiently, and in compliance with cGMP and ISO standards
Serve as a technical and operational resource for operators, providing guidance, training, and mentorship
Review and execute manufacturing documentation, including SOPs, batch records, and work instructions
Troubleshoot complex manufacturing equipment and process issues, escalating as appropriate
Support and drive continuous improvement initiatives, including lean manufacturing practices
Ensure strict adherence to safety protocols and clean room/controlled environment requirements
Collaborate cross-functionally with Quality, Engineering, and Supply Chain teams
Participate in documentation review, deviation investigations, and corrective action implementation
Maintain accurate records using manufacturing software systems and ERP platforms
Keys to Success Education
High School Diploma or equivalent required
Bachelors Dedree Preferred fields of study: Engineering, Chemistry, Biology, or a related discipline
Technical certifications in manufacturing or a related field are beneficial
Experience
Minimum of 4 years of manufacturing experience, with demonstrated leadership capabilities
Experience working in regulated manufacturing environments
Proven success leading teams, training operators, and managing multiple priorities
Experience with batch record review and documentation in cGMP-regulated settings
Knowledge, Skills, Abilities Knowledge
Strong understanding of cGMP, ISO standards, and regulatory requirements
Knowledge of lean manufacturing and continuous improvement methodologies
Skills
Advanced troubleshooting and problem‑solving skills
Proficiency with manufacturing software systems, ERP platforms, and Microsoft Office Suite
Strong communication and interpersonal skills
Abilities
Ability to lead, mentor, and develop team members
Exceptional attention to detail and commitment to quality
Strong analytical and decision‑making capabilities
Ability to coordinate cross‑functional teams and drive results
Physical Requirements / Work Environment
Ability to stand for extended periods of time
Ability to lift up to 50 lbs
Ability to work in PPE and clean room/controlled environments
Flexibility to work various shifts and overtime as required
Benefits We offer competitive remuneration, an annual incentive plan, healthcare, and a comprehensive range of employee benefits. Thermo Fisher Scientific provides employment with an innovative, forward‑thinking organization and outstanding career and development opportunities.
Our benefits include
Medical, Dental, and Vision benefits – effective Day 1
Paid Time Off & Designated Paid Holidays
Retirement Savings Plan
Tuition Reimbursement
Additional Information
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, including a drug screening
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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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, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift
Job Description Lead Operator, Manufacturing Operations
Thermo Fisher Scientific’s oral solid dose (OSD) site in Cincinnati, Ohio, supported by over 800 employees, offers various drug development and commercial manufacturing services. These services include controlled and sustained release solid oral dosage forms, osmotic release dosage forms (laser drilling), liquid fill hard capsules, controlled substances manufacturing, and abuse-deterrent dosage forms.
Discover Impactful Work
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Every day, our colleagues bring our Mission to life—enabling our customers to make the world healthier, cleaner, and safer. In this role, you’ll support critical manufacturing operations that contribute to protecting the environment, ensuring food safety, and advancing life‑saving therapies.
Position Summary Join our manufacturing team as a Lead Operator, where you will play a critical role in leading daily production activities while mentoring and developing team members. You will ensure consistent execution of manufacturing processes, uphold the highest standards of safety and quality, and drive continuous improvement initiatives. This role offers the opportunity to work with advanced manufacturing technologies while supporting operational excellence in a regulated environment.
Shift Monday-Wednesday 6:00pm-6:30am
A Day in the Life You will:
Lead and coordinate daily manufacturing operations to ensure production goals are met safely, efficiently, and in compliance with cGMP and ISO standards
Serve as a technical and operational resource for operators, providing guidance, training, and mentorship
Review and execute manufacturing documentation, including SOPs, batch records, and work instructions
Troubleshoot complex manufacturing equipment and process issues, escalating as appropriate
Support and drive continuous improvement initiatives, including lean manufacturing practices
Ensure strict adherence to safety protocols and clean room/controlled environment requirements
Collaborate cross-functionally with Quality, Engineering, and Supply Chain teams
Participate in documentation review, deviation investigations, and corrective action implementation
Maintain accurate records using manufacturing software systems and ERP platforms
Keys to Success Education
High School Diploma or equivalent required
Bachelors Dedree Preferred fields of study: Engineering, Chemistry, Biology, or a related discipline
Technical certifications in manufacturing or a related field are beneficial
Experience
Minimum of 4 years of manufacturing experience, with demonstrated leadership capabilities
Experience working in regulated manufacturing environments
Proven success leading teams, training operators, and managing multiple priorities
Experience with batch record review and documentation in cGMP-regulated settings
Knowledge, Skills, Abilities Knowledge
Strong understanding of cGMP, ISO standards, and regulatory requirements
Knowledge of lean manufacturing and continuous improvement methodologies
Skills
Advanced troubleshooting and problem‑solving skills
Proficiency with manufacturing software systems, ERP platforms, and Microsoft Office Suite
Strong communication and interpersonal skills
Abilities
Ability to lead, mentor, and develop team members
Exceptional attention to detail and commitment to quality
Strong analytical and decision‑making capabilities
Ability to coordinate cross‑functional teams and drive results
Physical Requirements / Work Environment
Ability to stand for extended periods of time
Ability to lift up to 50 lbs
Ability to work in PPE and clean room/controlled environments
Flexibility to work various shifts and overtime as required
Benefits We offer competitive remuneration, an annual incentive plan, healthcare, and a comprehensive range of employee benefits. Thermo Fisher Scientific provides employment with an innovative, forward‑thinking organization and outstanding career and development opportunities.
Our benefits include
Medical, Dental, and Vision benefits – effective Day 1
Paid Time Off & Designated Paid Holidays
Retirement Savings Plan
Tuition Reimbursement
Additional Information
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, including a drug screening
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
#J-18808-Ljbffr