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Full-time
bachelor degree, postgraduate degree
Posted 22d ago
~40 hrs/week
Responsibilities
The Manufacturing Sciences Supervisor will lead technical operations in a GMP-regulated environment, supporting scientists and engineers while serving as the technical owner for customer programs. They are responsible for overseeing process execution, standardizing methodologies, and driving continuous improvement initiatives to ensure operational efficiency and regulatory compliance.
Requirements
Candidates must possess an advanced degree with 3 years of experience or a bachelor's degree with 5 years of experience in the GMP-regulated pharmaceutical or biologics industry. Strong knowledge of pharmaceutical manufacturing processes, cGMP requirements, and demonstrated leadership experience are essential for this role.
Full job description
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION: Join our collaborative team at Thermo Fisher Scientific as a Manufacturing Sciences Supervisor, where you'll guide technical operations in a GMP-regulated environment. You'll support a team of scientists and engineers while serving as the technical owner for customer programs in manufacturing. Working at the intersection of process development and production, you'll contribute to innovation and excellence in pharmaceutical technologies while ensuring compliance with quality standards. This role offers the opportunity to contribute to life-changing therapies while developing your leadership skills in an innovative organization.
In this position, you'll oversee process execution, standardize methodologies, review critical documentation, and provide technical expertise for manufacturing operations. You'll collaborate across functions to optimize processes, implement improvements, and ensure efficient operations. Your expertise will be valuable in supporting team members, managing timelines, and maintaining productive partnerships with stakeholders to deliver exceptional results for our customers.
Essential Functions:
Lead by developing and empowering staff; cultivating relationships; managing performance and career development; building effective teams through hiring and training to apply diverse skills and perspectives; driving engagement and creating a climate where our staff are motivated to do their best.
Actively participate in team meetings and interact with operational, analytical and project management staff to meet customer objectives. Contribute to development of realistic work plans and lead technical meetings with customers.
Recommends and assists in implementing organizational and technical improvements designed to enhance the efficiency, reliability, and productivity of operations all conforming to applicable regulatory standards.
Integrate a risk-based approach during project execution and design mitigation strategies in alignment with our customers. We lead problem solving for equipment and processes, including investigation of incidents on the manufacturing floor, and drive to the true root cause. Design experiments and formulate statistics to support findings.
Draft and review quality batch production records, reports, and protocols to support client and project milestones. Ensure the collection and interpretation of data and conduct scientific review to substantiate conclusions and recommendations.
Role model compliance with Standard Operating Procedures (SOP), Good Manufacturing Practices (GMP), Environmental, Health & Safety (EH&S) and other regulatory requirements related to pharmaceutical development.
Develop and maintain an in-depth knowledge of pharmaceutical processes, equipment, instrumentation, and procedures, including assisting in implementing organizational and technical improvements to enhance reliability, productivity and follow regulatory standards.
REQUIREMENTS:
Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in GMP-regulated Pharmaceutical/Biologics industry.
3 Years leadership experience preferred
Preferred Fields of Study: Chemistry, Chemical Engineering, Materials Science, Pharmaceutical Science or related science or engineering field
Advanced knowledge of pharmaceutical manufacturing processes for solids, liquids, and semi-solid dosage forms.
Strong understanding of cGMP requirements and US/EU regulatory standards
Demonstrated ability to manage teams and complex projects
Experience with process validation, technology transfer, and scale-up activities
Proficiency in technical writing and documentation (batch records, validation protocols, technical reports)
Strong problem-solving skills for deviations and implementation of corrective actions
Excellent interpersonal and communication skills for cross-functional collaboration
Proficient in Microsoft Office Suite and relevant manufacturing systems
Ability to work in manufacturing areas wearing appropriate PPE
Ability to support manufacturing operations as needed
Experience with continuous improvement methodologies (Lean, Six Sigma, or PPI)
Knowledge of risk assessment and root cause analysis techniques
Experience in developing and supporting technical staff
Location, Work Authorization & Pre-Employment Requirements
Please review the following requirements before applying:
Relocation: Relocation assistance is not available for this position.
Work Authorization: Applicants must be legally authorized to work in the United States without current or future employer-sponsored work authorization.
Pre-Employment Screening: Employment is contingent upon successful completion of all applicable pre-employment requirements, including a background check and drug screening, in accordance with company policy and applicable law.
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
For more information, please visit www.thermofisher.com.
Offices: 168 Third Avenue, Waltham, MA, US
Analytical InstrumentsLaboratory Supply Chain Programs and eCommerceLaboratory EquipmentLab ServicesSpecialty DiagnosticsLife SciencesPharma Servicesand CDMOElectronicsHealth Care
How many Manufacturing jobs are open in Cincinnati, OH right now?
There are currently 957 open manufacturing positions in Cincinnati, OH listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Cincinnati, OH?
Companies currently hiring include Thermo Fisher Scientific, Baxters North America, Quest Defense, CREMER North America, LP, Givaudan, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Manufacturing jobs in Cincinnati, OH?
Yes — 77 of the 957 open manufacturing positions offer remote or hybrid work (28 remote, 49 hybrid).
How do I apply for Manufacturing jobs in Cincinnati, OH?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.