Formulations Manufacturing Manager

Thermo Fisher Scientific · Cincinnati

Work Schedule

Standard (Mon-Fri)

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), Office, Rapid flashing lights, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products 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:
Guide a collaborative team in manufacturing high-quality pharmaceutical and diagnostic products while ensuring compliance with cGMP standards and regulatory requirements. Support operational excellence through effective resource management, process optimization, and continuous improvement initiatives. Collaborate across teams to meet production goals, maintain quality standards, and deliver products on time. Support a culture of safety, quality, and innovation while developing team members' capabilities and fostering engagement.

REQUIREMENTS:
• Advanced degree plus 6 years of experience

Bachelor's degree plus 8 years of experience, in cGMP manufacturing environment, preferably in pharmaceutical or diagnostic manufacturing
Preferred Fields of Study: Chemistry, Engineering, Life Sciences, or related scientific/technical field
3+ years of demonstrated management/leadership experience supervising manufacturing teams
Strong understanding of cGMP regulations, quality systems, and regulatory compliance requirements
Demonstrated success in operational excellence and continuous improvement initiatives
Experience with manufacturing documentation, batch record review, and change control processes
Ability to conduct investigations, implement CAPAs, and support quality improvements
Strong project management and organizational skills to manage multiple priorities
Skilled in cross-functional collaboration and stakeholder management
Strong verbal and written communication skills in English
Proficiency with ERP systems, Microsoft Office suite, and quality management software
Ability to work in cleanroom environments and comply with gowning requirements
Physical capability to stand for extended periods and occasionally lift up to 25 lbs
Ability to work various shifts including nights/weekends as business needs require

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.

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