Work ScheduleStandard (Mon-Fri)
Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, 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 DescriptionTitle: Manufacturing Process Manager Division/Site Specific InformationPosition will sit onsite at the Florence, SC site and will support the Drug Substance Division (DSD) at Thermo Fisher Scientific. This role, reporting to the Production Planning Manager, ensures the flawless import of materials and goods at our Florence, South Carolina locations.
Discover Impactful Work:Join us as a Process Manager (Area Manager) in Manufacturing and contribute to excellence in process development and manufacturing optimization of active pharmaceutical ingredients. You'll provide technical leadership in developing, validating, and implementing robust manufacturing processes while collaborating across multiple departments to ensure successful scaling and optimization of new and existing processes. Make meaningful contributions to innovative solutions that help our customers make the world healthier, cleaner, and safer.
A Day in the Life:- As a key technical expert, you'll lead complex projects, provide manufacturing support, conduct process improvements, and drive technology transfer initiatives.
- You'll collaborate with cross-functional teams including R&D, Quality, Engineering, and Production to achieve project goals and maintain high quality standards.
- Your expertise will be essential in troubleshooting, optimizing processes, and implementing data-driven solutions while ensuring compliance with regulatory requirements.
Keys to Success:Education- BS Degree Required. Preferred Fields of Study: Chemical Engineering, Chemistry, Polymer Chemistry, Process Engineering, or a similar background.
- Advanced degree preferred.
Experience
- Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of experience in process development, scale-up, and manufacturing optimization required.
- Experience leading cross-functional teams and managing complex technical projects.
- Experience with quality systems and risk assessment methodologies.
- Experience developing and supporting team members.
Knowledge, Skills, Abilities- Deep technical expertise in process development, scale-up, and manufacturing optimization
- Strong background in GMP manufacturing and regulatory compliance (FDA, EMA, ISO)
- Advanced analytical and problem-solving skills with expertise in statistical analysis and DOE
- Proven ability to troubleshoot complex process issues and implement corrective actions
- Strong documentation skills including SOPs, batch records, validation protocols and reports
- Expertise in data analysis, process modeling, and trending
- Excellence in technical writing and presentation skills
- Strong interpersonal and communication abilities for collaborating with internal/external stakeholders
- Ability to work in cleanroom/GMP manufacturing environments
- Proficiency with statistical software and standard business applications
- Travel may be required (
- Knowledge of Lean/Six Sigma methodologies preferred
Benefits
We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.
