When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
 
Location/Division Specific Information
Cincinnati, OH – Pharma Services Group
 
How will you make an impact?
Supports execution for the development of new formulations and manufacturing processes of solids, liquids, and semi-solid dosage forms.  Increase and develop knowledge regarding drug toxicology, pre-clinical – phase III, scale-up, registration, validation and commercialization.  Communicate with technical leads, supervisors and project team peers (analytical and project management) on the progress and timely completion of activities and critical milestones. 
 
What will you do?

• Participates/supports the design, evaluation and execution of formulations for pre-clinical studies, clinical trials, registration, scale-up, and process validation to be commercialized as defined by client requirements.  
• Assures manufacturing and documentation is in accordance with cGMPs.  
• Participates in problem solving and stage gates for formulations, equipment and processes.  
• Supports or writes master batch records, reports, memos, and protocols as required or to support client regulatory submission to the United States Food & Drug Administration (FDA), European Medicines Agency (EMEA) or other regulatory agencies.  
• Supports technically challenging projects for upper level scientist and may lead simple projects on case by case basis. 
• Evaluates results and draft subsequent reports for all client projects.

How will you get here?
Education 

Minimum Bachelor of Science (BS) in science/engineering related field.  Pharmaceutical science or experience in pharmaceuticals development for solid oral dosage forms (preferred). 

Experience
 
Education or Experience in the pharmaceutical industry and/or a fast-paced pharmaceutical environment (CMO) focused on solid oral dosage form product development (preferred). 
 
Knowledge, Skills, Abilities

• Understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory compliance. 
• Basic knowledge of pharmaceutical manufacturing practices 
• Communicates and co-operates with others to meet project and team objectives 
• Proficiency using Microsoft (MS) Office applications (statistical knowledge preferred) 
• Demonstrated proficiency in written and oral communication skills 

• Demonstrated commitment to our 4i Values 
• Proficiency with the English language 

 
At Thermo Fisher Scientific, each one of our 75,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
 
Apply today! http://jobs.thermofisher.com
 
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.