Process Engineer III

Full-timeSENIOREngineeringOncologyPhDMay Not Sponsor
$97K - $146K/yr(estimated)
Estimated based on industry data, role level, and location. Actual compensation may vary. Required by CO/NYC/CA salary transparency laws.
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Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

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 team as a Process Development Scientist III, where you'll contribute to innovation in developing and optimizing critical processes for therapeutic development. You'll apply your expertise to design, implement, and validate scientific methodologies for manufacturing pharmaceutical products across pre-clinical through commercial stages. Working with advanced technology and collaborating with cross-functional teams, you'll address complex technical challenges while ensuring the highest quality standards. Your work will directly impact patient lives by helping deliver breakthrough therapies in areas including cell therapy, viral vectors, and biologics manufacturing.

REQUIREMENTS:
•Bachelor’s degree required in a scientific field, preferably an engineering field.  

5+ years of experience in GMP regulated Biologics / Pharma Industry, or equivalent experience (or master's degree in a scientific field + 3 years' experience or Ph.D.). 

• Expertise in analytical techniques including HPLC, PCR, flow cytometry, and cell-based assays
• Strong knowledge of cGMP regulations and quality systems in pharmaceutical manufacturing
• Demonstrated ability to manage multiple complex projects independently
• Experience with technology transfer and process scale-up activities
• Advanced skills in experimental design, data analysis, and statistical methods
• Demonstrated expertise in documentation including SOPs, protocols, and technical reports
• Strong problem-solving abilities and scientific creativity
• Excellent written and verbal communication skills
• Ability to work effectively in cross-functional teams
• Proficiency with relevant software including MS Office, statistical analysis tools
• Experience mentoring colleagues and serving as technical subject matter expert
• Schedule flexibility including occasional evenings/weekends as needed
• Up to 20% travel may be required

Benefits

We offer competitive remuneration, annual incentive plan bonus, 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!

Other

Relocation assistance is not provided.

Must be legally authorized to work in the United States now and in the future, without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

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OncologyEngineeringSt. Louis, Missouri, USA
TF

Thermo Fisher Scientific

OTHER

LocationWALTHAM, MA
Employees50000+
Open Jobs1998

Pipeline

Retrospective Cohort EnrollmentN/A
Technical Evaluation of Brahms PCT DirectN/A
Blood sample collectionN/A
Blood samplingN/A
RimegepantN/A