Manufacturing Sciences Scientist

Work Schedule

Standard (Mon-Fri)

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, Laboratory Setting, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials

Location:

Miami, FL. Relocation assistance is NOT provided.

Must be legally authorized to work in the United States without sponsorship.

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

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.

Join our team at Thermo Fisher Scientific as an entry level to early career Scientist where you'll contribute to our mission of enabling customers to make the world healthier, cleaner and safer. In this role, you'll support manufacturing operations by developing, optimizing and implementing production processes while ensuring compliance with quality standards. You'll collaborate with cross-functional teams to manufacture critical products for diagnostics, research, and therapeutic applications.

The position offers opportunities to enhance processes, solve technical challenges, and directly impact patient care through high-quality manufacturing.

• Contributes to investigations, support, and implementation of products and processes.
• Responsible for creating and reviewing SOPs and Batch Records for accuracy.
• Assist with technical transfers.
• Communicates any gaps, errors, or improvement recommendations.
• Contributes to analysis and documentation of data summary reports.
• Models our 4i values, integrity. Innovation, intensity, and involvement.
• Complies with our Quality Policy by continuously improving the quality of our products & services and by ensuring global regulatory compliance.
• Generates data tables/slides and record drafts.
• Contribute to investigations and deviations.
• Accurately capture information and perform calculations within documents.
• Draft documents, e.g., batch records, summary reports, and SOPs.

• Minimum
  
  Education required:
  
  Bachelor's degree (Preferred Fields of Study: Chemistry, Biochemistry, Chemical Engineering, Biotechnology, or related scientific field)
• Minimum Experience
  
  Required:
  
  1 year of hands‑on experience or related coursework

• Previous experience in a scientific research laboratory.
• Prior experience in updating controlled documentation such as SOPs, batch records, and product specifications.
• Experience with chromatography, spectroscopy, and other analytical instrumentation
• Demonstrated proficiency in standard laboratory techniques and equipment operation
• Experience with responsible use of language learning models and generative artificial intelligence (ChatGPT etc.)

• Proficiency in Microsoft Office applications including Excel, Power
  
  BI, as well as laboratory information systems
• Ability to use QMS and other documentation systems with guidance.
• Understanding of bioanalytical methods, wet chemistry protocols, and good documentation practices
• Ability to grasp a working knowledge of GMP, GDP, and other relevant regulatory requirements
• Strong technical writing skills.
• Strong analytical, critical thinking and problem‑solving abilities
• Effective written and oral communication skills and ability to work collaboratively in teams
• Ability to work various schedules including potential…