Formulation Scientist II

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly.

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, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs 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.

Join our Clinical Next-Generation Sequencing Division (CSD) Manufacturing Operations team as a Formulation Scientist II, where you will play a critical role in delivering innovative scientific solutions. In this role, you will perform complex formulation and manufacturing activities within a GMP-regulated environment, leveraging advanced technologies to support the development and production of high-quality biopharmaceutical products.

You will collaborate across cross-functional teams to support technology transfer, process validation, and commercial manufacturing, while continuously driving process improvements and maintaining the highest standards of quality and compliance.

• Perform complex formulation and manufacturing operations in a GMP environment
• Execute and support technology transfer and process validation activities
• Maintain accurate and compliant documentation in accordance with GMP standards
• Operate and troubleshoot analytical and manufacturing equipment (e.g., HPLC, PCR, cell culture systems)
• Apply aseptic techniques and work effectively in cleanroom environments
• Collaborate with cross-functional teams including Quality, R&D, and Manufacturing
• Analyze data, identify trends, and contribute to continuous process improvement initiatives
• Support deviation investigations, root cause analysis, and CAPA implementation
• Train and mentor team members as needed
• Advanced degree (Master’s or PhD) in a scientific field with no prior experience required, OR Bachelor’s degree with 2 years of experience in pharmaceutical/biotechnology manufacturing or laboratory environment
  
  

Preferred Fields Of Study

• Chemistry, Biology, Biochemistry, Biotechnology, Chemical Engineering, or related scientific discipline
• Demonstrated experience with GMP manufacturing processes and documentation practices
• Strong understanding of aseptic techniques and cleanroom operations
• Hands-on experience with analytical techniques (e.g., HPLC, PCR, cell culture)
• Knowledge of process validation and technology transfer activities
• Familiarity with regulatory requirements (FDA, EMA, etc.)
• Experience with process improvement methodologies (Lean, Six Sigma)
• Strong troubleshooting, analytical, and problem-solving skills
• Excellent documentation and data analysis capabilities
• Proficiency in Microsoft Office and laboratory information systems
• Strong organizational skills and attention to detail
• Effective written and verbal communication skills
• Ability to work both independently and collaboratively
• Ability to lift up to 20 lbs regularly and up to 45 lbs with assistance
• Ability to work in a laboratory/manufacturing environment, including cleanrooms
• Flexibility to work varying schedules, including weekends or holidays as needed
  
  

Compensation And Benefits

The hourly pay range estimated for this position based in Maryland is $31.73–$47.60.

This Position May Also Be Eligible To Receive a Variable Annual Bonus Based On Company, Team, And/or Individual Performance Results In Accordance With Company Policy. We Offer a Comprehensive Total Rewards Package That Our U.S. Colleagues And Their Families Can Count On, Which Includes

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs
• Employee assistance and family support programs, including commuter benefits and tuition reimbursement
• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
  
  

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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