Formulation Scientist II

Thermo Fisher Scientific • Frederick, MD

4d • $32 - $48 • Onsite

About The Position

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.

Requirements

• 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

Nice To Haves

• 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

Responsibilities

• 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

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees