Scientist I, Analytical Research & Development

Thermo Fisher Scientific • Florence, SC

1d • Onsite

About The Position

The Scientist I develops, qualifies, validates, and implements analytical methods for Quality Control (QC) use, primarily supporting pharmaceutical development and manufacturing of small-molecule active pharmaceutical ingredients (APIs). The role applies critical thinking and scientific judgment to plan and execute experiments, troubleshoot analytical challenges, and progress complex method-related work independently while seeking guidance when appropriate. The Scientist follows applicable cGMP and laboratory safety requirements, maintains accurate and complete records, and communicates methods, data, and conclusions clearly. The role collaborates with colleagues and cross-functional teams to support method implementation and manufacturing needs.

Work is scheduled standard Monday through Friday in a laboratory setting. Analytical techniques and equipment may include high-performance liquid chromatography (HPLC), gas chromatography (GC), mass spectrometry, and wet chemistry. The position requires movement around office and laboratory locations, periodic and extended standing or walking, and other physical activities. Personal protective equipment may be required depending on the work.

A bachelor’s degree in Chemistry is required. No prior laboratory experience is required, and new graduates are encouraged to apply; laboratory experience and experience in a GLP or GMP/cGMP environment are preferred. The employee must be legally authorized to work in the United States without sponsorship and pass a comprehensive background check, including drug screening. Relocation assistance is not provided.

Requirements

• Bachelor’s degree in Chemistry.
• Working knowledge of chemistry, analytical instrumentation, and qualitative and quantitative analysis.
• Ability to follow technical procedures and interpret analytical results.
• Logical problem-solving skills and sound scientific judgment.
• Clear written, verbal, and interpersonal communication skills.
• Ability to contribute to technical documents such as SOPs, protocols, and reports.
• Proficiency with Microsoft Office applications.
• Ability to organize work and contribute to multiple projects.
• Must be legally authorized to work in the United States now or in the future, without sponsorship.
• Must be able to pass a comprehensive background check, which includes drug screening.
• Ability to meet the described physical requirements, including moving about office and laboratory locations; standing, walking, stooping, kneeling, or crouching; moving items weighing approximately 10 to 35 pounds; and performing laboratory and computer work.

Nice To Haves

• Laboratory experience.
• Experience in a GLP or GMP/cGMP environment.
• Experience with analytical instrumentation such as HPLC, GC, inductively coupled plasma (ICP), or mass spectrometry.

Responsibilities

• Follow current good manufacturing practices (cGMP), applicable safety requirements, standard operating procedures (SOPs), and laboratory procedures.
• Maintain a clean, organized, and safe work area, including laboratory equipment, instruments, and testing materials.
• Develop, qualify, validate, and implement analytical methods for QC use, primarily supporting small-molecule APIs and their manufacturing.
• Plan and execute analytical work, troubleshoot method and instrument issues, and progress complex problems independently, seeking input or escalation when appropriate.
• Use analytical techniques and equipment appropriate to assigned work, which may include HPLC, GC, mass spectrometry, and wet chemistry.
• Evaluate analytical data for accuracy, completeness, and scientific relevance.
• Promptly communicate unexpected results, method performance concerns, and other issues through established procedures.
• Document experimental work, data, observations, and conclusions accurately in required laboratory systems and records.
• Prepare or contribute technical information for analytical methods, qualification and validation protocols and reports, SOPs, and other technical documents.
• Communicate work progress, technical challenges, and results clearly to colleagues and project teams.
• Plan and manage assigned work across multiple projects.
• Support analytical method implementation for QC use through technical documentation, knowledge transfer, and collaboration with relevant teams.

Benefits

• Medical, dental, and vision benefits effective Day 1.
• Paid time off and designated paid holidays.
• Retirement savings plan.
• Tuition reimbursement.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level