Scientist I, Analytical Research & Development

Thermo Fisher Scientific • Florence, SC

1d

About The Position

The Scientist I develops, qualifies, validates, and implements analytical methods for Quality Control (QC) use to support pharmaceutical development and manufacturing, primarily for 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, seeking guidance when appropriate.

The Scientist I 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 successful method implementation and manufacturing needs.

Requirements

• Bachelor’s degree in Chemistry.
• Working knowledge of chemistry, analytical instrumentation, and qualitative and quantitative analysis.
• Familiarity with pharmaceutical quality and regulatory requirements, including GMP.
• 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.

Nice To Haves

• Laboratory experience is preferred; no prior laboratory experience is required.
• Experience in a GLP or GMP/cGMP environment is preferred.
• Experience with analytical instrumentation such as HPLC, GC, inductively coupled plasma (ICP), or mass spectrometry is preferred.
• New graduates are encouraged to apply.

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 Quality Control (QC) use, primarily to support small-molecule active pharmaceutical ingredients (APIs) and their manufacturing.
• Plan and execute analytical work, troubleshoot method and instrument issues, and progress complex problems independently.
• 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, progressing tasks independently and seeking input or escalation when appropriate.
• 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