Associate Scientist - Synthetic Molecule Analytical Chemistry

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

This is a fully onsite role based at our customer’s site in South SF, CA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

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

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

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Our Laboratories Functional Service Partnership (FSP) team plays a direct role in advancing drug development by creating sustained groups of talent within our customers’ organizations to provide long-term support. Through this collaborative approach, our professionals bring their commitment to excellence, industry knowledge, and operational strength directly into customer environments, helping to enhance capabilities and advance the delivery of life-changing therapies.

Key responsibilities:

• Method Development & Execution: Develop, optimize, and execute chiral and achiral HPLC, alongside other analytical methods, to characterize synthetic molecule drug substances and drug product samples in both R&D and/or GMP settings.
• Cross-Functional Support: Execute various analytical methods (e.g., LC-MS, GC, IC, KF, UV, CAD, and dissolution) to support samples requests, and advance process and formulation development.
• Data Management: Rigorously document experiments and studies in an Electronic Lab Notebook (ELN), summarize findings, and interpret complex data.
• Troubleshooting: Identify and resolve instrument and technical method problems to ensure highly efficient laboratory operations.

Education and Experience:

• Bachelor's degree in lab sciences such as Chemistry, Biochemistry, or similar
• Assoc Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0-2 years’)
• Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’)
• OR Masters degree

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

• Laboratory Expertise: Strong foundation in general wet laboratory practices, analytical/organic chemistry, and hands-on experience with chromatography (HPLC and/or LCMS, including data handling and reporting).
• Professional Skills: Excellent time management, problem-solving, and written/oral communication skills with strong attention to detail.
• Team Dynamics: A collaborative mindset with the proven ability to work seamlessly in a team-oriented, fast-paced environment.
• Preferred Knowledge: Familiarity with applying cGMP/GLP guidelines to everyday documentation and instrument use, as well as knowledge of applicable regulatory authority, compendia, and ICH guidelines.

Working Environment:

Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

Able to work upright and stationary and/or standing for typical working hours.

Able to lift and move objects up to 25 pounds

Able to work in non-traditional work environments.

Able to use and learn standard office equipment and technology with

proficiency.

May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Benefits

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