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Thermo Fisher Scientific · 1 day ago

FSP - Scientist - Analytical Development , Small Molecule

New Brunswick, NJ

Full-time

Onsite

Entry, Mid Level

2+ years exp

Thermo Fisher Scientific is a global leader in scientific services, dedicated to making the world healthier, cleaner, and safer. The Scientist in Analytical Development will conduct analytical testing and support method development for small molecule pharmaceuticals, ensuring quality and accuracy in drug product development.

BioinformaticsBiotechnologyCloud Data ServicesConsultingHealth CareLife ScienceManagement Information SystemsOffice SuppliesPrecision Medicine

No H1B

Responsibilities

Support analytical method development and drug product development

Hands-on experience and knowledge in small molecule pharmaceutical analysis

Critical analysis of analytical results with the goal of improving the robustness of analytical methods and enhancing understanding of key drug product quality attributes

Reviewing, interpreting, and communicating analytical results and conclusions effectively, both orally and in writing

Qualification

HPLC/UPLCDissolutionAnalytical method validationPharmaceutical industry experienceEmpowerProblem-solving skillsCommunication skillsWork independentlyWork collaboratively

Required

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

Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years')

OR Masters degree

Experience with various analytical techniques including HPLC/UPLC, Dissolution and KF

Pharmaceutical industry experience in the core analytical techniques of HPLC and Dissolution

Knowledge in analytical method validation and knowledge of analytical method validation requirements as defined by ICH

Experience in analytical development in support of drug product formulation development

Ability to execute and document scientific experiments and effectively communicate study results

Experienced in drafting and delivering analytical studies, with a strong ability to follow written procedures and protocols

Demonstrated ability to work independently as well as collaboratively within cross-functional teams to achieve shared objectives

Strong problem-solving and troubleshooting skills

Strong written and oral communication skills

Preferred

Experience with GC is a plus

Experience with Empower is desirable

Experience in performing dissolution testing using biorelevant media, for active ingredients and drug formulations to facilitate biopharmaceutics risk assessment and support drug product development is a plus

Familiar With USP, ICH And Other Compendial Requirements