Associate Formulations Scientist

Eurofins USA PSS Insourcing Solutions•San Diego, CA

5d•Onsite

About The Position

Eurofins PSS West is seeking an Associate Formulations Scientist to support preformulation and formulation development at a client site in San Diego, California. Under guidance, the scientist prepares and characterizes prototype formulations for preclinical research, including oral, subcutaneous, and/or intravenous dosage forms for feasibility work and routine solutions and suspensions for preclinical studies. The role also evaluates formulation properties, stability, and performance, and conducts quantitative analyses using HPLC and supporting techniques. The scientist writes laboratory study protocols, records experimental procedures and observations in an electronic laboratory notebook, follows procedures consistently, and recognizes and escalates issues as appropriate. This is a full-time position with an 8 a.m.–5 p.m. schedule and occasional overtime. Candidates within commuting distance of San Diego are encouraged to apply. The position requires authorization to work indefinitely in the United States without restriction or sponsorship.

Requirements

Bachelor’s degree in Chemistry or a related field.
1–3 years of related experience, including at least 1 year in formulation development.
Experience with drug formulation and preformulation techniques and an understanding of drug candidate properties.
Experience preparing formulations and running feasibility studies, including small-scale operations with guidance.
Quantitative analytical HPLC experience.
Experience running routine laboratory work on time, productively, and with consistent quality, including HPLC, DSC, PXRD, spectroscopy, solubility determinations, dissolution testing, and suspension processing.
Ability to learn new techniques, handle multiple tasks, maintain accurate records, and comply with company policies.
Strong computer, scientific, and organizational skills.
Excellent oral and written communication skills and attention to detail.
Ability to work independently and on a team, with self-motivation, adaptability, and a positive attitude.
Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

Prepare prototype formulations, including solutions and suspensions, for exploratory in-vitro and in-vivo studies.
Prepare oral, subcutaneous, and/or intravenous (sterile) dosage forms for feasibility work and routine solution and suspension formulations for preclinical studies.
Measure properties of active compounds and formulations, including solubility, pH, isotonicity, color, and gelling tendency.
Assess the chemical and physical stability of prototype formulations.
Evaluate prototype formulation performance using in-vitro tests such as non-sink dissolution and precipitation.
Run quantitative analyses using HPLC and supporting techniques, including DSC, PXRD, and spectroscopy.
Write protocols for laboratory studies.
Record experimental procedures and observations in an electronic laboratory notebook (ELN).
Follow procedures consistently and recognize and escalate issues as appropriate.