Associate Formulations Scientist

Eurofins•Groton, CT

6h•$22 - $27

About The Position

Preparation of prototype formulations (solutions, suspensions, tablets, capsules, powder blends, semi-solid dosage forms, sterile and non-sterile liquids) for exploratory studies in in-vitro and in-vivo models Development of oral, topical, and intravenous (sterile) dosage forms for feasibility studies and small-scale manufacturing operations Measurement of key active compound and formulation properties (such as solubility, tablet hardness, disintegration, pH, isotonicity, color, gelling tendency, etc.) Assessment of the chemical and physical stability of prototype formulations, as well as the performance of prototype formulations using in-vitro tests (non-sink dissolution, precipitation, etc.) Identify potential stability and performance issues with prototype formulations Development of protocols for preparation of formulations at preclinical and clinical study site

Requirements

Experience with drug formulation and pre-formulation techniques, and an understanding of drug candidate properties
Basic chemistry (wet or solid state) laboratory experience.
Experience working with laboratory equipment, mechanically inclined.
Ability to follow procedures reliably and consistently,
Strong computer and organizational skills
Adept in Microsoft office
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivared, adaptable, and a positive attitude
Ability to learn new techniques, keep accurate records, follow instructions, and comply with company policies

Responsibilities

Preparation of prototype formulations (solutions, suspensions, tablets, capsules, powder blends, semi-solid dosage forms, sterile and non-sterile liquids) for exploratory studies in in-vitro and in-vivo models
Development of oral, topical, and intravenous (sterile) dosage forms for feasibility studies and small-scale manufacturing operations
Measurement of key active compound and formulation properties (such as solubility, tablet hardness, disintegration, pH, isotonicity, color, gelling tendency, etc.)
Assessment of the chemical and physical stability of prototype formulations, as well as the performance of prototype formulations using in-vitro tests (non-sink dissolution, precipitation, etc.)
Identify potential stability and performance issues with prototype formulations
Development of protocols for preparation of formulations at preclinical and clinical study site