Analytical Method Development Scientist (Pharma)

Eurofins • Groton, CT

5h • $22 - $24

About The Position

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Ability to work in a GLP or GMP environment with appropriate documentation and safety practices.
Using routine laboratory techniques, support drug substance/drug product formulation development through hands-on generation of accurate and precise analytical chemistry data
Techniques such as liquid chromatography (HPLC, UPLC), NMR (liquid), mass spectrometry, vibrational spectroscopy, gas chromatography, USP/EP dissolution testing, and/or Karl Fischer titration
Development and execution of studies to ascertain degradation mechanisms in the solution and solid state.
Development of assay/purity methods and assessment of method robustness/ruggedness
Development and execution of method validation protocols.
Development of dissolution methodology that will provide some measure of an in vivo / in vitro relationship and serve as a quality control procedure.
Transfer of analytical methods to other laboratories and remote sites.
Hands-on generation of data in support of accelerated and registration stability studies.

Requirements

• Bachelor’s degree in science or other related degree concentration, or equivalent directly-related experience
• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Ability to work in a GLP or GMP environment with appropriate documentation and safety practices.
• Authorization to work in the United States indefinitely without restriction or sponsorship

Responsibilities

• Support drug substance/drug product formulation development through hands-on generation of accurate and precise analytical chemistry data
• Development and execution of studies to ascertain degradation mechanisms in the solution and solid state.
• Development of assay/purity methods and assessment of method robustness/ruggedness
• Development and execution of method validation protocols.
• Development of dissolution methodology that will provide some measure of an in vivo / in vitro relationship and serve as a quality control procedure.
• Transfer of analytical methods to other laboratories and remote sites.
• Hands-on generation of data in support of accelerated and registration stability studies.

Benefits

• Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level