Analytical Chemist- Method Development & Validation

Eurofins USA BioPharma Services•Lancaster, PA

1d•Onsite

About The Position

Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The role requires expertise in chromatography and method validation and applies GMP in all areas of responsibility, as appropriate. The position performs a variety of analytical tasks to validate methods used for testing drug products and raw materials, using procedures such as HPLC, GC, UV/Vis, and dissolution. It involves reading, understanding, and interpreting analytical procedures; conducting analytical investigations; troubleshooting instrumentation and communicating with vendors when needed; training and mentoring junior staff in laboratory procedures; and managing and discussing projects with clients. This is a full-time, first-shift, onsite position scheduled Monday through Friday, 8 a.m. to 4 p.m. Candidates within commuting distance of Lancaster, Pennsylvania, are encouraged to apply. Travel of up to 25% may be required.

Requirements

Bachelor's or master's degree in analytical chemistry or another related degree concentration.
Industry experience: 4 or more years with a bachelor's degree, 2 or more years with a master's degree, or 1 or more year with a PhD.
At least 3 years of industry experience with chromatography.
At least 3 years of experience with LC chromatographic validation in a GMP environment.
Authorization to work in the United States indefinitely without restriction or sponsorship.
Excellent oral and written communication skills 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.

Nice To Haves

Candidates currently living within a commutable distance of Lancaster, Pennsylvania, are encouraged to apply.

Responsibilities

Perform method validations, method transfers, and method verification activities for APIs and finished products.
Apply GMP in areas of responsibility, as appropriate.
Perform analytical tasks to validate methods used to test drug products and raw materials using procedures including HPLC, GC, UV/Vis, and dissolution.
Read, understand, and interpret analytical procedures.
Conduct analytical investigations.
Troubleshoot instrumentation and communicate with vendors when required.
Train and mentor junior staff in laboratory procedures.
Manage and discuss projects with clients.