Scientist - Analytical Plate Based Assays

Responsibilities

The Scientist will support the Quality Control Method Transfer and Validation team by performing method validation activities including drafting protocols and reports, executing validation assays, and conducting data analysis

This role also involves procedural updates, reviewing various reports, and ensuring compliance with cGMP and data integrity principles

Independently conceptualize, plan, and execute laboratory experiments

Collaborate with colleagues and subject matter experts to determine the most suitable analytical methodologies to support project initiatives, including the use of computational predictive tools, modeling software, and data visualization tools

Lead and manage multiple projects, assisting teams in developing effective strategies for analytical needs and controls

Engage with the method development team and participate in both in-process and final product sample analyses

Author relevant sections of technical reports to support interdepartmental technology and method validation and transfer processes

Prepare technical reports, critically review data, and evaluate new instrumentation and analytical techniques/approaches as required

Independently analyze experimental data and provide conclusive insights

Mentor junior scientists and offer technical guidance

The position follows a 1st shift schedule from Monday to Friday, 8 AM to 5 PM, with occasional weekend work on a rotating basis

We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form ( . The EEOC "Know Your Rights" Poster is available here ( .

To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: .

Skills and Requirements

-5-6 years of experience

-Experience executing laboratory assays, drafting protocol deviations under supervision, and performing data reviews

-Skilled in Anthrone, Lowry, Softmax, Spectramax and ELISA null

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to ....