Quality Control Chemist I - Virginia

Novo Nordisk•Petersburg, VA

39d•Onsite

About The Position

Novo Nordisk is seeking a Quality Control Chemist I for its new Petersburg, Virginia site, which focuses on Emerging Technologies (ET) within Chemical API development and production. This role is crucial for strengthening the Small Molecule (SMOL) strategy and amplifying operational capacity to support ET's SMOL projects. The position involves conducting analytical testing on materials and products in accordance with cGMP, site, and corporate procedures and policies. The company has a long history of tackling unmet medical needs in serious chronic diseases like diabetes and obesity, and this role contributes to improving the quality of life for millions worldwide.

Requirements

Bachelor’s degree in Chemistry, Microbiology or science-related field from an accredited university required and a minimum of one (1) year of experience with laboratory procedures and analytical chemistry techniques required.
Experience with GMP regulations and quality control procedures required.
Ability to troubleshoot laboratory equipment a plus.
Comprehensive knowledge of chemistry or microbiology and laboratory techniques required.
Good judgement and an understanding of chemistry theories and concepts required.
High consciousness for personal and laboratory safety required.
Detail-oriented with good documentation and record-keeping abilities required.
Good communication skills to effectively report findings and collaborate with other departments required.
Good collaboration skills with and interaction with many departments required.

Nice To Haves

May consider an Associate’s degree in Chemistry, Microbiology or science-related field from an accredited college or university with a minimum of three (3) years of experience with laboratory procedures and analytical chemistry techniques required.
May consider a High School Diploma or GED with a minimum of five (5) years of experience with laboratory procedures and analytical chemistry techniques required.

Responsibilities

Conduct analytical testing on materials and products in accordance with cGMP, site & corporate procedures & policies.
Analyze raw materials, intermediate and final API drug substance, pharmaceutical compounds and samples, which may include compiling & analysing data.
Ensure cleanliness of lab and restock supplies as needed.
Conduct review of peer data.
Maintain and adhere to cGMP guidelines.
Support communicating status and timing of analytical testing to internal clients.
Provide support in investigations of laboratory samples and help determine appropriate corrective and preventive actions.
Provide support to Deviations.
Follow all safety & environmental requirements in the performance of duties.
Other duties as assigned.