Job Description:

Duties and Responsibilities:

• Lead/support investigations through data gathering or interview process.

• Performs routine testing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment.

• Executes routine procedures based on methodologies/responsibilities of the specific QC sub-team.

• Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s).

Knowledge and skills:

• BS or Associate Degree - knowledge of science generally attained through studies resulting in a BS in the physical or life sciences, a related discipline, or the equivalent in related experience. 0-3 years of experience.

• Knowledge of basic laboratory techniques such as pH, volumetric measurement, pipetting, analytical weighing and basic laboratory safety practices preferred.

• Attention to detail and demonstrated organizational skills.

• Demonstrated manual dexterity.

• Knowledge of basic electronic systems (email, MS Office, etc.)

About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities

ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

Contact:

Full Name: Akash Mehra

Email ID: akashm@askconsulting.com

Phone: 908-224-9613