Job Description

• Job Type:Contract

Posted about 7 hours ago

• Expiry Date: 19 May 2023
• Referral: 225936@accuick.com

: Purpose and Scope Of Position: The primary focus of the Quality Control Associate I role will be to support drug product lot release and in-process testing within a cGMP environment. Required Competencies: Knowledge, Skills, and Abilities:

• Education BS in Scientific discipline

Experience:

• 0-3 years of regulated industry experience, or equivalent combination of education and experience.

Knowledge, Skills, and Abilities:

• Ability to work in a high paced team environment, meet deadlines, and prioritize work from multiple projects.
• Strong analytical and communication skills.
• Computer proficiency as well as the ability to master new software programs.
• Experience working in a GMP environment is preferred.
• Demonstrated success working in a high-performing, business results-driven environment.

Duties and Responsibilities: Key Responsibilities:

• Perform or support cGMP lot release, in-process, and stability testing using various software packages. Ensure timely completion of testing and tasks as assigned.
• Support assay transfer and method validation of by executing cross-site validation protocols and providing data to support final reports.
• Identify opportunities for continuous improvements.
• Maintain instrumentation and equipment preventative maintenance and supporting documentation in a cGMP compliant manner.
• Assist in the implementation of new assay methodologies and the associated instrumentation
• Identify and support initiation of Deviations, CAPAs and Laboratory Investigations.

Working Conditions (US Only):

• While performing the duties of this job, the employee is frequently required to stand; walk; sit; bend; stretch; use hands and fingers, with various manipulations; reach with hands and arms; and effectively communicate with others in the workplace, including the ability to make and promptly respond to audible cues and warnings.
• Work in areas that may have strong magnets. May work in areas with exposure to vapor phase liquid nitrogen.
• Must have ability to work assigned shift (Day, Night, Weekends and/or holidays).
• Will be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include, but not limited to: safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hairnets, gloves, and hearing protection. Require to work in and around laboratories and controlled, enclosed, restricted areas, included clean rooms.
• Require to carry and/or lift up to 10 pounds several times a day.

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.