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Quality Control Manager in Chicago at Next Level Performers

Date Posted: 10/25/2018

Job Snapshot

Job Description

Quality Control Manager

Are you a Quality Control Manager looking for a career with a 100-year-old high growth company who is a leader in biopharmaceutical and pharmaceutical industry?

Does your biopharmaceutical Quality Control Manager experience include High Purity Ingredients and are you current with cGMP’s?

Are you looking for a company where your aptitude for learning will determine your career path?

If so, we would love to talk to you!

A Day in the Life of the Quality Control Manager:

Reporting to the VP of Research and Development, you will manage departments and direct report QC scientists responsible for the testing of raw materials, in-process samples, finished products, and cleaning samples in support of the release of materials.

•       You are responsible for assigning and prioritizing the workload for the group to meet defined due dates, while also evaluating and managing initiatives for departmental process improvements.

•       Coordinate testing at external laboratories.

•       Lead laboratory investigations, document deviations and develop corrective and preventive action plans.

•       Additionally, this position will support other activities associated with laboratory operation and will review data for compliance, review policy and procedure documents as necessary to meet cGMP regulations and applicable guidelines. Perform training of other scientists. Act as a resource for instrument troubleshooting and guidance as well as mentoring to other scientists. 

Job Requirements

What it takes to be Successful:

•       Ability to work in a complex, fast-paced environment.

•       Manage a team of QC scientists through testing assignments, prioritization, and training

•       Develop and drive process improvement initiatives to improve QC departmental efficiencies

•       Perform testing, including raw materials, in-process samples, finished products, and cleaning samples in support of the release of materials

•       Effectively communicates with management on product status and problems encountered

•       Review analytical data for compliance with PI policies and procedures, and cGMP regulations and ICH guidelines

•       Coordinate with Stability Supervisor when QC support is required

•       Lead laboratory investigations, document deviations and develop corrective and preventive action plans

What we are looking for:

•       BS degree or equivalent

•       10+ years of experience (Supervisor / Manager) in a related position

•       Working knowledge of the cGMP regulations

•       Working knowledge of safe handling practices of dangerous chemicals

•       Computer skills (spreadsheet, database, and word processing window based programs)

•       Hands-on experience with the operation and maintenance of analytical instrumentation. (Preferred: HPLC and GC using Empower, Polorimitery, Automatic titrators, TOC and LAL)

Compensation and Benefits

$100,000

Excellent union Benefits

Next Level Performers and their clients are Equal Opportunity Employers

Key Words: Quality Control, Quality Assurance, Manufacturing, Pharmaceutical, QC, QA

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