Senior Chemist

Posted Nov 10, 2022 Grand Rapids, Michigan

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Expires Dec 10, 2022

Description

Description

If you want to be a part of launching a new analytical lab, transferring in new products, mentoring a growing team, and having your hard work recognized, we have a wonderful opportunity for you! Join a growing, fast-paced Grand Rapids based contract pharmaceutical manufacturer.

Job SUMMARY:

Support quality systems as they relate to the onboarding of new QC analytical testing related to cGMP drug products.

Examples of responsibilities include:

· Train Quality Control Chemists in new or revised test methods/procedures.

· Work cross functionally to transfer projects into the QC Analytical lab.

· Qualify new laboratory equipment.

· Work to author and execute CAPAs and Change Controls.

· Perform data review for accuracy, clarity, and adherence to GMP and/or GLP regulations.

Full job description available during formal interview process.

REQUIREMENTS: (education) 

Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology) and 6 years to 8 years of pharmaceutical or chemical testing experience. Or Master’s degree and a minimum of 4 years of pharmaceutical or chemical testing experience. Previous experience in Quality Control preferred.

What sets GRAM apart from other employers:

BENEFITS Starting day 1! Blue Cross/Blue Shield medical and dental with the company paying for 75% of the cost is available to you and your family on your first day of work. We also offer vision, life, disability, a 401(k) program, and off-shift premiums.

Paid VOLUNTEERISM Starting day 1! GRAM encourages giving back to your community by offering 16 hours of volunteer time per calendar year.

PTO! Full-time employees accrue up to 3 weeks of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!

HOLIDAYS: We celebrate diversity in offering 8 paid holidays per calendar year.

Pay: Depends on Experience JOB SUMMARY

Support quality systems as they relate to the onboarding of new QC analytical testing related to cGMP drug products. These duties include, but are not limited to document authoring and review, test method validation/verification execution and continuous improvement projects.

Company/Organization

Grand River Aseptic Manufacturing

https://www.grandriverasepticmfg.com/