Quality Assurance Associate

Millipore Corporation • Miamisburg, OH • 3d ago

Work Location: Miamisburg, Ohio Shift: No Department: LS-SC-PEMQ Quality Control Recruiter: Michelle Matthews This information is for internals only. Please do not share outside of the organization. Your Role: To ensure that all aspects of site production operate within all established quality systems. You will support the cGMP and/or ISO 9001 quality systems such as training, batch record reviews and documentation control. Responsibilities and tasks include:

Safely perform operations to meet quality expectations.

Improve quality systems in both GMP and ISO production and packaging environments.

Drive quality improvement in multiple departments

Be the "voice of quality" on the production and packaging floors performing routine walk through. o Review quality documents in production and packing areas.

Assist Quality Team issuing and reviewing batch records for GMP manufacturing.

Review ISO and GMP in-process batch records and form for good documentation.

Communicate the status of operations and bring critical deviations to the attention of the appropriate parties.

Communicate with coworkers and interact with other departments regularly.

Complete and have accurate work consistently with quality guidelines.

Take note of details and ensure others do as well.

Assist in maintaining department KPIs through on time CAPAs, Deviations, and Complaints.

Assist in compliance with Life Science and site quality policies and procedures.

Ability to serve on committees to improve department, site, or company performance. Committees may focus on safety, quality, inventory, output, costs, etc.

In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles.

Who You Are Minimum Qualifications:

High School Diploma or GED

2+ years of experience in a quality role at a GMP manufacturing facility OR

Associate's degree in any discipline.

1+ years of experience in a quality role at a GMP manufacturing facility.

Preferred Qualifications:

Bachelor's degree in chemistry, Biology, or other science discipline.

Previous QA experience in a GMP manufacturing or testing facility.

3-5 years' work experience in a GMP Manufacturing Facility.

Experience with quality management systems such as Trackwise, electronic document management systems, etc.

Ability to multitask and prioritize.

Understanding of ISO and cGMP quality standards.

Computer literacy, including Microsoft Word and Excel.

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination. Apply here: https://www.aplitrak.com/?adid=YmJnZW5lcmljLjk2MTY0LjEwNTA4QGVtZG1pbGxpcG9yZWNvbXAuYXBsaXRyYWsuY29t

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