QA Inspector

Merck•Indianapolis, IN

8d•Onsite

About The Position

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. In this role you will be part of the quality system, and ensure that components, in process products, and finished product meet their designated quality standards, and that the facility follows proper GMPs.

Requirements

Bachelor’s Degree in Biology, Chemistry, or other Life Science discipline and 1+ years of GMP pharmaceutical industry experience. OR High School Diploma or GED and 3+ years of GMP pharmaceutical industry experience.

Nice To Haves

Experience with computer software applications including Microsoft Excel, Word, and Access.
Experience with Quality Management computer systems and SAP.
Excellent interpersonal and team skills; work independently and carry out QA decisions based on GMPs and appropriate procedures.
Experience reading and interpreting documents such as quality standards, safety rules, operating and maintenance instructions, and procedure manuals.

Responsibilities

Ensure that all retain samples are logged in and stored according to standard operating procedures, as well as ensuring the annual review of Finished Packaged Product Retain Samples occurs on a quarterly basis, providing a written report of results to quality management each quarter.
Coordinate inspection of Finished Packaged Product Retain Samples for customer complaints and provide written report of results as needed.
Inspects incoming components for adherence to quality standards and documents results.
Assist in inspection and labeling of raw materials.
Work closely with Receiving and Production to ensure status is appropriate and up to date, both on the materials and in SAP.
Performs document revisions, deviation reviews, and processes change controls in existing Quality Systems.