QA Inspector

MilliporeSigma; Indianapolis (IN); On-site; USD 40,000 - 61,000; Full time

Benefits offered by this job

Health insurance

PTO

Retirement contributions

Job summary

MilliporeSigma in Indianapolis seeks a Quality Assurance professional to ensure that components, in-process products, and finished products meet GMP standards. You will help maintain the quality system, log retain samples, and support inspections and documentation.

The role requires a life science background with GMP experience, strong Excel/Word/Access skills, and familiarity with SAP. Collaboration across Receiving and Production is essential, with a focus on accurate QA decisions and

Qualifications

• Bachelor’s Degree in Biology, Chemistry, or life science with 1+ year GMP pharmaceutical industry experience.
• Alternatively, High School Diploma/GED with 3+ years GMP pharmaceutical industry experience.
• Experience with Excel, Word, and Access.
• Experience with Quality Management systems and SAP.
• Excellent interpersonal and team skills; work independently and make QA decisions based on GMPs and procedures.
• Experience reading and interpreting quality standards, safety rules, operating instructions, and procedures.

Responsibilities

• Ensure retain samples are logged and stored per SOPs, and quarterly annual review reports to QA management.
• Coordinate inspection of Finished Packaged Product Retain Samples for customer complaints and provide written reports.
• Inspect incoming components for adherence to quality standards and document results.
• Assist in inspection and labeling of raw materials; coordinate with Receiving and Production and SAP updates.
• Perform document revisions, deviation reviews, and change controls in existing Quality Systems.

Skills

Attention to detail

Teamwork

Independence

Interpersonal skills

Education

Bachelor’s degree in Biology, Chemistry, or Life Science

High School Diploma or GED with GMP experience

Tools

Microsoft Excel

Microsoft Word

Microsoft Access

SAP

Job description

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.

Your Role

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.

Responsibilities Include But Are Not Limited To

• 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.

Physical Attributes

• Lift and/or move up to 25 pounds.
• Wear appropriate Personal Protective Equipment.

Who You Are

Minimum Qualifications:

• 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.

Preferred Qualifications

• 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.

Pay Range for this position: $29 - $44 / hour

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.

RSREMD

What we offer:

We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!