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Shipyard Quality Assurance Inspector Jobs in Indiana

Merck Group

QA Inspector

Indianapolis, IN

$29 - $44/hr

Coordinate inspection of Finished Packaged Product Retain Samples for customer complaints and ... Excellent interpersonal and team skills; work independently and carry out QA decisions based on ...

Merck Group

QA Inspector

Indianapolis, IN · On-site

$29 - $44/hr

Coordinate inspection of Finished Packaged Product Retain Samples for customer complaints and ... Excellent interpersonal and team skills; work independently and carry out QA decisions based on ...

Keystone RV

Quality Assurance Inspectors

Goshen, IN · On-site

QA inspector desired experience and skills: * Reliable and professional with proven track record of good attendance * Strong communication and organizational skills * Ability to adapt and operate in ...

Amcor

Quality Assurance Inspector

Evansville, IN · On-site

... inspection reports 3. Gather samples of product from thermoformers. 4. Weigh / gauge parts and ... 9. Place nonconforming product on QA hold using JDE & Containment Report procedures.

Keystone RV

Quality Assurance Inspectors

Goshen, IN · On-site

QA inspector desired experience and skills: * Reliable and professional with proven track record of good attendance * Strong communication and organizational skills * Ability to adapt and operate in ...

RBC Bearings

QA Inspector - 2nd shift

Plymouth, IN · On-site

* Inspect product to ensure conformance with work orders and specifications. * Conduct dimensional checks on sample audits from inspection. * Sets up gauges to determine diameter and length. * Change ...

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Infographic showing various Shipyard Quality Assurance Inspector job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

QA Inspector

The businesses of Merck KGaA, Darmstadt, Germany

Indianapolis, IN • On-site

$29 - $44/hr

Full-time

Medical, Retirement, PTO

Posted 17 days ago

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. For more information click here.

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!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Employment Type: FULL_TIME

Apply