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Quality Assurance Specialist - 2nd Shift

MilliporeSigma

St. Louis (MO)

On-site

USD 60,000 - 80,000

Full time

6 days ago
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Job summary

A leading company in St. Louis is seeking a Quality Assurance Specialist for the 2nd shift. This role involves ensuring compliance with quality standards and continuous improvement of quality systems. The ideal candidate will have a science degree and relevant experience in quality assurance, with strong communication and problem-solving skills. Join a diverse team committed to innovation and excellence in science and technology.

Qualifications

  • 3+ years of industry experience in Quality Assurance.
  • Experience in a regulated environment.

Responsibilities

  • Implement and maintain Quality Systems and processes.
  • Assist in compliance with Life Science and site quality policies.
  • Conduct internal audits and represent the site during customer audits.

Skills

Communication
Problem-Solving
Time Management

Education

Bachelor’s Degree in a Science field
Bachelor’s Degree in any field

Tools

MS Word
MS Excel
SAP

Job description

Quality Assurance Specialist - 2nd Shift

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Quality Assurance Specialist - 2nd Shift

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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

The Quality Assurance Specialist - 2nd Shift, at our Ewing location, provides compliance oversight across the St. Louis ISCO MilliporeSigma Quality Management System (QMS) in collaboration with site personnel. As a QA Specialist you are responsible for the implementation and maintenance of Quality Systems and processes to ensure internal and external compliance and the promotion of quality practices that meet or exceed required guidelines and regulatory requirements. Responsibilities include maintenance and continuous improvement of the overall Quality Program.

  • Shift : Monday-Thursday 1:30pm - 12am OR Tuesday- Friday 1:30pm- 12 am
  • Improve quality systems in ISO and non-GMP production environments and drive quality improvement in multiple departments.
  • Complete a high volume of work to meet department goals.
  • Communicate the status of operations and bring critical deviations to the attention of your manager.
  • Communicate with coworkers and interact with other departments on a regular basis.
  • Complete and have accurate work consistently with quality guidelines.
  • Assist in maintaining department KPIs through on time CAPAs, Deviations, Complaints and Change Controls.
  • Assist in compliance with Life Science and site quality policies and procedures.
  • Represent the site during customer and regulatory audit and perform internal audits.
  • Assist in the investigation of customer complaints.
  • Contribute to Root Cause Investigations & Effectiveness Checks of Nonconforming Incidents and conduct Quality System Training
  • Documentation control activities include management of the electronic documentation management system, and the ability to write, review or approve Operation Procedures, Specifications, Master Manufacturing & Packaging Procedures and other controlled documents.

Who You Are

Minimum Qualifications:

  • Bachelor’s Degree in a Science field (e.g., Chemistry, Pharmacy, Chemical Engineering, etc.), with 3+ years’ of industry experience

-OR-

  • Bachelor’s Degree in any field with 5+ years experience in a Quality role

Preferred Qualifications

  • Knowledge of ISO 9001 and ISO 13485 and regulatory compliance issues (i.e., FDA, USDA, EXCiPACT, ICH, EDQM, IVDR) related to biologic derived materials, and prior experience working in a controlled/regulated environment
  • Current fine chemical industry knowledge &/or experience
  • Good computer skills, including proficiency in MS Word, MS Excel, MS Access, MS Project, MS PowerPoint, and ability to learn and operate using other specific application software (SAP, Trackwise, etc.)
  • Excellent communication (verbal & written) and customer services skills
  • Good writing skills and experience writing technical documentation & reports
  • Ability to simultaneously manage multiple tasks/priorities
  • Good problem-solving skills/abilities
  • Good time management and negotiating skills

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!

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Quality Assurance and Science

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