Quality Assurance Specialist - 2nd Shift
Join to apply for the Quality Assurance Specialist - 2nd Shift role at MilliporeSigma
Quality Assurance Specialist - 2nd Shift
2 days ago Be among the first 25 applicants
Join to apply for the Quality Assurance Specialist - 2nd Shift role at MilliporeSigma
Get AI-powered advice on this job and more exclusive features.
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
Job function
Job function
Quality Assurance and Science
Referrals increase your chances of interviewing at MilliporeSigma by 2x
Sign in to set job alerts for “Quality Assurance Specialist” roles.
Quality Assurance Product Release Specialist
Sr. Quality Assurance Associate Specialist
Quality Assurance Manager (OSSS-L3) NGA - St Louis
Quality Assurance Analyst, Accounts Receivable
Software Quality Assurance Specialist in Saint Louis, MO(Hybrid Full Time, Local USC Only)
Granite City, IL $100.00-$130.00 3 weeks ago
Quality Assurance Software Tester 2 **Hiring bonus $1,500**
Greater St. Louis $70,000.00-$130,000.00 4 hours ago
LOCAL to St. Louis only - Manual QA Analyst - US Citizen or GC only
St Louis, MO $55,000.00-$65,000.00 3 months ago
Food Manufacturing Quality Assurance Manager
St Louis, MO $70,000.00-$90,000.00 4 weeks ago
Greater St. Louis $40.00-$45.00 2 days ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.