Apply now »

We are experiencing a technical issue with the Careers Website. At the moment, applications are not possible. We are working on resolving the issue as soon as possible. Thank you for your patience.

Sr. Quality Assurance Associate Specialist

 

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

 

At MilliporeSigma, the QA Product Release Specialist will perform a variety of functions according to established protocols to support quality review and release of purchased and produced goods prior to downstream use and delivery to customers. Role responsibilities include the following:

 

  • Evaluate raw material or final products (repack or manufactured) to determine acceptability to meet import/export requirements that are derived from animal by-product (ABP).
  • Ensure that all aspects of routine product assignment and release for raw materials and finished goods meet analytical, packaging, and labeling specifications in accordance with established quality systems and regulatory/industry requirements.
  • Technical/consultative expert for risk assessment evaluations & implementation of mitigationstrategies related to; pathogenic agents, sourcing origin, genetically modified organisms, residual solvents, and/or heavy metals within the supply chain.
  • Review vendor documentation (certificate of origin, customer or regulatory questionnaires, etc.) as part of product release or as requested by Project Management, Technical Services, Customers, Sales, Marketing and/or regulatory agencies.
  • Assist with customer related documents, including supply chain declaration/affidavits and Certificate of Origin creation.
  • Perform product specific projects to improve product quality performance, product quality information and/or improve customer satisfaction as requested by Project Management, Technical Service, Sales, and/or Marketing.
  • Act as an auditor of the Internal Auditing Program.
  • Conduct Training (individual, group).
  • Batch review and usage decision.

 

Physical Attributes:

 

  • Environmental conditions: Varies depending on specific job responsibilities.
  • 70%-90% office environment, 10-30% production, QC, and packaging on the floor engagement.

 

Who You Are:

 

Minimum Qualifications:

 

  • Associate Degree in Life Sciences, Chemistry, Pharmacy, Chemical or Process Engineering.
  • 5+ years applicable experience in a QA job function as deemed appropriate by QA Management. 

Preferred Qualifications: 

 

  • Bachelors Degree in Life Sciences, Chemistry, Pharmacy, Chemical or Process Engineering.
  • 2+ years experience in industry.
  • Knowledge of ISO 9001:2008 required, ISO 13485 desired.
  • Knowledge of other regulatory requirements (i.e. USDA, FDA, EC, DEFRA, ICH, and EDQM).
  • Knowledge of animal/human pathogens desired.
  • Knowledge of transgenic plants and animals desired.
  • Current fine chemical industry knowledge and/or experience desired.
  • Knowledge of SAP – Resource Planning (ERP) Business tool related to COA generation and release of products required.

RSREMD


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team!

 

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html

 

Job Requisition ID:  286076
Location:  St. Louis
Career Level:  C - Professional (1-3 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

Notice on Fraudulent Job Offers
Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information.


Job Segment: Genetics, QA, Quality Assurance, Project Manager, Science, Technology, Quality

Apply now »