Document Control Quality Assurance 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:

The Quality Assurance Document Control Specialist is responsible for supporting the documentation system for the St. Louis Cell Marque group, ensuring accuracy, consistency and compliance with regulatory requirements.  This role involves managing document creation, revision, distribution, and archiving as well as providing training and support to employees on document control procedures. 

Key Responsibilities:

• Maintain a comprehensive document control system.
• Control the issuance, distribution, and retrieval of documents.
• Ensure documents are accurately indexed, filed, and archived.
• Manage electronic and physical document repositories.
• Maintain accurate records of document changes and approvals.
• Generate document control reports.
• Collaborate with various departments to ensure document accuracy and availability.
• Provide training and support to employees on document control procedures.
• Respond to document requests and inquiries promptly.
• Assist in the creation of documentation.

Who You Are:

Minimum Qualifications:                                                                                            

• Bachelor’s Degree in a scientific discipline (e.g., Biology, Chemistry, Microbiology, etc.)

Preferred Qualifications: 

• Experience in quality documentation and/or learning management systems
• Highly developed interpersonal, written, and verbal communication skills
• Ability to establish collaborative relationships with various departments to deliver on quality commitments
• Ability to work autonomously, effectively manage time and deliver results on time
• Strong problem-solving skills
• Strong computer skills, including Microsoft Office and quality systems software
• Understanding or experience with ISO & FDA regulations 

RSREMD

Cell Marque STL

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