Validation Technician

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

Validation Technicians are recognized as a quality presence and technical resource. The Technicians are responsible for the periodic review program, assisting validation engineers with the execution and review of validation documents and ensuring that the qualifications are consistent with quality standard. They will also be interacting cross-functionally with Manufacturing, Project Management, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance. This position is based in St. Louis at 3300 South Second.

 Responsibilities:

• Utilize GDP in a GMP atmosphere while executing protocols and reviewing documents
• Assist with the management and execution the periodic requalification program
• Conduct annual temperature mapping qualifications on controlled temperature units
• Execute periodic requalification packages and technical reports while adhering to GDP standards
• Responsible of maintaining the Validation Documents room
• Ensure that all validation protocols are stored and maintained electronically in internal quality management systems
• Retroactively ensuring that historical documents are maintained physically and electronically
• Conduct the execution of protocols for equipment, analytical instrumentation, cleaning, process controls, and facility qualifications (including but not limited to FAT/SAT/IOQ and PQ documents)

Who You Are
Minimum Qualifications:

• High School Diploma or GED
• 1+ years of technical writing experience

Preferred Qualifications:

• Bachelor’s Degree in Electrical Engineering, Chemical Engineering, or other Engineering discipline OR Biology, Chemistry, or other Life Science discipline
• Experience in a GDP setting (e.g. chemical laboratory, pharmaceutical manufacturing, engineering, etc.)
• Knowledge of GMP and knowledge to utilize GDP during document execution and review
• Proficiency with Microsoft Office products and ability to learn and operate new computer applications
• Detailed oriented

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