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Scientist

 

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.  

 

Your Role:

Perform laboratory operations associated with the manufacture of reagents in compliance with quality and regulatory requirements, such as tissue sectioning and staining, antibody activity evaluation, and developing formulations to manufacture reagents. Assist in development and commercialization of new product offerings by developing and executing a broad range of protocols. Establish manufacturing procedures, analyze and review methods as needed during processes, and ensure all quality requirements and scheduled deadlines are met. Job responsibilities below:

  • Perform laboratory operations such as tissue staining, antibody activity evaluation, and formulations to manufacture reagents according to established manufacturing procedures; analyze and review methods as needed during processes.
  • Contributes ideas and suggestions to improve standard laboratory techniques, improve protocols, processes, and equipment.
  • Ensure all quality requirements and scheduled deadlines are met.
  • Develop, write, and update documents pertaining to lab procedures and product manufacturing to maintain cGMP and ISO compliance; write lab reports or project summaries as requested.
  • Collect, analyze, and interpret data from verification testing to ensure that products meet all specifications.
  • Assist in the development of new assays.
  • Assist in training and oversight of new staff members.
  • Complete all work in compliance with established cGMP, FDA, OSHA, USDA, EPA, ISO and Quality System regulations, as applicable, to assure output meets established quality and regulatory specifications.
  • Assist in developing and transferring manufacturing processes, including instrumentation and training of staff.
  • Assist in training other staff members as requested.
  • As requested, participate in the implementation of cGMP and ISO compliance standards and assist with investigations dealing with manufacturing processes.
  • Cleaning of labware as well as general lab cleaning
  • Maintain inventory of all chemicals and supplies required for manufacturing.
  • Provide equipment maintenance as necessary.
  • Follow regulatory and standard requirements as applicable to the site, i.e., MDSAP, ISO 13485, IVDR, and compliance with the site Quality Manual.
  • Additional duties as assigned or required to support the business.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

 

Who You Are:

Minimum Qualifications:

  • Bachelor’s Degree in Biology, Biotechnology, or other Life Sciences discipline with 3+ years of laboratory experience.
  • Master’s degree in Biology, Biotechnology, or other Life Sciences with 1+ years of laboratory experience.
  • Experience following Standard Operating Procedures, accurate completion of Manufacturing Procedure batch records, adherence to Quality and Regulatory requirements.
  • Good oral and written communication skills.
  • Good organizational, time management, and project management skills
  • Experience with Microsoft Office: PowerPoint, Excel, Word.
  • Proficiency in the use of basic laboratory techniques, equipment, and materials
  • Technical skills should include but are not limited to histology, immunohistochemistry, immunoassays (eg, ELISA), molecular biology techniques (eg, qPCR, nucleic acid isolation)  

Preferred Qualifications:

  • Broad working knowledge of various immunoassays (eg, immunostaining, ELISAs)
  • Familiarity with both manual and automated staining of FFPE tissue
  • Ability to work independently and group setting.
  • Multi-tasker who can handle multiple projects at one time.
  • Ability to troubleshoot problems in experimental design.
  • Experience following Standard Operating Procedures, accurate completion of Manufacturing Procedure batch records, adherence to Quality and Regulatory requirements.
  • Good oral and written communication skills.
  • Good organizational, time management, and project management skills
  • Experience with Microsoft Office: PowerPoint, Excel, Word.
  • Proficiency in the use of basic laboratory techniques, equipment, and materials
  • Technical skills should include but are not limited to histology, immunohistochemistry, immunoassays (eg, ELISA), molecular biology techniques (eg, qPCR, nucleic acid isolation)  

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:  277827
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.

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