Scientist 1 - Flow, Elisa & GMP - 2nd Shift

 

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, as the Scientist 1 - 2nd shift, your activities will support assay development through commercial application of new and innovative service offerings within the biosafety testing space. You are responsible for the scientific integrity of technical work performed in the laboratory, and are required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Requirements also include maintaining a thorough understanding of company testing services, technical principles and applications as they apply to your position.

 

• Shift hours:  Monday - Friday 11am - 7:30pm 
• Act as subject matter expert (SME) for specific defined area(s) of the business.
• For GLP studies, acts as Study Director.
• Fully responsible for the technical conduct of a GMP/GLP study, as well as for the interpretation, analysis, documentation, and reporting of results.
• Assure that appropriate technical specifications and standard operating procedures are followed.
• Assure that all experimental data, including observations of unanticipated test system responses are accurately recorded and reviewed.
• Assure that computerized systems used in the study have been validated or are under appropriate controls.
• Utilizes problem solving/ trouble shooting skills.
• Leads the completion of deviation investigation records in a timely manner.
• Liaise with Quality Assurance and appropriate cross-functional departmental areas to close the events and corrective actions identified during GxP laboratory testing.
• Maintains a working knowledge of lab procedures and assays.
• Creates/ revises SOPs, laboratory records and other related documentation as assigned.
• Writes technical reports for internal use and collaborates on papers for external use.
• Performs training of laboratory personnel as needed/ assigned.
• Contribute ideas and suggestions to improve standard laboratory techniques, protocols, processes, and equipment.
• Acts as key driver/ champion on project teams.
• Complies with company health and safety regulations and procedures.

 

Who You Are

 

Minimum Qualifications:

• Ph.D. in scientific discipline (Immunology, Chemistry, Biology, etc. ) with 1+ years of experience in a laboratory environment – OR –
• Master’s degree in scientific discipline (i.e., Immunology, Chemistry, Biology, etc) with 3+ years of experience in a laboratory environment – OR –
• Bachelor’s degree in scientific discipline (i.e., Immunology, Chemistry, Biology, etc) with 5+ years of experience in a laboratory environment 

 

Preferred Qualifications:

• PhD in Immunology 

• Extensive hands-on experience with Flow Cytometry/cell sorting techniques (potency, titer, viability or identity)
• Hands-on experience with Mammalian cell-based Immunoassays (preferred cell line, adherent cells e.g. HEK293; suspension T cell (SupT1, MT4, H9) and primary hematopoietic cells (CD34+ cells))
• Hands-on experience with Quantitative ELISA (Relative potency, titer, host cell protein, etc.)
• Experience with industry GMP or GxP compliance and Client facing experience 
• Deviation investigation experience
• Intermediate skills in applicable computer programs (Softmax, PLA, or FACSDiva)