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) Hand-on experience with equipment (FACSCanto, Cell sorters, Cell counter, Stemvision, automatic liquid handler, etc.)
• Excellent verbal and written communication skills that have been demonstrated through presentations/seminars, oversight of projects, implementation of new services, etc.
• Excellent time management skills, highly collaborative as well as independent and excellent multi-tasking abilities
• Demonstrates a high level of initiative and leadership capabilities.
• Effective coaching and training skills for complex and highly technical work
• Highly, technically competent
  
  

Pay Range for this position - $71,700 - $132,000

Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!