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Scientist 1 - Product Characterization

 

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, you will be the primary scientific resource for a given study with the Product Characterization Laboratory within the overall Biologics department. The Scientist will act as subject matter expert in bioassay development for studies performed in the Product Characterization Lab and will oversee a wide variety of safety testing required to manufacture clinical and commercial products.  You will be responsible for ensuring current regulatory requirements are met and the technical & regulatory needs are appropriately met, effectively interpreted, and then communicated to the client and performing analysis of testing performed within the Product Characterization.

 

  • Shift:  Monday -Friday 12-8:30pm (weekend optional)
  • Performs testing in accordance with SOPs and regulations (cGMP and GLP)
  • Act as subject matter expert (SME) for specific defined area(s) of the business.
  • Applies laboratory techniques and skills to complete experiments designed to address a variety of specific problems.
  • Independently applies basic scientific principles in the design of experiments and the development of assays.
  • For GLP studies, acts as Study Director.
  • Maintains complete and comprehensive records for study integrity.
  • Makes detailed observations, documents result and performs data analysis.
  • Operates and maintains lab equipment as required by SOPs and testing procedures.
  • Utilizes applicable computer programs during testing and routine tasks (i.e. Word, Excel, Oracle, LIMS, BRIQS, etc.).
  • Utilizes problem solving/ trouble shooting skills.
  • Communicates deviations/ events, progress and interim results to Study Management.
  • Leads the completion of event records.
  • 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 (i.e., Immunology,  Biology, Biochemistry, etc.) with 1+ years of experience in a laboratory environment – OR –
  • Master’s degree in scientific discipline (i.e., Immunology,  Biology, Biochemistry, etc ) with 3+ years of experience in a laboratory environment – OR –
  • Bachelor’s degree in scientific discipline (i.e., Immunology,  Biology, Biochemistry, etc ) with 5+ years of experience in a laboratory environment 
  • 6+ months experience with Flow Cytometry (potency, titer, viability or identity) -OR- 6+ months experience with Elisa 

 

Preferred Qualifications:

  • Experience with some or all of the following technical disciplines
    • Molecular qPCR and/or ddPCR
    • Cell-based bioassays
    • Experience with industry GxP compliance
  • Intermediate skills in applicable computer programs (Softmax, PLA, or FACSDiva)
  • 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
  • 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 - $49,500 - $148,900

 

Our ranges incorporate all levels and career types available within this specific role, and are derived from 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 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:  281516
Location:  Rockville
Career Level:  D - Professional (4-9 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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Job Segment: Immunology, Biochemistry, Laboratory, QA, Quality Assurance, Science, Healthcare, Technology, Quality

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