Senior Associate Scientist

Job description

A career with MilliporeSigma is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.

 

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

  

 

Your Role:  

At MilliporeSigma, as a Senior Associate Scientist (SAS) within the Molecular Development Services (MDS) team, you will work in a group-based environment to perform laboratory testing for custom and internal projects, including assay development and validation. You will be expected to make scientific observations related to test data, maintain detailed workbooks, and ensure that documentation fulfills accepted professional and industry standards.  Additionally, you will maintain a thorough understanding of services, technical principles, and applications as they apply to your position.  

·  Perform all routine and relevant laboratory techniques in compliance with regulatory standards
·  Perform a wide variety of routine or custom tasks to support GLP/GMP assay development
·  Perform a wide range of laboratory techniques, such as conventional, real-time & digital PCR, nucleic acid extraction, capillary & gel electrophoresis, sanger-based sequencing, and gain experience using standard molecular automation for nucleic acid extraction and liquid handling
·  Use standard molecular automation for nucleic acid extraction and liquid handling
·  Train other members of staff and drive quality improvement
·  Perform laboratory housekeeping, preparation of reagents, inventory management and general equipment maintenance

  Who You Are:
  Minimum Qualifications:  

·  PhD in a Biological Sciences field (e.g., Molecular Biology, Microbiology, etc.) with 1+ years’ experience in a GLP/GMP laboratory environment – OR –
·  Master’s Degree in a Biological Sciences field (e.g., Molecular Biology, Microbiology, etc.) with 3+ years’ experience in a GLP/GMP laboratory environment – OR –
·  Bachelor’s Degree in a Biological Sciences field (e.g., Molecular Biology, Microbiology, etc.) with 5+ years’ experience in a GLP/GMP laboratory environment 

Preferred Qualifications:

·  Good technical knowledge and problem-solving skills
·  Knowledge of GLP/cGMPs and relevant regulatory guidelines
·  Experience with bio/pharmaceutical equipment / systems
·  Experience conducting custom contract testing in accordance with defined proposals or statements of work
·  Experience with Microsoft Office and database management systems
·  Ability to work well under minimal supervision and in a team environment
·  Working knowledge of lab policies and assays to conduct a wide range of laboratory methods 
·  Ability to organize workload efficiently to complete tasks effectively 

 

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. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology.
We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons.
Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!

 

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

 

If you are a resident of Colorado or New York City, 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

 

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

 

As an employee of the Company, you will be required to comply with all of the Company’s COVID-19 safety protocols and policies. The organization has currently suspended enforcement of its COVID-19 Vaccination Policy, but that policy may be reinstated by the Company in its discretion.

Job Requisition ID:  258190

Location:  Rockville

Career Level:  D - Professional (4-9 years)

Working time model:  full-time .buttontext1722e80f7dc3f6d2 a{ border: 1px solid transparent; } .buttontext1722e80f7dc3f6d2 a:focus{ border: 1px dashed #eb3c96 !important; outline: none !important; }

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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