Senior Scientist, Genetic Toxicology

Posté 22 sept. 2020

Rockville, Maryland - United States

Demander un identifiant 210152

Détails

A career with MilliporeSigma is an ongoing journey of discovery: our 57,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. 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 supports Millipore Sigma’s BioReliance Genetic Toxicology services.

 

Your role:

The Study Director will perform all aspects of the GLP role of Study Director with overall scientific responsibility for the study design, interpretation and reporting study results.  The role will also serve as a scientific resource in Genetic Toxicology and is responsible for the study design interpretation and reporting of study results. You will interact with sponsors or clients to present and interpret results, and to ensure the client expectations are met or exceeded.  You will also provide technical advice and support for internal and external interactions such as client and regulatory audits/inspections, meetings, teleconferences.  You will also contribute to and author scientific publications and presentations at conferences/ seminars.  This role will also monitor industry trends to ensure that Millipore Sigma remains at the forefront in the field of Genetic Toxicology and review and recommend potential assay developments to upper management.  You will lead by example, offer scientific insight to other staff members, and promote a culture of continuous improvement.  You will participate in initiatives and/or projects to drive improvement in quality and/or client service.

 

Who you are:

Minimum Qualifications:

  • MA/MS in scientific discipline with 6+ years of industry experience within genetic toxicology.
  • Relevant working knowledge and experience in executing and overseeing technical projects.
  • Laboratory Experience in conducting and/or overseeing GLP-regulated studies.
  • External customer facing experience.

 

Preferred Qualifications:

  • Ph.D. in scientific discipline with 2+ of industry experience in genetic toxicology.
  • In vivo micronucleus, Ames assay, chromosomal aberration experience.

What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

Curious? Apply and find more information at https://jobs.vibrantm.com


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.

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