Senior Scientist
Senior Scientist
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1 Vacancy
Job Description
A career with MilliporeSigma is an ongoing journey of discovery: our 57000 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 does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
In this role you will be responsible for analytical workflow application and product design and development. You will work collaboratively with the R&D marketing commercial teams and customers on multiple aspects of design method development and testing. You must be motivated to both learn from others and effectively transfer knowledge and processes to others. Come be a part of a dynamic innovativeand collaborativeteam.
MilliporeSigma is seeking to hire a Senior Scientist in the Reference Materials and Workflow Development R&D Department at its Cerilliant Corporation site in Round Rock TX. The Round Rock site manufactures high quality quantitative chemical reference standards for a diverse group of industries including forensic clinical pharmaceuticals environmental and food. The Workflow Team is responsible for design and development of workflows products and applications to support growth of MilliporeSigmas Analytical business.
Who You Are:
Minimum Qualifications:
- Bachelors Degree in Chemistry Biochemistry or other related Science discipline and 5 years in bioanalytical or biopharmaceutical testing experience
OR
- Masters Degree in Chemistry Biochemistry or other related Science discipline and 3 years in bioanalytical or biopharmaceutical testing experience
Preferred Qualifications:
- PhD in Chemistry or other related Science discipline
- Experience in clinical or bioanalytical mass spectrometry proteomics oligonucleotide or biopharmaceutical
- Expertise in method development for proteomics or oligonucleotides
- Experience with method validation and technology transfer
- Demonstrated motivation ability to learn new techniques and to collaborate well with others
- Experience working under regulated quality system requirements such as GMPs GLPs ISO CLIA and other regulatory requirements
- Experience with product development
- Experience with leading and coaching teams
- Demonstrated ability to effectively manage your time and to manage multiple projects
- Excellent written and verbal communication skills and ability to interact and collaborate with peers are critical to succeed in this role.
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
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.
Required Experience:
Senior IC
Employment Type
Full Time
