Senior Associate Quality Scientist

Posted 18 Mar 2022

Miamisburg, Ohio - United States

Req Id 244095

Details

 

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, the Senior Associate Quality Scientist will manufacture or evaluate stable isotope products according to established protocols, provide technical support to others and perform operations in support of the group and department.

 

  • Safely perform operations to meet quality expectations.
  • Ensure safety and quality throughout the process.
  • Assure you are adequately trained to perform tasks/assignments.
  • Perform multi-disciplined, established synthetic processes, assays, and/or unit operations, primarily those requiring a higher level of skill and knowledge involving stable isotope compounds.
  • Clean up equipment and working areas during and after operations.
  • Complete the volume of work required to achieve group/departmental goals and meet deadlines.
  • Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal).
  • Communicate the status of operations and bring deviations to the attention of supervisor.
  • Provide complete and accurate records consistent with quality guidelines.
  • Ensure all applicable logbooks have been filled out completely as required by current procedures.
  • Interface with other departments as needed.
  • Participate as needed in quality audits.
  • Accurately perform procedures independently.
  • Identify problems and limitations of analysis.
  • Perform routine troubleshooting
  • Review of final assays and procedures.
  • Interface with external customers.
  • Serve on committees to improve department, site, or company performance which may focus on safety, inventory, output, costs, etc.
  • In compliance with change control procedures, improve processes through the application of scientific knowledge, experience, and principles.
  • Identify opportunities for process improvement.
  • Participate in process improvements under the guidance of a Supervisor or Production Scientist.
  • Take the necessary action to resolve any unsafe conditions.
  • Develop improvement ideas, review the impact of changes, and document all work.
  • Train personnel and act as a technical consultant as needed. Perform and interpret analytical evaluations of products and intermediates.
  • Supply information based on experience and knowledge.

 

Physical Attributes:

  • Wear appropriate protective gear, (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protection equipment (PPE) to protect from toxic or corrosive chemicals in the forms of liquids, solids, vapors, or airborne particles
  • Work in outdoor weather conditions while moving material and waste handling.
  • Lift, push, and or pull up to 50lbs
  • Sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch or crawl for extended periods of time.

 

Who You Are:

 

Basic Qualifications:

  • Bachelor’s Degree in Chemistry, Biochemistry, or other life science discipline
  • 1+ year of independent lab research, and or industrial laboratory experience  

 

Preferred Qualifications:

  • 1+ year experience in a GMP testing environment
  • Mechanical skills
  • Troubleshooting skills
  • Interpersonal skills
  • Organizational skills
  • Laboratory and analytical skills
  • Knowledge of ISO Quality standards
  • Process techniques and unit operations
  • Analytical techniques and equipment
  • Safe chemical handling methods
  • Communication skills, oral and written
  • Computer skills
  • Knowledge in chemistry or biochemistry, math, and general science
  • Familiar with laboratory instruments and production equipment

RSRMS MilliporeSigma Millipore Sigma


 

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!

 

Curious? Chat with one of our curious minds on our interactive Q&A platform and catch a glimpse of our people, values, and culture. You can also apply and find more information at https://jobs.vibrantm.com

 

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 NYC, 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.

 

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.

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