Scientist, Quality Control

Posté 30 déc. 2021

Verona, Wisconsin - United States

Demander un identifiant 236625

Détails

 

A career with EMD Serono is an ongoing journey of discovery: our 58,000 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. EMD Serono is a business of Merck KGaA, Darmstadt, Germany.

 

 

US employees must be fully vaccinated against COVID-19 prior to your start date unless an accommodation is granted by The Company. The Company uses the definition of fully vaccinated assigned by the Centers for Disease Control & Prevention for purposes of considering satisfaction of this requirement which is a condition of employment.

 

 

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 

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

 


 

MilliporeSigma is currently looking for a Scientist, Quality Control for our Verona, WI location to exercise judgment within defined procedures and practices to obtain solutions.

 

  • Write stability protocols, & SOP to maintain stability chambers/programs, review/manage stability reports, interact with customers to support stability program.
  • Work on complex problems in which analysis of data requires an in-depth evaluation of various factors.  
  • Apply critical thinking and good problem-solving skills to thoroughly investigate deviations, identify root causes, and propose appropriate corrective/preventive actions with minimal assistance from supervisor & participate in OOS investigations via testing and good documentation.
  • Perform instrument calibration (IQ/OQ/PQ/PM) and routine equipment maintenance/repair.
  • Perform requalification of reference standards and maintain reference standard inventory/documentation.
  • Work in compliance with effective procedures and regulatory requirements outlined in ICH Q7 and 21 CFR Parts 11, 210 and 211 as applicable
  • Work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines.

 

Minimum Qualifications:

  • B.S. in Chemistry or related biological science discipline.
  • 5+ years in a GLP or cGMP analytical laboratory environment 

 

Preferred Qualifications:

  • Excellent written and verbal communication skills, as well as excellent documentation practices and attention to detail 
  • Ability to work in analytical testing lab with hazardous and toxic chemicals
  • Knowledge and understanding of organic analytical chemistry 
  • Adequate technical writing skills to author training memos and operating procedures 
  • Thorough understanding of 21 CFR Parts 11, 210 and 211 as applicable

 


 

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!

Our Benefits - http://jobs.vibrantm.com/emd/content/Benefits-at-a-Glance/?locale=en_US

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

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.

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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