cGMP Associate Production Scientist

Posted 21 Jan 2020

St. Louis, Missouri - United States

Req Id 202374

Details

 

A career with MilliporeSigma is an ongoing journey of discovery: our 56,000 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.

 


Your Role:

 

The cGMP Associate Production Scientist is responsible for the manufacturing of active pharmaceutical ingredients (APIs), chemicals, and bulk pharmaceuticals which are regulated by the Food and Drug Administration (FDA). They are responsible for following manufacturing protocols, consistent with and according to current Good Manufacturing Practices (cGMP), and ensuring the accuracy of documentation. This position is on third shift, with scheduled work hours of 9PM – 9:30AM and weekend work required every other week.

 

  • 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)
  • Assure you are adequately trained to perform tasks/assignments
  • Communicate the status of operations and bring deviations to the attention of supervisor
  • Provide complete and accurate records consistent with quality guidelines and Good Documentation Practice (GDP) requirements.

 

Physical Attributes:

 

  • May perform tasks while wearing personal protective equipment such as a respirator or chemical protective clothing for extended periods of time.  May perform occasional lifting and pushing of up to 80 pounds.

 

Who you are:

 

Minimum Qualifications:

 

  • Bachelor’s Degree in Chemistry, Biochemistry, Biology, Chemical Engineering or related life science. 

 

Preferred Qualifications:

 

  • Experience in a cGMP environment
  • Solid foundation in chemistry or biochemistry, math, and general science
  • Knowledge of safe chemical handling methods
  • Demonstrated oral and written communication skills
  • Strong organizational skills

 

RSRMS

 


 

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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