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Sr Associate Production Scientist

 

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 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.

 

Your role:
Position primarily involves the safe and efficient manufacturing of API’s according to cGMP requirements. The role of Production Scientist, Senior Associate is an iterative expansion of the Associate Production Scientist position and is primarily focused on performing and improving required production operations to support the end users and patients of the compounds produced at MilliporeSigma. These responsibilities include but are not limited to executing/updating existing production procedures, updating/drafting ancillary documents, and improving the safety and quality of the manufacturing environment.

 

Second Shift (M-Th, 1300 - 2330)

 

Essential job functions:

  • Show positive attitude, be respectful of others, and display MilliporeSigma values and competencies.
  • Become a role model for other employees through superb work habits and excellent occupational behavior.
  • Demonstrate proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines.
  • Function as a primary operator for multiple GMP Production areas.
  • Effectively execute non-GMP processes.
  • Author and execute project level Corrective and Preventative Actions.
  • Perform and author deviation investigation reports of moderate impact/scope.
  • Utilize and provide major updates to a wide variety of written procedures, including batch records and existing operating procedures with little to no assistance from a supervisor.
  • Function as a tier 2 project lead, as defined by department management.
  • Assume temporary project lead responsibilities during the absence of a coworker leading a tier 1 project.
  • Draft process specific reports and documents without the use of a previously approved template.
  • Function as a shift subject matter expert on a chemical process or piece of equipment.
  • Train secondary operators to help them achieve primary operator status in one GMP area.
  • Actively participate in internal and/or external calls and interactions as a representative of manufacturing for general information.
  • Identify and implement process improvements of moderate impact/scope.
  • Complete action items of moderate scope or impact for a PI initiative or safety committee.

 Physical Attributes 

  • Able to stand for long periods of time
  • Lifting and moving up to 50 pounds with the assistance of equipment or teammates as necessary
  • Working with highly potent / hazardous materials
  • Able to utilize proper personal protective equipment which could include but is not limited to:
  • Wearing respiratory protection (dust masks, half/full face respirators, supplied air, etc)
  • Wearing full body protection (disposable coveralls, hazmat suits, etc)

 


Who you are:

Minimum qualifications:

  • Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or related Life Science AND 2+ years of regulated pharmaceutical or chemical production manufacturing experience

          OR

  • High School Diploma or GED equivalent AND 6+ years of regulated pharmaceutical or chemical production manufacturing experience


Preferred qualifications:

  • Ability to read and understand written protocols
  • Strong computer literacy (Microsoft Office and Outlook tools, Electronic Document Management Systems, etc.)
  • Effective oral and written communication skills
  • Ability to write technical documents
  • Mechanical and technical aptitude
  • Able to operate hand tools, calculators and weighing / measuring devices
  • Strong mathematical skills
  • Possess a high degree of motivation and are a self-starter
  • Ability to multi-task while paying close attention to detail
  • Able to stand for long periods of time
  • Must be able to lift and move up to 50 pounds with the assistance of equipment or teammates as necessary

 

 

 

 

 

 

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.

Job Requisition ID:  218489
Location:  Madison
Career Level:  B - Recent University Graduate(<1 year of experien
Working time model:  full-time

Careers during Covid-19
Thank you for visiting our careers website, we are always looking for curious minds to join our teams. We understand how much the world is being impacted by the Covid-19 crisis and we want to assure you that your safety is very important to us. To ensure that everyone’s health is protected, instead of a standard face-to-face interview, it is likely that you will be offered alternative digital interview options.

US Disclosure
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.

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our HR Services team at 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday.


Job Segment: Chemistry, Biochemistry, Scientist, Pharmaceutical, Respiratory, Science, Healthcare

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