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Analytical Development 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:

A Scientist in the Analytical Development group is responsible for the coordination of the analytical aspect of incoming and existing projects for the MilliporeSigma Madison.  This includes but is not limited to use of state-of-the-art instrumentation to develop methodologies for the analysis of active pharmaceutical ingredients as well as the synthetic intermediates, contributing to discussions and communications with customers to achieve a desired endpoint, initiating documentation and methodologies needed to support cGMP manufacturing, troubleshooting instrumentation, and generating and compiling results to solve or diagnose a problem.

 

Use and troubleshoot HPLC, GC, DSC, TGA, KF, IR, MS, NMR and XRPD, among other instrumentation, and wet chemical assays.  The Scientist is responsible for development, or directing the development, of analytical methods to support Process and Analytical Development (PAD) for eventual validation and or use in cGMP.  The Scientist is responsible for reviewing and evaluating analytical data for identification of products, intermediates and raw materials as well as troubleshooting and guiding development.  The Scientist is responsible for maintaining project timing and interacting with clients to assure project goals are met in an efficient and well documented manor. 

 

Working with colleagues in PAD, the Scientist is part of a team of professionals advancing pharmaceutical candidates to cGMP manufacturing.  The Scientist is an expert in analytical chemistry and the requirements for cGMP manufacturing.  Executes and troubleshoots experiments as well as provides sound judgement in scientific and technical situations.  The Scientist is recognized as a significant individual contributor in the scientific and technical areas within PAD.

 

Essential Job Functions:

  • Independently lead project teams, provide guidance and oversee other group members​.
  • Develop test methods for Process and Analytical Development (PAD) products, intermediates and raw materials.
  • Initiate documentation and methodologies needed to support cGMP manufacturing.
  • Work on and be able to both independently and in a group, solve problems of significant scope.
  • Analytically test PAD final products, intermediates and raw materials. Testing will involve the use of HPLC, GC, DSC, TGA, KF, IR, MS, NMR and XRPD among other tests and instruments.
  • Properly document and review group members lab work.
  • Ability to manage and prioritize daily and project activities​.
  • Suggest specifications for final products, intermediates and raw materials.
  • Transfer analytical test methods to Quality Control.
  • Train Analytical and Quality Control personnel in operation of analytical equipment and methods.
  • Write and evaluate reports, protocols, SOP’s and other documentation.
  • Work with clients (internal and external) to achieve project goals.
  • Interpretation of analytical data (including FT-IR, NMR, MS).
  • Maintain and calibrate/verify analytical and related equipment.
  • Proactively consider impact of quality, regulatory, manufacturing, and safety requirements when planning activities. ​
  • Work in a safe manner and maintain the cleanliness of the work environment.
  • Work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines.

 

 

Who you are:

Minimum Experience

  • Bachelors degree in Chemistry, Biochemistry or related biological sciences AND 5+ years of experience in an analytical laboratory environment operating under GLP or cGMP conditions.

         OR

  • Masters degree in Chemistry, Biochemistry or related biological sciences AND 2+ years of experience

         OR

  • PhD in Chemistry, Biochemistry or related biological sciences AND 0+ years of experience in an analytical laboratory environment operating under GLP or cGMP conditions.

Preferred Qualifications

  • Excellent communication skills. 
  • Ability to work in a team environment. 
  • Ability to work in an Analytical testing lab with hazardous and toxic chemicals. 
  • Adequate technical writing skills to generate development reports.

 

 

 

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:  215005
Location:  Madison
Career Level:  D - Professional (4-9 years)
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.


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