Work Your Magic with us! Start your next chapter and join MilliporeSigma.

 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

 

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

 

Your Role:

 

The Scientist – Analytical Development plays a pivotal role in coordinating the analytical aspect of incoming and ongoing projects for Millipore Sigma-Madison. This role involves utilizing state-of-the-art instrumentation to develop methodologies and analyze active pharmaceutical ingredients and synthetic intermediates. The Scientist contributes to discussions and communications with customers to achieve a desired project endpoint. Additionally, they are responsible for documenting methodologies needed to support the project in cGMP manufacturing, troubleshooting instrumentation, and generating and compiling results to solve or diagnose a problem.

 

The Scientist is tasked with developing or overseeing the development of analytical methods to support Process and Analytical Development (PAD), ultimately for validation and/or use in cGMP manufacturing. 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 the subject matter expert (SME) in analytical chemistry and the requirements for cGMP manufacturing. Demonstrates a documented ability to execute and troubleshoot experiments as well as provides sound judgement in scientific and technical situations.

Specific Responsibilities Include:  

 

 

Independently lead project teams, provide guidance, and assist in the development of other group membersDevelop test methods for Process Development (PD) products, intermediates, and raw materialsInitiate documentation and methodologies needed to support cGMP manufacturingWork in the scope of the project independently and in a group settingTesting will involve the use of HPLC, GC, LCMS, DSC, TGA, KF, FTIR, NMR, and XRPD among other tests and instrumentsAbility to troubleshoot HPLC, GC, LCMS, DSC, TGA, KF, FTIR, NMR and XRPD, among other instrumentation, and wet chemical assays is essentialProperly document and review group members lab workManage and prioritize daily and project activitiesSuggest specifications for final products, intermediates, and raw materialsTransfer analytical test methods to Quality ControlTrain Analytical and Quality Control personnel in operation of analytical equipment and methodsWrite and evaluate reports, protocols, SOP’s, and other documentationWork with clients (internal and external) to achieve project goalsInterpretation of analytical data (including NMR, MS, FTIR)Maintain and calibrate/verify analytical and related equipmentProactively consider impact of quality, regulatory, manufacturing, and safety requirements when planning activitiesWork in a safe manner and maintain the cleanliness of the work environmentWork in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelinesRegular use of phones, computers, computer monitors, and all office / laboratory equipmentThe employee will also utilize computer keyboard and can read CRTS / computer monitors

 

 

Physical Attributes:
 

Regularly sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch, or crawl for long periods of timeUse all human senses (speak, hear, smell)  Lift or push up to 50 pounds unassistedJob involves use of close vision, distance vision, color vision, peripheral vision, depth visionWear appropriate (PPE) while working around mechanical parts and hazardous material(hard hats, glasses / goggles, chemical resistant suites, gloves, safety shoes, respirator)

 

Who You Are:
 

Minimum Qualifications:

 

Bachelor’s Degree in Chemistry, Chemical Engineering, or other Life Science discipline5+ years of experience in an cGMP or GLP analytical laboratory environment

OR

Master’s Degree in Chemistry, Chemical Engineering, or other Life Science discipline2+ years of experience in an cGMP or GLP analytical laboratory environment

OR

PhD in Chemistry, Chemical Engineering, or other Life Science discipline

 

Preferred Qualifications:

 

Excellent written and verbal communication skillsExcellent documentation practices and attention to detailAbility to excel in a team environmentExperience working in an analytical testing lab with hazardous and toxic chemicalsSuperior technical writing skills to generate development reports

RSREMD

 

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.