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, Quality position is responsible for validating methods and technical transfers as well as providing technical and analytical leadership to the Quality Control department at Millipore Sigma.  Analysis involves the use of HPLC, GC, KF, DSC, TGA, IR, MS, NMR and XRPD among other tests and instruments.  The position demonstrates the ability to work on, and solve,  problems independently with some guidance. Other responsibilities may include initiation and review of deviations, OOS/OOT’s, change controls, and CAPA’s. Additionally, participation in process improvement initiatives, and working in a team environment.  The Scientist, Quality position, like all positions at SAFC, will require a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.  

Perform method validations, transfers and analytical testing cGMP materials (samples, reference standards) and ensure accuracy and quality of data by using proper laboratory techniques and documentation.Perform peer review.Train new or less experienced personnel in SOP content, analytical techniques, and instrument use.Work in a safe manner and ensure the lab stays in an audit ready and clean state.Maintain the laboratory by ordering reagents or supplies, ensuring clean glassware is available, disposing of waste properly, and completing general housekeeping chores.Work on complex problems in which analysis of data requires an in-depth evaluation of various factors. Perform technical review of data including, but not limited to, HPLC, appearance, KF, and GC for accuracy and quality.Exercise judgment within broadly defined procedures and practices to select technique, methods, and evaluation criteria for obtaining results.Solve problems and make decisions with minimal assistance.Maintain projects and timelines with minimal oversight.Meet with internal and external groups to keep projects on track.Perform instrument Performance Verifications (PV) and Operational Qualifications (OQ) as needed.Participate in OOS and OOT investigations via testing and good documentation.  Apply critical thinking and good problem-solving skills to thoroughly identify root causes and propose appropriate corrective/preventive actions with minimal assistance.Author and revise SOPs including raw material specifications, intermediate specifications, final product specifications, and stability protocols.Work cooperatively within the QC department and with other departments to achieve project goals.Work in compliance with effective procedures and regulatory requirements outlined in ICH Q7 and 21 CFR Parts 11, 210, and 211 as applicable.Support all data integrity initiatives and strive for right first time.

Physical Attributes:

Wear appropriate protective gear (hard hats, lab coats, safety glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protective equipment “PPE”to protect from toxic or corrosive chemicals in the forms of liquids, solids, vapors, or airborne particles.Work with highly potent/hazardous materials requiring the use of proper PPE, which could include half/full face respirators, Saranex and/or Tyvek suits with powered respiration.Regularly sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch, or crawl for extended periods of time.Occasionally lift and/or move up to 30 pounds unassisted and be capable of pushing and pulling and pulling heavy materials to complete assignments and may need to lift more poundage with assistance.Will speak, hear, taste, and smell.Use close vision, distance vision, color vision, peripheral vision, depth vision and adjust focus.

Who You Are:

Minimum Qualifications:

Bachelor’s Degree in Chemistry, Chemical Engineering, or other Life Science discipline.5+ years of experience in a GLP or cGMP analytical laboratory environment.

Preferred Qualifications:

Experience with method validation.  Experience as a project lead.Experience with team and client interactions.Experience with  technical writing skills to author operating procedures, protocols and reports.Ability to work in analytical testing lab with hazardous and toxic chemicals.Knowledge and understanding of organic analytical chemistry.

 

 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!

 

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html