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 Quality Scientist (QC Microbiology) is responsible for microbiology related analysis specifically including but not limited to in-process, drug substance, raw material and water sample analysis. Job duties include:

 

Conduct and lead testing of raw materials and products using a variety of equipment and compendial methodology and non-compendial methods, including analytical and microbiological testing for quality compliance and release.Perform technical review of assays and assist in method development, process improvements and resolves complex technical issues through analytical thinking and troubleshooting using established or advanced technologies.Ensuring that suitable written records and work undertaken are kept in accordance with cGMP and company procedures.Working within various internal departments to improve and execute processes used in an ICHQ7 environment. Assisting with OOS/OOT investigations and root cause analysis investigations.Interacting with the production and laboratory personnel regularly to ensure adequate communication and feedback for quality-related services to internal customers.Maintaining and updating relevant Ops.

 

Who You Are

Minimum Qualifications:

 

Bachelor’s Degree in Biology, Chemistry, or other Life Science discipline.5+ years of microbiology experience in a cGMP environment.

 

Preferred Qualifications:

 

API knowledge.Knowledge of SOPs, cGMPs, GLP, GDP and quality control processes.Knowledge and understanding of endotoxin (USP ) and Bioburden (USP) testingExperience with ICH Q7, 21CFR210, USP and EP.Experience writing technical documents and reports.Knowledge of aseptic technique and practices.Ability to perform minor troubleshooting on microbiological processes and associated laboratory equipment.Experience with documentation control: writes, reviews, and approves operating procedures, reports, protocols, and other QC controlled documents.Familiar with basic scientific/regulatory principles.Excellent written and verbal communication skills.Capacity to work independently.Ability to simultaneously manage multiple tasks/priorities good computer skills, including proficiency in MS Word, MS Excel, MS PowerPoint, and the ability to learn and operate other specific application software.Strong problem-solving and time management skills.

#RSREMD

 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!