Work Your Magic with us!

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 Control Analyst 3 is a senior level technical position that will be responsible for performing analytical work on new methods for finished product and raw materials. In addition, this position will execute and manage method development, method transfer protocols, method validation protocols, investigation protocols, and instrument qualification protocols.

• Perform routine chemistry testing on raw materials, in-process samples, finished product samples, and stability samples according to validated methods

• Technical training and mentorship of lesser experienced chemistry personnel

• Develop and supervise the execution of protocols for method transfers, method validations, stability studies, and cleaning validations

• Develop and supervise special studies/projects applicable to the Chemistry Laboratories
• Management of periodic reviews of analytical test procedures and SOPs as required
• Review and approval of Analytical testing procedures and protocols
• Represent QC department as technical expert on special studies and validations when required
• Responsible for project managing assigned QC capital projects
• Support manufacturing process control & process improvement projects
• Performs special projects and other duties as assigned
• Handling wastes, including hazardous wastes

• Attending mandatory annual hazardous waste training meeting(s) and show competency in that training by passing test(s) administered by the company or consultant providing such training

Minimum Qualifications:

• Bachelor's Degree in Chemistry
• 4+ years' experience in a quality role within the pharmaceutical industry

Preferred Qualifications:

• Master's Degree in Chemistry
• Experience in cGMP testing/manufacturing environments
• Ability to perform analytical testing (HPLC, GC, TLC, UV/VIS Spectroscopy, FTIR Spectroscopy, Particle Size, Electrophoresis)
• Working knowledge of Empower 3
• Strong technical knowledge of bio-analytical and chemistry analytical techniques
• Familiarity with analytical validations, method transfers, cleaning validations, and scientific research
• Ability to communicate at all levels in a pharmaceutical organization
• Good interpersonal skills

RSRMS

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