Sr. Investigator

About the role

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 Reports to QMS Manager and Quality Systems Team. 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!

Responsibilities

• Provide timely resolution of assigned deviations and complaints, ensuring investigations are thoroughly investigated to determine root cause and that robust CAPA’s are implemented whenever necessary.
• Be assigned specific areas for which you will be responsible for deviation investigation.
• Coordinate with the area, technical support, and other personnel to facilitate completion of deviation investigations.
• Keep track of deviations for assigned area(s) and help ensure deviations are evaluated and closed per timing requirements.
• Generally handle the more complex deviations that require greater experience and coordination to complete investigation.
• Process deviations and complaints within the quality management system and conduct thorough root cause investigations.
• Interview personnel involved and interact with technical support and other personnel to determine root causes of deviations and assess impact.
• Review instructions, reference material, and documentation to understand the processes being investigated and what went wrong.
• Track deviations for your assigned area to help ensure on‑time completion of each step.
• Scope, track, and complete deviation investigations for assigned areas and assist the manager in improving the quality of investigations.

Requirements

• Bachelor’s degree in a science or engineering field.
• Minimum of 5 years of experience in a pharmaceutical manufacturing site environment.
• At least 2 of those years directly supporting deviation investigations.

Skills

• Advanced user of Microsoft Office products, including Excel, Word, Access, and PowerPoint.
• Use and system knowledge and experience of Quality Management Systems.
• Ability to interface with personnel from multiple areas to deliver results (e.g., complete deviation investigation).
• Demonstrated ability to write thorough, clear, concise, and logically organized technical documents.

Pay

Pay range for this position: $104,10