Quality Control Operations Specialist

Descripción del puesto:

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 Operations Specialist, Quality Control position supports planning, execution, and governance for quality systems projects in the Quality Control (QC) department. This position will have an understanding of the analytical workflow and instrumentation (HPLC, GC, KF, DSC, TGA, IR, MS, NMR, LC-MS and ICP-MS among other tests) in a QC lab in order to be able to critically evaluate, coordinate, and implement changes and process improvements. This position demonstrates the ability to work on, and solve problems independently with minimal guidance. This position will participate in duties and actions that support the QC functional areas to maintain an audit ready state and participate in responses to audit findings. This position is also responsible for maintaining project timing/costs and interacting with internal/external clients to assure project goals are met. Other responsibilities include maintaining a clean and safe working environment, drafting and reviewing departmental documents, and participating in data integrity initiatives. The Operations Specialist, Quality Control position, like all positions at MilliporeSigma, have a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.

* Drive continuous improvement through leading cross function teams to implement system improvements, Respond to new regulations, address evolving business needs, and enhance training for QC functional areas.

* Manage the full lifecycle of deviations, investigations, CAPA's, audit responses, and change controls within QC, ensuring timely closure, robust root cause analysis, and effective preventive actions.

* Assist in identifying, maintaining , and reporting functional KPIs to site management, enabling data-driven decision making and performance tracking.

* Participate in data integrity initiatives and processes related to QC functional areas.

* Work cross-functionally to support and expand digitization operations within QC (such as: STARe, Ommnis, Diffracto suite, Chromeleon, LIMS, and other software systems).

* Assist in drafting and reviewing of QC-related SOP's, technical reports, user requirements, and other documentation using the principles of ALCOA+.

* Represent QC interdepartmentally on QC projects, facilitating efficient and collaborative interactions with internal and external stakeholders.

* Other duties as assigned.

* Adhere to the GMP requirements defined within 21 CFR parts 210 &211, 820, ICH Q7, Safety standards set under ISO 14001 & 45001.

Who You Are

Minimum Qualifications:

* Bachelor's Degree in Chemistry, Biology, or other Life Science discipline.

* 5+ years in cGMP analytical laboratory environment.

Preferred Qualifications:

* Master's Degree in Chemistry, Biology, or other Life Science discipline.

* Work cross-functionally and to develop and maintain strong business partner relationships.

* Work with teams that work across various shift schedules that cover 24 hours/7 days.

* Manage multiple projects simultaneously with minimal supervision.

* Proficient with Microsoft Office Product (Outlook, Word, Excel, and PowerPoint).

Pay Range for this position: $63,600-$95,500.

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here

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!

Job Requisition ID: 300572

Location: Verona

Career Level: D - Professional (4-9 years)

Working time model: Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request. You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.
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