Quality Engineer

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All . We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone , we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo . We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

The Quality Engineer provides support for data analysis and continuous improvement projects related to product and process quality. In addition, the QE provides Quality Assurance review and approval for annual product reviews, as well as support for review of deviation investigations, laboratory investigations, and other cGMP documentation and studies conducted at Perrigo New York, and ensures that all information and documentation conforms to company policy, cGMP's and all other applicable FDA guidance.

Please note - We do not offer relocation for this position, and it is an onsite role

Salary Range: $85,000 - $100,000

Scope of the Role

• Data analysis projects including APR analysis, Ppk improvements, stability assessments, and the development of real-time statistical analysis using Minitab Connect.
• Participates in quality driven initiatives in the continuous support of Quality improvements, using data analysis techniques and other improvement tools.
• Works with operations, laboratory, engineering, and maintenance managers and staff to develop, evaluate and implement action plans which maintain or improve product and process quality.
• Supports the reviewing and approving of documents such as deviations, Annual product reports, non-routine batch status change requests, CAPA closures, calibration non conformances, etc.

Experience Required

• Bachelor's Degree in a scientific discipline or closely aligned field, with a minimum of two years experience working in an FDA regulated industry.
• Demonstrated understanding of and ability to apply cGMPs and US FDA laws and requirements in an FDA regulated industry.
• Strong functional knowledge of SAP systems.
• Demonstrated ability to organize multiple tasks and change priorities to meet project deadlines.

Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about at Perrigo.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more

Applicants please note:  To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo