Sr Quality Engineer

Cencora • Juncos, PR

10d • Onsite

About The Position

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Summary of Role: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University).

Requirements

• Engineering degree: Mechanical, Electrical or Chemical preferred (not Science)
• min. 5 yrs on field (quality – excluding experience laboratory micro/chemistry ) or engineering
• Seasoned individual contributor.
• Works independently under limited supervision to determine and develop approach to solutions.
• Coaches and reviews the work of lower level specialists .
• Requires advanced knowledge of job area combining breadth and depth, typically obtained through advanced education combined with experience.
• May have practical knowledge of project management.

Nice To Haves

• Experience with Risk management documentation: pFMEAs
• Basic knowledge in statistics (preferably using Minitab)
• Basic knowledge in designing validation strategies (e.g requirements flow down from design to manufacturing)
• Experience investigating manufacturing operations events in support to product disposition
• Experience assessing and tracing manufacturing defects/rejects trends
• Perform and/or review process validation (not cleaning processes) and equipment documents: URS, FAT, IQ, OQ, PQ, TMV (not laboratory)
• Knowledge in Medical Devices regulations
• Experience with projects: design requirements validation, manufacturing controls (not Operational Excellence)

Responsibilities

• Develops, modifies, applies and maintains quality standards.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Develop and implements methods and procedures for inspecting, testing and evaluating products and production equipment.
• Performs statistical analysis.
• Ensures that documentation is compliant with requirements.
• May specialize in the areas of design, production control, product evaluation and reliability, as they apply to product or process quality.

Benefits

• We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members’ ability to live with purpose every day.
• In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness.
• This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave.
• To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees