Product Quality Specialist - Orem

The Quality Support team works very closely with most teams across our corporate and field divisions as a group of subject matter experts.We specialize in assisting installers with day of install issues. · Our dedicated team is committed to making solar energy accessible and affo ...

The Quality Control Reverification Specialist ensures accuracy and validity of information provided in mortgage loan applications through detailed verification processes. · Responsibilities include contacting employers and other parties to confirm employment and data, · Conduct r ...

At doTERRA we encourage all employees to seek out opportunities that will expand their skill set. · We strive to help achieve personal career goals by providing opportunities of growth and movement throughout the company. · Works closely with Global Complaint Leader to manage com ...

The Quality Specialist will execute tasks related to regulatory and quality system functions, as well as participate in product development and operational tasks. Execute incoming inspection of raw materials, oversee in-process and final product QC. · The job requires working wit ...

We are looking for a Quality Compliance Specialist to maintain digital records and handle quality and regulatory aspects of food, supplements and cosmetics. Prior industry experience is not required but collaboration with cross-functional teams and focus on continuous improvement ...

This position assists in quality event management in compliance with regulations, Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs). · ...

We are seeking to add an experienced Project Manager to our team. The ideal candidate for this job is resourceful, a good problem solver, and organized. · Manage project timelines and ensure milestones are being met in each stage. · Negotiate prices and terms with factories. · ...

You'll be working for a liquids manufacturing company in an office with the option to occasionally work from home. · ...

The Quality Assurance Specialist supports the Quality Manager in maintaining Aspen Co-Pak's compliance with cGMP, · FDA (21 CFR 111/117), NSF/455-2, Organic, Kosher, · and customer quality requirements.Create Master Manufacturing Records (MMRs) · Evaluate Certificates of Analysis ...

The Quality Assurance Specialist supports the Quality Manager in maintaining Aspen Co-Pak's compliance with cGMP,FDA (21 CFR 111/117),NSF/455-2, Organic,Kosher,and customer quality requirements. · Ensures accurate records,strong GMP compliance,effective execution of key quality s ...

The Specialist II Quality will primarily support activities related to document and record control. · ...

This position is onsite in our West Jordan UT facility and supports Route 92 Medicals efforts to sustain a best practice Quality System by ensuring compliance to regulatory requirements such as FDA QSR ISO 13485 and the EU MDR Ensure all products meet all applicable internal and ...

We welcome team members who approach their work with courage, flexibility, persistence and a willingness to assist others. · Adaptable to a fast-paced environment · Attention to detail and focus on the identification of potential issues and continuous improvement · ...

We welcome team members who approach their work with courage flexibility persistence and a willingness to assist others Teamwork matters here We are committed to collaboration finding innovative solutions that advance neurovascular intervention establishing Route 92 Medical as on ...

Selective processing of customer complaints and maintenance of complaint files. Training will be provided regarding processing of MDR's and ADE's. · A bachelor's degree in Health Science is preferred but an associate degree with applicable experience will be considered. · The man ...

The Quality System Specialist I will review complaint detail and write/processing of customer complaints specifically Medical Device Reports (MDRs) under the direction of Sr. Manager Quality Assurance. · ...

We are seeking Quality System Specialist I to process customer complaints and maintain complaint files under the direction of Sr. Manager Quality Assurance. The ideal candidate should have a background in Medical Lab Technician or Medical Technologist. · ,Under the direction of t ...

The Staff Quality System Specialist II will be responsible for processing of customer complaints specifically Medical Device Reports (MDR's) and Adverse Drug Events (ADE's), including maintenance of complaint files, responses to customers and complaint reports. · ...

The Senior Compliance Specialist plays a key leadership role in ensuring the organization's GLP, GMP/QMSR, and ISO 17025 operations remain compliant. · ...

Under the direction of the Sr. Manager Quality Assurance the Staff Quality System Specialist II will be responsible for processing of customer complaints specifically Medical Device Reports (MDRs) and Adverse Drug Events (ADes), including maintenance of complaint files, responses ...