AMVETS Jobs

Position: Corporate Quality Coordinator Location: Cincinnati, OH Job Id: 1422

of Openings:

0 Corporate Quality Coordinator Reporting directly to the Total Quality Manager (TQM), the Corporate Quality Coordinator (CQC) supports the Corporate Quality team by ensuring the company's policies and practices meet regulatory requirements in a food, cosmetic and pharmaceutical environment. The CQC will control, organize, and maintain proprietary documentation for the company and customers. The CQC will also support the organization by participating in quality auditing, document writing, product statements, document control and employee training. This position will work with all levels of management and associates to facilitate problem-solving and ensure customer and regulatory quality standards are achieved. Why work for us We offer competitive hourly pay and a comprehensive suite of health & financial benefits to full time employees, including medical, dental, vision, company paid life insurance & disability, as well as: Annual Bonus up to 2k Retirement: 401K with company match & 401K profit sharing contribution (up to 9%). Time off w/ Pay: Vacation + 10 paid holidays + Personal Days Perfect Attendance Recognition Rewards Advancement Opportunities - skill-based increases Tuition Assistance Overtime available $1500 Referral Bonus Program for current employees (come work for us and refer your friends and family) And more! POSITION REQUIREMENTS Education, Credentials, Licenses: Associates or Bachelors degree in science or technical degree and/or combination of education and experience is required. Quality Assurance training or certification preferred. Kind & Length of Experience: Minimum of 2 years of experience in quality or scientific in a regulated industry is required. Familiar with customer and regulatory audits (ie. ISO, SQF, GFSI, RSPO, FDA) Proven technical writing skills and attention to detail is a plus. Must be comfortable with repetitive task oriented work. Strong working knowledge of editing, proofreading, spelling, grammar, and punctuation. Skilled at organizing information into a clear and concise written form. Ability to work independently as well as in a team environment. Strong Computer skills with MS Office Suite experience Experience in an ERP system, document control software, Enovia / Spec Reader, or SharePoint software This position involves customer specific software and data processing software daily to input the technical parameters from the documentation so that production can meet the specifications. Internal auditing skills to a quality standard, a plus. Facilitation of training materials or experience presenting to a group preferred PERFORMANCE MEASURES AND STANDARDS Work independently on assigned projects and daily QA maintenance functions. Assist with the development of Quality Management Systems (QMS) based on company's global standards and regulations by collecting and analyzing data. Creation and/or editing of procedures, product documents, quality newsletter articles, training documentation, and other support materials. Produce electronic documentation in addition to hard copy manuals. Provide support in the development and maintenance of a Document Control program that can be utilized across several sites. Provide support in vendor quality approval program for materials and services including quality agreements, incoming specifications, and incoming test methods using the new processes & systems established. Provide support in the development of onsite education and training programs including new employee orientation and annual GMP training. Provide training and education of the quality management syst