Quality Coordinator, Product Quality

Nestle Operational Services Worldwide SA•Leonia, NJ

2d•$51,250 - $73,250

About The Position

Under the direction of a Manager or Supervisor, the Quality Coordinator, Product Quality reviews batch-manufacturing documentation for accuracy and completeness in accordance with Good Documentation Practices (GDP). The role follows applicable Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs) to help assure product quality and quantity, and establishes priorities aligned with daily schedules. The work environment may include exposure to powders, chemicals, and food allergens.

Requirements

Proficient computer skills, including Microsoft Office.
Proficient basic mathematical and analytical skills.
Computer literacy and proficiency in math, basic statistics, office, and technical applications.
Proficiency with AS400, SharePoint, Excel, Word, PowerPoint, Veeva, and SAP.
Familiarity with GMP and Good Documentation Practices.
Good English verbal and written skills.
Positive attitude regarding work and responsibilities.
Creativity and intellectual curiosity, with an ability to try different approaches to solve obstacles.
Continuously look for ways to improve speed and quality.
Ability to remain effective through major changes in work tasks or environment and adjust to new structures, processes, requirements, or cultures.
Ability to work collaboratively within teams.

Nice To Haves

Associate's or bachelor's degree.

Responsibilities

Check in-process data, including weights, seams, and other information, for compliance with established specifications.
Check and complete final reconciliations for compliance.
Ensure required investigations, deviation reports, and rework documents are present and properly dispositioned; initiate and participate in investigations when documents or data are missing.
Bring Good Documentation Practice issues to the attention of the Lead or Supervisor as required.
Update batch status in AS400 and SAP.
Comply with company policies and procedures and maintain regular work attendance.
Follow safety rules, SOPs, and cGMP guidelines.
Run and maintain reports.
Track and trend key indicators related to batch review as needed.
Perform other duties as assigned.