Quality Coordinator,Product Quality Job Leonia area,New Jersey USA,Quality Assurance

At Nestlé Health Science, we believe that nutrition, science, and wellness must merge, not collide. Here, we embrace the intrinsic connections of these three pillars, harnessing their collective strength to empower healthier lives. Our broad product portfolio includes renowned brands like Garden of Life®, Nature's Bounty®, Vital Proteins®, Orgain®, Nuun®, BOOST®, Carnation Breakfast Essentials®, Peptamen®, Compleat Organic Blends®, and more. We also have extensive pharmaceutical expertise, offering innovative medicines that aim to prevent, manage, and treat gastrointestinal and metabolic-related diseases.

At Nestlé Health Science, we bring our best for better lives. Our people are challenged to bring fresh, diverse views and make bold moves to empower healthier lives through nutrition. We know brilliant ideas can come from anyone, anywhere. Here we embrace the entrepreneurial spirit and collaborate with teams that champion focused and forward thinking. We are committed to fostering professional growth and celebrating the achievements of our people along the way.

We offer dynamic career paths, robust development, opportunities to learn from talented colleagues around the globe, and benefits that support physical, financial, and emotional wellbeing.

Join us to innovate for impact and reimagine the future of health and nutrition for patients and consumers.

POSITION OVERVIEW:

Under the direction of the Manager/Supervisor, the Quality Coordinator, Product Quality is responsible for reviewing the accuracy and completeness of all documentation pertaining to the manufacturing of a batch by following GDP (Good Documentation Practices).

The Coordinator is also responsible for adhering to the Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs) that are in effect, assuring the quality and quantity of the product produced. The Coordinator will establish priorities that align with daily schedules

KEY RESPOSIBILITIES:

Checks in-process data, including weights, seams, and other information, for compliance with established specifications.
Checks and completes final reconciliations for compliance.
Assures the presence and disposition of investigations, deviation reports, and rework documents when required. If documents or data are missing, the individual will initiate and participate in the investigation.
Brings any Good Documentation Practice (GDP) issues to the attention of the Lead or Supervisor, as required.
Updates batch status in AS400 and SAP.
Complies with company policies and procedures and maintains regular work attendance.
Takes personal responsibility for following safety rules, SOPs, and cGMP guidelines.
Runs and maintains reports.
Tracks and trends key indicators related to batch review, as needed.
Performs other duties as assigned.

EXPERIENCE AND

EDUCATION REQUIREMENTS:

Associate's or bachelor's degree preferred.
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.
Work environment may include exposure to powders, chemicals, and allergens, including peanuts, tree nuts, milk, dairy, eggs, wheat, gluten, soy, fish, sesame, and shellfish.

SKILLS:

Good English verbal and written skills.
Positive attitude regarding work and responsibilities.
Creativity and intellectual curiosity; tries different and novel ways to solve obstacles.
Continuously looks for ways to improve speed and quality.
Ability to remain effective during major changes in work tasks or the work environment and adjust to new structures, processes, requirements, or cultures.
Ability to work…