Product Quality Coordinator

 

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. 
 

 

Under the direction of the Manager/Supervisor, the QA Document Review Coordinator is responsible for reviewing accuracy and completeness of all documentation pertaining to the manufacturing of a batch. Also, responsible for adhering to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) that are in effect assuring the quality and quantity of product produced. Will establish priorities which are in line with the daily schedules.

 

General responsibilities:

• Checks In-process data (weights, seams, etc.) for compliance to established specifications
• Checks and completes the final Reconciliations for compliance
• Assures the presence and disposition of investigations, deviation reports and rework documents when required.   If documents/data are missing, individual will initiate and participate in the investigation
• Any GDP issues are brought to the attention of the Lead/ Supervisor as required
• Update batch status in AS400 and SAP
• Complies with company policies and procedures and maintains regular work attendance
• Personal responsibility for following safety rules, SOPs and cGMPs guidelines
• Runs and maintains reports
• Track and trend key indicators related to batch review as needed
• Performs other duties as assigned.

 

Qualifications:

• High School diploma or GED required
• 1-3 years of Previous Quality Assurance experience in related field preferred
• Batch Record/Documentation Review experience preferred
• Technical proficiency including Microsoft Word  and Excel
• High level of organizational skills, good written and oral communication skills
• Excellent mathematical skills
• Exhibit positive attitude regarding work and responsibilities
• Ability to work collaboratively within teams