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Quality Specialist; Day Shift

Job in Boca Raton, Palm Beach County, Florida, 33481, USA
Listing for: Nestlé Health Science
Full Time position
Listed on 2026-06-02
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Quality Specialist (Day Shift)

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 Quality Lab Services, the Specialist is responsible for performing routine and specialized non-routine laboratory procedures in a Quality Control (QC) laboratory. Duties are performed under limited supervision. Ability to take on a larger scope of support functions and increased responsibility for managing a range of projects.

KEY RESPONSIBILITIES
  • Manages and performs root cause analyses and investigational studies for out-of-specification (OOS) and out-of-trend (OOT) results, including partnering with QC Analysts, Analytical Services, R&D, CTAG, Quality, and/or Operations to address problematic bulks and finished goods.
  • QC representative for material review board (MRB) meetings. Discuss non-conformance reports (NCRs) related to QC OOS investigations and responsible for executing any follow up actions required by QC.
  • Follow up on requests for additional or location samples for investigations (approximately 20 samples/month).
  • Print, report, and follow up on results reports daily for samples being sent to external laboratory: (approximately 3000 tests/month; 600 samples x 5 tests/sample).
  • Perform Gluten testing in-house for all samples submitted to the QC laboratory (approximately 350 samples per month).
  • Follow up on results for allergen testing: 10 samples for allergen test sent out / month.
  • Interpret the microbial test results and countersign the Product Evaluation Forms with results: 600 PEFs per month.
  • Collect samples for Environmental monitoring (water samples, air samples and compressed air samples) for both facilities 901 and 1297 buildings (approximately 100 samples per month).
  • Create graphs and data to store the environmental monitoring results for audits (once per month). Interpret Environmental monitoring sample results (approximately 100 samples per month) (water and air samples) for the facility (two buildings 901 and 1297).
  • Provide support during audits (getting information and data ready as requested before and during the audit) as needed to provide data/results from microbiological perspective. (about 10 audits per year.
  • Records data, performs calculations, evaluates and reports results. Performs peer review of data and provides critical analysis of laboratory systems. Keeps management apprised of progress.
  • Prioritizes workload and meets scheduled timelines, including managing multiple priorities.
  • Follows and complies with all testing procedures, operating procedures, GMPs, and safety and health requirements, as applicable.
  • Demonstrates good housekeeping practices to minimize analytical mix ups, potential laboratory contamination and safety hazards. Understanding and handling of hazardous materials and waste using proper and safe techniques. Selected qualified associates, at the discretion…
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