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Associate Specialist - Technical Group

Job in Boca Raton, Palm Beach County, Florida, 33431, USA
Listing for: Stouffers
Full Time position
Listed on 2026-07-05
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Manufacturing Engineer
Job Description & How to Apply Below
Position: Associate Specialist - Technical Applications Group

Associate Specialist - Technical Applications Group

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 SUMMARY

The Associate Specialist Technical Applications Group (TAG) supports the development, formulation, scale-up, and commercialization of nutritional and solid dose products, including capsules and tablets. This entry-level, hands-on role works across laboratory and manufacturing environments to support industrial trials, troubleshooting, data analysis, and technology transfer, partnering with cross-functional teams to ensure successful product implementation and compliance with quality and regulatory standards. This is an onsite, Monday–Friday role at the factory location in Boca Raton, FL.

RESPONSIBILITIES

  • Support formulation development, evaluation, and process improvement for nutritional and solid dose products
  • Execute laboratory studies, development trials, and assist with industrial trials and production support
  • Collect, analyze, and report data; prepare technical summaries and documentation
  • Support scale-up, validation, and technology/process transfer to internal and external manufacturing sites
  • Provide technical support for manufacturing, including troubleshooting, process improvements, and cost savings initiatives
  • Create and maintain technical documentation (raw material specifications, batch records, change controls, deviations, transfer documents)
  • Maintain laboratory records, equipment, and work spaces
  • Identify and support continuous improvement initiatives and elimination of non-value-added activities
  • Research and share scientific and technical information with the team
  • Perform documentation review and audits to ensure accuracy and compliance with SOPs, GLP, and cGMP standards
  • Support change control activities and track project approvals
  • Collaborate cross-functionally (Manufacturing, Quality Assurance, Quality Control, Regulatory, Procurement) to ensure compliance and resolve issues

REQUIREMENTS

  • Bachelor's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Food Science, or related scientific discipline
  • 0–1 year of relevant experience (internships, co-ops, or entry-level experience considered)
  • Basic understanding of formulation development and manufacturing processes
  • Familiarity with laboratory or manufacturing environments and nutraceutical, pharmaceutical, or consumer health products
  • Working knowledge of GLP and cGMP practices
  • Proficiency with Microsoft Office (Word and Excel)
  • Strong technical writing and documentation skills
  • Knowledge of scientific principles related to formulation and manufacturing processes
  • Ability to work in environments with exposure to powders, chemicals, and allergens

SKILLS

  • Strong communication (written and verbal) and collaboration skills
  • Analytical thinking and basic mathematical skills
  • Strong organizational skills and attention to detail
  • Ability to…
Position Requirements
10+ Years work experience
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