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Nestle

Associate Specialist – Technical Applications Group

Nestle

Associate Specialist in Technical Applications Group supporting development of nutritional and solid dose products at Nestlé Health Science. Collaborating across teams for product formulation and compliance in Boca Raton, FL.

Posted 7/2/2026full-timeBoca Raton • Florida • 🇺🇸 United StatesJuniorMid-LevelWebsite

About the role

Key responsibilities & impact
  • 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 workspaces
  • 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

What you’ll need
  • 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

Benefits

Comp & perks
  • dynamic career paths
  • robust development
  • opportunities to learn from talented colleagues around the globe
  • benefits that support physical, financial, and emotional wellbeing

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
Formulation DevelopmentManufacturing ProcessesTechnical DocumentationData AnalysisProcess ImprovementChange ControlDocumentation ReviewScientific PrinciplesCost Savings InitiativesContinuous Improvement
Soft Skills
CollaborationTroubleshootingCommunication