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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in formulation development and manufacturing processes, with a strong focus on compliance with GLP and cGMP standards. Proficient in technical writing and documentation, supporting cross-functional collaboration in a laboratory or manufacturing environment.

Highest-signal resume keywords

Formulation DevelopmentGLP and cGMP PracticesTechnical WritingLaboratory Environment FamiliarityCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Formulation DevelopmentManufacturing ProcessesTechnical DocumentationData AnalysisProcess ImprovementChange ControlDocumentation ReviewScientific PrinciplesCost Savings InitiativesContinuous Improvement

Soft Skills

CollaborationTroubleshootingCommunication

Tools & Technologies

Microsoft OfficeLaboratory Equipment

Industry Keywords

Nutraceutical ProductsPharmaceutical ProductsConsumer Health ProductsSOPsBatch RecordsRaw Material Specifications

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