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Technical Applications Specialist
Job in
Boca Raton, Palm Beach County, Florida, 33481, USA
Listed on 2026-07-20
Listing for:
Jobtailor
Full Time
position Listed on 2026-07-20
Job specializations:
-
Engineering
Process Engineer, Quality Engineering, Manufacturing Engineer, Regulatory Compliance Specialist -
Manufacturing / Production
Quality Engineering, Manufacturing Engineer, Regulatory Compliance Specialist
Job Description & How to Apply Below
- Support product development, renovation, and formulation optimization across formats (solid dose, liquid RTD, powders)
- Design and execute formulation studies, development trials, and industrial trials
- Support scale-up, validation, and production startup activities from pilot to commercial manufacturing
- Assist with technology transfer to internal sites and external manufacturers (CMOs), including documentation
- Prepare and maintain technical and manufacturing documentation (batch records, specifications, protocols, change controls)
- Define and support manufacturing processes, equipment parameters, and operational controls
- Troubleshoot manufacturing and process issues and implement corrective actions
- Apply scientific principles and material characteristics to formulation and manufacturing processes
- Analyze and report data to support process improvements and statistical evaluation
- Ensure compliance with SOPs, GMP, quality standards, and regulatory requirements
- Collaborate cross-functionally (Manufacturing, Quality, Regulatory, Procurement, Supply Chain, R&D, Marketing, Finance) to resolve product, process, and supply issues
- Support continuous improvement efforts to enhance product quality, yield, and efficiency
- Provide technical support for investigations, risk assessments, and process improvements
- Engage with suppliers and external partners and stay current on industry trends
- Communicate project updates, risks, and changes to stakeholders and management
- Bachelor’s degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Food Science, or related technical field
- 1+ year of experience in product development, process development, scale-up, or technology transfer
- Experience with development and characterization of nutritional or solid dose products
- Experience supporting manufacturing or industrial trials
- Familiarity with solid dose manufacturing processes (blending, encapsulation, tablet compression, coating preferred)
- Knowledge of laboratory activities, Quality by Design, Operational Excellence, and process capability concepts (e.g., statistical process control, process robustness)
- Proficiency with MS Office and Excel
- Ability to perform data collection, analysis, and reporting
- Ability to work in environments with exposure to powders, chemicals, and allergens
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