Position Details

Salary $71K – $113K USD / year

Type Full-Time

Experience entry

Exp. Years 0+ years

Education Bachelor of Science degree in Chemical Engineering, Biomedical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field (with expected completion no later than June 2026)

Category Science & Research

About this role

This role supports clinical manufacturing of oral solid dosage forms, ensuring quality and compliance through GMP documentation and process analysis.

Key Responsibilities

Lead batch manufacturing
Draft GMP documentation
Analyze process data
Build cross-functional partnerships
Support process improvements

Technical Overview

Focus on pharmaceutical process engineering, GMP documentation, data analysis, and unit operations like spray drying and hot-melt extrusion.

Ideal Candidate

The ideal candidate is an entry-level process engineer with a strong foundation in pharmaceutical manufacturing processes, GMP documentation, and data analysis. They should be eager to learn, detail-oriented, and capable of supporting clinical supply manufacturing in a collaborative environment.

Must-Have Skills

Data visualizationGMP documentationBatch record draftingProcess data analysisProcess engineering

Nice-to-Have Skills

Knowledge of drug product processingCommissioningQualification and ValidationUnit operations for solid oral dosage form manufacturingExperience with spray dryingExperience with hot melt extrusion

Tools & Platforms

ExcelGMP systems

Required Skills

Data visualizationGMP documentationBatch recordsProcess data analysisProcess engineeringPharmaceutical unit operationsSpray dryingHot-melt extrusionChange controlDeviation management

Hard Skills

ExcelData analysisGMP documentationBatch record draftingProcess data analysisProcess engineeringPharmaceutical unit operationsSpray dryingHot-melt extrusionChange controlDeviation management

Soft Skills

Interpersonal skillsCommunicationTechnical writingProblem-solvingCollaborationLearning mindset

Industry & Role

Industry Pharmaceuticals & Biotechnology

Job Function Support clinical supply manufacturing through process engineering and GMP documentation

Keywords for Your Resume

Process EngineerGMP documentationBatch recordsProcess data analysisProcess engineeringSpray dryingHot-melt extrusionDeviation managementChange controlGMPPharmaceutical unit operationsProcess improvementData visualizationGMP systems

Deal Breakers

Lack of GMP documentation experience, No pharmaceutical manufacturing background, Inability to work in a hybrid environment in Rahway, NJ

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Associate Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite)

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