Process Engineer

Jobtailor; New York (NY); On-site; USD 90,000 - 140,000; Full time

Job summary

Jobtailor in New York, NY is seeking a Process Engineer to provide technical and scientific support for Rx, OTC, and cosmetic topical products, and to lead technology transfer for new products.

You will collaborate with Regulatory Affairs, Quality, R&D, Operations, and Legal teams, develop and optimize manufacturing processes, investigate issues, and manage multiple projects while ensuring compliance with cGMP and FDA regulations.

Qualifications

• Bachelor's degree in a related scientific discipline is required.
• Experience in regulated pharmaceutical manufacturing is required.
• Strong technical writing and problem-solving skills.

Responsibilities

• Provide technical and scientific support for Rx, OTC, and cosmetic topical products
• Collaborate with Regulatory Affairs, Quality, R&D, Operations, and Legal teams
• Conduct technical assessments and provide ongoing process support
• Lead technology transfer activities for new products
• Develop and optimize manufacturing processes
• Investigate manufacturing issues and recommend corrective actions
• Prepare technical reports and documentation for process changes
• Manage multiple projects simultaneously

Skills

Pharmaceutical Manufacturing

CGMP Requirements

FDA Regulations

Technical Writing

Process Engineering

Problem Solving

Project Management

Interpersonal Skills

Organizational Skills

Communication Skills

Laboratory Processing

Commercial Processing

Education

Bachelor's degree in Pharmaceutical Sciences, Chemical Engineering, Pharmaceutical Engineering, Chemistry, or a related scientific discipline

Tools

SAP

Microsoft Office Suite

Job description

Responsibilities

• Provide technical and scientific support for Rx, OTC, and cosmetic topical products
• Collaborate with Regulatory Affairs, Quality, R&D, Operations, and Legal teams
• Conduct technical assessments and provide ongoing process support
• Lead technology transfer activities for new products
• Develop and optimize manufacturing processes
• Investigate manufacturing issues and recommend corrective actions
• Prepare technical reports and documentation for process changes
• Manage multiple projects simultaneously

Requirements

• Bachelor's degree in Pharmaceutical Sciences, Chemical Engineering, Pharmaceutical Engineering, Chemistry, or a related scientific discipline
• 2–5 years of pharmaceutical manufacturing, process engineering, technical services, or process support experience in a regulated environment
• Strong understanding of pharmaceutical manufacturing processes
• Knowledge of cGMP requirements and FDA regulations
• Excellent interpersonal, organizational, and communication skills
• Strong technical writing and problem‑solving skills
• Hands‑on experience with laboratory‑scale and commercial‑scale pharmaceutical processing equipment
• Proficiency with Microsoft Office applications, including Excel, Word, PowerPoint, and OneNote; experience with SAP is preferred

Core Competencies

Demonstrates expertise in pharmaceutical manufacturing processes, regulatory compliance, and technical documentation. Capable of leading technology transfer activities and optimizing manufacturing processes while managing multiple projects in a collaborative environment.

Highest‑signal resume keywords

• Pharmaceutical Manufacturing
• CGMP Requirements
• FDA Regulations
• Technical Writing
• Process Engineering

Key Skills

• Pharmaceutical Sciences
• Chemical Engineering
• Process Support
• Technical Assessments
• Manufacturing Process Optimization
• Laboratory‑Scale Processing
• Commercial‑Scale Processing
• Problem‑Solving
• Project Management
• Technical Documentation
• Interpersonal Skills
• Organizational Skills
• Communication Skills
• Microsoft Office
• Excel
• Word
• PowerPoint
• OneNote
• SAP