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Job Details

Skills

Quality Management
Manufacturing Operations
Process Improvement
KPI
Technology Transfer
Risk Assessment
Continuous Improvement
Technical Support
Manufacturing
Process Engineering
Pharmaceutics
Biotechnology
Medical Devices
Lean Manufacturing
Mechanical Engineering
Manufacturing Engineering
GMP
Regulatory Compliance
Root Cause Analysis
Corrective And Preventive Action
Technical Writing
Data Analysis
Collaboration
Conflict Resolution
Problem Solving

Quality Management
Manufacturing Operations
Process Improvement
KPI
Technology Transfer
Risk Assessment
Continuous Improvement
Technical Support
Manufacturing
Process Engineering
Pharmaceutics
Biotechnology
Medical Devices
Lean Manufacturing
Mechanical Engineering
Manufacturing Engineering
GMP
Regulatory Compliance
Root Cause Analysis
Corrective And Preventive Action
Technical Writing
Data Analysis
Collaboration
Conflict Resolution
Problem Solving

Summary

Job Description:
The Process Engineer II supports manufacturing operations by optimizing production processes, implementing process improvements, and ensuring compliance with quality and regulatory standards. This role partners closely with Operations, Quality, Maintenance, and Engineering teams to improve efficiency and product reliability.
Roles & Responsibilities:

Support daily manufacturing operations and troubleshoot process issues.
nalyze production data to identify process improvement opportunities.
Develop and update manufacturing procedures and work instructions.
Lead process validation and equipment qualification activities.
Collaborate with Quality on deviation investigations and CAPAs.
Monitor KPIs and recommend corrective actions.
Support technology transfer and new product introductions.
Participate in risk assessments and continuous improvement initiatives.
Ensure compliance with GMP, FDA, and company policies.
Provide technical support to manufacturing personnel.

Requirements:

3-5 years of manufacturing or process engineering experience.
Experience in pharmaceutical, biotechnology, or medical device industries.
Knowledge of Lean Manufacturing principles.
Experience with process validation activities.
Bachelor's Degree in Chemical, Mechanical, Industrial, or Manufacturing Engineering.

Mandatory Skills / Competencies:

GMP Compliance
Process Validation
Root Cause Analysis
CAPA
Technical Documentation
Data Analysis
Cross-functional Collaboration
Problem Solving

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: f5deb59c36f483810e8c95039714278
Posted 19 hours ago

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