Chemical EngineerGL Staffing • Davie, FL, US

Chemical Engineer

GL Staffing • Davie, FL, US

8 days ago

Job type

Full-time

Job description

Job Description

We are seeking a skilled Chemical Engineer to design, analyze, and optimize pharmaceutical manufacturing processes. The role involves leading process improvement and development projects, resolving complex technical and operational challenges, and ensuring compliance with Good Manufacturing Practices (GMP), quality standards, and regulatory requirements. The ideal candidate will have strong technical expertise, project management experience, and a continuous improvement mindset.

Shift / Working Hours

Hours : 8 : 00 AM – 5 : 00 PM Mon- Fri

Key Responsibilities

Analyze, design, and optimize pharmaceutical manufacturing processes (e.g., formulation, mixing, granulation, coating, sterilization)

Lead process improvement and development projects from concept through implementation

Apply structured problem-solving methodologies (Root Cause Analysis, 5 Whys, Fishbone, FMEA) to address deviations and operational issues

Drive process improvement initiatives focused on yield, efficiency, robustness, and scalability

Collaborate with Production, Quality, Validation, Engineering, Maintenance, and R&D teams

Ensure all process changes comply with GMP, regulatory requirements, and quality standards

Develop, review, and maintain process documentation, SOPs, batch records, and technical reports

Support process validation, revalidation, and technology transfer activities

Analyze process data and KPIs to drive continuous improvement and risk reduction

Lead or support CAPA investigations related to process deviations, non-conformances, and OOS results

Participate in internal and external audits (FDA, EMA, local authorities)

Train manufacturing and technical personnel on process changes and best practices

Required & Preferred Qualifications

Education

Bachelor’s degree in Chemical Engineering

5–10 years of experience in chemical engineering, process improvement, or pharmaceutical manufacturing

Proven experience in process development and project execution

Strong technical problem-solving and root cause analysis skills

Experience supporting validation and regulatory inspections preferred

Technical Knowledge

Pharmaceutical manufacturing processes and unit operations

GMP / cGMP, FDA, EMA regulations

Process validation, scale-up, and technology transfer

Risk management tools (FMEA, HACCP)

Statistical analysis and process capability (Cp, Cpk)

Process data analysis tools and advanced Excel

Apply now

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Chemical Engineer • Davie, FL, US

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