Senior Process Engineer - Pharmaceutical Manufacturing

Placements24

Noord-Kaap

Hybrid

ZAR 900,000 - 1,200,000

Full time

14 days+
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Benefits offered by this job

Competitive salary
Health insurance
Retirement plan
Paid time off
Career advancement

Job summary

Placements24 seeks a highly experienced Senior Process Engineer to oversee and optimize pharmaceutical manufacturing processes in Kimberley, South Africa. The role focuses on process development, validation, troubleshooting, and continuous improvement within a GMP environment.

You will collaborate with R&D, Quality Assurance, and Production to transfer and scale new processes, ensuring compliance with GMP and regulatory standards, delivering high-quality products and cost-efficient operations.

Qualifications

  • Bachelor's degree in Chemical or Mechanical Engineering.
  • 6+ years of pharmaceutical process engineering experience.
  • Strong GMP knowledge and regulatory understanding.
  • Experience in validation, scale-up, and troubleshooting.
  • Analytical mindset with project management skills.

Responsibilities

  • Design, develop, and optimize manufacturing processes to improve yield and product quality.
  • Lead process validation activities per regulatory requirements.
  • Troubleshoot and implement CAPAs for process issues.
  • Drive continuous improvement using Lean/Six Sigma methodologies.
  • Collaborate with R&D, QA, and Production for tech transfer and scale-up.
  • Ensure GMP compliance and regulatory standards across manufacturing.

Skills

Process engineering
GMP compliance
CAPA management
Root cause analysis
Project management
Process optimization

Education

Bachelor's degree in Chemical/Mechanical Engineering
Master's degree preferred

Tools

Process modeling software

Job description

About the Role

Our client is seeking a highly experienced and skilled Senior Process Engineer to oversee and optimize pharmaceutical manufacturing processes in Kimberley . This role is integral to ensuring the efficient, compliant, and high-quality production of pharmaceutical products. You will be responsible for process development, validation, troubleshooting, and continuous improvement initiatives within a GMP-regulated environment. This position offers a significant opportunity to contribute to the operational excellence of a leading pharmaceutical manufacturer, working collaboratively with production, quality, and engineering teams.

Key Responsibilities
  • Design, develop, and optimize pharmaceutical manufacturing processes to improve yield, reduce costs, and enhance product quality.
  • Lead process validation activities, including protocol development, execution, and report generation, in accordance with regulatory requirements.
  • Troubleshoot and resolve complex process-related issues, identifying root causes and implementing effective corrective and preventive actions (CAPAs).
  • Develop and implement continuous improvement initiatives using methodologies such as Lean Manufacturing and Six Sigma.
  • Collaborate with cross-functional teams, including R&D, Quality Assurance, and Production, to ensure smooth technology transfer and scale-up of new processes.
  • Ensure all manufacturing activities comply with Good Manufacturing Practices (GMP) and other relevant regulatory standards.
Requirements
  • Bachelor's degree in Chemical Engineering, Mechanical Engineering, or a related field.
  • Master's degree preferred.
  • Minimum of 6 years of experience in process engineering within the pharmaceutical manufacturing industry.
  • Strong understanding of GMP regulations and pharmaceutical manufacturing principles.
  • Proven experience in process validation, scale-up, and troubleshooting manufacturing operations.
  • Proficiency in process modeling and simulation software is a plus.
  • Excellent analytical, problem-solving, and project management skills.
Benefits
  • Competitive annual salary and performance-based bonus.
  • Comprehensive health, dental, and vision insurance.
  • Retirement savings plan with company contributions.
  • Generous paid time off and company holidays.
  • Opportunities for career advancement and specialized training in pharmaceutical manufacturing.
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