Process Engineer - Pharmaceutical Manufacturing

Placements24; Kimberley; Hybrid; CAD 51,000 - 77,000; Full time

Benefits offered by this job

Medical aid

Retirement planning

Hybrid work arrangement

Job summary

Placements24 seeks a detail-oriented Process Engineer to optimize pharmaceutical manufacturing processes in Kimberley. You will design and validate processes for APIs and finished dosage forms, ensuring GMP compliance.

The role requires 4+ years in pharma/biotech, strong GMP experience, and hands-on exposure to unit operations and process simulation. Hybrid role with opportunities for professional growth.

Qualifications

• Bachelor's degree in Chemical Engineering and 4+ years of experience in pharmaceutical/biotech manufacturing.
• Strong GMP and validation principles understanding.
• Experience with unit operations (crystallization, filtration, drying, blending, tablet compression).
• Proficiency in process simulation and data analysis tools.
• Excellent problem-solving and organizational skills.
• Strong communication and cross-functional teamwork abilities.
• Lean Six Sigma experience a plus.
• Cleanroom/aseptic processing familiarity an advantage.

Responsibilities

• Optimize existing manufacturing processes to improve yield, efficiency, and product quality.
• Develop process documentation, including SOPs, batch records, and validation protocols.
• Troubleshoot production issues, identify root causes, and implement effective solutions.
• Participate in process validation activities (IQ, OQ, PQ) and ensure GMP compliance.
• Collaborate with R&D, QA, and Manufacturing to support new product introductions and process improvements.
• Conduct process hazard analyses and implement safety measures.
• Evaluate and recommend process equipment upgrades and modifications.
• Monitor process performance data and prepare reports on key metrics.
• Stay updated on pharmaceutical regulations and industry best practices.
• Contribute to a culture of continuous improvement and operational excellence.

Skills

Regulatory compliance

GMP knowledge

Process optimization

Data analysis

Cross-functional collaboration

Problem solving

Lean Six Sigma

Cleanroom familiarity

Education

Bachelor's degree in Chemical Engineering

Tools

Process simulation tools

Job description

About the Role

Our client, a rapidly growing pharmaceutical company, is seeking a detail-oriented Process Engineer to enhance their manufacturing operations in Kimberley, Northern Cape . This role is focused on optimizing processes for the production of active pharmaceutical ingredients (APIs) and finished dosage forms, ensuring compliance with stringent regulatory standards (e.g., GMP). You will be involved in process design, troubleshooting, validation, and continuous improvement initiatives. The ideal candidate possesses a strong understanding of pharmaceutical manufacturing principles and a commitment to quality and safety. This is a key position within a thriving company contributing to healthcare solutions in the region.

Key Responsibilities

• Optimize existing manufacturing processes to improve yield, efficiency, and product quality.


• Develop process documentation, including SOPs, batch records, and validation protocols.


• Troubleshoot production issues, identify root causes, and implement effective solutions.


• Participate in process validation activities (IQ, OQ, PQ) and ensure compliance with GMP guidelines.


• Collaborate with R&D, Quality Assurance, and Manufacturing teams to support new product introductions and process improvements.


• Conduct process hazard analyses and implement necessary safety measures.


• Evaluate and recommend process equipment upgrades and modifications.


• Monitor process performance data and prepare reports on key metrics.


• Stay updated on relevant pharmaceutical regulations and industry best practices.


• Contribute to a culture of continuous improvement and operational excellence.

Requirements

• Bachelor's degree in Chemical Engineering or a related scientific field.


• Minimum of 4 years of experience as a Process Engineer in the pharmaceutical or biotechnology industry.


• Strong understanding of GMP regulations and validation principles.


• Experience with pharmaceutical unit operations (e.g., crystallization, filtration, drying, blending, tablet compression).


• Proficiency in process simulation and data analysis tools.


• Excellent problem-solving, analytical, and organizational skills.


• Strong communication and interpersonal skills, with the ability to work effectively in cross-functional teams.


• Detail-oriented approach and a commitment to quality.


• Experience with Lean Manufacturing or Six Sigma methodologies is a plus.


• Familiarity with cleanroom environments and aseptic processing is an advantage.

Benefits

Our client offers a competitive salary, comprehensive benefits package including medical aid and retirement planning, and opportunities for professional growth within the pharmaceutical sector. This hybrid role allows for a balance between on-site process involvement and off-site analysis and reporting. Working in Kimberley provides exposure to key manufacturing operations. Our client is dedicated to fostering a productive and collaborative work environment.