Senior Process Engineer (Pharmaceutical Manufacturing)

Placements24; Willows (CA); On-site; USD 54,000 - 78,000; Full time

Benefits offered by this job

Medical Aid

Retirement Contributions

Performance Bonuses

Job summary

Placements24 client seeks a Senior Process Engineer to optimize pharmaceutical manufacturing processes in Welkom, Free State. You will design, validate, and implement new technologies to boost yield, efficiency, and product quality while ensuring GMP compliance.

Key duties include leading scale-up initiatives, writing technical documentation, and delivering training to the operations team. Strong collaboration with QA, R&D, and maintenance is essential.

Qualifications

• 5–7 years of pharmaceutical/process engineering experience.
• Experience in scale-up, validation, and optimization.
• Knowledge of GMP and FDA regulations.
• Strong documentation and project management skills.
• Willingness to work on-site in Welkom, ZA.

Responsibilities

• Lead process development and optimization initiatives for pharmaceutical manufacturing.
• Design, specify, and implement new process equipment and technologies.
• Develop and execute IQ/OQ/PQ validation protocols for equipment and processes.
• Analyze process data to identify improvements and implement corrective actions.
• Troubleshoot complex manufacturing issues and provide technical solutions.
• Ensure GMP and safety regulatory compliance across processes.
• Collaborate with Production, QA, R&D, and Maintenance teams.
• Deliver training to staff on new processes and equipment.
• Stay updated on industry best practices and emerging technologies.
• Prepare technical reports and documentation for regulatory submissions.

Skills

Chemical Engineering

Process Engineering

GMP Compliance

FDA Regulations

Validation

Project Management

Technical Writing

Cross-functional Collaboration

Education

Bachelor's degree in Chemical Engineering

Master's degree

Tools

Process simulation software

Job description

About the Role

Our client, a leading pharmaceutical company, is seeking a highly skilled Senior Process Engineer to enhance and optimize manufacturing processes at their facility in Welkom, Free State, ZA . This critical role involves designing, implementing, and validating new manufacturing technologies and processes to improve efficiency, yield, and product quality. The ideal candidate will possess a strong engineering background coupled with extensive experience in pharmaceutical manufacturing environments. You will be instrumental in driving innovation and ensuring operational excellence within our client's production operations in Welkom, Free State, ZA .

Key Responsibilities

• Lead process development and optimization initiatives for pharmaceutical manufacturing.


• Design, specify, and implement new process equipment and technologies.


• Develop and execute validation protocols (IQ/OQ/PQ) for manufacturing equipment and processes.


• Analyze process data to identify areas for improvement and implement corrective actions.


• Troubleshoot complex manufacturing process issues and provide technical solutions.


• Ensure all processes comply with GMP, safety regulations, and environmental standards.


• Collaborate with cross-functional teams including Production, Quality Assurance, R&D, and Maintenance.


• Develop and deliver training to technical staff on new processes and equipment.


• Stay abreast of industry best practices and emerging technologies in pharmaceutical manufacturing.


• Prepare technical reports, process flow diagrams, and documentation for regulatory submissions.

Requirements

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


• Master's degree preferred.


• Minimum of 5-7 years of experience in process engineering within the pharmaceutical or biotechnology industry.


• Proven experience in process design, scale-up, validation, and optimization of pharmaceutical manufacturing processes.


• In-depth knowledge of GMP, FDA, and other relevant regulatory requirements.


• Strong understanding of unit operations in pharmaceutical manufacturing (e.g., granulation, tablet compression, sterile filling).


• Experience with process simulation and modeling software is a plus.


• Excellent analytical, problem-solving, and project management skills.


• Proficiency in technical writing and documentation.


• Strong interpersonal and communication skills to effectively collaborate with diverse teams.


• Must be willing to work full-time on-site in Welkom, Free State, ZA .

Benefits

Our client offers a competitive salary commensurate with experience, along with a comprehensive benefits package including medical aid, retirement contributions, and performance bonuses. Opportunities for professional growth through advanced training, workshops, and conference attendance are readily available. The company fosters a collaborative and innovative work culture, prioritizing employee well-being and a sustainable work-life balance in Welkom, Free State, ZA . This role provides a significant opportunity to impact pharmaceutical manufacturing advancements.