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Process Engineer (Operations & Supply Chain Specialist)

West Coast Personnel

Wes-Kaap

On-site

ZAR 200,000 - 300,000

Full time

11 days ago

Job summary

A leading company in the manufacturing sector is seeking an experienced Process Engineer to join their operations team in Wes-Kaap, South Africa. The successful candidate will support the team's efforts in tooling, plastic molding, and global supply chain management while ensuring compliance with quality standards and regulatory documentation. Candidates should have at least 5 years of experience in a regulated industry, alongside a degree in engineering or similar fields. This is an exciting opportunity for those who excel in fast-paced environments.

Qualifications

  • A degree in Engineering, Supply Chain, Business, or a related field.
  • 5+ years' experience in operations, process engineering, or supply chain management ideally in a regulated industry.
  • Strong knowledge of manufacturing, logistics, and inventory systems.

Responsibilities

  • Lead new product introductions (NPI) and support the scale-up of manufacturing processes.
  • Take ownership of tooling and plastic molding, ensuring robust verification and validation of components.
  • Manage global supply chain operations including procurement, supplier performance, inventory, and logistics.
  • Oversee validation of new equipment, including documentation in line with quality and regulatory requirements.
  • Ensure compliance with ISO 13485 and support the creation of regulatory documentation as needed.

Skills

Tooling
Plastic Molding
Supply Chain Management
Process Development
Manufacturing
Logistics
Inventory Systems
ERP Systems
Problem-solving

Education

Degree in Engineering, Supply Chain, Business

Tools

Excel
MS Project

Job description

About the Role
Were looking for a hands-on, experienced Process Engineer with a strong background in tooling, plastic molding, and supply chain management to join our operations team. Youll report directly to the COO and play a critical role in managing our global manufacturing, logistics, procurement, and supplier relationships.
This role is ideal for someone who thrives in a fast-paced, high-impact environment and enjoys taking products from concept to customer with efficiency, repeatability, and regulatory compliance, especially in industries governed by ISO 13485.

Key Responsibilities

  • Lead new product introductions (NPI) and support the scale-up of manufacturing processes.
  • Take ownership of tooling and plastic molding, ensuring robust verification and validation of components to support repeatable production.
  • Manage global supply chain operations including procurement, supplier performance, inventory, and logistics.
  • Oversee validation of new equipment, including documentation in line with quality and regulatory requirements.
  • Ensure compliance with ISO 13485 and support the creation of regulatory documentation as needed.
  • Coordinate production, inventory control, and distribution planning.
  • Manage change control processes (ECRs/ECNs), maintain technical documentation, and ensure quality compliance.
  • Work closely with suppliers to reduce lead times and improve operational efficiency.
  • Collaborate with Sales, Marketing, and Finance to support product launches, customer audits, and cross-functional initiatives.
  • Provide regular updates on operational KPIs and project performance.

Experience:

  • A degree in Engineering, Supply Chain, Business, or a related field.
  • 5+ years' experience in operations, process engineering, or supply chain managementideally in a regulated industry.
  • Proven experience in tooling, plastic moulding, and hands-on process development.
  • Strong knowledge of manufacturing, logistics, and inventory systems.
  • Experience with ERP systems, Excel (PivotTables), MS Project, and other planning tools.
  • Strong communication, collaboration, and problem-solving skills.
  • Comfortable working in a fast-paced, evolving environment.
  • Willingness to travel to engage with suppliers and partners as needed.


Bonus Points For

  • Familiarity with medical device regulations and documentation.
  • Experience with Lean, Six Sigma, or Kaizen continuous improvement methodologies.
  • Working knowledge of ISO 13485 and validation protocols in a regulated environment.
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