Senior Process Engineer

HCLTech; Leeds; On-site; GBP 40,000 - 60,000; Full time

Job summary

HCL, a global technology company, seeks a Process Engineer for permanent roles in Leeds. You will contribute to establishing and optimizing manufacturing processes across the product lifecycle.

Candidates should have 3+ years’ hands-on experience in process engineering, familiarity with ISO13485/ISO14971, Six Sigma and Lean tools, and exposure to medical device manufacturing.

Qualifications

• Hands-on process engineering in manufacturing.
• End-to-end support for establishing manufacturing processes.
• Optimization and efficiency improvements of processes.
• Support IQ OQ PQ validation.
• Knowledge of manufacturing processes in medical device manufacturing.
• Six Sigma, Kaizen, Lean techniques and related tools.
• Statistical methods including MSA, SPC, DOEs, reliability.
• Exposure to ISO13485 and ISO14971 medical standards is advantageous.
• Knowledge in cleaning and packaging processes.
• Familiarity with 3D CAD software.

Responsibilities

• Lead process engineering activities in manufacturing environments.
• Collaborate with cross-functional teams to optimize processes.
• Drive continuous improvement using Six Sigma and Lean methods.
• Support validation activities (IQ/OQ/PQ) for manufacturing setups.
• Ensure compliance with relevant ISO standards and quality systems.

Skills

Process engineering

Manufacturing

Six Sigma

Lean

MSA

SPC

DOEs

ISO13485

ISO14971

Kaizen

Tools

3D CAD

Job description

HCL is a $11 billion leading global technology enterprise consisting of over 200,000 professionals operating from 52 countries. Founded in 1976, HCL is one of India's original IT garage start-ups. For more on HCL, please visit www.hcl.com

Job Role -

Job Role : Process Engineer

Mode of Hiring- Permanent

No. of positions: 2

Experience: 3+ years relevant experience

Job Description-

• Hands on experience in process engineering in manufacturing industry
• End to end support for establishing manufacturing processes
• Optimization and efficiency improvement of processes
• Support IQ OQ PQ Validation
• Knowledge on various manufacturing processes in medical device manufacturing
• Six Sigma, Kaizen, Lean Techniques and/or other improvement tools and programs
• Technical training and experience using Statistics, Lean and Six Sigma Methodologies are required including Measurement System Analysis, SPC, DOEs, Reliability, etc.
• Exposure to ISO13485 and ISO14971 medical standards - Advantage
• Knowledge in cleaning and packaging process
• Knowledge of any 3D CAD software
• Strong Technical Knowledge in Manufacturing Engineering