Pharma Packaging Process Engineer | Lean Six Sigma

Kindeva; Loughborough; Hybrid; GBP 45,000 - 65,000; Full time

Benefits offered by this job

Company pension

25 days holiday

Private medical insurance

Life assurance

Cycle to work scheme

On-site parking

Employee assistance program

Job summary

Kindeva is seeking a Process Engineer for Pharmaceutical Packaging at its Loughborough site. You will support manufacturing, filling and packaging operations, analyse performance data and implement improvements to enhance productivity, quality and regulatory compliance.

You will work with cross-functional teams, apply Lean Six Sigma methods, and lead validation activities while ensuring adherence to GMP and related standards. Strong communication and documentation skills are essential.

Qualifications

• Educated to degree level in Chemical/Pharmaceutical engineering or related field.
• Knowledge of GMP, FDA, EMA requirements is advantageous.
• Lean manufacturing principles or Six Sigma experience is a plus.

Responsibilities

• Drive improvements to process capability, capacity and unit costs.
• Lead introduction of new technology and processes within operations.
• Apply Lean Six Sigma to lead continuous improvement projects.
• Create and manage detailed project plans for activities with foresight to avoid constraints.
• Lead validation activities with timely execution of validation protocols.
• Document deviations and implement corrective/preventive actions promptly.
• Develop understanding through experience, training and external courses.

Skills

Communication

Cross-functional teamwork

Lean Six Sigma

Data analysis

MS Word & Excel

Education

Degree in Chemical/Pharmaceutical Engineering

Tools

Microsoft Word

Microsoft Excel

Job description

Kindeva is seeking a Process Engineer for Pharmaceutical Packaging at its Loughborough site. You will support manufacturing, filling and packaging operations, analyse performance data and implement improvements to enhance productivity, quality and regulatory compliance.

You will work with cross-functional teams, apply Lean Six Sigma methods, and lead validation activities while ensuring adherence to GMP and related standards. Strong communication and documentation skills are essential.