Process Engineer - Pharmaceutical Packaging

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

Process Engineer - Pharmaceutical Packaging

Bishop Meadow Rd, Loughborough LE12, UK

Job Description

The Impact You Will Make:

We are expanding our team and looking for a Process Engineer to support our manufacturing, filling and packaging operations.

From analysing performance data, identify improvement opportunities, to implementing solutions to enhance productivity, reduce waste, and strengthen product quality, whilst ensuring regulatory compliance.

In this role you will work closely with cross‑functional teams, apply lean and continuous‑improvement methodologies, and play a key part in shaping how our operations evolve.

Key Responsibilities include, but are not limited to:

• Drive improvements to process capability, capacity and reduction in units cost for areas of ownership.
• Lead introduction of new technology and processes within operations.
• Apply Lean Six Sigma techniques to lead continuous improvement projects.
• Creation, management and communication of detailed project plans for project activities with foresight to escape constraints.
• Lead validation activities, by the preparation and timely execution of validation protocols for the validation of equipment/processes.
• Prepare detailed and effective documentation to record deviations, to assign and document corrective and preventative actions or facilitate change in a timely manner.
• Acquire a depth of understanding and knowledge in field of specialisation through experience, on the job training and external courses/conferences.
• Work in compliance with company procedures to maintain quality and safety e.g. GMP, EHS, specifications, methods.
• Understand the role of other sites, business functions and customers.
• Front information for regulatory inspectors and complete actions within target time.

Skills & Experience:

• Educated to degree level or equivalent in a Chemical Engineering, Pharmaceutical Engineering, or related field.
• Relevant work experience within the field of the medical device / drug product industry is preferred.
• Good understanding of the pharmaceutical industry standards and regulatory requirements (cGMP, FDA, EMA) is an advantage.
• Knowledge of lean manufacturing principles, Six Sigma, or other continuous improvement methodologies is a plus.
• Computer literate, familiar with Microsoft Word and Excel

Key Capabilities:

• Excellent interpersonal and communication skills, both written & oral at all levels.
• Able to work both as part of a cross‑functional team but also act independently.
• Enthusiastic and determined to achieve set objectives.
• Comfortable working with detailed technical information but also able to see the overall business picture.
• Possess strong computer skills and excellent organizational capabilities.
• Demonstrate flexibility, strategic thinking and drive to succeed.
• Adapt to changing priorities, timelines, and expectations without compromising on quality.
• Maintains a high standard of accuracy, completeness, and documentation.
• Champion data integrity and a right first-time culture.

What we Offer:

• Attractive compensation package.
• Company pension scheme (up to 10% employer contribution).
• 25 days holiday per year (plus bank holidays) plus service days after 5 years.
• Private Medical Insurance.
• Company sick pay.
• Employee Assistance Program with 24/7 confidential helpline support for employee and immediate family.
• Life assurance of four times life cover salary.
• Wellness programmes.
• Employee recognition program.
• Free on-site parking.
• Discount and cashback at many retailers.
• Cycle to work scheme.

Additional Information:

Location: Derby Road, Loughborough

All applicants must be eligible to work in the UK.

We believe our people make the difference at Kindeva, we look for skilled, passionate, and driven professionals to come and work with us to help us excel in manufacturing technologies and processes, which bring lifesaving products to patients worldwide.

#LI-AC1

Kindeva is an Equal Opportunity Employer