Process Engineer - Pharmaceutical Packaging

Kindeva Drug Delivery; Loughborough; On-site; GBP 45,000 - 60,000; Full time

Benefits offered by this job

Private Medical Insurance

Company pension scheme (up to 10%)

25 days holiday per year (plus bank)

Life assurance of four times life‑sail

Flexible working hours

Wellness programmes

Employee development

Free on-site parking

Cycle to work scheme

Flu vaccinations

Employee referral scheme

Job summary

Kindeva Drug Delivery in the UK is seeking a Process Engineer to support manufacturing, filling and packaging. You will analyse performance data to identify improvements and implement solutions to boost productivity, reduce waste, and maintain product quality under GMP requirements.

Working with cross-functional teams, you will apply Lean Six Sigma methods, lead validation activities, and contribute to evolving our operations while ensuring regulatory compliance and safe, efficient processes.

Qualifications

• Degree in Chemical Engineering, Pharmaceutical Eng or related field.
• Knowledge of cGMP, FDA, EMA is advantageous.
• Lean manufacturing principles or Six Sigma knowledge preferred.

Responsibilities

• Improve process capability, capacity and cost efficiency for owned areas.
• Lead introduction of new technology and processes in operations.
• Apply Lean Six Sigma to lead continuous improvement projects.
• Prepare and manage detailed project plans for activities with timeline controls.
• Lead validation activities and execute validation protocols for equipment/processes.
• Document deviations and assign/corrective actions promptly.
• Develop knowledge through experience, training and conferences.
• Maintain GMP/EHS compliance per company procedures.

Skills

Chemical Eng

Pharma Eng

Lean Six Sigma

Data analysis

Cross-functional collaboration

Microsoft Excel

Documentation

Education

Bachelor's degree in Chemical/Pharma Eng

Tools

Microsoft Word

Excel

Job description

Kindeva Drug Delivery

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 escal[e] 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.
• Flexible working hours.
• Wellness programmes.
• Employee recognition program.
• Employee development.
• Free on-site parking.
• Discount and cashback at many retailers.
• Cycle to work scheme.
• Flu vaccinations.
• Employee referral scheme.

Additional Information

Working Hours: 37.5hrs per week

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.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Kindeva is an Equal Opportunity Employer