Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Process Engineer

Whitley, Coventry
2 days ago
Create job alert

Process Engineer
Location: Coventry, CV3 2RQ
Salary: Competitive, DOE + Benefits
Contract: Permanent, full time
Benefits:
• Competitive salary
• Contributory pension scheme
• Life cover
• Incapacity benefits
• Cash Back Medical Scheme
About the Company:
We are an innovative medical devices manufacturer of advanced wound care products, including combination products, from gelling fibres and fabrics. We deliver innovative, cost effective and quality products and solutions for the advanced wound care industry helping to improve patient care and wellbeing.
Are you an experienced Process Engineer looking for a new challenge
If you are a natural problem solver and facilitator of change, passionate about optimizing processes and not afraid to get stuck in, we have the perfect role for you! We are looking for an experienced Process Engineer to join our Process Engineering Team and take on full responsibility for our process implementation and improvement.
Process Engineer - The Role:
As a Process Engineer, you will be responsible for developing and implementing process strategies, managing process resources, optimizing current processes, and maintaining process documents. Ultimately, your job is to maintain the efficiency of our production lines to reduce costs.
Duties to include:
• Prepare process documentation and operating instructions.
• Oversee and assess new and existing processes and workflows.
• Develop and implement metrics to monitor and improve performance of processes.
• Analyse data to discover areas that need improvements and upgrades.
• Perform risk assessments.
• Devise, implement and test new strategies to help optimise productivity.
• Maintain operational efficiency and deliver operational cost savings.
• Assess compliance and adherence to safety and quality standards and report to higher management about the findings and proposals.
• Work in conjunction with Maintenance, RAQ, R&D and Commercial teams to support new products launches.
• Lead the design, development, installation and validation of equipment and process for new product platforms.
• Liaise, project manage equipment suppliers and contractors in line with project budget.
• Represent Operations throughout the Design Control Process to assess and manage the risks and impact of new processes.
• Investigate and troubleshoot issues/problems.
• Production process development with full documentation support.
• Maintain KPI targets in line with business strategy.
• Identify and implement new technologies, specification of requirements, Capex justification, planning and implementation.
• Develop a Continuous Improvement culture to ensure opportunities for continuous improvement are identified, prioritised, and executed.
• Provide clear work instructions, training, and design systems to promote sustainability of improvements.
• Report process trend analysis
Process Engineer - Key skills / abilities:
• Proven work experience as a process engineer with a minimum of 10 years’ experience.
• Experience with process simulations and standard operating procedures.
• Knowledge and application of Kaizen and Lean Manufacturing techniques.
• High-level knowledge of process engineering software systems.
• Advanced technical skills.
• Analytical thinker.
• Familiarity with health and safety regulations.
• Ability to project manage.
• Previous experience of working in a highly regulated industry such as Medical Device, Pharmaceutical, Automotive, Aerospace or Food manufacturing.
• Thinks outside the box, highly motivated, team player and full of energy.
• An excellent problem solver with resilience and determination to identify and implement solutions
• Highly competent in document and report writing.
Advantageous Skills / Experience / Abilities
• Process scale-up and design transfer experience
• Project management experience
• Experience working with CAD and AutoCAD.
• Knowledge of SPC / DOE / analytical methods
• Knowledge of domestic and international Medical Device regulations, such as ISO 13485, FDA QSR, Medical Device Directive.
• Qualified Chemical background would be advantageous.
If you have the skills and experience we require for this role and are looking for a new challenge, please click APPLY with your updated CV today!
Important Information:
Due to the number of applications we receive, we will only contact those candidates that we want to take forward to interview; if you do not hear from us within 4 weeks, please assume that your application has been unsuccessful on this occasion.
No Agencies please

Related Jobs

View all jobs

Mechanical Design & Process Engineer

Project Engineer - Manufacturing - Implantable Medical Devices in Cambridge)

Project Engineer - Manufacturing - Implantable Medical Devices

Senior Manufacturing Engineer - Implantable Medical Devices

Senior Manufacturing Engineer - Medical Devices - Cambridge

Senior Manufacturing Engineer - Implantable Medical Devices in Cambridge)

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.

Why Medical Technology Careers in the UK Are Becoming More Multidisciplinary

Medical technology (medtech) is transforming healthcare in the UK — from wearable sensors to AI diagnostic tools, from surgical robots to telemedicine platforms. Advances in hardware, software, data and connectivity are enabling more personalized, efficient and accessible care. But with great power comes great responsibility. As medical devices and health technologies enter hospitals, clinics and consumers’ homes, professionals in this domain must master much more than engineering and algorithms. They must also understand law, ethics, psychology, linguistics & design. That is, medtech careers are now deeply multidisciplinary. In this article, we explore why medical technology careers in the UK are becoming more multidisciplinary, how these five allied fields now intersect with medtech work, and what job-seekers and employers should do to succeed in this evolving ecosystem.

Medical Technology Team Structures Explained: Who Does What in a Modern MedTech Department

Medical technology (MedTech) spans everything from wearable health devices and surgical robots to diagnostic imaging, in-vitro diagnostics (IVD), digital therapeutics, AI-driven triage, and Class I–III medical devices. In the UK, the sector touches NHS care pathways, private providers, and global markets—with stringent expectations for safety, clinical evidence, cybersecurity, and data privacy. As ventures scale from prototype to regulated product, clear team structures become the difference between promising pilots and licensed, market-ready devices. Whether you’re hiring your first clinical specialist or applying for a role in QA/RA, this guide explains who does what in a modern MedTech department, how functions collaborate across the product lifecycle, UK-typical skill sets and salaries, common pitfalls, and best practices for building a resilient team.