Associate Technician, Jasmine & Packaging

JenaValve is a global medical device company focused on developing and manufacturing innovative Transcatheter Aortic Valve Replacement (TAVR) systems for the treatment of patients with severe aortic regurgitation and aortic stenosis.

Our mission is to raise awareness of aortic regurgitation and transform treatment options for patients living with this condition.

Our Leeds manufacturing facility produces the proprietary porcine pericardial tissue valves used within the JenaValve TAVR System.

Joining JenaValve means becoming part of a team that is dedicated to delivering high-quality medical devices and supporting advancements in patient care across the world.

We are looking for a motivated and enthusiastic Associate Technician for our Jasmine & Packaging process within our manufacturing team. This is an excellent entry-level opportunity for someone looking to build a career within medical device manufacturing.

Working under the guidance of experienced Technicians and Managers, you will complete a structured training programme while learning the Jasmine treatment and packing processes used in the manufacture of transcatheter heart valve products. You will gain experience working in a cleanroom environment, following Good Manufacturing Practice (GMP), quality requirements and approved manufacturing procedures while developing the knowledge and skills required to become an independent Technician.

• Complete Jasmine treatment and packing activities under the supervision of trained and authorised colleagues.
• Follow approved work instructions, procedures and training requirements at all times.
• Assist with the preparation and packing of clinical and non-clinical valves in accordance with approved processes.
• Learn the correct identification, handling and labelling of valves, serial tags and product labels.
• Use production tooling and equipment following completion of appropriate training and authorisation.

• Learn and apply Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and Quality Management System requirements.
• Accurately complete Device History Records and associated production documentation.
• Carry out basic checks of work against approved specifications and instructions.
• Escalate errors, concerns, deviations or quality issues promptly.
• Maintain accurate, complete and traceable production records.

• Maintain a clean, organised and compliant work area.
• Follow all contamination-control, cleanroom and hygiene requirements.
• Complete training in the safe use and handling of production equipment and chemicals.
• Adhere to all Environmental, Health and Safety requirements, risk controls and PPE standards.
• Support a culture of safety, quality and compliance within the manufacturing environment.

• Complete all assigned training modules and competency assessments.
• Demonstrate competence and proficiency before working independently.
• Maintain reliable attendance and full participation in the training programme.
• Support other manufacturing activities within the scope of training and competence as required.

• Strong attention to detail and ability to complete repetitive tasks accurately.
• Good hand-eye coordination and manual dexterity.
• Ability and willingness to learn new skills and complete structured training.
• Process-driven approach with strong organisational skills.
• Ability to work effectively within a team environment.
• Able to work independently once trained while following detailed instructions.
• Good communication and documentation skills.
• Basic computer literacy.
• Flexible, reliable and punctual approach to work.
• Understanding of GMP principles or willingness to learn.
• Positive attitude with a strong commitment to quality and continuous improvement.

• GCSEs or equivalent qualification.
• Experience using small tools, microscopes and production equipment is essential.
• Experience with label printing would be advantageous.
• Previous experience within manufacturing, medical devices, GMP or cleanroom environments is desirable but not essential.
• A genuine interest in developing a career within medical device manufacturing.

• Based within a controlled cleanroom and office environment.
• Wear appropriate cleanroom gowning and personal protective equipment (PPE).
• Work with small components, labels, packaging materials and specialised manufacturing equipment.
• Follow strict contamination-control, hygiene and chemical safety procedures.
• Perform detailed production activities requiring sustained concentration and attention to detail.

Working Hours:

Monday to Thursday: 7.00am to 3.30pm

Friday: 7.00am to 1.30pm

• Casual dress
• Company pension
• Free parking
• Health & wellbeing programme
• Private medical insurance
• Employee Referral programme
• Sick pay

Pay £27,360 per year