Are you passionate about revolutionising medical device manufacturing? Do you have experience in validation and technical report writing within a highly regulated environment? If so, we have an exciting opportunity for you!
Our clients are a well-established company based near Blackpool, operating with the agility and innovation of a start-up. Their current focus is on transitioning products from metal to PEEK (Polyether Ether Ketone), a cutting-edge material known for its high strength, durability, and biocompatibility, making it ideal for medical applications.
The Role: We are seeking a dedicated professional to join their team full-time, on-site, five days a week.
The ideal candidate will have:
* Experience in Validation and Technical Report Writing: Ensuring their products meet the highest standards of quality and compliance.
* Background in Medical or Highly Regulated Manufacturing: Familiarity with the stringent requirements and best practices of regulated industries.
* Adaptability and Team Collaboration: Ability to thrive in a dynamic environment and work effectively with cross-functional teams.
Nice to Have:
* Experience with Injection Moulding: While not essential, knowledge in this area would be beneficial.
Why join them? This is a unique opportunity to be at the forefront of innovation in medical device manufacturing. You'll work in a collaborative environment that values creativity and initiative, contributing to products that make a real difference in healthcare.
If you're ready to take on this challenge and be part of a team that's shaping the future of medical technology - please apply below. (Sponsorship also available)