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Validation Manufacturing Engineer

JR United Kingdom

Blackpool

On-site

GBP 30,000 - 60,000

Full time

Yesterday
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Job summary

An established industry player is seeking a Validation Manufacturing Engineer to join their innovative team in Blackpool. This role offers a unique opportunity to contribute to the transition of medical devices to advanced materials like PEEK, known for its strength and biocompatibility. You will be at the forefront of medical device manufacturing, ensuring compliance and quality through technical report writing and validation processes. Join a collaborative environment where your creativity and initiative will make a real impact on healthcare solutions. If you are ready to embrace this challenge and shape the future of medical technology, this position is for you.

Qualifications

  • Experience in validation and technical report writing in regulated environments.
  • Background in medical or highly regulated manufacturing.

Responsibilities

  • Ensure products meet quality and compliance standards.
  • Collaborate effectively with cross-functional teams.

Skills

Validation
Technical Report Writing
Adaptability
Team Collaboration

Tools

Injection Moulding

Job description

Social network you want to login/join with:

Validation Manufacturing Engineer, Blackpool
Client:

Medical Engineers Recruitment

Location:

Blackpool, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

7

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

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:

  1. Experience in Validation and Technical Report Writing: Ensuring their products meet the highest standards of quality and compliance.
  2. Background in Medical or Highly Regulated Manufacturing: Familiarity with the stringent requirements and best practices of regulated industries.
  3. Adaptability and Team Collaboration: Ability to thrive in a dynamic environment and work effectively with cross-functional teams.

Nice to Have:

  1. 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)

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