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Pratap Partnership

Technical Manager

Huddersfield
Posted about 17 hours ago
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Technical Manager - Regulated Medical Devices, Huddersfield (hybrid)

Salary: Competitive + benefits

Paxman is a global leader in scalp cooling technology, improving the lives of cancer patients worldwide. As they continue to innovate and expand internationally, we're looking for an experienced Technical Engineering Manager to have responsibility for the Technical Files for all Paxman products, ensuring compliance globally.

Areas of Responsibility

Technical Files

  • Management of the Design Control Matrix and Risk Management File
  • Accountable for the Clinical Evaluation File and Usability File
  • Overall sign-off of the Technical File along with other heads of departments
  • Leading audits of the technical file

Other Areas of Responsibility

  • Plan and manage technical CAPAs
  • Manage the introduction of engineering changes to product development
  • Ensure all devices meet efficacy and safety standards when used during its intended use and possible misuse
  • Provide technical specs to suppliers and work closely with suppliers to agree processes
  • Ensure labelling and documents are compliant with regulatory legislation
  • Supporting new product development and ongoing product lifecycle management.
  • Support and strategic planning for any new products from a technical perspective

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£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Requirements

We're looking for someone with:

  • Experience at a senior level of managing technical documentation within a regulated manufacturing or medical device environment.
  • A strong understanding of medical device regulations and quality management systems (ISO 13485/MDR desirable), as is ISO 14971
  • Exposure to technical documentation and a regulatory compliance environment
  • Experience with design control, risk management, and technical file maintenance.
  • Excellent organization skills with the ability to manage multiple projects and stakeholders.
  • Team leadership and mentoring skills

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Benefits

In return you will have the opportunity to:

  • Lead a growing technical function
  • Mentor and develop your team
  • Have significant autonomy
  • Gain exposure to a newly launched medical device
  • Work in a supportive, people-focused culture

About the Company

This is a business that:

  • Is making a genuine difference to patients across the globe.
  • Invests heavily in innovation and product development.
  • Offers the opportunity to work with talented cross-functional teams.
  • Provides a competitive salary and benefits package with genuine career development opportunities.
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Skills

Technical Documentation
Regulatory Compliance
Design Control
Risk Management
Quality Management Systems
Team Leadership
Project Management
Clinical Evaluation
Usability Testing
Product Development
CAPA Management
Stakeholder Management
Innovation
Medical Device Regulations
Technical Specifications

Location

Huddersfield, England, United Kingdom

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