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Quality Assurance Manager

Nottinghamshire
Posted 1 day ago
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Interim Quality Manager

4-Month Contract | Nottinghamshire Area | 2 Days Onsite Per Week

The Opportunity

An established medical device manufacturer is seeking an experienced Interim Quality Manager to provide hands-on support during a critical period of growth and operational activity.

This is a practical manufacturing quality role requiring someone who can quickly integrate with production and engineering teams, lead investigations and support day-to-day quality decision-making.

The successful candidate will be visible on the shop floor, capable of challenging issues constructively and experienced in driving quality improvements within a regulated manufacturing environment.

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I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£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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Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Key Responsibilities

  • Provide quality leadership across site manufacturing operations.
  • Lead investigations into product quality issues, customer complaints and non-conformances.
  • Facilitate RCCA and CAPA activities with Engineering, Manufacturing and Operations teams.
  • Support manufacturing teams with problem solving and quality improvement initiatives.
  • Drive improvements in product quality, defect reduction and process performance.
  • Support customer audits, complaint reviews and quality discussions.
  • Coach site personnel on quality best practice and GMP expectations.
  • Ensure quality risks are identified, escalated and managed appropriately.
  • Partner with suppliers and internal stakeholders to resolve product-related quality concerns.

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Required Experience

  • Previous experience as a Quality Manager, Site Quality Manager, Manufacturing Quality Manager or Head of Quality.
  • Medical device, healthcare, plastics manufacturing or related regulated industry experience.
  • Strong understanding of ISO 13485.
  • Hands-on experience managing customer complaints, non-conformances and RCCA investigations.
  • Experience supporting manufacturing teams within a production environment.
  • Strong stakeholder management and communication skills.
  • Ability to operate independently as the senior quality representative on site.
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Skills

Quality Management
ISO 13485
RCCA
CAPA
GMP
Customer Complaint Management
Non-Conformance Management
Stakeholder Management
Problem Solving
Defect Reduction
Process Performance
Audit Support

Location

Nottinghamshire, England, United Kingdom

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