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Quality Assurance Manager

Siemens Healthineers

Llanberis

On-site

GBP 40,000 - 80,000

Full time

Yesterday
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Job summary

An established industry player is seeking a Quality Assurance Manager to join their dedicated team. In this pivotal role, you will oversee all Quality Assurance activities, ensuring compliance with regulatory standards while driving process improvements. Your expertise in Quality Management and risk assessment will be crucial as you lead a team focused on supplier quality and incoming material inspection. This role offers a unique opportunity to contribute to innovative healthcare solutions in a supportive environment that values diversity and personal growth. If you're passionate about quality and eager to make a difference, this position is perfect for you.

Benefits

26 days' holiday
Up to 10% employer pension contribution
Share and bonus scheme
Private medical insurance
Dental cover
Paid volunteering days
Employee assistance programme

Qualifications

  • 5+ years in Quality Management in a regulated environment.
  • Experience with FDA regulations and writing quality procedures.

Responsibilities

  • Lead Quality Assurance activities and manage Incoming Material Inspection.
  • Drive process quality improvements and update quality system procedures.

Skills

Quality Management
Risk Management
FDA Regulations
Complaint Handling
Process Improvement

Education

Degree in Quality Management
Degree in Mechatronics
Degree in Electronics
Degree in Mechanical Engineering

Job description

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

Apply now for the position of Quality Assurance Manager and you will act as a key member of the site Quality Management team with combined responsibility for all general Quality Assurance activities at the site and at corporate level.

Your Role:

  • Designated as the primary point of focus for all Quality Related matters associated with Instrumentation Quality.
  • Leading a team responsible for Incoming Material Inspection and Supplier Quality for all aspects of the business.
  • Contributing and leading in a broad range of activities including process change, risk assessment, CAPA, non-conforming material, complaint handling, manufacturing process deviations, non-conformance handling and validation.
  • Active in change management via verification and validation of product, process change, technology transfer plans, equipment commissioning, deviations, non-conforming material, out of tolerances, complaints, continuous improvement changes, and post-production (proactive surveillance). This will require a systems mindset incorporating a cross technology understanding, in addition to a core appreciation of risk and regulatory requirements.
  • Act as a key liaison and knowledge transfer champion among Quality Assurance, Manufacturing Engineering, R&D, Production and Documentation Control.
  • Focus on and be responsible for process quality design improvements and updating quality system procedures to achieve both fully compliant and lean processes.

Your Expertise:

  • 5 years minimum Quality Management experience in a similar role.
  • 5 years minimum of relevant experience in a regulated environment with a core appreciation of FDA regulations and Risk Management incl. writing and / or reviewing Quality related procedures, plans, and reports.
  • Minimum of a third level qualification (Diploma/Degree) in an appropriate discipline (Quality Management, Mechatronics, Electronics or Mechanical Engineering) OR appropriate and commensurate experience.

Our Benefits:

  • 26 days' holiday with the option to buy or sell an additional 5
  • Up to 10% employer pension contribution
  • Share and bonus scheme
  • Access to our flexible benefits from private medical insurance to dental cover
  • Corporate Social Responsibility opportunities including 2 paid volunteering days per year and support from our 24/7 employee assistance programme

Who we are:

We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.


How we work:

When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.


As an equal opportunity employer, we welcome applications from individuals with disabilities.


We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities.


To all recruitment agencies:

Siemens Healthineers' recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with us. Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees. We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices. Your adherence to our policies is appreciated.

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