Quality Systems Specialist - Document Control (Hybrid, Belfast)
Quality Systems Specialist - Document Control (Hybrid, Belfast)

Quality Systems Specialist - Document Control (Hybrid, Belfast)

Belfast Full-Time 28800 - 43200 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Manage and maintain essential documents for compliance with FDA and ISO standards.
  • Company: Leading medical device company with a focus on quality and innovation.
  • Benefits: Hybrid work model, collaborative environment, and career development opportunities.
  • Why this job: Join a team making a difference in healthcare while growing your skills.
  • Qualifications: Level 6 qualification and basic knowledge of regulatory standards required.
  • Other info: Great opportunity for recent graduates to kickstart their career.

The predicted salary is between 28800 - 43200 £ per year.

A leading medical device company is seeking a Quality Systems Specialist - Document Control in Belfast. This role involves managing and maintaining essential documents to ensure compliance with FDA regulations, ISO 13485, and QMS requirements.

The ideal candidate will have a Level 6 qualification and 0-2 years of experience, alongside basic knowledge of regulatory standards and effective communication skills.

The position offers a hybrid work model and opportunities for collaboration within cross-functional teams.

Quality Systems Specialist - Document Control (Hybrid, Belfast) employer: Stryker Corporation

As a leading medical device company, we pride ourselves on fostering a collaborative and innovative work culture in Belfast, where our employees are empowered to grow and develop their skills. With a hybrid work model, we offer flexibility alongside comprehensive training and development opportunities, ensuring that our team members can thrive in their careers while contributing to meaningful projects that impact healthcare. Join us to be part of a dynamic environment that values compliance, quality, and teamwork.
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Contact Detail:

Stryker Corporation Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Systems Specialist - Document Control (Hybrid, Belfast)

✨Tip Number 1

Network like a pro! Reach out to professionals in the medical device industry on LinkedIn or at local events. We can help you connect with people who might know about job openings or can give you insider tips.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of FDA regulations and ISO 13485. We suggest creating a cheat sheet of key points to discuss, so you can impress your interviewers with your understanding of quality systems.

✨Tip Number 3

Practice your communication skills! Since this role involves collaboration within cross-functional teams, we recommend doing mock interviews with friends or family to get comfortable articulating your thoughts clearly.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we often have exclusive job postings that you won’t find anywhere else.

We think you need these skills to ace Quality Systems Specialist - Document Control (Hybrid, Belfast)

Document Control
FDA Regulations
ISO 13485
Quality Management Systems (QMS)
Regulatory Standards Knowledge
Effective Communication Skills
Collaboration
Cross-Functional Teamwork

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your relevant experience and qualifications. We want to see how your skills align with the Quality Systems Specialist role, so don’t be shy about showcasing your Level 6 qualification and any experience you have with regulatory standards.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about the role and how your background makes you a great fit. We love seeing candidates who can communicate effectively, so let your personality come through!

Showcase Your Knowledge: If you’ve got any knowledge of FDA regulations, ISO 13485, or QMS requirements, make sure to mention it! We’re looking for someone who understands the importance of compliance in the medical device industry, so don’t hold back on sharing what you know.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the Quality Systems Specialist position. Plus, it’s super easy – just follow the prompts!

How to prepare for a job interview at Stryker Corporation

✨Know Your Regulations

Familiarise yourself with FDA regulations, ISO 13485, and QMS requirements. Being able to discuss these standards confidently will show that you understand the core of the role and are ready to contribute from day one.

✨Showcase Your Communication Skills

Since this role involves collaboration within cross-functional teams, prepare examples of how you've effectively communicated in past experiences. Highlighting your ability to convey complex information clearly can set you apart.

✨Prepare for Document Control Scenarios

Think about potential challenges in document control and how you would address them. Be ready to discuss your approach to maintaining compliance and managing essential documents, as this will demonstrate your problem-solving skills.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's quality systems and team dynamics. This not only shows your interest in the role but also helps you gauge if the company culture aligns with your values.

Quality Systems Specialist - Document Control (Hybrid, Belfast)
Stryker Corporation
Location: Belfast
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  • Quality Systems Specialist - Document Control (Hybrid, Belfast)

    Belfast
    Full-Time
    28800 - 43200 £ / year (est.)
  • S

    Stryker Corporation

    10000+
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