At a Glance
- Tasks: Lead quality projects, ensuring compliance and smooth operations at our new Melton site.
- Company: Smith+Nephew crafts innovative technology to enhance lives and promote well-being.
- Benefits: Enjoy flexible vacation, private health plans, and discounts on gyms and more!
- Why this job: Join a diverse team committed to innovation and making a positive social impact.
- Qualifications: Experience in Quality Assurance within Medical Devices or Pharmaceuticals is essential.
- Other info: This is a 2-year fixed-term contract with opportunities for personal growth.
The predicted salary is between 28800 - 43200 £ per year.
Social network you want to login/join with:
Quality Workstream Leader (2 years FTC), Hull
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Client:
Smith+Nephew
Location:
Hull, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
0226ada69efa
Job Views:
41
Posted:
22.06.2025
Expiry Date:
06.08.2025
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Job Description:
Life Unlimited. At Smith+Nephew, we craft and manufacture technology that takes the limits off living!
In this pivotal quality role, you\’ll be at the forefront of driving success for our workstream goals at S+N. You\’ll own the charge in planning, organising, and managing Quality resources to ensure our new Melton site is fully compliant and ready for seamless business operations.
Your role encompasses comprehensive project management, where you\’ll focus on quality plans and systems to bring processes and products from our Hull site to our Melton site. You\’ll coordinate operations to guarantee uninterrupted market supply, champion strong stakeholder relationships, and uphold the highest quality standards. You\’ll provide Quality governance on the design, specification, and validation of the new facility, ensuring that our manufacturing spaces, laboratories and processes meet all regulatory requirements.
What will you be doing?
Project Management
- Schedule and report Quality workstream activities.
- Integrate schedule activities and achievements into the overall program plan.
- Document and handle risks, issues, and dependencies.
- Deliver workstream objectives timely and on-budget.
- Provide regular project status updates using dashboards and critical metrics.
Facility Design, Specification & Validation
- Set up QA processes for inspection and release in Melton.
- Approve facility/equipment qualification and process validation.
- Ensure manufacturing spaces meet regulatory standards.
- Ensure readiness for facility quality audits.
Budget & Resource Management
- Handle workstream deliverables within agreed resources, dates, and budgets.
- Coordinate budgeting process for CapEx and identified costs.
Compliance & Safety
- Ensure project compliance with QMS and S+N procedures.
- Lead audit readiness for the project.
- Ensure appropriate document approvals and training requirements.
What will you need to be successful?
You will need strong experience in Quality Assurance within the Medical Device or Pharmaceutical Industry, including experience with validation and change control. You\’ll have good analytical and communication skills, and be able to handle workloads efficiently to ensure compliance and high standards.
If you have Project Management Tools experience and Auditing experience, thats a huge bonus!
You. Unlimited
We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
- Inclusion, Diversity and Equity: Committed to Welcoming, Celebrating and Thriving on Diversity, Learn more about Employee Inclusion Groups on our website (
- Your Future: Generous annual bonus and pension Schemes, Save As You Earn share options, and car allowance.
- Work/Life Balance: Flexible Vacation and Time Off, Paid Holidays and Paid Volunteering Hours, so we can give back to our communities!
- Your Wellbeing: Private Health and Dental plans, Healthcare Cash Plans, Income Protection, Life Assurance and much more.
- Extra Perks: Discounts on Gyms and fitness clubs, Salary Sacrifice Bicycle and Car Schemes and many other Employee discounts.
Applications:
If you share our passion for pioneering innovation and can demonstrate how you meet the criteria outlined, we would love to hear from you.
We continue to actively build an environment where every individual can fulfil their potential and be proud ambassadors for Smith & Nephew, our customers and their patients.
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Quality Workstream Leader (2 years FTC) employer: Smith+Nephew
Contact Detail:
Smith+Nephew Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Workstream Leader (2 years FTC)
✨Tip Number 1
Familiarise yourself with the specific quality standards and regulations in the medical device industry. Understanding these will not only help you in interviews but also demonstrate your commitment to compliance and quality assurance.
✨Tip Number 2
Network with professionals in the quality assurance field, especially those who have experience in project management within the medical sector. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss your previous experiences with validation and change control in detail. Be ready to share specific examples of how you've successfully managed quality processes in past roles.
✨Tip Number 4
Research Smith+Nephew's recent projects and initiatives. Being knowledgeable about their work will allow you to tailor your conversation during interviews and show that you're genuinely interested in contributing to their goals.
We think you need these skills to ace Quality Workstream Leader (2 years FTC)
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the key responsibilities and requirements for the Quality Workstream Leader position. Tailor your application to highlight relevant experience in Quality Assurance, project management, and compliance.
Highlight Relevant Experience: In your CV and cover letter, emphasise your experience in the Medical Device or Pharmaceutical Industry, particularly focusing on validation, change control, and any project management tools you have used. Use specific examples to demonstrate your skills.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also conveys your passion for quality assurance and innovation. Mention how your values align with Smith+Nephew's commitment to diversity and inclusion.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role focused on quality.
How to prepare for a job interview at Smith+Nephew
✨Understand the Role
Make sure you thoroughly understand the responsibilities of a Quality Workstream Leader. Familiarise yourself with project management, quality assurance processes, and compliance standards specific to the medical device industry.
✨Showcase Relevant Experience
Prepare to discuss your previous experience in Quality Assurance, particularly in the medical or pharmaceutical sectors. Highlight any specific projects where you successfully managed quality systems or compliance audits.
✨Demonstrate Analytical Skills
Be ready to provide examples of how you've used analytical skills to solve problems or improve processes. This could include discussing how you handled risks or issues in past projects.
✨Prepare Questions
Have insightful questions prepared for your interviewers about the company's quality goals and challenges. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.