At a Glance
- Tasks: Manage quality documentation and ensure compliance with industry standards.
- Company: Uniphar Medtech is a leading medical device provider across 21 markets.
- Benefits: Enjoy a collaborative work culture, opportunities for growth, and a focus on sustainability.
- Why this job: Join a team that values quality and innovation while making a real impact in healthcare.
- Qualifications: 1+ years in a similar role; ISO 9001:2015 experience preferred.
- Other info: Travel between sites in Manchester and Northampton is required.
The predicted salary is between 28800 - 43200 Β£ per year.
The Quality Administrator will play a pivotal role in maintaining and improving the quality management system (QMS) at Uniphar Medtech. This position will involve extensive management of quality documentation, ensuring compliance with industry standards, and supporting continuous improvement initiatives. The ideal candidate will have a keen eye for detail, strong organizational skills, and a solid understanding of quality assurance processes. Candidates will be required to travel between different Medtech sites across the UK (Manchester and Northampton).
Specific duties and responsibilities
- Maintain and update quality management system documentation, including policies, procedures, work instructions, forms, and records.
- Create, revise, and archive quality documents ensuring they meet regulatory and organizational standards.
- Coordinate the review and approval process for quality documents, ensuring timely completion and dissemination.
- Ensure that all documentation is up to date and accurately reflects current practices and regulatory requirements.
- Prepare and organize documentation for internal and external quality audits, ensuring readiness and compliance.
- Conduct internal audits β ISO 9001:2015 standard and internal procedures.
- Track audit findings and follow up on action items, ensuring timely resolution and documentation of corrective actions.
- Manage document control processes, including version control, approvals and distribution.
- Document non-conformance reports (NCRs) and corrective action requests (CARs), ensuring accuracy and completeness.
- Support the QMS Manager with external audits β Supplier, Customer and Competent authority.
Qualifications & Experience
- Minimum of 1 yearsβ experience in a similar role.
- Internal Quality auditor experience within the medical device manufacturing, distribution or other regulated environment would be advantageous.
- ISO 9001:2015 Auditors Course.
Skills
- Knowledge of the Q-Pulse program is preferred but not required.
- Be well organised, with strong time management skills.
- Excellent communication and listening skills.
- Ability to obtain, analyse and present information.
- Computer literate, including Outlook, Excel, Word and PowerPoint.
- Strong analytical and problem-solving abilities.
- Ability to work independently and as part of a team.
How weβd like to work together
Our core values, titled our Medtech Mindset, guides our culture and work environment:
- We Go Forward Together: We operate as a unified team, leveraging diverse specialties to make swift, collaborative decisions and embrace progress over perfection.
- We Take Our Business Seriously: We prioritise compliance and risk management to ensure the best outcomes for our patients and partners, supported by our innovative portfolio and commitment to sustainability.
- We Deliver Exceptional Results: We focus on quality, customer satisfaction, and commercial success to achieve outstanding results for our patients, customers, and business.
The Company
Uniphar Medtech comprises 10 businesses across 21 markets and is the medical device arm of the Uniphar Group. Uniphar Medtech represents global leading medical device manufacturers across a multitude of specialities. We train, we educate, and we support our customers through dedicated clinical specialists across Sales & Technical Service, Clinical IT, Clinical Applications, Training and Education and Customer Service. We are more than a distributor; we are a total solutions provider. Each of our businesses compete under their individual brand identity and respective specialities. Uniphar Medtech is the umbrella structure for all 10 brands and in addition incorporates our centralised support functions across Quality and Compliance, Logistics, Warehousing, Operational Excellence, Marketing, HR, Finance & IT. Uniphar Medtech is an equal opportunities employer.
Quality Administrator employer: Uniphar Medtech
Contact Detail:
Uniphar Medtech Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Quality Administrator
β¨Tip Number 1
Familiarise yourself with ISO 9001:2015 standards, as this is crucial for the Quality Administrator role. Understanding these standards will not only help you in interviews but also demonstrate your commitment to quality management.
β¨Tip Number 2
Network with professionals in the Medtech industry, especially those who have experience in quality assurance. Engaging with them can provide insights into the role and may even lead to referrals or recommendations.
β¨Tip Number 3
Prepare to discuss specific examples of how you've managed quality documentation or conducted audits in previous roles. Being able to articulate your hands-on experience will set you apart from other candidates.
β¨Tip Number 4
Showcase your organisational skills by discussing any tools or methods you use to manage documentation and compliance. This could include software like Q-Pulse or even simple strategies that ensure accuracy and efficiency.
We think you need these skills to ace Quality Administrator
Some tips for your application π«‘
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Quality Administrator at Uniphar Medtech. Familiarise yourself with quality management systems and the specific duties mentioned in the job description.
Tailor Your CV: Highlight your relevant experience in quality assurance and document management. Emphasise any internal auditing experience or familiarity with ISO 9001:2015 standards, as these are crucial for the role.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the position and how your skills align with Uniphar Medtech's core values. Mention your attention to detail and organisational skills, which are essential for maintaining quality documentation.
Proofread Your Application: Ensure that your CV and cover letter are free from errors. A well-presented application reflects your attention to detail, which is vital for a Quality Administrator. Consider asking a friend to review your documents before submission.
How to prepare for a job interview at Uniphar Medtech
β¨Know Your Quality Management Systems
Familiarise yourself with quality management systems, especially ISO 9001:2015. Be prepared to discuss your understanding of these standards and how they apply to the role of a Quality Administrator.
β¨Demonstrate Attention to Detail
Since the role requires a keen eye for detail, be ready to provide examples from your past experiences where your attention to detail made a significant impact on quality outcomes.
β¨Showcase Your Organisational Skills
Prepare to discuss how you manage documentation and ensure compliance with industry standards. Highlight any tools or methods you use to stay organised, especially in a fast-paced environment.
β¨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities and how you handle non-conformance reports or corrective actions. Think of specific scenarios where you successfully resolved issues in quality assurance.