At a Glance
- Tasks: Ensure quality standards are met and assist with document control and audits.
- Company: Join a leading company committed to quality and compliance.
- Benefits: Competitive salary, inclusive workplace, and opportunities for growth.
- Other info: Great chance to develop skills in a supportive and collaborative setting.
- Why this job: Be part of a team that ensures high-quality standards in a dynamic environment.
- Qualifications: 3 years in administration and document control experience required.
The predicted salary is between 30000 - 40000 £ per year.
We are currently recruiting for a Quality Specialist. This is an excellent opportunity to join the business at a skilled professional level.
About the Role
The Quality Specialist will be responsible for assisting in administration of the quality functions on site to assure adherence to ISO 13485, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This role coordinates document control transactions and site record retention. In addition, the Quality Specialist will assist in audit coordination and support validation and risk management activities where appropriate.
Responsibilities
- Process document control transactions.
- Review DHRs and support batch record release.
- Support record retention practices within the site.
- Coordinate site calibration activities and recordkeeping.
- Coordinate site inspection activities and recordkeeping.
- Support internal and external auditing processes.
- Support targeted Lean activities.
- Complete other duties as assigned.
Required Experience
- Administration – 3 years experience
- Document control QMS experience
Skills
- Teamwork: Collaborates with others and works in a professional manner to support team actions.
- Results: Effectively manages work tasks, details-oriented, strives for continuous improvement, analyzes technical issues, and copes with change and shifting priorities.
- Communication: Constructs clear written communication and keeps manager and co-workers informed.
- Job Knowledge: PC experience and working familiarity with common desktop applications including Excel and Word.
Equal Opportunities
STERIS plc provides employment and advancement opportunities without regard to age, disability, gender reassignment, marriage or civil partnership, pregnancy and maternity, race, religion/belief, sex (gender), sexual orientation or any other legally protected characteristic as defined by UK employment law. The Company bases all employment decisions on merit, qualifications, skills, and abilities with the intention that the best candidate is selected for each position.
null in Syston employer: STERIS
Joining STERIS plc as a Quality Specialist offers a unique opportunity to be part of a dynamic team dedicated to maintaining high standards in quality assurance. With a strong commitment to employee growth and a collaborative work culture, STERIS provides comprehensive training and development opportunities, ensuring that you can thrive in your role while contributing to meaningful projects that impact healthcare. Located in a supportive environment that values diversity and inclusion, STERIS is an excellent employer for those seeking a rewarding career in quality management.
StudySmarter Expert Advice🤫
We think this is how you could land null in Syston
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry and let them know you're on the lookout for a Quality Specialist role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ISO 13485 and FDA regulations. We recommend creating a cheat sheet with key points and examples from your experience that showcase your skills in document control and quality management systems.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you, and tailor your approach to each company’s culture and mission.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. It’s also a great chance to reiterate why you’re the perfect fit for the Quality Specialist position.
We think you need these skills to ace null in Syston
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience with document control and quality management systems. We want to see how your skills align with the responsibilities of the Quality Specialist role.
Showcase Your Teamwork Skills:Since teamwork is key for us, include examples of how you've collaborated with others in previous roles. This will help us see how you can fit into our team and contribute to our goals.
Be Detail-Oriented:Pay attention to the details in your application. Double-check for any typos or errors, as clear written communication is crucial for this role. We appreciate candidates who take pride in their work!
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 Specialist position. Don’t miss out!
How to prepare for a job interview at STERIS
✨Know Your Standards
Familiarise yourself with ISO 13485, FDA 21 CFR Part 820/211, and EU MDR. Being able to discuss these standards confidently will show that you understand the regulatory landscape and are ready to contribute from day one.
✨Showcase Your Document Control Skills
Prepare examples of your experience with document control transactions and quality management systems (QMS). Be ready to explain how you've managed records and ensured compliance in previous roles.
✨Emphasise Teamwork and Communication
Think of specific instances where you've collaborated effectively with a team. Highlight your communication skills by discussing how you keep colleagues informed and manage tasks in a professional manner.
✨Be Ready for Change
Demonstrate your adaptability by sharing experiences where you've successfully coped with shifting priorities or changes in processes. This will show that you're results-oriented and can thrive in a dynamic environment.
