At a Glance
- Tasks: Ensure quality standards in medical and pharmaceutical industries to keep patients safe.
- Company: Join STERIS, a leader in sterilization technology and patient care.
- Benefits: Gain valuable experience in a supportive environment with growth opportunities.
- Other info: Dynamic role with a focus on continuous improvement and innovation.
- Why this job: Make a real difference in healthcare while developing your skills.
- Qualifications: 3 years in administration and document control; teamwork and communication skills essential.
The predicted salary is between 30000 - 40000 € per year.
HOW YOU WILL MAKE A DIFFERENCE
About you: Do you want to spend your working time making a difference in the world around you? Are you passionate about supporting the medical and pharmaceutical industries? Do you care about keeping patients and people safe? If so, then a career with Steris could be a great fit for you.
About Us: At STERIS we are the technological leader in design, production, and supply of sterilization equipment and monitoring systems. 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.
What's involved:
- Process document control transactions.
- Review DHR’s and support batch record release.
- Support the record retention practices within the site.
- Coordinate site calibration activities and record keeping.
- Coordinate site inspection activities and record keeping.
- 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. Works in a professional manner to support team actions.
- Results: Effectively manages work tasks. Is detail oriented and strives for continuous improvement.
- Ability to analyze technical issues.
- Ability to cope with change and shifting priorities.
- Communication: Constructs clear written communication. Keeps manager and co-workers informed.
- Job Knowledge: PC experience and working familiarity of common desktop applications including Excel and Word.
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. STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. STERIS strives to be an Equal Opportunity Employer.
Quality Specialist in Syston employer: STERIS Canada Corporation
At STERIS, we pride ourselves on being a leading employer in the healthcare sector, dedicated to making a meaningful impact on patient safety and care. Our collaborative work culture fosters teamwork and continuous improvement, while our commitment to employee growth ensures that you will have ample opportunities to advance your career in a supportive environment. Located in a vibrant area, we offer a unique chance to contribute to innovative solutions in infection prevention and quality assurance, making every day at STERIS rewarding and fulfilling.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Specialist in Syston
✨Tip Number 1
Network like a pro! Reach out to people in the medical and pharmaceutical industries, especially those who work at STERIS. A friendly chat can open doors and give you insights that might just help you land that Quality Specialist role.
✨Tip Number 2
Prepare for the interview by brushing up on ISO 13485 and FDA regulations. Show us you know your stuff! Being able to discuss these standards confidently will definitely impress the hiring team.
✨Tip Number 3
Don’t forget to showcase your teamwork skills! During interviews, share examples of how you've collaborated with others to achieve results. We love candidates who can work well in a team environment.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re genuinely interested in joining our mission to create a healthier and safer world.
We think you need these skills to ace Quality Specialist in Syston
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Specialist role. Highlight your experience in document control and quality management systems, as these are key for us at STERIS. Use specific examples that showcase your skills and how they align with our mission.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Share your passion for supporting the medical and pharmaceutical industries and explain why you want to work with us. Make it personal and show us how you can make a difference in the world around you.
Showcase Your Teamwork Skills:We value collaboration, so be sure to mention any experiences where you've worked effectively in a team. Highlight how you’ve supported team actions and contributed to achieving results, as this is crucial for the Quality Specialist role.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team at STERIS.
How to prepare for a job interview at STERIS Canada Corporation
✨Know Your Standards
Familiarise yourself with ISO 13485 and FDA regulations. Being able to discuss these standards confidently will show that you understand the importance of quality in the medical and pharmaceutical industries.
✨Showcase Your Teamwork Skills
Prepare examples of how you've collaborated with others in previous roles. Highlighting your ability to work well in a team will resonate with their emphasis on teamwork and professional support.
✨Be Detail-Oriented
Since the role requires managing document control and record retention, be ready to discuss how you ensure accuracy and attention to detail in your work. Share specific instances where your meticulousness made a difference.
✨Communicate Clearly
Practice articulating your thoughts clearly and concisely. Since the job involves constructing written communication, demonstrating your communication skills during the interview will be crucial.
