At a Glance
- Tasks: Ensure quality compliance and manage documentation for innovative diabetes care products.
- Company: Join Abbott Diabetes Care, a leader in glucose monitoring technology with over 135 years of experience.
- Benefits: Enjoy competitive salaries, flexible benefits, private healthcare, and career development opportunities.
- Why this job: Make a real impact on people's lives while working in a supportive and innovative environment.
- Qualifications: Secondary education required; prior experience in regulated product development is essential.
- Other info: Be part of a small, high-achieving team in a state-of-the-art facility.
The predicted salary is between 28800 - 43200 £ per year.
Location: Witney, UK
About Abbott Diabetes Care: Bring your passion, ideas, and purpose to life in a company that can truly help you achieve your full potential. Known globally for the development of revolutionary technologies, Abbott Diabetes Care designs, develops, and manufactures glucose monitoring systems for use in both home and hospital settings. Abbott has been around for 135+ years, developing solutions for the world's health issues and creating a workplace that enables employees to live full lives. We have a Centre of Excellence in Witney for the manufacture of electrodes and biosensors used by patients and healthcare professionals for the day-to-day management of diabetes. The site has been instrumental in the research, development, and manufacture of the FreeStyle Libre Continuous Glucose Monitoring System as well as exciting developments in the Libre family including FreeStyle Libre 2, FreeStyle Libre 3, and the Libre Sense system.
The Role: We are passionate about doing work that improves the quality of people’s lives. As a result of strong business growth and industry-leading product development in the biosensor business, we have an opportunity for a Quality Associate 1 to join our team. This is an opportunity to make a difference and bring your best self to Abbott. In this role, you will be at the forefront of ensuring our Quality Management System remains robust and compliant. You will perform the creation and progression of items, assets, or events in ADC quality systems, supporting compliance with industry regulations, audits, managing documentation, and following quality control procedures to ensure the safety and efficacy of ADC products.
Main Responsibilities:
- Check and complete your own training records/status in a timely manner and perform functions in a manner that is compliant with the quality training system.
- Ensure the completion of records strictly adheres to defined procedures and associated quality standards, and that they are stored securely and appropriately.
- Support project tasks for the development, implementation, and improvement of ADC quality systems to ensure effective and compliant processes and procedures which meet the needs of ADC and its customers.
- Support audits and inspections for process or functional areas.
- Be responsible for your own and support the team's Health and Safety within the working environment; highlight opportunities for improvement to EHS performance.
- Ensure that all communication, interpersonal interactions, and business behaviours are consistent with the Abbott Code of Conduct.
Qualifications:
Education: Secondary level education necessary, including English and Maths or equivalent.
Experience: Prior experience in the development and/or manufacture of regulated products is essential to ensure familiarity with cGMP and/or ISO Quality System requirements.
Why Abbott: This is an exciting opportunity to join a small, high-achieving team that offers structured career development opportunities within a state-of-the-art manufacturing and development facility, working on a range of exciting and complex new products. Abbott offers a benefits platform that provides security to you and your family. As you’d expect from an innovative global healthcare company, we offer an excellent range of benefits including competitive salaries, a defined contribution pension scheme, share ownership scheme, private healthcare, life assurance, and a flexible benefits scheme you can tailor to your own requirements.
Quality Associate 1 – Final Release employer: Abbott Laboratories
Contact Detail:
Abbott Laboratories Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Associate 1 – Final Release
✨Tip Number 1
Familiarise yourself with the specific quality management systems and regulations relevant to the role, such as cGMP and ISO standards. This knowledge will not only help you understand the expectations of the position but also demonstrate your commitment to quality assurance during interviews.
✨Tip Number 2
Network with current or former employees of Abbott Diabetes Care, especially those in quality roles. They can provide valuable insights into the company culture and the specific challenges faced in the Quality Associate position, which can help you tailor your approach.
✨Tip Number 3
Prepare to discuss your previous experience with regulated products in detail. Be ready to share specific examples of how you've ensured compliance with quality standards in past roles, as this will highlight your suitability for the position.
✨Tip Number 4
Showcase your passion for improving people's lives through quality work. During interviews, express how your values align with Abbott's mission and how you can contribute to their goal of enhancing diabetes care through quality assurance.
We think you need these skills to ace Quality Associate 1 – Final Release
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and qualifications required for the Quality Associate 1 position. Tailor your application to highlight relevant experiences that align with these requirements.
Highlight Relevant Experience: In your CV and cover letter, emphasise any prior experience you have in the development or manufacture of regulated products. Mention specific examples where you adhered to quality standards or participated in audits.
Showcase Your Skills: Make sure to include skills that are pertinent to the role, such as attention to detail, compliance knowledge, and teamwork. Use concrete examples to demonstrate how you've applied these skills in previous roles.
Craft a Strong Cover Letter: Write a compelling cover letter that not only expresses your enthusiasm for the role but also explains why you want to work at Abbott Diabetes Care specifically. Mention how your values align with their mission to improve people's lives.
How to prepare for a job interview at Abbott Laboratories
✨Understand the Company and Its Products
Before your interview, take some time to research Abbott Diabetes Care and its products, especially the FreeStyle Libre systems. Understanding their mission and how they impact people's lives will help you align your answers with their values.
✨Familiarise Yourself with Quality Standards
Since the role involves compliance with cGMP and ISO Quality System requirements, brush up on these standards. Be prepared to discuss how your previous experience relates to maintaining quality in regulated environments.
✨Prepare for Behavioural Questions
Expect questions that assess your problem-solving skills and teamwork. Use the STAR method (Situation, Task, Action, Result) to structure your responses, showcasing how you've contributed to quality assurance in past roles.
✨Show Enthusiasm for Continuous Improvement
Abbott values innovation and improvement. Be ready to share examples of how you've identified opportunities for process enhancements in your previous work, demonstrating your proactive approach to quality management.