Senior Quality Assurance Specialist
2 weeks ago
Job Title: Senior Quality Assurance Specialist
Job Summary:
We are seeking a highly skilled Senior Quality Assurance Specialist to join our team at ATL Technology. As a Senior Quality Assurance Specialist, you will be responsible for managing and improving quality systems processes to ensure EU and US regulatory compliance with relevant company standards and Good Manufacturing Practice (GMP).
Key Responsibilities:
- Support established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and Preventive Action (CAPA), Complaints, Post Market Surveillance, Non-conformance Report (NCR), Document Control, Incoming Inspection and Product Release.
- Participate in the interpretation of EU and US regulatory Requirements to produce effective working policies and procedures.
- Manage and conduct internal and inter-company Quality System Audits with responsibility for the audit process lifecycle.
- Analyse data, including the use of statistical techniques, to provide reports to management to enable them to monitor system performance.
- Review and authorise documentation and processes in the Quality Management System to ensure compliance with established quality procedures and applicable regulations and alignment with other related documentation.
- Identify and collaborate in the implementation of changes to the Quality System to increase efficiency and/or effectivity whilst ensuring compliance with applicable regulations.
- Support and perform training throughout the company to maintain awareness of the Quality System requirements.
- Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of GDP and GMP.
- Adhere to the standards of behaviours, policies and procedures as laid out in the Employee Handbook.
- Deputise for the Head of Quality & Regulatory when required, to ensure progression of departmental commitments.
Requirements:
- Diploma level Science/Engineering/Quality orientated qualification
- Lead Auditor qualification (ISO 9000 series based quality system essential, ISO13485 preferred)
- Minimum of 3 years' experience working in a QA/QS environment within the medical device or pharmaceutical industry.
- Knowledge of ISO13485, Medical Device Directive MDD 93/42/EEC, Regulation (EU) 2017/745 and FDA QSR Part 820
- Computer literate to include MS Word and Excel and MRP
- Ability to work with minimal supervision and use initiative.
- Good inter-personal skills and the ability to communicate well in English both written and orally.
Benefits:
- Generous Pension scheme
- Bonus
- Life Assurance
- Private Health Insurance
- Retailer Discounts/Cycle to Work Scheme
- 33 days holiday (including bank holidays)
- Hybrid Working (role dependant)
- Employee Assistance Programme
About Us:
ATL Technology is a fast-growing provider of outsourced design, development and manufacturing services to the medical device market, and its UK site (GML Medical Ltd - an ATL Technology owned Company) is based in St Mellons, Cardiff, UK.
We believe there is a better way to bring medical devices to market. We use an engineer-to-engineer approach to develop custom interconnect solutions for medical devices that improve the quality of one's life. It is our mission to be the leading provider of custom engineered solutions for top medical device manufacturers.
ATL has operations in the UK, China, Costa Rica, Taiwan, UT-USA, plus remote staff in strategic global locations and we're growing.
You will be required to provide evidence of your eligibility to work and reside in the UK, in accordance with the requirements of Section 15 of the Immigration, Asylum and Nationality Act 2006. The role that you are applying for may require you to undertake a basic/standard/enhanced Disclosure & Barring Service (DBS) check.
We are an equal opportunity employer.
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