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This range is provided by Mediq UK. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
Mediq UK are a supplier of healthcare consumables, healthcare equipment, cleaning, and hygiene products, as well as healthcare devices to hospitals, care homes, and other facilities serving the healthcare sector in the UK.
We are recruiting for a QA Compliance Adviser to join our Quality team based at our brand new site in Castle Donington.
Reporting into the Head of Quality and Regulatory, the QA Compliance Adviser will execute non-conformance Reporting and CAPA tracking to ensure corrective actions are addressed for all quality activities and will progress the Quality, Regulatory and Technical activities.
You will provide support for all supplier quality related activities ensuring relevant standards are met.
Responsibilities:
* Completion of allocated actions in the QA Shared Inbox (priority to supplier recalls and FSN’s, complaints, MHRA checks (Supplier and Customer Verification for suspended and revoked WDA).
* Progress complaints and recall activities in a timely manner ensuring attention to detail and ensuring records and registers are accurately maintained.
* Co-ordinate complaint samples or other evidence to be received from the customer and sent to the supplier.
* Support activities such as Supplier Approvals liaising with procurement as requested to obtain additional information.
* Support on LSAS related activities and Own Brand manufacturer audits.
* Execute non-conformance Reporting and CAPA tracking to ensure corrective actions are addressed for all quality activities. Liaising with internal and external customers or suppliers to ensure an effective outcome.
* Support improvements in supplier performance, shown through risk assessments, Audits, CAPAs and PMS reviews.
* Conduct Batch Release inspection for 365 Healthcare and generate conformance documentation as required by customers in a timely manner.
* Support other QA departmental activities such as internal auditing (after appropriate training) and support in the development and review of the QMS documentation.
* Support in the update of product technical files.
* Take part in Regulatory Body and customer audits where applicable.
* Ensure significant non-conformances are escalated to Line Manager in a timely manner.
* Maintain records of all communications for traceability purposes.
What are we looking for?
* High attention to detail with a thoroughness and methodical approach to work.
* Experience working in a QA position.
* Flexibility and resilience to be able to deal with time constraints.
* Good time management and interpersonal skills.
* Proficient in Microsoft Office.
* Ability to establish and maintain relationships.
Please note that this job description is not exhaustive and additional duties may be assigned as needed.
Seniority level
Associate
Employment type
Full-time
Job function
Quality Assurance
Industries
Hospitals and Health Care
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