QA/RA Specialist

Job OverviewDentsply Sirona is seeking a highly skilled Quality Assurance Specialist to join our team. As a key member of our regulatory affairs department, you will play a critical role in ensuring the compliance of our medical devices with UK and Ireland regulations.Key Responsibilities:Maintain and develop our local quality management system to ensure...

About the Job:In this role, you will work closely with our EMEA QA/RA Manager to ensure regulatory compliance and maintain an effective ISO 13485 certified Quality Management System (QMS). You will also support the supply of regulatory information to international divisions and external parties.Responsibilities:Ensure regulatory compliance with UK and...

Job DescriptionDentsply Sirona is looking for a highly skilled Regulatory Affairs Manager to join our team. As a key member of our QA/RA department, you will be responsible for maintaining and developing the local quality and pharmacovigilance management system.The ideal candidate will have a strong background in regulatory affairs and quality management,...

About the RoleWe are seeking a talented Regulatory Affairs Professional to join our team at Dentsply Sirona. This exciting opportunity will see you working closely with our regulatory affairs department to ensure the compliance of our medical devices with UK and Ireland regulations.Responsibilities:Maintaining and developing our local quality management...

Career OpportunityThis Medical Device Compliance Expert position offers a unique chance to work with Dentsply Sirona's regulatory affairs team. The ideal candidate will possess excellent knowledge of UK and Ireland regulations and be able to maintain and develop our local quality management system.Main Responsibilities:Maintaining regulatory compliance of...

The GSK Group of Companies is a world-leading consumer health company with a unique combination of deep human understanding and trusted science.We are improving everyday health for billions of people by growing and innovating our global portfolio of category-leading brands including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum.This...

Job DescriptionThis HR Systems and MI Specialist role plays a crucial part in providing world-class HR services across our organization.You will oversee HR operations tools, ensuring they meet organizational needs, and collaborate closely with Information Systems teams and HR Operations Service Delivery teams.The estimated annual salary for this position is...

QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects.Role...

Job Description QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. ...

Job Description QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. ...

QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. Role...

QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. Role...

QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. Role...

QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. Role...

QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. Role...

QARA Specialist Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. Role...

QA SpecialistWe are currently partnered with an exciting Medical Device Company looking to recruit a QA Specialist to join their growing team in Cambridge.The role reports into the Head of QA/RA and will be responsible for the QMS and wider QA activities.It is a really exciting time for the company, they are expanding globally and very well funded.The role...

Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects.Responsible for the regulatory...

Reporting to the EMEA QA/RA Manager, in this role your main functions will be to maintain and develop the local quality and pharmacovigilance management system, support the product registration with local competent authorities, undertake relevant training to deputise for Responsible Person (RP) and manage various projects. Responsible for the regulatory...

Planet Pharma is pleased to be recruiting for a QA specialist with a strong GCP background.You will be focused on writing SOPs and managing training assignments and you will support the management of the quality and compliance processes training.You will also be involved in GAP analysis - looking at new regulations and how they may affect current SOPs /...

Job Title: Principal QA Specialist – Global Biopharmaceutical Contract: 12 monthsLocation: Slough (onsite)Salary: £31.99 PAYE, £40.47 Umbrella per hour (Inside IR35)Hours: 37.5 hours per weekThe Principal QA Specialist will act as a Subject Matter Expert for Quality at the site level with the primary focus on SQC preparation and publishment, Deviation...

Quality Manager - Hybrid Opportunity in GMP and GDPAre you ready to advance your career with a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a business who have 3 key divisions, providing exposure to an area of the pharmaceutical industry being directly involved in saving the lives of some of the most vulnerable...

Salter Grange is working with a leading Engineering Contractor who is currently recruiting a QA/QC Electrical Inspector to join a specialist Engineering Contractor on a high-profile, major Data Centre Development with an Electrical Package Value of over £100m in London.The successful QA/QC Electrical Inspector will be joining a new division on a Hyper-Scale...

QA Vendor Qualification Manager - GMP / GDPPosition Overview:The QA Vendor Qualifier will play a pivotal role in assessing, qualifying, and monitoring external vendors to ensure compliance and documentation with our quality standards and regulatory requirements across GMP and GDP. You will collaborate with cross-functional teams to evaluate vendors'...

Outstanding opportunity to join a specialist, medical product, distribution business in a senior role. Reporting directly to the CEO, the Head of Regulatory Affairs will establish robust processes and systems to ensure compliance to relevant operating standards. With the support of a QA team you will lead a cultural change programme to embed best practice...

We are currently looking for a Quality Assurance Specialist to join a leading pharmaceutical company based in the Kent area. As the QA Specialist, you will be responsible for ensuring the highest standards of quality and compliance within the manufacturing and production processes.This will be a maternity cover (Fixed Term Contract).Your duties as the...

QA Specialist – Maternity CoverAn exciting position for a QA Specialist (3+ years experience) to join a start-up Medical Device company (regenerative medicine) for a fixed term contract. This is a 9-12 month maternity cover position and we are beginning interviews next week. The role is Hybrid, 2-3 days remote/2-3 days on site in Nottingham per week.The...