Average Quality Specialist salary in the UK

Contract: PermanentRecruitment Partner: Shannon LintonThe Quality Specialist is a part of the quality team which sets the standards and processes for our products throughout their lifecycle so that they can be sold in global markets and deliver the high quality that our customers expect from No7. Who we are No7 Beauty Company is made up of five iconic brands - No7, Liz Earle, Soap & Glory, Botanics and Sleek MakeUP. We believe in creating the best in beauty for everyone - we’re innovators with a passion for challenging perceptions with ground-breaking products, proven results and positive impact. We have built a reputation on scientific innovation, whilst being environmentally sustainable and socially responsible. We are an equal opportunity employer, empowering our team members to be their authentic selves as we share a culture where diversity, equity and inclusion are at the centre of everything we do. About the role You will be an integral part of a cross- functional product development team ensuring compliant products, consistent ways of working and effective risk management through efficient processes.• Support the Quality Manager OTC and functional teams in ensuring the OTC products in No7 BC brands are developed and marketed in compliance with the regulatory requirements for the US FDA and Health Canada.• Provide quality expertise to support change controls, deviations and CAPA as required and use learnings as continuous improvement for compliance and quality.• Investigating quality issues to determine root cause, identify corrective actions and CAPA.• Conduct quality release of product batches to the markets.• Manage the Quality & Technical Agreements process and support the checking and approval of technical documents procedures and product specifications.• Provide support for regulatory audits.• Champion the use of the eQMS and provide guidance & training to internal teams using the system.• Seek to challenge established processes with the goal to deliver simplification and business benefit.• Contribute to the Internal Audit program and manage any resulting CAPA actions.• Contribute to a Quality Culture via training and reviewing best practices. What you’ll need to have • Strong knowledge of Quality Management Systems.• Good understanding of the development and lifecycle management of consumer products.• Curious, analytical problem-solving mindset.• Good organisational capabilities and attention to detail.• Stakeholder relationship management.• Clear communicator (both oral & written) with good team working and networking skills.• Ability to manage own workload. It would be great if you also have • Experience of the GxPs and regulatory requirements for consumer products such as US and Canadian OTC drug products.• Experience of batch release of products.• Experience of setting up quality agreements with suppliers.• Experience of managing internal audits. Our benefits Retirement Savings PlanEnhanced maternity/paternity/adoption leave payDiscretionary annual bonusGenerous discount on our own brands and partner businessesFlexible benefits scheme including holiday buying, discounted gym membership, life assurance, activity passes and much more. We have a great range of benefits in addition to the above that offer flexibility to suit you - go to working-here to find out more. Please note, any salary estimates given on third-party sites are not provided or endorsed by No7 Beauty Company and may not be accurate. What's next Where a role is advertised as full-time, we are open to discussing part-time and job share options during the application process. If you require additional support as part of the application and interview process, we are happy to provide reasonable adjustments to help you to be at your best.This role requires the successful candidate to complete a Pre-employment check after receiving an offer. Depending on your location you will be asked to submit either a DBS (Disclosure & Barring Service), PVG (Protection of Vulnerable groups) or an Access NI Check.We are a Ban the Box employer and will consider the suitability of applicants with criminal convictions on a case-by-case basis.

TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver groundbreaking solutions in global diagnostics. Your key responsibilities will include document control and the ability to implement robust document control processes while working closely with the Head of Quality and Regulatory Affairs establish the QMS aligned with ISO 13485 requirements, driving continuous improvement and operation excellence. The successful candidate will also compile technical files with comprehensive documentation to support regulatory submission and product certification while conducting risk management activities in accordance with ISO 14971, identifying potential hazards, assessing risks and implementing effective mitigation strategies. Quality and Regulatory Specialist Key Responsibilities: Manage and organize quality and regulatory documentationEnsure timely and accurate filing per industry standardsMaintain compliance with regulatory requirementsCollaborate with teams for regulatory compliance trainingImplement robust document control processesMaintain compliance throughout the product lifecycleAssist with the development of comprehensive technical files for CE markingCollaborate with stakeholders to establish a QMS Quality and Regulatory Specialist Requirements: Bachelor's degree in a relevant field (e.g., Engineering, Life Sciences, Regulatory Affairs)2 years' experience in quality and regulatory affairs within the medical device industry, preferably with exposure to software (IEC 62304) and Software as a Medical Device (SaMD)Strong understanding of ISO 13485, ISO 14971, and other relevant regulatory standardsExcellent communication skills with the ability to collaborate effectively across multidisciplinary teamsDetail-oriented mindset with a commitment to maintaining the highest standards of quality and complianceExperience with CE marking processes and regulatory submissions is highly desirable This is an exciting opportunity to be part of a dynamic and innovative company dedicated to making a meaningful impact on the lives of millions affected by diabetes. If you are driven by excellence, passionate about regulatory compliance, and eager to contribute to the future of healthcare, the Head of Quality and Regulatory Affairs is driven to help you develop your career with a clear pathway set to develop up to a managerial level. If you're interested, please apply with an up to date CV as this role will not be available for long.

TEC Partners is pleased to have partnered with a pioneering medical device company dedicated to improving the quality of life for patients through next-generation orthopedic implant devices. Through events, resources, and patient information, my client aims to empower both medical professionals and patients on their journey to improved orthopedic health. Quality Specialist As the Quality Specialist, you will play a pivotal part in upholding the company's commitment to quality and compliance with ISO 13485 standards. As a key member of the quality assurance team, you will be responsible for conducting internal audits, leading lean manufacturing initiatives, driving supply chain improvements, and conducting supplier audits to ensure the highest standards of product excellence. Quality Specialist Responsibilities: Conduct internal audits to ensure adherence to quality management systems and regulatory requirementsLead lean manufacturing initiatives to optimise processes and drive operational efficiencyCollaborate with cross-functional teams to identify areas for improvement and implement corrective actionsDrive continuous improvement initiatives throughout the supply chain to enhance product quality and reliabilityConduct supplier audits to evaluate performance and ensure compliance with quality standards and regulatory requirementsDevelop and maintain documentation related to quality management systems and regulatory complianceProvide guidance and support to team members on quality assurance processes and best practices Quality Specialist Requirements: Bachelor's degree in a Scientific related field or equivalent experience in a commercial manufacturing organisationMinimum of 3 years of experience in quality assurance within the medical device industryStrong knowledge of ISO 13485 standards and regulatory requirementsExperience conducting internal audits and supplier auditsProficiency in lean manufacturing principles and process improvement methodologiesExcellent communication and interpersonal skillsAbility to work effectively in a fast-paced, dynamic environment and collaborate with cross-functional team If you are passionate about quality assurance and committed to driving excellence in orthopedic implant devices, please apply with an up to date CV.