Senior Marketing Specialist (Contract)

Job Title: Senior Post Market Surveillance Specialist Contract: until 31/1/26 Location: Remote Pay: £153 per day SRG are partnered with a global medical products and technologies company. Our client is seeking a Senior Post Market Surveillance Specialist to join their team. This position will have the objective of maintaining high quality standards for the product manufacturing and compliance with all applicable regulatory requirements. The Senior Post Market Quality Engineer is responsible and accountable for quality product surveillance deliverables required within the post market compliance & surveillance processes across Infusion Care business unit. Maintenance of product malfunction codes across Infusion Care business units. Participates in complaint escalation reviews. Demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Timely and accurate presentation of complaint analysis to all stakeholders. Support quality engineering activities for all post market product surveillance including collection, analysis, and evaluation of product safety and performance data, and detection of trends in data that may warrant further action Execute and maintain procedures and processes to address post-market surveillance activities such as product investigations, periodic and ad hoc risk reviews, and product monitoring (trending and tracking) across all product franchises. Partnering with team members (and cross-functional teams) to ensure the development and execution of streamlined robust solutions to post-market quality processes are effectively implemented. Develop understanding of the current risk profile for all products including reportable product harms and malfunctions Provide quality and compliance input to project teams for project decisions and deliverables, especially those related to risk. Participate in design control activities and provide input into identifying failure modes and risk assessment for new and existing products while providing expertise in product complaint history and occurrence levels Quality Management System: Adhere to all requirements of the Quality Management System. Support investigations arising from CAPA, complaints, Health Hazard Evaluations (HHE), Internal audits, third party inspections, and other business processes by applying typical quality/problem solving tools such as fishbone/cause & effect, Pareto, process mapping, etc. Continuously support Quality Master Systems Data update for Product Lifecycle, including but not limited to, New Product Introduction, Product Obsolescence, Heightened Product Surveillance and Manufacturing Site updates. Provide Post Market Surveillance Quality Input to Management Review slide decks as required. Overall responsibility for ensuring technical rigor and compliance to applicable procedures during risk management, complaint, CAPA, and design related processes. Support R&D, Operations, Marketing, Clinical Affairs, Regulatory, Post Market Surveillance, external customers and equipment suppliers. The job holder will demonstrate the highest Quality standards, be able to impart knowledge and increase best practice across site/s and will embrace/drive core mission, values and priorities Advanced MS Excel skills, including the ability to independently create and utilize pivot tables and charts, formulas, V-lookups, and other advanced data manipulation or equivalent experience, in a scientific/technical discipline is required. At least 5 years experience in quality role in a medical device or life sciences technology driven company. Practical experience and global mastery in global quality standards and regulations governing medical products. Experience with various phases of the product development lifecycle including concept, design, implementation, verification, and validation activities necessary for product commercialization Experience in product and process risk management.