Job Title

Join Our Team at Glyance – QA Associate (Medical Devices)Are you a proactive, detail-oriented QA professional ready to take ownership of core quality activities in a fast-growing medical aesthetics company? Glyance is seeking a QA Associate with the drive and competence to lead day-to-day QA operations and play a critical role in ensuring product quality, regulatory compliance, and patient safety.This role is ideal for someone with solid experience in QA for medical devices or pharmaceuticals who is eager to step into a key role within a small, dynamic team, where your work directly impacts product development, clinical execution, and market readiness.About the RoleAs QA Associate, you’ll own and lead the execution of Glyance’s QA activities. You’ll be responsible for maintaining and improving our Quality Management System (QMS), ensuring compliance with ISO 13485 and EU MDR, and supporting all operational and product quality processes — from batch release to audits and risk management.You’ll report directly to the Head of QA/RA/Clinical affairs but be expected to operate independently, make informed decisions, and drive quality practices across the company.Key ResponsibilitiesTake full ownership of the day-to-day operation and actively maintain the QMS in accordance with ISO 13485, EU MDR, and GMP.Lead and perform QA documentation efforts, including SOPs, validation protocols, quality records, and controlled forms.Manage CAPA processes end-to-end: identification, investigation, resolution, and effectiveness checks.Own QA support for batch documentation review and product release processes.Oversee document control, training records, and change control management.Actively lead supplier qualification and monitoring activities, including audits and evaluation records.Actively participate and perform process, packaging, and equipment validations (IQ/OQ/PQ). Manage risk management activities under ISO 14971, including preparing and reviewing risk documentation.Monitor compliance of environmental and cleanroom data; ensure control over sterile product handling and packaging integrity.Prepare for and support external audits, inspections, and notified body interactions.Promote a culture of quality within the team; serve as point person for quality-related training and awareness.Qualifications & Requirements3–5 years of QA experience in the medical device or pharmaceutical industry, preferably with Class III or implantable devices.Proven ownership of QA processes and documentation in a regulated environment.Strong working knowledge of ISO 13485, EU MDR, GMP, and ISO 14971.Experience with CAPAs, validations, batch release, and supplier audits.Fluent in English (written and spoken); strong documentation and communication skills.Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field.Independent, self-motivated, and capable of working in a small team with minimal oversight.What We OfferA chance to lead and grow within a fast-paced, innovation-focused medical aesthetics company.Direct exposure to the full lifecycle of medical device development and commercialization.A collaborative, agile team where your voice is heard and your work is highly valued.Room to expand your role as the company grows.