with cross-functional stakeholders within Traders, Markets Risk and Control, Quants, Technology and Risk Management and Finance, while leading engagements with InternalAudit and regulators. The program covers all asset classes. In addition, change skills to define, organize and co-ordinate a program of work across businesses … of the actions in line with change methodology Identify issues and collaborate with stakeholders to generate solutions Work with Control and InternalAudit stakeholders to ensure credible challenge throughout the remediation process and validation of results in line with InternalAudit requirements Present on More ❯
Relevant experience in risk identification, assessment, monitoring, and remediation will be highly desirable Experience in Front Line Risk, Operational Risk or InternalAudit is also beneficial Experience operating in a dynamic, project-based environment with variable stakeholders, shifting priorities, and tight deadlines Familiarity with end-to-end More ❯
documentation Lead Corrective actions deliverables to ensure implementation are robust enough to prevent reoccurrence of issues Assist with gathering evidence for internalaudit requests as needed as well as being able to conduct IA walkthroughs of key controls Close collaboration with the Global Business Execution team and More ❯
Currently, ophthalmic biologic drugs represent a $14B market worldwide with growth projections reaching more than $22B by 2024. Our dual strategy includes the internal development of sustained-release therapeutics alongside the development of external strategic collaborations with major pharmaceutical partners. To date, Re-Vana has achieved significant progress … key member of the Belfast-based team. Reporting to the COO, he/she will work extensively with the CEO, CTO, and the internal scientific team. This is an outstanding opportunity to help build and contribute significantly to the strategic success of a well-capitalized, highly innovative startup … federal, state, and international regulations and guidance documents, as applicable (QSR, cGMP, ISO, ICH, etc.). Support NCMR, CAPA, Complaint, and InternalAudit investigations as needed. Thoroughly document all issues related to quality control, QSR, cGMP, ICH, and ISO compliance. Support company goals and objectives, policies, and More ❯
belfast, antrim, United Kingdom Hybrid / WFH Options
VirtueTech Recruitment Group
organisational controls, overseeing incident response, vendor security, and external certifications. Drive compliance automation initiatives to minimise manual processes and support scalable growth, conducting internal audits and monitoring to maintain high standards. Collaborate across teams to embed proportionate, automation-friendly compliance and security practices, and communicate risks clearly to More ❯
communication. Ability to drive progress issue-by-issue and ensure deadlines are met. Experience managing inter-department dependencies (e.g., Compliance, Technology, InternalAudit). Demonstrated ability to think critically, strategically, and analytically, and to creatively problem solve. Proficiency in Word, Excel, PowerPoint, and MS Project. This role More ❯
including testing and CI/CD deployment Collaborate cross-functionally to deliver innovative, high-quality solutions Drive continuous improvement and system optimisation through internal audits What We're Looking For: 3-5 years’ experience in a Salesforce development role Strong experience with Lightning, Apex, and Salesforce APIs Excellent More ❯
including testing and CI/CD deployment Collaborate cross-functionally to deliver innovative, high-quality solutions Drive continuous improvement and system optimisation through internal audits What We're Looking For: 3-5 years’ experience in a Salesforce development role Strong experience with Lightning, Apex, and Salesforce APIs Excellent More ❯
robust controls in the defined target state solution. Identify issues and collaborate with stakeholders to generate solutions. Work with Control and InternalAudit stakeholders to ensure credible challenge and validation of results. Present program status to senior stakeholders. Essential Criteria At least 7 years of experience in More ❯
Ability to analyse detailed content while maintaining a strategic portfolio view. Ability to influence and collaborate across functions such as HR, Technology, and Internal Audit. Basic understanding of Markets operations, including risk, controls, and trade lifecycle. This role will be a hybrid role with 3 days in the More ❯
and Hardware) and Customer Support teams to investigate and identify root causes of quality issues from customer complaints, internal non-conformances, and audit findings. Assist with implementing CAPAs and closing non-conformances. Work with cross-functional teams on documentation, risk management, and validation activities. Support quality compliance … for SaMD products, including lifecycle and version control. Participate in internal and external audits. Analyze quality data and contribute to process improvements. Required Experience: At least 2 years of experience in a Quality role within the medical device industry. Hands-on knowledge of ISO 13485 and 21 CFR … to work independently and prioritize tasks. Excellent communication, interpersonal, organizational, and IT skills. Helpful Experience: Experience with electronic Quality Management Systems (eQMS). Internal auditor qualification. Exposure to software as a medical device/IEC 62304. Technical or procedural writing experience. Familiarity with medical device regulatory requirements in More ❯