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Overview of salaries statistics of the profession "Risk Specialist in Ireland"

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Overview of salaries statistics of the profession "Risk Specialist in Ireland"

1 200 £ Average monthly salary

Average salary in the last 12 months: "Risk Specialist in Ireland"

Currency: GBP USD Year: 2021
The bar chart shows the change in the level of average salary of the profession Risk Specialist in Ireland.

Regions rating Ireland by salary for the profession "Risk Specialist"

Currency: GBP
The bar chart shows the change in the level of average salary of the profession Risk Specialist in Ireland.

Similar vacancies rating by salary in Ireland

Currency: GBP
Among similar professions in Ireland the highest-paid are considered to be Audit Assistant. According to our website the average salary is 5417 GBP. In the second place is Insurance Manager with a salary 5417 GBP, and the third - Audit Manager with a salary 4584 GBP.

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QA Specialist
CPL,
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Identify and Implement Continuous Improvement opportunities.•    Ensure that change controls and automation change requests are compliant with applicable procedures and maintain the validated state.Customer Complaints•    Co-ordinate and Assist with the analysis and investigation of customer complaints •    Utilize both Corporate and local systems for management, investigation and reporting of customer complaints •    Ensure all complaints are closed within specified timeframes Stability •    Facilitate creating and maintaining the schedule for completion of Annual Stability Program. •    Initiates, authors or assists in out of specification investigations •    Key role in participating in Stability Review Board (SRB) process.•    Manage the Reserve/Retain samples management program Raw Material/Component/CPA Compliance •    Ensure site BSE/TSE status is maintained current •    Oversight of vendor investigations. •    Approval of GMP documentation in support of raw material testing •    Provide oversight to ’use of material at risk’ process.•    Packaging Component Quality •    Quality oversight on vendor performance management and vendor certification program for packaging component suppliers Supplier Quality Management •    Preparation of Supplier Quality Agreements in conjunction with supplier quality management teams.•    Liaising with business and purchasing as part of the supplier sourcing and assessment process •    Preparation / approval of supplier qualification packs •    Maintenance of supplier status on SMS •    Monitoring / reporting on supplier qualification metrics to meet re-evaluation requirements, including escalation of supplier quality issues / adverse audit findings •    Liaising with corporate to meet all requirements for Legacy plans / ongoing system maintenance•    Assist in the generation of the Supplier Audit schedule •    Review Supplier audit reports •    Act in an advisory capacity for all supplier audit related queries. Metrics/Tracking•    Maintain tracking system for batch/document review status. 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People / Values: •    Demonstrate the GC OWNIT values•    Adhere to all HR Policies as appropriate•    Personal  Development plans focus on the 70:20:10 guidelines•    CI tools/- capability is a key building block for learning & development - Trained and M1 certified.•    Proactive engagement with key stakeholders.•    Best practices developed and shared with other teams /sites.•    Best practices actively sought and copied.•    Proactive & effective communication within and across shifts6. 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Clinical Evaluation Specialist
CPL,
Clinical Evaluation SpecialistMedical Device CompanySuitable Locations: Bath, Bristol, Gloucester, Swindon, CardiffSalary: Up to £45,000Benefits: 2-3 days' home working, 9% pension, private healthcare, annual pay review, bonusAn exciting opportunity has arisen for a Clinical Evaluation Specialist to join an innovative, global medical device company.We are looking for a Clinical Evaluation Specialist who will be responsible for creating and maintaining Clinical Evaluation Reports for medical device regulatory compliance.Key Tasks:- Work alongside the Clinical Operations team and CRO to contribute to Clinical Protocols, data analysis, Clinical Study Report review, and handling any issues arising during the trial (such as device deficiencies and SAEs) within the company.- Support design control process in areas such as risk, labelling review and clinical data.- Coordination of Clinical Evaluation using literature review, PMS, PMCF, pre-clinical and clinical data- Creation of the Clinical Evaluation Report, and update to it during the product lifecycle (e.g. update to literature search or when new Clinical data exists).- Cross-functional collaboration with Marketing, Regulatory and Legal teams Experience Required:- Life Science Degree- Previous experience in the medical device sector- Experience of gathering, evaluating and critically interpreting information.- Experience of creating clear and concise technical documentation.- Significant experience in critical appraisal, literature review, and/or data analysis This is a permanent role with a respected global business. As well as a competitive salary and benefits, you will work with an innovative and progressive company that value their employees. If this role is of interest, please send your CV to George.Danchie@cpl.com or call 01189594990 for more informationPay range unavailable
Complaints Specialist
PokerStars, Dublin
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You will also be responsible in providing regular insights on process and continuous improvements back to the business and the department.Some of your responsibilities will include:Report to the Senior Management on a weekly basis.Support the management of the IBAS escalation and IBAS Ruling processes when required.Look for opportunities to drive improvements and upskilling within customer issue touchpoints.Work with Voice of the Customer and Customer Experience Teams to tell the customers story and remove Pain Points.Manage the reporting framework that drives customer centric improvements throughout the organisation.Work closely with internal stakeholders such as Safer Gambling, AML, Fraud, Customer Support, & Payments to ensure that risks are handled effectively with minimal friction to our customers.The above responsibilities are not exhaustive, and the post holder will be required to undertake such tasks as may reasonably be encouraged within the scope and expectations of the post. What happens next?If you’re what we’re looking for, next up will be a phone interview. And if that goes well, we’ll meet you for a Zoom interview.The GroupPokerStars is part of Flutter Entertainment Plc, a global sports betting, gaming and entertainment provider headquartered in Dublin and part of FTSE 100 index of the London Stock Exchange, which brings together exceptional brands, products and businesses and a diverse global presence in a safe, responsible and ultimately sustainable way.We are an equal opportunity employer that values diversity. We do not discriminate on any protected characteristic as defined by applicable law. Requirements: Who we’re looking for?We are looking for someone who can handle and resolve all customer complaint queries raised via all complaint channels, including Senior Management, Regulatory and Frontline channels. Also, to be a great partner to the complainant, and to handle all contacts with a full and up to date understanding of regulatory requirements per license. Liaise with the various business stakeholder channels in the resolution of customer queries.Your experience:Experience with implementation and maintenance of regulatory information management systems.Knowledge of dual brand products, processes, and procedures.Ability to improve and understand the value of all available data; to develop creative solutions as well as “quick wins”.Proficiency in using Microsoft office tools to view and use email, spreadsheets, presentations etc.Experience in dispute resolution.Validated investigative skills in relation to customer risk, i.e. Fraud, AML and Safer Gambling.At least 2-years’ experience in customer service.International gambling regulation exposure and experience, and experience of dealing with stakeholders in a national / global setting would be considered advantage.Your skills:Must be proficient in English both written and verbal.An excellent communicator to all levels both internally and externally, ensuring both the company and its employees understand the customer feedback and what is being carried out to improve their experience.Strong commercial awareness with a history of adding value across the wider business and a track record of developing flexible solutions in fraud and risk to changing business needs.To be able to multi-task and work with short deadlinesSolid understanding of sports, gaming, and the betting industry, along with regulated markets and licenses within the online sports, gaming and betting industry.Your behaviours:Maintaining a continuous focus on the customer experience.Excellent interpersonal and prioritisation skills.Innovative problem-solving skills.Ability to build strong working relationships inter and cross departmentally. Offer: What’s in it for you?Our experience-based salaries are competitive. Plus, there’s a discretionary annual performance bonus. And we provide advice and dedicated assistance to those moving to Dublin.Your package will include:health and dental insurance for you, your partner and your children (if you all live at the same address)a personal interest allowance to let you learn something new or pursue a hobbythe option to join our company pension schemelooking to extend your family? You will receive a cash gift of 1,000 EUR for your new addition whilst working for usin-house training and development to develop your skills, progressing your careerfree fresh fruit, snacks and drinks in the officeaccess to an onsite gym.
Quality & Safety Specialist
,
HCI is a professional services provider of patient safety, regulatory compliance, and quality improvement intelligence and support to health and social care organisations.Reporting to the Director of Quality and Safety the Quality and Safety Specialists role shall include, development, implementation and support of practical quality and safety management systems within health and social care organisations such as Hospitals, Disability Services, Nursing Homes, Regulatory Bodies, Home Care, Medical Transport and Primary Care.Responsibilities of the Quality & Safety Specialist shall include (but not limited to)Lead and support the development of the client Quality & Safety Management Systems, including:Lead and develop all aspects of Quality & Safety Management Systems to fulfil healthcare regulation and accreditation. This includes all quality development as well as clinical and non-clinical risk management.Lead and support the development of quality improvement initiatives to improve the effectiveness of care and service deliveryImplementation of risk management systems such as incident identification and complaints processes.Enhance systems for ongoing patient/client/resident involvement, e.g. focus groupsAssist and support Incident InvestigationsDevelop the use of performance measurement systems in healthcare, e.g. Clinical AuditDevelop clients understanding and fulfilment of regulations including:Joint Commission International (JCI)CHKSHIQAISOHPRANational and International Best PracticeDevelop and educate re process control and the use of Policies & Procedures Framework, includingUnderstand the needs and requirements of client regulationsDevelop policies and procedures based on evidence based best practiceWork with care staff implementing policies and proceduresProcess mapping key care and non-care processesProvide training and education programmes relating to:Quality & Safety Management SystemsPublic & Patient InvolvementIncident ManagementRisk ManagementUtilisation of the Q-Pulse software system:Management of HCI projects through Q-PulseConfiguration of client specific systemsReview and monitoring of informationProviding client liaison and support with regards to Q-PulseDevelopment of Client Relationships:Develop strong ongoing relationships with current clientsOngoing client communicationEnsure on-going evaluation of client satisfactionDeveloping and administer structured feedback from clientsSharing expertise with clientsUsing feedback from observations and participants, and ideas from research, training courses and colleagues to develop performance.General Responsibilities:The Quality & Safety Specialist is responsible for supporting the HCI Quality Management System (QMS) as follows:Developing, implementing, maintaining and improving the process, and associated procedures, of the services provided by HCI.Recording, managing and addressing all allocated non-conformances in a timely and effective manner and in accordance to the applicable procedure.Completing all specific audit activities as identified by the Quality Manager in accordance to the applicable procedure.Ensuring that all relevant regulatory requirements related to the service being provided by HCI, are considered and incorporated during provision of that service.​​Qualifications and ExperienceA Nursing Degree (desirable)A Masters Qualification (desirable)A Healthcare or Quality Management Qualification (essential)Knowledge of HIQA StandardsKnowledge of Quality Management SystemsPersonal attributes/skillsExcellent administrative and organisational skillsExcellent analytical and report-writing skillsMotivation and ability to work on own initiativeExcellent communication and inter-personal skillsExcellent IT skillsFull clean Driving License and own car
Health and Safety Specialist
Morgan McKinley, Cork City, ie
Health and Safety Specialist required for a busy manufacturing facility. A stand alone role with a varied remit! Monday to Friday role! Experienced Health and Safety Specialist with an ability to work on their own initiative. Proven experience leading and implementing change. Duties and Responsibilities: Monitoring of multiple waste streams.Reviewing Contractor safety statements, insurance, Risk assessments and method statements.Clearing contractors for travel to site - Pre entry Covid forms, temp checking and ensuring the contractors abide by the latest Government guidelines on Travel.Organising Training both in house and through outside contractors. Update site on the latest Covid-19 restrictions and government guidelines.Organise monthly OH clinics.Track all work related injuries and illnesses and log with OH team.Liaise with the Company Doctor and nurse to ensure all OH issues are closed out.Advise Management on the results of Vibration, noise, chemical and ergonomic assessments.Ensuring PPE is adequate for Roles specified.Risk assessment of new equipment (Cross functional with Engineering team)Maintaining and updating Safety statement.Updating senior management and staff on any H&S related issues via weekly management meetings, tool box talks and town hall meetings.Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
Global Collections Specialist
Morgan McKinley, Cork, ie
Fantastic opportunity for an experienced Collections Specialist to work in an established multinational in a Global Role This new opportunity in Cork, is looking for a Senior Collections Specialist who have worked in a fast paced multinational environment in a Global role. The ideal person for this role will need to have excellent interperonal and communication skills to work with clients around the world. Key Responsibilities:Evaluate, investigate and timely collection of outstanding accounts receivables.Manage high level customer accountsAct as primary contact for inquiries, requests and issues related to accounts receivable for large portfolio of customers.Partner with the credit team to recommend and establish credit lines and ensures that accounts remain within the assigned credit limits as well as assess and mitigate financial risk.Drive desired customer payment behavior through timely and insightful contact with customers.Implement collection technique and negotiation to maximize cash flow and create a favorable financial relationship and customer experience.Analyze data, trends, drivers and root cause in customer payment behavior.Partner with other internal functions to create appropriate action plans to remove barriers to payment as well as provides support for action planning with data/dashboards.Identify/ execute opportunities for process improvements to increase efficiency.Requirements:4-5 years experience working in a Collections role within a multinational environment.Strong customer services/ customer relationship management experienceSAP/Oracle experience desirableProactive involvement in projects and process improvementsIf you are interested in hearing more about this opportunity, then get in touch for a confidential chat. Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
NPI Operations System Specialist (Pfizer)
CPL,
Pfizer Grange Castle is looking for NPI Operations System Specialists to join their Drug Substance Proteins t in Grange Castle, Dublin.Job Purpose:The purpose of this role is to represents the Operations function and provide operational and system support to the ongoing NPI requirements of the Drug Substance Operating Unit. The breadth of this role includes working initially through detailed design & procurement and subsequently construction, commissioning, verification/qualification, and production start-up. The position is part of the New Product Introduction (NPI) operations team. The NPI Operations System Specialist is responsible for providing process, equipment, system support to the operating unit, ensuring that NPI Operations project deliverables and Operations Readiness deliverables are completed as intended to support the manufacture NPI related batches (e.g. water trial, engineering runs, DEMO batches and Process Validation studies). Responsibility includes all support activities and operational functions necessary to ensure successful completion of project objectives which may include short term shift based assignment during manufacture of NPI specific batches.This project role focuses on tasks including but not limited to; detailed design/process mapping, closure analysis, risk assessment, SOP & PBR document generation, technician training, standard work capability, 5S, EBR (PMX/AMPS) generation, process understanding in support of orchestrate model development. The role will also include supporting and resolving operational issues during NPI related batch execution.ResponsibilitiesParticipate in Operational Readiness Activities including Commissioning, Validation andVerification execution and trouble shoot technical issues.Responsible for right first time creation of SOP, paper batch record and other documentation, as well as all records requirements in MES or future electronic systemsTraining of colleagues in new processes and equipment which may involve short term shiftbased assignment during manufacture of NPI specific batchesCompletion of activities detailed within the Project schedule.Raise executes and manages change controls relating to NPI.SME for bio-processing operations providing expertise and insight to ensure that facility design enables safe and efficient operation and rapid product changeover to maximize facility utilization.Development of innovative, new and lean method of moving from one product to another.Specification and introduction of new materials and consumables for the Multi Product environment.Liaise with Tech Services, Engineering, EHS, Quality, Automation and external parties regarding aspects of operating a Multi-Product Facility.Support and lead key meetings on behalf of Operations.Participation in Factory Acceptance Testing for key equipment packages (Travel may berequired).Lead/participate in risk assessment activities.Develop standard work model to align with existing operations.Update 5S plans to include new products requirements.Qualifications, Education, Experience:Diploma / Bachelors or Equivalent.Familiarity of systems such as MCS, Orchestrate, MES, QTS, SAP, LIMS and PDOCs4+ years biopharmaceutical manufacturing experience.In-depth working knowledge of Biopharmaceutical processing.Knowledge of cleaning validation/verification execution.Experience of DS product specific equipment and materials (column resins) would be beneficial.Experience writing technical documents such as SOPs and batch records.Experience with standard work, 5S and structured problem solving would be beneficial.Excellent communications skills essentialThe candidateDemonstrate the GC OWNIT valuesCI tools/- capability is a key building block for learning & development - Trained and M1 certified.Proactive engagement with key stakeholders.Best practices developed and shared with other teams /sites.Best practices actively sought and copied.Proactive & effective communication within and different functional groups in the Operating Unit.
Regulatory Compliance Specialist
Brightwater, Dublin (Central)
 A regulatory compliance role has become available with a client in Fintech. Remote working/fully flexible working model is offered along with the opportunity to join an existing team and contribute towards strengthening and growing their compliance/risk function. This role will suit a candidate who enjoys a collaborative working environment and will appeal to candidates looking to join a fast growing company where they can really embed themselves into the compliance function. The role will report into the Senior Compliance Manager. Responsibilities •Support the delivery of the company compliance plan and compliance monitoring programme to ensure that sound and responsible business practices are incorporated into the day to day operations of the business.•Responsibility for advice on conduct of business rules, fitness and probity regime, relevant complaints handling, corporate governance, anti-money laundering, terrorist financing, permissions, and data protection.•Liaise with operational teams, as well as the risk function, to ensure compliance risks are properly understood and mitigated: conduct and report enterprise-wide testing of operational teams’ compliance controls to identify compliance risks; identify breaches and monitor until resolved.•Continuous improvement of risk-based AML/CFT regime including support for MLRO in preparation of STRs.•Maintain breaches logs and assist in the provision of reports to Business Risk Committee based upon breach log data.•Assist in the preparation of regulatory and Group reporting.•Update compliance policies and cascade changes to operational teams.•Promote a Compliance Culture including support the development and delivery of compliance education and training programmes.•Assist in monitoring changes in regulations that impact on the company with the aim of providing relevant and timely advice to the business.•Raise awareness of compliance risk appetite and tolerance levels throughout the business.•Providing accurate advice and guidance in response to Compliance queries and issues raised by the business or clients•Keeping abreast of all regulatory changes and developments in the regulatory environment and notifying senior management of any changes or developments that could impact the business.•Supporting and advising the business in the implementation of new regulation to ensure ongoing compliance, as assigned by the Head of Compliance or Compliance Managers•Assisting in the preparation of the weekly regulatory update to Management and the Board on relevant regulatory matters across the industry as well as emerging regulations•Provide training in compliance practices and procedures to all employees.br> Requirements: •An accredited qualification in regulatory and compliance assurance will be advantageous.•At least three years’ experience as a regulatory compliance specialist, or similar in a Financial Services/Payments environment.•Extensive knowledge of industry regulations and governing laws specifically Anti-Money Laundering legislation.•You are a driven individual who will carry and drive the Compliance culture with your colleagues and within your team.•Proficiency in office and compliance management software.•Exceptional analytical, investigative, and organisational skills.•Excellent interpersonal and communication skills. For a confidential and discreet conversation to understand more about the role, please contact Louise Morrissey on 01 662 1000 or email [email protected]
QA Specialist
, Cork, Republic of
QA Specialist A leading pharmaceutical manufacturer is recruiting for a Quality Assurance Specialist to join their team in Cork on a FTC covering maternity leave This role contributes to the implementation and maintenance of Quality Assurance actions in compliance with the current GMP regulations. In this role as part of a diverse team your primary responsibility will be for the quality assurance compliance activities in the Cork Site. Key Responsibilities:Reviewing the GMP documentation e.g, SOPs, reports, methods, specifications, validation protocols, quality contracts etc., and Exceptional Documents e.g. NCRs/PNCRs, Planned Deviations etc.Writing and reviewing QA department procedures and reports e.g. protocols, SOPs, environmental reports etc. Reviewing and Approving other departmental procedures and reports.Internal Auditing (when required) of FLI Departments and external auditing (when required) of Material and Service Suppliers (including Supplier Management).Alerting the QA Compliance Manager in case of detection of a discrepancy / non-compliance.Participation in change control activities on site.Assisting in the preparation and reviewing of QA department reports and metrics e.g. monthly quality report, discrepancy reports, exceptions reports, KPI reports.Reporting and communication to QA Compliance Manager on key events and issues etc. via normal in house reporting structure e.g. meetings, formal reports etc.Participate in initiatives and action plans for the development of QA and improvement of GMP compliance.Participating and follow-up the audits and/or inspections carried out at the site by the authorities or clientsAssist in preparation and presentation of GMP training programmes.Represent QA on BeX projects to ensure compliance to GMPEnsure QA activities are executed in line with in-house procedures and in compliance with requirements of cGMPSAP Local Key User for the QA DepartmentSupport supplier activities (qualification, risk management and notification management) are executed in line with in-house and Global Procedures and in compliance with requirements of cGMP.Assist in New Product Introduction Activities when required.Reviewing all documentation associated with batch release to ensure GMP compliance.Verifying the labelling of the raw material, packaging components, bulk and finished product.Ensuring the follow-up of the necessary corrective actions & preventative actions implemented in consequence of a quality failureBy performing investigations, and ensuring a follow-up, following discrepancy, failures and external complaints.Participate in KPI meetings to assist the batch release process.Education Educated to third level in science based discipline. Degree level preferable.Technical Skills and Experience: Minimum 3 years pharmaceutical experience in a regulated environment would be preferable. Experience in pharmaceutical environment a significant advantage.Experience with Solid DoseKnowledge of GMP.Good organisation skills and time management.Analytical approach to problem solving.Proficient with Microsoft Word, ExcelFor further information on this QA Specialist role in Cork please contact Clara Burke on (phone number removed) or Check out all our open jobs on our HERO Recruitment website