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Costa Coffee requires a Team Member for our store in Antrim. At Costa Coffee we are as passionate about our people as we are our great coffee! Being a part of our team gives you the chance to learn new skills in coffee excellence whilst letting your personality shine through. As a Costa Barista you receive full training in delivering every customer with an unbeatable coffee experience, through great customer service and great coffee. Are you: -
UHWM Risk Officer
*********PLEASE COMPLETE THE APPLICATION FORM FULLY, CV'S ARE NOT ACCEPTED************ Principal Duties and Responsibilities Under the direction of the Risk Manager the post holder will; The above Job Description is not intended to be a comprehensive list of all duties involved and consequently, the post holder may be required to perform other duties as appropriate to the post which may be assigned to him/her from time to time and to contribute to the development of the post while in office.
UHWN Clinical Nurse Manager Supplementary Campaign
*********PLEASE COMPLETE THE APPLICATION FORM FULLY, CV'S ARE NOT ACCEPTED*********** Principal Duties and Responsibilities Professional / Clinical The CNM1 (Medical Directorate) will: The above Job Description is not intended to be a comprehensive list of all duties involved and consequently, the post holder may be required to perform other duties as appropriate to the post which may be assigned to him/her from time to time and to contribute to the development of the post while in office.
Senior Social Worker, Perinatal Mental Health
The Hospital is inviting applications for the following post: Senior Perinatal Mental Health Social Worker - Permanent, Full-Time Intended applicants should submit an updated Curriculum Vitae by 12noon on Friday 19th September 2025. Full job description can be found attached. Details of Service Specialist perinatal mental health services are vital because of the potential detrimental impact of perinatal mental health disorders for the mother, the baby, their relationship and that with the partner and other children. The specific circumstances of pregnancy, birth and early mother/infant bonding requires staff who are knowledgeable, skilled, sensitive and experienced in this area. Hence the philosophy underpinning this model of care is its focus on: (i) The mother (ii) The baby (iii) Their relationship – all within the context of the family The model is informed by national and international epidemiological evidence of need. In 2016, there were approximately 64,000 births in Ireland. Approximately 2,240 women are likely to have suffered from more serious mental illness and so would likely benefit from advice from or referral to a specialist perinatal mental health service. Support for all other services involved with women in the perinatal period by the Specialist Perinatal Mental Health Service is an important part of the role. This includes clinical advice, training and education. The Model of Care is based on the maternity networks recommended in the National Maternity Strategy. This means the specialist perinatal mental health services will be aligned to hospital groups and developed in a hub and spoke format so all 19 maternity services are included in the model. In each hospital group, the maternity service with the highest number of deliveries will be the hub. These are: • RCSI Hospital Group (HG) – Rotunda Hospital • Dublin Midlands HG – Coombe Hospital • Ireland East HG – National Maternity Hospital • Saolta HG – Galway University Hospital • South/Southwest HG – Cork University Maternity Hospital • University of Limerick HG – University Maternity Hospital Limerick Each hub has a specialist perinatal mental health service. Its staffing is multidisciplinary and led by a Consultant Psychiatrist in perinatal psychiatry. Each specialist team will include a Senior Perinatal Mental Health Social Worker. Overall job role: The primary purpose of this Senior Perinatal Mental Health Social Worker (SPMHSW) post is to provide a recovery orientated, client centred social work service to women attending the Specialist Perinatal Mental Health Service. The SPMHSW will work as part of a multidisciplinary team delivering a co-ordinated approach to client care. The SPMHSW brings a systemic perspective to assessments and interventions on a multidisciplinary team emphasising the importance of assessing the person in their environment, assessing and providing expertise where the social aspects are factors impacting on the service user’s mental health and on her family. The SPMHSW emphasises the importance of Family Focused Practice and their psychosocial assessments and therapeutic interventions focuses not only on mother’s individual mental health needs, but on the mother-infant relationship, the Partner/Supporter and the broader family and community system. The Senior Perinatal Mental Health Social Worker (SPMHSW) is a member of the hub-based specialist Perinatal Mental Health team for the hospital group. A key function is close working with multidisciplinary colleagues in other hubs to ensure a seamless service is provided for women and their families.
Biocatalysis Chemist
Biocatalysis Chemist Hours : 37.5 hours per week, Monday – Friday. Flexible working hours. Ref No: HRJOB10264/1 Business Unit: Almac Sciences Location : Craigavon, Northern Ireland, UK Open To: Internal and External Applicants may apply The Role Almac Sciences are currently recruiting for a talented chemist to perform high quality biocatalytic chemistry for our clients in accordance with agreed timelines. The role involves carrying out contract research projects involving enzymes, gram scale synthesis and process development prior to the synthesis of larger amounts of the target molecules using enzymes. Working as part of a multi-disciplinary project team the post holder will plan carefully, carry out their work safely and document and communicate their methods and results accurately The team perform high quality chemistry for our clients, in accordance with agreed timelines. We are looking for chemists with an appetite for novelty, to be put to good use in development of new applications in the pharmaceutical industry. Essential Candidate Criteria · Bachelor’s Degree (or equivalent) in Chemistry / Biochemistry or other closely related discipline · Previous experience of enzyme screening and enzyme catalysed synthesis · Previous experience of screening assay development for rapid identification of active enzymes Desirable Criteria · Postgraduate Qualification i.e. MSc, PhD or equivalent in Chemistry, Biochemistry or other closely related discipline · Previous experience of the synthesis and analysis of organic molecules in industry · Previous practical experience of process development chemistry · Previous practical experience of performing synthetic chemistry to a deadline · Previous experience of colormetric assay development For more information, including postholder responsibilities and full candidate criteria, please review the attached Job Description. As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group. Closing Date : Sunday 14th September at 5pm RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited, and no fee will be payable. Thank you for your cooperation.
Quality Assurance Specialist
Quality Assurance Specialist Location: Loughborough, UK Hours: 37.5 hours, Monday-Friday, Flexible working hours Business Unit: Pharma Services Open To : Internal & External Applicants Ref No.: HRJOB10701 The Role We are currently recruiting for a Quality Assurance Specialist in Almac Pharma Services. In this role you will be responsible for supporting compliance of the Quality Management System (QMS) and supporting the releases of batches by working with the Qualified Persons. Key responsibilities include monitoring operations, conducting internal and external audits, assisting in process improvement initiatives, and providing QA support for various projects Please see attached job description for further details. Key Requirements To be successful in this position you will need A-Level qualification (or equivalent) and experience in a QA role within a Pharmaceutical Quality System. Whilst not essential, it would be an advantage if candidates have Bachelor’s degree (or above) in a scientific (Chemistry, Biology or Pharmacy) or technical (Engineering) discipline (or equivalent), previous experience in writing and producing detailed reports, review of executed manufacturing records and direct experience in the manufacture of solid oral dosage, suspensions and liquid fill capsule products Please see attached job description for further details of criteria. Apply Now: Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible. Closing Date: We will no longer be accepting applications after 5pm on Sunday 14th August 2025 RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CV’s received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation. Please be aware: This position is being readvertised. If you have submitted an application for this role within the last six months, we will not be able to consider your application at this time. Thank you for your understanding.
Senior Laboratory Instrument Specialist
Senior Laboratory Instrument Specialist Location : Loughborough, UK Hours : 37.5 hours per week Mon-Fri with flexible working hours. Business Unit: Pharma Services Open To : Internal & External Applicants Ref No .: HRJOB10895 The Role Almac Pharma Services are currently recruiting for a Senior Laboratory Instrument Specialist to join their Analytical team, at our Charnwood facility in Loughborough. The post holder will coordinate instrument validation, calibration, planned maintenance, and breakdown maintenance of analytical equipment in our Laboratories, ensuring the continued compliance of existing GxP critical equipment within the Analytical Operations department. Additionally, the Senior Laboratory Instrument Specialist will support the qualification of new scientific analytical equipment, and coordinate with multiple departments within the business to ensure Analytical Operations has the analytical capabilities required to support complex projects. Please see attached Job Description for further information on job specific responsibilities. Key Requirements · B.Sc. (or equivalent) in a Science, Engineering or Information Technology Subject ( Significant industry experience in a similar role may be considered in lieu of academic qualification ) · Experience in a similar role or a QC/QA within a Pharmaceutical Quality System · Experience in writing and producing detailed reports Desirable Criteria · Validation, Qualification & Data Integrity Assessments of Analytical equipment Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible. Closing Date: We will no longer be accepting applications after 5pm on Sunday 14th September 2025. RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Project Coordinator
OVERALL ROLE OBJECTIVE: The principle function of the Project Services department is the day-to-day management of all Almac Clinical Services customers at any Almac Clinical Services (ACS) site. The department coordinates all aspects of the delivery of a customer’s project as specified in the quotation. In order to achieve this, the department is divided into a customer support group which includes supply chain management and an operations support group. The operations support group is further divided into two key areas: production and distribution. The Project Coordinator working in production is responsible for performing all tasks associated with the successful management of the manufacture and packaging of clinical trial supplies at any Almac Clinical Services (ACS) site. The Project Coordinator working in distribution is responsible for performing all tasks associated with the successful management of the distribution and return of clinical trial supplies at any Almac Clinical Services (ACS) site. Project Coordinators provide a supportive role to the Project Distribution Lead or Project Production Lead. JOB SPECIFIC RESPONSIBILITIES: Production Schedule operations with production planning to meet customer timelines Track the progress of operations against the project plan and advise the Project Production Lead of any issues or delays arising throughout the course of the project, escalating to the Project Team or Project Group Manager as appropriate Draft detailed written instructions for the manufacture/packaging of each batch of material ensuring full compliance with current Good Manufacturing Practice Provide timely information/documentation required for the management of the materials required for upcoming manufacturing operations Track ordering and receipt of drug product and components for production activities, assisting Logistics and QC in the clearance upon receipt at Almac Expedite materials and documents through internal Almac systems Escalate project specific production issues to the Project Team or the Project Group Manager as appropriate Calculate quantities of drug product and input components needed per production operation Allocate drug product and components to production jobs Track the progress of the production operations against the project plan and advise the Project Team of any issues affecting the planned production dates Schedule and gather documents for QP release of Almac produced finished goods Schedule analytical services to meet customer timelines Monitor inventory levels and expiry dates of components to ensure adequate levels of inventory are available for production operations Initiate the order for ancillary supplies and components for production operations as required ensuring that the appropriate approvals are obtained Assist in progressing rework of returned material per customer request Generate change requests for material receipt and production related documentation Assist in the generation of quality incident reports and technical queries relating to project specific production issues Distribution Draft detailed distribution instructions and depot project instructions Draft instructions for return, accountability and destruction at Almac facilities and Almac contracted depots Establish distribution protocols in COSMOS to ensure accurate and complete set up of all items, Autoship, Depots, Returns, JIT, and distribution related activities Schedule and gather documentation for QP release of customer supplied finished goods, scheduling analytical testing if required Ensure required lots of finished goods are released for shipment to the appropriate countries in advance of the first shipment date Complete protocol setup in the inventory release file (IRF) generator if applicable and generate Inventory Release Files for lot release Set trigger levels, monitor inventory levels and expiry dates of shipping components (e.g. shippers, temp tales), ancillary supplies (e.g. syringes, dosing instructions/leaflets, alcohol swabs) and ancillary drug supplies (e.g. rescue medications) to ensure adequate levels of inventory are available for subsequent shipments from Almac warehouses and depots Notify the customer when inventory levels are low for customer supplied components and supplies Initiate the order for ancillary supplies and components supplied by Almac ensuring that appropriate approvals are obtained Monitor expiry dates of finished goods and notify the Clinical Supply Manager as required Arrange for shipment of samples to the customer or third party Generate memos providing instructions to the sites and depots on re-labelling activities and upon approval from the Clinical Supply Manager, assemble and distribute the notifications and materials for re-labelling to sites, depots and clinical monitors, tracking and reconciling the completion of the re-labelling activities Review and track the receipt of Drug Accountability Logs communicating with sites and/or clinical monitors as required ensuring that the logs are completed Track destruction of returns and forward Certificates of Destruction to the customer Generate change requests for distribution and returns related documentation Assist in the generation of quality incident reports and technical queries relating to project specific distribution issues Customer Service (All areas) Ensure all customer contact is carried out with a high level of professionalism in order to develop and maintain good working relationships with each customer Receive and follow through on all customer queries ensuring a response is supplied in a timely manner Attend teleconferences and meetings with customer as required Deal with customer complaints according to defined procedures and escalate to the Clinical Supply Manager as appropriate Maintain a professional approach at all times while representing Almac Fulfil any necessary administration duties required to assist the team Log all billable time against the correct project in the Timesheet system Other (Operational) Provide support and act as the backup to the Project Distribution/Production Lead when requested for routine customer communication and project team updates Perform all tasks within the necessary timeframe defined for each project Provide regular updates to the Clinical Supply Manager for global projects when required Complete departmental Key Performance Indicators (KPIs) for specific projects as required This role may require coverage beyond normal working hours on a regular basis. It is a condition of your employment that you are able to fulfil this requirement of the role. QUALIFICATIONS
Thoracic Transplant Service Data Manager
Job Purpose This post is dedicated to Thoracic Transplant and VAD data management and will be a step towards aligning the service with key aims of HSE Digital Health Strategic Implementation plan particularly facilitation of collaboration, communication, and data sharing among healthcare professionals, leading to improved coordination of care and better decision-making all key requirements for safe Organ Donation and Transplant services. Note NSP 2025 has provided funding for a Transplant Centre Management Software application which is part of a wider ODTI strategy. This post will have a coordination role for roll out of this application at National Thoracic service. The Heart/Lung Transplant Data Manager is responsible for managing and analysing data related to the MMUH Heart and Lung Transplant, Heart Valve Tissue Bank and VAD service. This includes collecting, validating, and reporting on patient data to support Heart Lung Transplant Quality, Clinical Audit, research and quality improvement initiatives. They work with the multidisciplinary team to ensure data accuracy, integrity and to facilitate data-driven decision-making and achievement of KPIs. For informal enquiries, please contact Karen Fitzpatrick, Data Co-Ordinator Lead, karenfitzpatrick@mater.ie For more information, please refer to the attached job description.
Chief Assistant Technical Services Officer, Hospital Engineer/project Manager
Job Purpose: The Chief Assistant Technical Services Officer will be responsible for: A panel may be formed as a result of this campaign, from which current and future, permanent and specified purpose vacancies of full or part-time duration may be filled. Informal Enquiries: John Reilly, Director of Estates. Email: johnreilly@mater.ie
