Armagh jobs in Armagh
Sort by: relevance | dateSenior Laboratory Instrument Specialist
Location: Craigavon Hours: 37.5 Hours Contract: Permanent Salary: Competitive Business Unit : Pharma Services Open To : Internal & External Applicants Ref No.: HRJOB10871 The Role Working as part of the Pharma Services Business Unit, the Senior Laboratory Instrument Specialist will coordinate instrument validation, instrument calibration, planned maintenance and breakdown maintenance of analytical equipment in our laboratories, to ensure the continued compliance of existing GxP critical equipment within the Analytical Operations department. Additionally, they 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. For a full list of job specific responsibilities please see attached Job Description. Essential Criteria Reward For the successful candidate, we offer an attractive benefits package which will include a competitive salary, annual bonus, employer pension contributions, 34 days paid annual leave, healthcare benefits and much more. Please see further details on the Benefits Tab. 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 Tuesday 16th 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 CV’s received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Housing Support Worker
Part Time Housing Support Worker Location: Housing Support for Young People in the Armagh/Dungannon Salary: £13,224 per annum Contract: Permanent Work hours: Monday-Friday, 20 hours per week Please note, we do not offer sponsorship for our roles. Applicants must demonstrate they have Right to Work in UK as part of the shortlisting process Belfast Central Mission (BCM) is an award-winning leading charity with social care projects and social enterprises across Northern Ireland. With over 300 staff and volunteers delivering services across Northern Ireland to support people at their point of need. Housing Support for Young People supports young people (aged 16-25) to access and maintain accommodation in the community. Support can be provided for up to 2 years depending on the needs of the Service User What we can offer you 4% employer pension contribution (after 3 months of service) 21 days annual leave per annum 12 statutory days Westfield Health Level 1 - Cash back plan and additional benefit of unlimited MRI and CT scans and 1 PET scan within a 12 month period Westfield Health Rewards Learning & Development opportunities Long service annual leave increments and scheme What we need from you GCSE English or equivalent At least one year’s experience supporting groups and/or individuals either a paid or voluntary capacity. Good communication skills A full driving licence and access to a car with Business insurance as you may have to transport Service Users. NISCC registration or willing to obtain within 6 months of start date Right to Work in UK Please refer to the job description for further details. Belfast Central Mission is an Equal Opportunities Employer. We reserve the right to close this vacancy early if we receive sufficient applications for the role. Therefore, if you are interested, please submit your application as early as possible.
Cleaning Operative
Mount Charles Group are one of the largest and privately owned soft Facilities Management, catering and ancillary service/product providers in Ireland. If you are a customer focused individual and want to join a fun and family orientated business which believes people are our greatest asset, then we have a role for you! Our family values speak for themselves: Do the right thing, Have fun & grow together, Take pride in what you do! We are currently recruiting for a Cleaning Operative to join our team based at Orchard Leisure Centre, Armagh. This is a great opportunity to join a world leading facilities management company. Working Pattern: Basic statutory training for the role will require all candidates to have basic reading, writing, speaking and listening skills to assist in understanding safety and work instructions and communicating with customers on a day-to-day basis. Please note the successful applicant's offer is subject to the Access NI (Enhanced) check prior to commencement of role. The Access NI Code of Practice is available upon request. Mount Charles Group has a policy on recruiting ex-offenders, a copy of which can be provided upon request. Having a criminal record will not necessarily prevent you from working for the Mount Charles Group. Due to the number of applicants Mount Charles receives, we only respond to short-listed applicants. If you have not been contacted within six weeks of the closing date, you have not been selected for interview. GREAT PEOPLE - GREAT SERVICE - GREAT FUTURE
Technical Quality Specialist
Technical Quality Specialist (FTC 9 - 12 months) Location: Craigavon Hours: 37.5 hours per week Salary: Competitive Business Unit : Pharma Services Open To : Internal & External Applicants Ref No.: HRJOB10902 (Please note this is a re-advertisement, if you have applied for this position within the past 6 months, we will be unable to accept your application at this time) ㅤ We warmly encourage recent graduates to apply for this exciting opportunity within the Technical Quality team at Almac Pharma Services. This role offers a dynamic entry point into the pharmaceutical industry, where you'll gain hands-on experience in validation activities, regulatory compliance, and cross-functional collaboration. It's an excellent chance to develop your skills in a supportive environment while contributing to high-impact projects that uphold global quality standards. If you're passionate about science, detail-oriented, and eager to grow your career. ㅤ The Role In this role within the Technical Quality team at Almac Pharma Services, the successful applicant will play a crucial part in ensuring compliance with GMP principles and the company's quality standards. The responsibilities include overseeing a variety of validation activities to ensure that essential facilities, systems, processes, and procedures meet the EU and FDA requirements in a timely manner. This involves active participation in the validation life cycle stages, such as developing project design documentation, risk assessment of validation requirements, generating validation plans, preparing protocols and reports, and analysing process validation data. The role involves collaborating with various stakeholders, providing advice on validation procedures, monitoring equipment and processes, managing workloads to meet client needs, and serving as the lead representative during the initiation of new projects. The position also entails monitoring and re-evaluating equipment, systems, and processes periodically, ensuring appropriate system access for users, supporting satellite Pharma Services sites, and updating management on validation project statuses. The successful applicant will work closely with project teams, plan validation tasks, participate in testing to meet operational needs, review and approve documentation for system and process releases, and assist in regulatory compliance remediation actions. By providing guidance to internal and external stakeholders, managing workloads effectively, and ensuring timely completion of validation tasks, the successful applicant will contribute significantly to maintaining high-quality standards and regulatory compliance within Almac Pharma Services. ㅤ Key Requirements ㅤ Further Information The working pattern for this role is a flex pattern between the hours of 07:00 – 19:00 with core hours of 10:00 – 16:00. You will also be eligible for hybrid working following the successful completion of probation. ㅤ 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. ㅤ Closing Date We will no longer be accepting applications after 5pm on 02 December 2024 ㅤ 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.
Associate Dentist
We have an exciting opportunity for an Associate Dentist to be part of our family run group of Practices and to join our team in Lurgan. There is an established list available which includes a number of private patients. Denplan is offered at this practice. We pride ourselves on offering an excellent quality of care and service to our patients. We can offer:
Associate Dentist, Maternity Cover
Job Summary We have an exciting opportunity for an Associate Dentist to be part of our family run group of Practices and to join our team for 6-9 months' maternity cover in our Lurgan practice. There is an established list available which includes a number of private patients. Denplan is offered at this practice. We pride ourselves on offering an excellent quality of care and service to our patients. We can offer:
Quality Auditor Nightshift
The Job Reporting to the Quality Specialist, the Quality Auditor will be responsible for inspecting products to ensure quality specifications and standards are met. Main responsibilities will include: •Reporting of quality issues to production management & Quality Specialist •Backtracking non-conforming product into finished goods store •Processing of product in the QC hold area •Ensure correct stock quantities are maintained •Record and analysis of quality inspection findings, to highlight key areas for improvement •Attend the production morning meeting, to highlight quality issues to wider operations team •Producing quality aides for production job files •Support in quality investigations •Attend & contribute to Quality Forum meeting The Person The successful candidate should: •Be educated to GSCE level or equivalent in Mathematics and English •Minimum 12 months experience in a FMCG manufacturing environment or previous experience within a quality assurance role •Have Awareness of good health and safety practices •Experience with problem-solving and knowledge and understanding of root cause analysis and CAPA •Computer literate with previous experience of MS Excel •Have strong attention to detail •Have good organisational & time management skills •Be confident in making decisions on product quality Whilst not essential, it would be advantageous to your application to have knowledge of management system standards, particularly ISO 9001 Quality Management System and BRC for Packaging Materials and also previous experience and involvement in quality improvement projects. Hours of work will be 12-hour continental nightshift (7pm-7am). This role is for a 12 month fixed term contract. Ideally the candidate will have knowledge & experience which can be applied in this role. Additional training will be provided where appropriate. Those wishing to apply for this position, should apply online by visiting: https://huhtamaki.getgotjobs.co.uk/home Completed applications must be returned by Friday 12th September, 5pm WE ARE AN EQUAL OPPORTUNITIES EMPLOYER
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.
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
Associate Dentist
Job Summary We have an exciting opportunity for a Private Dentist to be part of our family run group of Practices and to join our team in Armagh. There is an established list available which includes a number of private patients. We pride ourselves on offering an excellent quality of care and service to our patients. We can offer:
