Armagh jobs in Armagh
Sort by: relevance | dateAnalytical Learning & Development Specialist
Location: Craigavon Hours: 37.5 Hours per week Salary: Competitive Business Unit : Pharma Services Open To : Internal & External Applicants Ref No.: HRJOB9961 The Role: This role will be based within the Analytical Operations department of the Almac Pharma Services (APS) Business Unit. The Analytical Learning and Development Specialist will primarily deliver training within the Analytical Operations enabling all employees to perform analytical related activities in a GMP compliant manner. In the role, they will promote a culture of learning across this group, by creating learning environments where employees can continuously develop and thrive. The specialist will work with their team members to develop and deliver the Analytical Operations training strategy. The specialist will have a sound understanding of all analytical techniques and will competently provide theoretical and practical training on all aspects of the lab, including GMP compliance, sample preparation, and the use of a wide range of analytical instrumentation, for example HPLC (Including software training), Dissolution, FTIR, etc. Within the role the specialist will provide ongoing support and mentoring for trainees and will provide feedback on progress to their line managers. The specialist will also monitor the success of the training program, scrutinizing the results on a periodic basis, and implementing corrective actions to improve the program as required. For a full list of job specific responsibilities, please see attached Job Description. Key Requirements: 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 15th May 2024 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.
Quality Assurance Specialist
Quality Assurance Specialist ㅤ Location: Craigavon Hours: 37.5 hours per week Salary: Competitive Business Unit : Pharma Services Open To : Internal and External Applicants Ref No.: HRJOB9635 ㅤ The Role This role involves assessing and improving the Quality System of Almac Pharma Services and contributing to GMP (Good Manufacturing Practice) compliance and the quality of pharmaceutical products. The main responsibilities include monitoring and reviewing various operations such as manufacturing, quality control, analytical support, product development, and engineering to assess ongoing GMP compliance and product quality. The role also involves providing quality assurance support and advice to operational departments, implementing quality systems like deviation/CAPA (Corrective and Preventive Action) management and change controls, and actively improving quality systems to ensure GMP compliance and product quality. The successful candidate will also be involved in reviewing production and laboratory data, participating in the Supplier Management Process, conducting internal and external audits, and assisting in the compilation and review of various reports and agreements. ㅤ In addition to the above, the post holder will be the internal and external contact for queries related to product compliance and quality. They will also participate in audits of external suppliers and assist in hosting customer and regulatory audits. The role requires the identification, writing, approval, and implementation of critical GMP documents, as well as conducting internal audits and assisting in the compilation and review of Product Quality Reviews, Technical Agreements, and Risk Assessments. Additional duties related to ensuring GMP compliance and product quality may also be assigned. ㅤ The ideal candidate for this role should have a strong understanding of GMP compliance and quality systems. Attention to detail, analytical skills, and the ability to review data and reports for accuracy are crucial. Excellent communication and organizational skills are essential for interacting with internal and external stakeholders and ensuring timely delivery of projects while maintaining product quality. The role also requires the ability to conduct audits and participate in the Supplier Management Process. The successful candidate should be proactive in continuously improving quality systems and demonstrating a commitment to GMP compliance and the quality of pharmaceutical products. ㅤ Key Requirements ㅤ Further Information There is currently 1 x Permanent position available with future permanent & fixed term opportunities arising within the next 12 months. ㅤ These roles are based on a flex work pattern: Monday – Friday between the hours of 07:00 – 19:00 with core hours of 10:00 – 16:00. These roles 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 Sunday 5th May 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.
Lead Investigator
Lead Investigator Location: Craigavon Hours: 37.5 Hours Salary: Competitive Business Unit : Pharma Services Open To : Internal & External Applicants Ref No.: HRJOB9636 The Role Working as part of the Pharma Services business unit based in our global headquarters in Craigavon, the primary role of the Lead Investigator is to oversee and manage the timely investigation of deviations and CAPA’s. The successful candidate must ensure that investigations are performed and documented, with appropriate root cause determination and to ensure that CAPA actions are identified and implemented in line with procedural and regulatory expectations. Lead Investigators will be aligned with operational areas and must work closely with the senior manager of that area to communicate, educate and ensure continuous improvement within those areas. The successful candidate will be part of a Lead Investigator team working closely with Quality Assurance to manage and support investigations in all business areas. For a full list of job specific responsibilities please see attached Job Description. Essential 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 5th May 2024
Global Quality Specialist
Location: Craigavon Hours: 37.5 Hours per week Salary: Competitive Business Unit : Pharmaceutical Services Open To : Internal & External Applicants Ref No.: HRJOB9397/1 *Please note if you have applied for this role within the past 6 months and have been unsuccessful, your application cannot be reconsidered* The Role Working as part of the Pharma Services Quality Assurance department, the Global Quality Specialist (Regulatory Compliance) will be responsible for supporting the global regulatory intelligence program. The program monitors regulatory news/ feeds, hot topics and keeps abreast of new and changing legislation. The post holder will also be responsible for keeping the business informed about upcoming regulatory changes and supporting the management of change/risk as appropriate. 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 Monday 5th May 2024 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.
Senior Operator Grade Facility Cleaner
Job Title: Senior Operator Grade 2 Facility Cleaner Location: Craigavon Hours: 37.5 hours per week , rotating shift pattern Salary: Competitive Business Unit : Almac Pharma Services Open To : Internal and External Applicants The Role With a wealth of knowledge and experience, Almac Pharma Services have been manufacturing medicines in tablet, capsule and powder form for over 50 years. We also pack commercial drug products into bottles, blisters and sachets and provide specialised packaging solutions for medical kits, vials and syringes. The expert services we provide supports the provision of medicines and treatments to patients around the world. We are currently recruiting for a Senior Operator Grade 2 Facility Cleaner to join our highly skilled team. As a Senior Operator (Grade 2) you will be responsible for maintaining high standards of cleanliness in designated areas within the GMP manufacturing facility ensuring activities are carried out satisfying cGMP at all times. Tasks include; general cleaning of designated production areas including production corridors, toilets, changing areas and showers to a high standard as dictated by regulatory requirements, providing direction to other cleaners and assign their daily and weekly tasks and perfoming final sign off on cleaning completion and quality. Further details can be found in the attached job description. Reward A fantastic salary and benefits package is available, including annual bonus for all, generous holiday allowance, healthcare reimbursement scheme, and a rewarding role where the work you do will ultimately be contributing to the advancement of human health. Apply Now Apply online - please ensure your CV clearly outlines how you meet criteria for this role – refer to the job description attached to this advert for full details of the essential and desirable criteria required. Please upload your CV in PDF format where possible.
Technical Support Team Leader
Technical Support Team Leader (Packaging Operations) Location: Based at our Craigavon headquarters Hours: Monday to Friday 08:30 – 17:00 Salary: Competitive plus excellent benefits package Business Unit : Almac Pharma Services Ref No.: HRJOB9643 The Role Almac Pharma Services is an established and highly successful outsourcing partner working with leading pharmaceutical and biotechnology companies around the world. Our highly skilled team specialise in the manufacture and packaging of commercial drug products and medicines, and offer end-to-end management of product supply as well as a range of additional bespoke client services. The expert services we provide supports the provision of medicines and treatments to patients around the world. We currently have an opportunity to join our Packaging Operations department in the role of Technical Support Team Leader. The Technical Support Team Leader will lead the Production Technician Team, ensuring delivery of business objectives whilst driving cGMP compliance, efficiency, effectiveness, and continuous improvement. The role will support new product process validation, technical transfer activities, new equipment, and tooling validations. The postholder will be responsible for the quality, material consumption, labour cost, and process output in accordance with associated protocols and batch documentation whilst maintaining schedule adherence. This is a key role within our Packaging Team, working closely with the multidisciplinary team including Technical Support, Technical Quality, Quality, Business Development, and Client Project Management teams. It’s an excellent opportunity to progress your career within our Operations Department. Key Requirements **All applicants must be eligible to work in the UK, or hold a valid visa/work permit that allows you to work in the UK ** Further information on the essential criteria required for this role can be found in the Job Description attached to this advert. Reward A fantastic salary and benefits package is available, including annual bonus for all, generous holiday allowance, healthcare reimbursement scheme, and a rewarding role where the work you do will ultimately be contributing to the advancement of human health. Apply Now Apply online - please ensure your CV clearly outlines how you meet criteria for this role – refer to the job description attached to this advert for full details of the essential and desirable criteria required. Please upload your CV in PDF format where possible. Closing Date Closing date for receipt of applications is 7th May 2024 at 5pm.
Brand Manager
Brand Manager (FTC 9 – 12 months) Location: Craigavon Hours: 35 hours per week Salary: Competitive Business Unit : Galen Open To : Internal and External Applicants Ref No.: HRJOB9667 ㅤ The Role The overall role objective of the position is to provide hands-on management of marketed brands and launch products, with a focus on developing and implementing tactical plans to achieve budgeted sales and profit targets. This involves building strong relationships with key personnel across various departments such as Marketing, Medical, Commercial Operations, Finance, and sales management. The role entails developing robust tactical implementation plans in collaboration with internal stakeholders, ensuring effective communication to field teams and adherence to industry codes, managing external agencies and suppliers, and monitoring budget allocation and spend. Additionally, the role involves generating sales reports, reviewing implementation of tactical plans against key performance indicators, addressing issues management, and staying updated on product, competitor, therapy area, and market knowledge. The position also includes coordinating with the Medical Manager to deliver initial and ongoing field-force training and maintaining communication with the Sales Director regarding training needs. 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. This role will occasionally require coverage beyond normal working hours as and when required. 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 12 May 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.
Product Quality Auditor
Location: Craigavon Hours: 37.5 Hours Salary: Competitive Business Unit : Pharma Services Open To : Internal & External Applicants Ref No.: HRJOB9616 *Permanent & Fixed Term opportunities available - Please state on the application form which contracts you are open to* The Role Working as part of the Pharma Services Business Unit, based in our Headquarters in Craigavon, the Product Quality Auditor will work as part of the Product Quality Team responsible for review of batch records prior to QP certification and release. They will support the Product Quality department objectives in relation to the delivery of batches in line with OTIF timelines, including performing the associated electronic transactions required to generate KPI data. They will also ensure customer requirements for batch release are met in relation to Promise Date, escalate any anticipated issues in meeting these timelines to the Product Quality Team Leader and log constraints as required. 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. For a full list of job specific responsibilities please see attached Job Description. *Please note that if you have applied for this role within the past 6 months and have been unsuccessful, you will be ineligible to re-apply* Essential 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 19th May 2024 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.
Commercial Coordinator
OVERALL ROLE OBJECTIVE: The post holder is responsible for carrying out all duties relating to Commercial operations tasks. JOB SPECIFIC RESPONSIBILITIES: The post holder will: 1. Receipt of orders via post, fax, phone, EDI and email. Check customer accounts where necessary. Process all orders through Tropos system ensuring all prices, discounts and quantities adhere to relevant price lists/customers terms. 2. Send customer overdue letters and statements when necessary. 3. Apply to external companies for credit references for new customers. Set up new customer accounts on Tropos system and process relevant paperwork. 4. For new accounts and current accounts ensuring all schedule 5, GDP and WDA licences are available and checked in the Eudra/ MHRA website for legitimacy. Annual GDP reviews will be collated. Keeping the licencing file update to in preparation for any audits. 5. Liaise with Commercial Support Manager regarding availability dates for backorders. Regularly check stock status for product availability, expiry dates etc. Prompt invoicing of backorders when products become available. 6. Carry out end of day sales routine, which involves invoicing, processing daily sales reports, backorders report, despatch notes report and distribution of these to relevant personnel. 7. Collating the cash receipts, from the bank and into cash books, ensuring each payment is recorded correctly. Creating the weekly cashflow. 8. Manage debtor’s collection for all outstanding invoices. Ensuring accounts are kept up to date. 9. Process monthly sales reports, by customer, by products and by country and by commercial generic targets. Review the sales information and discuss any issues with sales with the Head of Commercial Operations and formulate a strategy to respond to customer needs. 10. Processing Iqvia monthly reports, for all direct pharmacies sales by product and list prices in the correct format. Ensuring these are available in time for submission to IMS. 11. Report the monthly rebates in the appropriate spreadsheets, to ensure the information is available for the monthly financial accounts. 12. Keep monthly sales report by product and average selling price up to date on monthly basis. Ensuring accurate calculations of the rebates. Review average selling prices are in line with budget. 13. Ensure customer invoices are sorted and posted on time. 14. Maintenance of price list files on Tropos to ensure prices are updated on time and accurately, to ensure the invoicing for all products are correct. 15. Maintenance of EDI customer system, listing the pricing and EAN codes, where necessary for changes in product details and adding new products. 16. Dealing with customer service queries with regards to deliveries, damages, shortages, price queries, account queries, short-dated stock/returns. Submit credit claims to distribution companies when necessary. Review the customer’s queries and report any reoccurring queries to try to improve our customer service levels. 17. Dealing with the transport companies, ensuring all orders are delivered on time and ensuring the wholesalers have enough stock for the demand. 18. Creating adhoc sales reports for the marketing and sales teams. 19. Arrange the samples for the Metabolics products to be despatched and delivered to the customer and keeping the traceability of the stock. 20. Complete the goods in book, for all stock delivered every month. 21. Complete the month end process for the Stock valuation. 22. Assist with new commercial projects, on an ongoing basis. QUALIFICATIONS
Product Leader
Business Unit: Almac Clinical Services Hours of work: 35 hours per week The role Almac Clinical Services provides services to over 600 Pharmaceutical and Biotech companies worldwide including 18 of the top 20 global pharma companies. We are recognised as one of the leading, multi-faceted, global solution providers within the niche and complex market of clinical trial supply. Our excellence in clinical supply chain management has been built over 25 years, providing our clients with the best and most comprehensive service offerings in the marketplace. In support of our ongoing Clinical Services Supply Chain Management business objectives, we are seeking an experienced Product Leader to lead on the development and delivery of a new end-to-end customised digital platform (Prime) which will be integral in managing the supply of clinical trials materials to support clinical trials globally. Planning and managing clinical trials is an increasingly complex task and unlike standard supply chains, there are many unpredictable factors. This role presents a fantastic opportunity to get involved with an exciting, challenging new project which will contribute to the achievement of our business goals, and contribute to improving patient health globally. The successful role holder will be responsible for defining the product vision and creating and managing product roadmaps to ensure timely and functional releases. They will oversee the product development from initial concept, through definition of MVS to launch, enhancement and maintenance of the platform. They will work closely with the PMO to balance scope, budget and time, collaborating with various internal engineering/development teams to ensure alignment. They will lead multi-disciplinary teams as necessary, engaging with many stakeholders, including executive and senior management teams members. What we are looking for.. To apply for this role, you should hold a Degree or equivalent qualification in a business administration, engineering, computer science or similar discipline. You should also have significant experience of performing or leading the delivery for a software product or a complex digital system with a wide range of functionality, along with working knowledge of software development in a GXP or other regulated environment. (Please see job description and person specification for further information on essential and criteria) Reward In addition to the excellent salary and management benefits package on offer, the successful candidate will also be afforded numerous personal and professional development opportunities which come from working as part of a busy team within a rapidly growing organisation, operating within an exciting, challenging industry. To apply: Please upload a copy of your CV to the online portal, ensuring you detail how you meet the requirements for the role. Please upload your CV in PDF format where possible. Closing date for receipt of applications: 5pm, Friday 17th May 2024
