List of R&D and Science job
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- Senior Materials Analyst –Pharma Our clients, a Mulit-national Pharmaceutical firm in Dublin 24, are looking to recruit an experienced Materials Analyst to work as part of their Supply Chain team. The role: The Planner is responsible for ensuring that the planning cycle is adhered to on a pre-determined basis. This will include: Generate Sales & Operations plan (S&OP) for each Stock Keeping Un ...
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- Our client a leading animal health company is currently seeking a Site Microbiologist (Sterility Assurance Expert) to join their organisation in the West of Ireland. Role/Opportunity: Provide microbiological support to the site ensuring facility and process sterility programme compliance to in-house, corporate and regulatory requirements. Provide microbiology related technical support for manufact ...
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- Our client a leading animal health company is currently seeking a Quality Manager to join the organisation in the West of Ireland. Role/Opportunity: To manage the Quality Department (Quality Control and Quality Assurance) and in doing so ensure the manufacture of quality product in accordance with existing product licences and with GMP. To provide direction and leadership for the site in meeting t ...
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- Our client, a medical device company, is currently recruiting Financial Analyst to join its Cork based team on a 12 month contract Role/Opportunity Responsibility for Intercompany pricing within the Ireland Finance group Liaise with all relevant Business Partners eg WW Finance, Customer Services, Marketing, WW Selling Entities in relation to queries/issues regarding Intercompany Pricing. Support ...
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- Our client, a pharmaceutical company, is currently recruiting a QC Manager to join its team in Belgium in a permanent role Role/Opportunity Manage a team of laboratory supervisors/coordinators Motivate employees toward operational excellence and in respect of Good Manufacturing Practices Analytical troubleshooting and problem solving for laboratory activities Guarantee and defend laborator ...
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- Berkley Pharmaceutical & Life Sciences is working with a dynamic leading healthcare provider. As a result, we are now recruiting a Regulatory Affairs Specialist for a permanent position based in Cork Assist the Regulatory Affairs Manager in managing Adverse Drug Event reporting, monitoring of multiple global contract manufacturer sites, analyse and trend safety data, generate metrics and prepare ...
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- Our Client pharmaceutical company is currently recruiting a QA specialist to join its team in the Netherlands in a permanent role. Role/Opportunity Compliance review and approval of all batch documentation related to disposition of clinical product (unlabeled product and incoming product like filters, comparators, co-medication etc.) Approval of class 1 and class 2 non-conformances (NC) and corr ...
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- Our client is a leading pharmaceutical company based in the North of Ireland is currently seeking a Product Quality Specialist to join the organisation. Role/Opportunity: The role of the Product Quality Specialist is to manage the day to day batch review activities in line with customer and business demands. A major component of the role will be to provide support to the company QP’s in fulfilling ...
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- Our client, a pharmaceutical company, is currently recruiting a QP to join its team in the Netherlands in a permanent role Role/Opportunity Responsible for the overall release process and ensuring quality within the IPT. Ensure GMP requirements, product-specific laws and regulations are adhered to Contribute to the quality strategy within the company by advising on compliance and quality related ...
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- MEMJET IS THE GLOBAL LEADER IN COLOR PRINTING TECHNOLOGIES THAT PROVIDE REMARKABLE SPEEDS AND AFFORDABILITY. Memjet-powered colour printers are at least twice as fast but only half the total cost of ownership of traditional printers, on average. We supply brand name customers across the printing industry the same way leading-edge chip makers supply OEM partners across the cellphone, smartphone and ...
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- A Senior Clinical Research Associate is required for a leading CRO based in Dublin. Within this position you will be responsible for: • Performing site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. • Providing monitoring visits and site management for a variety of protocols, sites and therapeutic areas. • Managing sp ...
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- PROCESS CHEMICAL ENGINEER Pharma Company in the Mid West looking for a Process Chemical Engineer to be responsible for process safety management, operational qualification of projects and changes, technology transfer, production support and process optimisation. Responsibilities include: Designing, installing and commissioning new production equipment, monitoring modifications and upgrades, and t ...
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- Biomedical Principle Scientist · 3 year contract · Cork based · Forefront of medical device research technology We have a fantastic opportunity for a Biomedical Principle Research Scientist/Engineer for a cutting edge opportunity with a medical device multinational. The successful candidate will be responsible for performing research to advance the understanding of medical applications of sensin ...
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- Microbiology Team Leader - Medical Device · Permanent role · Cork based Duties and Responsibilities: · Manage day to day activities of the Micro(QA) Team (Recruitment, training, reviews and development of Team) · Assist in managing regulatory compliance program · To review and develop procedures for all microbial assurance activities · Ensure compliance with documented quality system, develop qu ...
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- Our client is a leading pharmaceutical company based in the North of Ireland is currently seeking a Quality Compliance Manager to join the organisation. Role/Opportunity: The role of the Quality Compliance Manager is to ensure that all requirements of the company’s QMS are managed on a day to day basis. This role will also be fundamental in driving continual improvement in line with customer expec ...
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- Our client, based in Ringaskiddy, requires a QC Analyst for a 6 month contract. Third Level Science Qualification and 4 years equivalent work experience gained in Pharmaceutical GMP regulated laboratory environment Analyse Raw Materials, In-Process Materials and Finished Products. To maintain all laboratory notebooks, records, chromatograms to an acceptable GLP standard. Entering and approving r ...
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- Our client, based in Ringaskiddy, requires a compliance specialist for a 6 month contract. · You will be working, in an FDA / IMB approved GMP manufacturing facility, ensuring compliance to new and established systems and global regulations and guidelines for a wide range of complex active pharmaceutical ingredients and drug substances. · Implementation and maintenance of all site Quality/Complia ...
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- Our client requires a Manufacturing Engineer to join its team on a permanent basis. Role requirements: Provide ongoing support to the manufacturing team Lead site continuous improvement initiatives Aid in the transfer of new products or processes to the new production or manufacturing facilities Develop and implement all necessary documentation Maintain and develop preventative maintenance and ...
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- Primary activities/responsibilities: * Supervision and leadership of personnel * Co-ordination of Laboratory resources * Training and Development of Laboratory personnel. * Delivery of area performance to meet or exceed functional unit goals. * Investigations (Lab LIRs / NOEs) * Development and co-ordination of Continuous Improvement Initiatives. * Contribute to site operational and strategic init ...
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- Technical Writer Our client requires a Senior Technical Writer for a role based in Limerick The contract will be of 12 months duration, with the work being paid hourly. Job Role and Responsibilities: l To provide support for the technical/validation documentation activities l Ensuring that all compliance issues and requirements of Company Validation/Quality Policies and Procedures are addres ...
