The position you are looking for is no longer available, but here are some similar jobs that might interest you
… validation of the Biotech facility initial qualification activities for lab and/or manufacturing equipment. Key Responsibilities. Implement qualification programme for initial qualification of lab and/or manufacturing equipment. Document preparation for. Equipment Qualification Assessments. IQs, OQs, … more
… activities for cleaning validation on site. Key Duties. Taking cleaning validation samples alongside Upstream/Downstream processing. Work closely with manufacturing to ensure the CIP/SIP are operating to schedule. Technical writing, deviation/change control writing. Generate, review, approval of protocols. Maintain … more
… activities for cleaning validation on site. Key Duties. Taking cleaning validation samples alongside Upstream/Downstream processing. Work closely with manufacturing to ensure the CIP/SIP are operating to schedule. Technical writing, deviation/change control writing. Generate, review, approval of protocols. Maintain …
Apple Recruitment are delighted to be recruiting for an AREA MANAGER, reporting to the business unit manager, sought for a leading automotive manufacturing company based on the outskirts of Lisburn. This role covers a evening/night shift. 4 evenings per week, Mon-Thurs 4pm-2am. Salary offered is €37 …
6 month day rate contract. Leading award winning consultancy. Dublin based primarily Our client is a leading Irish consultancy with international offices and customers. They have won several top awards by their various vendor partners in the last few years and have gone from strength to strength …
… successful candidate will be a point of contact for products or functional areas within the company, including Supply Chain, Information Systems, Manufacturing, Process Development, Validation, Engineering and Quality Control. Responsibilities. Provide overall quality direction and oversight for key functional … more
Senior Associate QC- LIMS/ LMES/ CIMS/ Empower. A requirement has arisen for a Senior QC Associate responsible for LIMS/ LMES/ CIMS/ Empower support within a Dublin based pharmaceutical multinational. This role will be responsible for administration and technical support for the QC Enterprise … more
… control system definition, development and support to include coordinating the design and updating of PLC's, both hardware and software, used in our manufacturing and facilities process. The successful candidate will join a senior automation engineers in supporting a busy maintenance department within a 24 …
VMP, IQ's, OQ's, PQ's as required according to procedure QAP 030 and other related procedures. Our expectations. Level 8 degree in Engineering/Manufacturing/Quality with emphasis on Medical Devices/Biomedical. 2-3 yrs previous experience as Quality/Validation Engineer in Medical Device/Pharma Environment …
Automation Application Engineer. Euro Executive Recruitment has been retained to recruit an Automation Application Engineer for a leading manufacturing company based in Killarney, Co. Kerry. The ideal candidate will be qualified in a relevant engineering discipline and have excellent knowledge of automation …
QC Project Manager. Headcount Engineering is seeking a Project Manager QC for our client's biopharma facility in Dublin. The role will be a key role for the QC Department responsible for collating and planning for all QC projects and non-routine requests including transfers and NPI. They will also … more
Apple Recruitment are delighted to be recruiting for an AREA MANAGER, reporting to the business unit manager, sought for a leading automotive manufacturing company based on the outskirts of Lisburn. This role covers a evening/night shift. 4 evenings per week, Mon-Thurs 4pm-2am. Salary offered is €37 … more
Qualifications & Requirements. Third level degree in Engineering, Computer Science, or other technical discipline. 2-5 years of experience with Manufacturing Execution Systems such as Emerson Syncade, Werum PAS X and CSV in biotechnology/ pharmaceutical industry. Excellent communication skills (written … more
… role you will have. A Degree (or equivalent) in an engineering discipline is preferred. 5 Years' manufacturing experience gained in a similar role. Experience in the implementation of Lean Manufacturing initiatives. It would be desirable if candidates had any of the following. Masters degree (or equivalent … more
Shift Team Leader. Are you fed up working weekends? Fancy a Monday to Friday role. Are you a people manager who enjoys a good balance of factory floor versus the office. Working for a global brand you'll provide leadership for the day to day operations of within a highly regulated product … more
6 month day rate contract. Leading award winning consultancy. Dublin based primarily Our client is a leading Irish consultancy with international offices and customers. They have won several top awards by their various vendor partners in the last few years and have gone from strength to strength … more
Automation and Control Engineer. My client, an innovative, Irish company have an urgent requirement for an Automation and Control Engineer to join their expanding R&D team in Cork. This company specialises in using advanced, market-leading automation technology which is developed in-house. My … more
… looking for a Manufacturing Process Specialist for our multinational pharmaceutical client based in the Cork area on an initial 12-month contract with the potential to extend. Job Purpose. Reporting to the Purification Business Unit, this position is responsible for supporting manufacturing activities associated … more
Reporting to the Purification Business Unit, this position is responsible for supporting manufacturing activities associated with the purification and process support of monoclonal antibodies. Main duties and responsibilities. Technical Lead for purifcation process and providing process and equipment … more
… all product builders in your designated area of manufacturing. Write, revise and review Standard Operating Procedures related to all manufacturing practices where and when required. Make appropriate decisions on a daily basis, using the Manufacturing Manager (and/or the Director of QA/Reg and the … more
… world leading provider of products and services to the Life Science industry. We are focused on improving our customers' performance across the manufacturing enterprise through the application of innovative technologies. Zenith Technologies is embedded in numerous world leading Life Science multinational … more
… requirements. You will be required to comply with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions. Qualifications & Requirements. Relevant Computer … more
Candidate needs to Ideally Irish national or be willing to do a permanent move to Ireland with no rotation requirements. 3 to 5 years experience in QA/Cx management and capable of leading a team. Experince in learge scale construction projects required, ideally processor … more
Automation / Controls Engineering, or similar manufacturing support role required. Familiarity with Rockwell Automation Software family (RSLogix500, Control Logix 5000). Knowledge and understanding of GAMP5, experience preferred. Familiarity with batch manufacture, mixing, extrusion, plastic converting, and … more
… control system definition, development and support to include coordinating the design and updating of PLC's, both hardware and software, used in our manufacturing and facilities process. The successful candidate will join a senior automation engineers in supporting a busy maintenance department within a 24 … more
Our client, a large production/manufacturing based company in the Duncrue area of Belfast, are seeking to recruit a number of Production Operatives to work on ongoing temporary assignments, starting immediately. Hourly rate of pay will commence at €10.21ph, rising to €10.95ph after a successful training … more
Auditor experience. Reference Number: RTR88990c. Technical Manager, Quality, Hygiene, Lead, Director, Supervisor, Head of, Food, FMCG, Production, Manufacturing, ISO, Audit, Senior, Drinks, Quality Control, Manager, Auditor, Project, Quality Assurance, Systems, Process. To apply for this role or for to be … more
Auditor experience. Reference Number: RTR88990. Technical Manager, Quality, Hygiene, Lead, Director, Supervisor, Head of, Food, FMCG, Production, Manufacturing, ISO, Audit, Senior, Drinks, Quality Control, Manager, Auditor, Project, Quality Assurance, Systems, Process. To apply for this role or for to be … more
VMP, IQ's, OQ's, PQ's as required according to procedure QAP 030 and other related procedures. Our expectations. Level 8 degree in Engineering/Manufacturing/Quality with emphasis on Medical Devices/Biomedical. 2-3 yrs previous experience as Quality/Validation Engineer in Medical Device/Pharma Environment … more
MEDDEV 93/42/EEC. Deputising for the Management Representative in their absence. Provision of support to all departments to ensure that products manufactured meet customer requirements. Ensuring that product introductions & change controls are effectively managed in accordance with the requirements of … more
We currently require a Multi Skilled Operative for our client based in Belfast. Main Duties / Accountability. To receive lists of defects from Clerk of Works, site staff and from Supervisors. To maintain lists of completed and uncompleted works. To maintain lists of access records. To report back … more