QC Analyst Micro
2 weeks ago
Duties & Responsibilities Provide Microbiological support to the site Develop, maintain and update microbiological methods, specifications and SOP's in compliance with quality and regulatory requirements to allow the execution of the analysis in a GMP environment. This will include trending data, monitoring Out of Specifications and participating in laboratory investigations. Testing of In-process, Drug Substance and Drug Product Batches manufactured. Co-ordinating all site Utilities testing-environmental monitoring and water testing programmes. Lead all environmental investigations, root cause analysis, and report close out. Lead monthly environmental review meetings and present all relevant trends to a cross departmental team. Provide annual contamination control training to all personnel. Provide aseptic technique training to all new employees. Validation of microbiological methods e.g. bioburden and endotoxin. Support autoclave validation programme. Stability testing of Drug Substance and Drug Product Batches Participate in Quality and Safety regulatory audits. Support raw material testing when required for GMP manufacture Input into the identification of equipment requirements and work with vendors to ensure execution of all deliverables, including equipment qualification and validation. Troubleshooting equipment and techniques within the Analytical team. Participation in other projects/duties as defined by the Quality Director POSITION SPECIFICATION Qualifications, Experience, Skills, Knowledge and Attributes Third level degree in a life Science discipline 2-5 years' experience in a microbiology role with relevant experience in environmental monitoring and utilities testing, bioburden testing and endotoxin testing. Experience in validation of microbiological methods also required. Strong analytical and technical skills Ability to learn quickly and take responsibility for tasks/projects. Highly organised and structured approach to task completion. Strong time management awareness and the ability to drive projects forward. Excellent verbal and written communication skills, including ability to present work in clear, concise reports or presentations. Full time Legal statement as below This job advert indicates the general nature and level of work expected. It is not designed to cover or contain a comprehensive listing of activities or responsibilities required of the incumbent. Incumbent may be asked to perform other duties as required. Additional position specific requirements/responsibilities are contained in approved training curricula. Visa status re must be eligible to work and live in Ireland as below Colleague must be legally eligible to live and work in Ireland. Summary of our Benefits In addition, to being part the world leading animal health company focused on the needs of those who raise and care for animals we offer a range of benefits such as competitive salary, bonus, 25.5 days holiday per annum plus public holidays, a defined contributory pension plan, private medical insurance for you and your family and empowered flexible working, to name a few. Please note that the benefits outlined are subject to change based on organization decision. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process click the Apply button below to Login/Register.
-
Micro Lab Manager
3 weeks ago
Sligo, Co. Sligo, Ireland Next Generation Recruitment Full timeJob Title: Micro Lab Manager Location - Sligo A rapidly expanding biopharmaceutical manufacturer are at a pivotal time in our growth. They are in the late stages of developing and commercialising a new portfolio of innovative biopharmaceutical products. As they continue to expand, they are looking for a dedicated Microbiology Manager to lead their Micro...
-
QC Analyst
3 weeks ago
Carlow Town, Co. Carlow, Ireland Next Generation Recruitment Full timeThis is a contract based role for an Associate Quality Control Specialist as part of the Incoming Quality team reporting to the Quality Control Manager. You will support all aspects of New Material Introduction process and associated supplier changes ensuring effective interaction with other departments/global teams on matters related to new material...
-
GMT Analytical Scientist
3 weeks ago
Birr, Co. Offaly, Ireland Zoetis EUAFME Full timeThe GMT Analytical Scientist role encompasses 4 levels (LI - L4) based on the experience/knowledge of the analyst and the complexity of the role being performed. This role, within Global Manufacturing Technologies - Analytical (GMT-A), is responsible for supporting the provision of analytical technical services. This role supports GMT on projects such as...
-
Sterility Assurance Coordinator
1 month ago
Sligo, Co. Sligo, Ireland FRS Recruitment Full timeSterility Assurance Coordinator Biotech Scale-Up Join a leading biotech company in an exciting growth phase, working on the forefront of microbiology and cleanroom management currently seeking a Sterility Assurance Coordinator to lead key projects Key Responsibilities: Lead and manage cleanroom upgrades from Grade D to Grade A. Develop and implement action...