QC Microbiology Specialist
1 day ago
QC Associate Microbiology Specialist.We are actively recruiting for a QC Microbiology Specialist to provide technical support to the QC Microbiology Lab & operations to ensure the continued manufacture and supply of quality pharmaceutical products within a leading Pharmaceutical Manufacturing multinational.Key Responsibilities: * Development and execution of Microbiology test methods and project validations. * Troubleshooting of issues which arise during the execution of validation studies and routine tests. * Development of training modules. * Microbiology Support to Site Investigations * Driving Continuous Improvement initiatives, including lean lab initiatives, method optimization/redevelopment. * Authoring and managing change controls, procedures, test methods and deviations. * Result authorization for microbiological samples to support batch release. * LIMS System updates * Assessing compendial and quality manual updates pertaining to the Microbiology Lab & environmental control. * Supporting lab stock management and financial control as required. * Supporting the environmental control program by trend analysis and implementation of appropriate corrective and preventative measures.Qualifications and Experience * Bachelor’s Degree or higher preferred; ideally in Microbiology or a closely related discipline. * Demonstrated change management skills (CEM) with continuous improvement. * Strong knowledge in execution, validation and development of microbiology related test methods i.e. Bioburden, Endotoxin and Sterility testing. * At least 5 years’ experience in the Microbiology Pharmaceutical industry or a similar operating environment * Strong Planning and Organising skills * In-depth knowledge of the veterinary market * In depth knowledge of pharmacovigilance legislation and guidelines * Wide-ranging and sound communication skillsFor more information and a full job spec contact Nicola on (phone number removed) or email your CV in the strictest confidence to (email address removed)
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QC Associate Microbiology Specialist
2 weeks ago
Carlow, Ireland Life Science Consultants (LSC) Full timeLSC have a great contract opportunity for a QC Associate Microbiology Specialist to join a global Biopharmaceutical company in Carlow. This is a state-of-the-art vaccines and biologics manufacturing facility currently producing many products in various therapeutic areas including: oncology, autoimmunity, pneumonia, and infectious disease. If you have 5+...
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QC Associate Microbiology Specialist
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Carlow, Ireland Life Science Recruitment Ltd Full timeQC Associate Microbiology Specialist RK22609 Contract 11 months Carlow Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. This role holds more senior...
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Carlow, Ireland Life Science Recruitment Ltd Full timeQA Validation Specialist (New Product Introduction) 11 month contract On site Carlow AMC22404 I am on the lookout for a QA Specialist for Validation and NPI for a rapidly expanding biotechnology manufacturer in Carlow. You will be an essential member of the Technical transfer and Validation team responsible for managing development and manufacturer of...
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▷ Apply Now: QA Specialist
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Carlow, Ireland Life Science Consultants (LSC) Full timeLSC have a great contract opportunity for a QA Specialist to join a global Biopharmaceutical company in Carlow. This is a state-of-the-art vaccines and biologics manufacturing facility currently producing many products in various therapeutic areas including: oncology, autoimmunity, pneumonia, and infectious disease. If you have 3 years of experience working...
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▷ Immediate Start! QA Validation Specialist
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Carlow, Ireland Recruitment by Aphex Group Full timeThis is an 11-month contract and is a 2-shift cycle. This is an onsite role. Purpose Responsible for ensuring that the process for the manufacture of drug products at our Carlow site complies with cGMP and the associated regulatory requirements. Responsible for reviewing and approving GMP documentation to support corporate compliance/regulatory expectations...