QC / QA MICROBIOLOGIST | PHARMACOVIGILANCE & DRUG SAFETY | MEDICAL AFFAIRS

Company Description Arundathi Institute of Medical Sciences & Hospital is a healthcare institution dedicated to delivering comprehensive medical services and advancing clinical excellence. The organization focuses on providing patient-centered care supported by modern facilities and evidence-based practices. It encourages collaboration among multidisciplinary teams to improve health outcomes and support continuous learning. Professionals joining the institute can expect an environment that values ethical standards, clinical safety, and ongoing professional development.
Role Description This is a full-time, on-site role based in Dublin for a QC / QA Microbiologist with responsibilities in Pharmacovigilance & Drug Safety and Medical Affairs. The role involves performing microbiological quality control testing, supporting quality assurance activities, and contributing to quality management systems to ensure compliance with regulatory and internal standards. Daily tasks include reviewing batch records, monitoring GMP practices, assisting with quality audits, and documenting investigations and corrective actions. In pharmacovigilance and drug safety, the role includes collecting, assessing, and reporting safety data, supporting risk management activities, and collaborating with clinical and medical teams on safety-related documentation. The position also supports medical affairs by contributing to scientific materials, responding to medical information requests, and coordinating with cross-functional teams to maintain accurate and compliant medical communications.
Qualifications

• Candidates should possess strong Quality Control skills, including microbiological testing, data analysis, and documentation of laboratory findings.
• Candidates should possess Quality Assurance expertise, including SOP adherence, deviation handling, and implementation of corrective and preventive actions.
• Candidates should possess Quality Management capabilities, including participation in continuous improvement initiatives and support of quality system maintenance.
• Candidates should possess knowledge of Good Manufacturing Practice (GMP), including regulatory compliance, cleanroom and aseptic techniques, and validation processes.
• Candidates should possess Quality Auditing skills, including preparation for internal and external audits, conducting inspections, and compiling audit reports.
• Relevant experience in pharmacovigilance, drug safety, or medical affairs, including safety data handling and medical documentation, is highly beneficial.
• Bachelor’s or Master’s degree in Microbiology, Pharmacy, Life Sciences, or a related discipline is preferred.
• Strong analytical and problem-solving abilities, attention to detail, and proficiency in scientific and technical writing are desirable.
• Effective communication skills, ability to work collaboratively in multidisciplinary teams, and adaptability to a regulated healthcare environment are important.