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Job Description
full-time
Our client, a leading pharmaceutical company, is actively seeking a meticulous and experienced Pharmaceutical Quality Assurance Manager to ensure compliance with stringent regulatory standards. This role is fully remote, providing a unique opportunity to contribute to global health initiatives from your home office. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS) to meet international regulatory requirements (e.g., GMP, ICH, FDA). Key responsibilities include overseeing internal and external audits, managing deviations and CAPAs (Corrective and Preventive Actions), reviewing batch records, and ensuring the quality of all pharmaceutical products throughout their lifecycle. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, quality control principles, and regulatory affairs. Excellent analytical skills, meticulous attention to detail, and exceptional written and verbal communication abilities are crucial. You will lead and mentor a team of QA professionals, fostering a culture of quality and continuous improvement. This position requires a proactive approach to identifying and mitigating quality risks. Collaboration with cross-functional teams, including R&D, manufacturing, and regulatory affairs, is essential. The successful applicant will demonstrate leadership in quality assurance strategy and execution. Experience with validation processes, change control, and supplier quality management is vital. This is an exceptional opportunity to make a significant impact on patient safety and product quality within a dynamic and growing pharmaceutical organization. We are looking for a dedicated professional who is passionate about upholding the highest standards of quality in the pharmaceutical industry. The role involves staying current with evolving regulatory landscapes and implementing best practices. A deep understanding of pharmacovigilance and product complaint handling is also required. This is a critical role that demands integrity, expertise, and a commitment to excellence in pharmaceutical quality.
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