Sample Coordinator

1 week ago

Singapore No deviation Full time

Description About No deviation At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation. We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally. Position Overview Responsible for performing microbiological testing, environmental monitoring, and related quality control activities in compliance with USP, GMP, and regulatory standards. The role supports manufacturing operations, ensures the microbiological integrity of products and facilities, and contributes to continuous improvement, validation, and compliance efforts. This position also assists in investigations, training, and audit readiness to maintain a high standard of laboratory performance and product quality. Key Responsibilities Perform and interpret microbiological and microbial limits testing for raw materials, finished products, and stability samples in accordance with USP and GMP guidelines. Conduct environmental and water monitoring to ensure aseptic conditions and facility compliance. Support and lead investigations, CAPA, and change control processes to maintain quality standards. Develop, review, and implement microbiology-related SOPs, test methods, and validation protocols. Train analysts and serve as a backup to the Microbiology Team Leader when required. Coordinate third-party testing, manage documentation (e.g., CoAs, logs, records), and ensure proper maintenance of laboratory equipment and supplies. Participate in audits, continuous improvement initiatives, and enforce safety and sustainability practices within the laboratory. Required Qualifications Experience of working within a GMP environment is highly desirable Customer-focused and solutions-driven. Excellent written and verbal communication skills. Strong IT skills, including proficiency in Microsoft Office. Self-motivated, with a flexible and proactive approach. High attention to detail and strong observational skills. Why join us? Generous Leave Policy. Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs. Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company. Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated. Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career. How to apply Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team Please submit your resume, outlining your qualifications and experience relevant to the role, here. #J-18808-Ljbffr Industry Other Category Management & Operations Sub Category Project & Process Management

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