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A pharmaceutical solutions provider in Singapore is seeking a CQ Manager Drug Linker to oversee the commissioning and qualification of chemical synthesis equipment. Candidates should have over 10 years of CQV experience in relevant environments and a degree in chemical engineering or chemistry. This role ensures compliance with GMP standards and requires coordination with multiple teams. The company offers benefits like generous leave, health coverage, and professional development opportunities.
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.
We are seeking a dedicated CQ Manager Drug Linker to lead the commissioning and qualification of a specialized chemical synthesis and conjugation facility. This role is critical in ensuring that all systems used in linker synthesis and conjugation processes comply with GMP standards and regulatory expectations. You will oversee complex chemical and bioconjugation equipment, coordinate with EHS and Engineering teams on containment and safety requirements, and ensure seamless integration with downstream processes. This is a highly visible role where your expertise ensures safe, compliant, and efficient manufacturing of high-potency drug substances.
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.