Jobs / Singapore / Astrazeneca Pharmaceuticals Lp
Manufacturing Specialist
Astrazeneca Pharmaceuticals Lp · 🌍 Singapore
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- Last confirmed live 1 day agoWhen a source last listed this job as open.
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Sponsor Radar — Astrazeneca Pharmaceuticals Lp
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About the role
Job Title: Manufacturing Specialist GCL D Introduction to role: Be part of history in the making. AstraZeneca is building its first biologics manufacturing campus in Singapore — a groundbreaking USD 1.5 billion investment that will serve as a global hub for innovation and excellence. This state-of-the-art facility will deliver end-to-end Antibody-Drug Conjugate (ADC) capabilities with different manufacturing units/buildings in one campus • Small molecule- chemical API production • Large molecule- monoclonal antibody manufacturing • Conjugation • Fill-and-finish operations, including sterile filling and lyophilization • Final secondary packaging The campus will be equipped with modern digital and automation infrastructure, enabling autonomous manufacturing powered by artificial intelligence. In addition, it will be designed for carbon neutrality, embedding sustainability into every aspect of operations and setting a new benchmark for environmentally responsible biologics' manufacturing. We are looking for passionate individuals with relevant experience who thrive in dynamic environments and bring a “make-it-happen” attitude. Joining us means contributing to a project that will not only transform AstraZeneca’s global supply chain but also advance life-changing medicines for patients everywhere. If you’re ready to shape the future of biologics and be part of a once-in-a-generation project, we want you on our team. We are recruiting Manufacturing specialist for all the five different manufacturing units Job Title: Manufacturing Specialist Introduction to role Are you passionate about transforming innovative manufacturing technologies into reliable medicines for patients? As a Manufacturing Specialist, you will play a key role in bringing our pioneering Singapore biological campus from project execution through qualification and into commercial operations. Working within one of our manufacturing areas, API manufacturing, mAb Drug Substance, Conjugation, Aseptic Filling, or Secondary Packaging—you will provide technical expertise and shopfloor leadership to ensure safe, compliant and efficient manufacturing. You will work closely with Engineering, Quality, MSAT, Validation, Supply Chain and EHS to support equipment start-up, process optimization, trouble-shooting and continuous improvement while building operational excellence from Day One. 3. Accountabilities • Equipment Ownership and Lifecycle: Serve as the technical owner for assigned manufacturing unit, ensuring equipment is installed, qualified, and maintained in a state of readiness for GMP operations throughout its lifecycle. • Start-up and Qualification Leadership: Plan and support FAT, SAT, commissioning, qualification, validation, and handover activities; prepare, review, and implement protocols and technical - documentation to site standards and GMP requirements. • Shopfloor Technical Support: Act as primary contact for equipment-related issues; provide rapid trouble-shooting, performance monitoring, and breakdown investigations to protect safety, quality, and schedule. • Operational Readiness and GMP Execution: Drive SOP development, batch record inputs, equipment setup, line readiness, material flow reviews, and operator training; ensure execution aligns with validated states and production plans. • Digital and Data Integrity: Ensure alignment between DCS recipes and MES - master batch records, and maintain complete, compliant documentation that supports audit readiness and knowledge transfer. • Safety, Quality, and Regulatory Oversight: Apply a safety-first mind-set; participate in risk assessments and hazard reviews; support deviations, CAPAs, change controls, and corrective actions tied to equipment and operations. • Cross - functional Collaboration: