No deviation Jobs in Singapore

We are seeking an experienced CMMS Engineer to support the deployment of a Computerized Maintenance Management System (CMMS) at our client's site. · ...

No deviation is looking for individuals who are excited to contribute to impactful projects and drive innovation. · ...

The QC Raw Material Analyst performs routine and non-routine analyses on incoming and raw materials to ensure compliance with approved specifications and quality standards. · ...

The Incoming Quality Assurance (IQA) Support role provides administrative and operational support to the Incoming Quality Assurance team within the Lot Disposition function of Quality Assurance. · ...

Wearelookingforindividualswhoreadytcontribute to impactful projects and drive innovation. · We support process engineers with product characterization , metrology , and continuous improvement activities in a regulated biotech or medical device setting . · Thisroleassistsprocessen ...

We are looking for individuals who are excited to contribute to impactful projects and drive innovation.The QC Analytical Analyst is responsible for performing analytical testing to support product release, stability, and manufacturing operations in a regulated environment. · ...

The Project CQV Engineer is responsible for planning and executing commissioning and qualification activities for GMP manufacturing and laboratory equipment within a project environment. · ...

The Lead HVAC & Cleanroom Engineer is responsible for designing and implementing HVAC and cleanroom systems across manufacturing buildings. · ...

The Material Handler role provides hands-on operational support to manufacturing activities within cleanroom environments. · ...

No Deviation busca un experto en validación para apoyar la vida útil de sistemas automatizados principalmente DeltaV dentro de un ambiente farmacéutico regulado. · ...

We are seeking a dedicated CQ Manager Drug Linker to lead the commissioning and qualification of a specialized chemical synthesis and conjugation facility. · Lead CQV activities for chemical synthesis equipment, conjugation reactors, chromatography systems, solvent handling syste ...

We are looking for individuals who are excited to contribute to impactful projects and drive innovation. · The MSAT Engineer provides technical MSAT support for routine upstream manufacturing operations, with a focus on cell culture harvest and clarification via centrifugation. · ...

We are seeking an experienced Project Scheduler / Planner to support an ongoing large-scale manufacturing expansion project. · ...

The role is responsible for supporting Quality Assurance operations within a multi-product cGxP contract manufacturing environment. · Manage the GMP document lifecycle within the Documentation Management System (DMS), including archiving and handling of inactive records · Maintai ...

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 ...

No deviation is looking for an Operations Engineer to support project and start-up phase activities for Media and Buffer Preparation systems within a GMP biologics manufacturing environment. · ...

We are seeking a knowledgeable CQ Manager QC Laboratory · to lead commissioning and qualification of analytical laboratories that support critical testing and quality assurance operations. · ...

We are seeking a skilled Validation Engineer with 3 to 5 years of hands-on experience in aseptic operations and fill–finish environments. · Plan, execute, and document Aseptic Process Simulations (APS/media fills) in compliance with regulatory requirements. · ...

We are looking for a Sustainability & Permitting Manager to develop and execute projects' sustainability strategy in alignment with corporate ESG goals and regulatory requirements. · Degree in Sustainability, Environmental Engineering, or related field. · 5-10 years experience in ...

+We are seeking a skilled Validation Engineer with 3 to 5 years of hands-on experience in aseptic operations and fill–finish environments. · +Degree in Engineering, Life Sciences, Pharmaceutical Sciences or related field. · 3 to 5 years of experience in pharmaceutical aseptic ope ...