Job Description

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Your Role

The Associate Scientist II – Biosafety Testing is responsible to perform a wide variety of routine tasks to support GMP operations and primarily focusses on Virology and Cell Culture work related to Biosafety Testing. Responsibilities include performing Biosafety assays in Virology and Cell Culture laboratories which required to characterize product, maintenance of cell culture detector cell lines, preparing and qualifying of reagents, monitoring stock levels, and conducting general equipment maintenance to sustain seamless workflow and optimal performance of laboratory equipment.

The Associate Scientist II may require to provide training and / or mentoring junior members of lab personnel. The ability to maintain effective working relationships with Scientists, Lab Scientists, support services, and laboratory personnel will be critical for success in this role. Training will be provided upon onboarding to ensure you are train to qualify level before performing any routine testing.

What You Do

• Works within the Virology, and Cell Culture laboratories following Standard Operating Procedures and compliance regulations.
• Adherence to Standard Operating Procedures (SOPs) and Compliance Regulations: Ensure all work is carried out according to established protocols and regulatory standards.
• LearningManagementSystem: EnsurezerooverdueLMSrecords,timely complete training required to perform the assay or task.
• TimelyCompletionofStudiesandRecordKeeping:Completeroutineand custom studies on time, maintaining accurate records that meet scientific and Good Manufacturing Practice (GMP) standards.
• Assays transfer: Perform assays transfer following relevant protocols as required.
• Document Control: Maintain SOPs, laboratory books, and forms, ensuring outdated versions are removed promptly. Review and improve working documents through document control processes.
• StockControlandProcurement:Managestocklevels,orderconsumables,and handle procurement through designated systems.
• Laboratory Maintenance: Conduct housekeeping, equipment checks, and environmental and personnel monitoring to ensure compliance and safety.
• Health and Safety: Maintain a clean, tidy, and safe work environment, adhering to health and safety policies and procedures.
• Training and Mentoring: May require to train and mentor newer or junior members of the lab personnel.
• QualityAudits andRegulatoryCompliance: Participateininternalqualityaudits and regulatory audits as required.
• Audit Readiness: Maintain a constant state of readiness for audits across all laboratory areas.
• ProtocolandSOPDevelopment:Authorlaboratoryprotocols,SOPs,and workbooks for projects.
• Peer Review and Data Management: Conduct peer reviews of raw data records and ensure accurate data management practices on a timely manner.
• Deviation/Discrepancies:RaiseandprogressdeviationandCorrectiveand Preventive Action (CAPA) records promptly.
• Continuous Improvement: Proactively identify and implement improvements to laboratory processes and procedures to enhance efficiency and reduce waste.
• SiteorGlobalInitiatives:participateinsiteorglobalinitiatives

The above list of job functions is not exclusive or exhaustive and the post holder will be required to undertake such tasks as may reasonably be expected within the scope of the post. Job descriptions will be regularly reviewed to ensure they are an accurate representation of the post.

Who You Are

• MinimumDegreeinBiologicalSciences orhigherqualification in relevant scientific subject
• 3plusyearsofworkingexperiencein biologics orbiopharmaceuticalindustry
• 3plusyearsofworkingexperienceinaregulatedenvironment (GMPor equivalent)
• 2plusyears of working experience in specific area of expertise (molecular biology, virology, microbiology/mycoplasma) with demonstrated ability to trouble-shoot
• Quality mindset and good understanding of GMP
• Demonstratableexperienceinimplementingprojects toset-up/improvelab processes/systems
• GoodoralandwrittencommunicationskillsinEnglish
• Capability on problem solving and planning skills
• ERPexperienceisanasset(OracleSAP/LIMS/Trackwise)
• ProficientinMicrosoftprograms(Word,Excel,PowerPoint,etc)
• AdherestosafetySOPsandfollowssafeworkpractices
• Always ensures a safe and healthy work environment
• Teamplayer,proactiveandwillingtotakeownership
• FlexibilitytoworkovertimeorshiftstocoverBusinessspikes/needswhen necessary.
• Working on Public Holiday (except weekends) for on-going studies.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!