APAC Logistics & Distribution Lead (Transformation Mandate)
OverviewWe are looking for a senior logistics leader to drive operational transformation across APAC distribution and 3PL operations.This role will lead a regional Distribution Centre (recently relocated to Johor Bahru) and stabilize, optimize, and modernize logistics processes across multiple markets. The mandate includes strengthening accountability, improving system integration, driving automation, and elevating 3PL governance standards.This is a high-impact leadership role requiring strong operational ownership, data-driven decision-making, and executive-level stakeholder engagement.
Key Responsibilities
Regional Distribution LeadershipLead and oversee APAC Distribution Centre operationsDrive operational stabilization following recent relocationEstablish clear governance, ownership structures, and performance KPIsEnsure service level performance across APAC Region
3PL & Contract GovernanceManage strategic relationships with regional 3PL providersDefine and enforce KPIs, SLAs, and performance review frameworksLead contract negotiations and cost optimization initiativesDrive accountability and corrective action when required
Operational Optimization & Systems IntegrationImprove WMS visibility, inventory control, and tracking processesStrengthen integration between warehouse systems and ERP (e.g., SAP)Identify automation opportunities to reduce manual interventionImplement data-driven dashboards and performance metrics
Financial & Strategic ManagementDevelop and manage regional logistics budgetsDrive cost control, ROI analysis, and efficiency improvementsBuild business cases for technology investments (e.g., tracking systems, GPS, automation)
Stakeholder LeadershipServe as the primary logistics representative in cross-functional discussionsPartner closely with Procurement, Manufacturing, and Commercial teamsProvide clear reporting and executive-level updatesFoster a culture of accountability and ownership within the DC and 3PL teams
Ideal Candidate Profile10–15+ years of experience in regional logistics, manufacturing supply chain, or 3PL operationsProven experience managing regional Distribution CentresStrong background in freight management and warehouse operationsDemonstrated experience turning around underperforming logistics operationsExperience integrating WMS with ERP systems (SAP preferred)Strong contract negotiation and vendor management capabilitiesExperience handling large, high-value or oversized industrial equipment preferredExposure to APAC markets with multi-country responsibilityBachelor’s degree required; MBA or advanced degree preferred
Leadership Attributes RequiredStrong sense of ownership and accountabilityCrisis management and problem-solving capabilityAbility to operate in complex, evolving environmentsData-driven and financially astuteClear communicator with executive presenceHands-on yet strategic mindset
We are partnering with a leading healthcare organization to appoint a forward-thinking Regional Medical Affairs Lead with a strong scientific foundation and a passion for innovation across cardiometabolic health.We are looking for someone commercially aware, digitally savvy, and excited to evolve with the changing healthcare landscape.Key RequirementsSolid medical/scientific background (MD, PharmD, PhD or equivalent preferred)Experience within Cardiometabolic therapy area strongly preferredDemonstrated experience in digital engagement strategies, including medical engagement with digital partnersExposure to Medical Excellence initiatives (metrics, processes, capability building) is highly attractiveExperience in Consumer Health is a strong plusComfortable operating regionally with cross-functional stakeholdersOpen to travel and excited by industry transformationIdeal ProfileStrong in scienceAgile, curious, and adaptableComfortable bridging medical, commercial, and digital conversationsPassionate about evolving Medical Affairs in a more data-driven, patient-centric directionThis is a fantastic opportunity for someone who wants to shape the future of Medical Affairs across APAC and work at the intersection of science, digital health, and innovation.If this sounds like you — or someone in your network — feel free to reach out confidentially to kay@barringtonjames.com
Job Description: Supply Chain Project Manager (Global)Location: SingaporeSalary: Competitive Market RateType: 12 Months contract role
Position SummaryThe Supply Chain Project Manager is responsible for driving the successful delivery of highly complex, strategic divestiture and transformation programs across all regions within Enterprise Markets (i.e. ISEA, WCE, EETI, MEA, LATAM). This role works across cross-functional teams through all phases of major programs, ensuring high levels of confidentiality, governance, and stakeholder alignment. The position plays a critical part in enabling operational continuity for warehousing and transportation networks, ensuring seamless transition plans and robust execution during periods of significant change.
Key Responsibilities1. Strategic Program & Project LeadershipLead end-to-end delivery of high-complexity projects, ensuring alignment with enterprise strategic objectives.Set project governance frameworks, milestones, KPIs, and reporting mechanisms to enable timely, on-budget delivery.Navigate high levels of uncertainty and interdependencies across multiple regions and functions.
2. Cross-Functional Leadership & Stakeholder ManagementLead large cross-functional teams across EM, including Supply Chain, Logistics, Operations, Finance, Legal, IT, and Commercial.Engage senior leaders to ensure buy-in, risk mitigation, and effective decision-making.Influence decisions across a complex matrix organization.
3. Warehousing & Transportation Transition PlanningSupport operational teams in ensuring smooth execution of operational separation and transition planning for warehouses, distribution centres, and transportation partnerships impacted by program.Drive optimization opportunities related to network flows, contract changes, service-level design, and cost structures.This will include project management to ensure necessary processes (UATs etc.) are completed on time without any business disruptions.
4. Business Continuity & Technology StandardizationDeploy supply chain continuity projects to ensure resilience across end-to-end networks.Lead the standardization of tools, platforms, and processes across multiple markets.
Qualifications & SkillsRequiredMaster’s degree and 6+ years of relevant supply chain or transformation experience.Proven track record leading complex, multi-market strategic programs in matrix organizations.Deep understanding of warehousing and transportation operations globally, including 3PL management, service-level agreements, and network design principles.Strong negotiation capability with external partners and senior internal stakeholders.Ability to lead through ambiguity and manage confidential information at senior levels.Demonstrated success in delivering projects on time, within scope, and within budget.Expertise in governance, PMO frameworks, risk management, and stakeholder communication.
Advantageous Skills:Experience with divestitures, carve-outs, or major organizational transformations.Certification in Project Management (PMP, Prince2) or Agile methodologies.Experience with major SC digital and planning platforms and process standardization initiatives.
We are seeking a highly skilled Senior Specialist – Design & Visualisation to support product development and commercial initiatives through high-quality technical and 3D visual content. This role plays a critical part in translating complex medical device designs into clear, accurate, and compelling visual assets for engineering, regulatory, and customer-facing applications.
Key Responsibilities
Product & Technical Visualisation
Develop high-quality 3D renderings, animations, and exploded views of medical devices and components.Translate CAD models into photorealistic visuals for product presentations, training, and marketing.Produce technical illustrations for Instructions for Use (IFU), regulatory submissions, and technical documentation.
Cross-Functional Collaboration
Partner with R&D, Engineering, Quality, Regulatory, and Marketing teams to ensure visual accuracy and compliance.Support new product development by creating visual assets that communicate design intent and functionality.Collaborate with commercial teams to create customer-facing visuals and sales tools.
Design & Brand Alignment
Ensure all visual outputs align with corporate branding and design standards.Maintain consistency across product visual assets and documentation.
Process Improvement
Establish best practices for visualization workflows and asset management.Evaluate and implement new tools and technologies to enhance visualization quality and efficiency.
Requirements
Education & Experience
Bachelor’s degree in Industrial Design, Product Design, Biomedical Engineering, Medical Illustration, or related field.5–8+ years of experience in design visualisation, product visualisation, or technical illustration.Prior experience in medical devices, life sciences, or regulated industries is highly preferred.
Technical Skills
Proficiency in CAD and visualization tools such as:SolidWorks, Creo, or Fusion 360KeyShot, Blender, 3ds Max, or Cinema 4DAdobe Creative Suite (Illustrator, Photoshop, After Effects)Strong understanding of product design workflows and engineering drawings.Experience creating visuals for regulatory or technical documentation is an advantage.Experience with medical illustration or scientific visualization.Familiarity with GMP and regulated product documentation requirements.Knowledge of human factors or usability design in healthcare products.
Job Title: Senior Process Engineer – Biologics (1 year contract - renewable)Location: SingaporeIndustry: Biopharmaceutical / Biotechnology Manufacturing
Job Overview
We are seeking a Process Engineer – Biologics to support the development, optimization, and scale-up of biologics manufacturing processes. The successful candidate will play a key role in ensuring robust, efficient, and compliant upstream and downstream manufacturing processes for biologic products.
This role will collaborate closely with manufacturing, quality, and technical teams to improve process performance, troubleshoot production issues, and support technology transfer activities.
Key Responsibilities
Process Development & OptimizationSupport development and optimization of upstream and downstream biologics manufacturing processes.Monitor and analyze process performance to identify opportunities for improvement in yield, efficiency, and cost.Conduct process characterization, validation, and scale-up activities.
Manufacturing SupportProvide technical support to GMP manufacturing operations.Troubleshoot process deviations, investigate root causes, and implement corrective actions.Support batch record review, deviation investigations, and CAPA implementation.
Technology TransferSupport process technology transfer from R&D to manufacturing or between manufacturing sites.Develop process documentation including process descriptions, SOPs, and technical reports.
Process Validation & ComplianceParticipate in process validation activities, including IQ/OQ/PQ.Ensure processes comply with GMP, regulatory, and quality requirements.Collaborate with Quality and Regulatory teams during audits and inspections.
Data Analysis & Continuous ImprovementAnalyze process data using statistical tools to drive continuous improvement initiatives.Support implementation of Lean, Six Sigma, or operational excellence programs.
RequirementsEducationBachelor’s or Master’s degree in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field.
Experience3–8 years of experience in biologics or biopharmaceutical manufacturing.Experience with cell culture, fermentation, purification, or biologics processing.Experience supporting GMP manufacturing environments.
Technical SkillsKnowledge of upstream (cell culture, bioreactors) or downstream processing (chromatography, filtration).Familiarity with process validation and technology transfer.Experience with data analysis and process optimization tools.
Preferred QualificationsExperience with monoclonal antibodies, vaccines, or recombinant proteins.Knowledge of regulatory guidelines (FDA, EMA, ICH).Experience with bioprocess equipment and automation systems.Key CompetenciesStrong problem-solving and analytical skillsExcellent cross-functional collaborationAbility to work in a fast-paced GMP manufacturing environmentStrong documentation and communication skills
I am currently looking for a Regional Demand Planning Manager for one of my Global Medical Devices MNC client. This position is responsible for the overall demand and supply of each BU through the execution of a robust S&OP process for Greater Asia.
He/She is responsible for business demand forecasts by business units and countries to align with financial and business objectives. This role requires strong partnerships with the Worldwide Business Planning team to support regional requirements and act as the main contact for demand forecast and supply needs. He/ She also plays an influential role in managing escalations and participates in Global and Regional Supply chain initiatives.
Job Title: Regional Demand Planning ManagerType: Full TimeLocation: SingaporeSalary: SGD 7,000 - SGD 10,500
Job DescriptionStrategic Planning and Implementation: support and implement planning strategies and plans based on the global and regional Supply Chain's overall strategy. This includes but is not limited to inventory strategy, replenish strategy, demand forecast strategy, master data management, logistics network, etc.Demand Management : Managing Greater Asia demand, ensuring market intelligence and business changes are captured, and establishing supply chain action plans in collaboration with business / Marketing.Data analysis and decision support: Use advanced supply chain data analysis tools to conduct in-depth analysis of supply chain performance, identify potential problems and opportunities, and provide data support for improvement and decision-making.Risk management: Early warning and management of potential supply chain risks through risk identification, assessment and monitoring to ensure the stability and continuity of the supply chain.Continuous improvement: Promote and implement continuous improvement and optimization of the supply chain, improve supply chain efficiency, and reduce operating costs by improving processes, introducing new technologies or optimizing strategies.Cost management: Comprehensive control and analysis of supply chain costs to ensure that the cost of the supply chain plan is controlled within industrial leading range. Through in-depth analysis of cost data, potential cost-saving opportunities are discovered, and corresponding measures can be taken.S&OP : Building collaborative relationships across functions, maintaining formal S&OP process with clear accountability, leading S&OP meetings to deliver clear business objectives and supporting the Planning Lead to drive the S&OP maturity roadmap.Cross-department collaboration and communication: Maintain good communication and collaboration with other departments (such as sales, marketing, finance, etc.) to ensure that supply chain plans are consistent with the needs and goals of other business departments.Project management and execution: Responsible for project management, including project plan formulation, progress control, quality management, etc. Ensure projects are completed on time and meet expected goals and quality requirements.
Principal FPGA Verification EngineerRole OverviewThe Principal FPGA Verification Engineer is responsible for leading the development and implementation of comprehensive verification and validation strategies for FPGA-based systems. This role focuses on ensuring the functionality, performance, integrity, and reliability of FPGA designs used in advanced digital imaging and microscopy products.
This is a dedicated verification role, not a design/development position. The engineer will primarily work at the sub-system and simulation level, ensuring strong design coverage before product integration and build. The role bridges hardware and firmware verification and supports early-stage product development.
The position is on-site and reports to the Verification Manager within the Research & Development team.
Key Responsibilities
🔹 Verification Strategy & DocumentationDevelop detailed verification plans, test strategies, and validation protocols.Define test cases to ensure functional and performance compliance.Establish measurable coverage criteria (targeting high coverage levels).Prepare structured verification reports with findings, analysis, and recommendations.Ensure all verification activities are properly documented in accordance with internal quality procedures.
🔹 FPGA Verification & ValidationPerform simulation-based verification of FPGA designs.Validate functional correctness, timing behavior, performance metrics, and power considerations.Ensure FPGA modules meet defined requirements before integration into the final product.Work closely with design engineers to ensure issues are identified and resolved early in the development cycle.
🔹 Issue Identification & DebuggingIdentify, document, and analyze design issues discovered during verification.Collaborate with development teams to support root cause analysis and resolution.Ensure traceability between requirements, test cases, and verification results.
🔹 Automated Testing DevelopmentDevelop and maintain automated test frameworks to improve efficiency and repeatability.Utilize scripting languages (e.g., Python) to support simulation and regression testing.Enhance verification coverage through structured automation approaches.
🔹 Continuous Improvement & Quality AssuranceContribute to improvements in verification methodology and processes.Support compliance with applicable industry standards.Ensure verification activities align with structured documentation and quality management systems.Promote best practices in FPGA verification across the development lifecycle.
Essential RequirementsBachelor’s or Master’s degree in Electrical Engineering, Computer Engineering, or related field.Strong understanding of FPGA technologies and digital electronics.Experience with FPGA development and simulation tools (e.g., Xilinx, Altera, or equivalent).Knowledge of FPGA verification methodologies.Experience with scripting/programming for test automation (e.g., Python; familiarity with VHDL/Verilog).Strong analytical and problem-solving skills.High attention to detail with disciplined documentation practices.
Preferred QualificationsExperience in the medical device, life sciences, or regulated product environment.Understanding of quality systems and structured verification documentation.Experience verifying subsystem-level designs prior to full system integration.Familiarity with digital imaging or microscopy-based systems is an advantage.Experience achieving high verification coverage in structured development environments.
Role Focus SummaryVerification-focused (not FPGA design role).Primarily simulation and subsystem-level validation.Ensures strong coverage (targeting high design coverage before integration).Bridges hardware and firmware verification.Contributes to product robustness prior to final build and release.Works closely with cross-functional teams including R&D and Quality.
I am currently looking for a Antibody Scientist - Early Discovery for one of my R&D client specialized in RNAi and siRNA therapeutics development.
Job Title: Antibody Scientist - Early DiscoverySalary: Competitive Market RateType: Full TimeLocation: Singapore, Central
The Antibody Scientist will lead the discovery and optimization of antibodies for AOC/PCC conjugates targeting extrahepatic tissues, applying strong expertise in antibody engineering and characterization to drive programs from early discovery to PCC nomination.
Responsibilities 1. Lead the discovery and screening of antibodies for extrahepatic targeting applications, using established antibody discovery platforms and technologies.Design and execute antibody engineering strategies to optimize affinity, specificity, and developability properties for AOC/PCC conjugates.Perform comprehensive antibody characterization including binding affinity assessment, epitope analysis, and cross-reactivity profiling.4. Collaborate closely with Senior Chemist and Senior Biologist teams to co-develop and optimize new AOC/PCC platforms for extrahepatic targeting.Establish and maintain a seamless and effective working model with the Suzhou discovery team, including regular scientific alignment, joint experimental design, transparent data sharing, and synchronized project timelines to ensure efficient cross-site collaboration.Manage external CRO collaborations for antibody discovery and characterization, including study design oversight, quality control, data review, and timeline management.Drive innovation in antibody discovery workflows and contribute to IP generation and scientific publications.
Requirements:Ph.D. in Molecular Biology, Immunology, Protein Engineering, or a related discipline with minimum 5 years of industry experience in antibody discovery and engineering.Demonstrated industry expertise in antibody discovery technologies and antibody engineering for therapeutic applications.Proven experience in antibody characterization including binding kinetics analysis, functional assays, and binding site characterization.Direct experience with AOC/PCC modalities or conjugate technologies in an industry setting is highly preferred.Strong hands-on skills in molecular biology and protein biochemistry techniques relevant to antibody development.Proven ability to work effectively in cross-functional, cross-site project teams, with experience in establishing efficient collaboration models across geographically distributed teams.Experience in managing external CRO collaborations for antibody discovery and characterization projects.
We are currently looking for QC System Specialist for one of my Global Pharmaceutical MNC client on a long term contract. This is an exciting opportunity to join a huge MNC in a huge brownfield project.
Role: QC System Specialist Location: Singapore, TuasType: 12 months contract (extendable)Salary: SGD 6,000 - SGD 8,000
Key Attributes/Responsibilities:Looking for candidates with 5+ years QC/Lab Equipment Validation experience.Provide technical support to run and validate necessary test methods on lab equipment and in developing method transfer/validation protocols and reports.Perform qualification and validation for in process, release and stability equipment (HPLC, UV, TOC, pH, GC etc).Conduct thermal mapping and temperature uniformity studies of laboratory temperature-controlled equipment (e.g., refrigerators, freezers, incubators, ovens) to ensure compliance with regulatory and quality standardsManage day-to-day Quality Control/LAB Validation activities in accordance with approved Project Plans and Policies for a fast-paced brownfield project.Help with lab system validation, develop and oversea system qualificationReview and Approve C&Q plans/protocols/reports and GxP SOPs/recordsReview validation life-cycle documents during the commissioning, qualification (IQ/OQ), and validation (PQ) phase e.g., pre and post-execution commissioning/ qualification plans and test specifications, validation summary reports & etc.Ensure that documents are in compliance with quality standards and applicable regulatory requirementsReview engineering change control to evaluate the validation/quality impact(s).Support in the resolution of validation deviations and approval.Participate in the qualification coordination meeting to ensure correct event sequence in compliance
