Role Description We're hiring a Senior or Staff-level Data Scientist to help design and build the powerflow and optimisation engines at the core of our platform. This role sits at the heart of our work on calculating safe, real-time capacity for distributed energy resources within network constraints and turning those calculations into forecasts and dispatch, resource allocation, and grid management decisions that affect how networks actually operate. This is applied optimisation work. You'll formulate constrained optimisation problems, implement algorithms, and build systems that run in real-time or near-real-time operational contexts. You'll work closely with the rest of the Grid Modelling team to translate network physics into optimisation constraints and get solutions into production. What you'll do - Develop powerflow engines for grid modelling and forecasting - Solve constrained optimisation problems related to grid operations, resource dispatch, and network management - Design optimisation solutions that balance multiple objectives (safety, efficiency, customer impact, operational constraints) - Collaborate with others in the grid modeling team to formulate network models and constraints as optimisation problems - Build scalable optimisation solutions that perform in real-time or near-real-time operational contexts - Establish best practices for optimisation model development, validation, and monitoring - Contribute to technical strategy for data science, optimisation capabilities and future applications Qualifications - Powerflow and/or optimisation expertise - Deep experience with one or both of: - AC optimal powerflow (AC-OPF) calculations, including the use of key open-source packages such as OpenDSS, pandapower and lf-energy - Constrained optimisation, operations research, or similar fields (linear programming, convex optimisation, mixed-integer programming, familiarity with optimisation solvers and frameworks such as Pyomo, CBC, Gurobi, CPLEX, OR-Tools, etc.) - Data science foundations: Statistical modeling, numerical programming, algorithm design, data analysis - Senior/Staff level experience: 5+ years in data science/ML/optimisation roles with demonstrated impact - Python proficiency: Capable of writing quality code for optimisation algorithms and data analysis; familiar with architectural principles, system design, version control, testing practices, code review, CI/CD Requirements - Grid domain knowledge (electrical networks, power systems, operational constraints) - Experience with market dispatch, energy economics, or resource scheduling problems - Real-time or near-real-time optimisation system experience - Understanding of DER integration challenges and VPP operations - Experience in highly parametric statistical model fitting, e.g. state estimation for energy networks - Experience with optimisation in high-performance contexts, e.g. use of metaheuristics, HPC - Experience in load forecasting - Ability to work with customers to incorporate their existing forecasts into your own calculations - Software engineering depth (system design, testing, deployment, MLOps) - Familiarity with Databricks - Familiarity with data cleaning and data exploration Benefits - $160k–$220k depending on experience, plus equity - Remote-first, with head office in Sydney - A talented team of engineers, data scientists, and power systems specialists working on hard problems that matter Sound interesting? We'd love to hear from you! Apply directly and we'll be in touch shortly.

Role Description We’re looking for an Associate Clinical Data Manager (ACDM) based in Costa Rica to support the acquisition, quality, and compliance of external clinical trial data across multiple studies. - Support the end‑to‑end acquisition of third‑party (non‑EDC) clinical data for assigned studies - Ensure data integrity, quality, compliance, and audit readiness throughout the data lifecycle - Collaborate with external vendors to align on timelines, processes, and issue resolution - Partner with cross‑functional study teams to support study objectives - Monitor data deliverables and proactively identify and resolve risks or inconsistencies - Represent ACDM activities in study team meetings, audits, and inspections - Support and informally train coordinators and peers on study and vendor‑specific considerations - Contribute to process improvements and data integration optimization initiatives Qualifications - 3–5 years of experience in Clinical Data Management and/or drug development - Experience supporting third‑party clinical data acquisition and vendor oversight - Solid understanding of clinical trial processes, ICH‑GCP, and global regulatory requirements - Clinical data standards (CDISC, SDTM, ADaM) and data governance practices - Non‑EDC data sources and data integration processes - Strong organizational, problem‑solving, and project coordination skills - Effective communication and collaboration across functional teams - High attention to detail and commitment to quality and compliance Requirements - BS/BA required, preferably in Life Sciences, Health, Technology, or equivalent experience Important - This position requires candidates to be based in Costa Rica Benefits - Exposure to multiple therapeutic areas and development phases - Collaboration with global teams and innovative data technologies - Opportunity to make a meaningful impact on clinical development programs

Role Description The Senior Scientist - MSAT is responsible for acting as a primary point of contact for technical inquiries from Cytiva’s biopharmaceutical customers. In this role, you will provide high-quality scientific support and guidance on the use of Cytiva filtration and separation technologies in customer processes. This position reports to the Senior Manager - MSAT and is part of the MSAT (Manufacturing Science and Technology) team working remotely to cover the eastern USA and Canada. What you will do: - In coordination with commercial and technical colleagues, you will use your expertise and training to support customer success with Cytiva filtration products. - You will interact with customers to educate them on the use of Cytiva bioprocessing technologies. - You will perform and report on scientific application studies in customer processes from bench-scale to manufacturing-scale. - You will provide guidance on process optimization, troubleshooting and scale-up. - You will use your knowledge of customer needs to help guide Cytiva’s new product development programs. Qualifications - You have a bachelor’s degree in a natural science or chemical engineering. - You have 4+ years’ experience in the biopharmaceutical industry, ideally in PD (process development) or MSAT. - You have a practical aptitude for performing bench-scale scientific studies and are adept at writing technical reports. - You have demonstrable expertise in bioprocessing and GMP manufacturing. - You have experience delivering technical training and presenting scientific material in group settings. Requirements - As you will support customers throughout the eastern USA and Canada, with travel away from home up to 60% of the time, you must live within a reasonable distance of a major airport. - You must have a valid driver’s license with an acceptable driving record. - You must be able to lift, move or carry equipment up to 45lb. - You must be able to put on and remove a cleanroom garment in a manner typically encountered in biopharmaceutical manufacturing facilities. Benefits - Comprehensive, competitive benefit programs including paid time off. - Medical/dental/vision insurance. - 401(k) to eligible employees. - Bonus/incentive pay eligibility.

Role Description The Scientist I in CMC supports regulatory activities for pre-approval, post-approval changes, and lifecycle management across client Rx and non-Rx products. Working as a consultant, this role assists in the preparation, review, and coordination of regulatory documentation, while ensuring alignment with applicable regulatory requirements and client expectations. The individual will collaborate closely with cross-functional teams and contribute to the timely delivery of high-quality regulatory submission content. - Support the development, authoring, and compilation of regulatory documentation related to post-approval changes and lifecycle management activities. - Assist as an authoring strategist by organizing and maintaining submission-ready documents in accordance with regional regulatory requirements. - Collaborate with cross-functional teams (e.g., CMC, Quality) to gather and verify required information for regulatory submissions. - Ensure documentation consistency, accuracy, and compliance with internal standards and client expectations. - Track and manage document timelines and deliverables to support regulatory milestones. - Maintain clear and proactive communication with client stakeholders while operating in a contractor capacity. - Ensures an established level of billable hours per fiscal year. Qualifications - 0-2 years of experience, open to new graduates. - Bachelor's degree in related field, or equivalent work experience, preferred. - Proactive, self-motivated, and able to work independently in a client-facing role. - Strong attention to detail and organizational skills. - Effective written and verbal communication skills. - Ability to manage multiple tasks and meet deadlines in a dynamic environment. - Basic proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). - Working knowledge of Adobe Acrobat for document editing, formatting, and publishing. - Team-oriented mindset with the ability to collaborate across functions. Requirements - Applies basic concepts, principles and technical capabilities to perform routine tasks with attention to detail. - Works on projects of limited scope and complexity. - Follows established procedures to resolve readily identifiable technical problems. - Works under direct supervision and executes detailed instructions. - Develops competence by performing structured work assignments. - Support client projects as a consultant. - Ability to work remotely from home office. - Requires adaptability and responsiveness to changing project priorities. Benefits - Medical, dental and vision coverage. - Paid time off plan. - Health savings account (HSA). - 401k savings plan. - Access to wages before pay day with myFlexPay. - Flexible spending accounts (FSAs). - Short- and long-term disability coverage. - Work-Life resources. - Paid parental leave. - Healthy lifestyle programs.