Jobs at Argenta

Act as primary client contact to translate forecasts into an 18-month Master Production Schedule (MPS), manage MRP parameters, coordinate material deliveries, track artwork/version control and packaging change controls, resolve capacity constraints, and ensure on-time, in-full delivery aligned with production.

Lead FP&A for US CMO business units: produce monthly management accounts, variance analysis, budgeting and consolidation. Partner with general managers, provide cost modelling and operational performance recommendations, act as primary finance contact for non-transactional queries, and deliver projects as assigned by the CFO.

Perform qualitative and quantitative chemical analyses for APIs and products, support analytical method development and technology transfer, generate technical/CMC documentation, and support R&D projects and client interactions.

Lead design, implementation, maintenance, and optimization of plant automation systems (PLCs, HMIs, SCADA). Manage automation scope for capital projects, develop software and HMI graphics, maintain documentation, and drive operational efficiency and compliance.

Lead US CMO FP&A including monthly management accounts, variance analysis, cost modelling, budgeting, and financial reporting. Act as business unit finance partner, support general managers, handle non-transactional finance queries, and complete CFO-assigned projects to improve operational performance and costing.

Provide first- and second-level IT support, maintain IT infrastructure, assist onboarding/offboarding, support databases and reporting, and research, test, and implement AI and digitalisation initiatives across departments.

Manage CRO/CDO projects from initiation to closure: define scope, plans, budgets, timelines and milestones; monitor progress and risks; ensure FDA/CVM compliance and facility safety; drive decisions, implement process improvements, and train project personnel.

Provide engineering support for production and process equipment in a cGMP pharmaceutical/sterile manufacturing environment. Lead projects, manage capital expenditures and budgets, ensure compliance with FDA/EU regulations, perform equipment lifecycle support, validations, risk analyses, and coach junior engineers to improve reliability and manufacturing processes.

Lead end-to-end sterile product tech transfers and lifecycle programs, coordinating cross-functional teams, managing budgets, schedules, regulatory and validation activities, and ensuring site/product launch readiness while mitigating contamination and supply risks.

Lead and support product/technology transfers, process development, and optimization for oral solids, soft chews, non-sterile liquids and injectables. Author technical protocols/reports, manage schedules and cross-functional teams, identify critical quality attributes, support validation/quality, and troubleshoot manufacturing/process issues while interfacing with customers and internal stakeholders.

Lead cGMP analytical method development, transfer, verification, and validation for active ingredients, raw materials, and finished products. Manage multiple analytical projects, mentor staff, qualify laboratory equipment, perform routine analyses, maintain detailed GMP documentation, and design and execute cleaning validation protocols while interfacing with client teams.

Lead regulatory strategy and support for animal health product development for clients and internal projects. Provide regulatory advice, prepare submissions and documents, navigate regulatory challenges, engage industry associations, pursue consulting opportunities, and manage stakeholder expectations with clear communications and regulatory expertise.

Lead proposal development, costing, pricing governance, and change‑order activities across a multi‑site CDMO. Create and maintain standardized costing models, SOPs, and centralized quote/change registers; perform quality control on proposals; liaise with Commercial, Manufacturing, MSAT, and Finance; support customer due diligence and continuous improvement of pricing methodology and tools while ensuring GMP and quality compliance.

Lead execution of US clinical strategy and business plan, manage clinical staff and client expectations, ensure GCP-compliant trial conduct, develop and deliver training for CTM/CRA teams, and provide reporting to leadership to drive high-quality clinical data delivery.

Prepare monthly management accounts, balance sheet reconciliations, and variance analyses for CMO Americas. Manage fixed assets and asset WIP, maintain costings and standard cost reviews, update cash flows, and forecast trends to identify overspends. Provide timely project spend updates to sponsors and support tax fixed asset register reconciliation to ensure financial statement integrity.

Lead and take scientific responsibility for GLP animal health studies: approve protocols, ensure regulatory compliance, oversee animal care/data collection, address deviations, interpret results, and write/sign final study reports while coordinating sponsors, QA, and cross-functional teams.

Lead Argenta's CDMO commercial strategy across the Americas by building client relationships, identifying growth opportunities, preparing and negotiating proposals and contracts, and collaborating with scientific and manufacturing leaders to win integrated service business.

Lead and execute R&D transformation initiatives across CRO and CDO business units to improve operational effectiveness, simplify processes, implement continuous improvement, enhance KPIs and reporting, and drive cross-functional collaboration and data-driven decision-making.