Jobs at Acino

Lead budgeting, forecasting, and financial planning; monitor performance and variance analysis; manage product costing, inventory valuation, and working capital; evaluate capital investments; ensure IFRS compliance and internal controls; support audits; drive ERP optimization and Power BI reporting; partner across functions and mentor junior finance staff.

Oversee accounting, tax, and financial reporting, ensuring compliance with regulations. Lead functions in accounting, manage audits, and tax filings while developing the team.

The role involves ensuring compliance with GMP and CSV requirements by planning and executing validation activities for computerized systems in sterile manufacturing operations.

The Quality Control Senior Specialist performs and reviews chemical and physical analyses for finished products, prepares documents, records results on SAP, calibrates lab equipment, and participates in investigations related to analysis.

The Quality Assurance Specialist at Acino manages document and record compliance, ensures adherence to GMP standards, and participates in audits and training while maintaining quality assurance in pharmaceutical production.

The QC Senior Expert oversees the review and approval of analytical data and records, ensuring compliance with regulatory standards and data integrity principles while supporting batch release processes.

Certify and release medicinal product batches per marketing authorization, GMP and regulations; oversee batch release, deviations, CAPAs and supply chain integrity; ensure third-party GMP compliance; maintain legal/technical knowledge and contribute to the quality team.

Act as finance business partner for the Gulf cluster, leading FP&A, budgets, forecasts, MBRs, commercial insights, distributor performance, G2N management, S&OP partnership, cost optimization, controls, reporting, and finance team development across UAE, Qatar, Oman, Kuwait, and Bahrain.

Provide administrative and operational support across functions: coordinate HCP engagement logistics, manage vendors and procurement documents (PR/PO/DocuSign), maintain marketing records, support campaign and event execution, ensure compliance and confidentiality, and assist People & Culture with onboarding, offboarding, and employee engagement activities.

Lead site-wide computer system validation and data integrity for manufacturing, lab instruments, and utilities. Implement technical controls (user access, audit trails, backups), perform DIRA and CSV risk assessments, support regulatory inspections, investigate deviations, and drive CAPA to ensure GxP and 21 CFR Part 11 compliance.

Lead global data integrity strategy and governance across manufacturing to ensure ALCOA+ compliance. Oversee policies, DIRA risk assessments, audit defense, CAPA remediation, metadata archiving, audit trails, and cultivate a culture of transparent GxP data practices.

Provide end-to-end sterility assurance and quality oversight for liquid sterile manufacturing lines. Own and update the site's Contamination Control Strategy (CCS) to ensure Annex 1 compliance. Supervise microbiological laboratory activities, review EM and bioburden trends, approve APS/media fills, lead method validation, perform gap analyses and QRM, design and track CAPA remediation, and serve as SME during regulatory inspections.

Lead national sales for the Clones, Generics & OTC Business Unit in South Africa by implementing sales strategies, driving profitable growth, coaching and managing the sales team, expanding market share, recruiting customers, maintaining KOL and hospital relationships, ensuring compliance, delivering business plans and targets, and forwarding quality/adverse event reports to QA/Pharmacovigilance/Medical Affairs.

Administer and optimize Microsoft-based on-premises, cloud, and hybrid IT systems. Responsibilities include Windows Server and AD management, Microsoft 365 administration, VMware, monitoring, patching, automation with PowerShell, incident response, security compliance, user support, documentation, and asset/inventory management.

Lead end-to-end demand planning and commercial supply chain for Egypt: develop 36-month forecasts, align supply plans with commercial objectives, lead monthly S&OP, optimize inventory and logistics, manage 3PL relationships, ensure OTIF and customer service, mitigate supply risks, drive process improvements and digitalization, and coach a high-performing planning team.

Lead deployment and operation of the Integrity & Compliance program in Egypt. Conduct compliance reviews, risk assessments, monitoring, investigations, policy localization, training, and speak-up management while coordinating with regional and global teams.

Manage and improve QMS processes related to training and documentation archiving. Ensure compliance with GMP, develop training programs, and promote data integrity best practices.

Manage all legal affairs for Egypt region, support business and Headquarters Legal, act as company secretary where applicable, draft/review/and negotiate commercial and regulatory agreements, advise on corporate governance, support BD/M&A, monitor legislative developments, maintain contract repositories, and implement risk-mitigation processes and training.

Lead development and execution of regional market access, pricing, and reimbursement strategies across META. Support country teams on P&R submissions, HTA readiness, and pricing projects; build payer and policymaker relationships; develop value dossiers, economic models, and RWE/HEOR evidence; align access with commercial and regulatory plans; monitor access KPIs and strengthen local capabilities through training and tools.

Perform microbiological testing and environmental monitoring for raw materials, packaging, products, and utilities; review media preparation, method validation, calibration, sterilization, documentation; investigate OOS/OOT/deviations and support CAPA to ensure GMP compliance.