Jobs at Acino

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.

Support quality oversight across manufacturing, facilities, utilities, and warehouses to ensure GMP/GDP compliance. Conduct GMP walk-throughs and Gemba activities, participate in investigations, RCA and CAPA management, review SOPs and QMS gaps, promote data integrity and quality culture, and support training and mentoring of junior staff to ensure timely resolution of quality events and continuous improvement.

Lead oversight of analytical method development, validation, transfer, and stability studies in QC labs ensuring ICH/USP/GLP and 21 CFR Part 11 compliance. Ensure data integrity, troubleshoot chromatographic systems (HPLC/GC), manage OOS/OOT investigations, support regulatory submissions and CTD dossiers, drive continuous improvement, and provide technical training and audit readiness for analytical teams.

Lead and govern the site deviation lifecycle, driving investigations, root cause analysis, risk-based impact assessments, CAPA linkage and effectiveness verification. Provide quality oversight, ensure GMP and data integrity compliance, maintain trending and reporting, support inspections and audits, and enable continuous improvement across GxP operations.

Serve as single point of contact for assigned external CMOs to oversee GMP compliance and quality performance, implement QMS, coordinate audits and lifecycle changes, manage product launches, escalate complaints and adverse events, and maintain cross-functional communication with suppliers and internal teams.

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.

Develop and execute marketing strategies, design tools, engage stakeholders, lead product training, and drive digital transformation for brand success.

Manage, control, and maintain material specifications and analytical methods to ensure compliance with GMP, pharmacopoeias, and site QMS. Coordinate cross-functionally, track document status, support change control, audits, inspections, and eQMS implementation, and maintain data integrity and version control.

The Accounts Receivable Accountant is responsible for reviewing orders, managing credit risks, processing customer payments through SAP, and generating sales reports to ensure compliance with financial deadlines.

The Finance Analyst will support budgeting, inventory control, and financial reporting, ensuring compliance and accurate accounting in line with local regulations.

The Accountant role involves managing accounts payable, financial reporting, bank reconciliations, and compliance, while supporting financial objectives and improvements.

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

The FP&A Manager leads financial planning and analysis, budgeting, forecasting, and performance analysis to support business decisions and improve performance.

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

Ensure GMP and SOP compliance across production by managing deviations, CAPAs, audits, inspections, and trainings. Support manufacturing teams, lead investigations and process improvements, track quality KPIs, and drive continuous improvement and documentation to maintain product quality and regulatory readiness.

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.

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.

Lead QA and QC functions, certify product batches, ensure compliance with regulations, and develop a high-performing quality team in a pharmaceutical manufacturing setting.

As an R&D Specialist, you will formulate, research, and test product specifications, conduct analyses on raw materials and finished products, and ensure compliance with export requirements.

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.