Technical Manager

About the Role

GSK Saudi Arabia is seeking a Technical Manager to lead technical functions at its pharmaceutical manufacturing site in Jeddah Warehouse City. This full-time role involves overseeing all technical aspects of the product lifecycle on-site, driving performance and capability, and ensuring full compliance with Saudi Food and Drug Authority (SFDA) and other regulatory requirements. The position supports GSK's commitment to Vision 2030 and the Saudi Arabian National Agenda, including Saudization initiatives.

Key Responsibilities

• Lead the site technical function at Jeddah Warehouse City and serve as a core member of the Site Leadership Team, contributing to overall site performance and business goals within a GMP framework.
• Provide strategic direction for technical activities across the product lifecycle, ensuring robust technical support for manufacturing operations and product-related decisions.
• Champion safety, quality, and compliance, embedding GMP and QMS principles in daily operations and long-term improvement plans.
• Represent the Jeddah Warehouse City site in interactions with SFDA, Ministry of Health (MOH), and other regulatory bodies regarding licensing, inspections, and regulatory submissions.
• Lead regulatory and internal audits, ensuring effective follow-up, alignment of Level 2 processes, and implementation of Corrective and Preventive Actions (CAPAs).
• Hold formal responsibility for product recalls and complaints, coordinating with relevant departments to secure timely corrective and preventive actions.
• Oversee preparation, review, and approval of technical registration documentation and product files submitted to SFDA and other authorities.
• Ensure manufacturing operations adhere to GMP requirements, including approval of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
• Authorise site quality improvement plans, technical change controls (facilities, production lines, product components), and annual product review reports.
• Review and approve the self-inspection plan (Inspection Audit Universe), and audit and CAPA reports generated by relevant departments.
• Provide finished product batch release during the absence of the Quality Lead and authorise any reprocessing/rework requests as required.
• Approve quality risk assessments, incident/deviation management, and associated CAPAs, ensuring robust documentation and governance.
• Drive proactive talent management within the technical team, including succession planning, capability building, and support for graduate and industrial placement programmes.

Qualifications and Experience

• Education: Bachelor’s degree in Pharmacy or Doctor of Pharmacy (PharmD) is required.
• Experience: 3-5 years of experience, with a minimum of 3 years in a pharmaceutical manufacturing environment. Proven experience in a senior technical or leadership role within pharmaceutical manufacturing, or at the interface of R&D and manufacturing.
• Track Record: Strong track record in leading technical teams and delivering technical solutions in a GMP setting.
• Knowledge: Excellent knowledge and practical application of GMP guidelines and Quality Management System (QMS) requirements.

Licensing and Eligibility

• Saudi national, in line with local regulatory and licensing requirements.
• Valid practitioner licence from the Saudi Commission for Health Specialties and compliance with SFDA requirements.

Required Skills and Competencies

• Demonstrated ability to drive change, deliver solutions, and develop people in a complex, matrixed environment.
• Strong knowledge of regulatory requirements and pharmaceutical product development.
• Solid operational understanding of manufacturing unit operations, plant, and laboratory equipment.
• Strong analytical skills with the ability to interpret data and use it for tactical and strategic decision-making.
• Excellent communication and influencing skills at all levels of the organisation and with external regulators.

Work Type

This is a full-time position based in Jeddah, Saudi Arabia.