Pharmaceutical Process Supervisor - (MALTA, Ħal Far)

Position based in Malta (Ħal Far), at the manufacturing site of a leading global pharmaceutical company.

Main Duties and Responsibilities

• Oversees the daily operations of the Pharmaceutical Technology – Process team, ensuring scientific and technical aspects of projects are executed efficiently and on schedule (including planning, evaluation, implementation, monitoring and documentation).
• Serves as the key liaison with cross-functional departments to promote seamless coordination and timely delivery of project milestones across the organization.
• Supports the preparation, review, and approval of documentation related to Regulatory Submissions, Process Optimization, Process Validation, and Cleaning Validation, in line with internal standards and GMP requirements.
• Works closely with QC, Production, and Supply Chain to coordinate manufacturing activities for submission, optimisation, and validation batches.
• Provides support in managing and resolving any deviations or investigations that may occur during manufacturing or testing phases.
• Participates in drafting manufacturing instructions that align with the specifications outlined in regulatory dossiers and market filings.
• Acts as a central point for all new project information regarding product transfers, submissions, and scale-ups, helping to assess potential inventory impacts, tooling or equipment requirements, and related interdepartmental procurement activities.
• Functions as a reference point for the Pharmaceutical Technology – Process section, and ensures effective collaboration with the equivalent team at HQ to share knowledge, align resources, and track joint initiatives.

Requirements

Benefits