Pharmaceutical Process Supervisor - (MALTA, Ħal Far)

JUST ONE; Palermo; In loco; EUR 30.000 - 35.000; Tempo pieno

Descrizione del lavoro

A leading global pharmaceutical company is seeking an experienced professional in Palermo to oversee the Pharmaceutical Technology - Process team. The role involves ensuring project milestones are met and requires a university degree in a scientific field alongside 5-10 years of hands-on experience in solid oral dosage form production. The ideal candidate will have strong knowledge of pharmaceutical formulations and excellent interpersonal and leadership skills.

Servizi

€ 30.000 Net Yearly

Private health insurance plan

Ongoing training and career development opportunities

Supportive and stimulating work environment

Relocation support for eligible candidates

Competenze

• 5-10 years of hands-on experience in solid oral dosage form production.
• Proactive and adaptable, with a results-driven mindset.
• Excellent organizational and coordination capabilities.

Mansioni

• Oversees daily operations of the Pharmaceutical Technology - Process team.
• Acts as liaison with cross-functional departments.
• Supports documentation related to regulatory submissions.

Conoscenze

Pharmaceutical formulations knowledge

Process dynamics understanding

Interpersonal skills

Leadership abilities

Communication skills

Formazione

University degree in a scientific field

Descrizione del lavoro

Overview

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

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

• University degree in a scientific field or equivalent professional experience within pharmaceutical manufacturing.
• Minimum of 5-10 years of hands-on experience in solid oral dosage form production.
• Strong knowledge of pharmaceutical formulations and process dynamics.
• Proactive, adaptable, and results-driven mindset.
• Strong interpersonal and leadership skills with an ability to motivate and manage a team effectively.
• Excellent written and verbal communication abilities.
• Demonstrated organizational and coordination capabilities.

Benefits

• € 30.000 Net Yearly
• Private health insurance plan
• Ongoing training and career development opportunities
• Supportive and stimulating work environment
• Relocation support for eligible candidates