Our Client, who specialises in the Pharmaceutical industry is looking for an experienced Pharmaceutical Process Specialist to coordinate and manage Pharmaceutical Technology projects, ensuring timely execution in line with regulatory and company standards. Reporting to the Pharm Tech Supervisor your roles and responsibilities will include:
- Lead the planning, coordination, and follow-up of pharmaceutical technology projects.
- Collaborate across departments (QC, Production, Supply Chain) to align project timelines and deliverables.
- Prepare, review, and approve documentation related to submissions, process optimisation, validation, and cleaning validation in compliance with GMP.
- Oversee manufacturing activities for submission, optimisation, and validation batches.
- Support investigations and resolve issues arising during manufacturing and testing phases.
- Coordinate product transfer activities, acting as the main point of contact for all related information.
- Ensure smooth execution of process transfers to meet submission, launch, and regulatory deadlines.
- Provide technical support and troubleshooting for formulation and process-related challenges.
- Identify and implement process improvements where needed.
Working Hours: Monday - Friday: Office Hours
Requirements
- Minimum of two (2) years’ experience in the manufacturing or quality assurance of solid oral dosage forms.
- Strong understanding of pharmaceutical formulations.
- Hold an excellent level of written and verbal English.
- Candidates must already be based in Malta, with the legal right to work in Malta
Education and Experience
- A university degree in a science-related field or several years of experience in pharmaceutical manufacturing or a related industry.
Benefits
- Private medical scheme
- Continuous training
Job Reference: US040
