Pharmaceutical Development Technician

You will provide technical and operational support to formulation and process development activities under the guidance of the Process & Formulation Development Manager, scientists, senior scientists or project leaders, ensuring equipment readiness, accurate documentation and effective organisation of the preformulation laboratory in compliance with GMP and internal procedures.

Key Responsibilities:

• Support the cleaning, organisation and routine maintenance of the R&D preformulation area and related equipment.
• Assist formulation and process development activities under the guidance of the R&D Manager, Specialists, Senior Specialists, Scientists or Project Leaders.
• Assist with laboratory-scale, pilot-scale, engineering, PO, clinical, registration and validation batches in accordance with relevant SOPs, instructions and protocols.
• Check equipment readiness, calibration status and basic functionality before use, and report any malfunction or issue to the supervisor.
• Participate in R&D and pilot-scale manufacturing activities and carry out assigned operational tasks under supervision.
• Record experimental data, process parameters and activities accurately and in compliance with GMP and GLP requirements.
• Support material management activities including receipt, labelling, stock control and storage of raw materials, excipients and packaging materials.
• Assist with dispensing, weighing and preparation of materials for development trials and production runs.
• Perform assigned in-process checks, cleaning, labelling and packaging activities for laboratory or pilot batches.
• Maintain complete and traceable records including logbooks, laboratory records and batch documentation.
• Perform other duties assigned by R&D management in compliance with company SOPs, GMP, GLP, regulatory and health & safety requirements.

About you:

• Leaving Certificate or equivalent qualification.
• Minimum 4 years’ experience in pharmaceutical manufacturing or a similar GMP regulated operational environment.
• Strong knowledge and hands-on experience of pharma manufacturing equipment and machinery, prep, cleaning and maintenance.
• You will work as part of a collaborative team, contributing to high-quality data delivery in a fast-paced, GMP-regulated environment
• Opportunity to work in lab environment working on development-stage and commercial products
• Collaborative and quality-driven environment

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