PRINCIPAL QUALIFICATIONS:

A third level Science Qualification
Skills REQUIRED:
Good communications skills, excellent time management skills, flexibility and agility will be required. Openness to change. Proven ability to work on own initiative and deliver expectations.

DESIRED WORK EXPERIENCE:

Pharmaceutical experience in a GMP regulated laboratory environment.

MAIN RESPONSIBILITIES

Graduate role specific:

• Raw Material team project & Testing Support
• Running Team Boards & Metrics
• Consumables management support

ROLES AND RESPONSIBILITIES:

• Carry out routine analysis in QC Raw Material Team samples ensuring compliance with cGLP/cGMP and that turnaround times are met. The testing carried out is on In coming materials.
• Actively involved in Investigations
• Always ensure compliance with EHS, actively participate in EHS activities and 5s.
• Perform routine instrument calibration checks at appropriate times.
• Preparation and control of Standard Operating Procedures and always ensuring compliance with cGMP guidelines.
• Completion of Documentation for Batch Release process.
• Assisting in the provision of trends
• Assist in audits.
• Generation/ reporting of Key performance indicators for the group.
• Ensure compliance with current pharmacopoeias and all regulatory/company guidelines.
• Interaction with other departments e.g., QA, BU, Sterility assurance etc.
• Keep colleagues informed of current issues and developments as appropriate.
• Reasonable level of overtime will be required to facilitate the business needs.
• Carry out additional duties as deemed necessary by your PTL/Senior Analyst