KEY RESPONSIBILITIES:

• Manufacture / pack product to GMP / regulatory standards as outlined in company documentation

• Accurate completion of all necessary documentation
• Carry out IPC checks as outlined in company documentation
• Ensure machines / equipment are maintained and working correctly
• Carry out minor machine / equipment adjustments as appropriate
• Clean machines / work area in accordance with standard operating procedures
• Assist with training as required
• Attainment of targets relevant to work centre
• Adherence to health and safety procedures
• Ensure compliance to documented procedures and cGMP requirements as outlined in company procedures
• Maintenance of hygiene / housekeeping standards in all production areas
• Comply to terms and conditions as outlined in your contract of employment

COMPETENCIES:

• Ability to build relationships and collaborate with others is vital
• Demonstrate and practice company values on a daily basis
• Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks

QUALIFICATIONS:

• At least 1 years’ experience in a Pharmaceutical FDA/HPRA or manufacturing environment preferable
• Excellent knowledge of GMP & GDP requirements desirable
• Good communication, leadership and people management skills are essential
• Strong organisational and problem solving ability
• Availability to work on shift cycle based on company requirements