Overview
Visual Inspection Technician
Team Horizon is seeking a Visual Inspection Technician for a client in Sligo.
This person will be visually inspecting vials against a black and white surface for visual defects.
Why you should apply
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people's lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
Responsibilities
To work as a team member to support biologics operation in pharma operations in line with all safety, regulatory and organizational requirements.
Visual Inspection Technician will be assigned to the daily production operations.
Documentation of all activities in line with cGMP requirements.
Perform final product visual inspection.
Perform product intermediary packaging, as applicable.
Perform in process testing methods.
Monitor Process Alarms.
Material receipt from warehouse, verifying all pertinent documentation.
Transfer of final material to warehouse inventory.
Ensure all manufacturing documentation is completed on a timely manner without errors, following cGMP's.
Diagnose and resolve events or exceptions of VI process.
Disposal of domestic, biomedical, and hazardous waste from their respective area as applicable, ensuring compliance with regulations following the procedures and policies of the plant, division, and the corporation.
Keep detailed records, manual or electronic, of the operations carried out during the work shift.
Active Participation in Factory Acceptance testing, Site Acceptance Testing and commissioning and qualification of equipment.
Adhering to all relevant policies relating to Quality & Safety.
Ensure successful external inspections, and Division and Corporate audits.
Active participant in the development of batch records and electronic batch records for the site.
Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures
Qualifications
Leaving Certificate and 1 years' experience in GMP manufacturing
1 year plus of Knowledge of GMP and regulatory requirements relating to the pharma/biologics industry.
1 year in Batch processing operations in an FDA/ HPRA regulated industry is highly desirable.
Annual visual test certification for colour blindness and ***** vision is essential.
A good knowledge of cGMP and regulatory requirements relating to the biologics/pharmaceutical industry is desirable.
Experience in handling of dangerous chemicals is highly desirable.
Good I.T. skills are required.
Possessing previous Inspection experience in a Pharma/Biologics facility is a distinct advantage for operators assigned to VI.
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