Job Description

Team Horizon is seeking a Visual Inspection Technician for our client based in Sligo.

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

What you will be doing:

* 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.

What you need to apply:

* 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.

* Requires annual visual test certification for colour blindness and 20/20 vision.

* 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