Visual Inspection Technician

2 weeks ago


Sligo, Sligo, Ireland Team Horizon Full time

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 year's 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.
Seniority level

Entry level

Employment type

Full-time

Job function

Engineering and Information Technology

Industries

Pharmaceutical Manufacturing

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