Pharmaceutical & Biotechnology

Visual Inspection Technician

  • Contract
  • Sligo, County Sligo, Ireland
  • 42040777

PE Global is currently recruiting for a Visual Inspection Technician for a leading multi-national Biotech client based in Sligo.

This is an initial 6-month contract position working on a 16/5 shift pattern, 07:00 – 15:00 and 15:00 – 23:00 which rotate each week (Monday-Friday), No Weekends.

 

ROLE:

  • To work as a team member to support biologics operation 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.

 

REQUIREMENTS:

 

  • Leaving Certificate minimum education requirement 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.
  • Essential: 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.

 

 

Interested candidates should submit an updated CV.

Please click the link below to apply, call Seán on +353 86 3514962 or alternatively send an up-to-date CV to sean.molloy@peglobal.net 

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***