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***
Similar Jobs
Pharmaceutical & Biotechnology
Lead Biotech Associate
- Contract
- County Meath , Dunboyne , Ireland
Similar Jobs
Pharmaceutical & Biotechnology
Bioprocess Associate
- Contract
- North Dublin , County Dublin , Ireland
Similar Jobs
Pharmaceutical & Biotechnology
Senior QA Speciaist
- Contract
- Dún Laoghaire , County Dublin , Ireland
Similar Jobs
Pharmaceutical & Biotechnology
QA Specialist
- Contract
- County Dublin , South Dublin , Ireland
Similar Jobs
Pharmaceutical & Biotechnology
Quality Systems Specialist
- Contract
- County Cork , Cork , Ireland