Visual Inspection Technician
| Job Type | Contractor |
| Area | Sligo, Ireland |
| Sector | Operations & Manufacturing |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1003470 |
| Job Views | 20 |
- Description
Team Horizon is seeking a Visual Inspection Technican 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.
