Quality Control Inspector - Almac Clinical Services
CPL have partnered with ALMAC Group to recruit for a Quality Control Inspector to join their team on a temporary, on-going contract.
· Pay Rate - £14.36 per/hr + 16.7% shift premium
· Location – ALMAC Global Headquarters, Craigavon
· Benefits – 34 days holiday per annum
· Hours – 37.5 hours per week
· Shift - Evenings 15.30 to 23.30 (Monday to Friday)
OVERALL ROLE OBJECTIVE:
The post holder will be expected to sample, inspect and release labels and shipments in accordance with relevant SOPs, agreed specifications and timelines.
JOB SPECIFIC RESPONSIBILITIES:
The post holder will be required at a minimum level, to fulfil the following responsibilities detailed below. Further development opportunities exist within this role and are also outlined.
The post holder will:
1. Perform the following tasks:
· Inspection of labels
· Sampling and inspection of distribution orders
· Destruction activities
· Checks on material returned to stock
· Approval of randomisation files and label verification projects
2. Ensure any customer specific requirements have been carried out during processing and by Quality Control during the inspection process.
3. Travel, when required, to other buildings to aid in the inspection and sampling of materials for Almac Clinical Services.
4. Ensure adherence to cGMPs, SOPs and customer instructions through performance of job function.
5. Maintain a regular presence on the floors in order to monitor compliance with cGMP and general housekeeping within the Label Control/Distribution areas.
6. Check documentation for completeness and accuracy. Identify any deviations from written procedures and inform relevant personnel.
7. Be forthcoming with ideas/suggestions regarding process simplification and improved compliance. Be proactive regarding implementation of such through good engagement with Supervisors.
8. Report/escalate serious/potentially serious breaches of GMP compliance or matters of concern to the QC Supervisor in an open and timely manner for appropriate resolution.
9. Provide information to support the Lead Investigators during the conduct of an investigation.
10. Work to a consistently high standard, even when under pressure.
11. Maximise efficiency through successful time management and the ability to prioritise daily activities independently.
12. Fulfil any necessary administrative duties associated with the role, as and when required.
Development opportunities exist within the role. The following additional job responsibilities will be the focus of the most experienced members of the team.
1. Perform the role of key-trainer and mentor personnel in the team providing advice and guidance in order to build on their competence and experience.
2. Assist QC Supervisors with the allocation and prioritisation of tasks to relevant QC personnel in line with business needs and customer expectations.
3. Attend teleconferences/meetings/customer visits/supplier visits, as required, representing the Quality department.
a. This task may be on delegation from the QC Supervisor.
ESSENTIAL REQUIREMENTS
GCSE (or equivalent) in English Language at Grade C or above
and
A minimum of 2 A Levels (or equivalent)
DESIRABLE REQUIRMENTS
Previous experience working within the Pharmaceutical industry, GMP manufacturing, packaging, or Quality Assurance/Control.
For further details please apply directly below or contact Luke Bush directly on 028 3025 3460.
If successful you will be required to complete a criminal record check through Access NI, having a criminal conviction will not necessarily exclude you from this process. Cpl have a policy on the recruitment of ex-offenders, for a copy of this policy please email [email protected].
Cpl is an equal opportunities employer and welcomes applicants from all backgrounds. We recognise that a diverse and inclusive workplace will better our relationships and services with our clients, our candidates, our communities, and one another. Be You, Be Kind, Be Proud.
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