QC Compliance Specialist
- Midlands (Ireland)
- Contract
- Compliance / Quality Assurance
This vacancy has now expired
QC Compliance Optimisation Specialist opportunity to work with a Global Bio-Pharmaceutical Organisation at their Manufacturing facility in County Westmeath, Ireland.
Working hours: 40 hours per week
Working from home: Mixture of remote/ on site. You will need to come to site to get familiar with the lab and facility but then there would be flexibility to work from home on an ongoing basis.
Ireland is a hive of activity for the Life Sciences Sector at present, with Global Players investing heavily in manufacturing facilities here.
An excellent opportunity has arisen for an experienced QC Compliance Specialist to join a Global Bio-Pharma facility in County Westmeath. In the role you will be responsible for actively identifying opportunities for process and compliance improvement and translating these into practice.
Principal Responsibilities to include:
- Support implementation of effective shift handover/QC internal communication
- Identify and implement improvements to Lab Processes, Layout/flow and 6S type activities
- Training: design of induction training to lab, up to area SME level; define the training requirements and implement simplified training program
- Planning, scheduling and facilitating continuous improvement workshops and translation of the output to procedural/process updates.
- Documentation flow and paperwork practices: Improving Right First Time and reducing GDP errors within QC and implementing processes to track and trend performance against target
- Develop simplified and effective scheduling for routine/non routine activities to maximise available resource
- Implementation of real time review and real time trending of all QC data
- Support Implementation of in-house microbial identification using the Vitek including the design of process, documentation and training program
- Maintain regular and proactive communication with all stakeholders.
Desired Experience:
- Strong experience working in a GMP Quality Control Laboratory
- Knowledge and understanding of GMP/GDP standard
- Strong problem solving and leadership experience
- Experience in workshop facilitation
- Experienced in leading and executing continuous improvement initiatives
- Experience of SOP authoring and document management processes
- Experience of provision training to other
- Good working knowledge of QC Microbiology and Chemistry instrumentation and methods
Interested in hearing more? Apply today to be considered for this position!
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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