Quality Auditor
- Midlands (Ireland)
- Contract
- Compliance / Quality Assurance
This vacancy has now expired
With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a Quality Auditor to join their team to support multiple capital projects taking place onsite in Leinster.
This is a fantastic opportunity to work on a state-of-the art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US.
Role Summary:
- Responsible for helping to ensure that the validated equipment on site maintains validated status.
- Act as quality support for validation and qualification activities of equipment, facilities, and associated processes on site to ensure they are maintained in accordance with global and local procedures.
- Ensure that quality issues are identified, addressed, and resolved in a timely manner.
- Responsible for supporting deviation close out and initiating/following up on corrective and preventative actions.
- Partner with colleagues cross functionally to provide support and advice on day-to-day basis and on a project, basis including communications, training, project work, audit/inspection duties, investigations etc.
Requirement:
- Bachelor’s degree or higher preferred; ideally in a related Science discipline
- Lean Six Sigma Methodology experience desired.
- Demonstrated ability in pharmaceutical equipment validation/qualification or quality support for same
- Knowledge of EU/US quality related pharmaceutical regulations
- Experience of Sterile manufacture preferred.
- Ideally a minimum of 3 years’ experience in the FDA and/or EU regulated pharmaceutical environment; preferably in a manufacturing site in quality and/or engineering roles.
- Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices requirements.
- Knowledgeable in Industry Best Practices for quality and compliance related topics
- Proven ability to effectively initiate and drive change.
- Strong verbal and written communication skills, project management skills
- Report, standards, policy writing skills required.
- Proficiency in Microsoft Office and job-related computer applications required (electronic validation systems)
If this role is of interest to you, please apply now!
#LI-CH3
I have always received a highly professional & personable service from the team at QCS Staffing. 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 QCS Staffing for seven years now and have always received a professional service. QCS Staffing'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 QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
Save as job alert
WE’RE NOT JUST
ABOUT THE WORK
Although That’s Pretty Awesome
We’re about an unmatched company culture and a huge range of benefits you’ll love, both on and off the clock.
Check out all our perks hereSimilar Jobs
Salary
Competitive
Location
Clonmel
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
Ireland
East
Description
Quality Auditor - Life Science - Contract - Clonmel Our Partner in Tipperary area develops and supplies the active ingredients and final formulated product for a range of innovative medicines at
Reference
TE31997
Expiry Date
01/01/0001
Author
Tom EvansAuthor
Tom EvansSalary
Competitive
Location
Clonmel
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
Ireland
East
Description
Quality Specialist - Life Science - 11-Month Contract - Clonmel Our Partner in Tipperary area develops and supplies the active ingredients and final formulated product for a range of innovative
Reference
TE32461
Expiry Date
01/01/0001
Author
Tom EvansAuthor
Tom EvansSalary
Competitive
Location
Clonmel
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
Ireland
East
Description
QA Specialist - Life Science - Contract - Clonmel Our Partner in Tipperary area develops and supplies the active ingredients and final formulated product for a range of innovative medicines at its
Reference
31714
Expiry Date
01/01/0001
Author
Tom EvansAuthor
Tom EvansInsights
Send us your CV
Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.
Christopher
I manage this role.