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Quality Assurance Specialist, Laboratory Services EU
CTI Clinical Trial Services, Inc —Bilbao, Vizcaya provincia
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Quality Assurance Specialist, Laboratory Services EU
CTI Clinical Trial Services, Inc —Bilbao, Vizcaya provincia
The Quality Assurance Specialist, Laboratory Services is responsible for the assessment of quality and compliance according to CLIA and CAP requirements, ISO…
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Quality Assurance Specialist, Laboratory Services EU

CTI Clinical Trial Services, Inc -
Bilbao, Vizcaya provincia

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Teletrabajo opcional

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Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Outlook
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Quality Assurance Specialist, Laboratory Services EU

Job Purpose/Summary

The Quality Assurance Specialist, Laboratory Services is responsible for the assessment of quality and compliance according to CLIA and CAP requirements, ISO 15189 requirements, GCP, GLP and CTI Laboratory SOPs

What You’ll Do

Author, review and maintain Standard Operating Procedures (SOP) for the laboratory.
Provide training and guidance regarding quality and regulatory compliance for laboratory staff.
Participate and support Risk Assessments within the Quality Management System to continuously improve processes
Participate in outside qualification audits for vendors supplying services or products, subcontractors, including contract laboratories; resolve and follow-through on any quality issues
Conduct in-study and facility-based audits, including equipment/instrument qualifications, equipment calibration and maintenance, software validation and laboratory processes in compliance with QA SOPs.
Conduct reviews of protocols, final reports and contributing scientists reports, when applicable.
Effectively report quality issues to supervisor, and CTI Laboratory management, as appropriate.
Provide input for process investigations, nonconforming quality events, client concerns and the associated CAPA plans.
Support quality-led sponsor audits
Support inspections and help ensure laboratory maintains current federal, state, and local licensure and accreditation (as applicable)
Support regulatory authority inspections
Maintain properly indexed quality assurance records. Assure all QA records are up-to-date and accurate and compile the appropriate records for archiving.
Attend pre-initiation, pre-planning, or operational team meetings as needed.
Participate in quality projects as assigned
Promote strong relationships with CTI sponsors.

What You Bring

Working knowledge of clinical laboratory regulations (e.g. CAP/CLIA), ISO 15189, and licensing requirements
Working knowledge of instrument/equipment qualification, calibration, and software validation
Working knowledge of quality assurance GLP GCLP best practices
Knowledgeable with electronic data collection systems used in data generation, including proper use, reporting, audit trails, security/Part 11 compliance, data correction, QC, etc.
Must possess excellent analytical, critical thinking, oral and written skills
Well organized and ability to meet deadlines
Ability to work independently and within a team environment
High level of attention to detail
Proficient in MS Excel, Word, Outlook, and PowerPoint
2 years of related experience in a clinical laboratory in a Quality Assurance role
Bachelor’s Degree or equivalent combination of education and experience
CLIA and/or CAP laboratory inspection experience
SQA, CQA or other quality related certification
Fluent in English

Why CTI?

At CTI, we recognize that our people are what make our company successful. Our work moves medicine forward.

For that reason, we treat our team members with the respect they deserve, and our numbers show it:

We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward
We value education and training – We provide tuition assistance, partner with universities and colleges to create programs in our field, and have a dedicated training department
We value our people - We have never had a layoff in our three decade history and we guaranteed full pay for our employees during the COVID-19 shut-down regardless of the number of hours worked. We support a work-life balance and the importance of time with family by offering generous vacation time, a hybrid work from home schedule, and paid parental leave.
Our culture is unparalleled – We've received multiple awards recognizing CTI as one of the best places to work in the greater Cincinnati area, as well as one of the top CROs in the industry
We think globally and act locally – With employees across 60 countries, we have global reach but maintain culture and connections to the local communities in which we work. Our CTI Cares Committees are dedicated to ensuring the CTI culture and values translate around the world.
We are looking toward the future – We have had a consistent double-digit growth rate over the last decade, invest in cutting-edge technology, and pride ourselves on our average annual retention rate of 95%, which is much higher than many other CROs
Our work makes a difference – We focus our work on treatments for chronically and critically-ill patients, who are depending on us to bring these life-changing therapies to market

Are you interested? Then we look forward to your electronic application, with a tabular CV in English.

CTI Clinical Trial and Consulting Services

Filipa Magalhães

www.ctifacts.com

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