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QC Analyst

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About the role

This vacancy has now expired. Please click here to view live vacancies.
"At ICON, it's our People that set us Apart"
 
 Do you have experience conducting quality control (QC) inspections to identify deficiencies?
 
Quality Control Analyst role within ICON: 
 
ICON has a strong reputation in our approaches to clinical development.   We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients.   We work with top pharmaceutical organizations on emerging therapeutic areas which include but are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain.  We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally. 
 
The Quality Control Analyst will perform quality control (QC) inspections to identify deficiencies in sample handling/preparation, reagent preparation, laboratory methods, notebooks, raw data, and report tables.  Review study materials for compliance with the protocol, standard operating procedures (SOPs), and applicable regulations.  Perform verification of operational activities including review of notebooks, raw data, and report tables.  Employ rapid feedback loop to resolve deficiencies found during QC inspection. Ensure subsequent correction(s) are made.  Assist in the implementation of the quality management system, including both corrective and preventive actions and maintain accurate and complete records and ensures QC documentation is incorporated into appropriate study files.
 
Benefits of working at ICON:
In addition to partnering with the top pharmaceutical and biotech companies in the world we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, bonus plans, vacation, and other incentives.  
 
To succeed you will need:
We are seeking candidates with an Associate’s degree in science however we strongly prefer a Bachelor’s degree in science (i.e. Biology/Chemistry/Med Tech).
 
To be successful you will be expected to have previous lab experience in a regulated environment and/or a minimum of 2 years’ experience in a quality role, document control, and/or record-keeping desirable. The ability to follow directions with minimal supervision, organizes and managers large quantities of documentation, and possesses excellent organizational, communication, and interpersonal skills. 
 
We invite you to review our opportunities at www.iconplc.com/careers.
 
What’s Next?
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
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