Quality Administrator

Posted 9 Days Ago
Be an Early Applicant
Hiring Remotely in New York, NY
Remote
60-65
Senior level
Consulting
The Role
The Quality Administrator will manage audit program records, extract pre-audit information, maintain audit schedules, and coordinate meetings. The role involves handling data within computerized systems, working with suppliers, and ensuring adherence to quality standards.
Summary Generated by Built In

Introduction:


We are searching for a Quality Administrator for one of our clients. They are a global biotechnology company that focuses on discovering, developing, and delivering innovative therapies for patients with neurological, neurodegenerative, and rare diseases.


Their portfolio includes treatments for MS, such as Tecfidera and Tysabri, and Spinraza, a groundbreaking treatment for SMA. The company is also investing heavily in the development of therapies for Alzheimer's, Parkinson's disease, and other neurodegenerative disorders, using cutting-edge research in gene therapy and other advanced technologies.

They collaborate with various research institutions, universities, and biotech companies, aiming to address unmet medical needs and improve the quality of life for patients with complex conditions. Their mission is to improve the health and well-being of individuals through transformative medicines, a vision that drives its continued innovation and growth in the biopharmaceutical industry.


Responsibilities:

 

-Create, coordinate, maintain, and update records for the Audit Program, including uploading audit reports and CAPAs to the main database/Computerized system.

-Extract pre-audit information from databases and provide it to audit execution teams.

-Maintain the audit schedule and audit adherence and coordinate stakeholders' pre-audit meetings.

-Experience with administrative tasks within quality, a good understanding of Microsoft Office, databases, and managing large amounts of data, including uploading information into different systems and databases.

-Working with suppliers in the receipt and exchange of information.

-Good Manufacturing Practices experience is a plus.


Qualifications: 

5 year's of experience working in Quality Assurance, Audit Programs, at a Life science/Healthcare company, or related industry


The Company
HQ: Palos Verdes Peninsula, California
350 Employees
On-site Workplace
Year Founded: 1995

What We Do

Welcome to the SQA Services, Inc. home on LinkedIn! Follow us to stay up to date on all things quality - including industry events, news, and ways to get involved with #TeamSQA. Also, keep an eye out for job postings! SQA is always looking for quality professionals and new team members!

WHAT IS SQA SERVICES, INC.?
SQA provides global supplier quality services for quality-critical industries. With quality, manufacturing, and regulatory experts located in over 50 countries, SQA provides a cost-effective, local supplier presence.

Managed, on-demand services include supplier quality audits, supplier remediation, quality engineering, source inspection, corrective action management, and real-time supplier quality data via SQA's world-class STEPQ technology.

HOW CAN I GET IN TOUCH WITH SQA?
We look forward to connecting with you and discovering how Team SQA can help you and your team reach your quality goals. Contact our team by heading over to http://www.sqaservices.com/contact

If you think you or someone you know would be a great fit for our team, please send your resume to our Associate Development team at: [email protected]

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