QA Associate I
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Quality Assurance Associate for a global pharmaceutical company located in El Segundo, CA.
Job Responsibilities:
- Perform receipt and disposition of incoming apheresis material.
- Perform verification/inspection and ensure timely issuance of production documents and labels
- Review batch-related documentation and ensure resolution of issues to release and ship product.
- Ensure timely resolution and escalation of issues in operations
- Ensure all product-related Deviations are initiated, investigated and resolved.
- Ensure that associated CAPAs are initiated and resolved, as needed.
- Ensure approval and timely delivery of final product.
- Ensure products are manufactured in compliance with regulatory and GMP guidelines.
- Provide Quality Assurance support resolving material, in-process product, final product, environmental, facility and equipment manufacturing issues.
- Gather metric information for use in continuous improvement of areas of responsibility.
Skills and Requirements:
- BS/BA + multiple yrs. experience in a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.
- Works on multiple assignments in collaborative and dynamic environment.
- Working knowledge and ability to apply GMPs in conformance to U.S., EU, and ROW standards
- Ability to effectively negotiate and build collaboration amongst individuals
- Strong teamwork and collaborative skills
- Experience with manufacturing investigations, deviations, and CAPA.
- Experience with change control practices and strategies.
- General knowledge of aseptic manufacturing processes.
- Proficient in MS Word, Excel, Power Point and other applications.
- Strong interpersonal, verbal and written communication skills
- Comfortable in a fast-paced environment and able to adjust workload based upon changing priorities
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Brendan Thalheimer at
(+1) 215-531-5299 or upload your resume on our website - www.proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-BT1
#Compliance/Quality
Related jobs
Highly Competitive
Visp, Switzerland
Join a leading Swiss team as a QC Associate driving excellence in biopharmaceutical quality control.
Highly Competitive
Rockville, USA
Step into a role where precision meets purpose-become a Materials Technician supporting essential pharma and respiratory operations
Highly Competitive
Liverpool, England
Are you passionate about quality and precision? Join our client in this Quality Assurance Representative and help ensure top-tier standards every day.
Highly Competitive
Bristol, USA
Drive cGMP excellence by powering large‑scale downstream manufacturing that brings life‑changing therapies to reality.