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QA Specialist
- Permanent
- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), Good Laboratory Practice (GLP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking to hire a QA Specialist located in Houston, TX.
Job Responsibilities:
- Inspection of incoming raw materials, in-process and finished products
- Assist manufacturing with batch release and other relevant documentation
- Assist with post-market monitoring of the company's products
- Assist with training as required
- Assist with maintaining equipment calibration logs
- Assist with maintaining proper documentation of incoming and outgoing product
- Facilitate the periodic review of documents to comply with internal QMS requirements
- Ensure completed documentation meets internal quality standards
- Support the Internal Quality Audit program
- Manage relevant record logs for Quality Events
- Assist in other duties as assigned by the QA Manager
Skills and Requirements:
- Have at least 4-5 years of relevant experience and a relevant bachelor's degree OR at least 8-10 years of relevant experience without a degree, preferably in the Medical Device industry
- Be able to work with a cross-functional team on an international stage
- Be able to communicate effectively in written and spoken English
- Be able to troubleshoot as necessary
- Be able to prioritize tasks effectively
- Show initiative and be proactive in their day-to-day tasks
If you are having difficulty in applying or if you have any questions, please contact Eric White at (+1) 512-354-1710 or e.white1@proclinical.com.
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.
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