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Quality Assurance Director
| Details |
Country: USA
Location: California CA
Total applied: 40
Location:US-CA-California
Base Pay:$90,000 - $110,000/Year
Commission:
$0.00
Other Pay:
Excellent Benefits & 401kEmployee Type:Full-Time Employee
Industry:Biotechnology Pharmaceutical Medical Equipment
Manages Others:yes |
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Quality Assurance Director
National Careers Corp. has an excellent opportunity for a Regulatory Affairs and Quality Assurance Director. This outstanding position is with Santa Barbara/Ventura County's most innovative and successful industry leaders.
The ideal candidate for this opportunity will direct RA/QA and will be responsible for implementation and maintenance of the company’s regulatory affairs and quality systems to ensure compliance with internal policies, procedures, customer requirements, external regulations and standards (FDA). Responsibilities also include internal and external auditing, training, document control, product complaints and final technical review of commercial and clinical products. The selected candidate will make recommendations for quality and compliance. Additional duties will be assigned. Some travel will be required.Please send your resume to Dixie Vargas, [Click here for email] for immediate consideration. You may call with your inquiry to (800) 639-3640 ext. 243.The competitive salary for this opportunity is based on each individual candidate’s professional experience and includes excellent benefits and 401k.National Careers Corp. offers many career opportunities. If you are interested in sales, management, executive, senior administration and much more, National Careers Corp. can find you competitive compensation and benefits with full time, permanent positions always available. Be sure to visit our website and register, http://www.nccx.com.
REQUIREMENTS
Requirements of this opportunity include and are not limited too;Bachelor’s degree- related fieldMasters preferred but not required
10 – 12 years related experience (medical device, pharmaceutical, in vitro diagnostic pref)
Problem solving ability
Multi tasking and prioritizing ability
Project management experience
Ability to make presentations written and orally
Experience with FDA 501 (k)
Experience with reporting on compliance with Federal and International regulations and standards including EN 46001, ISO 13485, ISO 9001, IVDD
Computer literacy including MS Word, Excel, Outlook, Power Point, Access
Experience using ERP/MRP
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