Here is an opportunity for an aspiring Quality Assurance professional in the medical industry to take their career to the next level.

Our client, located in Arcadia, CA is a leading manufacturer in their niche and their business continues to grow, even in this recession.  They had a record year in 2008 and are poised for another record year in 2009.

Why you might want to work for this company?​

• They have been in business for over 70 years and have very little employee turnover.​
• Moral is quite high at this company.​
• They continue to introduce new products into the marketplace and are setting record sales numbers even in 2009.
• In their industry this company is highly respected and the products it makes are high quality and in high demand.​
• If you are looking for a stable career position with a company that is growing and can offer you personal career growth--take a further look.​

As a Quality Assurance Specialist for this company here is what you will be doing.  (We are looking for someone that has experience doing this in a similar role):

• Assist the Quality Manager in developing and maintaining quality procedures and reports that measure the quality system.
• Assist the Quality Manager in implementing and maintaining FDA compliance ISO 13485 Certification.
• Assist the Quality Manager in maintaining Internal Audit Program.
• Assist the Quality Manager in maintaining the Corrective and Preventative Action System.
• Assist the Quality Manager in interfacing with various company departments to support the Quality Documentation system.

Requirements:

• Must have 1-3 years of Quality Assurance experience in an FDA/ISO regulated manufacturing environment.
• Must have experience developing operational procedures, including FSA QSR and ISO 13485 Standards.

There is a tremendous opportunity for personal growth within this industry leading company.  If you would like to learn more about this position, please submit a confidential resume to:  mmyers@greaterjob.com .