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Quality Assurance Specialist III
Job ID:00004J5N
Category:Quality Control
Location:CA Camarillo
Hours:40 Monday to Friday 8am to 5pm
Pay:$55,000.00 $70,000.00
Career Opportunity Available in Camarillo
Job Description
Collaborate with stakeholders to the management of the Quality System. Recommend and implements changes to the existing quality system with regards to nonconforming product, correctivepreventive actions, document control, quality control inspections and product release, internal audits, validations and equipment calibration and maintenance programs. Responsible for all activities involving quality assurance and compliance with applicable regulatory requirements. Regulatory submissions and compliance with applicable national and international regulations. Conducts audits and reviewsanalyzes data and documentation. Manage internal audit program and support QMS related activities. Host customer audits. Perform supplier audits, support supplier audit program. Initiate, investigate and complete corrective actions CA. Participate in the MRB meetings. Includes ability to apply problem solving tools and methods to coordinate andor lead investigation teams. Participate in the management and execution of equipment, process and software validation. Manage the equipment calibration and maintenance program. Provide directions for all aspects of testing related to manufacturing. First article inspections. In-process release inspection. Final QC release of finished goods. Document review. Ensures that all inspections and procedures are properly completed and documented. Review all quality assessment results and determine whether to accept or reject manufactured products during the inspection process. Perform environmental monitoring of cleanrooms and bioburden results. Provides solution for microbial failures. Assists department with continuous improvements initiatives or lean projects. Can serve as Quality Assurance representative on facility projects. Respond to customer complaints and collaborate with internal departments for resolution and preventative corrective actions.BENEFITS include Medical, Dental and Vision Insurance, 401K plan with company match, 3 weeks of PTO, 9 pa
Skills Required
BA Degree in Business, Science or Engineering. 5+ yrs exp in quality operations within a biotech or pharmaceutical manufacturing facility. Exp w root cause analysis and investigations. Initiation closure of CAPAs.
Skills Preferred
Exp with quality audits, validation of manufacturing processes, or product development in a pharmaceutical or medical device environment.