|Interested? Email Us||Never Applied? Apply|
|Quality Associate I|
|Hours:||40 Monday Friday 8AM to 5PM|
|Pay:||DEPENDS ON EXP|
|Great opportunity in Camarillo CA|
Collaborate with the Quality oversight of manufacturing operations. Supports investigationsdeviations of non-conformance reports. Management of GMP documentations for area of operations and associated processes. Management of documentation, including real time manufacturing review, approval and archiving. Provide plant floor Quality oversight to maintain an inspection ready facility.ResponsibilitiesResponsible for all activities involving quality assurance and compliance with applicable regulatory requirements.Supports the generation of product Certificate of Compliance CoC.Responsible for creating GMP labels, and reviews and reconciles GMP generation Ensures that all inspections and procedures are properly completed and documented.Verify logs, and other data to track and flag quality concerns and improvements.Ensures documents are entered in the quality databases, scanning, indexing, filing and archiving.Work with organization team members to audit, identify quality problems, and improve operational processes. Performs logbook documentation audits for GMP regulated logs and SOPs. Responsible for the scanning and organization of the Batch Records and supporting documents within the Document Management Systems.Backup support for QC Inspection to assist with first article, in-process inspections and final QC release of finished goods.
HS. 0 to 3 years of experience in quality assurance or technical documentation for quality activities such as quality inspections, corrective actions,change control in a pharmaceutical or medical device environment.
Bachelors degree in a technical or scientific skill