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Quality Assurance Mananger

Details
Posted By:
Teddi Franklin Hammer
Posting ID:
3869s3318
Location:
Los Angeles, Ca
Telephone:
310-798-6979
Tags:
 iso   lead   audit   health   and   beauty   industry 
Category:Biotech / Science
Listing Type:Job
Employment:Full Time
Company:Zimmerman and Associates staffing firm

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Basic Purpose
Oversee daily QA/QC activities, ensure raw material, component, in-process and finished products are released properly. Supervise QA/QC staff including QA & QC Supervisors, Lab Technicians, QA Floor Inspector, and Incoming QA. Perform and manage Nonconforming materials and products. Evaluate and validate production processes including compounding manufacturing processes, filling and packing processes, water system, cleaning and sanitization.
Essential Duties and Responsibilities
Review daily component and raw material receiving reports, ensure each raw material and component have specifications and are released properly.
Review batch record for in-process and finished products to ensure products are released properly.
Manage production records, component and raw material receiving records, master formula records, raw material and finished product retain samples.
Oversee daily QA/QC staff activities and needs.
Initiate and investigate any nonconforming materials or products, issue and manage corrective action to prevent reoccurrence if necessary.
Establish testing requirements for each product, manage testing by outside testing laboratories, and validate testing methods.
Evaluate new raw material, component, and product.
Manage chemical waste disposal.
Evaluate validation requirements for manufacturing and production processes.
Conduct validation activities and prepare reports for approval.
Train department and other departments as required.
Assist the head of Quality Department to ensure quality records meet FDA and ISO 9001-2000 requirements.
Other duties and responsibilities as may be required by the head of Quality Department or management team

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