Quality Engineer (Otc And Cosmetic Sterile/Non:Sterile)

Quality Engineer (Otc And Cosmetic Sterile/Non:Sterile)
Empresa:

Sqa Services


Quality Engineer (Otc And Cosmetic Sterile/Non:Sterile)

Detalles de la oferta

Job Description

This is temp. to a permanent hire job. All expenses are paid for anyone not local for the first three months, including hotel, rental car, meals and one weekend a month of home trip for the first three months.

The Quality Engineer will be responsible for the execution of assigned activities for technical support and process validation related to new products, process, equipment, and troubleshooting of current processes associated with OTC and Cosmetic Sterile/Non:Sterile Liquids (Compounding, Filling, and Testing ) and Powder Products (Blending, Capsule and Reservoir Filling of Devices). Interacts with production personnel, equipment engineering and QC Lab as well as provides some assistance and direction for less experienced engineering and technical personnel. Responsible for the execution and processing of product complaint investigations.

Execute assigned projects for the implementation of new processes, problem solving for existing processes, process optimization and process validation activities. Generate related documents including SOPs, Batch Documentation, Validation Plans, Protocols and Evaluations. Develop and execute design of experiments (DoE) to support the development and registration of manufacturing processes used to produce clinical and commercial products. Provide technical and operational support to meet customer commitments (internal and external). Support technology transfer from client or product development into the facility and, when applicable, to commercial manufacturing.

Requirements

Bachelors degree in chemical engineering or life sciences
5+ years relevant experience
Direct experience with MDI and Sterile/Non:Sterile Processes
Conduct DOEs for process development and process improvement
Ability to statistically analyze data in support of technical and regulatory documents
Knowledgeable in cGMPs and regulatory requirements
Familiar with the activity sequence for process investigations and/or Root Cause Analysis
Knowledgeable in principles of process validation and cGMPs
Company Description
SQA Services is a leading Supply Chain and Quality Assurance consulting firm specializing in the management of Supplier Audit, Quality Engineering, Inspection, and Remediation programs in the Aerospace/Defense, Medical Device, Pharmaceutical, Cosmetic, and Automotive manufacturing industries. Clients leverage our network of quality professionals in more than 50 countries as an extension of their own supplier quality teams.


Fuente: Tiptopjob_Xml


Área:

  • Production - Manufacturing / Manufacturing Engineer
  • Production - Manufacturing / Manufacturing Quality Engineer
  • Production - Manufacturing / Manufacturing Coordinator

Requisitos

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