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Quality Assurance Specialist - Birmingham, AL, United States - BuildSubmarines
Description
Complaint Handling
• Work with multifunctional teams (R&D, Manufacturing, Operational Compliance, and Engineering to drive resolution to product complaints
Verification, Validation and Qualification
o Process validation
o Cleaning validation
o Facility/cleanroom validation
o Equipment qualification
JOB DESCRIPTION SUMMARY
This position is responsible for providing quality and technical support to the production team providing oversight to manufacturing rooms and laboratories by reviewing and approving data and all other Quality Management System documentation. The position utilizes risk management, quality planning and statistical analysis to complete assigned tasks.
PRINCIPAL ACCOUNTABILITIES
Routine Quality Assurance functions, to include but not limited to:
Manufacturing Support
Provide real time production floor QA oversite
Evaluate manufacturing data for trends and other special causes
Review and disposition manufacturing / packaging batch documentation
Perform room / line clearances as needed
Review and disposition raw materials / components for manufacturing
Support resolution of quality issues in manufacturing
Product and Process Development
Represent quality department on development project teams
Review and approve product and process-related documentation
Support the generation and justification of product and materials specifications
Deviations/ CAPA
Support Deviation / CAPA investigations
Support interdisciplinary teams for root cause analysis of quality deficits using known of problem solving tools
Failure reports for products in the field
Identification of potential failure modes and risks
Resolving of customer issues appropriately
Continuous Improvement
Support product quality and System improvements activities
Support collection and analyze data to identify opportunities for quality improvement
Complaint Handling
Work with multifunctional teams (R&D, Manufacturing, Operational Compliance, and Engineering to drive resolution to product complaints
Risk Management
Support to facilitate risk assessment activities such as design and process FMEA
Ensure product risks are identified and risk mitigation controls are put in place to eliminate product risk to an acceptable level
Verification, Validation and Qualification
Provide support for the development of validation strategies and validation plans
Review / approve protocols and reports
Design verification
Process validation
Cleaning validation
Facility/cleanroom validation
Equipment qualification
REQUIREMENTS
Bachelor of Science degree in Chemistry, Biology, or Engineering , preferred.
Minimum two to three years' experience in pharmaceutical or medical device manufacturing
Minimum two to three years' experience in a pharmaceutical or medical device Quality Assurance role
Proficient computer skills, Microsoft Word, Excel, Access
High attention to detail, organization, and accuracy
Strong written and verbal communication skills
Good interpersonal skills
Knowledge or understanding of FDA's cGMP and / or QSR quality system requirements
Experience in Regulatory Agency inspections , preferred
Experience in aseptic techniques and manufacturing , preferred.
Your Application
To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal . Further information about Evonik as Employer can be found at .
Please address your application to the Talent Acquisition Manager, statingyour earliest possible starting date and your salary expectations.
Your Talent Acquisition Manager:
Vincent Szewczyk [C]
Company is
Evonik Corporation