R&D Partners is seeking to hire a Quality Specialist Validation in Indianapolis, IN.
Your main responsibilities as a Quality Specialist - Validation :
Assists in the development of cGMP operating procedures that relate to process, computer systems, and equipment validation.
Assures compliance with SOPs upon implementation. Investigates and proposes additional corrective actions as required.
Communicates with Field Quality/Operations and other Operational and Quality Assurance personnel where necessary on Donor Center compliance and cGMP issues.
Assists in ensuring validation approaches are current to regulatory expectations and standards within the industry:
Write test cases to validate critical control points, user requirements, and functional designs.
What we are looking for in a Quality Specialist - Validation:
Bachelor's degree
Work is performed in an office and a laboratory/manufacturing environment.
Exposure to biological fluids with potential exposure to infectious organisms.
Exposed to occasional extreme cold below 32* and high levels of noise in production areas.
Exposure to electrical office and laboratory equipment.
Why Choose R&D Partners ?
As an employee, you have access to a comprehensive benefits package including:
Pay Scale:
$69,409 $104,124 Dependent on Experience)
R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&D Partners is an equal-opportunity employer.
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