Vacancy expired!
- Develop protocols
- Provide execution support, data analysis, and report generation for multiple installation, operational, and performance qualification activities
- Analyze and troubleshoot validation problems
- Ensure qualification activities are in accordance with internal, cGMP industry, and regulatory guidance
- Act as initiator and owner of validation related change controls and corrective and preventative actions
- Ensure all aspects of facilities meet policies and procedures, including safety and training
- Executing thermal mapping of the facility
- Support implementation of validation programs (e.g., requalification)
- Initiate and/or assist with investigations into protocol non-conformances and site deviations
- Provide input to standard operating procedures related to validation practices
- Bachelor’s degree in Science, Engineering, or related field
- At least 2 years of experience in pharmaceutical or biotech industry
- Proven understanding of cGMP
- Familiarity of compliance and regulations
- Strong problem solving and analytical skills
- Excellent verbal and written communication skills
- ID: #40279562
- State: Rhode Island Cumberland 02864 Cumberland USA
- City: Cumberland
- Salary: USD70,000 - USD75,000
- Job type: Permanent
- Showed: 2022-05-05
- Deadline: 2022-07-03
- Category: Et cetera