What are the responsibilities and job description for the Quality Specialist - Validation position at The Fountain Group?
The Fountain Group is currently seeking a Quality Specialist - Validation for a prominent client of ours. This position is located in Durham, NC. Details for the position are as follows:
Title: Quality Specialist - Validation
Location:Durham, NC
Shift: 1st shift
Duration: 4 months (Possible extension/conversion based on performance and budget)
Hourly Rate on W2: $35- $40
Position Summary:
Ensures current Good Manufacturing Practices (cGMP) and FDA/*** Quality Systems are adhered to throughout the evaluation, review and approval of validation and quality assurance/control documentation
Key Responsibilities:
Required Qualifications:
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Title: Quality Specialist - Validation
Location:Durham, NC
Shift: 1st shift
Duration: 4 months (Possible extension/conversion based on performance and budget)
Hourly Rate on W2: $35- $40
Position Summary:
Ensures current Good Manufacturing Practices (cGMP) and FDA/*** Quality Systems are adhered to throughout the evaluation, review and approval of validation and quality assurance/control documentation
Key Responsibilities:
- 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.
- Execute test cases as needed.
- Interacts with Donor Center and Field Quality/Operations personnel to facilitate validation testing to ensure timely and documented approval prior to implementation for routine use. "
- Assists in analyzing validation data to ensure acceptance criteria are met.
- Assists in writing validation summaries.
- Ensure milestones and timelines are met on assigned projects.
- Prepares validation reports for distribution.
- Evaluates adequacy of corrective actions.
- Participates in the evaluation of processes, systems, and individual center equipment needs and final approval process:
- Prepares validation equipment for use at the Donor Center and for evaluation upon return.
- Assists in identifying and determining actions to add, remove, and/or revalidate processes, systems, and equipment, including evaluation of new/updated methodologies/applications/equipment and resolution of issues or problems with performance, transfer, or service. "
- Tracks and monitors process/system failures/events. Provides feedback to Donor Center management regarding requirements, results from data collected, and validation processes. "
- Tracks and monitors equipment calibration due dates and calibration failures/events. Provides feedback to Donor Center management regarding equipment calibration due dates, requirements, results from data collected, and validation processes. "
- Monitors and trends customer complaints and nonconformance related to equipment failures.
Required Qualifications:
- Bachelor's degree
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy
Salary : $35 - $40