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Backtrace:

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Line: 144
Function: strpos

File: /home/optresume/public_html/application/controllers/Inhouse.php
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A PHP Error was encountered

Severity: 8192

Message: strpos(): Non-string needles will be interpreted as strings in the future. Use an explicit chr() call to preserve the current behavior

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Backtrace:

File: /home/optresume/public_html/application/controllers/Inhouse.php
Line: 146
Function: strpos

File: /home/optresume/public_html/application/controllers/Inhouse.php
Line: 207
Function: inhouse_job_details

File: /home/optresume/public_html/index.php
Line: 315
Function: require_once

A PHP Error was encountered

Severity: 8192

Message: strpos(): Non-string needles will be interpreted as strings in the future. Use an explicit chr() call to preserve the current behavior

Filename: controllers/Inhouse.php

Line Number: 146

Backtrace:

File: /home/optresume/public_html/application/controllers/Inhouse.php
Line: 146
Function: strpos

File: /home/optresume/public_html/application/controllers/Inhouse.php
Line: 207
Function: inhouse_job_details

File: /home/optresume/public_html/index.php
Line: 315
Function: require_once

Sterility Assurance Job In Splintpharma At Kankakee, IL

Sterility Assurance Specialist senior QA Consultants Details

splintpharma - Kankakee, IL

Employment Type : Full-Time

Sterility Assurance Specialist senior QA Consultants, Kankakee, IL on site near Chicago with a possibility of extensionResponsibilities
• Conducts Minor / Major / Critical Deviation investigations in their respective areas as necessary and documents such investigations appropriately
• Leads Root Cause Analysis to identify the most probable root cause, determine product impact, and assign appropriate CAPAs with responsibilities and due dates
• Performs trending to identify and report adverse trends that may require further action
• Completes investigations within the specified time-frames
• Develops corrective and preventative actions to prevent problem recurrence and establishes an effective follow-up system to ensure corrective and preventative actions have been implemented and are effective
• Reports performance metrics to Project Leader on a periodic basis

Requirements
• Bachelor’s degree from an accredited college/university
• Appropriate written and verbal communication skills in English and in any other relevant language(s)
• At least 7 years of experience in Pharmaceutical industries, with biologics and/or biotech products preferred
• Knowledge and experience with aseptic processing
• Expert level understanding of deviation resolution for manufacturing processes and CAPA management
• Previous experience with remediation plans for the FDA
• Expertise in other QA tasks that include PQR, auditing, change control, complaints management, OOS, batch record review, documentation management, training, supplier management)