Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Manufacturing Specialist
Posted: 02/20/2025
2025-02-20
2025-04-24
Employment Type:
Contract
Job Category: Engineering
Job Number: 617940
Is job remote?: Yes
Country: United States
Job Description
Target PR Range: 34-44/hr
*Depending on experience
Remote - Any time zone
IDEAL CANDIDATE: B.S. + 3-5 YOE
Quality records experience working with suppliers would be a home run candidate.
The ideal candidate should have previous experience managing quality records as owner (such as deviations, change control, supplier investigations/etc. Preferred experience managing in Track Wise or Veeva Systems
Basic project management skills required.
The Specialist Manufacturing is expected to own and execute under minor supervision all the processes related to deviations (minor and majors), Corrective and Preventive Actions (CAPAs), CAPA-Effectiveness Verifications, Supplier Event Notifications and Investigations (SICAR /EN), and Change Control quality records. This Specialist Manufacturing will act as the External Supply representative across functional teams and drive closure of quality records in a timely manner. The Specialist Manufacturing, External Supply owns and manages quality records originating from manufacturing sites across the network.
Responsibilities:
- Address and close quality records (Deviations, Corrective and Preventive Actions (CAPAs), CAPA-Effectiveness Verifications, Supplier Event Notifications and Investigations (SICAR /EN), and Change Control) under the company's quality management system procedures and ensures compliance with regulatory agency requirements.
- Monitors and investigate deviations owned by External Supply and implements corrective / preventive actions. Partner cross-functionally across the site to ensure maturity and execution of robust Deviations / CAPA process
- Build and present quality records summaries for Senior Management review. Provide timely and comprehensive process and status updates to senior management
*CO/NYC candidates might not be considered
*Depending on experience
Remote - Any time zone
IDEAL CANDIDATE: B.S. + 3-5 YOE
Quality records experience working with suppliers would be a home run candidate.
The ideal candidate should have previous experience managing quality records as owner (such as deviations, change control, supplier investigations/etc. Preferred experience managing in Track Wise or Veeva Systems
Basic project management skills required.
The Specialist Manufacturing is expected to own and execute under minor supervision all the processes related to deviations (minor and majors), Corrective and Preventive Actions (CAPAs), CAPA-Effectiveness Verifications, Supplier Event Notifications and Investigations (SICAR /EN), and Change Control quality records. This Specialist Manufacturing will act as the External Supply representative across functional teams and drive closure of quality records in a timely manner. The Specialist Manufacturing, External Supply owns and manages quality records originating from manufacturing sites across the network.
Responsibilities:
- Address and close quality records (Deviations, Corrective and Preventive Actions (CAPAs), CAPA-Effectiveness Verifications, Supplier Event Notifications and Investigations (SICAR /EN), and Change Control) under the company's quality management system procedures and ensures compliance with regulatory agency requirements.
- Monitors and investigate deviations owned by External Supply and implements corrective / preventive actions. Partner cross-functionally across the site to ensure maturity and execution of robust Deviations / CAPA process
- Build and present quality records summaries for Senior Management review. Provide timely and comprehensive process and status updates to senior management
*CO/NYC candidates might not be considered
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