QA Associate Quality Engineer - Night Shift Job in , Operations Career, Full Time Jobs in Novartis Pharmaceuticals
Sign in
Create a candidate account
Create a candidate account
Create an employer account
Sign in to an existing account
Create a candidate account
Create an employer account
Sign in to an existing account
Forgot password
Forgot password
Sign in
Create a candidate account
Sign in
Create an employer account

Hirelifescience_728x90

QA Associate Quality Engineer - Night Shift job

Vacancy has expired

Sign in
Create a candidate account
Novartis Pharmaceuticals jobs
Job Code:  249117BR
Employer:  Novartis Pharmaceuticals
Category:  Operations
Job Type:  Full Time
Country:  United States
Map: 
09/05/2018

Description
The Assoc Quality Engineer - Operations will lead activities involving product impact assessments, product quarantine, non-conformance reporting/issue resolution, auditing of production areas, and procedural updates to ensure the process and documentation is compliant to 21CFR820, ISO and internal requirements.

Audits personnel and processes in manufacturing areas for practice versus procedures and against current regulatory requirements (FDA, ISO, etc.). Analyse audit results for trends and provide feedback to QA Ops Management and QA team. Actively participates in Production Triage team as the lead Quality member by providing direction and support on the non-conformance process, product impact assessment, root cause analysis and product quarantine as non-conformances arise. Ensures non-conformance reports are initiated per established requirements and applicable activities are identified and implemented. Responsible for performing Product Quarantine activities, such as entering product into quarantine, completing quarantine documentation, reviewing/disposition non-conformance records for quarantine release and removal of product from quarantine area. Initiates and leads QA Ops process improvements from start to implementation including creating /revising procedures using the Change Control process. Interact in a team environment with Operations, Quality Engineering, Compliance, and Engineering personnel and participate in work groups to help improve the process and increase product quality while keeping within compliance with site Quality Systems procedures.
Develop quality system processes that meet corporate, government and international regulations Identification of issues and non-conformances Prioritizing workload to meet compliance and quality requirements. Recommending actions for continuous process improvement, increased product quality and compliance risk reduction. Shutting down production equipment and processes suspected of having quality issues. Placing non-conforming product on hold.Bachelor's Degree or equivalent years of directly related experience. The ability to fluently read, write, understand and communicate in English. No experience required.
ref: (249117BR)
Back to search results

Popular locations: New Jersey (NJ) (514) | Maryland (MD) (346) | Pennsylvania (PA) (186) | Texas (TX) (173) | California (CA) (119) | Massachusetts (MA) (116) | Delaware (DE) (106) | North Carolina (NC) (95) | Indiana (IN) (66) | Wisconsin (WI) (36)

Popular categories: Research and Development (457) | Sales (266) | Operations (149) | Clinical Research (120) | Information Technology (94) | Business Development (83) | Other (79) | Sales and Marketing (68) | Laboratory (63) | QA (60)

Popular jobs: Manager (474) | Director (383) | Sales (371) | Associate Director (156) | Account Manager (131) | Business Development (84) | Project Management (83) | Senior Specialist (42) | Clinical Data Management (32) | Bioinformatics Scientist (26)