Supplier Quality Specialist Job in New Jersey (NJ), Laboratory 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

Supplier Quality Specialist job in Morris Plains

Sign in
Create a candidate account
Novartis Pharmaceuticals jobs
New Jersey (NJ), Morris Plains
Job Code:  247845BR
Employer:  Novartis Pharmaceuticals
Category:  Laboratory
Job Type:  Full Time

Location
Country:  United States
State:  New Jersey (NJ)
City:  Morris Plains
Map: 
09/05/2018

Description
• Support the audit function for vendors, suppliers, service providers and contracts. Assists with supplier qualification activities of new and current suppliers in support of Clinical and Commercial Manufacturing activities. • Maintain the Supplier Quality program, policies, and procedures ensuring that performance and quality of the of the program conform to established standards, such as QSR/GMP, Novartis Quality Modules and policies and procedures • Coordinate / Support the communication of the audit schedule and executing to plan as required by local procedures and regulatory requirements. • Conducts Supplier Quality Audits in accordance with Novartis Morris Plains Audit Plan. Travel is approximately 30%. Maintain adherence to the supplier audit schedule and in line with Quality System requirements. • Provides written reports and observations in a timely manner and assure correctives are adequate and timely. Support the AQWA FURP and QARP Coordination for the Morris Plains facility as needed with external audits. • Maintain supplier monitoring program for all commercial suppliers and provide feedback to sup-plier on a routine basis. • Assists with ensuring site quality metrics are compiled and submitted per established deadlines for the Novartis Dashboard and Site Management Reviews. • Initiates, reviews and approves Deviations, CAPA's, change controls, Raw Material Specifications and any other site/product related documents in support of the Novartis Morris Plains facility ensuring adequate levels of documentation are adequate and compliant to existing procedures. • Write, review and approve Standard Operating Procedures (SOPs), Quality Risk Assessments (QRAs), specifications,), as needed. • Coordinate / Support the Supplier Quality Review Board and Supplier Quality Vendor Changes meeting and the approval process for new vendors / materials. • Lead / participate on quality manual implementation teams in area of technical expertise as required.Bachelors or higher in Chemistry, Pharmacy, Microbiology or another related science. English: fluent in reading, speaking, and writing. Additional language(s) preferred. Minimum: 5+ years GMP manufacturing and/or QA related experience, at least 3 years of which are in the area of Sup-plier Quality. Preferred: 7+ years in a medical device/ pharmaceutical manufacturing environment or applicable industrial experience. Applicable Certifications (i.e. ASQ certified like Certified Quality Auditor (CQA), or Certified ISO 9000 Assessor (RAB).
ref: (247845BR)
Back to search results

Popular locations: New Jersey (NJ) (521) | Maryland (MD) (340) | Pennsylvania (PA) (189) | Texas (TX) (175) | California (CA) (117) | Massachusetts (MA) (111) | Delaware (DE) (106) | North Carolina (NC) (106) | Indiana (IN) (68) | Wisconsin (WI) (38)

Popular categories: Research and Development (460) | Sales (266) | Operations (147) | Clinical Research (118) | Information Technology (92) | Other (84) | Business Development (83) | Other (81) | Sales and Marketing (64) | Laboratory (59)

Popular jobs: Manager (469) | Director (380) | Sales (348) | Associate Director (160) | Account Manager (132) | Business Development (90) | Project Management (79) | Senior Specialist (39) | Bioinformatics Scientist (25) | Clinical Data Management (21)