Expires soon SANDOZ

Validation Specialist

  • Morris Plains (Morris)

Job description

Job Description

The Validation Specialist is responsible for ensuring compliance to the regulatory requirements of the facilities, utilities, equipment and analytical instruments qualification processes and activities performed in the Novartis, Morris Plains, NJ facility. Recommends and implements improvements of the qualification process. Performs a variety of routine and non-routine tasks related to facilities, utilities, equipment and analytical instruments qualification, as managing and overlooking qualification projects and changes. Prepares risk and impact assessments and other evaluations. Supports Process Unit (PU), Manufacturing, Science and Technology (MS&T), Operations (OPS), Quality Control (QC) and Quality Assurance (QA) departments.

Responsibilities:
• Coordinates Qualification activities in compliance with corporate policy, local procedures and regulatory expectations
• Coordinates and develops with PU, MS&T, OPS, QC and QA Teams qualification projects and plans and identifies the “critical to quality” parameters impacting qualification activities
• Prepares Qualification Master Plans, Risk and Impact Assessments, Protocols and Summary Reports and coordinates review and approvals of the documents
• Authors/reviews/updates/assists in developing departmental standard operating procedures (SOPs) and qualification programs
• Conducts field execution of Installation, Operational and Performance Qualification protocols
• Assists PU, MS&T, OPS, QC and QA colleagues, as necessary
• Ensures that all activities are in compliance with cGMP, Health Authority regulations and the Novartis Policies
• Determines of Qualification requirements based on a worst case matrix approach for the site
• Provides qualification solutions that meet regulatory requirements within budget, where applicable.
• Supports/assists 3rd party/ vendor qualification activities, if applicable.
• Support qualification/validation projects as allocated.
Posting Title

Validation Specialist

Desired profile

Minimum requirements

Education:
BS degree in Scientific discipline or other related field with significant prior experience (5+ years) or equivalent.

Langauge:
Fluent in English General, 3-5 years of Pharmaceutical industry experience required.

Experience / Skills:
2-5 years of Facilities, Utilities, Equipment and Analytical Instruments Qualification experience or applicable experience in a related area in the Pharmaceutical industry.
Job Type

Full Time
Country

USA
Work Location

Morris Plains
Functional Area

Quality
Division

Novartis Technical Operations
Business Unit

NTO BTDM
Employment Type

Regular
Company/Legal Entity

Novartis Pharmaceuticals
EEO Statement

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

Make every future a success.
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