Work as Analyst in Artwork Ops at Novartis

 

 

Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

Post : Analyst - Artwork Ops

Job Description
TechOps Support, part of the Operations Services Practice (OSP) within Product Lifecycle Services (PLS), delivers a portfolio of services and solutions to manufacturing and supply processes of Novartis, creating value for the internal customers across all Novartis divisions and geographies.
Analyst Artwork Operations has responsibility to support PLS-M&SO delivery in compliance with cGMP regulatory requirements. The appointed candidate will need to assist and coordinate various Artwork Operations activities in the site and in global projects to ensure regulatory compliant artwork creation for printed packaging materials based on essential parameters.
Analyst Artwork Operations need to provide end-to-end documentation support for artwork activities.
•  Assist in mass Artwork creation / changes in the day to day environment and support major projects in the Novartis Artwork space.
• Supports the Manager – Artwork Ops Artwork Specialists for meeting business priorities to ensure timely delivery of the approved artwork, especially for launches, safety-related changes and transfers to guarantee fast and successful implementation of the Novartis Pharma products on the market (avoid stock-out situations).
• Perform and deliver quality reviews and trends, performance reporting, artworks review and monitoring, audit support and application user support related to Artwork Ops
• Ensure on time In full delivery of service to internal Artwork customers and stakeholders
• Accountable for high-quality artworks fully compliant with Novartis standards and in-country regulatory, marketing, manufacturing and legal compliance.
• TechOps Support, part of the Operations Services Practice (OSP) within Product Lifecycle Services (PLS), delivers a portfolio of services and solutions to manufacturing and supply processes of Novartis, creating value for the internal customers across all Novartis divisions and geographies.
• Generate and analyze predefined and ad-hoc reports in various applications (like AGILE PLM, SALTO, AQWA etc.) and perform follow-up actions if required.
• Create and review GxP documents and reports like trend analysis, performance, qualification, validation and technical investigations.
• Responsible for GMP compliant documentation following external and internal regulatory aspects and processes. Create and review GxP documents and reports like trends, performance, qualification, validation and technical investigations.
• Ensure adherence to Novartis standards and quality manuals
• Ensure compliance to the Novartis internal quality standards, relevant regulatory requirements, filed product quality standards and service level agreements.

Candidate Profile
University or academic degree in Chemistry, Microbiology, Biotechnology, Pharmacy or equivalent Excellent written and verbal communication skills in English as a language Experience in chemical/pharmaceutical industry. Min. 4-7 yrs Experience in Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances or products.

Additional Information
Experience :  4-7 years
Qualification : 
M.Sc, M.Pharm
Location : Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Technical Operations
End Date : 25th May, 2019

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