Bsc Chemistry & Pharma Analyst Job Vacancy @ Novartis

Bsc Chemistry & Pharma Analyst Job Vacancy @ Novartis

Pharmaceutical Science Analyst – ARTWORK OPERATIONS. Applications are invited for the post of Analyst @ Novartis.Career @ Novartis. Pharma job opportunity at Novartis. Analyst vacancy. Interested candidates may apply online. Check out all the details on the same below:

Job Id: 259858BR


Eligibility: Bachelors or University degree in Chemistry, Pharmacy or equivalent


Excellent written and verbal communication skills in English as a language Experience in the chemical/pharmaceutical industry. Min. 4-7 yrs Experience in Artwork Change Coordination, Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances or products.

Job Description:

  • 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 creation and implementation of CAPAs for deviations and performance improvement for all involved parties. Escalate, lead or support service-related GxP and non-GxP issues to ensure timely investigation and compliance with local and global operating procedures.
  • Support in enhancing quality drivers like upgrading standard operating procedures, working procedures and process charts as per business requirements.
  • Create, maintain and archive all documents related to Artwork Operations. Ensure that sufficient and relevant records are in place in line with Novartis standards.
  • Adherence to the service KPI’s and ensuring

Apply Online

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