Novartis is hiring for Specialist – Quality Operations roles, this typically involves responsibilities related to ensuring product quality, regulatory compliance, and overseeing manufacturing or operational processes within the pharmaceutical or healthcare sectors, If you are interested for this position please check below details;
Specialist – Quality Operations
Job ID REQ-10015988
Summary:
Provide quality services in compliance with cGMP requirements and Novartis Quality Management System as defined and agreed between QOP and business partners. Manage Quality aspects & projects within area of responsibility.
Major accountabilities:
· Coordination and management of analytical method transfers and stability studies. Compilation of data reports
· Life-cycle management of analytical methods, including control of method performance, pharmacopoeia and health authority compliance and definition of method improvements. Handling of deviations, investigation, OOS/OOE/OOT cases as well as changes and complaints
· Perform statistical data analysis to report Out of Expectations (OOE), out of trends (OOT), etc
· SAP master data management: Maintenance of master data, creation of Q-info records and other SAP related activities.
· Validate spreadsheets
· Collect, transcribe and/or compile data from various repositories (SAP, LIMS, external COAs)
· Author, approve and archive Impurity risk assessments – Nitrosamines, residual solvents, etc
· Trend and report all QMS elements as per the request
· Monitor, trend and report Health Safety and Environmental parameters
· Implementation of GMP requirements. Compilation and Review of documents (analytical protocols and reports, annual performance quality reports, ongoing process verification reports, registration documents (Common Technical Document modules)).
· Perform activities of a Quality Control expert as defined by the respective sites
· Support regulatory requirements – routine queries, Chromatogram requests
· Compile Quality performance management decks
· Create and review GxP documents including SOPs, working procedures, trend reports, qualification reports and technical investigations, as and when needed
Key performance indicators:
· On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand -Successfully support continuous improvement projects -Executes batch release in compliance with registration
Minimum Requirements:
· Pharmacy/ Science/ MBA / Engineering/ equivalent from a reputed institute
· Min 3 years of experience in Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances/ products/ medical devices
· GxP knowledge, Basic IT knowledge
· Good communication, presentation and interpersonal skills
· Experience of working closely with the global stakeholders
Skills:
· Continuous Learning.
· Dealing With Ambiguity.
· Gmp Procedures.
· Qa (Quality Assurance).
· Quality Control (Qc) Testing.
· Quality Standards.
· Self Awareness.
· Technological Expertise.
· Technological Intelligence.
Languages :
· Fluent in English (written and spoken)
