Job Description Summary
-Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.
Job Description
Major Accountabilities
*Execute the main activities according to prepared SOPs and laboratory rules.
*Fulfill the responsibilities, which are given by AS&T team Lead and QC manager at the right time and correctly in conformance with methods, procedures and workflow.
*Following the global analytical method development studies, current guidelines and pharmacopoeias.
*Prepare analytical method development, re-validation, validation, transfer and stability protocols and reports.
*Create and revise SOPs, FRMs.
*Participate in laboratory investigations.
Minimum Requirements
*University degree in Pharmacy, Chemical Engineering or Chemistry.
*Approx. 3 to 5 years in pharmaceutical industry and/or analytical laboratory in GMP environment.
*Experience with equipment e.g. HPLC, GC, UV/Vis.
*Knowledge of cGMP&cGLP.
*Ability to work in a fast-paced changing environment.
*Team working and costumer-oriented mindset.
*Strong interpersonal written and verbal communication skills.
*Good knowledge of MS Office and other standard IT applications.
*Fluent in English.
Skills
*Communication skills
*Continuous learning
*Decision making skills
*Self-awareness
Skills Desired
Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence
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What We Do
Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.
