Job Opportunities in Turkey
July 2, 2024
Sandoz
Gebze
OTHER
AS&T Specialist-1
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 pharmacopeia.
•Routinely assess testing monographs and proactively sustain compliance of all activities with current official regulations, pharmacopeias, QM, QD, GOP and SOP.
•Evaluate and implement new technologies required to maintain state-of-the- art analytical methods for development and marketed products.
•Execute analytical method development, pre-validation and validation studies.
•Ensure right first time in all analysis and documentation.
Minimum Requirements:
•University degree in Pharmacy, Chemical Engineering or Chemistry
•Minimum 5 years of Analytical Laboratory experience with equipment e.g. HPLC, GC, UV/Vis and Wet Chemistry preferably at a pharmaceutical company with FDA approval.
•Knowledge of c GMP& c GLP and basic SAP
•Ability to work in a fast-paced changing environment
•Team working and customer-oriented mindset
•Good analytical thinking skills
•Strong interpersonal written and verbal communication skills
•Good knowledge of MS Office applications
•Good command of English is required
Work Experience:
• Sound technical & scientific knowledge of pharmaceutical/ chemical.
• analytics/QC/R&D/ equivalent.
Skills:
• Communication Skills.
• Continuous Learning.
• Dealing With Ambiguity.
• Decision Making Skills.
• Gxp.
• Industry Standards.
• Laboratory Equipment.
• Laboratory Excellence.
• Self Awareness.
• Technological Expertise.
• Total Quality Management.
Languages :
• English (Advanced)
•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 pharmacopeia.
•Routinely assess testing monographs and proactively sustain compliance of all activities with current official regulations, pharmacopeias, QM, QD, GOP and SOP.
•Evaluate and implement new technologies required to maintain state-of-the- art analytical methods for development and marketed products.
•Execute analytical method development, pre-validation and validation studies.
•Ensure right first time in all analysis and documentation.
Minimum Requirements:
•University degree in Pharmacy, Chemical Engineering or Chemistry
•Minimum 5 years of Analytical Laboratory experience with equipment e.g. HPLC, GC, UV/Vis and Wet Chemistry preferably at a pharmaceutical company with FDA approval.
•Knowledge of c GMP& c GLP and basic SAP
•Ability to work in a fast-paced changing environment
•Team working and customer-oriented mindset
•Good analytical thinking skills
•Strong interpersonal written and verbal communication skills
•Good knowledge of MS Office applications
•Good command of English is required
Work Experience:
• Sound technical & scientific knowledge of pharmaceutical/ chemical.
• analytics/QC/R&D/ equivalent.
Skills:
• Communication Skills.
• Continuous Learning.
• Dealing With Ambiguity.
• Decision Making Skills.
• Gxp.
• Industry Standards.
• Laboratory Equipment.
• Laboratory Excellence.
• Self Awareness.
• Technological Expertise.
• Total Quality Management.
Languages :
• English (Advanced)
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