Armando Carlone
Quality Assurance Officer at Micro-Sphere SA- Claim this Profile
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Bio
Federico Antonelli
Armando was part of my team and always show great commitment and proactiveness. The team was in a difficult phase of change but he brought passion for the result and quality for his work. Point of strength of Armando are quality, precision, commitment and passion. You always can count on him
Federico Antonelli
Armando was part of my team and always show great commitment and proactiveness. The team was in a difficult phase of change but he brought passion for the result and quality for his work. Point of strength of Armando are quality, precision, commitment and passion. You always can count on him
Federico Antonelli
Armando was part of my team and always show great commitment and proactiveness. The team was in a difficult phase of change but he brought passion for the result and quality for his work. Point of strength of Armando are quality, precision, commitment and passion. You always can count on him
Federico Antonelli
Armando was part of my team and always show great commitment and proactiveness. The team was in a difficult phase of change but he brought passion for the result and quality for his work. Point of strength of Armando are quality, precision, commitment and passion. You always can count on him
Credentials
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Time Management: Working from Home
LinkedInOct, 2020- Sep, 2024 -
Project Management Foundations: Quality
LinkedInMay, 2020- Sep, 2024 -
Analytical Skills
HPLC, LC-MS / MS, UV, Dissolution Rate Testing, Karl Fischer Chromelon, Analyst, SAP P75, AQWA Trackwise System QC Release and Stability Analysis for Inhalation Drug Products Using Andersen Cascade and Next Generation Impactor
Experience
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Micro-Sphere SA
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Switzerland
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Quality Assurance Officer
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Jan 2022 - Present
Quality Officer in Production and Quality Control Area: Ensure batch records are prepared for production per production schedule Review all batch documentation for accuracy and completeness Adhere to site policies and cGMP requirements while reviewing batch documentation Ensure work instructions and SOPs are followed Effectively resolve documentation discrepancies and issues with manufacturing operations personnel in a timely manner to allow for material release Address deficiencies and ensures timely completion of all follow-up actions for resolution to all batch review issues according to cGMP Assist in resolving quality problems/concerns related to batch review Build quality into all aspect of the product manufacturing and release process by maintaining compliance to all quality requirements Assist in Regulatory and Internal Audits / Inspections Actively collaborate as QA member during GMP training sessions for production Personnel Collaborate in the definition, management, and implementation of CAPAs Actively collaborate for continuous improvement making proposals to improve inefficient processes Show less
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Novartis
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Switzerland
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Pharmaceutical Manufacturing
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700 & Above Employee
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Novartis Facility Manager and Site SAP Super User
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Jan 2021 - Jan 2022
In this capacity, I coordinate the planning and prioritisation of team activities to attain individual and corporate goals. I esure each member operate at optimal performance level through implementing process improvement and conducting investigation. I purchase chemical and chromatographic materials and consumables within competitive pricing. I maintain an appropriate stock level in line with needs of the laboratories by means of external provider. I ensure smooth execution of warehouse operations by establishing security procedures and protocols in collaboration with HSE department. I facilitate employees in resolving technical problems related to SAP WM/MM management module software. Related Skills: Stock Level Maintenance, Corrective Action Implementation, Operational Excellence, Effective Communication Following are the highlights of the value I achieved at Novartis Pharmanalytica SA: ☛ Optimised performance of internal and external warehouse staff through executing training and implementing corrective action. ☛ Drove operational excellence through improving current processes in coordination with external service provider. Show less
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Method Development Specialist at Novartis
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Apr 2016 - Dec 2020
In this capacity, I perform detailed QA investigation and determined analytical deviation with the training module. I transfer the stability testing of the products passed under property of Novartis to Pharmanalityca through successful collaboration with GSK. Introduce Chromeleon 7.2 CDS for LC-MS screening and quantitation of Nitrosamines in several kind of Drug Substances and Drug Products. I coordinate the management of laboratory balance digitalisation project called LabX to gain accurate research results. I liaise with team member in overseeing all aspects of Nitrosamine Project, including development and evaluation of analytical procedures by LC-MS / MS. Related Skills: Stability Testing, Analytical Procedures Implementation, Cross-functional Collaboration Following are the highlights of the value I brought to Novartis Pharmanalytica SA: ☛ Played an integral role in conducting stability studies within Novartis Targu Mures (Romania) and Novartis Strykow (Polonia). ☛ Enahnced personal knowledge regarding SAP warehouse management Tool, while supporting team members in handling reference standards and reagents / consumables. Show less
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Junior Method Development Specialist
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Apr 2012 - Apr 2016
In this capacity, I developed and implemented effective test procedures for ensuring top-quality of finished products. Managed all facets of assigned transfer project from conception to successful completion. I initiated a wide range of analytical techniques, including HPLC, UV, Dissolution Rate by HPLC/UV, Karl Fisher, Appearance, Densimeter, Viscosimeter, TLC, Andersen Cascade Impactor for Inhalation Products, Next Generation Impactor for Ihalation Produts to determine chemical and physical properties of a substance. Related Skills: Test Procedures Implementation, Method Validation Evaluation, Productivity Gains Improvement Following are the highlights of the value I achieved at Elcom Systems Funding Solutions: ☛ Evaluated method validation and transfer protocols and reports to produce reliable results. ☛ Reviewed analytical GMP documentation to ensure accuracy and quality of the information presented. ☛ Conducted analysis of Chromeleon to ensure top quality and drive significant productivity gains. Show less
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Master Thesis
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May 2011 - Apr 2012
- Conducted thesis on determining the size distribution of fine inhaled drug particles Foradil 12 micrograms Inhalation Powder HGC, by Andersen Cascade Impactor: Review and improvement of the analytical procedure- Excellent collaboration with department of Analytical Science & Technologies to review/improve/development analytical procedures indicated for stability studies and release of drug products and drug substances (APIs) under responsability of Novartis
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Education
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Università degli Studi di Pavia
Laurea, Chimica e Tecnologie farmaceutiche
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