Marcio Almeida
Senior Analytical Chemist at Intertek Melbourn- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
Topline Score
Bio
Experience
-
Intertek Melbourn
-
United Kingdom
-
Pharmaceutical Manufacturing
-
1 - 100 Employee
-
Senior Analytical Chemist
-
Aug 2023 - Present
Targeted work with advanced analytical techniques and methods, including HPLC, GC and spectroscopy, to analyse and validate pharmaceutical formulations, with a commitment to excellence, extending to method development, validation and troubleshooting, contributing to the overall success of our projects , promoting collaboration in multifunctional teams. Targeted work with advanced analytical techniques and methods, including HPLC, GC and spectroscopy, to analyse and validate pharmaceutical formulations, with a commitment to excellence, extending to method development, validation and troubleshooting, contributing to the overall success of our projects , promoting collaboration in multifunctional teams.
-
-
-
AMFRESH Group
-
Spain
-
Food and Beverage Services
-
200 - 300 Employee
-
Quality Control Analyst
-
Nov 2021 - Present
Quality Control in fresh fruit, specialty Citrus Quality Control in fresh fruit, specialty Citrus
-
-
-
Zydus Brasil
-
Brazil
-
Pharmaceutical Manufacturing
-
200 - 300 Employee
-
Full Validation Analyst
-
Aug 2018 - Aug 2022
Develop analytical methodologies to assist in the development of new products, evaluate the incompatibility and degradation of assets in formulation and mass balance, matrix effect evaluation in complex matrices, and protocol work and validation report. Process validation, support and training of the quality and control team. Develop analytical methodologies to assist in the development of new products, evaluate the incompatibility and degradation of assets in formulation and mass balance, matrix effect evaluation in complex matrices, and protocol work and validation report. Process validation, support and training of the quality and control team.
-
-
-
GSK
-
United Kingdom
-
Pharmaceutical Manufacturing
-
700 & Above Employee
-
Full Validation Analyst
-
Apr 2014 - Aug 2018
Develop analytical methodologies to assist in the development of new products, evaluate the incompatibility and degradation of assets in the formulation and stability in accelerated chamber and room zone 4. And protocol work and validation report. Team Training . System Validation and Equipment Qualification. Support with computer systems of chemical control laboratory. Develop analytical methodologies to assist in the development of new products, evaluate the incompatibility and degradation of assets in the formulation and stability in accelerated chamber and room zone 4. And protocol work and validation report. Team Training . System Validation and Equipment Qualification. Support with computer systems of chemical control laboratory.
-
-
-
Novartis
-
Switzerland
-
Pharmaceutical Manufacturing
-
700 & Above Employee
-
Quality Control Analyst
-
Aug 2012 - Apr 2014
Analyzes Control Quality of Petrochemicals, active raw materials and solvents , and stability in Accel camera Erada and living room area 4 laboratory organization, 5S, BBS, working with SAP and Chromeleon in instrumental laboratory. Analyzes Control Quality of Petrochemicals, active raw materials and solvents , and stability in Accel camera Erada and living room area 4 laboratory organization, 5S, BBS, working with SAP and Chromeleon in instrumental laboratory.
-
-
-
Diffucap
-
Brazil
-
Pharmaceutical Manufacturing
-
200 - 300 Employee
-
Full Validation Analyst
-
Nov 2010 - Nov 2012
Develop analytical methodologies, quality control analyzes to assist the pharmacist in the development of new products, evaluate the incompatibility and degradation of assets in accelerated chamber and zone room formulation and stability. Organize the validation and galenic team with elaboration master validation plan, protocol drafting and validation report . Team Training. Develop analytical methodologies, quality control analyzes to assist the pharmacist in the development of new products, evaluate the incompatibility and degradation of assets in accelerated chamber and zone room formulation and stability. Organize the validation and galenic team with elaboration master validation plan, protocol drafting and validation report . Team Training.
-
-
-
Laboratório Daudt Oliveira Ltda
-
Brazil
-
Pharmaceutical Manufacturing
-
1 - 100 Employee
-
Analyst Galenic and Validation Junior
-
Aug 2009 - Nov 2010
Develop analytical methodologies, to assist the pharmacist in the development of new products, evaluate the incompatibility and degradation of assets in the formulation and stability in accelerated chamber and zone room 4. Organize the validation and galenic team with elaboration of master validation plan. , protocol drafting and validation report . Team Training. Develop analytical methodologies, to assist the pharmacist in the development of new products, evaluate the incompatibility and degradation of assets in the formulation and stability in accelerated chamber and zone room 4. Organize the validation and galenic team with elaboration of master validation plan. , protocol drafting and validation report . Team Training.
-
-
Education
-
Extracurricular Courses and Related Knowledge
Professional Improvement course -
Unigranrio University
Teaching and Bachelor degree, Chemistry, Química