Maria Rubio Email & Phone Number | Regulatory Affairs professional with regulatory expertise in the Medical Device Regulations. Responsible for wide range of regulatory activities, including, but not limited to, prepared and submitted to Health Authorities , determined and developed regulatory strategies for changes to devices, supported change assessments, and other regulatory and compliance activities. Detail-oriented ensuring completeness and accuracy in all regulatory documents with strong organizational and time management skills. Master’s Degree in Biomedical Engineering and bachelor’s degree in Chemistry and Biology. Knowledge of FDA Quality System Regulations (21 CFR), EU Medical Device Directives (MDD), EU Medical Device Regulation (MDR). FDA GLP and GMP Laboratory Certifications.

Maria Rubio

Regulatory Affairs professional with regulatory expertise in the Medical Device Regulations. Respons...
Bloomfield, New Jersey, United States

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Maria Rubio’s Phone Numbers +1 408-260-****

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Maria Rubio’s Location Bloomfield, New Jersey, United States

Maria Rubio’s Current Industry Stryker Depuy Synthes

Maria Rubio’s Prior Industry Cerenovus | Ethicon | Sgs | Clean Earth | William Paterson University

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Senior Regulatory Affairs Specialist

2022-01-01 00:00:00 - Present

MDR Regulatory Specialist II

2020-12-01 00:00:00 - Present

Regulatory Affairs Specialist II

2018-12-01 00:00:00 - 2020-11-01 00:00:00

Regulatory Affairs Specialist

2017-12-01 00:00:00 - 2018-12-01 00:00:00

Wet Chemistry Analyst

2015-04-01 00:00:00 - 2015-08-01 00:00:00

Assistant Laboratory Manager/ Supervisor

2012-02-01 00:00:00 - 2015-04-01 00:00:00

Research Student

2008-09-01 00:00:00 - 2010-12-01 00:00:00

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Maria Rubio is a Regulatory Affairs professional with regulatory expertise in the Medical Device Regulations. Responsible for wide range of regulatory activities, including, but not limited to, prepared and submitted to Health Authorities , determined and developed regulatory strategies for changes to devices, supported change assessments, and other regulatory and compliance activities. Detail-oriented ensuring completeness and accuracy in all regulatory documents with strong organizational and time management skills. Master’s Degree in Biomedical Engineering and bachelor’s degree in Chemistry and Biology. Knowledge of FDA Quality System Regulations (21 CFR), EU Medical Device Directives (MDD), EU Medical Device Regulation (MDR). FDA GLP and GMP Laboratory Certifications.

Maria Rubio has prior
experience in the following industries:
Cerenovus | Ethicon | Sgs | Clean Earth | William Paterson University

Maria Rubio has the following professional experience:
Stryker | Depuy Synthes | Cerenovus | Ethicon | Sgs | Clean Earth | William Paterson University