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Maryam K. に連絡

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プロフィール詳細

プロジェクトを作成

★★★★★

☆☆☆☆☆

★★★★★

☆☆☆☆☆

Dr. Maryam K.に依頼

United Kingdom

Analytical method development and validation, Risk management, Root cause analysis, Change Control, Audit, CAPA, Deviat

プロフィール概要

As a scientist with over 10 years of experience working with pharmaceutical companies, I have had the opportunity to develop a comprehensive understanding of internationally recognized quality processes. I have excelled at adapting, gathering, and analyzing data while simultaneously working with different departments and organizations to identify ways to create processes that are more efficient and profitable.
Through my work at Abidi Pharmaceuticals, I had the opportunity to perfect my knowledge about the pharmaceutical industry, including drug product formulation & scale-up development knowledge. I have a robust array of experience in liquid chromatography (HPLC and UPLC-MS) (maintenance, calibration, and repairment), GC & GC-MS, UV-Vis, KF, FT-IR as I worked on this on a daily basis and additionally with drug design and formulation, analytical method development, and validation, stability studies, feasibility study, the use of pharmacopeia (BP, USP, EP), ICH & PICS and CTD writing.
Through my work at IOCB and my education, I have the opportunity to perfect my knowledge about organic synthesis and characterizing organic compounds. I bring academic and real-world experience with both independent and team-based research on API and finished products; these experiences have taught me how to respond quickly and methodically in high-pressure situations and how to organize and make the best decision for each situation. Additionally, my outstanding communication skills have been proven in a practical environment and my colleagues often describe me as an effective, innovative, resilient, and flexible worker. 
I have specialized in good manufacturing practices, pharmaceuticals, audits, self-inspection, risk management, change control, GMP documentation, deviation (& OOS) investigation, CAPAs & root cause analysis, ISO 9001/2015, ISO 14001/2015, and planning and performance an on-site audit for materials suppliers. I have a robust array of experience with activities required to plan, prepare for, conduct, report and close the assigned audits (internal and external). I consider myself to be a dynamic and detail-oriented scientist with hands-on experience working in laboratories all over the world. These experiences enabled me to possess a broad experience in organic chemistry and pharmaceutical industries. Moreover, I am proficient in the design and execution of experiments that I have worked on individually. These opportunities have given me the skills to successfully execute project planning, data and analysis, and interpretation for project progress.

専門分野

サービス

Research
Consulting
Product Development

Research Feasibility Study, Gap Analysis, Scientific and Technical Research

Consulting Scientific and Technical Consulting

Product Development Formulation, Stability/Shelf Life Testing, Product Evaluation, Product Validation, Manufacturing, Quality Assurance & Control (QA/QC), Product Compliance , Concept Development, Product Launch Support

職務経験

Senior QC validation analyst

EuroAPI

7月 2022 - 現在

Research And Development Specialist

Dr.Abidi Pharmaceuticals

4月 2020 - 現在

Postdoctoral Research Position

Institute of Organic Chemistry and Biochemistry of Czech Academy of Science Prague

10月 2021 - 6月 2022

Senior Formulation and Analysis Scientist (Research and Development Expert)

Abidi Pharmaceutical co.

6月 2017 - 9月 2021

Scientist

Institute of Organic Chemistry and Biochemistry

9月 2019 - 4月 2020

Responsible person

Modaberan Teb Salamat ( hager werken)

4月 2017 - 10月 2019

Research And Development Specialist

Dr.Abidi Pharmaceuticals

6月 2017 - 9月 2019

expert

Dr.Abidi Pharmaceuticals

9月 2013 - 6月 2017

QA GMP leader

Abidi pharmaceutical company

8月 2013 - 6月 2017

Responsible person

Arya Borhan (Dorco)

2月 2015 - 2月 2017

QA leader

Tolid darou pharmaceutical co

12月 2011 - 7月 2013

学歴

Ph.D., Chemistry

Kharazmi University

9月 2015 - 9月 2020

Ph.D (Science department)

Kharazmi University

9月 2015 - 9月 2020

Master (Organic chemistry)

Chemistry and Chemical Engineering Research Center of Iran

9月 2007 - 3月 2010

bachelor (science)

University of Mazandaran

9月 2003 - 6月 2007

認定資格

認定資格の詳細は未入力です。

level-one heading

Analytical method development and validation, Risk management, Root cause analysis, Change Control, Audit, CAPA, Deviat

Senior QC validation analyst

EuroAPI

Research And Development Specialist

Dr.Abidi Pharmaceuticals

Postdoctoral Research Position

Institute of Organic Chemistry and Biochemistry of Czech Academy of Science Prague

Senior Formulation and Analysis Scientist (Research and Development Expert)

Abidi Pharmaceutical co.

Scientist

Institute of Organic Chemistry and Biochemistry

Responsible person

Modaberan Teb Salamat ( hager werken)

Research And Development Specialist

Dr.Abidi Pharmaceuticals

expert

Dr.Abidi Pharmaceuticals

QA GMP leader

Abidi pharmaceutical company

Responsible person

Arya Borhan (Dorco)

QA leader

Tolid darou pharmaceutical co

Ph.D., Chemistry

Kharazmi University

Ph.D (Science department)

Kharazmi University

Master (Organic chemistry)

Chemistry and Chemical Engineering Research Center of Iran

bachelor (science)

University of Mazandaran