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Erum Akhtar
Erum Akhtar
Assistant scientist | Organon
Pennsylvania, Chalfont, United States
Erum Akhtar
Summary
Erum Akhtar is an accomplished Director of Global Regulatory Affairs CMC with a robust background in regulatory affairs, process validation, and drug development. With over a decade of experience in the pharmaceutical industry, she has a proven track record of managing complex regulatory submissions and ensuring compliance with industry standards. Erum has held significant roles at major companies like Merck and Teva Pharmaceuticals, where she honed her skills in product development and validation. Her current position at Organon showcases her leadership in navigating global regulatory landscapes. Erum is not only focused on compliance but is also passionate about mentoring the next generation of regulatory professionals. Her educational foundation in Biochemistry from Temple University complements her extensive professional experience. Based in Pennsylvania, she is well-versed in both the scientific and regulatory aspects of drug development, making her a valuable asset in the pharmaceutical sector.
Erum Akhtar
Work Experience
Executive Director, Global Regulatory Affairs CMC at
Organon
July 2024 - Present
Erum Akhtar
Education
Temple University, B.S., Biochemistry
January 2004 - January 2006
Frequently Asked Questions about Erum Akhtar
What is Erum Akhtar email address?
Erum Akhtar's primary email address is ***********@merck.com. To view the full verified email and additional contact details, sign up for free with Muraena.
What company does Erum Akhtar work for?
Erum Akhtar is a Assistant scientist at Organon.
Where Erum Akhtar graduated from?
Erum Akhtar holds a degree in null from Temple University.
How can I directly contact Erum Akhtar?
To contact Erum Akhtar directly, you can use the email address ***********@merck.com. Complete contact information is available upon registration with Muraena.
Who is Erum Akhtar?
Erum Akhtar is an accomplished Director of Global Regulatory Affairs CMC with a robust background in regulatory affairs, process validation, and drug development. With over a decade of experience in the pharmaceutical industry, she has a proven track record of managing complex regulatory submissions and ensuring compliance with industry standards. Erum has held significant roles at major companies like Merck and Teva Pharmaceuticals, where she honed her skills in product development and validation. Her current position at Organon showcases her leadership in navigating global regulatory landscapes. Erum is not only focused on compliance but is also passionate about mentoring the next generation of regulatory professionals. Her educational foundation in Biochemistry from Temple University complements her extensive professional experience. Based in Pennsylvania, she is well-versed in both the scientific and regulatory aspects of drug development, making her a valuable asset in the pharmaceutical sector.
Erum`s contact details
***********@merck.com
***********@organon.com
Colleagues
Associate
Senior Manager
Sr Project Scientist
Logistic Assistant
Senior Consultant
Captain
Director, PV Licensing
Compliance Lead, US Medical Affairs
Various Roles at Merck & Co., Inc
VP Regulatory Affairs