Anette GruesshaberMuth Email & Phone Number | Compliance driven scientific professional with expertise in research & development, quality control and quality assurance in the biopharmaceutical industry, covering pre-clinical to phase 3 product development as well as post-marketing commitments. Experienced with common analytical techniques. Familiar with ICH guidelines, USP and PhEur. Proficient in authoring, revising, and managing technical documents including protocols, reports, analytical methods and SOPs. Experienced in supporting IND and NDA preparations, as well as PAI inspections. Accustomed to working in a GMP-regulated environment throughout the product lifecycle. Organizationally skilled with the ability to work independently or on cross-functional teams in a fast paced, dynamic and complex environment. Ability to collaborate with internal and external business partners. Experienced with investigations, change control, method transfer and method validation, and analytical data review.

Anette GruesshaberMuth

Compliance driven scientific professional with expertise in research & development, quality control...
Moorpark, California, United States

*50 free lookup(s) per month.

Anette GruesshaberMuth’s Email agruesshabermuth@amgen.com

Anette GruesshaberMuth’s Phone Numbers

Get ANETTE’s Phone Number (For Free)

Social Media

Anette GruesshaberMuth’s Location Moorpark, California, United States

Anette GruesshaberMuth’s Current Industry Amgen

Anette GruesshaberMuth’s Prior Industry 3m Pharmaceuticals | Ciba Vision

Find accurate emails & phone numbers for over 700M professionals.

Senior Associate Scientist

2005-09-01 00:00:00 - Present

Quality Control and Quality Assurance

1998-12-01 00:00:00 - 1999-10-01 00:00:00

Scientist IV

1996-10-01 00:00:00 - 1998-06-01 00:00:00

No Skills Available

No Languages Available

Anette GruesshaberMuth is a Compliance driven scientific professional with expertise in research & development, quality control and quality assurance in the biopharmaceutical industry, covering pre-clinical to phase 3 product development as well as post-marketing commitments. Experienced with common analytical techniques. Familiar with ICH guidelines, USP and PhEur. Proficient in authoring, revising, and managing technical documents including protocols, reports, analytical methods and SOPs. Experienced in supporting IND and NDA preparations, as well as PAI inspections. Accustomed to working in a GMP-regulated environment throughout the product lifecycle. Organizationally skilled with the ability to work independently or on cross-functional teams in a fast paced, dynamic and complex environment. Ability to collaborate with internal and external business partners. Experienced with investigations, change control, method transfer and method validation, and analytical data review.