Cheryl Anderson
Senior Specialist@ Merck
New York, New York, United States
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Cheryl Anderson is a highly experienced professional with 36.1 years of work experience in the pharmaceutical industry. She has expertise in HPLC, drug development, GMP, and validation. Cheryl is a cGMP-Driven and a team player, known for her quick learning abilities and flexibility. She has extensive experience in Regulatory Affairs and Quality Assurance, with a focus on documentation compliance. Cheryl is skilled in fast-paced environments and is adaptable to changing needs and priorities. She is available to assist co-workers on an as-needed basis.
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Emails and Phone Numbers

@spcorp.com
@merck.com
@merck.com
@merck.us
+1 503430****
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About

I am a cGMP-Driven, team player, quick learner, and very flexible with experience in Regulatory Affairs and Quality Assurance. Extensive pharmaceutical experience in Research and Development (R&D) with a focus on documentation compliance. Functions in a fast paced environment and anticipates/adapts to changing needs and priorities. Detail-oriented reviewer for investigational products batch records to ensure that the records meet cGMPs and regulatory requirements. Available to assist co-workers on an as-needed basis.

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Work Experience

126 E Lincoln Ave, Rahway, New Jersey, 07065, US

Pharmaceutical Manufacturing

67379
Phone
+1 5034305821
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Cheryl Anderson's Professional Milestones

  • Associate Scientist Through Scientist Ii (1987-09-01~2008-12-01): Conducted groundbreaking research, revolutionizing the field and advancing scientific knowledge in the field.
  • Senior Specialist (2018-07-01~): Implementing effective strategies to improve operational efficiency and enhance overall productivity.
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Education

Felician University
Felician University

Biology,

Bachelors,

General

1985-1987
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