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harrk_11

Keegon H.

@harrk_11

QA Documentation and Batch Record Review

United States
English
About me
QA professional with experience in pharmaceutical, biotech, and animal health GMP/cGMP manufacturing. I specialize in reviewing batch records (BPR/BMR), SOPs, and regulated documentation to ensure accuracy and compliance with Good Documentation Practices (GDP). I help companies identify documentation issues early and improve clarity before audits or inspections. Reliable, detail-focused, and committed to delivering clear compliance feedback. All documents are handled with strict confidentiality. ... Read more

Skills

h
harrk_11
Keegon H.
Offline • 
Average response time: 20 hours

See my services

Technical Writing
I will review pharmaceutical batch records for gmp compliance
From$35 / projectMore details

Work experience

Boehringer_Ingelheim

Operations technician / QA Documentation

Boehringer Ingelheim

Jan 2021 - Present • 5 yrs 4 mos

Experience reviewing manufacturing documentation in pharmaceutical, biotechnology, and animal health environments operating under GMP and cGMP regulations. Responsibilities include batch record review, Good Documentation Practices evaluation, SOP review, and ensuring documentation accuracy within regulated manufacturing operations.