h
harrk_11

Keegon H.

@harrk_11

QA Documentation and Batch Record Review

Verenigde Staten
Engels
Sommige informatie wordt in het Engels weergegeven.
Over mij
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. ... Lees meer

Skills

h
harrk_11
Keegon H.
offline • 
Gemiddelde reactietijd: 20 uur

Bekijk mijn diensten

Technische teksten
I will review pharmaceutical batch records for gmp compliance
VanafUS$ 35 / projectMeer informatie

Werkervaring

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.