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harrk_11

Keegon H.

@harrk_11

QA Documentation and Batch Record Review

États-Unis
Anglais
Certaines informations sont présentées en anglais.
À propos de moi
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. ... Plus d’infos

Compétences

h
harrk_11
Keegon H.
hors ligne • 
Temps de réponse moyen de 20 heures

Voir mes services

Rédaction technique
I will review pharmaceutical batch records for gmp compliance
De35 $US / projetPlus de détails

Expérience professionnelle

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.