

BSc (Hons) Pharmaceutical Science graduate with hands-on experience in GMP-regulated pharmaceutical manufacturing and a strong academic foundation in pharmaceutical quality systems. Experienced in high-potency API handling, containment isolators, SAP, MES, PAS-X and LIMS, with strong knowledge of data integrity and GMP documentation. Additional experience with Lean Manufacturing, 5S, continuous improvement and Document changes.
Approximately 460 hours of laboratory experience across 140 practical sessions, including Chemistry, Biology and Validation. Practical exposure to analytical testing, pharmaceutical manufacturing, microbiological techniques and validation principles
LinkedIn - www.linkedin.com/in/paulpearse