Manna Pathan

Background

About Manna Pathan

Detail-oriented and highly adaptable pharmaceutical professional with hands-on experience in cGMP environments, regulatory documentation, and cross-functional collaboration. My professional experience includes supporting both early-phase engineering initiatives and full-scale manufacturing for vaccine production, authoring and revising critical documentation such as SOPs, BPRs, and logbooks, as well as participating in system testing, inspections, and audits. My technical acumen is backed by a strong command of key industry software, including MES, DeltaV, MODA, LIMs, and S/4HANA, with a demonstrated ability to meet tight production deadlines and drive process improvements on the shop floor. My academic foundation has equipped me with a strong understanding of compliance and regulatory standards. I’m passionate about continuous learning and thrive in dynamic, fast-paced environments where precision, communication, and quality are essential. I'm eager to continue growing within the pharmaceutical industry and contribute to projects that enhance patient safety and product quality. Let’s connect! I'm always open to new opportunities and knowledge sharing in the pharmaceutical field.