
Sumedha Sharma
Pharmaceutical / Bio-tech
About Sumedha Sharma:
Quality & Compliance Engineer with expertise in GMP/GDP/GLP, ISO (9001, 13485, 14001), MHRA, FDA, EU/UK MDR. Skilled in QMS, CAPA, audits, risk, complaints, and driving ethical, compliant, continuous improvement.
Experience
Results-driven Quality Assurance professional with over 3 years of hands-on experience in the pharmaceutical and healthcare manufacturing sectors. Demonstrated expertise in GMP compliance, internal and external auditing, deviation investigations, and CAPA management. Adept at supporting site quality systems, driving continuous improvement initiatives, and ensuring adherence to regulatory standards including MHRA, FDA, and ISO guidelines. Skilled in interpreting and applying quality principles across manufacturing, packaging, and laboratory environments to maintain product integrity and patient safety. Recognized for a proactive, detail-oriented approach and strong collaboration with cross-functional teams to uphold high-quality standards and achieve operational excellence.
Education
MSc. Pharmaceutical Sciences
Professionals in the same Pharmaceutical / Bio-tech sector as Sumedha Sharma
Professionals from different sectors near Alton, East Hampshire District, Hampshire
Other users who are called Sumedha
Jobs near Alton, East Hampshire District, Hampshire
-
Quality Engineer
1 day ago
Ferrovial LondonThe Quality Engineer is responsible for ensuring that Ferrovial Construction projects at Heathrow Airport meet client requirements, company procedures, and industry standards. · ...
-
Quality Engineer
4 days ago
Acteon WokinghamWe are seeking an experienced Quality Professional to join our team on a full-time, permanent basis. This newly created Quality Engineer role is ideal for someone with several years of QA/QC experience in electronics and mechanical manufacturing, preferably with experience in off ...
-
Quality Engineer
1 month ago
Premier Group Southampton, EnglandThe Quality Engineer will support all quality activities across the manufacturing process. · Key Responsibilities:Lead root cause analysis and implement corrective and preventive actions · Support internal and external audits, maintaining ISO/AS quality standards · ...