PharmEng Technology
Ts. Ahmad Safuan Dzakuan Hj. Mokhtar has a diverse and extensive work experience in various roles and companies. Ts. Ahmad Safuan Dzakuan began their career in 2012 as a Project Director at PharmEng Technology Asia. Ts. Ahmad Safuan Dzakuan then joined Alcon in 2021, where they held multiple positions, including Principle Validation Consultant, Validation Lead Consultant, and Validation Consultant, working on projects related to surgical products and spreadsheet validation. In the same year, they also worked at Tiger Balm (M) Sdn Bhd as a Project Governance specialist.
In 2022, Ts. Ahmad had roles at ROVI Pharma Industrial Services as a Lead Auditor for USFDA and FDA Mock Pre-Approval Inspections. Ts. Ahmad Safuan Dzakuan also served as a CQV Project Manager at Samil Pharmaceutical Co Ltd.
Additionally, Ts. Ahmad Safuan has gained experience in risk assessment and supplier audit support roles. Ts. Ahmad Safuan Dzakuan worked at Givaudan as a GMP & HAZOP Risk Assessment Lead Consultant, Insulet Corporation for GMP Assessment for Warehouse Lead Consultant, Moderna for ROVI PhIS as an Offsite Supplier Audit Support Auditor, and Catalent Pharma Solutions for ROVI PhIS as an Offsite Supplier Audit Support Auditor. Ts. Ahmad Safuan Dzakuan also served in the same capacity at Lonza for ROVI PhIS.
Overall, Ts. Ahmad Safuan Dzakuan Hj. Mokhtar has demonstrated expertise in project management, validation, audit, and risk assessment in the pharmaceutical industry.
Ts. Ahmad Safuan Dzakuan Hj. Mokhtar obtained their education from Universiti Teknologi Malaysia, where they pursued a degree in Chemical Engineering from 1998 to 2003. In addition to their formal education, they have obtained several certifications throughout their career. These include being certified as an End User by Kneat Solutions in September 2022, as a Panel of Assessors by the Malaysia Board of Technologists in November 2020, and as a Professional Technologist by the Malaysia Board of Technologists in September 2019. Ts. Ahmad Safuan Dzakuan also obtained certifications such as Graduate Technologies from the Malaysia Board of Technologists in March 2019, Six Sigma Green Belt Certification from EPCOS in July 2009, ISO/TS 16949 Auditor from Det Norske Veritas in September 2007, ISO 14001 Auditor from SQC Management (Penang) Sdn Bhd in April 2006, ISO 9001 Auditor from BSI Neville Clarke – A BSI Professional Services Company in March 2005, and Graduate Engineer from the Board of Engineers Malaysia in February 2005.
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PharmEng Technology
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PharmEng Technology is a leading global provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes. Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique needs and challenges. At PharmEng Technology, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives and develop customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs. As a trusted partner to some of the world's largest pharmaceutical companies, we have a proven track record of success in delivering high-quality technical services and solutions that drive operational efficiency, reduce costs, and enhance overall performance. We are dedicated to helping our clients succeed in an ever-evolving and highly competitive industry. At PharmEng Technology, we are passionate about what we do, and we are committed to delivering excellence in everything we do. Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).