PharmEng Technology has been providing quality services to the manufacturers of health care products for over 20 years. In highly regulated industries, there is a need for experienced specialists who can provide solutions in a cost effective and timely manner. PharmEng Technology is a full service consulting firm that specializes in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering and Training. We provide a wide range of services to the pharmaceutical, biotechnology, medical device and nutraceutical industry. We are a global company and we are here to assist your company with any issue you may be facing.
At PharmEng Technology, we have a highly qualified and dedicated professional team who believes quality plays an integral role in every facet of our activities. Our international presence ensures we are current with regulatory practices and ahead of the emerging trends around the globe. Our staff brings a variety of disciplines to the table, to ensure every aspect of your project needs are met. PharmEng Technology is a multicultural company with staff all over the world servicing companies of all sizes. We are confident that we are the solution you need to operate in this highly regulated industry.
PharmEng Technology is one of the leading consulting firms in the world with offices in USA, Canada and Asia. We have developed a stable client base and provide services all around the world including USA, Canada, Asia, Europe, Australia and Africa.
Alan Kwong, P.Eng, M.Sc., M.B.A.
Alan Kwong established PharmEng Technology in 1997 and is currently the CEO and Chairman with over 120 staff in Asia, USA and Canada.
Mr. Kwong has been in the pharmaceutical, biotechnology and medical devices industries for over 20 years and has leveraged that experience into the global expansion of consulting operations, serving 7 of the top 10 pharmaceutical companies in the world.
Ben Lee P.Eng, B.Sc., I.E.
Ben Lee brings over 25 years experience in all aspects of Project Management. He has successfully delivered over $1B in major projects in the biotechnology, pharmaceutical, hospital and manufacturing sectors from concept to completion.
Mr. Lee has comprehensive knowledge and practice of current GMP, GLP, FDA and CFR 21 Part 11. He possesses direct and extensive experience in project planning such as benefit-cost analysis, life cycle costing, feasibility studies, change control, operational/technical requirements, analysis & optimization, functional/space programming, land use and environmental approvals.
Kenny Peng P.Eng, M.A.Sc., R.A.C.
Managing Director, Asia
Kenny Peng is based inSingapore and Taiwan and possesses 10 years of experience as a Project Manager and Business Manager.
Mr. Peng is a consulting professional whose experiences have spanned start-up, technology transfer, commissioning, validation, audits, regulatory affairs, and engineering, having worked with clients in pharmaceutical, biotechnology, medical device, and food industries across North America and East Asia, including multinational and domestic clients.
Alex Della Mora
Alex Della Mora has 20 years experience in various areas of drug development including cGMP Manufacturing, Quality Systems, Compliance, Audits (cGMP), Validation, Clinical Operations and Quality Assurance.
Mr. Della Mora has successfully lead the management of projects in a fast paced environment, with limited resources and implemented various procedures/systems. His excellent communication and customer service skills have resulted in successful project completion and soaring client satisfaction.
David Mayers, B.Cs., M.B.A.
David Mayers brings over 25 years of pharmaceutical leadership, with extensive experience in corporate strategy, Quality, Lean Manufacturing, Supply Chain, product launch and product transfer, general management, R&D, capital procurement and implementation and facility expansion.
Prior to joining PharmEng, Mr. Mayers was formerly President of WellSpring Pharma Services, and VP of Manufacturing Operations at Purdue Pharma.
Nizamil Fairuz Yahya, B.Eng., M.Eng., Ph.D.
Nizamil Fairuz Yahya has a diverse global experience in R&D, Medical devices and Pharmaceutical industries..
Mr. Fairuz has demonstrated excellent compliance solutions in GxP enforcement. His current advisory roles focus on quality system, commissioning, qualification and validation, compliance remedication, GxP training and quality behavior coaching. Mr. Fairuz's professional career traverses from consulting to project management experience within Americas and Asia Pacific region, serving multinational and domestic clients focused on GMP.
Yeeju Chen, B.Sc.(Pharm)(Hons)
Yeeju Chen, as a registered pharmacist in Singapore, brings with her a diverse and valuable knowledge of the Asian pharmaceutical market.
Ms. Chen's insight into the pharmaceutical industry encompasses quality assurance and regulatory compliance, spanning from drug discovery to biomedical development, manufacturing and to market access. She now leads the Regulatory Affairs team in South East Asia, overseeing various product registration projects across different product classifications, ranging from Biologics/Biosimilars to Pharmaceuticals to Medical Devices etc.