Saleh Allababidi, Ph.D.

Senior Development Scientist

Dr. Allababidi is an experienced pharmaceutical professional with +20 years of industrial and academic roles both locally and internationally.  He has expertise in formulation development and manufacturing of various dosage forms, including pharmaceuticals, nutraceuticals and cosmetics.

Dr. Allababidi is a registered pharmacist and he held different positions in the pharmaceutical continuum (retail and hospital pharmacies, formulation R&D, pharmaceutical and nutraceutical industry, CMOs, CROs, training and academia). Currently, he is teaching cGMP, Cosmetics, Compounding and Formulation courses at the URI College of Pharmacy and working as Senior Development Scientist with the URI Pharmaceutical Development Institute.


Currently Instructing

Introduction To Cosmetics Development
The course addresses the basics for formulating and developing elegant and functional cosmetic products. The course is a great steppingstone towards exploring the vast world of cosmetics.

Cahil McGovern, Ph.D.

Manager of Operations

Dr. McGovern has more than 20 years of experience in the biotech industry including expertise in cell therapy, manufacturing, validation, quality, and facility design. He currently serves as the Manager of Operations of the University of Rhode Island’s College of Pharmacy’s Product Development Institute.

Prior to his current role, Dr. McGovern served as Vice President of Manufacturing Operations at Neurotech Pharmaceuticals. In this role, he developed and aseptically validated the manufacturing process for the company’s encapsulated cell therapy platform for multiple Phase 1 and 2 US and ex-US clinical trials to treat retinitis pigmentosa, wet and dry macular degeneration, glaucoma, and a Phase 3 clinical trial to treat macular telangiectasia. He also held positions at CytoTherapeutics in manufacturing and product development for the treatment of chronic pain and contributed multiple patents, scientific articles and oral presentations related to the fields of drug delivery and cell-based therapeutic. 

Malcolm G Pluskal, Ph.D.

Instructor, Purification

Dr Pluskal has worked in the Biotechnology field in the Boston area for 40+ years gaining a wide range of experience in chromatography, protein and nucleic acid purification, molecular biology, electrophoresis, synthesis of macromolecules and development of devices and hardware for analysis and sample preparation. Former positions included, Executive Vice President of New Technology and Business Development based in the Proteome Systems, Inc facility in Woburn, MA; Director of Bioseparations and Production for Unisyn Technologies, Inc; Director of Custom DNA and PNA Synthesis group in the Biosearch Division of Millipore Corporation: Senior Consulting Scientist in Corporate R&D at Millipore Corporation; Senior Scientist in Chemical R&D Waters Division of Millipore Corporation.

Dr. Pluskal received his Ph.D. in 1976 and was a Muscular Dystrophy Post-Doctoral Fellow in the area of aging influence’s on muscle protein synthesis and regulation of gene expression in developing muscle at the level of translational control. On leaving academia for a career at Millipore Corporation, Dr. Pluskal developed key technology in PVDF based blotting membranes, 2D-gel electrophoresis hardware, pre-cast gel technology, carbohydrate analysis by electrophoresis, membrane base chromatography resin development and purification applications. His work has led to several successful products in use today in Proteomics and protein purification leading to 4 granted US patents with several pending. He has published extensively in sample preparation, Proteomics, protein purification and synthetic chemistry areas. More recently, Dr Pluskal has held leadership positions focused on biomolecule chromatography applications at Pall Corporation, Thermo-Fisher Scientific and JNC Corporation. His wide experience has also been applied in education leading to the development of range of lectures and "hands on training" courses supporting academic training in Biotechnology. 

Beth Zielinski-Habershaw, Ph.D.

Coordinator of Training

Dr. Zielinski-Habershaw has extensive biopharmaceutical experience in both academia and the private sector, covering all aspects of the biopharmaceutical and biomedical industry. She came to the PDI in 2019 after a two-year stint in business development at Advanced BioScience Laboratories in Rockville, MD. This is her second stint with the University of Rhode Island, having previously served as Co-Director of Biotechnology Manufacturing at the university.

She has also served as a Director with the Center for Biological Engineering at Brown University, a Contract MSL with Medtronic Endovascular in California, and a Medical Writer with CRBard, Inc. in Warwick. Dr. Zielinski-Habershaw’s varied experience is a valuable benefit to the industry partners she works with as Coordinator of Training for the PDI.


Currently Instructing

Best Practices in Cleaning (CIP/SIP) and Environmental Monitoring
This course introduces biopharmaceutical personnel to best practices, regulatory expectations and industry trends in the disciplines of facility cleaning, validation and environmental monitoring.

Upstream Aseptic Processing
This course is designed for biopharmaceutical manufacturers to ensure that their employees, who are working in upstream processing, have clear understandings of and technical accumen for aseptic cell culture and scale up. Lectures and hands-on laboratories prepare participants to work effectively in upstream bioprocessing suites which includes maintenance and monitoring of aseptic environments while culturing mammalian cells.