"Give a man a fish, feed him
for a day. Teach him to fish,
he'll eat for a lifetime."

Lao Tzu
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After ten years servicing the pharmaceutical industry as a consultant and an employee, I established LSM Consulting in 2008 to deliver my expertise and knowledge in the areas of documentation and training directly to you helping you avoid the costly overhead of agency support.

Whether you need to outsource program development, need assistance with strategy (e.g., developing best practices, transitioning to low-cost e-Learning, or training internal staff to facilitate and develop), want help refining existing processes or developing new ones, or could simply use an extra set of hands, our team 
proudly boasts a diverse skill set that will add value to your organization and help you design the best solution to address your current needs.

Liimu McGill, Principal


Vince D'Esposito, Senior Training Consultant

Vince D'Esposito has nearly 15 years of experience in the pharmaceutical industry including vaccines manufacturing, liquid/solid dose manufacturing, QA, and Pharmacovigilance. His experience includes training design, development, facilitation and administration for several major pharmaceutical companies. 
Vince’s specific skill set includes design and development of cGMP Training Programs, including classroom and eLearning, training facilitation and project management, as well as curriculum development and maintenance within a variety of learning management systems. He is also extremely well-versed in the development and administration of MS SharePoint sites.
Vince has a proven track record in harnessing the capabilities of the many training tools available to industry to build sound, compliant, meaningful and efficient training process/programs.  Over the years, Vince’s strong work ethic, and creativity have made him an asset to many project teams and resulted in significant business impact and improvements.

Peggy Newfield, Documentation Specialist

Peggy Newfield brings a wealth of expertise serving the technology, financial and pharmaceutical industries in the areas of project management, documentation, and software development. She has more than twenty years experience identifying, designing, and creating the appropriate types of documentation, both hard-copy and web-based, necessary for business and technical development, implementation and training, management acceptance, regulatory compliance, and marketing and distribution.     She is also experienced in the conversion of legacy documents for single source use and html import. Her project management and coordination experience includes the editorial life cycle for documentation, the software and infrastructure development life cycle, and hardware procurement and installation scheduling.

Monica Mount, Quality & Compliance Specialist

Monica Mount has more than fifteen years of experience as a Senior Quality Engineer and Training Professional. She has extensive experience working Quality Systems, including managing procedural documents, compliance training, complaint handling, deviations and CAPAs. She has been directly involved with inspections and audits, and has designed and implemented process improvements as a result of findings.

As a Training Professional, she has designed and implemented Validation and Compliance training to global personnel, has developed global curricula, and managed learning management system upgrades and migrations, including the development of validation methods, IQ, PQ, and OQ protocols. She has also managed teams of administrators responsible for day to day tasks, including training assignment and reporting.

She has also supported manufacturing environments in Statistically Based Continuous Improvement efforts, including Statistical Process Control and Design of Experiments, as well as management of supplier audits and other quality-related activities.

Caroline Collins, Quality & Compliance Specialist

Caroline Collins is a quality and compliance professional with over fifteen years of experience supporting the pharmaceutical industry. She is experienced in change control, product release, GMP training, documentation and data integrity, auditing, deviation management, root cause analysis and CAPA. Her experience includes all phases of drug development from Phase I through post approval. She holds a masters degree in Quality Assurance/Regulatory Affairs from Temple University.

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