With both academic background in pharmaceutical development, engineering and operations and experience in each of these areas, I can provide support in any project a pharmaceutical manufacturing company would like to endeavor. This support will include:
> Identification of critical resources required prior to initiation of projects
> Establishment of key milestones for the project
> Evaluation of scientific, regulatory and quality implications of the project
> Creation of project plans detailing how project should ideally be executed
> Provision of documentation and reliable sources of information to support execution of project
> Write-ups of any risk assessment, protocols and/or reports required for completion of the project
> Training to personnel involved in project to ensure your company has full independence regarding the project and other similar endeavors without having to rely on outside support every time.
> Ongoing support, if needed, post-execution of projects, especially with regards to regulatory-focused projects.
Each of the above support can be provided on a separate basis i.e., I can provide support on ongoing projects for specific tasks such as risk assessments or summary reports without obliging the company to employ my full list of services.
I will always ask for a 1-hour discussion (free of charge) before accepting the job to better understand the nature of the request and ensure that my services will be of use to your company.