Experience managing a complete project launch Responsible for delivering and meeting project deadlines with multiple clients

Write, prepare, review, audit and control R&D documents including: protocols, reports, laboratory notebooks, SOP’s, material specification and compliance. Quality Reviewer - cGMP, FDA, USP and ICH guidelines

Direct Report to the Marketing ManagerDeveloped long term relationships with existing and prospective customersManaged regular contact with all customersCoordinated all Conferences, Seminars and Vendor Shows. Provided project plans and client timelines to the project management team, able to manage multiple priorities with a commitment to delivering quality, on-time results. Reviewed Client Marketing Material prior to printing. Assisted in the layout of new marketing material and provided support for the Marketing and Sales department. Designed the basic layout of all client requests and contracted the project out.

Lead and trained all new critical reagents group members in the conjugation, biotinylation, data reduction and process for the group. Responsible for protein Conjugation of critical reagents used for all chemiluminescent NID assays, both automated and manual. •Tested/ released all final components used in manufacturing•Trained in cGMP, FDA, Six Sigma and ISO 9001. Certified in Women in Management

Tested and released raw materials such as active pharmaceutical ingredients (API) and peptides and complex organic molecules.