Patrick Kenny Email & Phone Number

Waltham, Ma, Us

Waltham, Ma, Us

Perform product marketing for Chromeleon Chromatography Data System (CDS) software with an emphasis on its compliance functionality. This is a global role that includes responsibilities of: - Content creation (brochures, whitepapers, product spotlights, technical notes, blog posts, videos, webinars, etc.) - Education of sales specialists and customers through face-to-face meetings, seminars and webinars - Representing the company and product at industry tradeshows - Development and testing of new product features related to compliance

The mission of Meghan's Light is to support finding a cure for cystic fibrosis and to inspire hope and courage in patients, families and communities impacted by the disease.www.meghanslight.com

Little Rock, Arkansas, Us

Started the company's first Analytical Chemistry Testing Laboratory at their expansion site in Connecticut. Activities/responsibilities included: - Planning the layout of the lab and working with contractors to ensure the build-out went according to plan - Purchase, installation and validation of all equipment (testing, stability chambers and support) - Creation and implementation of the lab's quality systemResponsible for all aspects of GMP chemistry testing for the products manufactured at the Connecticut site. Activities included: - Development and validation of 15 stability-indicating UHPLC test methods (which covered >300 commercial products) - Setup and execution of bracketed stability studies to cover all commercial productsRepresented Chemistry department in all meetings with C-level/Sr. executives, regulatory agencies and customers

East Rutherford, New Jersey, Us

Responsible for meeting revenue and quality goals, capex decisions, client outreach and developing new test offerings for the chemistry and stability groups. My groups focus on the analysis of pharmaceutical and medical device products. Testing is routinely performed on raw materials, final product testing, stability, water system validation, cleaning validation and ethlyene oxide sterilization residuals. Specific testing includes HPLC, GC, Container Closure Integrity, FTIR, Electrophoresis, UV-Vis, Particulate Counting, Moisture Determination, Osmolality, pH, Total Organic Carbon as well as many wet chemistry methods.Avista Pharma Solutions is a contract testing, development and manufacturing organization encompassing over 200,000 square feet of laboratory and manufacturing space across three locations (Agawam, MA – Durham, NC – Longmont, CO), providing pharmaceutical, animal health and medical device clients with a broad suite of scientifically-differentiated services ranging from early drug development and drug product manufacturing to stand-alone analytical and microbiology testing support.OUR CAPABILITIES INCLUDE:Drug Substance Development & ManufacturingDrug Product Development & ManufacturingProcess ChemistryAnalytical Development, Validation & TestingMicrobiology & Environmental MonitoringAnimal Health Anti-Parasitic Screening & Discovery

Signature authority on batch records, certificates of analyses and stability results for 70+ drug products (4 commercial), totaling more than 200 lots, from our aseptic fill/finish manufacturing operation.Author and reviewer of SOPs and method validation/transfer protocols, Study Director for GLP projects.

Supervised analysts responsible for supporting manufacturing operations as well as contract testing. Review and signature authority on raw data, test results and testing certificates.

Performed GMP & GLP testing on manufacturing and contract testing samples, method transfer protocols and method validation protocols. Developed and validated HPLC and GC methods approved as part of NDA and ANDA submissions.

West Springfield, Ma, Us

Performed organic synthesis in research and development of chemiluminescent devices.Analyzed strategic partners’ and competitor’s products using analytical testing equipment (HPLC, GC, wet chemistry).

East Hartford, Connecticut, Us

Performed research and development of IR instruments in a company funded by SBIR grants. Authored monthly research updates provided to funding agencies.Prepared the combustion gas FTIR spectrum reference library to be sold commercially.

Performed multi-step organic synthesis and purification of chemiluminescent diagnostic substrates.Authored SOPs in support of successful ISO 9000 registration.

Ms, Chemistry

Bs, Chemistry