Mark O'Riordan Email & Phone Number

Thousand Oaks, Ca, Us

Thousand Oaks, Ca, Us

Thousand Oaks, Ca, Us

Thousand Oaks, Ca, Us

• Developed procedures to improve the scheduling process with Production planners and internal departments for daily, weekly and monthly cycles.• Development of planning tools to assess production demand and possible capacity constraints across multiple area's in Manufacturing.• Implementation of standard work.• Creation of documents such as an Operating Master document for general information purposes.

Thousand Oaks, Ca, Us

Key member of the Amgen ADL Operational Excellence Team working in the Patient Supply Organisation. Patient Supply encompasses Manufacturing, Engineering, Maintenance, Warehouse and Supply Chain. The Operational Excellence Team enables teams and business functions to reduce waste by improving efficiencies, improving productivity, and reducing rework and waste through the use and application of Lean Six Sigma tools, techniques, and methodologies.On a day to day basis I engage with internal customers to support their efforts to solve complex problems and improve performance through Kaizens, 5S, VSM, TPM, Problem Solving, Kanbans and visual Management. I also deliver training on Lean tools, techniques, and methodologies to staff and leaders, coach and mentor site staff involved in Lean activities, and perform data analysis to identify opportunities for improvement and make recommendations to management.

St. Petersburg, Florida, Us

• Led Teva molding and automation validations which included FAT/SAT/IQ/OQ/PQ/PV.• Conducted detailed equivalency studies to drive cross tooling validations.• Generated and drove the implementation of cross departmental change controls.• Conducted process characterization / optimization such as PFMEA’s, DOE’s.• Conducted risk assessments on non-standardize work, new tooling, process changes and validation activities.• Led systematic technical root cause investigations for Roche clinical trial devices.• Provided technical input into Non-conforming events and investigations from an automation/manufacturing stand point. • Drove improvements in manufacturing metrics including OEE, scrap, cost, productivity and utilization through daily data analysis and lean six sigma methodologies. • Applied and supported lean manufacturing principles through A3 projects and DMAICs - achieved over 50K in savings over the course of the financial year 2016.• Coached maintenance and other technical team members on problem solving and improvement projects. • Drove continuous improvement projects such as automation design changes to improve OOE.• Revised CPS for continued improvement projects – scrap reduction project (~10K).• Managed assigned project budgets; liaised with customers and contractors for decommissioning of automation equipment.

Santa Clara, California, Us

I was a Project/Process engineer for Intel Ireland. In February 2013 I began working as a Process engineer in the Chemical Vapor Deposition (CVD) module of the Dielectrics department. This was a particularly interesting role as I worked on collecting data required to make improvements and modifications, utilised complicated process simulation software, investigated and troubleshot process problems, ensured that equipment worked to its specification and to appropriate capacities, and ensured safe working conditions and compliance with Intel’s health and safety policies.Following on from my role in CVD sustaining I moved into CVD De-installation Qualification (DIQ). This role saw me working with various vendors and third parties in the decontamination and de-installation of CVD tools. This involved a vast amount of networking and invaluable communications skills. Over that time I built strong working relationships with various companies as well as other engineering departments within Intel. The role also involved:(i) purchasing and installing equipment(ii) scheduling and co-ordinating work to tight deadlines and within financial budgets(iii) assessing safety and environmental issues(iv) liaising with installation/project engineers and specialists

Minneapolis, Mn, Us

•Compilation and revision of installation qualifications for manufacturing equipment.•Validation activities for new pieces of automated equipment.•Process characterisation activities and gauge R+R studies on new pieces of equipment for a new stent project.•Investigation of the geometrical influences that affected the production and manufacture of bare metal stents prior to drug application.•Creation and application Design of Experiment's (DOE's)•Reconfiguration and maintenance of lasers.

Minneapolis, Mn, Us

Master Of Science (Ms), Bioengineering And Biomedical Engineering

Certificate, Medical Sciences

Beng, Biomedical Engineering

Education record