Neyazi (Nick) Haddadin

773-***-****, mp4n00@r.postjobfree.com

Objective

To utilize and develop my knowledge, education and skills in the pharmaceutical industry in order to participate in improving work process quality as a result achieving department goals.

Education

MBA-Finance at Roosevelt University, 2010 (GPA: 3.7).

Masters of Science in Analytical Chemistry: 2006. NEIU, GPA: 3.72 out of 4.00.

Experience

ABBOTT LABORATORIES, 08/03 – Present:

Chemist (R&D):

Working on project (method development and validation) closely with Managers as well as Pilot Plane (manufacturing) and Formulators to meet the dead lines of Drug development Process.

Communicate results and issues within department’s team or other departments through written reports and/or oral presentations. As well as, Summarize results in reports that are used in FDA submissions.

Interact closely with third party in case of outsourcing studies by taking the leadership of the analytical analysis of the drug, and coordinate results and plans with CMC team.

Evaluate and bring new technology in order to improve drugs method development process.

Experience with USP, EU, and ICH regulations and requirements, as well as, GMP and GLP.

Evaluating result of drug analysis using statistics in order to measure, evaluate, manage risk against benefit.

Familiar with (Quality By Design) of drug analysis development, Minitab and pHstab, which are used in controlling system quality and predicting risk associated with analytical methods.

Has a general knowledge of drugs development process and manufacturing, as well as, clinical studies.

Participate in creating and revising protocols, reports, analytical memos, and procedures.

System Event owner (Lab Results Investigation).

EHS member. (Environment and Health safety)

Sr. Lead Analyst QC/QA (08/2003-02/2008):

Worked independently, multi-tasks and prioritize daily work schedule as well as long term goals.

Performed analytical testing within a GMP/GLP environment to support one of these areas: Raw materials, in process, final substance, stability, and validation samples.

Reviewed, verified, approved, and released lab data generated by others to determine conformance with product specifications.

Fill in for an absent Group Leader.

Independently troubleshoot and resolved analytical techniques and instrument issues like: HPLC, GC (FID, TCD and Head Space), ICP, UV-VIS, FTIR, as well as wet chemistry, TOC and Nitrogen analysis.

Maintain reference standard inventory.

Environmental Monitoring and Technologies, (EMT), 4/2000-8/2003.

Chemist

Performing analytical testing and samples clean up for wastewater, slag and soil by different techniques.

• Chromatographic technique (IC) and Spectroscopy techniques (UV-vis, FTIR).

• Wet chemistry/physical-testing techniques.

Jordanian Air Force

First lieutenant (Administrator)

Supervising up to 50 people, including performance evaluation, assign weekly responsibilities, vacations approval as well as, participate with budget spending (~1000 $).

Presentations and Publications:

Received “Abbott of Excellence Award” (Silver Award From department) in 2010 for the significant contribution in ABT-888. (GARD)

Speaker in Roosevelt University for the international business class about ” Effect of Culture on the Multinational Companies”.

Received “Abbott of Excellence Award” and “Golden Award” in 2009-10, for the significant contribution in Simcor 40mg. (GARD)

Received “Abbott of Excellence Award” in 2009, for the contribution of SOPs consolidations. (GPO)

Received several Awards of Merit in recognition of outstanding researchs at the Student Research & Creative Activities Symposium at Northeastern IL University in April 2006, April 2005, & April 2003

Skills

Knowledge of Microsoft Word, Excel, Microsoft Power Point, Lotus Notes and Microsoft MathCAD.

Knowledge of DryLab (A computer assistant for method development).

CDA (controlled drugs agent).

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