Associate Scientist Resume
New Jersey, NJ
ANALYTICAL CHEMIST Specializing in product development—synthesis, analysis and manufacturing. Extensive experience with a Fortune 100 corporation in developing products from design to full scale manufacturing by utilizing excellent chemical, analytical, communication and teamwork skills. Trained and experienced in GMP/GLP while following rigid Standard Operating Procedures. Professional strengths include:
- Substantial experience in industrial laboratory and scale-up manufacturing.
- Technical proficiency: HPLC, UV-VIS, FT-IR, NMR, TLC, Dissolution, KF, Silverson.
- Formulations, quality control and manufacturing.
- Excellent teamwork, oral and written communication skills.
- Organized, detail-oriented with the ability to handle volumes of simultaneous tasks.
Confidential NJ 2005- 2011
Associate Scientist (2006 – 2011)
- Protocol preparation (writing, reviewing, amending and cross functional facilitation)
- Ensured compliance with all applicable regulations and company policies
- Maintained detailed records used in formulations for dosing preclinical studies.
- Developed and validated methods of formulations for stability and homogeneity testing.
Confidential
(2005 – 2006)
Responsibilities:
- Worked on ongoing method development for new drugs.
- Performed degradation studies, accelerated and real-time stability studies.
- Tested through HPLC, UV and dissolution stability and bulk sample of a new drug following GMP.
- Performed Pharmaceutical Active Ingredient extraction for new drugs
- Entered and reviewed accuracy of contract laboratory data into LIMS for FDA submission of a new drug.
- Supported investigations from the out of specification results test.
- Performed calibration and maintenance of laboratory instrument
Accomplishments:
- Developed a method for testing new drugs using dissolution, HPLC and UV.
- Followed GMP while using HPLC, UV, dissolution for stability and bulk products
- Finalized all the data from contract labs into LIMS for FDA submission of a new drug
- Resolved the compliance issues of investigated results of the testing
- Calibrated and maintained the laboratory instruments on time.
Confidential
Organon USA, West Orange, NJ 2001 – 2004Responsibilites:
- Responsible for testing of raw materials used for production of the company products.
- Conducted stability and released testing of oral, protein and sterile products.
- Supported the routine testing of sterile bulk following the GMP.
- Monitored testing to ensure timely turnaround of both release and stability samples.
- Maintained monthly maintenance and calibration of laboratory instrumentation
Accomplishments:
- Facilitated the raw materials were tested before productions
- Generated results of stability and released testing of oral, protein and sterile products
- Reported results on timed turnaround of both release and stability samples
- Analyzed the routine testing of sterile bulk following GMP
Confidential
Abbott Laboratories, Abbott Park, IL 1996 – 1999
- Collected routine Nuclear Magnetic Resonance (NMR) spectra in both manual and automated modes on several spectrometers and plotting the resulting spectra for chemical research.
- Monitors test results of samples collected from NMR Spectrometers.
- Evaluates and reports results of testing through formal reports or in conversation with managements.
- Advised chemist regarding questions pertaining to samples and techniques.
- Responsible for setting up experiments in spectrometers through robotic systems.
- Exercises proficiency in archiving and plotting all spectra results using UNIX operating systems.
- Ordered and maintained inventory of laboratory supplies and instrument.
- Assisted in training of new employees.
PRIOR RELEVANT EXPERIENCE
Confidential
Waukegan, IL
Pharmacy Technician
Confidential
Philippines
Operations Manager
Confidential
Philippines
Pharmacist
EDUCATION
BS, Pharmacy
