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RYAN SINGH
857 Anderson Road • Jackson, NJ 08527 • ryansingh2244@gmail.com • (551) 358-7163
A driven research scientist with a wide range of lab skills.
BIOTECHNOLOGY ● RESEARCH SCIENCE ● PHYSICAL SCIENCE ● NUCLEAR
ENGINEERING
SUMMARY OF QUALIFICATIONS
 Excellent computational, analytical, and problem-solving skills.
 Training in both organic and inorganic synthetic techniques, and characterization by NMR, IR, LC-
MS, GC, HPLC, AA, UV Visible Spectroscopy.
 Familiarity with pharmaceutical compound screening using animal models.
 Strong ability to work in teams with superb communication and interpersonal skills.
 Inherent dedication to consistency.
 Adept at encouraging compliance to a set of standards.
 Detail-oriented with exceptional documentation skills.
 Proven ability to handle multiple tasks and prioritize accordingly.
 Quick and keen learner, always striving for excellence.
 Highly adaptable – calmly, intelligently, and readily responding to circumstances.
 A strong asset to any team by enhancing the commitment to achieve in others.
 Highly experienced and familiar with USP, EP, BP, and FCC Compendia.
Professional Experience
QC CHEMIST October 2015 to Presemt
AUROLIFE PHARMA Dayton, NJ
Healthcare product manufacturer and distributor with more than $20 billion in 2015 revenues.
• Executes all tasks and responsibilities in accordance with SOPs and in a fast-paced FDA regulated
environment.
• Provide leadership, training, and guidance to peers as a senior level chemist.
• Tests CII, CI controlled substances, as well as generic, OTC,non-OTCand uncontrollesd, finished,
bulk goods and raw materials using HPLC, GC, UV, Mv, Potentiometric, and KF methods.
Decreased amount of time materials remain on hold by 20%.
• Inventories and orders laboratory chemicals and supplies. Reduced wasted spending by up to 35%.
• Reviews laboratory notebooks, analysis sheets and other FDA regulated documentation.
• Ensures adherence to GMP and FDA rules and regulations throughout testing and analysis.
• Coordinates with multiple departments as needed.
• Regularly perform laboratory and safety audits as directed by the department manager.
• Responsible for the inspection and calibration all equipment, standards and controls to confirm
specifications and standardization’s are current.
RYAN SINGH
857 Anderson Road • Jackson, NJ 08527 • ryansingh2244@gmail.com • (551) 358-7163
R&D SCIENTIST - RAW MATERIAL CENTER August 2012 to October 2014
JOHNSON & JOHNSON Skillman, NJ
Multi-national manufacturers of pharmaceutical, diagnostic, therapeutic, surgical, and biotechnology
products with more than $65 billion in 2011 revenues.
• Revise raw material and process/formulation specifications as needed.
• Provides the necessary technical writing to justify project changes made globally.
• Evaluates the impact on the marketed product due to revisions on the raw material specification.
• Effectively works with various cross-functional groups (Stability, Analytical, Microbiology, etc) in
order qualify new raw materials in currently marketed products and successfully closed projects in
a timely manner.
• Prepare lab batches of all formulations of semi-solid and liquid products to ensure safety and
efficacy before implementing the raw material changes.
• Advised other cross functional groups of any potential risks associated with the given chemical
changes.
• Successfully determined route cause analysis
• Performs periodic stability studies in FDA regulated lab notebooks while adhering to cGDP’s.
• Effectively manage 50+ qualification projects at once while meeting strict project deadlines.
• Qualify new materials and suppliers, validate supply chains, write and maintain specifications, and
troubleshoot day-to-day issues with suppliers and manufacturing sites.
LABORATORY CHEMIST January 2010 to August 2012
CHURCH & DWIGHT, ARM & HAMMER Lakewood, NJ
Healthcare product manufacturer and distributor with more than $2 billion in 2010 revenues.
• Executes all tasks and responsibilities in accordance with SOPs and in a fast-paced FDA regulated
environment.
• Provide leadership and guidance to peers as a Shift Lead on an off-shift.
• Tests dental care, antiperspirant, household, OTC and non-OTC finished, bulk goods and raw
materials. Decreased amount of time materials remain on hold by 20%.
• Inventories and orders laboratory chemicals and supplies. Reduced wasted spending by up to 35%.
• Reviews laboratory notebooks, analysis sheets and other FDA regulated documentation.
• Ensures adherence to GMP and FDA rules and regulations throughout testing and analysis.
• Coordinates with multiple departments and attend daily production meetings to ensure quality is
maintained and production runs proceed without incident.
• Regularly perform laboratory audits as directed by the department manager.
• Assists in the development of new product formulations through the use of small scale lab batches.
• Responsible for the inspection and calibration all equipment, standards and controls to confirm
specifications and standardizations are current.
• Reviews testing by other analysts to ensure compliance, completeness and accuracy.
• Conduct minor investigations related to Out-of-Specification procedures and test results.
In charge of reviewing and presenting new and updated SOPs.
RYAN SINGH
857 Anderson Road • Jackson, NJ 08527 • ryansingh2244@gmail.com • (551) 358-7163
• Successfully developed new ideas and implemented ways to improve existing processes.
RESEARCH ASSISTANT August 2004 to March 2009
RIDER UNIVERSITY Lawrenceville, NJ
Private university ranked in top tier by US News and World Report.
• Successfully synthesized lipid lowering compounds using Pyrrole derivatives.
• Successfully synthesized many 2,3,4-trisubstituted Pyrrole Nucleosides.
• Tested the purity of the compounds by TLC, C13,and 1H-NMR.
• Administer compounds to mice via IP dosing at 8mg/kg/day for 14 days.
• Collect serum and assay for total cholesterol and triglycerides.
• Compounds were determined to lower both serum cholesterol and triglyceride levels in mice buy
24% and 33% respectively.
Additional EXPERIENCE
 Hospital Intern, Capital Health Systems, Fuld and Mercer Campus, Trenton, NJ, January 2005 to
May , 2005.
 Automotive Technician, K&S Diagnostics, Pt. Pleasant, NJ, March 2009 to January 2010.
Education And Training
BACHELOR OF SCIENCE 2008
RIDER UNIVERSITY Lawrenceville, NJ
Area of Study: Biochemistry
Coursework
Advanced Cell & Molecular Biology, Genetics, Organic Chemistry, Physical Chemistry I and II,
Analytical Chemistry, Advanced Organic Synthesis & Characterization, Biochemistry.
Laboratory Skills
Agarose gel electrophoresis; culturing and handling of bacterial samples; PCR techniques;
spectrophotometry, microscopy, recrystalization, distillation, extraction, column chromatography, Ion
Chromatography, collecting and analyzing data, Infrared Spectroscopy, 1H-NMR, 13C-NMR, GC,
Normal and Reverse Phase HPLC. UV Visible Spectroscopy , pH and mV testing, Atomic Absorbtion
Spectroscopy, and Refractive Index Analysis, Primer creation (Primer3 Website) and select
Bioinformatics (ORF finder programs, BLAST, and MFold).
• Presentation, 235th National American Chemical Society meeting in New Orleans. Diaa Nimer,
RYAN SINGH
857 Anderson Road • Jackson, NJ 08527 • ryansingh2244@gmail.com • (551) 358-7163
Kelsey Brown, Sophie Song, Ryan Singh, Katiana Bordenave, Lipid-Lowering Pyrrole Derivatives
and their Biological Effects, April 2008.
Professional associations and skills
 Member, American Chemical Society.
 Microsoft Word, Excel, PowerPoint.
 Proficient in WMS and SAP systems.
 Proficient in Chromeleon Chromatographic Software.
 Proficient in Empower 3 Chromatographic Software.
 Proficient in LIMS software.

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RyanSingh - CV1

  • 1. RYAN SINGH 857 Anderson Road • Jackson, NJ 08527 • ryansingh2244@gmail.com • (551) 358-7163 A driven research scientist with a wide range of lab skills. BIOTECHNOLOGY ● RESEARCH SCIENCE ● PHYSICAL SCIENCE ● NUCLEAR ENGINEERING SUMMARY OF QUALIFICATIONS  Excellent computational, analytical, and problem-solving skills.  Training in both organic and inorganic synthetic techniques, and characterization by NMR, IR, LC- MS, GC, HPLC, AA, UV Visible Spectroscopy.  Familiarity with pharmaceutical compound screening using animal models.  Strong ability to work in teams with superb communication and interpersonal skills.  Inherent dedication to consistency.  Adept at encouraging compliance to a set of standards.  Detail-oriented with exceptional documentation skills.  Proven ability to handle multiple tasks and prioritize accordingly.  Quick and keen learner, always striving for excellence.  Highly adaptable – calmly, intelligently, and readily responding to circumstances.  A strong asset to any team by enhancing the commitment to achieve in others.  Highly experienced and familiar with USP, EP, BP, and FCC Compendia. Professional Experience QC CHEMIST October 2015 to Presemt AUROLIFE PHARMA Dayton, NJ Healthcare product manufacturer and distributor with more than $20 billion in 2015 revenues. • Executes all tasks and responsibilities in accordance with SOPs and in a fast-paced FDA regulated environment. • Provide leadership, training, and guidance to peers as a senior level chemist. • Tests CII, CI controlled substances, as well as generic, OTC,non-OTCand uncontrollesd, finished, bulk goods and raw materials using HPLC, GC, UV, Mv, Potentiometric, and KF methods. Decreased amount of time materials remain on hold by 20%. • Inventories and orders laboratory chemicals and supplies. Reduced wasted spending by up to 35%. • Reviews laboratory notebooks, analysis sheets and other FDA regulated documentation. • Ensures adherence to GMP and FDA rules and regulations throughout testing and analysis. • Coordinates with multiple departments as needed. • Regularly perform laboratory and safety audits as directed by the department manager. • Responsible for the inspection and calibration all equipment, standards and controls to confirm specifications and standardization’s are current.
  • 2. RYAN SINGH 857 Anderson Road • Jackson, NJ 08527 • ryansingh2244@gmail.com • (551) 358-7163 R&D SCIENTIST - RAW MATERIAL CENTER August 2012 to October 2014 JOHNSON & JOHNSON Skillman, NJ Multi-national manufacturers of pharmaceutical, diagnostic, therapeutic, surgical, and biotechnology products with more than $65 billion in 2011 revenues. • Revise raw material and process/formulation specifications as needed. • Provides the necessary technical writing to justify project changes made globally. • Evaluates the impact on the marketed product due to revisions on the raw material specification. • Effectively works with various cross-functional groups (Stability, Analytical, Microbiology, etc) in order qualify new raw materials in currently marketed products and successfully closed projects in a timely manner. • Prepare lab batches of all formulations of semi-solid and liquid products to ensure safety and efficacy before implementing the raw material changes. • Advised other cross functional groups of any potential risks associated with the given chemical changes. • Successfully determined route cause analysis • Performs periodic stability studies in FDA regulated lab notebooks while adhering to cGDP’s. • Effectively manage 50+ qualification projects at once while meeting strict project deadlines. • Qualify new materials and suppliers, validate supply chains, write and maintain specifications, and troubleshoot day-to-day issues with suppliers and manufacturing sites. LABORATORY CHEMIST January 2010 to August 2012 CHURCH & DWIGHT, ARM & HAMMER Lakewood, NJ Healthcare product manufacturer and distributor with more than $2 billion in 2010 revenues. • Executes all tasks and responsibilities in accordance with SOPs and in a fast-paced FDA regulated environment. • Provide leadership and guidance to peers as a Shift Lead on an off-shift. • Tests dental care, antiperspirant, household, OTC and non-OTC finished, bulk goods and raw materials. Decreased amount of time materials remain on hold by 20%. • Inventories and orders laboratory chemicals and supplies. Reduced wasted spending by up to 35%. • Reviews laboratory notebooks, analysis sheets and other FDA regulated documentation. • Ensures adherence to GMP and FDA rules and regulations throughout testing and analysis. • Coordinates with multiple departments and attend daily production meetings to ensure quality is maintained and production runs proceed without incident. • Regularly perform laboratory audits as directed by the department manager. • Assists in the development of new product formulations through the use of small scale lab batches. • Responsible for the inspection and calibration all equipment, standards and controls to confirm specifications and standardizations are current. • Reviews testing by other analysts to ensure compliance, completeness and accuracy. • Conduct minor investigations related to Out-of-Specification procedures and test results. In charge of reviewing and presenting new and updated SOPs.
  • 3. RYAN SINGH 857 Anderson Road • Jackson, NJ 08527 • ryansingh2244@gmail.com • (551) 358-7163 • Successfully developed new ideas and implemented ways to improve existing processes. RESEARCH ASSISTANT August 2004 to March 2009 RIDER UNIVERSITY Lawrenceville, NJ Private university ranked in top tier by US News and World Report. • Successfully synthesized lipid lowering compounds using Pyrrole derivatives. • Successfully synthesized many 2,3,4-trisubstituted Pyrrole Nucleosides. • Tested the purity of the compounds by TLC, C13,and 1H-NMR. • Administer compounds to mice via IP dosing at 8mg/kg/day for 14 days. • Collect serum and assay for total cholesterol and triglycerides. • Compounds were determined to lower both serum cholesterol and triglyceride levels in mice buy 24% and 33% respectively. Additional EXPERIENCE  Hospital Intern, Capital Health Systems, Fuld and Mercer Campus, Trenton, NJ, January 2005 to May , 2005.  Automotive Technician, K&S Diagnostics, Pt. Pleasant, NJ, March 2009 to January 2010. Education And Training BACHELOR OF SCIENCE 2008 RIDER UNIVERSITY Lawrenceville, NJ Area of Study: Biochemistry Coursework Advanced Cell & Molecular Biology, Genetics, Organic Chemistry, Physical Chemistry I and II, Analytical Chemistry, Advanced Organic Synthesis & Characterization, Biochemistry. Laboratory Skills Agarose gel electrophoresis; culturing and handling of bacterial samples; PCR techniques; spectrophotometry, microscopy, recrystalization, distillation, extraction, column chromatography, Ion Chromatography, collecting and analyzing data, Infrared Spectroscopy, 1H-NMR, 13C-NMR, GC, Normal and Reverse Phase HPLC. UV Visible Spectroscopy , pH and mV testing, Atomic Absorbtion Spectroscopy, and Refractive Index Analysis, Primer creation (Primer3 Website) and select Bioinformatics (ORF finder programs, BLAST, and MFold). • Presentation, 235th National American Chemical Society meeting in New Orleans. Diaa Nimer,
  • 4. RYAN SINGH 857 Anderson Road • Jackson, NJ 08527 • ryansingh2244@gmail.com • (551) 358-7163 Kelsey Brown, Sophie Song, Ryan Singh, Katiana Bordenave, Lipid-Lowering Pyrrole Derivatives and their Biological Effects, April 2008. Professional associations and skills  Member, American Chemical Society.  Microsoft Word, Excel, PowerPoint.  Proficient in WMS and SAP systems.  Proficient in Chromeleon Chromatographic Software.  Proficient in Empower 3 Chromatographic Software.  Proficient in LIMS software.