Experienced Laboratory Analyst with GC Training and Experience who brings formal education along with on hands experience to the workplace. A trained professional who can function in the field as well as in a corporate setting. A motivated problem solver who utilizes all available resources to complete a given task. I can work independently or on a team. Outstanding communication skills that enable me to present a proposal in a boardroom or teach a safety class in the laboratory. Safety 1st!
Experienced Laboratory Analyst with GC Training and Experience who brings formal education along with on hands experience to the workplace. A trained professional who can function in the field as well as in a corporate setting. A motivated problem solver who utilizes all available resources to complete a given task. I can work independently or on a team. Outstanding communication skills that enable me to present a proposal in a boardroom or teach a safety class in the laboratory. Safety 1st!
Experienced Laboratory Analyst with GC Training and Experience who brings formal education along with on hands experience to the workplace. A trained professional who can function in the field as well as in a corporate setting. A motivated problem solver who utilizes all available resources to complete a given task. I can work independently or on a team. Outstanding communication skills that enable me to present a proposal in a boardroom or teach a safety class in the laboratory. Safety 1st!
I am in quest of senior level assignments as Functional Lead - Quality Control/ Quality Assurance with an organization of repute in Denmark or nearby Schengen countries.
Experienced Laboratory Analyst with GC Training and Experience who brings formal education along with on hands experience to the workplace. A trained professional who can function in the field as well as in a corporate setting. A motivated problem solver who utilizes all available resources to complete a given task. I can work independently or on a team. Outstanding communication skills that enable me to present a proposal in a boardroom or teach a safety class in the laboratory. Safety 1st!
I am in quest of senior level assignments as Functional Lead - Quality Control/ Quality Assurance with an organization of repute in Denmark or nearby Schengen countries.
Idling your engine may seem harmless. But it can have countless dangerous effects on your vehicles, your drivers, and your business. Not only that, but it can severely hurt your wallet.
Luckily, there are ways to reduce idling that won't eat up your time or dramatically change how you operate. Teletrac is a fleet management software provider based in Southern California, specializing in helping fleets reduce costs and waste. Reducing idle time with Teletrac software is one of the best ways fleets can become more efficient.
A Global perspective on Energy Securityrainowbrocks
The fossil fuels reserves will no longer be able to supply the growing global demand before 2050. Mankind has to reduce dependence on oil, gas and coal by 2030 to avoid the global economy being thrown into a 1930s style slump by the inevitable rapid increase in oil prices when Peak Oil finally happens. To guarantee UK's Energy Security the Government needs to treble investment in Renewable Energy, expand and sustainably harvest the UK's biomass resource, manufacture synthetic gas, mass produce electric cars and build an electric transport infrastructure, refurbish all buildings with insulation and energy conservation measures and replace all boilers with heat pumps. The benefits could be huge, investing in the alternative technologies creates jobs, energy security will give UK business a competitive advantage, a stronger economy reduces the debt burden and the UK may even survive the global slump ensuring that the UK's future as a prosperous nation. The Zero Carbon Britain - rethinking the future, published by The Centre of Alternative Technology, describes a viable business plan that the UK Government should adopt.
GoGreen Communications has posted this important documentation in support of its market-leading research and practice on idle reduction.
GoGreen is focused on driver behavior modification training, certification and branding for fleet operators.
GoGreen’s Point of View on Idle Reduction.
As of September, 2020, idle reduction from driver behavior modification in a fleet’s gasoline and diesel-burning assets, is the biggest combined cost reduction, greenhouse gas reduction, and air pollution reduction opportunity for fleet operators in the United States and Canada in all fleet industry sectors.
Further, GoGreen believes that cost reduction, greenhouse gas reduction and air pollution reduction should be a fleet operator’s priority at this time of economic crisis, accelerated climate change, and a lung virus pandemic. Currently, idle reduction is not an area of priority for most operators (GoGreen is actively surveying the market, documenting the barriers to creating an idle reduction fleet culture).
It is GoGreen’s view that the typical addressable opportunity for North American fleet operators who have not addressed driver idling behavior (as an aggregate of all fleet industry sectors and all fleet departments) is about 40% of engine hours and its associated downstream cost impact on operation and maintenance expenses* This assumes driver idling behavior only and excludes ‘PTO’ or business function idling in park.
GoGreen has identified the following cost metrics regarding driver idling behavior:
Fuel.
Added maintenance, lost warranties.
Lifecycle costs.
Vehicle downtime.
Employee productivity.
Carbon emissions.
Air quality.
Safety risk (vacant vehicle idling).
Fleet reputation.
Get our A Point of View Paper
Idle Cost Metrics U.S. and Canada
https://docs.goidlefree.com/Idle-Cost-Metrics-POV-Sept-2020
Focused Chemical/Microbiological technician highly effective at following USP methods and GMP practices with pharmaceutical and medical device experience.
Chemist accomplished in GC, HPLC, analytical and assay methods used on raw material and finished products to assure the quality and purity of products. Certified in Clinical Trials and Drug Development and worked side by side a chemical formulator R&D chemist for 3 years. Coordinated process validation procedures, stability program, chemical waste management system, calibration program, laboratory set up, ordering and SOP procedural writing.
Versed Microbiological surface and air quality testing, process validation, microbiological identification, trending, tracking, gram staining techniques and microbiological morphology. Certified in Pharmaceutical Microbiology.
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.