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JRF India

Head – Business Development

Manager – Business Development

Jr. Research Officer - Ecotox Section

Jr. Research Officer/ Research Officer - Genotox Section

Jr. Research Officer - Acute/ Chronic / Reptox Section

Jr. Research Officer/ Research Officer - Chemistry Section

Jr. Research Officer - Chemistry Section

JRF America

Lab Technician

Scientist I / Entry Level Chemist

JRF America, a member of the JRF Global group, established in 2008 is a Fully Independent Contract Research Laboratory (CRO) specialized in a higher tier regulatory chemistry services to the agrochemical sector. Our extensive expertise includes managing large study programs, field study components & understanding regulatory needs at a state, national, and international level. Studies are performed in accordance with GLP guidelines. We have the latest and most sensitive analytical instruments including HPLC/UPLC instruments with Sciex 4000 and 6500 Q Trap Mass Spectrometers, and a B-Ram radio analysis detector, to name a few.

JRF America strives to employ a varied and diverse range of dynamic people who understand and appreciate the importance of our mission and what we do. When you consider an opportunity at JRF America you will be joining a dedicated and professional group.

Experience and competencies in the following is a Plus -

Bachelor of Science or advanced degree from an accredited college or university in chemistry or other science-related field, or has comparable industrial credentials.
1-3 years of experience in a laboratory setting (QA experience preferred)

Key Job Responsibilities –

Set up experiments under the guidance of a Scientist II and/or Team Lead
Operate equipment, observe and log the progress of experiments
Promptly submit experimental data / findings to the supervisor
Promptly inform the supervisor of any problems encountered during the experiments.
Assist in data entry in various formats and verify accuracy of data entry
Assist in writing drafts of Protocols and Reports
Provide a daily update on the progress, findings and results for each experiment.
Compile the data as directed by the supervisor
Check the quality and accuracy of the data before submission to the supervisor

Additional Info –

Position Type - Full Time
Package - Commensurate with expertise and experience
Benefits: Medical, dental, and vision coverage, Flexible Spending Account, Employee Assistance Program, Company-paid Short Term & Long Term Disability coverage, Retirement savings with a generous company match, Paid holidays and vacation time

Apply Now

Scientist II

JRF America, a member of the JRF Global group, established in 2008 is a Fully Independent Contract Research Laboratory (CRO) specialized in a higher tier regulatory chemistry services to the agrochemical sector. Our extensive expertise includes managing large study programs, field study components & understanding regulatory needs at a state, national, and international level. Studies are performed in accordance with GLP and via EPA, OECD, and any other guidelines applicable. We have the latest and most sensitive analytical instruments including HPLC/UPLC instruments with Sciex 4000 and 6500 Q Trap Mass Spectrometers, LSC, and a B-Ram radio analysis detector, to name a few.

Experience and competencies in the following is a Plus:

Bachelor/Master’s Degree in Science with minimum 3-5 years’ experience in analytical chemistry & agrochemical.
Knowledge of extraction procedures and basic fundamental of separation chemistry.
Total knowledge of guidelines utilized to run high tier metabolism studies and residue studies.
Ability to independently run instruments such as: HPLC/MS/MS, GC/MS/MS, UV, and others.
GLP experience and have worked on GLP studies as they relate to the agro or pharmaceutical industries.
Team management experience and coordination
Report and protocol writing experience

Key Job Responsibilities:

Design experiments and studies, manage resources, both equipment and personnel, and organize experimental set up
Design new studies under the guidance of the team leads
Work with the Team Leads to develop protocols and run studies for our clients
Instrument operation and data interpretation as primary review
Act as study director in multiple studies and in different departments
Review data and provide timely updates to sponsors
Relationship Management for key accounts
Report writing
Organizing resources to improve the efficiency of the lab process
Review SOP’s to provide feedback and contribute towards improvement
Orient, mentor and teach laboratory methods, procedures and techniques to new chemists
Demonstrate effective teamwork skills by knowledge sharing
Take on formally assigned additional duties as a part of routine job performance
Participate on special project teams as requested by management
Volunteer to serve on various committees and panels to the benefit of the laboratory (e.g. Safety Committee)

Additional Information:

Position Type: Full-Time
Package: Commensurate with expertise and experience
Benefits: Medical, dental, and vision coverage, Flexible Spending Account, Employee Assistance Program, Company-paid Short Term & Long Term Disability coverage, Retirement savings with a generous company match, Paid holidays and vacation time

Apply Now

Team Lead

Experience and competencies in the following is a Plus:

Bachelor/Master’s Degree in Science with minimum 5-8 years’ experience in analytical chemistry & agrochemical.
Strong fundamental knowledge of the chemistry for extraction and concentration of the moieties of interest from complicated matrices like soil, water, waste-water, plant and animal tissues.
Ability to tune and optimize compounds for mass spectrometers as part of an HPLC/MS system.
GLP experience and total understanding of guidelines and study conduct as it applies to residue and metabolism

Key Job Responsibilities:

Design experiments and studies, manage resources (both equipment and personnel), and organize experimental set up
Interpret data and present the results and conclusions with scientific proof/references.
Act as a technical liaison with the sponsor, organize regular technical calls to explain experimental results,
suggest technically sound, innovative, and reliable ways to undertake the studies, and justify the scientific
findings using sound judgment on case-to-case basis, to produce scientifically defensible data.
Protocol and Report writing/reviewing
Guide and help Scientist II to develop into their roles and prepare for a new role, as applicable
Ensure all GLP processes are followed and adhered to
Ensure studies are on track and no delay will occur due to errors or lack of organization.
Manage resources to ensure that laboratory is effective and efficient.
Determine ways to improve in-house processes and develop new innovative way to do things.
Use management tools to ensure study directors are meeting their timelines with total scientific integrity
Present work at conferences, as applicable; SOP review and development
Provide weekly or monthly review of concurrent studies and their progress
Ensure safety protocols are always followed

Additional Info:

Position Type: Full-Time
Package: Commensurate with expertise and experience
Benefits: Medical, dental, and vision coverage, Flexible Spending Account, Employee Assistance Program, Company-paid Short Term & Long Term Disability coverage, Retirement savings with a generous company match, Paid holidays and vacation time

Apply Now

Quality Assurance Officer

Experience and competencies in the following is a Plus:

Bachelor of Science or advanced degree from an accredited college or university in chemistry or other science-related field, or has comparable industrial credentials.
1-3 years of experience in a laboratory setting (QA experience preferred)
Good verbal and excellent written communication skills and the ability to work within a highly government-regulated area.

Key Job Responsibilities:

Position provides quality assurance (QA) functions for the US based regulatory chemistry program, requiring knowledge and experience with local, state, federal, and foreign government regulations (e.g., U.S. Federal Insecticide, Fungicide, Rodenticide Act, U.S. Good Laboratory Practices (GLP), European and Canadian OECD, and JMAFF study requirements).
Assists in maintaining the QA database system for JRF America.
Assists in scheduling and conducting inspections of JRF America studies and facilities to ensure that all studies and facilities are conducted in accordance with the appropriate GLP regulations, including:
- Reviewing protocols, amendments, and deviations,
- Inspecting data and reports to confirm that the methods, procedures, and observations are accurately and completely described, and that the reported results accurately and completely reflect the raw data of the studies,
- Coordinating and responding to external audits (e.g., sponsor and regulatory agency audits) and ensuring adequate corrective actions to any findings.
Assists in GLP training and education; and miscellaneous support duties as needed.

Additional Info:

Position Type: Full-Time
Package: Commensurate with expertise and experience
Benefits: Medical, dental, and vision coverage, Flexible Spending Account, Employee Assistance Program, Company-paid Short Term & Long Term Disability coverage, Retirement savings with a generous company match, Paid holidays and vacation time

Apply Now

Lead Scientist/Test Facility Manager (TFM)

JRF America, a member of the JRF Global group, established in 2008 is a Fully Independent Contract Research Laboratory (CRO) specialized in a higher tier regulatory chemistry services to the agrochemical sector. Our extensive expertise includes managing large study programs, field study components & understanding regulatory needs at a state, nat ional, and international level. Studies are performed in accordance with GLP guidelines. We have the latest and most sensitive analytical instruments including HPLC/UPLC instruments with Sciex 4000 and 6500 Q Trap Mass Spectrometers, and a B-Ram radio analysis detector, to name a few.

Experience and competencies in the following is a Plus:

Master’s degree/PhD in Science.
12+ years of experience with GLP E-fate and Metabolism as well as residues studies, as an eminent scientist in a CRO of a corporate regulatory research set up. Any experience of outsourcing and monitoring the studies would be valuable, in addition to the hands-on research experience.
Expertise and experience in extremely low level detection and quantification of parent compounds, impurities,
metabolites and degradants.
Strong fundamental knowledge of the chemistry for extraction and concentration of the moieties of interest from complicated matrices like soil, water, waste-water, plant and animal tissues.
Ability to tune mass spectrometers as part of an HPLC/MS system.
Understanding and interpreting the regulatory requirements in the sciences preferably on a global basis.
Flexibility to travel throughout the US, Canada and some international travel.

Key Job Responsibilities:

Serves as the principal technical manager (Test Facility Management) for the laboratory. The incumbent will be responsible for ensuring that all studies performed at JRFA meet the highest quality standards, full EPA and Global GLP compliance. Adherence to the sponsor’s timelines while ensuring the conduct of the study with application of sound scientific principles. Responsible to perform the duties of Lead Scientist, which include but are not limited to:

Provides oversight and management for environmental fate/ metabolism studies, and residue studies, for the purpose of registering/reregistering new/existing compounds for agrochemical/ specialty chemical /pharmaceutical/veterinary uses.
Mentor, advise and provide training to the scientific personnel on a range of topics including (but not limited to
analytical chemistry (Mass spectrometry, HPLC, IR, UV, NMR, Raman etc.), Soil chemistry, protein chemistry,
Guidelines as per OECD, and EPA, conduct of studies for residue and metabolism, GLP, regulatory affair issues,
extraction procedures, new innovations in industry.
Communicate & trouble shoot techniques for all methods involving the following: gas and liquid chromatography, separations chemistry, radio tracer analysis (LSA and RFA-HPLC) and specialized trace level analytical procedures such as LC/MS, GC/MS, MS/MS, NMR, IR, or UV. Have hands-on proficiency with performing and troubleshooting, these techniques and associated instruments and equipment.
Perform (or oversee) method development and validation for residue and metabolism studies.
Review protocols and GLP reports for all studies in accordance with the expected Guidelines.
Ensure accurate interpretation of data and reviews reports produced by the Study Directors.
Ensure that the studies are performed and delivered efficiently and timely, to meet sponsors expectations.
Ensure that new software packages or modeling tools follow the experimental needs and GLP.
Study and work with new concepts and applies them to the work at hand.
Understand field trial studies as they relate to residue or metabolism, and the requirements set forth by guidelines and authorities.
Oversee all the research projects as per needs with sponsor requirements in mind.
Provide guidance to business development personnel, based on extensive knowledge of the agrochemical marketsector and science involved.
Ensuring sponsor engagement and satisfaction. Provide guidance to sponsor on agency requirements and assists in agency meetings.
Provide thorough knowledge of analytical procedures and appropriate skills for interpreting data in residue,
environmental fate, and metabolism studies.
Provide sound knowledge of regulatory requirements in accordance with the guidance documents of FIFRA, GLP, US-FDA, and EPA etc.
Act as study director when necessary, for any of the services offered by JRFA.
Work with the Quality Assurance Unit in the assessment of procedures and results, providing an awareness and understanding of EPA GLP and data reporting requirements.
Oversee assignments relating to general laboratory safety, Rad safety, and waste disposal safety.
Responsible to track and resolve sponsor complaints.

Additional Info:

Position Type: Full-Time
Package: Commensurate with expertise and experience
Benefits: Medical, dental, and vision coverage, Flexible Spending Account, Employee Assistance Program, Company -paid Short Term & Long Term Disability coverage, Retirement savings with a generous company match, Paid holiday s and vacation time

Apply Now