Current Job Openings

Job Description:

Our Business Development team consist of highly professional and strong background in Sales and Business Development they build professional relationship and coordinate various business development activities. The major task of the team is to achieve the business that contributes to the total target for JRF and ensure T-A=0 for the region.

Job Responsibilities:

• Oversee the sales process to attract new clients.
• Work with senior team members to identify and manage risks.
• Maintain a pleasant and fruitful professional relationship with clients and address their needs/ concerns effectively.
• Research and identify new market opportunities.
• Prepare and deliver pitches to potential investors.
• Foster a collaborative environment within the organization.

Qualification and Experience:

• Minimum Educational Qualification: Graduate in Science (preferably Pharmaceutical Science) or MBA will be an added advantage.
• Experience Range: 1 to 4 years.
• Relevant Experience: 1-2 years in Pharma/Biotech/CRO/CMO/CDMO or other allied industries.
• Computer/IT Skills: Laptop, Salesforce, Microsoft Excel and Power Point or similar Sheets and Presentation Platforms and Data analysis.
• Other skills: Sales, Marketing, Data analysis, Data presentation, English language proficiency, Communication skills, Team work.
• Salary: Negotiable for competent candidature.

Job Description:
JRF offers comprehensive nonclinical GLP research services for regulatory submissions, worldwide. JRF offers fast, transparent, cost-effective, and hassle-free services in Toxicology, Eco-toxicology, Chemistry, Environmental Fate and Metabolism, and other regulatory testing requirements.

Job Responsibilities:

• Participate and learn while conducting the scientific Regulatory Research/ studies, as per the Organizational requirements.
• Assist the Study Director and subsequently learn to operate the required instruments and machineries for performing the required research work.
• Assist the study Director in preparing and maintaining the required regulatory data.
• Ensure that studies are of the best quality and carried out in an expeditious manner.
• Constantly work towards improving self-competency; effectively maintain the performance improvement activities within the section.

Qualification:

• Relevant Experience: 0-2 years
• Education: M. Sc. (Zoology/Toxicology/Pharmacology/Life science), M.V.Sc.
• Computer Skills: Proficient.
• Other skills: Teamwork and Collaboration

Only for Experience candidate:

• Knowledge of conducting of animal toxicology studies mainly repeated dose toxicity studies.
• Should be aware of animal handling and care
• Should be aware of dosing procedure by different routes in different in different species.
• Should be aware of different regulatory requirement for toxicology studies.
• Should have experience in working under GLP conditions.

 
Salary: Negotiable for competent candidature.

Job Description:
JRF offers comprehensive nonclinical GLP research services for regulatory submissions, worldwide. JRF offers fast, transparent, cost-effective, and hassle-free services in Toxicology, Eco-toxicology, Chemistry, Environmental Fate and Metabolism, and other regulatory testing requirements.

Job Responsibilities:

• Develop and lead the unit.
• Establish Strategy and develop a time bound action plan for implementation of the strategy.
• Provide guidance to the team and mentor the supporting team.
• Use an integrated approach, leverage public data bases and novel technologies to address problems in research under preclinical settings.
• Research and design build in-silico models and tools for risk and toxicity assessment for prospect drug moieties, cosmetic ingredients and specialty chemicals using QSAR, Read Across approach and forward reverse docking approach.
• Guide the team to develop relevant SOPs.
• Interact with the other CROs and collaborators to augment capabilities that other are yet to be developed in-house.
• Identifying lead and implement proof of concept studies that can lead to publications white papers and can be leveraged to build solutions.
• Present work at internal and external meetings.

Qualification:

• Relevant Experience: 10-15 yrs. In Industry/Biotech/CRO in preclinical environment.
• Experience in planning, implementing, and delivering projects in the predictive toxicology space leveraging new technologies, best practices, and regulatory guidelines.
• Education: Minimum M.Sc. and maximum Ph.D. in Medicinal Chemistry or Bioinformatics or Molecular Biology or Biotechnology or related areas.
• Computer Skills: Basic Computer knowledge.
• Other skills: Team Player, Hardworking and keen learner
• Salary: Negotiable for competent candidature.

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:

• High School Diploma OR GED OR has comparable industrial credentials.

Key Job Responsibilities:

• Assist laboratory chemists in tasks revolving around chemistry, for regulatory studies in conformity with
  the principles of GLP.
• Laboratory and written task/s (with end-time target for completion) assigned by the Supervisor(s) are
  completed diligently, ensuring proper usage of the equipment and facilities.
• 90% - General laboratory washing of laboratory glassware; grinding and processing of samples; provide
  support to chemistry staff for studies; maintaining chemical inventory and laboratory supplies;
  receiving/delivering of materials; and general upkeep and maintenance of the laboratory.
• Receipt, storage, log-in, and inventory of samples in the walk-in freezer; and the disposal of samples as
  appropriate.
• Scheduled calibration of laboratory equipment (e.g., pipettes, thermometers)
• 10% - Work with the Archivist with archival duties, e.g., copying/scanning of documents; filing; packaging;
  and preparation of transmittal documentation to sponsors.

Additional Info:

• Position Type: Part-Time (30 hours/per week)
• Benefits: Retirement savings with a generous company match, Flexible Spending Account, Employee Assistance
  Program

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