Paramount to E-Merge tech is the sustenance of an exclusive work culture that has effectively driven the organization on the path of success. E-Merge tech’s winning blend comprises of teamwork, innovation, technology and vision, which takes shape to form a very unique work ethos.
The organization ensures that it absorbs highly talented people with problem-solving abilities. E-Merge tech truly values those who exhibit leadership abilities and prove to be highly intelligent with a creative bent of mind.
Jobs @ E-Merge tech
Product Compliance Analyst
E-Merge tech is seeking highly Energetic, Dynamic and Research mindset analyst for Chemical Regulatory and Product compliance services.
Roles & Responsibilities
Manage the product compliance projects
Work along with team
Analyse other EU regulatory compliance requirements related to chemicals
Participate in client interactions
Support business department through the Regulatory and Compliance knowledge
Collect, analyse and interpret regulatory information
Responsible for final regulatory outputs
Familiar with Regulations like – Chemical, Cosmetics, Medical Device, Toys, food etc
RoHS, REACH, WEEE, Prop65 etc
Knowledge in Toxicology
3+ years of relevant work experience
Chemical | Environmental | Pharma | Biotech Degree
E-Merge tech is seeking a Senior Data Curator to be a Lead on a project and provide solution for data curation.
Role involves reading scientific literatures, clinical trials, other related documents and curating or extracting information.
Roles & Responsibilities
Gather requirements from the customer and propose strategic directions and potential solutions.
Curating or extracting information such as gene, disease, drug, mutation, protein interaction, pathways, mechanisms etc. from different literature’s according to SOP and protocol.
Strong scientific knowledge, and a good understanding of molecular biology concepts
Team handling experience
Prior experience in curating information from scientific publications, related to the disease mechanism, protein interactions, genomics, genetic variants, BioMarker, Omics, microbiome is an advantage
Regulatory Documents such as Clinical Study Reports (CSRs), Case Studies, Investigators Brochures (IBs) Protocol and other Regulatory medical writing, Data Science Analytics, Scientific and Research Writing, Blog Content Writing, Content Development.
Responsible for Authoring Clinical Evaluation Reports, Clinical Evaluation Plans, Post-Market Surveillance reports, and Periodic Safety Update Reports Literature Search, Screening, and Summarization of articles Perform data Fact check of the Documents authored Ensure Documents Comply with the Regulatory Requirements Participate, Project requirements Compliance to Quality, Confidentiality, and Security Adhere and follow Quality Systems, Processes and Policies Comply to Training and Specifications.
Minimum of 2-3 years Experience in Scientific Writing / Regulatory-Medical Writing / Developing Requires an Extensive relevant Experience in Clinical or Regulatory Documents for Submission within the Pharmaceutical/Biotechnology / Medical Device industry.
Excellent Verbal Communication Skills
Well-Developed Computer Skills Including Proficiency in Word Adobe Excel and the Regulatory Document Management System
Knowledge in using standard checklists such as MEDLINE, EMBASE, Cochrane, CancerLit, AIDSLine, ToxLine, IndexMedicus