- 19
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Active Jobs Found
(Last Updated: Jul 18, 2026)
- /> Neurology (16)
- 2+ years
- Not Disclosed
- Delhi, India
- Post Date: Jul 07, 2026
- End Date: Sep 07, 2026
- 2+ years
- Not Disclosed
- Delhi, India
- Post Date: Jul 07, 2026
- End Date: Sep 07, 2026
Qualification & ExperienceEligibility: Ph.D. in Life Sciences with 2-3 years' research experience (ICMR/DBT/DST/CSIR or equivalent) and expertise in human physiological monitoring, molecular biology, cell culture and related techniques.
- Operations
- Inspection
- Management
- 5+ years
- Not Disclosed
- Mumbai, Maharashtra, India
- Post Date: Jul 03, 2026
- End Date: Sep 03, 2026
- 5+ years
- Not Disclosed
- Mumbai, Maharashtra, India
- Post Date: Jul 03, 2026
- End Date: Sep 03, 2026
Qualification & Experience MSc Nursing with post M.sc minimum 5 years of teaching experience and should have some experience in leadership or administrative role of school.
- Nurse
- 1+ years
- Not Disclosed
- Mumbai, Maharashtra, India
- Post Date: Jun 29, 2026
- End Date: Aug 29, 2026
- 1+ years
- Not Disclosed
- Mumbai, Maharashtra, India
- Post Date: Jun 29, 2026
- End Date: Aug 29, 2026
Qualification & Experience M.Sc. Nursing or B.Sc. Nursing | Experience: 1–2 years
- Nurse
- 2+ years
- Not Disclosed
- Mumbai, India
- Post Date: Jun 23, 2026
- End Date: Aug 23, 2026
- 2+ years
- Not Disclosed
- Mumbai, India
- Post Date: Jun 23, 2026
- End Date: Aug 23, 2026
ResponsibilitiesIndependently lead end-to-end formulation development and process design for personal care products across formats (creams, lotions, gels, deodorants, body oils, cleansing) Drive fast-track NPD ensuring OTIF timelines and First-Time-Right (FTR) commercialization Translate marketing concepts and consumer insights into technically feasible, cost-effective, and scalable formulations Manage multiple projects simultaneously, ensuring timely delivery and stakeholder alignment Perform technical scoping including literature review, benchmarking, ingredient selection, and formulation strategy Apply DoE and scientific approaches to optimize formulations for performance, stability, manufacturability, and cost efficiency Conduct trend mapping and competitive intelligence to drive innovation and differentiation Identify opportunities and drive innovation, cost optimization, and sustainability initiatives Execute formulation trials, stability studies, and product evaluations considering performance, cost, packaging, regulatory, and safety requirements Lead pilot batches, scale-up, and technology transfer in collaboration with manufacturing and supply chain teams Collaborate with cross-functional teams (Marketing, QA, Analytical, Regulatory, Procurement, Supply Chain) and manage external stakeholders (vendors, third-party manufacturers, labs) Ensure compliance with GLP, GDP, regulatory, and internal quality standards, maintaining audit-ready documentation Create product demos and technical tools to support business and product understanding Draft and validate product claims based on formulation and ingredient functionality, ensuring regulatory alignment Act as a technical partner to marketing, supporting Key Visuals (KV), A+ content, and product storytelling Drive continuous improvement in safety, processes, and operational efficiency Maintain accurate documentation and digital systems for project tracking and data management
- pharma
- pharmacovigilance
- Management
- 4+ years
- Not Disclosed
- Hyderabad, India
- Post Date: Jun 23, 2026
- End Date: Aug 23, 2026
- 4+ years
- Not Disclosed
- Hyderabad, India
- Post Date: Jun 23, 2026
- End Date: Aug 23, 2026
ResponsibilitiesSupport reaction monitoring, scale-up and final analysis of samples as per monograph /in-house procedures including method development/validation if required. Prepare development reports for Synthetic Support projects. Execute projects per the approved test protocols if assigned. Plan, execute, and complete the projects as per specifications, timelines, and budget. Responsible for preparation and review of SOPs, protocols, reports, etc. Ensure project requirements by coordinating with external vendors and all internal relevant departments. Responsible for ensuring the required maintenance and calibrations of the equipment Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned Preparation and planning for ISO-9001 certification/recertification by participating actively, verification of protocols and related documents and take an active role in the internal as well as external QA audits and address the audit issues in a timely manner.Qualification & ExpeirenceSc. in Analytical Chemistry / Organic Chemistry/M. Pharm, having 8-10 years of experience in Analytical Research and Development or Ph.D. with 4-7 years of experience in Analytical Research and Development. Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, LC-MS, GC-MS, FTIR, UV-Visible, wet chemistry, etc.
- Quality control
- clinical research
- Management
- 2+ years
- Not Disclosed
- Gurugram, India
- Post Date: Jun 11, 2026
- End Date: Aug 11, 2026
- 2+ years
- Not Disclosed
- Gurugram, India
- Post Date: Jun 11, 2026
- End Date: Aug 11, 2026
ResponsibilitiesAssisting and supporting the development of thought-provoking insights through market analysis and in-depth review of trends. Drawing on both traditional and innovative data sources and research methodologies to explore key questions. Analyzing large datasets and interpreting results using statistical techniques and data visualization tools Updating our proprietary in-house models and provides results to the practice when needed. Developing research insights and compelling business narratives alongside research leads. Presenting key findings in a structured and concise manner (with focus on insights).
- clinical research
- Operations
- Clinical Trial
- Inspection
- 5+ years
- Not Disclosed
- Gurugram, India
- Post Date: Jun 11, 2026
- End Date: Aug 11, 2026
- 5+ years
- Not Disclosed
- Gurugram, India
- Post Date: Jun 11, 2026
- End Date: Aug 11, 2026
Responsibilities Assisting and supporting the development of thought-provoking insights through market analysis and in-depth review of trends. Drawing on both traditional and innovative data sources and research methodologies to explore key questions. Analyzing large datasets and interpreting results using statistical techniques and data visualization tools Updating our proprietary in-house models and provides results to the practice when needed. Developing research insights and compelling business narratives alongside research leads. Presenting key findings in a structured and concise manner (with focus on insights). “Hard” skills: Ability to use techniques such as secondary research, company and market analysis, strategic analysis frameworks, interview-based research and financial analysis. Strong analytical skills and a proven ability to make sense out of data, with ability to analyze, visualize, and interpret Able to learn and embrace new sources, tools, and skills, including alternative modes of research delivery/data visualization tools (e.g., Power BI, Qlik etc.). Compiling reports/analysis with clear storyline and results. A basic understanding of the role of digital / technology in disrupting chemical markets Able to write in a clear, concise, and compelling way Strong PowerPoint, Excel, and Word skills “Soft” skills: Strong interest in the Chemical industry and Technology Intellectual curiosity and desire to learn more and grow Problem solver approach to work Proven ability to work independently, collaboratively, and virtually - in a global, multi-cultural, multi-time zone team Ability to present research findings to team and Accenture executives Strong communications skills and good interpersonal skills Strong professional qualities: client focus, decisiveness, integrity, resilience to stress against stretch goals and deadlines Ability to work on multiple engagement. Qualification & Experience A bachelor’s degree, preferably in a science or engineering. A PG degree in business, such as business (MBA), economics or equivalent is a plus. Work Experience: 5-7 years of business experience, preferably in a consulting environment, think tank, financial institution, or other 3rd party business research organization or demonstrated equivalent skill."
- clinical research
- Operations
- Clinical Trial
- Inspection
- 8+ years
- Not Disclosed
- Bengaluru, India
- Post Date: Jun 11, 2026
- End Date: Aug 11, 2026
- 8+ years
- Not Disclosed
- Bengaluru, India
- Post Date: Jun 11, 2026
- End Date: Aug 11, 2026
ResponsibilitiesAnalyze industry and company data using research and visualization tools. Work with senior researchers to update internal models and produce client-ready outputs. Work with research leads and client teams to shape viewpoints, answer strategic questions, and contribute to publications or internal briefings. Craft clear and compelling research outputs (slides, visualizations, written summaries) for Accenture leadership and clients. Develop case studies, conduct surveys, and perform secondary data analysis. Comfortable with expert interviews. Leverage generative AI to enhance ways of working, identify novel insights, and deliver outputs in non-traditional ways “Hard” skills: Understanding of the Life Sciences (pharmaceutical) industry and its key challenges Experience applying a range of research methodologies, including secondary research, market and company profiling, strategic frameworks, and financial analysis. Strong analytical skills with the ability to make sense out of data, visualize, and interpret findings Comfortable using Generative AI tools (e.g., ChatGPT, Claude, Copilot) to enhance research and content creation. Business knowledge on the application of AI (including machine learning, deep learning, natural language processing, large language models (LLMs), generative AI, agentic AI, etc.) and related emerging topics in AI, Data, Automation, Analytics. Qualification & ExperienceA bachelor’s degree, preferably in business or STEM. A postgraduate degree in business or STEM, such as an MBA, MS, PhD., or equivalent is a plus. Work Experience: 8-10 years of experience, preferably in a consulting environment, think tank, financial institution, pharmaceutical/biotech company, CRO/CDMO or other business research organization or have demonstrated equivalent skill elsewhere
- clinical research
- Operations
- Clinical Trial
- Inspection
- 2+ years
- Not Disclosed
- Bengaluru, India
- Post Date: Jun 09, 2026
- End Date: Aug 09, 2026
- 2+ years
- Not Disclosed
- Bengaluru, India
- Post Date: Jun 09, 2026
- End Date: Aug 09, 2026
ResponsibilitiesAs Tech Lead or Change Owner, define, organize, plan and execute activities related to product design change and new product registration in compliance with current international/regional/national regulations with minimal support of senior colleagues or independently. Provide technical assessment for product changes related to design, labeling, raw material, manufacturing support, regulatory compliance, quality improvement and new registrations in collaboration with senior scientists Lead, and coordinate - including follow-ups as required with global stakeholders - of technical activities in collaboration with key stakeholders, with respect of project commitment, quality procedures and business needs. Provide technical information, &/or prepare reports based on internal or external data available to formulate response to authorities’ questions Propose options, work closely with stakeholders and develop action plan for problem-solving, product and process improvement Establish, maintain and update technical & Design documentation according to Good Documentation Practices Participate in and at times lead multi-functional and international project team for effective collaboration and deliverables Demonstrate excellent internal and cross-functional communication and provide regular status update of activities to senior management & stakeholder with some supervisions from direct manager and senior members of the organization. Draft technically accurate reports with in-depth analyses as required using statistics or other relevant tools and mentor/coach help junior members to create information that can go into such reportsQualification & ExperienceMaster’s in Chemistry or Pharmacy (or related disciplines) with minimum 4 years of relevant experience, or PhD in chemistry or Pharmacy (or related disciplines) with experience in Pharmaceutical product development and life cycle management, preferably sterile injectable/parenteral formulations. Demonstrated ability in clear and effective communication (written, oral) and presentation skills to global stakeholders Excellent stakeholder management (local and global) A proven track record of leading small size projects – especially Change Controls in Pharmaceutical industry Demonstrated ability to work in a matrix environment with multiple stakeholders A proven track record of effectiveness in a fast-paced environment working in global teams Proven ability to deliver results by owning & being accountable for budget, timeline, and product/project deliverables
- clinical research
- Operations
- Clinical Trial
- Inspection
- 2+ years
- Not Disclosed
- Mumbai, India
- Post Date: Jun 09, 2026
- End Date: Aug 09, 2026
- 2+ years
- Not Disclosed
- Mumbai, India
- Post Date: Jun 09, 2026
- End Date: Aug 09, 2026
ResponsibilitiesIndependently lead end-to-end formulation development and process design for personal care products across formats (creams, lotions, gels, deodorants, body oils, cleansing) Drive fast-track NPD ensuring OTIF timelines and First-Time-Right (FTR) commercialization Translate marketing concepts and consumer insights into technically feasible, cost-effective, and scalable formulations Manage multiple projects simultaneously, ensuring timely delivery and stakeholder alignment Perform technical scoping including literature review, benchmarking, ingredient selection, and formulation strategy Apply DoE and scientific approaches to optimize formulations for performance, stability, manufacturability, and cost efficiency Conduct trend mapping and competitive intelligence to drive innovation and differentiation Identify opportunities and drive innovation, cost optimization, and sustainability initiatives Execute formulation trials, stability studies, and product evaluations considering performance, cost, packaging, regulatory, and safety requirements Lead pilot batches, scale-up, and technology transfer in collaboration with manufacturing and supply chain teams Collaborate with cross-functional teams (Marketing, QA, Analytical, Regulatory, Procurement, Supply Chain) and manage external stakeholders (vendors, third-party manufacturers, labs) Ensure compliance with GLP, GDP, regulatory, and internal quality standards, maintaining audit-ready documentation Create product demos and technical tools to support business and product understanding Draft and validate product claims based on formulation and ingredient functionality, ensuring regulatory alignment Act as a technical partner to marketing, supporting Key Visuals (KV), A+ content, and product storytelling Drive continuous improvement in safety, processes, and operational efficiency Maintain accurate documentation and digital systems for project tracking and data management
- pharma
- pharmacovigilance
- Management

