Research Associate

Posted Yesterday
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Mumbai, Maharashtra, IND
In-Office
Mid level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Lead end-to-end formulation development and NPD for personal care products, applying DoE, stability testing, and pilot-scale transfers. Translate consumer insights into scalable, cost-effective formulations, manage multiple projects, ensure regulatory and quality compliance (GLP/GDP), collaborate cross-functionally, and drive innovation, sustainability, and continuous improvement while maintaining audit-ready documentation.
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Job Description

Research AssociateSeeking a dynamic R&D professional to drive end-to-end formulation development and New Product Development (NPD) in the personal care/FMCG space. The role focuses on delivering innovative, cost-effective, and scalable formulations across multiple formats with a strong emphasis on fast-track development and First-Time-Right (FTR) commercialization. The incumbent will work closely with cross-functional teams to translate consumer insights and business requirements into high-quality, market-ready products, while ensuring speed, robustness, and regulatory compliance.
§Independently 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

Skills Required

  • End-to-end formulation development experience in personal care products (creams, lotions, gels, deodorants, body oils, cleansing)
  • Experience applying Design of Experiments (DoE) and scientific optimization approaches
  • Experience executing formulation trials, stability studies, and product evaluations
  • Experience leading pilot batches, scale-up, and technology transfer with manufacturing/supply chain
  • Knowledge of and compliance with GLP, GDP, regulatory, and internal quality standards and audit-ready documentation
  • Ability to translate marketing concepts and consumer insights into technically feasible, cost-effective formulations
  • Project management skills to manage multiple projects and ensure OTIF delivery and stakeholder alignment
  • Experience with trend mapping, competitive intelligence, and driving innovation/cost optimization
  • Collaboration experience with cross-functional teams and external vendors/third-party manufacturers/labs
  • Capability to draft and validate product claims and support marketing assets (KV, A+ content)
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The Company
HQ: Lexington, KY
3,919 Employees
Year Founded: 2020

What We Do

Piramal Pharma Limited is a global pharmaceutical company that provides end-to-end drug development and manufacturing services (CDMO), complex hospital generics, and consumer healthcare products.

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