Responsibilities Coordinate with Principal Investigators (PIs), Institutional Review Boards (IRB), Sponsors/CROs, and research teams to execute clinical trials. Recruit and follow up with trial participants to ensure their well-being throughout the study. Maintain trial databases, logs, and documentation for regulatory compliance. Ensure adherence to Good Clinical Practice (GCP) guidelines and applicable regulatory requirements. Train staff on trial-related duties and ethical considerations in clinical research. Protect the rights and confidentiality of all trial participants. Ensure timely and accurate reporting of trial data, including adverse events and protocol deviations. Manage documentation, including informed consent forms, Case Report Forms (CRFs), and other regulatory submissions. Archive trial-related documents for the required retention period. Identify potential research opportunities and liaise with sponsors.  QualificationBachelors/Masters in Life Sciences w/ Certificate course in Clinical Research, OR Bachelors/Masters in Clinical Research Excellent written and oral communication skills. Preference for ICH-GCP trained professional.

ResponsibilitiesResearch Associate - AR&DResearch Associate - AR&D Capable to handle independent projects Analytical testing support to PDG synthetic group. Coordinate with QA regarding method transfer, CCF and investigation reports. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. API Stability knowledge. Capable to handle analytical method development, Implementation, Validation as per requirement. Should have experience of Analytical method transfer to QC. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. Should aware about GLP practices and 21 CFR part-11. Keep the work area clean and the laboratory under controlled temperature. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. Understand the safety and environmental aspect. Maintain the reagents and standardize the volumetric solutions as per schedule. Maintain the laboratory journals and instrument log books online. Ensure compliance to Hazardous waste and chemical management. Observe unsafe acts and conditions and take corrective & preventive Actions immediately.

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 

ResponsibilitiesTo perform Comparative, multimedia, discriminatory and other relevant dissolution activity for Drug Product as per regulatory requirement. To perform Method validation of drug product for Assay, RS, Dissolution etc. To perform calibration of Laboratory instruments. Preparation of protocol, Test Data Sheet and Report for Method Validation. To maintain the GLP practice in the Laboratory. Wet AnalysisQualification & Experience1-3 Years of related experienceMasters in Analytical Chemistry or Organic Chemistry

 Responsibilities As 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 reports Lead, and conduct activities related to exploration of innovation concepts and technology platforms, demonstrate critical mindset and “out-of-the-box” thinking. Qualification & 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

 Responsibilities Provide technical leadership and subject?matter expertise across product lifecycle management activities. Independently own and execute product design changes and new product registrations, ensuring compliance with international, regional, and national regulatory requirements. Lead technical assessments and define strategies for changes related to formulation, design, labeling, raw materials, manufacturing support, quality improvement, and regulatory compliance. Develop technically sound, data?driven solutions in collaboration with senior scientists and global partners. Project & Stakeholder ManagementLead and coordinate cross?functional technical activities with global stakeholders to meet project commitments, quality standards, and business objectives. Proactively follow up and drive alignment across functions such as R&D, Regulatory Affairs, Quality, Operations, and Supply Chain. Provide clear, concise, and timely technical updates to senior management and key stakeholders.Qualification & ExperienceMaster’s degree in Chemistry, Pharmacy, or a related scientific discipline. Minimum 10 years of relevant experience in pharmaceutical or medical products R&D, lifecycle management, or regulated product development.

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 

Responsibilities  Literature & Pre-Formulation Conduct detailed literature reviews to support new product development initiatives. Evaluate reference products, patents, regulatory status, and formulation strategies. Perform physicochemical characterization of API and excipients (solubility, particle size, hygroscopicity, polymorph). Assess API-excipient compatibility, solubility, and stability as part of pre-formulation studies.  Formulation & Process Development Design and develop robust formulations for tablets and pellets using extrusion-spheronization, layering, and coating (aqueous and non-aqueous). Develop tablets via wet / dry granulation or direct compression as per product strategy. Optimize process parameters through laboratory and pilot-scale equipment — extruder, spheronizers, FBD, Wurster coater, RMG. Apply DoE / QbD principles to identify critical process parameters and critical material attributes.  Stability, Validation & Documentation Conduct stability studies as per ICH guidelines and internal SOPs. Interpret results and recommend necessary formulation or process adjustments. Coordinate and execute process validation batches in the production department. Prepare and review technology transfer documents — TTD, FDR, protocols. Facilitate successful scale-up and handover of developed products to manufacturing.Qualification & ExperienceQualification B.Pharm / M.Pharm Experience 3 – 5 years; able to run an area or shift independently (OSD experience preferred).

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)