448 Formulation Jobs - Page 10

Conduct trials and to develop relevant products. Cost effective product formulation. Experienced in Formulation Exp Technical related to concrete admixture; conducting trails / testing and chemical analysis of various ingredients. Required Candidate profile Decent know - how on concrete related chemistry. Generating and analyzing of various technical trails report. Must have worked in Admixture / Construction Chemical Company or RMC plants in the region.

1.Establishing company as the world leader in Paracetamol, Paracetamol DC and other new molecules such as Mirabegron, Levosalbutamol, etc by Identifying potential Countries and responsible for penetrating the targeted markets and catering the customers. 2.To have the thorough understanding of the Sales Process, Product Knowledge, Market Knowledge, Customer Profile, Regulatory requirements, along with competitor's capacity, regulatory approvals, pricing strategy 3.Monthly Analysis of export data & import data of Indian & Chinese supplies of PARACETAMOL PAP, PNCB, evolving a mechanism of market demand and supply along with forecast of the month & sales promotion activities 4.Planning visit to targeted Market & customer visit for enhancing the customer base 5.Pricing, order finalization, execution of orders, follow-up, payment collection, customer bonding 6.Organizing for CPHI participation and enhancement of FARASON BRAND Visibility across globe. 7.Regulatory approvals worldwide listed out as we may go for it based on the volumes achieved from the country 8.Nurture Team members for future responsibility 9.Periodic review of Customer performance, Country Performance, performing market share enhancement activities 10..Achieving sales budgets as mutually discussed and decided. Note: Mandatorily required the experience of API, Export Marketing & Regulated Markets

1)Operate equipment and instruments as per SOP. 2)Adhere to GDP and cGMP practices. 3)Inspect equipment for required repairs/replacements. 4)Follow SOPs and BMR/BPR instructions. 5)Perform balance and instrument calibration as per SOP Required Candidate profile Previous experience 0.6 to 2 Year in formulation plant is preferred.

Walk In Drive for Production OSD Department In Formulation Division @ Kothur Qualification :- BA| B Com | Diploma | BSc | MSc| M Pharmacy Experience:- 2 to 8 Years Interview Date:-05-04-2025 Interview Time:- 9.00AM TO 2.0PM Work Location :- MSNF-II, Kothur, MSNF- IV, Mekaguda Venue Location :- MSN Laboratories Pvt Ltd,. Formulation Unit-02,Kothur, Nandigama. Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidates those who have experience in 1. Blister Cam, 2.Cam Cartonator 3. BQS, 4. ELMAC, 5. IMAPG, 6. Primary Packing & Secondary Packing 7. Capsule Filling Operator 8. CVC 9. Documentation. About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Walk In Drive For Microbiology Department In Formulation Division @ Kothur Department:- Microbiology Qualification :- B Sc | M Sc (Microbiology) Division :- Formulation Fresher's :- 2023 & 2024 Passed outs only. Experience:- 0 to 10 Years Interview Date:- 05-04-2025 Work Location :- MSNF Unit-II, Kothur Venue Location :- MSN Laboratories Pvt Ltd , Formulation Unit -II, Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-30438701 | 8785 Note:- Candidate should bring Update Resume , Offer Letter, Increment Letter, CTC, Pay slips ,Bank Statement, Certificates, Aadhaar Card & Pan Card We are looking for candidates those who have experience in Production OSD Department.(Coating Operator & Compression Operator) About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Hello Dear Greetings!! We are hiring for R&D Head profile vacant with Leading Chemical Industry for Vapi Location. Education:: Phd (Chemistry) Must Experience: Min 15 Years Industr Type : Chemical Key Roles & Responsibility: Implement norms for safety culture and 5S in laboratory Improve existing products Oversee management of laboratory to benchmark standards Prepare, review and ensure adherence to department policies and SOPs (as applicable) Comply with statutory and regulatory requirements Develop new products Perform the role of people manager Provide technical support to cross-functional teams and customers Develop R&D culture and protect intellectual property Keep abreast with latest trends in research, technology and competition Interested candidate can share their CV on hr6@sarthee.com or call on 9033033611. Regards Umang Parmar hr6@sarthee.com 9033033611

Job Title: Formulation and Development Executive Experience Required: Minimum 3 years Key Responsibilities: Develop and formulate cosmetic products across various categories such as skincare, hair care, and grooming products, ensuring high-quality formulations. Facilitate the successful transfer of formulations from R&D to production, ensuring seamless scaling up of manufacturing processes. Collaborate with production and manufacturing teams to ensure efficient and accurate technology transfer. Prepare and manage all necessary documentation related to technology transfer. Conduct stability testing to ensure the shelf life and quality of products under various environmental conditions. Analyze and interpret stability test results and recommend improvements to formulations. Maintain proper documentation of all stability testing and product evaluation data. Maintain well-organized records of formulations, test results, and production processes. Key Skills & Qualifications: A degree in pharmaceutical sciences, chemistry, cosmetology, or a related field. Minimum of 3 years within the cosmetic or pharmaceutical industry. Strong knowledge of formulation techniques, stability testing methodologies, and technology transfer processes. Proficient in preparing, maintaining, and reviewing technical documentation in line with industry standards. Familiarity with regulatory requirements for cosmetic products (e.g., FDA, EU Cosmetics Regulation, etc.). Ability to analyze and interpret data from stability testing, raw material testing, and formulation trials.

We are hiring for the following 2 positions: Senior Executive- Quality Control RM Section Head- 5-8 Years of Experience Executive- Quality Control- Analytical Method Validation- 4-6 Years of Experience 1. Senior Executive- Quality Control- RM (Raw Material) Section Head Raw Material Testing and Release: Supervise and ensure the testing of raw materials (active pharmaceutical ingredients, excipients, packaging materials) according to approved specifications. Lead the RM team in the timely testing and release of raw materials for production use, ensuring no delays in manufacturing. Ensure that the testing of raw materials is compliant with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other relevant regulatory standards. Supervision and Team Management: Lead, guide, and mentor a team of QC analysts in the RM section, ensuring effective training and development. Allocate tasks and manage workload distribution within the team to ensure smooth and efficient operations. Conduct regular performance appraisals, set objectives, and ensure team productivity and morale. Raw Material Specifications and Documentation: Review and ensure the accuracy and completeness of raw material specifications, test protocols, and related documents. Approve the testing methods and ensure compliance with the established standard operating procedures (SOPs). Ensure the proper maintenance of records related to raw materials, including stability studies, inventory control, and release certificates. Compliance and Regulatory Adherence: Ensure all raw materials and testing activities comply with the Indian Pharmacopeia (IP), USP, BP, and other regulatory standards. Ensure that all QC raw material processes are aligned with FDA, EMA, and other regulatory guidelines as applicable. Assist in audits (internal and external), and provide necessary data and reports during regulatory inspections. Equipment and Instrument Management: Oversee the calibration, maintenance, and qualification of equipment used in the RM section, ensuring accurate and reliable results. Ensure that the laboratory instruments and equipment are well-maintained and functioning optimally. Quality Control & Troubleshooting: Address any deviations, out-of-specification (OOS) results, or out-of-trend (OOT) findings related to raw material testing. Investigate and resolve any quality control issues, and recommend corrective and preventive actions (CAPAs). Lead root cause analysis and support the investigation of quality incidents related to raw materials. Vendor Management & Raw Material Supplier Interaction: Liaise with suppliers and vendors to ensure the timely and quality supply of raw materials. Participate in the selection and qualification of raw material suppliers and ensure they meet quality standards. Continuous Improvement and Efficiency: Identify opportunities for process optimization and recommend improvements to enhance operational efficiency. Ensure that the QC RM section continuously adheres to cost-effective practices, reducing wastage and improving turnaround time. Training and Knowledge Sharing: Train QC team members on analytical techniques, equipment usage, and quality control standards for raw material testing. Keep the team updated on industry trends, new regulatory guidelines, and best practices. Executive-Quality Control- Analytical Method Validation (AMV) Analytical Method Validation (AMV) : Conduct validation of analytical methods as per ICH, FDA, and other regulatory guidelines. Perform method development, optimization, and validation for raw materials, in-process materials, and finished products. Ensure adherence to validation protocols and documentation. Testing & Documentation : Oversee the execution of analytical testing for stability, release, and in-process samples. Review and verify analytical data, ensuring accuracy and completeness. Prepare and review validation reports, SOPs, and other related documentation. Compliance & Quality Assurance : Ensure compliance with GMP, GLP, ISO, and other relevant standards in laboratory activities. Support the QC team in audits (internal and external) and address any non-conformities. Ensure proper handling, storage, and disposal of chemicals, reagents, and samples in compliance with safety protocols. Equipment Maintenance : Coordinate with the maintenance team for the calibration and qualification of laboratory instruments. Perform routine checks and calibration of instruments used in testing and validation. Continuous Improvement : Actively participate in continuous improvement initiatives and training programs. Suggest and implement improvements in analytical methods and processes to enhance efficiency. Cross-Department Collaboration : Liaise with R&D, production, and regulatory teams to resolve technical issues. Assist in troubleshooting analytical issues in collaboration with the technical team

Associate Machine Learning Engineer Maersk, the world s largest shipping company responsible for moving 20 % of global trade, is on a mission to become the Global Integrator of Container Logistics. To achieve this, we are transforming into an industrial digital giant by combining our assets across air, land, ocean, and ports with our growing portfolio of digital assets to connect and simplify our customer s supply chain through global end-to-end solutions, all the while rethinking the way we engage with customers and partners. In this role as Machine learning engineer on the Global Data and Analytics (GDA) team, you will be working on our new strategic visibility initiative to develop recommendation solutions facing internal and external users. The overall objective is to develop actionable recommendations which enable unprecedented flexibility during supply chain execution and strategic planning and unlock new types of services for our internal users and our customers. Building on top of a best-in-industry visibility data foundation, you will be partnering with product managers and engineering counterparts to develop scalable solutions following industry best-practices. You will be empowered to take ownership of your domain and we expect you to proactively contribute to identifying opportunities and solutions. There is a lot of exciting challenges ahead of us, and the ideal candidate will have a passion for working on industry-transforming products and creating impact from the ground up in a fast-paced environment. You should have demonstrated ability to make sense out of large, integrated datasets, and build statistical and machine learning (ML) models on top of these data sets. For this role it is crucial to have prior hands-on experience developing prediction/forecasting models and/or recommendation systems, and with putting solutions to production in collaboration with data engineering and software engineering. Furthermore, you must have demonstrated experience in initiating and leading ML projects in a dynamic, international environment. Over time, and when you are ready, we will be looking to you to take on more leadership responsibility. No prior knowledge of logistics needed; we will help you learn what you ll need to succeed. Key responsibilities Develop, test, and deploy prediction, forecasting and recommendation system solutions and other analytical tools together with the team. In addition to the topics mentioned above, this can range from building integrated data sets over analyses to dashboards and machine learning models Lead model development, implementation and deployment end-to-end incl. MLOps (mindset and technical implementation). Specifically, you will drive problem formulation, modeling approach, implementation, testing, deployment and monitoring. Collaborate with software engineers and data engineers to deploy recommendation solutions to production Partner with product managers to drive maturation of ideas into production solutions, including challenging problem formulation Communicate effectively with technical and non-technical audiences Basic qualifications BSc/MSc in computer science, data science or related discipline with 10+ years of industry experience building cloud-based ML solutions for production at scale, including solution architecture and design experience 3+ years of hands-on experience building ML solutions in Python, incl knowledge of common python data science libraries ( e. g. scikit-learn, PyTorch , etc) Hands-on experience building end-to-end data products based on recommendation technologies Experience with collaborative development workflow: version control (we use github ), code reviews, DevOps ( incl automated testing), CI/CD Communication and leadership experience, with experience initiating , driving and delivering projects Team player, eager to collaborate Preferred qualifications Experience as tech lead or engineering manager (still hands-on) Experience with a common dashboarding technology (we use PowerBI for now) Experience working in cross-functional product engineering teams following agile development methodologies (scrum/Kanban/ ) Experience with Spark and distributed computing Strong hands-on experience with MLOps solutions, including open source solutions. Experience with cloud-based orchestration technologies, e. g. Airflow, KubeFlow , etc Experience with containerization: Kubernetes & Docker Maersk is committed to a diverse and inclusive workplace, and we embrace different styles of thinking. . We are happy to support your need for any adjustments during the application and hiring process. If you need special assistance or an accommodation to use our website, apply for a position, or to perform a job, please contact us by emailing .

Roles and Responsibilities Manage raw material procurement process from vendor development to final delivery. Develop and maintain relationships with vendors to ensure timely supply of high-quality materials. Ensure compliance with quality standards by conducting regular inspections at vendor sites. Collaborate with formulation team to understand their requirements and plan accordingly.

Knowledge of ich guidelines and different global regulatory authorities requirements related to products and its methods, control strategy towards critical quality attributes. Understand customer expectations on to-be manufactured product.

Location: Patalganga (Rasiyani) Role & responsibilities The requirement is for laboratory chemist, initially be involved majorly in lubricant development activities and subsequently transition to laboratory Chemist role for Lubricant Quality Control. New lubricant formulation and development and optimization Quality Control of lubricants formulations. Testing and benchmarking of lubricants in liaison with global and local laboratories. Localization of lubricant formulation Should be result oriented and be able to work with minimal supervision Working knowledge of relevant IT related tools such as MS office, E mails. Understanding and knowledge of Quality management systems Preferred candidate profile Technical Qualification in Chemistry ( Diploma Chemistry) Laboratory Experience is preferable

Greetings from Natco Pharma Limited We are conducting Walk-in interviews for the following requirements for our formulation division in Kothur. Job Requirements Department: QA (IPQA / AQA / Qualifications / Micro QA / Documentation) - 1 to 10 Years Positions: Sr Executive / Executive / Officer / Assistant Officer Qualification: M. Sc / B. Pharmacy / M. Pharmacy Hands-on experience in IPQA activities for OSD / Sterile operations. Experience in Qualification activities for all Equipments, Utilities, Instruments, and Facilities. Experience in Analytical QA & Micro QA and handling OOS, OOT, incidents, Investigations, and GLP activities. Department: Microbiology (OSD / Injectables) - 3 to 12 Years Positions: Assistant Manager / Sr Executive / Executive / Officer / Assistant Officer Qualification: M. Sc (Microbiology) Experience in QMS & GLP activities and Analytical Doc review Experience in Media Preparation and Method Validations of MLT & BET Experience in Vitek-2 Operation/Culture handling/Water Sampling / Analysis Experience in Environmental monitoring activities. Preferably Male candidates Department: Engineering (QMS / Process / Electrical) - 4 to 10 Years Positions: Executive / Officer / Assistant Officer / Sr Assistant / Assistant / Trainee Qualification: Diploma / B. Tech Hands-on experience in QMS, Documents & OQ protocol execution. Experience in Process maintenance and vendor follow-up activities. Experience in OSD Process / Packing Maintenance and Qualifications. Experience in Electrical Maintenance & Electrical substation. Should have knowledge about AutoCAD Department: Warehouse (OSD / Sterile) - 0 to 6 Years Positions: Assistant Officer / Sr Assistant / Assistant / Trainee Qualification: B. Com / B. Sc Handling of Raw / Packing Materials Knowledge of SAP & Isolator handling Experience in Dispensing & Material Management

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned, If any of the requirement is matching your current job profile, kindly walk-in with your latest resume. Role & responsibilities Injectable - Manufacturing & Packing & Visual Inspection (Senior Executive / Executive / Senior Officer / Officer / Associate) Experience - 01 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI with relevant functional experience in injectable manufacturing/ Aseptic area operations / Packing / Visual inspection / QMS activities OSD Manufacturing ( Executive / Senior Officer / Officer / Associate) Experience - 01 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing and Packing operations / QMS activities Time and Venue : 05th April 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. Preferred candidate profile *Having relevant qualification as mentioned above can attend the scheduled walk-in. Perks and benefits

Prepare CTD dossiers for regulated markets and other markets as per country specific guidelines. Attend to various queries raised by the importing countries wrt to Co.products & dossiers Coordinate with factory Required Candidate profile 1-3 Years Experience In Regulatory Affairs for formulations Excellent communication skills both written and verbal

Role & responsibilities Good knowledge of QMS documents, SOP preparation, Change control initiation as per GMP norms. Good knowledge and preparation of Equipment qualification documents URS, DQ, IQ, OQ and PQ. Preparation and maintain daily log book of utility equipment, water system and HVAC system. Handling of breakdown and operation of water system and HVAC system Handling breakdown of pharma process equipment and Preparation of Preventive maintenance schedule/planner. Schedule Preparation and performing HVAC validation, Instrument calibration. Knowledge and handling of utility equipment, DG, Transformer, Air compressor, Boiler and PCC and MCC panel. Good Knowledge of deviation and CAPA documents

Roles and Responsibilities Should be able to formulate and Develop Personal Care/Skin Care/Hair Care/Baby Care/Hygiene Care Cosmetics, Aerosol and Industrial Products in a cost-effective manner within time bound delivery by keeping in view of GMP Norms and quality. Lead the ideation process for new products and conduct market research to identify customer needs and trends. Manage customer relationships and perform reviews, customer visits, and product testing.Self driven and accountable will need to completely own the R&D space and achieve results with limited supervision. Collaborate with cross-functional teams, including design, formulation, and marketing, to develop product concepts and specifications. Monitor the development process, ensuring that all milestones are met on time and within budget. Review and approve product designs, packaging, and labeling to ensure they meet quality and regulatory standards. Manage the testing and evaluation of prototypes and samples, making adjustments/iterations as required. Liaison with manufacturing team to ensure the timely production and delivery of new products. Lead the launch of new products, including planning and executing product launches and coordinating with the sales and marketing teams to ensure successful market penetration. Continuously evaluate the performance of existing products and suggest improvements to maintain their competitive edge in the market. Should have grasp knowledge on costing to develop products according to customer budget Excellent Knowledge of raw materials & packaging material required to manufacture. Determines customers needs and desires by specifying the research needed to obtain market information. Assess market competition by comparing the company`s product to competitors products Determines product pricing by utilizing market research data, reviewing production and sales costs, anticipating volume, and costing special and customized orders Understand customer expectations on to-be manufactured products. Document all phases of research and development Monitor and maintain R&D laboratory and testing equipment including purchasing of testing equipment in a cost-effective manner, conduct or arranging equipment calibrations and preventative maintenance. Support marketing and quality assurance/control team in dealing with technical and quality issues raised by customers. Provide presentation to customers and travel with marketing team to meet customers as required.

- Assist in preparing and reviewing regulatory submissions for nail polish products, including product dossiers, safety data sheets, and labeling. - Support product registration and internal audits. - Collaborate with R&D, QA, and Marketing teams. . Required Candidate profile - Bachelor’s degree in Regulatory Affairs, Pharmacy, Chemistry, Cosmetic Science or related field. - 1-2 years of experience in regulatory affairs, preferably in the cosmetics or nail polish industry

Role & responsibilities Keen Knowledge on Regulatory guidelines for finished product registration. Dossier compilation as per guidelines. Compilation and review the product dossiers for submission in CTD, ACTD . Gap analysis of the dossier and addressing the gaps before submission to MOH. Handling the customer and MOH queries . Life cycle management of the product. Development report, scale up report , specification, COA, stability protocol and Process validation protocol. Documents review (Specification, STP, Analytical method validations, Development report and validation reports, BMR, BPR, PVP/R and stability). Post approval experience to file the applicable variations timely. Knowledge on EAEU, ICH and EMEA guidelines. Re-registration (Renewal) procedures. Administrative documents requirements (COPP, Mfg. License and Import License) . Registration information management system updates on regular basis.

SUMMARY Opening for an Top Branded Construction Chemical/ Admixture / Paints manufacturing Company About the company: our client is one of the leaing name in admixture & construction chemical manufacturing industry Designation : Concrete Technologist Experience : 2 to 3 years Location : Guwahati Job Description - In-depth knowledge about trials with concrete admixture in project sites, preferably some idea about admixture formulation also. - Establishing most economical solution with admixture, for meeting customer needs. - Support the sales team to improve wallet share of admixtures, & evaluate existing and new customers every year and prepare action plan for next year. - Handle and resolve issues of key users on technical parameters. - Thorough market mapping in that particular geography. - Drive admixtures business in B/C class RMC & prepare cost estimate for concrete. - Work towards site approval of admixture in small road projects (State highways at least) tapping in-site consultants & technically establishing suitable products. - Drive admixture in developer segment & create database for it. - Drive admixture business in paver block & AAC block manufacturing industry; including preparing cost estimate for concrete. - Connect with local consultants/engineers to get approvals of admixtures in major projects. - Benchmarking with widely used range of competition product by picking up their samples & maintain data on market development or changes of competitor’s activities. Requirements Experience: 2-3 years into admixture Age Group: 23-35 years Qualification: MSc ( Chemistry ) / B.Tech/M.Tech ( Polymer Science / Chemical Engineering/Civil Engineering/Concrete Technology )

Experience in maintenance and repair is must. Responsible for equipment preventive & breakdown maintenance. Responsible for boiler & Utility operation and maintenance. Technician and fitter shift planning. QMS Documentation & Logbook preparation Perks and benefits Accommodation & Transportation Mediclaim Policy

Documentation, compliance, and regulatory audits, analytical testing, formulation development and process optimization, microbial testing and sterility assurance, ensuring adherence to GMP, GLP, & ISO, managing deviations, CAPA, maintaining QMS & RC Office cab/shuttle Food allowance Annual bonus Provident fund House rent allowance Over time allowance Employees' state insurance

• Prepare/Review Design Drawings as project deliverables. • Prepare Documents as project deliverables. • Knowledge and understanding of relevant Design Guidelines & Statutory Requirements

Role & responsibilities 1. Routine analysis of incoming RM/PM/FG 2. Collection of RM/PM/FG control sample 3. Routine water testing CI/DM/Soft water 4. Weighing balance validation 5. Calibration of all lab instruments internally 6. Retain sample analysis 7. Rm standard sample 8. Reporting and documentation 9. Qc clearance in sap system Preferred candidate profile Fresher can apply Only Male candidate can apply Job location Howrah Jalan Salary Negotiable

Job Title: Senior Manager / Manager - Botanist Department: R&D Job description We are seeking a skilled Botanist to support our FMCG (Fast-Moving Consumer Goods) product development by researching and sourcing plant-based ingredients, ensuring quality, sustainability, and regulatory compliance. The ideal candidate will have expertise in plant sciences, raw material sourcing, and botanical formulations, playing a key role in the innovation and development of herbal, food, beverage, personal care, and wellness products. Key Responsibilities: Conduct research on plant-based ingredients for use in personal care, cosmetics, and other FMCG products. Herbs identification and sourcing Collaborate with R&D, product development, and procurement teams to source high quality and sustainable botanical raw materials. Analyze the chemical composition, benefits, and potential applications of various plants and extracts. Analysis of validated herbs/medicinal plants for Ayurvedic formulations Phytochemical analysis of herbs Ensure compliance with industry regulations, certifications (e.g., organic, fair trade), and safety standards. Develop new formulations or enhance existing ones using botanical extracts, essential oils, and plant derivatives. Work closely with suppliers to evaluate ingredient quality, traceability, and ethical sourcing practices. Maintaining relationship with existing vendors , developing new vendors for managing sourcing schedule. Stay updated on industry trends, scientific advancements, and market demands in plant-based products. Support sustainability initiatives by researching eco-friendly and renewable plant based alternatives Required Qualifications: Bachelors or Masters degree in Botany, Plant Science, Agriculture, Biotechnology, or a related field. Experience in botanical research, plant-based product development, or ingredient sourcing within the FMCG sector. Knowledge of phytochemistry, plant extraction methods, and botanical formulations Familiarity with regulatory standards such as FDA, FSSAI, EU Regulations, USDA Organic, or COSMOS certification. Strong analytical skills with the ability to assess ingredient efficacy and safety. Excellent collaboration skills to work across departments including R&D, procurement and marketing. Preferred Qualifications: Proven & Significant experience in Taxonomy Experience of working with R&D Team, for appropriate material selection for specific formulation. Ph.D / M.Sc. in relevant field. Experience working with herbal supplements, functional foods, beverages, or cosmetics. Understanding of good agricultural and collection practices (GACP) and sustainable sourcing. Knowledge of herbal pharmacology, ethnobotany, or nutraceuticals. Familiarity with lab testing methods and plant-based ingredient stability Work Environment & Benefits: Opportunity to work on innovative, plant-based FMCG products. Collaboration with a multidisciplinary team of scientists, researchers, and product developers. Professional development opportunities in the rapidly growing natural and organic products sector.