606 Formulation Development Jobs - Page 6

Role & responsibilities To handle the responsibility of Agri Business for an assigned zone and coordinate with entire zonal team to provide support & business growth. Understand Market requirements Vs Product Range & work to build products to bridge the gap. Close working with Plant for product development, price, policy formulation, sales release, managing sales forecasts & sales generation. Must be able to read pump curves, have understanding of MOC & pump parts. Get involved in pre-tendering activities & coordinate with Zones for deciding specifications for government projects. Responsible for understanding tender requirements, product selection/development, pricing & participation. Responsible to push plant team for BIS & Star rating activities. Travel in assigned territory and understand market scenario, competition etc to recommend action plan. Provide training to zonal colleagues for products, systems, software, policies etc Responsible for implementation of Digital transformation projects in his area of operation. MIS Prepare & analyse the data and derive & refine sales strategies after studying the same. Preferred candidate profile

-Formulation of trials for solid, liquid and semisolid formulations -To perform literature search & preparation of literature survey report -Execution of formulated/ Design trials and sample order batches -Preparation of R&D Departmental SOPs Required Candidate profile -To maintain GLP and GMP in the laboratory -Preparation & review of Technology Transfer Document and other relevant documents -To involve in scale-up and initial commercial batches preparation

1.Experience in Regulated Market (US, Europe) 2.Candidate should perform literature search 3.Should have some basic understanding of patent and generic formulation development. 4.Characterization of marketed product wrt market requirements Required Candidate profile 5.Knowledge of ICH stability conditions and compilation of analytical data 6.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

Walk -in drive at Hotel Parc Estique - Pune - Macleods Pharma Department : PDR Designation : Research Associate/ Sr. Research Associate Experience : 4 - 8 Years Location R&D Mumbai Qualification : M. Pharm/ PHD (Pharmaceutics) Job Responsibilities Candidates should have 4-8 Years of relevant experience in Solid Oral Dosage & Liquid Orals form in Formulation & Development Dept. for Regulated Market

Role & responsibilities Formulation Development (Solid Orals, Liquids, MUPS, Molten Mass, Roll Compaction) Technology Transfer & Scale Up. QbD & DoE Methodologies Regulatory Compliance (US, EU, Emerging Markets) Preferred candidate profile Leading Successful Technology Transfer of Multiple Site Transfer Products for US & EU Markets, Ensuring Zero Regulatory observations during Inspectoins.

To Work as a Team Lead To develop the pharmaceutical oral solids / oral liquids / Semi-Solids Finished product for Regulated / ROW markets To develop & execute the manufacturing process R&D Scale and Pilot Scale Edu. M.Pharm / Ph.D Exp. 08 to 12 (OSD Formulation)

Job Opening: Food Technologist (Beverage Formulation & Carbonation) Location: Noida Sec-142 Job Type: Full-time/ Freelancing/ consultant Experience Required: 2-5 years in beverage R&D / formulation About the Role We are looking for a Food Technologist with hands-on experience in beverage formulation, flavor optimization, and carbonation techniques. The candidate will be responsible for developing innovative beverages, ensuring stability, sensory appeal, and compliance with safety standards. Key Responsibilities Develop and optimize beverage formulations (herbal, functional, carbonated, and non-carbonated). Work on flavor setting, taste balancing, and mouthfeel enhancement. Manage carbonation levels for consistency and product differentiation. Conduct stability studies, shelf-life testing, and sensory evaluations. Collaborate with production and quality teams to ensure scalability and regulatory compliance. Stay updated with market trends, new ingredients, and flavor technologies. Requirements Bachelors/Masters in Food Technology, Food Science, or related field. Proven experience in beverage R&D and formulation. Strong understanding of flavors, sweeteners, emulsions, and carbonation processes. Knowledge of FSSAI/US FDA/EU beverage regulations (as per target market). Innovative mindset with a passion for functional and wellness beverages. What We Offer Competitive salary & benefits. Opportunity to work on next-gen functional and herbal beverages. Collaborative environment with R&D freedom to innovate.

Role & responsibilities Job Title: R&D Officer Job Summary: We are seeking a highly motivated R&D Officer to join our food business. The successful candidate will be responsible for handling the new product development work, including formulating recipes, conducting trials, and working on the shelf life of the products. The R&D Officer will play a critical role in ensuring that our organization stays competitive by developing innovative and high-quality products. Duties and Responsibilities: Developing new product concepts and formulations, based on market trends and customer demand. Conducting trials to test new product concepts and formulations, and making necessary adjustments to recipes and processes. Ensuring that all products meet regulatory and safety requirements. Working on the shelf life of the products and developing strategies to extend the shelf life of products. Keeping up-to-date with new technologies and innovations in the food industry, and providing recommendations for improvements. Collaborating with other departments, including production, and quality control, to ensure that products are developed and produced in accordance with company standards. Maintaining accurate records of all R&D activities, including recipes, trial results, and product specifications. Providing regular reports to senior management on the status of R&D activities, including updates on new product development and progress on existing projects. Requirements: Bachelors degree in food science, food technology, or a related field. Strong knowledge of food science, including ingredient functionality, processing, and formulation. • Strong analytical and problem-solving skills, with the ability to identify and resolve complex technical issues. Excellent communication and interpersonal skills, with the ability to work effectively with individuals at all levels of the organization. Strong organizational and time management skills, with the ability to manage multiple projects and priorities. Ability to work independently and as part of a team. Strong attention to detail and accuracy. Proficient in Microsoft Office Suite and other relevant computer software applications.

Key Responsibilities: Formulation Development: Design and develop formulations for injectable products such as solutions, suspensions, emulsions, lyophilized products, and pre-filled syringes. Conduct pre-formulation studies, compatibility studies, and stability testing. Process Optimization: Define and optimize manufacturing processes for sterile products. Work on scale-up and validation batches for tech transfer. Documentation & Compliance: Prepare and maintain development reports, batch manufacturing records (BMR), and related documentation as per cGMP. Ensure compliance with ICH, USFDA, EMA, and other regulatory guidelines. Technology Transfer: Support technology transfer activities from R&D to production. Assist in troubleshooting during exhibit and commercial batches. Cross-Functional Interaction: Collaborate with Analytical, Regulatory, QA, and Manufacturing teams. Required Skills & Competencies: In-depth knowledge of injectable dosage forms and aseptic processing. Hands-on experience in lyophilization, sterilization techniques, and formulation design. Familiarity with QbD principles and DoE approach. Strong understanding of regulatory guidelines (USFDA, EMA, WHO). Qualification & Experience: Education: M. Pharm / PhD in Pharmaceutics or related discipline. Experience: 10 to 15 years in sterile formulation development.

R&D executive required from a mobile accessories company Qualification - any electronic Exp- min 2 yrs salary- max 20000 Location - kundli, sonipat. Wtsapp me resume at 8295842337- Mr. Bansal

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Please see the following position summary: Client Name: US based C2C Complex Formulator for USA market Position: Sr. Executive / Asst. Manager - Formulation Development (Complex Formulations) Market: USA Products: Sterile Injectable, Ophthalmic + Nasal & Inhalation Location: Navi Mumbai Job Profile: Responsible for design & development of complex sterile formulations including Sterile Injectable, Ophthalmic (Solution, Emulsion, Suspensions formulations), Nasal, Inhalation solution targeted for the USA market. Planning and conduction daily project related activities, analysing the trial outcome and further planning towards product development. To conduct pre-formulation, prototyping, formulation optimization, process development, preparation of due diligence documents and tech transfer of an injectable / sterile products aimed at US market filing. To conduct pre-formulation, prototype development, preparation of due diligence documents of ophthalmic suspensions using instruments like microfluidizer and high pressure homoginiser. The products are being developed for regulated market. To do patent searches, scientific literature searches, and associated strategies for sterile products, particularly ophthalmic products, for US markets. Execution of the developmental trial and optimization of formulation by systematic approach as per Quality by Design (QBD). Preparation and monitoring of stability protocols as per ICH guidelines and compilation of relevant stability data of development batches. Execution of the various studies like Preservative Efficacy Study, Photo stability, Thermal Stability, filterability, filter validation, filter compatibility, drop size and Short-Term Excursion Study etc. Execution scale-up & Exhibit batch of optimized formulation. Troubleshoot formulation and process-related issues during development, scale-up, & validation. Guide and mentor junior scientists, providing technical oversight and project direction. Desired Profile: M.Pharm with 5 to 10 experience in Formulation Development for USA markets especially in Sterile Formulations. Ph.D would be added advantage. Should have Good understanding of product development life cycle for Complex Sterile Formulation (Solution, Emulsion, Suspensions formulations). Exposure in Complex Sterile Formulation for USA market is must. Sterile formulation along with additional knowledge of Solid Orals, Nasal & Inhalation will give added advantage. Should have Good understanding of product development life cycle for Nasal Formulation. Prior experience in a Pharma CRO/CDMO environment is highly desirable. Should have Good understanding of product development life cycle for Complex Sterile Formulation. Person must have proficiency in operating High Pressure Homogenizer (GEA Panda, Avestin Emulsiflex C5). Strong project management, leadership, and cross-functional collaboration skills. Should have excellent communication skills with good spoken and written English. Recruiter Details: BEST - FIT Recruitment Riders G-7, Amrit Complex, Opp: Mahavir Jain Vidhyalaya & Jain Derasar, Vadodara-390001, Gujarat, India Mobile: 09722052906, 09722042906 E-Mail: career@bfrr.in Website: www.bestfitrecruitment.co.in

Role & responsibilities Formulation Development (Solid Orals, Liquids, MUPS, Molten Mass, Roll Compaction) Technology Transfer & Scale Up. QbD & DoE Methodologies Regulatory Compliance (US, EU, Emerging Markets) Preferred candidate profile Leading Successful Technology Transfer of Multiple Site Transfer Products for US & EU Markets, Ensuring Zero Regulatory observations during Inspectoins.

We have requirement for Formulations AR&D. Exp: 2 to 16 Years Designation: Executive to Senior Manager Work Location: CRAMSN Research Park, Pashamylaram, Patancheru, Hyderabad. Interested can share there CV's to mail: manishankar.dadi@msnlabs.com

Sound Knowledge in Overall Plant formulation activities, and statutory compliances Operations Management, Leadership &Team Management,Safety Compliance,Knowledge in QA & QC, Process Optimization and Continuous Improvement, Resource Management

Roles & Responsibilities 1. To support and execute formulation development of mAbs 2. Conducting stability studies as per ICH guidelines. 3. Acquisition, recording, analysis and compilation of data in prescribed formats. 4. Responsible for maintenance and documentation of the developmental work carried out. 5. Supporting procurement/installation of appropriate equipment’s and consumables required for work, whenever applicable. 6. Capturing and compilation of the data generated contemporaneously in eLN (electronic Lab Notebook) and getting the same verified by the manager of the team regularly. 7. Ensuring proper usage and maintenance and calibration of equipment: entering the usage in log books and alerting appropriate personnel about any discrepancy and breakdown. 8. Implementation of the SHE management system in respective department/function. 9. Any other assignment given by group lead/team lead or assistance requested for compilation of urgent deliverables for the formulation development team. Additional Responsibilities: 1. Collection and review of the related literatures for specific methods/molecules and participation in various other forums for discussion and presentation. 2. Ensuring good house-keeping in the laboratory Qualification Educational qualification A M. Pharm/M. S in Pharmaceutical Sciences (specialization in Pharmaceutical Biotechnology, Pharmaceutics) or M. Tech (pharmaceutical Technology/ Biotechnology) Minimum work experience 6-9 years of experience in Biological drug product formulation development, Process development Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. The World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. " Benefits Offered At Dr. Reddy’s we actively help to catalyze your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. " Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions... For more details, please visit our career website at https://careers.drreddys.com/#!/ "

Greetings! We are looking for Formulation Research & Development Scientist - Injectables for a leading Pharmaceutical company based at Hosur location. Responsibility: 1. Develop robust formulations and processes for general products to various markets such as Regulatory, Semi-regulatory, ROW, and Domestic with application on QbD as needed. 2. Monitoring and supporting the formulation team for the completion of allocated projects within the timelines by trouble shooting the concerns involved. 3. Scale-up and optimization of manufacturing process; execution of pre-exhibit and exhibit batches; scale up and technology transfer from R&D to production to meet timeIines. 4. Plan and contribute to project-related scientific/technical activities (e.g., interpret results, critical assessment of data, draw relevant conclusions, and write reports). 5. Author technical documents including Product Development Report, Quality Overall Summary and other relevant documents for filing purpose. 6 Interaction with API/Excipient manufacturers, CROs and CMOs as needed. 7. Interaction with external testing laboratories as needed. 8. Work proactively with other cross-functional groups to execute all product related activities such as Manuticturing and Packaging master records, SOPs and protocols etc. 9. Co-ordination with other Dept. like Purchase. QC/QA, RA, ADD, Production Eng. etc. related to product development activity. 10. Review SOPs, as well as appropriate documentation and test results for accuracy and coin pleteness and coinpl iance with SOPs/GM P requirement. 11 . Coordinate with RA for fiI ing AN DAs and addressing deficiencies; provide relevant documents to Regulatory Affairs in a timely man ner for ANDA fil ings and Supplements filing. 1 2. Review of batch records, process characteri xation reports, validation reports and investigation reports. Interested Candidates Kindly share your updated cv to uma@bvrpc.com

Designation: F&D Manager External Preparations Job Location: Baddi Experience: 7 yrs above Notice: Immediate to 15 days Company: Leeford Healthcare Ltd. https://www.leeford.in/ https://www.linkedin.com/company/1464125/admin/dashboard/ Education: Graduation; Post Graduation: BSC/ B. Pharma Desired Candidate Profile: Required experience of 7-10 years, Exposure to work with one or more reputed organization. Knowledge of Topical manufacturing in Drug & Cosmetics - Manufacturing, Filling, Sealing and packing of products. Job Description: Work Profile: Troubleshooting in existing formulations. Formulation & Development of new trial batches for Domestic market and ROW market and Emerging Countries. Support entire drug product development process starting with first pre-formulation studies up to the manufacturing process transfer to production and the provision of the required documentation to allow worldwide registration. 4. Preparation of Bill of Materials, Master Formula Record, Product Development Report, Stability Study Protocol. Compilation of Physicochemical data and dissolution profile. Provide documentation of raw data, evaluation and contribute to interpretation of results. Provide input for the selection of next experiments. Communicate and address problems, perform safety and literature searches under guidance from more experienced team members. Interested one can share resume to talent@leeford.in or can whatsapp to 9875961129

Develop and optimize formulations for oral solids and liquids to meet quality, stability, and regulatory requirements. Conduct pre-formulation studies, compatibility studies, and excipient screening for both dosage forms.

Key Responsibilities: Design, develop, and execute behavioral and technical test cases for systems, applications, or products. Analyze requirements and user stories to create comprehensive test strategies. Conduct manual and/or automated testing as needed. Identify, log, and track defects or issues , and work with development/engineering teams for resolution. Validate system behavior under different conditions (e.g., performance, stress, usability). Participate in review meetings to provide test updates and insights. Maintain test documentation , including test plans, test cases, and test reports. Ensure compliance with quality standards and best practices in testing. Collaborate with cross-functional teams including developers, business analysts, and project managers. Support User Acceptance Testing (UAT) and assist users during testing phases. Skills/Experience: Realtime experience in BT-Stack, profile level testing, Tools like PTS, Python or Shell scripting Domain: BT Testt Experience (years) : 2 to 4 years Location - Bengaluru,Hyderabad,Chennai,Pune

Role & responsibilities 1. To undertake literature search & preparation of report for a new development project. 2. To execute development trials as part of prototype development till technology transfer of new drug products at the manufacturing sites. 3. To guide & supervise development trainees or associates during development of new formulations. 4. To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches. 5. Material Master creation of Material code/ Vendor code in ERP. 6. MIC creation of Raw material / Packing material / Finished products in ERP. 7. Applying Test / Import / Manufacturer Licenses 8. Involving all Development QA activities & ensure compliance. Preferred candidate profile M. Pharm/ Ph.D in Pharmacy Interested Candidates can share their resumes on shikha.mishra@walterbushnell.com

A leading manufacturing company in Chennai is looking for R&D Formulation Scientist in Chennai Interested candidates can contact us via email veena.k@prometoconsulting.com For quick response kindly, send your profile on whats app : +91 72006 29368 Position: R&D Formulation Scientist Experience: 08+ Years Job Location: Chennai. Education: M.Sc. in Chemistry Duties/Responsibilities: Develop and optimize formulation of friction materials (brake linings, pads, and related components). Research and evaluate new raw materials, binders, fillers, and fibers to enhance product performance. Conduct lab-scale trials and pilot plant experiments for new formulations. Perform physical, chemical, and performance testing on brake lining materials as per industry standards. -- Thanks & Regards, Veena K Prometo Consulting Pvt Ltd M : +91 72006 29368 E: veena.k@prometoconsulting.com L: https://www.linkedin.com/in/veena-k-6a9b5331a/ W: https://www.prometoconsulting.com/

Skills/Experience: Strong C programming, LSP, 802.11xx protocols, and realtime experience in WiFi firmware developent (eg: Atheroes chipset) Domain: WiFI Dev Design, develop, and maintain WiFi firmware and protocol stack based on 802.11 standards. Implement and optimize low-level drivers and firmware modules on WiFi chipsets, specifically Atheros or similar platforms. Work closely with cross-functional teams to integrate firmware with hardware and higher-layer software. Debug and troubleshoot complex wireless communication issues in real-time environments. Ensure firmware meets performance, reliability, and security requirements. Develop and execute test plans for validating WLAN firmware features. Participate in code reviews and contribute to continuous improvement of development processes. Stay updated with latest WLAN standards and industry trends to enhance product capabilities. Location - Bengaluru,Hyderabad,Chennai,Pune

Skills/Experience: Strong C, DS, LSP, Understanding of Linux Kernel, ARM Arch, Debugging with JTAG, T32, (GDB, KGDB optional), Python or shell and relevant project level experience Domain: Bare metal/ Firmware Experience (years) : 2 to 4 years Location - Bengaluru,Hyderabad,Chennai,Pune

Skills/Experience: GIT, Jenkins/Electric Commander/Hudson, Docker, Ansible, Python Domain: Devops Experience (years) : 2 to 10 years Location - Bengaluru,Hyderabad,Chennai,Pune

Job description Role Description This is a full-time on-site role for an Assistant Manager- R&D (Cosmetics & Skin Care) at A. G. Organica Pvt. Ltd. in Noida. The Assistant Manager will be responsible for conducting research and development projects in the field of cosmetics and skin care. Qualifications • Expertise in Research and Development (R&D) in cosmetics and skin care. • Experience with conducting research in the field related to cosmetics and skin care. • Strong team management and project management skills. • Excellent team leadership abilities. Relevant skills and qualifications that would be beneficial for this role include: • Knowledge of industry trends in cosmetics and skin care. • 4+ Yrs of experience in the R&D cosmetics and skin care. • Knowledge of the related documentation. • Experience in formulating skincare products. • Strong problem-solving and analytical skills. • Effective communication and interpersonal skills. • Master's degree in Chemistry, Cosmetology, or a related field. NOTE:- INTRESTED CANDIDATE CAN SHARE RESUME ON WHATSAPP ONLY Regards Priya Misra 9355010836