381 Formulation Development Jobs

As the Laboratory Manager at Motley Exim Co., you will be responsible for overseeing day-to-day lab operations to ensure safety standards are met and procedures are followed. Your role will involve the maintenance of lab equipment and efficient management of inventory for smooth workflow. You will be in charge of inventory control, tracking and managing all laboratory supplies, raw materials, and resources to maintain adequate stock levels and reorder timely when necessary. Additionally, you will be involved in Formulation Development, creating new formulations that meet project specifications while adhering to quality, performance, and regulatory standards. Conducting thorough product testing will be a key aspect of your responsibilities, where you will test formulations for stability, performance, and compliance. Documenting and analyzing test results will be crucial to support product development and enhancement. Staying updated on industry trends, materials, and technologies will be essential for Research & Innovation purposes. You will be expected to identify opportunities for innovative solutions in product offerings and enhance the company's competitive edge. Collaboration with cross-functional teams, including production, quality assurance, and marketing, will be vital to ensure product alignment and successful implementation across departments. Motley Exim Co. is a renowned company specializing in designing, developing, and manufacturing high-quality camouflage products. The flagship brand, Campro, offers innovative solutions for concealment and deception.,

DKSH's purpose is to enrich people's lives. For 160 years, DKSH has been marketing, selling, and distributing high-quality products and brands for multinational and Fortune 500 companies. Through Business Units Consumer Goods, Healthcare, Performance Materials, and Technology, DKSH delivers sustainable growth for partners, contributing to improving the quality of life for employees and people in the local communities where operations are conducted. Headquartered in Switzerland, DKSH is publicly listed and operates in 36 markets across Asia Pacific, Europe, and North America. With over 28,000 specialists employed, DKSH achieved net sales of CHF 11.1 billion in 2024. The strength of DKSH lies in the diversity of services, industries, clients, products, regions, and employees from various nationalities. DKSH is proud of its people, who are the key to its success. The employees are passionate about their career growth and business success, working as part of an energetic and committed team that positively impacts millions of lives through the products and services provided. Join DKSH today if you are ready to drive growth, be the difference, experience a world of learning and development, own your career, take business responsibility, and have a positive impact that touches people's lives. Job Summary: The Assistant Manager, Business Development, Pharmaceutical Excipients (Raw Materials) is responsible for technical business development for pharmaceutical excipients and nutraceutical actives. Job Responsibilities: - Promote and aggressively develop Pharma business in assigned geographical regions/customers. - Identify and introduce products of clients (existing and new) in the specified regions/customers. - Undergo technical training and support the Pharma sales team and customers with technical know-how and product application. - Ensure that targets set by Senior Manager-Pharma and Head, Pharma Business Line are met to achieve performance bonuses. - Analyze the potential of the pharma market and build the customer base. - Identify prospective customers, generate leads, and support new business development with the reporting manager. - Conduct market mapping and promote new segments while maintaining strong relationships with various functions at customers (R&D, QA, Technology Transfer, Procurement, etc.). - Send monthly and specified reports on business development to the Senior Manager Pharma and principals/suppliers. - Coordinate and organize supplier visits at customer R&D. - Provide technical solutions to customers and support them in shop floor trials. - Align with internal business processes like Salesforce and proactively fulfill digital updation requirements. - Be prepared for new responsibilities assigned by Senior Manager - Pharma based on industry clusters or product groups and the development of other regions. Work Experience: 3-4 years in pharma excipient business development, techno-marketing technical development, formulation research development. Functional Skills and Knowledge: - Knowledge of formulation development activities of solid orals like Tablets, Capsules, Liquid oral, and Topical formulations. - Experience with novel drug delivery systems, regulatory filing of products for US, EU, ROW, and domestic markets. - Problem-solving capabilities in terms of pharma product development and scale-up trials troubleshooting. Education: B.Pharm/M.Pharma,

Role & responsibilities Responsible for formulation and process development (QbD approach) of following categories of Pharmaceutical products: Oral Immediate-Release Dosage Forms. Oral Modified-Release Dosage Forms Including Pelletization technology and Wurster technology. Topical Semisolids (Creams, Ointment and Gels). Oral Liquid Dosage Forms Topical Liquid Dosage forms. Solid (Suppositories), Semisolid & Liquid dosage forms for Rectal and Vaginal applications. Design and execute formulation trials and evaluate stability data to finalize formulation composition. Execution of technology transfer batches for manufacturing processes from laboratory scale to production scale. Oral Immediate-Release Dosage Forms. Oral Modified-Release Dosage Forms Including Pelletization technology and Wurster technology. Topical Semisolids (Creams, Ointment and Gels). Oral Liquid Dosage Forms Topical Liquid Dosage forms. Solid (Suppositories), Semisolid & Liquid dosage forms for Rectal and Vaginal applications. Knowledge of patent non infringing strategy based product development Knowledge of Bioequivalence study & clinical study protocol and criteria Independent contributor for batch planning, batch execution & technology transfer Develop manufacturing processes for R&D formulations so that the technical transfer is successful for large-scale batches. Responsible for all formulation/ process related CMC documents which will be part of regulatory filings. Write/review master formulas, manufacturing procedures, SOPs, stability protocols, process validation protocols, Product Development Reports etc. Prepare/review specifications for pharmaceutical products and packaging components, etc. Support the manufacturing of exhibit/submission batches per regulatory requirements. Work with Cross-functional teams (Analytical, Regulatory Affairs, Pharmacovigilance, Bioequivalence, Quality Control, Quality Assurance, Inventory Control, etc.) to expedite the development and approval of new products by different Agencies for Regulated and ROW Markets. Assure that all formulation and process development activities are documented in the notebook as per company procedures and cGLPs. Provide recommendations for continuous improvements in practices and systems to improve performance and enhance efficiency and quality. Communicate with outside vendors and laboratories. Preferred Skill Set: Thorough knowledge of the pharmaceutical industry, particularly drug delivery industry, and formulation and process development including guidelines. Knowledge for development of formulations comes under category of medical devices, Dietary Supplements and Cosmetics. Knowledge of ICH/GMP regulations. Behavioral /Managerial Skill Sets Skills building and maintaining productive relationships with organizational partners including teamwork. Skills related to develop and deliver products well with in specified timelines. Being a team player Appropriate communication with all stakeholders

About Us: InSilicoMinds is a leader in the application of computational modeling and simulation (CM&S) for pharmaceutical research and development. We focus on harnessing cutting-edge in silico technologies to streamline drug design, formulation development, and regulatory submissions. Our innovative approaches help to accelerate drug discovery while optimizing formulations and ensuring high-quality manufacturing processes. Position Overview: We are looking for a highly skilled and motivated Computational Chemistry Expert with hands-on experience in retrosynthesis and reaction simulation. The ideal candidate will have deep expertise in computational chemistry tools and software, with a focus on optimizing reaction pathways to achieve high yields, minimal impurities, and selective production of specific isomers and polymorphs. Key Responsibilities: Lead retrosynthesis projects aimed at developing efficient synthetic routes for pharmaceutical compounds. Simulate reaction pathways and optimize reaction conditions, including solvent selection, temperature, and reagent concentrations, to maximize desired product yield. Address challenges related to regioselectivity, stereoselectivity, and polymorphism, ensuring the selective formation of specific isomers and crystalline forms. Collaborate with cross-functional teams, including synthetic chemists and formulators, to translate computational insights into experimental protocols. Utilize advanced computational chemistry tools and software to predict reaction outcomes, impurity formation, and scalability of processes. Continuously explore new computational methodologies and contribute to the development of in silico tools and workflows within the organization. Present and defend findings and strategies in project meetings, contributing to decision-making processes. Qualifications: Ph.D./ masters in computational chemistry, Organic Chemistry, or a related field, with strong knowledge of retrosynthesis and reaction mechanism modeling. Proven experience in simulating chemical reactions and optimizing reaction parameters to improve yield, reduce impurities, and control isomer or polymorph formation. Proficiency in computational chemistry software, such as Gaussian, Schrdinger, ORCA, or similar tools. Familiarity with molecular modeling techniques, including quantum chemistry, molecular dynamics, and thermodynamic simulations. Strong analytical skills and problem-solving abilities with attention to detail. Excellent communication skills and ability to work in a collaborative, interdisciplinary team environment. Preferred Experience: Experience with cheminformatics tools and databases for reaction prediction. Knowledge of AI or machine learning applications in retrosynthesis or reaction optimization. Experience in the pharmaceutical or chemical industry, especially in synthetic route design or process optimization.,

The role involves leading the Development of Dermatological OTC products across various markets like the US, Europe, Australia, New Zealand, CIS, and Rest of World. You will be responsible for end-to-end ownership of formulation activities, including both new product development and enhancements to existing products. The ideal candidate will have a strong track record in delivering robust, stable, and cost-effective formulations that align with target product profiles, timelines, and budgets. You should be able to drive innovation in formulation approaches, contribute to intellectual property generation, and ensure seamless technology transfer from development to commercial manufacturing. Key Responsibilities: Product Development: - Lead end-to-end formulation development for derma OTC products, ensuring formulations meet target product profiles, regulatory requirements, and manufacturing constraints. - Conduct stability studies and optimize existing formulations to improve efficacy, stability, sensory attributes, and cost-effectiveness. - Collaborate with packaging development to ensure compatibility between formulations and packaging components. Technical Leadership: - Provide scientific expertise on dermatological active ingredients, excipients, and delivery systems. - Stay updated with emerging technologies and scientific advances in topical/dermatological OTC products. Project Management: - Manage multiple development projects concurrently, prioritize resources effectively, and adhere to project timelines, budgets, and resource plans. - Identify and mitigate technical risks throughout the development process. Team Leadership: - Supervise and mentor formulation executives, foster a collaborative environment, and promote innovation and continuous improvement. - Collaborate effectively with cross-functional teams to ensure seamless product development and commercialization. Manufacturing Support: - Lead technology transfer of new formulations to manufacturing sites, support scale-up activities, and troubleshoot manufacturing issues related to formulation aspects. - Develop and maintain standard operating procedures for formulation processes. Qualifications: Education & Experience: - Master's or PhD in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field with 10 years of hands-on experience in formulation development of topical/dermatological products. - Proven expertise in developing OTC products in alignment with regulatory standards. Technical Expertise: - In-depth knowledge of dermatological product formulations such as creams, lotions, gels, and ointments, and familiarity with OTC monographs and regulatory requirements. Leadership & Strategic Skills: - Proven project management abilities, problem-solving skills, and scientific curiosity. - Strong verbal and written communication skills and experience in handling multiple projects simultaneously. If you are interested and meet the qualifications mentioned above, please send your updated resume to unitedtechit@uhr.co.in. We will contact you for a detailed discussion if your profile matches our requirements.,

At Lilly, the focus is on uniting caring with discovery to improve the lives of individuals worldwide. As a global healthcare leader headquartered in Indianapolis, Indiana, the organization is committed to developing and delivering life-changing medicines, enhancing disease management, and giving back to communities through philanthropy and volunteerism. The team at Lilly prioritizes putting people first and is dedicated to making a positive impact on a global scale. The Product Research and Development (PRD) organization at Lilly is instrumental in the development and delivery of quality medicines to patients. The diverse portfolio includes the development and commercialization of various medical products ranging from insulins to gene therapy systems. This multidisciplinary group collaborates closely with therapeutic business units and manufacturing teams to bring Lilly's clinical portfolio to patients worldwide. Located in Bengaluru, India, the Lilly Capability Centre India (LCCI) is a strategic investment aimed at attracting top talent from India's academic and professional landscape. The LCCI team works in tandem with the PRD team in Indianapolis to develop critical capabilities for Lilly and support the delivery of the organization's portfolio. As part of the PRD team, the role involves leveraging experience in solid drug product manufacturing unit operations to expedite the development of combination products and enhance manufacturability. Responsibilities include conducting risk assessments, defining critical quality attributes, implementing new manufacturing platforms, and designing manufacturing process control strategies. The position also entails leading development activities, collaborating with cross-functional teams, and contributing to regulatory strategies and submissions. The ideal candidate for this role possesses a Ph.D. in chemical engineering, pharmaceutical sciences, or a related field with relevant experience, or a B.S. or M.S. with extensive experience in a related field. Additional skills/preferences include familiarity with new platforms such as PAT and modeling tools, knowledge of oral drug delivery landscapes, project management experience, and demonstrated leadership abilities in a team setting. Lilly values diversity of thought and experience, encouraging creative solutions to address technical challenges. The organization is committed to engaging with the external environment and adopting innovative approaches across its drug product portfolio. The position may require some travel. Lilly is dedicated to providing equal opportunities for individuals with disabilities in the workforce. If accommodation is needed to apply for a position at Lilly, applicants can complete the accommodation request form for further assistance.,

As an Executive - Application Lab at Azelis India, your main objective is to develop innovation through formulation, application, sampling, and technical support in the Personal Care and Home Care products industry. You will be responsible for formulating a wide range of products, conducting stability studies, ensuring regulatory compliance, and working on sustainable product concepts aligned with market trends. Your role will also involve providing technical support to customers, conducting product demonstrations, and collaborating with suppliers on new ingredient innovations. In addition, you will manage the HPC application development lab, handle lab operations, support CAPEX planning, and maintain technical documentation. You will be required to provide internal technical training, evaluate market intelligence, develop marketing strategies, and monitor competition activities in the market. The ideal candidate for this role should have a B. Tech or M.Sc. in Chemistry/ M.Tech/Chemical Technology/cosmetologist with a minimum of 2-5 years of experience in technical/formulation development. Strong communication and collaboration skills, a sense of ownership, drive, and excellent organizational abilities are essential for this position. Fluency in English is a must, and proficiency in other languages is a plus. Adherence to work culture and ethics is also expected. Please note that the job requirements may evolve based on business needs, and you will be expected to adapt to changes and perform any tasks for which you are trained.,

Responsibilities: * Develop advanced cosmetic formulations using R&D techniques. * Lead new product development from ideation to launch. * Optimize delivery systems for skin care products.

Hiring for f&D Location- Baddi Experience- 4-7 years Salary Range- 40-50 k Industry - Pharma (injectable) interested candidates share resume on 9815675900

Responsibilities: * Conduct research on new chemical formulations * Develop processes for textile cleaning products * Prepare MSDS & TDS reports for chemical manufacturing * Collaborate with R&D team on product development Health insurance Annual bonus Leave encashment Mobile bill reimbursements Gratuity Provident fund

As an R&D Executive (Food Technologist) at our Mohali-based company, you will play a crucial role in leading New Product Development (NPD) and Technology Transfer projects with a specific focus on Nutraceuticals, Sports Nutrition, and Health Supplements. Your expertise in formulation, process innovation, and regulatory compliance will be vital in bringing science-backed products from the lab to the market. Your responsibilities will include managing NPD projects, ensuring compliance with FSSAI Nutraceutical Regulations, selecting ingredients based on scientific research, developing taste-masking strategies, conducting compatibility studies, validating nutritional information, and overseeing technology transfer to the production floor. Collaboration with cross-functional teams for cost optimization, process standardization, and sensory evaluation will be key aspects of your role. Preferred qualifications for this position include a B.Tech in Food Technology with a minimum of 3 years of industry experience in Sports Nutrition, Infant Nutrition, or Dietary Supplements. Proficiency in functional claim validation, regulatory documentation, and flavor optimization will be advantageous. This is a full-time position that offers health insurance, a yearly bonus, and requires fluency in Hindi. Your dedication to product innovation and commitment to quality will contribute significantly to our company's success.,

Responsibilities: * Diagnose & treat patients using Ayurvedic principles * Collaborate with healthcare team on patient care plan * Prescribe herbal remedies & dietary advice * Record Medical Detail & Data of Patients * Study Data to identify Patterns

Execution and documentation of the Pre-formulation studies Execution of Lab scale experiments (Feasibility trials), product and process parameter optimization employing the concept of Quality by Design. Execution of process evaluation, optimization, scale-up and exhibit batches. Record primary data of experiments performed and prepare data for reports; report and discuss results, issues and work-in-progress with the senior colleagues Coordinate with other departments for material procurement, analytical data etc. Prepare documents related to the product development such as Product development plan, Stability protocols and Product development reports Document the formulation activities in PLM as per SOP, handle QMS events, LIMS, OAMS and SAP Adhering to the GLP practices

We require candidates who are having prior experience in formulating and testing and development of aviation fluids and lubricants. Basically product development technologists/scientists required with strong command in development and formulation of varied products across applications in the aviation sector. Familiarity with GOST, MIL, CEMILAC, DEFSTAND. Proven years of experience and managerial level in aero lubes. Prior work in aero lubricants company is highly preferable.

We're looking for a motivated and detail-oriented R&D Chemist (Fresher) to join our R&D team in food and cosmetic colorants. A strong academic background in chemistry and passion for innovation in color formulation & testing is a must. Apply now!

1. Ensure QA oversight in product development lifecycle from pre-formulation to tech transfer 2.Review & approval of developmental protocols, reports & technical document 3. Readiness for audits and regulatory submissions - EU, USFDA, TGA Required Candidate profile 1. Work Location is Chengalpet 2. Qualified M.Pharm / M.Sc / B.Pharm 3. Minimum Exp of 7 to 10 yrs (in a DQA/QA role with pharma formulation R&D)

You will be part of the Formulation Development team, contributing your expertise in Biologic Formulations and pharmaceutical sciences. Your responsibilities will include conducting literature reviews, formulating biological products, designing and executing experiments, analyzing data using various techniques, calibrating instruments, performing proof-of-concept studies, conducting stability studies, writing scientific reports, and collaborating with cross-functional teams. To excel in this role, you should hold a minimum of a Postgraduate degree (MTech, MPharm) in Pharmaceutical Sciences, Chemistry, or a related field. Proficiency in analytical techniques like HPLC, GC, pH, Osmolality, KF, and UV spectroscopy is essential. Effective communication, strong analytical and research skills, teamwork abilities, and knowledge of pharmaceutical excipients and raw materials will be key to your success in this position.,

As the Head of R&D and Manufacturing at a Cosmetics & Personal Care Manufacturing Company in DR Congo, your primary responsibility will be to oversee the development and production of cosmetic formulations, including makeup, skincare, and hair care products. You will be tasked with researching and selecting appropriate raw materials, conducting product testing for stability, safety, and efficacy, and ensuring regulatory compliance with relevant cosmetic regulations and safety standards. Your role will also involve managing production processes, implementing production schedules to optimize efficiency, and overseeing quality control programs to maintain product standards. Additionally, you will be responsible for supervising and motivating production teams, identifying areas for process improvement, and staying up-to-date on industry trends and best practices. It is essential that you possess a B.E. in Chemical Engineering with over 15 years of experience in cosmetic manufacturing, with a strong background in managing teams and implementing operational strategies. Experience working in Africa, particularly in DR Congo, is a requirement for this role. Your ability to communicate effectively, collaborate with various departments, and ensure compliance with safety regulations and environmental standards will be crucial to your success in this position. If you are a results-driven individual with a passion for innovation and continuous improvement in cosmetic product development, we encourage you to apply for this challenging and rewarding opportunity. For further details or to express your interest, please contact Rina Arun at +91 9904322770 or via email at rina@uhr.co.in.,

The Assistant General Manager - Nasal Spray Formulation Development will play a crucial role in leading the development of innovative nasal spray formulations within the Research & Development (R&D) department of a Pharmaceuticals company. Reporting to the Head of R&D, you will be responsible for driving projects from concept to commercial scale-up, ensuring regulatory compliance and meeting quality standards. Your primary focus will be on designing, developing, and optimizing nasal spray drug products for global markets. Key Responsibilities: - Develop and technology transfer Nasal Sprays, Dry Powder Inhalers, and Soft Mist Inhalers dosage forms for regulated markets like EU and US. - Conduct literature search reports for drug substances and products, design product development strategies, and propose different formulation strategies based on the review outcomes. - Guide executives in lab development batches, provide expert input into formulation and process studies, and ensure compliance with specifications. - Evaluate packaging material vendors, monitor stability studies, and prepare/review Technology Transfer documents. - Coordinate with internal stakeholders, follow GLP & GMP, participate in stability and validation batch manufacturing, and prepare PDR for regulatory submission. Qualifications & Skills: - M.Pharm or Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related field. - Specialization in drug delivery systems or formulation science preferred. Experience: - 8-10 years of formulation development experience, with a minimum of 5 years focused on nasal spray or inhalation formulations. - Proven experience in nasal spray product development from early-stage to commercial scale-up. Technical Expertise: - Strong understanding of nasal spray formulation techniques, drug-excipient interactions, and delivery systems. - Experience with device development and knowledge of regulatory requirements for nasal spray formulations. Project Management: - Strong project management skills, ability to manage multiple projects, work with cross-functional teams, and deliver results. Regulatory Knowledge: - Experience in preparing and reviewing regulatory submissions, familiarity with CMC requirements for nasal formulations. Leadership & Communication: - Ability to lead and develop a team, excellent communication and presentation skills for conveying complex scientific information. Problem-Solving & Innovation: - Strong analytical and problem-solving skills, ability to innovate and apply new technologies to improve drug delivery processes. Work Environment: - Primarily based at the R&D center with occasional travel to manufacturing sites, vendors, and regulatory meetings. Join us in this exciting role to contribute towards developing high-quality nasal spray formulations for global markets.,

Key Responsibilities- Should be able to test Raw Materials, process the finished products in Lab using HSD, Hobart Mixer. Correction plan, issuing the correction plan to Stores & Production for return material, after Discussion with QCM Should able to conduct Lab experiments. Coin and implement processes to QC, Production after discussion with respective Manager. Performing sample testing using basic methods (UTM, Karl Fischer, Viscometer, Density, Titrations, pH testing etc.) Up keeping the general maintenance of laboratory equipment as per the quality assurance and standard operating procedures. Preparation of volumetric solutions/media/buffers Should have good communication skills and good handwriting Analysing data and developing new products or improving existing ones. Conducting research and development to create new products, processes, and technologies Ensure compliance with regulatory requirements and safety standards in all research and development activities. Foster a culture of continuous improvement, collaboration, and knowledge sharing within the R&D team. Establish and execute Laboratory work that align with the company's overall goals and objectives. Collaborate with cross-functional teams, including product development, Purchase, regulatory affairs, and manufacturing, to drive project success. Skills- 1.Basic Computer operating skills and proficiency in English 2. Basic knowledge of laboratory working in industry 3. Familiarity with raw materials, minerals, polymers, pigments 4. Basic knowledge of testing construction chemicals/ cements/paints 5. Strong understanding of chemical safety and hazard assessment procedures. Education Qualification- Bachelors Degree in Science (Chemistry) or Master Degree in Science or Polymers

Key responsibilities include literature reviews, pre-formulation, pellet formulation, stability studies, process validation, technology transfer, troubleshooting, and maintaining documentation like QAQN, MFR, FPS, and logbooks. Perks and benefits Accommodation, Transportation and Mediclaim.

Work closely with cross-functional teams including Production, QA, QC, and Regulatory Affairs Prepare and maintain laboratory records, batch documents, and technical reports Assist in the design and development of formulations for tablets, capsules and other dosage forms

Company website : www.microgenindia.co

Department: Formulation Development. Job Title: Research Associate / Sr. Research Associate - Formulation Development Experience: 2 - 4 Years Reporting to: Manager Formulation Development Location: Hosur, Tamil Nadu. Qualification M. Pharm in Pharmaceutics Candidate should be from English medium. Job Description: Preparation of product initiation from (PIF). Literature search/ Patent search/ Formulation strategy for formulation. Interpretation of stability study reports. Leading team in effective manner. Market sample / innovator sample procurement in coordination with the marketing team, providing training to team members. Reference/comparator product procurement and evaluation. Test license application. Preparation of costing formula. Execution of Bio batches. Procurement of Raw materials, Packing materials & Lab equipment. Preformulation studies / Drug excipient compatibility study review and further plans. Monitoring formula development activity for lab scale batches / pilot batches. Providing costs for new product development. Preparation of documents viz product development report, stability protocols, product specifications, formulation certificate, master formula record. Resource organization and coordination with relevant departments viz. purchase, R&D, Analytical, Quality Control, Quality Assurance, production and Engineering etc. Organizing seminars by internal staff and external vendors. Providing justification and response to queries received from regulatory authority. Formulation development and scale up. Stability Studies. Analytical data and stability data compilation. Maintenance of Lab Notebooks and Project files.

Develop & optimize makeup formulas; focus on texture, pigment, binding, and stability. Test performance, scale up to production, use clean ingredients, ensure global compliance & collaborate across R&D, packaging & suppliers. Accessible workspace House rent allowance