1025 Formulation Development Jobs - Page 3

Strong communication, presentation skills Ability to build trust-based relationships with healthcare professionals Required Candidate profile Good understanding of nutrition, protein supplements, or healthcare products (preferred) Basic computer proficiency for reporting Freshers are Ok

Role Purpose Responsible for managing formulation development activities of Oral Solid Dosage (OSD) forms including Tablets, Capsules, DC Granules, and related dosage formats, ensuring development from concept to commercialization in compliance with regulatory and GMP requirements. Key Responsibilities Formulation Development Lead design and development of robust OSD formulations for regulated and semi-regulated markets. Conduct pre-formulation studies, API characterization, excipient compatibility & selection. Design QbD-based formulation studies, DoE trials, and scale-up plans. Preparation & review of BMR, BPR, MFR, BOM, and process development documentation. Execute pilot batch, exhibit (...

Role & responsibilities Formulation development (solid, semisolid, liquid oral) Tech transfer & scale-up Troubleshooting & problem-solving QbD, DoE, FMEA Strong documentation skills Knowledge of regulatory requirements Project management & cross-functional coordination

Company Description Senores Pharmaceuticals is one of the fastest-growing pharmaceutical companies with a strong manufacturing presence in the USA. The company has a global footprint, with a marketing reach in over 30 countries. Senores Pharmaceuticals is committed to delivering high-quality products and maintaining excellence in pharmaceutical innovation. The company strives to meet the healthcare needs of a global population with effective and affordable solutions. Role Description This is a full-time, on-site role located in Ahmedabad, for a Formulation & Development & ADL Executive. The role involves developing and executing formulations for new product development, ensuring compliance w...

Assistant Manager PU Product Development (R&D) Company: Pon Pure Chemical India Private Limited Department: Research & Development (R&D) Location: Chennai Designation: Assistant Manager PU Product Development Minimum Qualification: M.Sc. Polymer Science / Chemistry B.Tech / B.E. Polymer Engineering Position Overview The Assistant Manager PU Product Development will be responsible for leading research and development activities in Polyurethane (PU) applications, including flexible foam, rigid foam, and specialty PU systems. The role involves formulation development, application testing, customer trials, and supporting innovation initiatives aligned with the company's product roadmap. This pos...

Role & responsibilities Job Responsibilities: 1. Handling of stability section independently. 2. Handling of additional stability studies, such as, Photo stability, In-use studies, freeze thaw studies. Split studies etc. 3. Preparation of stability protocols, reports and stability compilation. 4. Responsible for timely initiation, closure of QMS documents related Quality Control and implementation respective corrective and preventive action. (i.e. Change controls, Laboratory Incidents, OOS, OOT & CAPA) 5. Responsible to follow ALCOA + principle while doing the data recording. 6. Review of In-process, finished, stability, process validation, in-process, Raw material, Excipients, packing mater...

Position Purpose The role holder is responsible for working at the bench ensuring clear and on time delivery of products as planned by the department. This person should be responsible for developing formulations of different actives under the guidance of the Team Leader. The incumbent should be either a M.Sc./MTech/Ph.D. in any branch of chemistry (physical, analytical, agrochemicals, bio-technology). A few years hands-on experience in any organization is an advantage. Key Responsibilities: Strategic Actively imbibing the values and philosophy of PI Industries Efficient contribution to the overall success of R&D Chemistry by driving innovation and team performance according to objectives an...

Company Description Senores Pharmaceuticals is one of the fastest-growing pharmaceutical companies with a strong manufacturing presence in the USA. The company has a global footprint, with a marketing reach in over 30 countries. Senores Pharmaceuticals is committed to delivering high-quality products and maintaining excellence in pharmaceutical innovation. The company strives to meet the healthcare needs of a global population with effective and affordable solutions. Role Description This is a full-time, on-site role located in Ahmedabad, for a Formulation & Development & ADL Executive. The role involves developing and executing formulations for new product development, ensuring compliance w...

Role & responsibilities Position Title: HR Business Partner R&D Department: Human Resources Location: Dholka Reports To: Head – HR (Site) 1. Role Summary The HR Business Partner for the Research & Development Centre will act as the strategic HR advisor supporting scientists, technical teams, analytical functions, and support groups. The role focuses on driving people strategies, capability building, performance excellence, and creating a high-engagement culture aligned with R&D priorities such as innovation, compliance, and speed-to-market. 2. Key Responsibilities A. Strategic HR Partnership Partner with R&D leadership to understand talent needs and create HR strategies aligned with business...

Roles and Responsibility Develop and optimize formulations for various products. Collaborate with cross-functional teams to ensure successful product launches. Conduct research and stay updated on new trends and technologies in formulation development. Analyze data and provide insights to improve product performance. Ensure compliance with regulatory requirements and company standards. Manage multiple projects simultaneously and meet deadlines. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels bef...

Roles and Responsibility Oversee production processes to ensure compliance with regulatory requirements and company standards. Coordinate with cross-functional teams to optimize production efficiency and reduce costs. Develop and implement process improvements to increase productivity and quality. Conduct regular audits to identify areas for improvement and implement corrective actions. Collaborate with the quality control team to ensure products meet required standards. Analyze data to identify trends and opportunities for improvement. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourag...

JOB DESCRIPTION Title: Product Development Scientist - VMS (Vitamins, Mineral Supplements) Suggested Grade: Individual contributor role Minimum Qualification & Experience: Food Technology/Dairy Technology/Oils and Fats Technology with 5 – 10 yrs of experience in nutritional product development Preferred additional experience in VMS and other formats like bakery, Gummies,healthy Bar, Diskettes and Chocolate development & breakfast formats. Other requirements – familiar with manufacturing operations like spray drying, dry mixing, encapsulation techniques, liquids & beverages, etc Critical Skills Required : Knowledge of FSSAI standards, BIS norms, food laws and regulations in India Knowledge of...

Job Description / Responsibilities Optimize and refine system-level microprocessor operations to enhance printer efficiency and overall performance. Collaborate with mechanical, electronics, and ink technology teams to ensure synergy between unit operations, microprocessors, and consumables. Perform system-level performance analysis covering print head drive electronics, mechatronic technologies, and control systems for precise ink delivery. Provide technical leadership in selecting and integrating high-performance electronics, DSP architectures, electrical control systems, and real-time control platforms. Prepare technical documentation, specifications, and test reports, ensuring effective ...

1. Evaluation of Existing Products Conduct periodic technical reviews of all current product formulations. Analyze product performance, stability data, customer feedback, and competitive benchmarks. Identify gaps, inconsistencies, or performance improvements required in existing products. Recommend reformulations or process modifications to enhance quality, cost-effectiveness, safety, or regulatory compliance. Ensure all improved formulations meet company standards, statutory regulations, and industry benchmarks. New Product Development (NPD) Understand company needs, market trends, and customer requirements to propose new product concepts. Develop new formulations from concept to sample sta...

This is where your work makes a difference. At Baxter, we believe every personregardless of who they are or where they are fromdeserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. He...

Roles and Responsibility Conduct thorough research and analysis to identify trends and patterns in complex data sets. Develop and implement innovative research methods and techniques to drive business growth. Collaborate with cross-functional teams to design and execute research studies. Analyze and interpret large datasets to inform business decisions. Develop and maintain detailed reports and presentations to communicate findings. Stay up-to-date with industry trends and developments to identify new opportunities. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to veri...

Job Summary We are seeking a highly skilled Analytical Scientist in to join our Research and Development team for Injectable Division for developing and validating analytical methods for injectable products, ensuring compliance with the regulatory requirements, conducting literature reviews, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. This role demands a strong understanding of analytical principles, excellent documentation skills, and the ability to work effectively in a collaborative team environment. scaling up for manufacturing of batches, coordinating manufacturing readiness, ov...

About The Role Skill required: Regulatory Services - Life Sciences Regulatory Operations Designation: LifeScience Regulatory Svs Sr Analyst Qualifications: Master of Pharmacy Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes b...

Job Description: Qualification: B.Pharm / M.Pharm / M.Sc (Chem) / M.Sc (Microbiology) With Production experience of 510 years Experience required in sterile / Injectable / OSD / USFDA / EUGMP / PICS approved facilities API is not preferable Disclaimer: The job location mentioned in this description is based on publicly available information or company headquarters. Candidates are advised to verify the exact job location directly with the employer before applying

HCP Wellness is hiring a Key Account Executive (Cosmetics Skincare) to manage and nurture high-value clients while ensuring smooth coordination with our Product Development Officers, Product Development Coordinators, Formulation Development Coordinators, RD Chemists NPD Division. This role involves daily account communication, issue resolution, update tracking, product development follow-up, sample coordination, CRM updation, production tracking, packaging updates, and ensuring every assigned account receives complete support for building skincare, cosmetics, oral care, haircare personal care products with us. You will act as the single point of contact for all assigned clients and ensure th...

Lead the design, synthesis & scale-up of oleochemicals & additives, focusing on innovative, sustainable & commercially viable solutions Develop, optimize and scale up chemical processes Apply advanced analytical techniques Supervise R&D Chemists Required Candidate profile Experience in advanced analytical techniques (HPLC, GC-MS, FTIR) for product characterization & process monitoring Proficiency in process scale-up, technology transfer, and pilot plant operations

As a candidate for the position, you will be responsible for driving technology transfer for third-party manufacturing, loan license projects, and Abbott's own manufacturing plants. Your role will also involve supporting Abbott site MS&T team as per requirements and assisting in the qualification of alternate suppliers for raw materials & API. You will need to ensure compliance with regulatory, quality, statutory, EHS, and Pharmacovigilance requirements. Your primary job functions will include performing effective gap analysis between the sender & receiving site in process & equipment, preparing Master formula record & Technology transfer protocol for products identified for transfer, and re...

Dr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can't Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolve...

Role & responsibilities At least 8 years experience in formulation and development for oral liquid dosage and Injectable device dosage form for with US & EU Should have done active contribution in liquid products development which includes identification of excipients, prototype formulation based in innovator product characterization Identification of right primary packaging components. Initiate stability batches with generating required GxP documents Candidate should have detailed understanding of scale up and EB manufacturing Should independently monitor and prepare formulation development documents like development report, MFC, specifications, tech transfer documents. Candidate should sup...

Role Overview: As a candidate for this position, you will be responsible for developing, validating, and transferring analytical methods for raw materials, intermediates, and finished products in compliance with regulatory guidelines such as ICH, USP, EP, JP, etc. You will utilize techniques including HPLC, UPLC, GC, MS, FTIR, UV-Vis, and dissolution testing for method development. Your role will also involve supporting formulation development by providing analytical data for stability, compatibility, and process optimization studies. Additionally, you will troubleshoot analytical methods and instrumentation to ensure data integrity and reliability. Conducting forced degradation and stabilit...