1057 Formulation Development Jobs - Page 22

Pupose:Deliver formulations in defined timeframe to meet product delivery goals for I&D Development of different formulations either as generic or differentiated generics. To demonstrate successful stability and scale up at manufacturing site. Core Job Responsibilities Development of formulation using scientific rationale in use of excipients to create a reproducible prototype formulation. Ensure Proper documentation of every trial in the log note books and then using the information for creation of the Product Development Report for use in dossier for filing. Use of QbD wherever required for Product and process optimization. Ensure proper upkeep, maintenance and calibration of the equipment...

The Executive, Regulatory Compliance Europe (RCS) in Regulatory Affairs (RA) organization of the Business Unit Performance Materials (BU PM) is accountable for the Master Data Management and its regulatory compliance for Europe. Job Summary : Technical business development for pharmaceutical excipients and nutraceutical actives Job Responsibilities : Promote and aggressively develop Pharma business in assigned geographical regions/customers. Identifying and introducing products of clients (existing and new) in the specified regions/customers. To undergo technical training and support the Pharma sales team and customers with technical know-how and product application. Ensuring that the target...

Job Description Position: Junior research scientist (JRS)/Research scientist (RS) Job Location: - Plot No. 214, Borsad - Tarapur Road, Ta: Petlad, Dist: Anand, Gujarat, India. Department: R&D / Formulation Experience: 3-6 years in Nutraceuticals Formulations. Industry: Nutraceutical / Food / Pharma Manufacturing Reports To: Manager FRD. Job Type: Full-Time Company Profile: - Pharmanza Herbal Pvt. Ltd. is one of the few companies which is focusing on standardizing and proving the efficacy of Herbal products. Our strong supplier base, fully equipped R&D facility, FDA approved manufacturing facility, infrastructure for conducting human trials as well as our formulations unit provides a one stop...

Exciting Opportunity for Research associate - Alternate Vendor Development in Formulation & Development(PDR) We are looking for a skilled professional with 3-5 years of experience in alternate vendor development for diverse markets like US, EU, ROW, Domestic, WHO. Key Requirements: - B.Pharm/M.Pharm qualification - 3-5 years of relevant experience - Familiarity with various market guidelines - Expertise in technology transfer - Exposure to shopfloor operations is advantageous

Responsibilities: Review IP landscape reports, non-infringement& FTO analysis Devise strategies for patent non infringement and invalidations Collaborate with R & D Scientist to explore design around strategies for P-IV & NCE products Conduct IP due diligence for product selection/ new opportunity identification. Support RA for patent certification, PIL clearances and declaration Monitor, review and manage ANDA litigations Conduct patentability searches, draft and file patent applications and manage prosecutions Ensure timely and effective task delivery through strategic planning prioritisation and execution.

You will be the Formulation & Development Scientist for our Nutraceutical Division, leading the development of innovative dietary supplements, functional foods, and health products. Your responsibilities will include researching, formulating, and optimizing nutraceutical products in adherence to regulatory guidelines. In the realm of Formulation Development, you will design and develop new formulations for dietary supplements such as tablets, capsules, powders, gummies, and liquids. You will also enhance existing formulations to improve stability, bioavailability, and efficacy. Evaluating new ingredients, excipients, and delivery systems for nutraceuticals will be a crucial part of your role...

Design, conduct and or supervise formulation development, process development, process optimization, scale up and manufacturing of product. Prepare and review documents such as batch records, Batch Packaging Records, Product Development reports, SOPs, Stability protocols, Raw material specifications, Packaging material specifications and In-process/ Finished product specifications, labelling and stability loading. Review of test results in alignment with the project goals, identify causes of variances and recommend solutions to achieve goals. Schedule experiments and prioritize assignments to meet project objectives and deadline. Maintain laboratory equipment and follow company safety standa...

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 7 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improv...

Key skills required by this role includes: Understand Regulatory operations Gather, review and analyse data regarding the business and its operations; prepare models and process maps for improvements; and communicate findings and suggestions to key stakeholders Understanding software requirements, ability to translate business need into functional and technical requirements Skilled in documentation and timely response and sharing of information Ability to perform discussion with customer Ability to effectively report on status of work Break down requirements in user stories Ability to verify the functionality in the solution. Ability to write test cases/scripts and execute them.

Role & responsibilities Conduct formulation trials for solid, liquid, and semisolid dosage forms . Perform literature search and prepare survey reports. Execute design trials, sample batches, and submit for analysis. Prepare stability study batches and maintain related reports. Support scale-up, initial commercial batches, and process validation . Draft and review Technology Transfer Documents and product development reports. Ensure GLP & GMP compliance with laboratory safety standards. Prepare departmental SOPs and stage-wise development reports

"Opportunity for M.Pharm professionals in Formulation Development (R&D) to work on sterile and non-sterile dosage forms (ANDA/ROW/US-OTC) with leading pharmaceutical projects in Mumbai.

We are looking for a highly motivated and innovative Junior Chemist to join our Research and Development team. You will have a key role in formulating, developing, and improving new products and processes. As a Junior Chemist, you will collaborate with team members to conduct experiments, analyze data, and contribute to our organization's research initiatives. Your responsibilities will include preparing standard chemical solutions, conducting lab trials following instructions, handling chemicals, glassware, and equipment, analyzing data as per SOP, maintaining records, adhering to lab safety protocols, and being willing to work in shifts. To qualify for this position, you should have a Bach...

You will be joining CBC Corporation India Pvt. Ltd., a subsidiary of the Japanese conglomerate CBC Co., Ltd., with a rich history dating back to 1925 and a global presence in industries like pharmaceuticals, life sciences, chemicals, electronics, and machinery. In India, CBC Corporation primarily focuses on trading and distributing high-quality chemicals, specialized materials, advanced optics, and technology-driven solutions. As part of the company's diverse operations, you will play a crucial role in providing technical support to pharma customers using excipients from CBC's portfolio. Your responsibilities will include engaging in regular technical discussions with R&D teams of customers ...

You are required to join our team as an R&D Executive (Food Technologist) in Mohali, Punjab. Your main responsibilities will include leading and managing New Product Development projects, ensuring compliance with FSSAI Nutraceutical Regulations, selecting ingredients based on scientific research, developing taste-masking strategies, conducting trials, coordinating with cross-functional teams, and maintaining thorough documentation for regulatory submissions. The ideal candidate must possess a B.Tech in Food Technology with a minimum of 3 years of experience in the industry. You should have expertise in Nutraceuticals, Sports Nutrition, and Health Supplements. It is essential to have knowledg...

Key Responsibilities: Conduct research and development of innovative dental products such as dental cements, cavity varnishes, and related materials. Perform reverse engineering of existing dental/chemical products to enhance or develop improved formulations. Work extensively with silver-based products and silver nanoparticles , ensuring proper synthesis, handling, and stabilization. Carry out chemical characterization, testing, and analysis of materials to ensure product quality, safety, and performance. Collaborate with cross-functional teams (production, QA, regulatory) for product validation and compliance. Prepare detailed technical documentation, research reports, and regulatory submis...

We are seeking a motivated and detail-oriented Injectable Plant Compliance Manager to join our team. The ideal candidate will be responsible for ensuring compliance with all regulatory requirements and industry standards specific to the production of injectable pharmaceutical products. This role will serve as a key leader in maintaining quality assurance, overseeing audits, and implementing compliance systems to ensure the safety and efficacy of our products.

As a Product Development Manager in Animal Healthcare at AABT Group, you will play a crucial role in leading the design of cutting-edge animal healthcare products that meet global standards. Your responsibilities will involve analyzing market trends, identifying product opportunities, and developing innovative formulations and packaging to ensure our products stand out in terms of both performance and presentation. You will be required to manage the entire product development process from concept to launch, collaborating closely with R&D, production, regulatory, and marketing teams. Conducting product trials, ensuring regulatory compliance, and collecting customer feedback for product enhanc...

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company dedicated to providing innovative products that cater to the needs of underserved patients. As a leading player in the industry, Azurity focuses on delivering unique, accessible, and high-quality medications by leveraging its integrated capabilities and extensive partner network. The company's diverse product portfolio covers areas such as cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, positively impacting millions of patients. At Azurity Pharmaceuticals, we pride ourselves on fostering an inclusive workplace and being an Equal Opportunity Employer. Our success is at...

Conduct and document quality control tests on raw, in-process, and finished products while ensuring compliance with BIS, ISO, and internal standards. Operate and calibrate lab instruments, analyze test data, maintain QC records, and provide feedback

About IDP IDP is the global leader in international education services, delivering global success to students, test takers and our partners, through trusted human relationships, digital technology and customer research An Australian-listed company, we operate in more than 50 countries around the world, Our team is comprised of over 7,000 people of various nationalities, ages and cultural backgrounds Proudly customer-first, our expert people are powered by global technology Together, we offer unmatched services, helping local dreams become realities, all over the world, Learn more at careers idp Role purpose Key accountabilities

- New Product Development (NPD) in Topicals - Documentation (Product Dossiers, Manufacturing SoPs, Regulatory etc) - Pilot Scale Productions - Customer Side Communications - Project Management

Role & responsibilities: The candidate should be an expert in the area of drug product development. He/she should have high level of experience to be called a subject matter expert in concepts of product stability, role of excipients in protein stability, knowledge of higher order structure and its role on product stability The candidate should be well-versed on drug product formulation development. He/she should have knowledge on the concepts of developing a brand new formulation, evaluation of buffer systems, sugar excipients, role of surfactants such as polyols etc. Having experience of developing new formulations for Biosimilar products is a plus The candidate should have experience in r...

Assist in pre-formulation studies and compatibility testing of APIs and excipients. Support formulation trials for dosage forms liquids Operate and maintain F&D lab equipment such as granulators, blenders Assist in scale-up, process optimization.

As a Process Analyst – HR Contact Center, you are responsible for receiving calls, emails, or chats and resolving HR-related queries from employees.You should be flexible to work in shifts. Your primary responsibilities include:? Educate and document enquirers on processes whenever necessary. Provide quality customer service in every interaction. Identify, investigate, analyse, and resolve issues identified within the process. Monitor and process tickets in the ticketing system. Provide floor support for escalation and query resolution. Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise Graduate with 1-2 years of experience ...

"Macleods Pharmaceuticals Limited" Company Overview: A vertically integrated, Global Pharmaceutical Company. Established in 1989, we are engaged in developing, manufacturing, and marketing a wide range of formulations across several major therapeutic areas including anti-infectives, cardiovascular, anti-diabetic, dermatology, and hormone treatment. We develop, manufacture, and globally distribute a broad range of pharmaceutical products across therapies in multiple dosage forms such as solid orals, liquid orals, topical formulations, injectables (Dry Powder) metered dose inhalers and dry powder inhalers. Our Vision: To be a leading global pharmaceutical company by providing high quality, aff...