606 Formulation Development Jobs - Page 3

As Service Associate -Payroll,you will be supporting the end-to-end payroll related activities while ensuring you are in adherence to the policies and processes. Your primary responsibilities include: Process any payroll data in accordance with legal, IBM and the customer requirements related to personal data protection Ensure the timeliness of payroll processing (sending inputs to payroll services providers, approving payrolls) Ensure the timeliness of payroll payments processing (requesting uploads and payments releases, uploading payroll payments into the bank system, monitoring the rejected payments) Carry out the validation of payroll inputs and the reconciliation of output files and properly handle any discovered errors/discrepancies Monitor execution of compliance activities if required Perform any activities related to electronic payslips handling Communicate any risks to payroll process or deadlines in accordance with escalation paths Interact with employees, client, payroll stakeholders or third party providers to process payroll data and ensure the correct and timely pay Report the status of payroll cycle in a timely and accurate manner Support year end processes or any other country specific processes not related to monthly payroll cycle Initiate and actively supporting any continuous improvement activities or other process and/or tools improvements using the existing change management channels Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise 2-3 years’ experience in payroll operations for any International IT / ITES Company Good communication skills in English both oral & written Strong knowledge of MS Excel and MS Word Ability to pre-empt potential issues and reprioritize work to meet ever changing needs of customers both internal and external; proactively follows up with key customers on resolution and action plans Ability to think through complex issues and situations and develop robust, well thought out solutions which meet the need of the business Effectively Works with Others - Works well with internal customers and external suppliers and can positively influence others in problem solving and work process improvements Excellent Customer Service skills – ability to communicate to all people at all levels within the organization. Must have the ability to resolve difficult customer service issues High degree of numeracy skills with meticulous attention to details Team work – the ability to work well within the team is key to this role Preferred technical and professional experience Ambitious individual who can work under their own direction towards agreed targets/goals. Ability to work under tight timelines and have been part of change management initiatives. Proven interpersonal skills while contributing to team effort by accomplishing related results as needed Enhance technical skills by attending educational workshops, reviewing publications etc.

Develop and establish product formulations based on industry trends. Develop and optimize formulations for new and existing nutraceutical products. Conduct thorough research on ingredients and their interactions. Required Candidate profile Qualification: Bachelor's degree (Food Science & Food Technology) Exp: Min 3 year in any Nutraceuticals Industry/Manufacturing or production Required only Male Candidates

At Nouryon, our global team of Changemakers takes positive action every day, to reach higher goals collectively and individually. We create innovative and sustainable solutions for our customers to answer societys needs – today and in the future. Purpose/Key Objectives of the Job Identifying and creating new business development opportunities through product development /application with hydrocolloids. Foster and build business relationships with potential & existing customers, distributors, and all appropriate business channels. Enhancing customer experience. Coordinate internal interface between Customers, sales support and the Sales and Marketing Team. Developing and maintaining relationships with related key stake holders in the industry for the promotion of Nouryon innovative and sustainable solutions. Ensures that all technical & product development activities in strict compliance with Nouryon’s Business and Anti-Competition Principles. Competitive Market Intelligence, market mapping and watch Market development. About the job (Job Responsibilities) Responsible for conducting trials with Nouryon products for Ice cream and frozen desserts customers. Handling customer NPD projects end to end from product development to plant trials and commercial launch. Understanding of various hydrocolloids blend formulation & stabilizer for fruit juices, dairy & nondairy products, plant-based products, bakery & culinary applications. Experience of setting up an application lab for food & beverage industry. Work in accordance with Nouryon global and regional business strategies. Development of new functional solution blend for gaining market share in food & beverage industry. Liaise with Sales Support / Customer Support / Technical Service and address needs of Customers through visits & trials. We believe you bring (Education & Experience) Graduate or post graduate degree in food technology and dairy technology. Minimum of 7 years of Technical and Business Development experience in the food ingredient & additive industry. Knowledge, Skills & Abilities Result driven Ability to influence stakeholders (Internal and External) Ability to work as part of a team and good interpersonal skills. Be willing to develop and support company policies, procedures, and initiatives. Please apply via our online recruitment system. We will not accept applications via e-mail. Once it's with us we will review to see if we have a match between your skills and the role! For more information about our hiring process, visit: nouryon.com/careers/how-we-hire/ We look forward to receiving your application! We kindly ask our internal candidates to apply with your Nouryon email via Success Factors. We’re looking for tomorrow’s Changemakers, today. If you’re looking for your next career move, apply today and join Nouryon’s worldwide team of Changemakers in providing essential solutions that our customers use to manufacture everyday products such as personal care, cleaning, paints and coatings, agriculture and food, pharmaceuticals, and building products. Our employees are driven by the wish to make an impact and actively drive positive change. If that describes you, we will gladly make way for your ambitions. From day one we support you with your personal growth, through challenging positions and comprehensive learning and development opportunities, in a dynamic, international, diverse, and proactive working environment. Visit our website and follow us on LinkedIn . #WeAreNouryon #Changemakers .

Adobe Systems India Pvt. Ltd. is looking for Computer Scientist 1 (C++) to join our dynamic team and embark on a rewarding career journey Conduct research and development in computer science. Develop and implement computer algorithms and systems. Collaborate with computer science and engineering teams. Monitor and report on computer science performance. Ensure compliance with computer science standards and protocols. Provide support and guidance on computer science matters.

Responsibilities 1. Preparation of PFD, URS, FDS, Cycle Time Analysis etc. 2. Calculation for Utilities, Peak Loads, Pipe / Pump sizing, Equipment capacity, and other accessories capacity/load/size 3. Preparation of P&ID, TS, DS, BOQ, Tender, Validation documents (VMP, FAT, IQ, OQ, PQ etc). 4. Desired exposure/ hands-on experience include: • Engineering & Consultancy Biotech & Pharmaceuticals • Process Engineers Sterile API / Formulations / Biotech Facilities • QA (Validation Experts) – Sterile API / Formulations / Biotech Facilities

Hiring for Research associate for Alternate Vendor development in formulation & development. Desired candidate : - Should be B.Pharm / M.Pharm in pharmacy , having 3-5 years experience in development of alternate vendor for various market like US ,EU, ROW , Domestic , WHO etc. - Candidate should aware aabout various guidelines - Experience of technology transfer and exposure to shopfloor will be appreciated

About the Company RENE Cosmetics is an Indian makeup brand committed to redefining beauty through its range of high-quality, cruelty-free, and FDA-approved innovative products. At RENE, we believe in empowering women to embrace their bold, ambitious personas and express themselves through the art of cosmetics. Drawing inspiration from timeless beauty, we aim to meet the evolving needs of the modern woman. Key Responsibility As a Product Development Manager at RENE Cosmetics, your primary responsibilities will include: - Leading and managing the end-to-end product development process, from ideation to commercialization - Creating project timelines and ensuring timely delivery of new product launches - Conducting research on emerging beauty trends, consumer preferences, and competitor activities in color cosmetics - Collaborating with the Marketing team to identify gaps and opportunities in the product portfolio - Partnering with R&D to conceptualize and test formulations that align with brand guidelines and quality standards - Working with the packaging team to develop aesthetically pleasing and functional packaging solutions - Negotiating costs and maintaining vendor relationships to ensure quality and timely delivery - Ensuring product compliance with local and global regulatory standards, including labeling and safety requirements - Overseeing stability testing, safety testing, and consumer trials to ensure product efficacy and satisfaction - Conducting continuous quality checks during and post-production phases - Collaborating with Marketing, Sales, and Supply Chain teams to create product launch strategies and ensure a seamless transition to mass production - Monitoring budgets for product development, including formulations, testing, and packaging - Providing regular updates on costs and optimizing resources effectively Qualifications & Experience The ideal candidate should possess the following qualifications and experience: - MBA/Masters/Bachelor's degree in Cosmetics Science, Chemistry, or a related field - 3-6 years of hands-on experience in New Product Development within the cosmetics, beauty, or Skin/Personal Care industry - Strong knowledge of formulation development and packaging processes for color cosmetics How to Apply If you are passionate about driving innovation in the cosmetics industry and possess the required qualifications and experience, please share your updated resume with us at careers@reneecosmetics.in.,

As a skilled Formulation & Development Scientist for the Nutraceutical Division, your primary responsibility will be to lead the development of innovative dietary supplements, functional foods, and health products. This role involves conducting research, formulating new products, and optimizing existing formulations while ensuring adherence to regulatory guidelines. Your key responsibilities will include designing and developing new formulations for a variety of dietary supplements such as tablets, capsules, powders, gummies, and liquids. You will also be tasked with optimizing existing formulations to enhance stability, bioavailability, and efficacy. Evaluating new ingredients, excipients, and delivery systems for nutraceutical products will be an essential part of your role. You will conduct various tests and analyses, including stability studies, compatibility tests, and dissolution studies. Collaboration with analytical teams will be necessary to maintain quality and consistency in the formulations. Ensuring compliance with regulatory bodies such as FSSAI, FDA, EFSA, and other international regulations will be a critical aspect of the role. Additionally, you will be responsible for preparing technical documents like COAs, MSDS, and formulation dossiers. To stay abreast of the latest trends in nutraceutical science, herbal extracts, probiotics, and functional foods, you will need to engage in continuous research and innovation. Developing and implementing novel delivery technologies to enhance bioavailability will be key to your success. Collaboration with cross-functional teams including procurement, manufacturing, quality, and marketing will be essential for scale-up and commercialization of products. As a Formulation & Development Scientist, you will troubleshoot formulation challenges related to solubility, stability, and taste masking. Process optimization to improve manufacturing efficiency and product performance will be part of your responsibilities. Your expertise in nutraceutical formulation techniques, knowledge of herbal extracts, vitamins, minerals, amino acids, and probiotics, and familiarity with Good Manufacturing Practices (GMP) and Quality Control (QC) protocols will be invaluable. Strong analytical skills, experience with testing techniques such as HPLC, FTIR, and a problem-solving mindset with attention to detail are essential for this role. Good documentation and regulatory knowledge will also be required. Preferred experience includes working with tablets, capsules, soft gels, gummies, and effervescent formulations, ideally in an R&D, F&D, or Nutraceutical/Pharma company. This is a full-time, permanent position with benefits such as Provident Fund. The work schedule is during the day, and the location is in person.,

As a Formulation & Development Executive in the Formulation & Development department, you will be responsible for leading formulation development projects and identifying robust cosmetic and topical medicinal formulations for dermatology through lab experiments. Your role will involve serving as the technical project lead, authoring technical documents, and ensuring regulatory compliance. Additionally, you will be responsible for knowledge transfer for commercial manufacturing, collaborating with cross-functional teams, troubleshooting challenges, and staying updated on industry trends to drive continuous improvements in the product development process. Your key responsibilities will include designing and executing laboratory experiments for formulation and process development, conducting sample stability studies to ensure product performance and shelf life compliance, analyzing scientific data to advise on robust formulations, and selecting suitable cosmetic ingredients. You will also be tasked with drafting technical documentation such as formulation development reports, process development reports, and technical transfer documents. Furthermore, you will support commercial manufacturing through the technology transfer of developed formulations and production processes, and participate in information management including the management of procedures and status reports (PDRs, COA, MSDS, and Stability Reports). To qualify for this role, you should possess a Bachelors/Masters in Pharma and have 1-2 years of relevant experience. This position is based in Chandigarh.,

You will be responsible for the formulation development of Pharmaceutical and Nutraceutical products including tablets, capsules, effervescent tablets, sachets powders, and liquid formulations. This involves conducting literature search and patent search for the formulation, as well as developing cost-effective and fast production processes along with stable formulations. You will be required to create MFR and relevant specifications, facilitate tech transfer, and maintain documentation. Additionally, you will need to address any ongoing issues in the existing formulations. The ideal candidate should have 7 to 10 years of experience in this field. If you are interested in this opportunity, please reach out to hrd@stravahealthcare.com for further details.,

The Senior R&D Officer will provide technical support for product development within the Harpic and Lysol Innovation Team. Responsibilities include utilizing formulation development skills to create new products that address consumer needs, following SOP/ISO protocols for data generation, maintaining lab equipment, recording data accurately, and conducting lab tests and analysis. They will also be responsible for inventory management, collaborating with key stakeholders, ensuring health and safety standards, and maintaining a clean work environment. Professional qualifications include a minimum Bachelor's degree in chemical engineering or a Master's degree in Chemistry or Pharmaceutical Sciences. The ideal candidate should possess strong interpersonal skills, formulation expertise, oral and written communication skills, problem-solving abilities, and the capacity to work effectively in a team. They should be result-oriented, proactive, flexible, and eager to learn and grow. Proficiency in MS Office applications is required. Interested candidates are encouraged to share their updated CV at ruchika.kaushik@reckitt.com.,

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 - Worked in R&D Department /Formulation Department Planning and execution of Alternate Vendor batches for product development

Assist in formulation development of Solid Oral Dosage form. Perform literature & patent search, pre-formulation studies, documentation, data compilation & ensure SOP/GMP compliance for global market products. Required Candidate profile Execution of process evaluation, optimization,scale-up and exhibit batches/Meeting product development timelines/literature survey/ICH guidelines/Solid Oral- Share CV- stuti.naik@enaltec.com

Responsible for managing formulation development of Solid Oral dosage forms for global markets. Oversees pre-formulation, patent search, documentation, compliance, and team guidance as per regulatory standards. Required Candidate profile Pharma professional with 7–10 years in formulation development, strong regulatory knowledge, documentation, data analysis & proven team leadership skills. Share CV- stuti.naik@enaltec.com

Responsibilities: * Conduct literature reviews on drug discovery * Help draft study/experiment outlines, SOPs, COAs summaries * Collaborate on formulation development * Support clinical liaison activities

Support new product development for both Born Good and ETCC, from ideation to formulation. Prepare technical literature such as MSDS &TDS. Assist the procurement team in communicating with the supply chain for sourcing raw materials for new products. Required Candidate profile Assist the procurement team in communicating with the supply chain for sourcing raw materials for new products. Conduct market sampling and replicate competitive products.

You will be responsible for formulation and process development of oral immediate-release dosage forms, Liquid Oral Dosage forms, Injectable Dosage forms including oral film and other formulations for regulatory markets such as Europe, Canada, ANIVSA, ANZ, US and others. Your role will involve troubleshooting and problem-solving unresolved or new formula issues. Additionally, you will design and execute formulation trials and evaluate stability data to finalize formulation composition. It will be your responsibility to develop manufacturing processes for R&D formulations to ensure successful technical transfer for large scale batches. You will also be accountable for all formulation/process related CMC documents which will be part of regulatory filings such as PDR. The ideal candidate for this position should have an M. Pharm degree with over 8 years of experience in Research & Development. A strong understanding of solid oral dosage forms, including formulation development, processing, testing, and evaluation is required. Experience in scaling up processes from lab to commercial production scale is essential for this role.,

Formulation Development Assistant Santej (Nearby Ahmedabad) Position Formulation Development Assistant Vacancies 1 Location Santej (Nearby Ahmedabad) Education Bachelors or masters degree in chemistry, pharmacy, or a related field. Experience 0- 2 years Skills Job description Designation : Assistant Job Type : Full- time Location : Santej (Nearby Ahmedabad) Salary Range : 2. 40 LPA 3. 00 LPA Key Responsibilities: Collaborate with FD executives to execute trials of new cosmetic product formulations, ensuring accuracy and adherence to project timelines. Conduct thorough research on novel cosmetic ingredients, providing detailed technical insights to inform product development strategies. Perform comprehensive analytical tests on both intermediate formulated samples and final product batches to guarantee high- quality standards. Evaluate raw materials using a range of analytical tests during the inward inspection phase, contributing to the selection of premium- quality ingredients. Maintain and update established Standard Operating Procedures (SOPs) as directed by the organization and FD department. Organize and maintain records and reference documents related to Formulation and Development activities. Communicate effectively with cross- functional teams to exchange critical information and ensure seamless project coordination. Basic Skill Sets Required: Bachelors or masters degree in chemistry, pharmacy, or a related field. Thorough understanding of cosmetics product manufacturing and packaging processes. Deep knowledge of various cosmetic formulations and their corresponding manufacturing procedures. Proficiency in conducting detailed analyses of cosmetic products for quality assessment. Capability to perform comprehensive analysis of cosmetic ingredients, ensuring adherence to specifications. Strong proficiency in English, Hindi, and Gujarati languages. Basic to intermediate proficiency in computer applications: Microsoft Excel, Word, and PowerPoint. Excellent communication skills, both verbal and written, to effectively collaborate within cross- functional teams. Apply now Resume Submit

A good understanding of business objectives and market trends to guide R&D efforts effectively.Strong skills in planning, executing, and overseeing projects from start to finish.Excellent ability to lead, manage, and inspire a team.

Coordinate technology transfer activities for (OSD) formulations from R&D to manufacturing sites, Support scale-up, exhibit, and validation batches, participate in investigations, deviation handling, and change control activities.

Lead end-to-end tech transfer of OSD products from R&D to commercial manufacturing sites, conduct scale-up and process validation activities, and provide technical support during regulatory audits and inspections.

Role & responsibilities Job description Perform protocol for drug excipient compatibility studies and submit the protocol for review and approval Complete lab. experiment hands-on independently (Lab scale to exhibit batch and query handling). Dosage forms experience: Injectables predominantly more than 90% in career. Perform formulation development activities on differentiated formulations and innovative technologies as part of product development. Carry out /Support Scientific literature search (CVM/USFDA/Daily-med/publications). Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments. Compilation, interpretation and review of analytical results and stability data Maintain records of formulations, batch processes, and stability studies. Proficient in drafting, reviewing, and managing technology transfer document (MFR, MPR, stability protocols, justification of specifications etc. as part of TT). Exposure in oral liquids and oral solid dosage forms will have an added advantage Preparation of quality-based product development reports (PDR). Evaluation of alternate vendor Experience in preparing technical and regulatory submissions. Coordinate outsourced activities at the partner site by a regular communication plan. Provide timely technical inputs and timely escalation to ensure successful task completions. Communicate effectively with R&D, production, QA/QC, supply chain teams clients, vendors, and stakeholders regarding project progress and requirements. Qualifications M. Pharm or Ph.D. in Pharmacy with minimum industrial experience of 2 to 5 years in pharmaceutical development and scale-up of products. Support in Technical troubleshooting/ root cause identification/ Investigation/Corrective Action and Preventive Action pertaining to product development or manufacturing activities.

You should be an experienced and motivated formulation development professional with 10-15 years of experience in Oral Solid Dosage forms. As an Asst Manager/Manager, you will be responsible for leading the development of new formulations, improving existing ones, and ensuring compliance with regulatory standards. Your expertise in formulation development will be crucial in driving the success of our projects and meeting our business objectives. Strong leadership skills, attention to detail, and a proactive approach to problem-solving are essential for this role. If you are looking for a challenging opportunity to showcase your skills and contribute to the growth of our organization, we encourage you to apply for this position.,

JOB DESCRIPTION: 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. . Ensure scale up of the developed formulation works at engineering batch level. Key Deliverables: . Literature/Patent search to create drug profile . Prototype development with rationale use of excipients . Preformulation study as may be required for formulation development . Conduct 6 months accelerated stability studies to ensure stable formulation . Proof of concept studies to demonstrate BE or comparative PK as the case may be . Scale up studies at 1/10th scale or engineering batch . Technology transfer and manufacturing of Bio/Clinical batch Job Title: Jr Research Scientist Formulation Job Function: Innovation & Development Location: Mumbai (Andheri MIDC) Reporting to:Sr Group Leader Formulation Critical Success Factors: Functional/ Technical: Functional / Technical: 1. Formulation and Product Development a. Schedule and follow all the steps to deliver the drug as per QTPP b. Select the suitable polymers / excipients based on either properties or scientific rationale c. Evaluation of CQA of drug / excipients and estimate its implications for product development d. Designs the process which is reproducible and scalable with higher yield, cost effective, and environment friendly 2. Design of Experiments a. Executes the experiments as per DOE to optimize product and process 3. Pharmaceutical Development Report (PDR) a. Prepares PDR as per Common Technical Document (CTD) module 3 requirements b. Complies with regulatory requirements as defined in QTPP 4. Project Management a. Is able to plan and prioritize multiple project deadlines to meet product delivery goals Education & experience: . M. Pharm/Ph. D. . 5 to 7 yrs The base pay for this position is N/A In specific locations, the pay range may vary from the range posted. JOB FAMILY: Product Development DIVISION: EPD Established Pharma LOCATION: India Mumbai : BKC Building ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

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. Ensure scale up of the developed formulation works at engineering batch level. Key Deliverables: Literature/Patent search to create drug profile Prototype development with rationale use of excipients Preformulation study as may be required for formulation development Conduct 6 months accelerated stability studies to ensure stable formulation Proof of concept studies to demonstrate BE or comparative PK as the case may be Scale up studies at 1/10th scale or engineering batch Technology transfer and manufacturing of Bio/Clinical batch Job Title: Jr Research Scientist Formulation Job Function: Innovation & Development Location: Mumbai (Andheri MIDC) Reporting to:Sr Group Leader Formulation Critical Success Factors: Functional/ Technical: Functional / Technical: 1. Formulation and Product Development a. Schedule and follow all the steps to deliver the drug as per QTPP b. Select the suitable polymers / excipients based on either properties or scientific rationale c. Evaluation of CQA of drug / excipients and estimate its implications for product development d. Designs the process which is reproducible and scalable with higher yield, cost effective, and environment friendly 2. Design of Experiments a. Executes the experiments as per DOE to optimize product and process 3. Pharmaceutical Development Report (PDR) a. Prepares PDR as per Common Technical Document (CTD) module 3 requirements b. Complies with regulatory requirements as defined in QTPP 4. Project Management a. Is able to plan and prioritize multiple project deadlines to meet product delivery goals Education & experience: M. Pharm/Ph. D. 5 to 7 yrs JOB FAMILY: Product Development LOCATION: India > Mumbai : BKC Building t SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)