606 Formulation Development Jobs - Page 5

Research mycelium-based biomaterials using R&D principles | Develop formulations with microbiologists & scientists | Conduct quality control analysis | Enhance existing biomaterial products.

HI, We have an urgent opening for Research Development role for one of leading Chemical company for Bharuch location. Job Responsibilities: Do lab experiments for R&D projects with guidance from seniors. Help in developing, improving, and testing new formulations and products. Use and take care of lab equipment and testing instruments. Record test results correctly, prepare simple reports, and keep proper lab notes. Follow all lab safety rules and practices. Support in pilot plant trials and scale-up work when needed. Help manage chemicals, consumables, and lab inventory. Work with other teams (Quality, Production, Marketing) for product testing and validation. Quantifiable Dimensions of Responsibilities: Experience in laboratory experiments and analytical equipment operation. Timely and accurate preparation of experimental data and reports. Complexities of the position: Requires ability to handle multiple experiments simultaneously with attention to detail. Working knowledge of handling hazardous chemicals and laboratory safety is critical. Balancing routine testing with research-driven development work.

Responsibilities Global Pay Plus Testers. MT MX messaging , SWIFT payments Preferred Skills: Banking->GPP Financial Services Domain->Payments->GPP Generic Skills: Banking Roles and Responsibility Manage and process payments transactions efficiently. Collaborate with cross-functional teams to resolve payment-related issues. Develop and implement new payment systems and processes. Analyze payment trends and provide insights for improvement. Ensure compliance with regulatory requirements and industry standards. Provide excellent customer service and support to clients. Job Requirements Strong knowledge of payment processing and reconciliation. Experience with payment gateways and payment systems. Excellent analytical and problem-solving skills. Ability to work in a fast-paced environment and meet deadlines. Strong communication and interpersonal skills. Familiarity with industry-standard protocols and technologies. Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering

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 targets set by Senior Manager-Pharma and Head, Pharma Business line; are met to achieve performance bonus Analyzing the potential of pharma market and building the customer base. Identify prospective customers, generate leads and support new business development with reporting manager. Market mapping and promotion of new segments and maintaining strong relantionship with various functions at customers (RD, QA, Technology Transfer, Procurement etc). Sending monthly and other specified reports business development to the Senior Manager Pharma and to principals/suppliers. Coordinating and organizing supplier visits at customer R D. Provide technical solutions to customers. To support customers in Shop floor trials. Well aligned with internal business processes like as Salesforce and efficient proactive measures to fulfill digital updation and its requirements. New responsibilities may be assigned from time to time by Senior Manager - Pharma based on industry clusters or product groups and 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 as Tablets, Capsules, Liquid oral and Topical formulations Experience of 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

As a Formulation and Process Development Scientist, you will be responsible for the formulation and process development of Solid Orals, Liquid Orals, and Semi Solids dosage forms. Your main tasks will include designing protocols and development plans for new products, conducting formulation trials, and evaluating stability data to finalize formulation compositions. You will also be involved in tentative costing Bill of Materials (BOM) and trial BOM preparation for trial execution. Additionally, you will prepare supporting documents for stability studies, resolve product stability issues, and develop manufacturing processes for R&D formulations to ensure successful technical transfer for large-scale batches. Your role will also involve writing master formulas, manufacturing procedures, stability protocols, and validation reports, as well as supporting technology transfer for manufacturing processes from laboratory scale to production scale. Furthermore, you will be responsible for developing FSSAI / AYUSH, EU, and US FDA compliant Supplement Facts and Nutrition Facts labels from product formulas. You will also create and review production Master Formula records and Manufacturing batch Records. The ideal candidate for this position should have 5-6 years of relevant experience in formulation and process development. If you are a detail-oriented professional with a strong background in pharmaceutical development and regulatory compliance, we encourage you to apply for this exciting opportunity.,

Develop and optimize rubber compound formulations as per product requirements and customer specifications. Conduct lab trials and validations to evaluate compound properties and performance. Analyze and adjust raw material proportions to achieve targeted physical and chemical properties. Collaborate with production and quality teams to ensure successful scale-up of developed formulations. Maintain documentation of formulations, trial reports, and process parameters systematically. Evaluate alternative raw materials for cost optimization while maintaining quality standards. Assist in troubleshooting formulation-related issues in production and provide technical support. Skill Requirement: Strong knowledge of rubber polymers, chemicals, and compounding processes. Understanding of physical and rheological testing of rubber compounds. Ability to analyze compound failures and take corrective actions. Knowledge of rubber processing equipment and lab testing instruments. Good analytical, documentation, and problem-solving skills. Experience 0 5 years in rubber compounding and formulation development. Qualifications Diploma/Degree in Polymer/Rubber/Mechanical Engineering.

Works closely with the Lead Scientist to develop and refine pouch formulations, Focuses on ingredient optimization, flavor blending, and pilot-scale testing Supports transition from lab to production. Required Candidate profile M. Pharma with 8+ years of experience in oral formulations and operations in pharmaceuticals.

Oversee all R&D initiatives for nicotine pouches and related oral dosage innovations Leads formulation strategy, raw material research, stability studies, and new product concepts acts as the technical head for regulatory submissions and IP. Required Candidate profile Experience in pharma and oral drug delivery products.

We are looking for a highly enthusiastic & passionate candidate for the post of R&D Associate to develop next-generation dental materials, including cements, 3D printing resins, sealers, and composites. You will be part of a high-energy team driving innovation from concept to commercial launch. 3-5 years of hands-on R&D experience for mid-level roles in polymer or biomaterial development, including formulation, characterization, and scaling from lab to production Relevant sector : Dental Materials & Products, Medical Device & Biomaterials, Polymer & Chemical manufacturing, Additive Manufacturing/ 3D printing, Advanced Materials Science & nanotechnology Role & responsibilities : Formulate and optimize dental materials (UV-curable resins, composites, sealers, cements) Modify fillers/monomers for improved adhesion, toughness, and antimicrobial properties Develop photopolymerization processes for dental 3D printing applications Test and validate material performance, ensuring biocompatibility compliance (ISO 13485 / CE MDR / FDA) Lead R&D projects, align research with business goals, and meet project milestones Preferred candidate profile : BSc/MSc in Chemical Engineering, Materials Science, Polymer Science, or Chemistry Experience in polymer chemistry, dental materials formulation, and photopolymerization Strong problem-solving, analytical, and time-management skills Familiarity with dental-specific applications a plus

Educational Requirements Bachelor of Engineering Service Line Enterprise Package Application Services Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Preferred Skills: Technology->BPMI - IBM->IBM Integration Bus (IIB)

Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Additional Responsibilities: Ability to work with clients to identify business challenges and contribute to client deliverables by refining, analyzing, and structuring relevant data Awareness of latest technologies and trends Logical thinking and problem solving skills along with an ability to collaborate Ability to assess the current processes, identify improvement areas and suggest the technology solutions One or two industry domain knowledge Technical and Professional Requirements: Primary skills:Technology->XML->SOAP UI Preferred Skills: Technology->XML->SOAP UI Educational Requirements Bachelor of Engineering Service Line Enterprise Package Application Services

Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Technical and Professional Requirements: Technology->4GL->4G - All,Technology->Networking->Routing technologies Preferred Skills: Technology->4GL->4G - All Technology->Networking->Routing technologies Educational Requirements Master Of Comp. Applications,Master Of Science,Master Of Technology,Bachelor Of Computer Science,Bachelor of Engineering,Bachelor Of Technology Service Line Engineering Services

Role & responsibilities Basic to intermediate understanding of Lead Acid Battery chemistry and materials. Familiarity with lab-scale battery testing techniques charge/discharge cycles, impedance analysis). Ability to interpret test data, charts, and performance trends. Proficiency in data analysis tools (e.g., Excel, Origin, MATLAB) and technical reporting. Preferred candidate profile Key Deliverables Conduct lab experiments and pilot-scale trials to evaluate new materials, additives, or processes. Support prototype development, electrochemical testing, and validation activities. Record and analyse experimental data, prepare technical reports, and present findings to senior R&D management. Analyse critical data related to product field performance and failures including failure modes and analytics related to same Assist in benchmarking studies of competitor products and new technologies. Ensure timely execution of test plans aligned with NPD and R&D programs. Collaborate with cross-functional teams including Quality, Manufacturing, and Procurement during trials and scale-up. Interfacing with customer on NPD and quality complaint related issues. Prior experience of APQP preparation and submission of Production part approval process

Greetings from Vistas HR! We are currently looking to hire a Scientist specializing in Food Technology or Food Nutrition for a Food Nutrition company based in Bhubaneswar, Odisha. As a Scientist in the R&D Food and Functional Ingredients department, you will play a crucial role in developing innovative food and beverage formulations utilizing plant-derived alternative proteins. As the ideal candidate, you should hold a Master's or Ph.D. in Food Science or Food Technology with at least 6 to 10 years of hands-on experience in food/nutraceutical product development. Your primary responsibility will be to design and create food and beverage products such as dairy alternatives, bakery items, beverages, and snacks using plant-based alternative proteins. In this role, you will be instrumental in ensuring the nutritional validation of formulations by analyzing and optimizing nutritional profiles, including amino acid balance, digestibility, and bioavailability. You will also lead prototyping and application trials in collaboration with FMCG partners and work towards validating health/nutritional claims while ensuring compliance with international food safety regulations. Moreover, your duties will involve supporting sensory testing protocols, acting as a technical liaison with R&D teams of partners, preparing technical dossiers, and engaging with external research bodies and academic partners for joint studies and knowledge exchange. Additionally, your role may require familiarity with marine-derived or botanical ingredients, experience in clean-label and health-focused product formulation, and an understanding of sustainable food systems or green ingredient innovation. If you possess a strong background in nutrition science, functional ingredients, and regulatory frameworks, along with effective communication and documentation skills, we encourage you to apply for this exciting opportunity. Candidates with prior experience in seaweed, algae, or dietary fiber-based products, research publications, or clinical validation experience will be given preference. If you meet the desired qualifications and are passionate about advancing the field of food technology and nutrition, we invite you to share your updated CV with us at CV.VISTASHR@GMAIL.COM. Join us in shaping the future of food innovation and making a positive impact on global consumer products. #foodtechnology #Foodnutrition #appliednutrition #clinicalnutrition #foodscience,

Role & responsibilities Job Responsibilities: 1.Market samples receiving, entry and stock maintenance. 2.List updations, equipment and SOPs, Product code list updation 3.RM BOM preparation and checking of new product solid, liquid and semi-solid dosage form. 4.Preparation of MFR/MPR/PDR of solid, liquid and semi-solid, injectable dosage form. 5.Sample upkeep Withdrawal and Storage of Sample. 6.RA related mail communication, document follow ups, preparation and send as per urgency and priority of documents. 7.List updations (RM/PM/Stability samples)/ Innovator samples/ Equipments. 8.BOP preparation and corresponding mail correspondence. Responsible for QMS activity ,MFR preparation and corresponding change control documentation. 9.Document preparation as per regulatory requirement and commercial MFR preparation and revision with change control. 10.BMR/BPR filling as per dossier requirement/ Dossier related documentation 11.Filing of documents and list updation. 12.Commercial Work Order Request form entry & Clearance. 13.Audit related documentation 14.New item code creation 15.Change control initiation for new product development & tech transfer Preferred candidate profile Reputed Pharma background

Experience in Solid Oral Dosage & Liquid Orals form in Formulation & Development Dept. for Regulated Market. Required Candidate profile Candidates should have 4-8 Years of relevant experience.

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

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

KEY RESPONSIBILITIES: Develop new processes, or refine existing ones, to optimize the scale up of lab batches in factory. plan, carry out and supervise process trials in laboratories & pilot trials. Develop tech transfer documents along with formulation team. Plan the scale up batches aligning with stakeholders. scale up the production process via trials, making changes to raw materials or components, and process parameters to ensure quality is maintained during large-scale production. To run the stability studies of pilot batches, assist the lab team in running stability studies. work with product pipelines at various stages of development and provide guidance on scalability. develop formulae specifications by taking pilot trials. advise on equipment modification to enable process changes for new product development. read and write technical reports and specifications, maintaining appropriate records. initiate and generate ideas based on reading and research. Adhere to GMP practices. Adhere to safety & quality standard operating procedures. Identify and Implement Process improvement projects. Follows and supports current Good Manufacturing Practices and current Good mfg/Laboratory Practices Cross-functional collaboration: to work closely with R&D, Quality Assurance, Quality Control and Manufacturing SKILLS: a. scale up of lab batches in factory. b. Read and write technical reports and specifications. c. Experience in cosmetic production facility, worked as manufacturing chemist handled production d. Having good exposure on ISO 9001-2015 & ISO 22716 requirements e. Mastery of office tools such as Excel, Word, Power Point, and Sharepoint f. Problem-solving mindset g. Excellent communication

You will be joining Be Clinical, a company dedicated to creating a science-backed, clinical-grade, anti-aging skincare brand tailored for the modern Indian consumer. Your role as a Scientific Researcher in New Delhi will involve conducting laboratory experiments, writing research papers, collaborating with fellow scientists, and innovating new skincare formulations. Working closely with the product development team, you will ensure that all products meet clinical standards and deliver effective results. To excel in this role, you should possess laboratory experience, skills in experimental design and data analysis, scientific writing proficiency, and a knack for research paper publication. Knowledge in formulation development, skincare product testing, collaboration, and teamwork is crucial. Strong written and verbal communication skills are essential, along with the ability to work independently, meet deadlines, and ideally, experience in the skincare or pharmaceutical industry. A Masters or PhD degree in Biochemistry, Chemistry, Pharmacology, or a related field would be advantageous.,

As an R&D Executive at PTC - SIGMA, you will be responsible for a wide range of activities related to documentation, product development, collaboration & coordination, and team training. Your primary responsibilities will include preparing various Technology Transfer documents such as LIF, PIF, PBOM, BOM for VAQ review, FBOM, and MFC. You will also be initiating AIF and Change control in the portal and handling SAP related activities including BOM loading, New SAP code generation, and Code extension. Additionally, you will be involved in LnB Issuance, PDR review, LnB and Project Files Archival, SOP preparation, review, and training, as well as Form 29, Form-11 application activities. In terms of product development, you will be conducting literature searches, monitoring raw material availability, aligning formulation development activities, preparing project presentations, loading products in stability studies, and analyzing stability data. You will also be responsible for preparing regulatory submission documents and ensuring compliance with SOPs during practical work. Collaboration and coordination with other departments such as ADL, PKG, RA, GDSO, and CQA will be crucial for the successful execution of day-to-day activities. Additionally, you will be expected to deliver presentations on assigned topics and share execution learnings within the team. Overall, as an R&D Executive at PTC - SIGMA, you will play a key role in driving the successful development and documentation of products, ensuring regulatory compliance, and fostering effective collaboration within the organization.,

UMEDICA is a vertically integrated company engaged in the manufacturing and export of a wide range of finished formulations including Injectables, Tablets, Capsules, Suspensions, Dry Syrups, etc. Our manufacturing facility, situated in Vapi (Gujarat), holds approval from global regulatory authorities. Founded in 1983, UMEDICA operates in over 85 countries across the globe, encompassing EU, UK, USA, Canada, Australia, Middle East, Central & South American countries, Africa, Asia & CIS countries. Upholding a culture of innovation & continuous improvement, we at UMEDICA constantly strive for excellence. We are currently looking for a dynamic and experienced Manager/ Sr. Manager specializing in Formulation Development for Oral Liquid products to join our R&D Centre located at Turbe. This role will directly report to the GM Formulation Development. The remuneration package will be competitive and aligned with the candidate's professional experience and prevailing market standards. Key Responsibilities: - Minimum 8 years of experience in formulating and developing oral liquid dosage forms compliant with US & EU regulations. - Actively involved in the development of liquid products, including excipient identification, prototype formulation based on innovator product characterization, and selection of primary packaging components. - Proficient in initiating stability batches and generating necessary GxP documentation. - Thorough understanding of scale-up and EB manufacturing processes. - Independent preparation of formulation development documents such as development reports, MFC, specifications, and tech transfer documents. - Support in addressing regulatory queries for the US & EU markets. - In-depth knowledge of excipients, their functions, and applications. Other responsibilities: - Execution of product development activities in adherence to GMP requirements. - Assistance in scale-up and EB batch operations. - Maintenance of laboratory environment as per GXP requirements, formulation of SOPs, and system development. - Comprehensive understanding of regulatory agency prerequisites. - Independent handling of plant operations. Required Skills & Competencies: - Expertise in Oral Liquid formulation. - Strong grasp of regulatory stipulations from FDA, EMA, ICH guidelines, QbD, and BCS-based biowaivers. - Knowledge of intellectual property considerations in formulation design such as FTF and PIV. - Hands-on experience with formulation equipment and scale-up processes including granulators, compression, encapsulation, and coating. - Proficiency in data interpretation, scientific writing, and regulatory documentation. Qualifications & Experience: - M.Pharm in Pharmaceutics, Pharmaceutical Sciences, or related field. - 8 to 12 years of experience in the formulation development of oral liquid dosage forms. - Demonstrated success in technology transfer, global regulatory filings, and team leadership.,

As a Research Associate at Naari Pharma, you will play a crucial role in the execution of formulation development activities for solid dosage forms across regulated and semi-regulated markets. Your responsibilities will include conducting literature search and pre-formulation studies, evaluating innovator/RLD products, executing R&D trial batches and scale-up activities, and preparing stability batches. You will also be responsible for documentation tasks such as preparing Master Formula Cards, Product Development Reports, and Stability Protocols, as well as supporting regulatory submissions. You will work closely with cross-functional teams to monitor scale-up and exhibit batches, troubleshoot formulation challenges, and ensure adherence to development timelines and project goals. The ideal candidate for this position should hold an M. Pharma degree in Pharmaceutics, have at least 3 years of hands-on experience in solid dosage formulation development, possess knowledge of pre-formulation, DoE, and scale-up activities, and be familiar with stability studies and regulatory documentation. Strong problem-solving skills, attention to detail, and good communication and teamwork abilities are also essential for this role. If you are passionate about advancing women's health through pharmaceutical innovation and are looking for an opportunity to contribute to a global company with a focus on hormonal therapies, we encourage you to apply for the Research Associate position at Naari Pharma.,

As a Principal Analyst, you will be part of our deliverability team working directly with our customers. You will provide guidance on best practices, reporting and recommendations to improve their email programs and get the most out of Zeta Global. Teams at Zeta work collaboratively to deliver great customer experiences. You will partner with our Client Services, Technology and Sales Teams to develop strategies that improve both our customers and our teams. Job Description Provide guidance to clients to improve deliverability for their email programs Support an assigned portfolio of paid deliverability services clients Own the client relationship for your portfolio Manage onboarding projects including discovery, IP and domain provisioning, email authentication, reputation warming plan development and execution Manage retainer based strategic projects focused on optimizing inbox placement and driving response Monitor and manage IP & Domain Reputation and Block Listings Monitor client email metrics/effectiveness and report on performance Collaborate on Mail System Infrastructure and DNS Management Utilize 3rd party Deliverability Monitoring Tools Provide email best practices consultation to clients and Internal stakeholders Your Skills and Experience 5+ years of experience at an ESP Strong attention to detail, dedicated work ethic, organized, and strong communication skills Strong critical thinking and analytical skills Thorough understanding of email technology Experience analyzing large data sets to derive insights Advanced Excel Experience Knowledge about ESPs, Mailbox providers, and email authentication vendors Understanding of email, SMTP, IP and domain strategies, authentication, reputation strategies, data hygiene, privacy, permission policies, anti-spam policies Ability to work with cross-functional teams.

Roles and Responsibilities Develop new polymer products through formulation development, process development, and technology transfer. Conduct consumer trials to test product performance and provide technical support to sales teams. Clarify customer requirements and develop solutions using analytical skills. Provide technical expertise on polymer products to internal stakeholders. Desired Candidate Profile MS/M.Sc(Science) degree from a recognized university. Minimum 7-9 years of experience in R&D, in the polymers industry. Strong understanding of formulation development, process development, and technology transfer processes. Excellent analytical skills with ability to clarify complex issues.