659 Formulation Jobs - Page 3

About this role Role Summary: We re seeking a dynamic System Engineer to design and deliver intelligent, scalable, and reliable data systems. This hybrid role combines data engineering, AI/ML integration, system reliability, and DevOps to accelerate data collection, enable intelligent workflows, and drive business impact. You ll collaborate across engineering, data analytics, and business teams to build reusable frameworks, reduce time-to-value, and uphold engineering excellence. Key Responsibilities: Data & AI Workflow Engineering Accelerate data collection at scale from millions of sources using robust, scalable pipelines. Design, build, and deploy workflows that combine AI/ML models with human-in-the-loop systems. Operate as a full-stack data engineer , taking projects from problem formulation to production. Develop APIs and services to expose data and model outputs for downstream consumption. System Engineering, Reliability & DevOps Build and maintain CI/CD pipelines for data and ML services using Azure DevOps or GitHub Actions. Implement observability (metrics, logs, traces) and reliability features (retries, circuit breakers, graceful degradation). Optimize data workflows and infrastructure for performance, scalability, and fault tolerance . Lead incident response, root cause analysis, and postmortems for data and ML systems. Contribute to infrastructure-as-code (IaC) for provisioning and managing cloud-native environments. Platform & Framework Development Elevate development standards through reusable services, frameworks, templates, and documentation. Champion best practices in code quality, security, and automation across the engineering lifecycle. Collaborate with engineering teams across the business to improve time-to-value and share internal solutions. Collaboration & Business Impact Collaborate with stakeholders, ensure that risks are mitigated timely and drive through metrices. Collaborate with engineering teams across the business to improve time-to-value and share internal solutions. Translate business problems into data science/ML solutions with measurable outcomes. Propose pragmatic, diverse approaches to solving business challenges using data and AI. Present results and recommendations clearly to technical and non-technical audiences using compelling storytelling and visualizations. Required Skills and Qualifications: 10+ years of experience in data engineering , machine learning , or system/platform engineering . Strong programming skills in Python/DotNet or Java ; proficiency in SQL , DBT , and data orchestration tools (e.g., Airflow). Experience with containerization (Docker) and Kubernetes on Azure and/or AWS. Proficiency in CI/CD , Git , and cloud-native development . Familiarity with observability tools (Azure Monitor, Prometheus, Grafana) and data validation frameworks (e.g., Great Expectations). Familiarity with data science libraries (Pandas, NumPy, scikit-learn) and deploying ML models to production. Strong understanding of distributed systems , microservices , and API design . Excellent communication and stakeholder engagement skills. Bachelor s or Master s degree in Computer Science, Data Science, Engineering, or a related field. Our benefits . Our hybrid work model BlackRock s hybrid work model is designed to enable a culture of collaboration and apprenticeship that enriches the experience of our employees, while supporting flexibility for all. Employees are currently required to work at least 4 days in the office per week, with the flexibility to work from home 1 day a week. Some business groups may require more time in the office due to their roles and responsibilities. We remain focused on increasing the impactful moments that arise when we work together in person aligned with our commitment to performance and innovation. As a new joiner, you can count on this hybrid model to accelerate your learning and onboarding experience here at BlackRock. . This mission would not be possible without our smartest investment the one we make in our employees. It s why we re dedicated to creating an environment where our colleagues feel welcomed, valued and supported with networks, benefits and development opportunities to help them thrive. For additional information on BlackRock, please visit @blackrock | Twitter: @blackrock | LinkedIn: www.linkedin.com / company / blackrock BlackRock is proud to be an Equal Opportunity Employer. We evaluate qualified applicants without regard to age, disability, family status, gender identity, race, religion, sex, sexual orientation and other protected attributes at law.

MSN Laboratories Hiring for professionals Roles and Responsibilities To conduct FTO and novelty searches on various databases for Biosimilar / various Formulations and API To search on various country patent databases to retrieve equivalent patent information, legal status etc., in different geographies To prepare patent landscapes, analyze the patent content to summarize their claims and specification. Patent analysis: i) to check novelty ii) FTO analysis iii) due diligence reports for different geographies To retrieve, analyze and interpret the file histories of patents and patent applications for different geographies To prepare patent landscapes for each project To assist in IP in turn development strategy for each project To assist in Patent drafting, filing and prosecution procedures Tracking patents, approvals, filings and litigations etc., To assist in drafting and responding to customer queries To assist in drafting and responding to regulatory queries Dep: IPM( Intellectual Property Management) Designation: Executive to Asst Manager Job Location: Pashamylaram- Hyderabad Experience: 5 to 10 Years Please apply only if your profile is matching the above requirements to dinesh.baratam@msnlabs.com

Job Title: R&D Senior Executive Softgel Formulation Department: Research & Development (R&D) Softgel Formulation Job Summary: A reputed softgel manufacturer in Gujarat is seeking an accomplished R&D professional with 8-10 years of experience in softgel formulation and drug development. The ideal candidate will demonstrate expertise in pharmaceutical or nutraceutical softgel product development, process optimization, technology transfer, and the creation of QA/QC documents from scratch. Willingness to relocate to Gujarat is essential. Key Responsibilities: Softgel Formulation Development: Lead the complete development process for softgel products, including excipient compatibility, fill and shell formulation for pharmaceuticals and nutraceuticals. Process Scale-up & Optimization: Design, execute, and optimize laboratory and pilot scale batches using rotary die or relevant softgel encapsulation technologies. Product Development (NCE & Generics): Drive projects involving both new chemical entities and generic softgel drugs, ensuring robust formulation and regulatory compliance. QA & QC Documentation: Independently develop and implement all necessary Standard Operating Procedures (SOPs), batch manufacturing and packing records, product specifications, method validation documents, and stability protocols. Technology Transfer: Prepare required documentation and ensure smooth transfer of technology and processes to manufacturing, QA, QC, and regulatory teams. Cross-Functional Collaboration: Coordinate with Quality Assurance, Quality Control, Regulatory, Procurement, and Production teams for successful project execution. Regulatory & Compliance: Support global regulatory filings, address queries, and maintain compliance with cGMP, ICH, and international regulatory standards. Continuous Improvement: Keep abreast of industry trends and proactively recommend improvements in formulation and manufacturing processes. Qualifications & Requirements: Educational Qualification: M.Pharm in Pharmaceutics, Pharmaceutical Sciences, or a related discipline. 8-10 years of hands-on experience in softgel formulation and product development within the pharmaceutical or nutraceutical industry. Strong technical expertise in softgel encapsulation, fill/shell composition, and process troubleshooting. Proven ability to create all QA and QC documentation from the ground up. Solid knowledge of cGMP, ICH, FDA, and other global regulatory requirements. Experience in analytical method development and stability studies is an advantage. Excellent teamwork, communication, problem-solving, and documentation skills.

Role & responsibilities Asst. Manager (Regulatory Affairs) 1. The Candidate must be M.Sc or B.Pharma or M.Pharma with 7-12 years of experience out of which minimum 3-4 years in regulatory affairs in EU, US markets, WHO GMP certified pharmaceutical formulation company. He will be responsible for all regulatory functions- domestic as well as exports. He will coordinate with other departments on regular basis. He will provide documentation support required for regulatory submission independently, including preparation and submission of dossiers for product and plant registrations in different countries as per latest guidelines. Exposure to Regulatory Audits & QMS system. Knowledge of Drug & Cosmetic Act, DPCO & All other guidelines related to pharmaceutical industries Responsible for monitoring of critical processes for R&D in compliance of operations, Quality Management and regulatory affairs. Preparation or Review of SOPs, BMRs, MFRs, PVP, PVR, PDR, Chemical compatibility of drug product/Drug substance specifications, MOA and change control to ensure compliance. To ensure new products registration and license renewal compliance to local regulations, as well as GMP, GDP and ISO requirement. Review of formulation development protocols, and technology transfer dossier (TTD) Performing literature reviews and staying up-to-date with the latest advancements in pharmaceutical research to contribute to the development of new products. Ensure compliance with regulatory requirements, including FDA and global regulations, and maintain up-to-date knowledge of industry regulations and guidelines. Oversee R&D tasks, ensuring proper documentation of records and prepared of reports submitted to regulatory authorities. R&D document and their findings to support quality assurance, and regulatory affairs processes. Co- ordination with Quality assurance, Quality control, Production, Warehouse & Engineering department, ensure GMP and EHS related to R&D functions. Establish operational, analytical and documentation standards aligned with industry best practices. Preferred candidate profile

Role & responsibilities Job Title: International Regulatory Affairs (IRA) Sr. Manager Location: Ahmedabad -HO Markets: CIS (Including EAEU), LATAM (Central and South America), Middle East, Africa, South East Asia. Key Responsibilities: 1.Prepare monthly regulatory MIS reports and present status updates, key metrics, and strategic insights to senior management. 2. Manage relationships with external regulatory consultants, in-country partners, submission vendors, and the external regulatory team to ensure timely regulatory filings and ongoing compliance. 3. Collaborate cross-functionally with Formulation, QA, QC, Packaging Development, Production, RA, PV, and BD teams for data collection, gap analysis, and submission readiness. 4. Liaise with regulatory authorities including (EU, CIS, LATAM, ROW, Asia) and others. 5.Develop and implement regulatory strategies across international markets (EU, CIS, LATAM, ROW, Asia, Middle East, and Georgia) to ensure timely submissions and approvals for product registrations and lifecycle maintenance. 6. Lead the preparation, review, and submission of CTD/eCTD/ACTD dossiers for multiple dosage forms including solid orals, injectables, topicals, and liquids for pharmaceutical and nutraceutical products, as per country-specific guidelines. 7.Manage lifecycle regulatory activities such as renewals, variations, line extensions, and prompt responses to health authority queries across global jurisdictions. 8.Maintain up-to-date knowledge of global regulatory and provide strategic recommendations based on updated guidelines and country-specific requirements. 9.Ensure regulatory compliance for labeling, artworks, inserts, and packaging as per regional regulations and internal quality standards. 10 .Support and participate in regulatory audits and inspections by ensuring the availability of complete and updated documentation and responses. 11.Lead and train junior regulatory staff, encourage cross-market knowledge transfer, and ensure consistent alignment with global regulatory processes and corporate objectives. Preferred candidate profile

Prototype formulation design to Lab scale development, process optimization using DOE, Characterization of complex formulations by advanced techniques, and Interpretation of data, handling of regulatory queries, and preparation of justifications.

HIRING FOR OSD - PRODUCTION & QC PRODUCTION(OSD) Experience: (01-07Years) Compression, Granulation, Coating, Capsule filling, Inspection QC Experience: (02-09Years) HPLC, GC, RM,PM, Stability, IP/FP, Method Development, Method Transfer QUALIFICATION : ITI/DIPLOMA/BSC/MSC/B PHARM/M PHARM With relevant Experience ITI/DIPLOMA/BSC/MSC/B PHARM Freshers can Apply DESIGNATIONS: Operator/Sr Operator/Jr Officer/Officer/Jr Executive/Executive INTERVIEW VENUE: SK Consultancy Services, H.No-1-77, 3rd Floor, Bachupally X Road, Opposite Sri Swastik Multi Specialty Hospital, Towards Nizampet Road DATE &TIME: 26th July 2025 ( Saturday); From 09.00 A.M. to 03.00 P.M NEED TO CARRY: Resume 3 Month Pay slips Increment letter Previous company relieving letters Education Documents and ID Proofs Help Us Spread the Word (Refer): Circulate it in your Social Networking sites and groups for better reach and Refer your friends and colleagues, it could be a great opportunity for someone in need! WORK LOCATION: Hetero Labs Limited, UNIT V Polleypally, Jadcherla, Mahabubnagar CONTACT INFO: E-mail: Ashok.ch@hetero.com & Contact:8555912639 for further info.

Roles and Responsibilities Perform calibration, electrical maintenance, formulation, HVAC operations, process engineering, and process maintenance tasks to ensure smooth plant operations. Conduct quality control checks on equipment and processes to identify areas for improvement. Collaborate with cross-functional teams to resolve issues related to OSD (Oral Solid Dose) production. Ensure compliance with safety protocols and regulations in the pharmaceutical industry. Maintain accurate records of work performed and report any defects or anomalies.

Job Description: As a key member of the Bold Care team, you will play a crucial role in supporting and leading the development of packaging initiatives for the Category. Your primary responsibility will be to oversee the New Product Development (NPD) process and packaging for all new launches and existing products. You will work closely with Brand Development and Supply Chain teams to ensure the successful execution of all sourcing and development activities for Bold Care Brands. Your duties will include managing packaging specification, developing optimal solutions for primary, secondary, and tertiary packaging components, and building strong relationships with key stakeholders such as customers, suppliers, and partners. Additionally, you will focus on cost optimization by reducing packaging and product costs through new vendor developments and negotiations. You will be responsible for monitoring project timelines and milestones to ensure on-time delivery, as well as handling tasks such as PO generation, inventory management using tools like Zoho and Unicommerce, and quality control. Your role will also involve conducting research and development on new products, coordinating lab testing, and actively engaging with stakeholders from Marketing, Quality, Consumer Science, and Procurement to maintain a consumer-centric packaging research and development approach in all relevant initiatives and projects. In addition to your packaging expertise, you will contribute your skills in NPD projects, with at least 3-4 years of experience in Formulation, New Products, and an understanding of various packaging types including Flexible, Plastic bottles and containers, and Rigid Packaging. Experience in D2C/Consumer goods will be beneficial, and previous exposure to beauty/personal care, nutraceuticals, and FMCG industries will be advantageous. Monthly reporting and cost optimizations will also be part of your responsibilities, ensuring continuous improvement and efficiency in the packaging development process. If you are a proactive and innovative professional with a passion for packaging and product development, we encourage you to join our dynamic team at Bold Care and contribute to revolutionizing men's wellness through cutting-edge solutions and consumer-centric approaches.,

You will be responsible for developing and implementing strategic R&D plans and initiatives in the Nutra segment. Your role will involve overseeing all stages of product development from concept to commercialization. It is essential to stay updated on the advancements in food science and nutrition to ensure the products meet the required standards. The ideal candidate should have prior experience in any Nutra company with a good understanding of Nutra and its application in food product development. Knowledge of food science, formulation, and product formulation will be crucial for success in this role. This is a full-time position with a day shift schedule. The work location is in person.,

The candidate will be responsible for the proper receipt, storage, and GMP-compliant dispensing of raw materials used in pharmaceutical production Perform raw material dispensing activity in designated dispensing booths under controlled conditions.. Required Candidate profile Receive, inspect & label incoming raw materials as per SOP Coordinate with the QA, Production & QC department during material movement Ensure adherence to GMP, GDP & safety guideline during dispensing

Roles and Responsibilities Manage warehouse operations, including inventory management, storage, and dispatch. Coordinate with production team to ensure timely delivery of raw materials (RM) and packaging materials. Ensure accurate recording of stock levels, orders, and deliveries using ERP systems. Desired Candidate Profile Experience: 2-5 years Qualification: B.A/ B.Sc./ B. Com Must have experience in OSD Formulation Warehouse operations Should be willing to work in shift operations Interested candidates can share their updated CV to jahnavi.kodali@granulesindia.com

Walk In Drive For Engineering Services Department Formulation's Division @ Burgula Interview Date : 26-07-2025 Department : Engineering Services OSD, Formulations Qualification : Diploma | B Tech ( Mechanical | Electrical | Instrumentation ) Work Location : MSN Formulations Unit-VI, Burgula Interview Venue Details :- X59Q+P95, Mothighanapur, Burgula, Telangana 509202

RESPONSIBILITIES Ensure achievement of budgeted targets on a monthly and yearly basis. Ensure site is in state of compliance for multiple authorities inspections and guide / coordinate during inspections and local statutory authorities. Work out areas of improvement in product cost, engineering cost and implement the same. Create and maintain an environment of mutual trust, respect, and customer centricity. Build and maintain a high performing team and culture. Ensure manpower management and engagement. Brand ambassador of Unichem for any internal and external stakeholders at the plant. DESIRED SKILLS Excellent Experience in manufacturing formulations (Tablets & Capsules). Exposure in Managing and working with International Regulatory Authorities like MHRA, EU etc. is a must. Should have strategic, operational excellence, collaboration, and customer-centric mindset. Excellent experience in general management, team management, and networking Should have experience in budgeting and cost optimization. Should have functional knowledge of LEAN Aptitude for automation and use of technology. Should have experience of working in a matrix environment. Should be ready to work in a dynamic environment. Excellent negotiation skills and interpersonal skills Experience in Site Transfer, New Product Launch & Green field Project will be appreciable.

About Company: Come be part of a rocket ship that s creating a massive impact in the world of higher education! On the one hand, over a million college graduates have barely 5% employability rates yearly, while thousands of companies need help finding talent. Newton School of Technology aims to bridge this massive gap through its industry-oriented Computer Science and AI degree program. Newton School of Technology s vision is not just to be an alternative to IITs but to redefine the landscape of higher education. We aspire to be a modern, industry-led institute that focuses on a future-ready curriculum, deep industry engagement through faculty & mentors, advance-tech subjects like AI & robotics, and a strong focus on coding from day Zero. At the same time, we are committed to providing the best exposure to students through international treks, fully funded conferences, and hackathons. This vision presents a unique opportunity to shape the future of higher education and make a significant impact in the field. We have a strong core team consisting of alumni from IITs and IIM who have several years of industry experience in companies like Unacademy, Inmobi, Ola, and Microsoft. On this mission, we are backed by some of the most respected investors around the world - RTP Global, Nexus Venture Partners, and a slew of angel investors, including CRED s Kunal Shah, Flipkart s Kalyan Krishnamoorthy, Unacademy and Razorpay founders, Udaan s Sujeet Kumar among others. Requirements: Min 3-4+years of experience working as a Performance Marketing Associate or similar role Leverage paid channels to drive, website traffic, top funnel, lead velocity and conversions Solid and ongoing understanding of appropriate third party tools, and ability to integrate these tools Proficiency in Ad Content Creation, Fluency in Microsoft Office suite (Outlook, Excel, Word, PowerPoint, etc.) Use data-driven marketing strategy to identify trends/patterns and opportunities for innovation, and make optimization recommendations across the user s journey Measure, track and report on performance marketing efforts through structured dashboards Responsibilities: Assist in the formulation of strategies to build a lasting digital connection with consumers Plan and execute all digital marketing, including SEO/SEM, marketing database, email, social media and display advertising campaigns Launch optimized online adverts to reach the target audience through Google Adwords, Facebook, LinkedIn, etc. to increase company and brand awareness Continuously improve by capturing and analyzing the appropriate social data/metrics, insights, and best practices across digital marketing campaigns, and then acting on the information to meet marketing goals (ROI and KPIs) Be actively involved in SEO efforts to optimize web content to increase traffic (keyword, image optimization, etc.) Collaborate with internal teams to create landing pages and optimize the user experience. Prepare online newsletters and promotional emails and organize their distribution through various channels Conduct market research to identify new opportunities Monitor competitors marketing activities About Company: Come be part of a rocket ship that s creating a massive impact in the world of higher education! On t ...

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Experience: 2 to 6 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 7600033423 Free Job Required Candidate profile Autoclave Operator Granulation Operator Mixing Operator Grinding Operator Cartonator Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling Operator Vial Sealing Operator Lyo Operator

Interview for SVP & Injectible Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Experience: 2 to 6 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 7600033423 Free Job Required Candidate profile Autoclave Operator Granulation Operator Mixing Operator Grinding Operator Cartonator Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling Operator Vial Sealing Operator Lyo Operator

Multiple Positions open for Officer/Manager Role & responsibilities : Managing the production line with end to end responsibility for Quality and Quantity. Also required to complete requisite documentation and MIS as desired by management. Preferred candidate profile: S cience Graduate with 3-11 years of experience in managing Filling Lines/Batch Manufacturing/Packing operations in the pharmaceutical industry. Preference will be given to candidates with Injectable operations experience. Should be able to handle 6-10 supervisors Perks and benefits : Best in Industry salaries, growth opportunities within the organization and a fair minded organization which respects individuals as contributors.

Roles and Responsibilities Should Have Formulation Experience. Having vacancies in RoW (ASIA , MENA, LATAM, AFRICA) Regions Responsible for product registration RoW (ASIA , MENA, LATAM, AFRICA) Regions region Preparation, compilation and review of dossiers for region in eCTD/CTD/country specific format. Co-ordinating with cross functional departments like API, R&D, QC, QA, PDD, Micro for documents required for dossier compilation for initial submission, query responses or other submission like tender activities. Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration. Responding to queries with in the time lines received from client/agency. Preparation of check list as per country specific requirements region. Review of documents like specifications/ MFC/ BMR/ PV/ Stability/ PDR/ DMF/ CoAs/Artworks and other quality related documents for their suitability for registration in MENA region. Co-ordinating for CoPP, GMP, License and other required documents/certificates legalization activity required for dossier compilation and registration. Archiving/Maintenance of the dossiers, renewal files and variation approvals along with supporting documents in regulatory data base. Identifying gaps in approved dossier, compiled and submit the post approval changes (Minor variations) to agent/agency. Filing of variations if any and registration renewals. Compilation and circulation of product approval package up on receipt of product approval/Minor variation approvals to concern departments. Maintaining the product status (Registered and Under registration) in excel sheet. Desired Candidate Profile Should Have Regulatory Affairs Relevant Formulation Experience Perks and Benefits

Role & responsibilities Handling of pre and post approval regulatory activities of US/EU/CA submissions. Review of developmental documents for regulatory submission. Good knowledge of handling CMC documentation for Dossier submission Compilation and Submission of Annual reports and Supplements. Having the experience of solid orals and injectables. Preparation of Sterility Assurance Package for injectable Dossiers. Preparation of Pre-IND/scientific advice meeting packages Drafting, compiling & eCTD publishing of dossiers for regulatory filings. Review of specifications and test procedure as per pharmacopoeia requirements. Providing regulatory support for customer filings and customer queries. Evaluation of regulatory authority deficiencies and preparation of action plan accordingly. Also follow up of response documents with concern stake holders. Evaluation and approval of QMS documents, wherever applicable. To update cross functional teams for different regulatory compliance & requirements. Responsible for outlining requirements for labelling, storage and packaging. Review of product development report and QBD concepts. Updating product approval package to plant team. Preferred candidate profile Should Have Formulation Regulatory Affairs Relevant Experience in US/EU/Canada Perks and benefits

Role & responsibilities Required for Quality Control(Formulations) Quality Control(QC)- Need 1 to 5 years of experience. *Analysis of Finished Product & Stability *GLP and LIMS, Documentation Preferred candidate profile Perks and benefits

Role & responsibilities Product Development: Lead the formulation and development of new construction chemical products. Enhance existing product formulations to improve performance, cost-effectiveness, and sustainability. Research Initiatives: Identify and evaluate new raw materials, technologies, and methods relevant to construction chemicals. Keep abreast of industry advancements and leverage them to drive innovation. Project Management: Plan and execute R&D projects from concept to commercialization. Develop project timelines, allocate resources efficiently, and monitor progress to meet deadlines. Testing and Analysis : Oversee lab testing to ensure product performance meets established standards. Analyse test data to optimize formulations and resolve technical challenges. Collaboration: Work closely with the Quality Control, Production, and Marketing teams to ensure R&D projects align with quality and production requirements and meet customer expectations. Documentation: Maintain detailed records of experiments, formulations, and test results. Prepare technical reports, product specifications, and regulatory documentation as needed. Compliance: Ensure that R&D activities comply with all applicable safety regulations and environmental guidelines. Stay updated with industry standards and regulatory changes. Supplier Interaction: Collaborate with suppliers for sourcing and testing new raw materials. Assess the quality and suitability of materials for product development. Team Management: Manage and mentor a team of R&D chemists and technicians. Provide training and support to enhance their technical expertise and performance. Market Analysis: Conduct market research to identify emerging trends, customer needs, and opportunities for product innovation. Incorporate market insights into the development process. Problem-Solving: Address technical issues related to product performance and development. Provide innovative solutions and optimize processes to overcome challenges. Reporting: Prepare and present R&D reports to senior management, highlighting progress, challenges, and opportunities for new product development Preferred candidate profile Education: Bachelors degree in Chemistry, Chemical Engineering, or a related field. A Master's degree is preferred. Experience: 5-7 years of experience in R&D roles within a manufacturing environment, preferably in the construction chemicals industry. Technical Expertise: Strong knowledge of construction chemicals, raw materials, and formulation techniques. Familiarity with analytical and testing methods. Innovation: Demonstrated ability to innovate and develop new products or enhance existing formulations. Project Management: Experience in managing multiple R&D projects, with excellent organizational and time management skills. Problem-Solving Skills: Strong analytical and problem-solving abilities to address complex technical challenges. Leadership: Proven leadership and team management skills to motivate and guide an R&D team. Communication: Strong communication and presentation skills for effectively sharing technical concepts with internal teams and external stakeholders. Safety and Compliance : Knowledge of safety regulations and compliance requirements related to R&D and manufacturing environments.

At Umami Bioworks, we are a leading bioplatform for the development and production of sustainable planetary biosolutions. Through the synthesis of machine learning, multi- omics biomarkers, and digital twins, UMAMI has established market-leading capability for discovery and development of cultivated bioproducts that can seamlessly transition to manufacturing with UMAMI s modular, automated, plug-and-play production solution By partnering with market leaders as their biomanufacturing solution provider, UMAMI is democratizing access to sustainable blue bioeconomy solutions that address a wide range of global challenges. Umami Bioworks is looking to hire an inquisitive, innovative, and independent Machine Learning Engineer to join our R&D team in Bangalore, India, to develop scalable, modular ML infrastructure integrating predictive and optimization models across biological and product domains. The role focuses on orchestrating models for media formulation, bioprocess tuning, metabolic modeling, and sensory analysis to drive data-informed R&D. The ideal candidate combines strong software engineering skills with multi-model system experience, collaborating closely with researchers to abstract biological complexity and enhance predictive accuracy. Responsibilities Design and build the overall architecture for a multi-model ML system that integrates distinct models (e.g., media prediction, bioprocess optimization, sensory profile, GEM-based outputs) into a unified decision pipeline Develop robust interfaces between sub-models to enable modularity, information flow, and cross-validation across stages (e.g., outputs of one model feeding into another) Implement model orchestration logic to allow conditional routing, fallback mechanisms, and ensemble strategies across different models Build and maintain pipelines for training, testing, and deploying multiple models across different data domains Optimize inference efficiency and reproducibility by designing clean APIs and containerized deployments Translate conceptual product flow into technical architecture diagrams, integration roadmaps, and modular codebases Implement model monitoring and versioning infrastructure to track performance drift, flag outliers, and allow comparison across iterations Collaborate with data engineers and researchers to abstract away biological complexity and ensure a smooth ML-only engineering focus Lead efforts to refactor and scale ML infrastructure for future integrations (e.g., generative layers, reinforcement learning modules) Qualifications Bachelor s or Master s degree in Computer Science, Machine Learning, Computational Biology, Data Science, or a related field Proven experience developing and deploying multi-model machine learning systems in a scientific or numerical domain Exposure to hybrid modeling approaches and/or reinforcement learning strategies Experience Experience with multi-model systems Worked with numerical/scientific datasets (multi-modal datasets) Hybrid modelling and/or RL (AI systems) Core technical skills Machine Learning Frameworks: PyTorch, TensorFlow, scikit-learn, XGBoost, CatBoost Model Orchestration: MLflow, Prefect, Airflow Multi-model Systems: Ensemble learning, model stacking, conditional pipelines Reinforcement Learning: RLlib, Stable-Baselines3 Optimization Libraries: Optuna, Hyperopt, GPyOpt Numerical & Scientific Computing: NumPy, SciPy, panda Containerization & Deployment: Docker, FastAPI Workflow Management: Snakemake, Nextflow ETL & Data Pipelines: pandas pipelines, PySpark Data Versioning: Git API Design for modular ML blocks

At Umami Bioworks, we are a leading bioplatform for the development and production ofsustainable planetary biosolutions. Through the synthesis of machine learning, multi- omics biomarkers, and digital twins, UMAMI has established market-leading capability for discovery and development of cultivated bioproducts that can seamlessly transition to manufacturing with UMAMI s modular, automated, plug-and-play production solution By partnering with market leaders as their biomanufacturing solution provider, UMAMI is democratizing access to sustainable blue bioeconomy solutions that address a wide range of global challenges. Umami Bioworks is looking to hire an inquisitive, innovative, and independent Research Associate for either Cell Line and Media Development to join our R&D Team in Bangalore, India with hands-on experience in animal cell culture and media formulation to support the development of scalable, serum-free cell culture platforms for marine species. This role involves the isolation, characterization, and optimization of cell lines from fish and crustaceans, as well as the formulation and screening of food-grade, cost-effective culture media to support proliferation and differentiation. You ll work directly with senior technical leadership and cross-functional teams to meet scientific and commercial milestones. Responsibilities: Develop, characterize and optimize cell lines derived from fish and crustacean species Primary cell isolation & suspension adaptation Plan and execute experiments to evaluate cell growth, viability, and differentiation potential towards muscle or fat cells etc. Optimize protocols for cell lines characterization Sourcing of animals of various developmental stages for cell line isolations Design and execute experiments using high-throughput screening approaches to identify optimal media compositions. Formulate and produce novel, food-grade, serum-free media formulations for cell proliferation and differentiation. Collaborate with external vendors, suppliers, and internal teams to source raw materials and animal tissue samples. Prepare reports and technical presentations in coordination with senior scientists for internal and external updates. Core competencies: Minimum 2 years of experience in cell line development, preferably in aquatic species Proficient in animal cell culture techniques, including primary cells, stem cells, suspension culture, and primary cell culture Experience working with high-throughput screening in multi-well plate formats for molecular biology or cell biology applications. Familiarity with statistical analysis tools and DoE methodologies for data interpretation and process optimization. Strong experimental design skills and attention to detail in documentation and data analysis. Experience Master in Biology/Life Science, or related field with more than 2 years of relevant industry experience Bachelor in Biology/Life Science, or related field with more than 5 years of relevant industry experience

Role & responsibilities : Only for male candidates Shri Kartikeya Pharma [Jadcherla / India] located in JADCHERLA TELANGANA, India had its last known inspection on 04 Jan 2024. There are 1 known inspections on record Preferred candidate profile Freshers,1-2 yrs