176 Scale Up Jobs

As a Process Development Chemist, you will be responsible for designing and conducting experiments to create new chemical processes and enhance existing ones. You will scale up laboratory procedures to pilot and production levels, ensuring scalability and reproducibility. Analyzing current processes, identifying areas for enhancement, and implementing modifications to boost efficiency, yield, and safety will be a key aspect of your role. Utilizing statistical methods and tools to assess process performance will be crucial. You will collaborate closely with cross-functional teams, such as R&D, quality assurance, production, and regulatory affairs, to seamlessly integrate processes. Providing technical support and expertise to production teams will be essential. Additionally, you will prepare detailed documentation for processes, including protocols, reports, and standard operating procedures (SOPs), while ensuring compliance with safety, environmental, and quality standards. In the event of issues during production, you will investigate and resolve them promptly to minimize downtime. Conducting root cause analysis and implementing corrective actions will be part of your troubleshooting responsibilities. Staying updated on the latest advancements in chemical processes and technologies, and evaluating and recommending the use of new tools and technologies to enhance process performance will be vital for research and development. To qualify for this role, you should hold a Bachelors or Masters degree in Chemistry, Chemical Engineering, or a related field, along with years of experience in chemical process development or a related area. A strong understanding of chemical reactions, kinetics, thermodynamics, and safety regulations is required. Proficiency in analytical techniques such as HPLC, GC, NMR, and others relevant to process chemistry is essential. Excellent problem-solving skills, attention to detail, and strong communication and teamwork abilities are desired qualities. This is a full-time, permanent position with benefits such as provided food, paid sick time, and Provident Fund. The work schedule may involve day shifts or rotational shifts, with the work location being in person.,

Responsible For Design & Development, Optimization And implementation Of Chemical Processes within a Manufacturing Plant Lead Executives , Manage Projects, Ensure Safety And Quality Leading Role In Process Development, Innovation And Optimization Required Candidate profile BE - ME - Chemical From Reputed Institute Candidate Should Have Worked In Pilot Plant & Plant Deep Knowledge Of Troubleshooting And Problem-Solving Capable To Allocate Responsibility To Team Member

Position Title: Research Chemist / Research Scientist Department: Research and Development (R&D) Location: Boisar, Tarapur Reporting To: HOD R&D Date of Request: 24th July 2025 Type of Position: New Position Number of Positions: 3 1. Job Purpose / Objective To conduct chemical reactions as per the experimental processes provided, support new product development, and contribute to expanding the organization's product portfolioultimately enhancing company growth and innovation. 2. Key Responsibilities / Duties S. No.Responsibility / TaskWeightage (%) 1Conduct reactions/experiments as per the given process60%2Record and maintain experimental data systematically30%3Handle different types of chemicals5%4Maintain lab cleanliness and ensure equipment upkeep5% 3. Required Qualifications FieldDetails Education QualificationM.Sc. in Organic ChemistryProfessional CertificationNot RequiredExperience6 months to 1.5 yearsIndustry PreferenceAPI and Chemical IndustryLanguages KnownMarathi, English, Hindi 4. Technical / Functional Skills Technical Skills: Process Development Chemical Handling Glassware Handling Behavioural / Soft Skills: Team Collaboration Soft Communication Skills 5. Key Performance Indicators (KPIs) Accuracy and quality of conducted experiments Timely documentation and reporting of experimental data Adherence to safety protocols and chemical handling guidelines Maintenance and cleanliness of lab area and equipment 6. Internal & External Interactions Internal: R&D team, Quality Control, Production team External: May occasionally interact with vendors or suppliers for chemicals or instruments (as needed) 7. Additional Notes / Special Requirements Basic physical effort involved in handling lab equipment Candidate must be comfortable with chemical handling procedures May require extended lab hours during trials or critical experiments Fresher Can Also Apply Compensation: As per Market Standard & Experience

Responsible for software development projects involving design, development, testing, debugging and implementation of software applications and source code to support end users needs. This is an operational role, responsible for driving day-to-day operations. Responsibilities Participate in designing discussions, planning meetings. Developing the new application/software based on the business requirements. Translating designs into high quality code at all levels of SDLC Involve in defining infrastructure and deployment requirements. Build and maintain operational tools for testing, deployment, monitoring, and analysis. Integrate software components and third-party programs. Develop, test, troubleshoot, debug and upgrade software across a wide array of services and functional areas. Create technical documentation for reference and reporting. Involve with Product Owners and teams in story grooming, backlog maintenance and prioritization and planning. Prepare Test Strategies and Test Design Identify tools and approach for automated testing. Generate Test reports and based on the features, modules, severity, and releases based.Desired Skill sets Expert code/test case writing skills Ability to develop unit testing of code components or complete applications. Understand concepts of software engineering. Experience with software design, coding, testing and development. Knowledge and/or experience in scrum/Agile techniques.

-Conduct feasibility studies, scale up studies and technology transfer. -P&ID, BFD, heat balance & mass balance & HAZOP studies & provide technical inputs. -Design and calculate heat exchangers, utilities, pipe sizing, and for other equipment Required Candidate profile -Drive demo-commissioning scale-up in lab & pilot plant and to ensure successful transfer to commercial scale. -To do process improvements cost reduction and troubleshooting in plants.

The role is responsible for software development /testing/deployment/debugging process. This is an operational role that may seek appropriate level of guidance and advice to ensure delivery of quality outcomes. Responsibilities Writing effective and scalable code/test case Debugging and deploying applications Providing support for production environment Preparing software development calendar Preparing reports and dashboards on project time deviations, rework time etc Conducting development testing and reports testing issues to supervisor Identifying and tracking bugs, assessing nature of bugs, and executing corrective actionsDesired Skill sets Good programming skills Familiar with software applications and tools Good Knowledge on coding/testing environment

Dear Candidate, Greetings from Sanmar Group! We are looking for R&D Process Development Group Leader for our plant located in Berigai, Hosur. Details Below, Company Name : Chemplast Sanmar Ltd https://www.sanmargroup.com/organic-chemicals.php Key Responsibilities: To systematically undertake R&D process development activities, to interpret analytical data, identification of impurities based on acquired fundamental knowledge. 1. Design of experiments 2. Handling Milligram to Kilogram scale reactions 3. Multistep route synthesis 4. Literature collection , route selection and norms preparation 5. Need based support to scale-up on new products, 6. Guidance and work extraction from Team 7. Review of action items for internal and external meetings 8. Inter and intra departmental communication - Planning document review, review of MSDS 9. Preparation of Safety Assessment report related to synthesis of molecules and reactions 10. Overview trouble shooting activity and review of instruments in R&D Lab Qualification : PhD in Organic Chemistry Required : Minimum of 5 - 10 years of experience post Doctorate. If you are interested, kindly send your resume to pt8@sanmargroup.com

You will be responsible for conducting literature searches, gaining a thorough understanding of the product, and interpreting data for product development purposes. Additionally, you will design primary product strategies and prepare product strategies for discussion with group leaders or team leaders. Your role will involve planning and executing product development work to achieve the desired product profile, as well as compiling data. You will be required to schedule work plans in consultation with group leaders or reporting authorities to ensure timely project completion based on assigned priorities. Furthermore, you will carry out the execution and evaluation of various formulation optimization trials, process optimization trials, and data compilation. It will also be your responsibility to write laboratory notebooks and assist in documenting controlled documents, as well as compiling development data. You will be involved in the execution of scale-up, exhibit batches, characterization batches, process validation batches, and commercial batches at manufacturing locations. Additionally, you will prepare documents to ensure the smooth execution of scale-up and exhibit batches, including Justification of specification, QbD elements, MFC, etc.,

As a Process/Project Engineer at GFCL EV Products Limited in the Technical Services department, your primary responsibility will be to assist in process/project engineering and front-end engineering for the commercialization of in-house and licensed processes. You will be instrumental in generating Technology Transfer Data from R&D Kilo Lab Scale and Pilot Plant scale to facilitate the transfer of technology to the Commercial Plant. Your duties will include generating and reviewing various engineering documents such as mass balance, energy balance, process engineering calculations, PFDs, P&IDs, layouts, isometric drawings, project cost estimates, and project schedules. Working closely with the R&D team, you will plan Design of Experiments and organize studies on material compatibility, effluent minimization, solvent recovery, and more. In addition, you will be responsible for selecting appropriate equipment and agitation patterns for scaled-up plant operations, preparing proposals for trial and validation batches in the Pilot Plant, and conducting Process HAZOP and Risk Assessment. Your role will also involve collaborating with the Process Engineering Team to finalize the scaled-up version of the commercial plant and arranging trials at vendors" shops for various operations as per process requirements. Furthermore, you will assist the ADL team in transferring analytical methods to the Plant, support the commissioning of new plants, and collect data for process improvements and modifications. Troubleshooting process problems, ensuring equipment works to specifications, and providing information throughout project phases will be essential aspects of your job. To excel in this role, you must have a minimum qualification of B.E./B. Tech in Chemical Engineering along with at least 5 years of relevant experience in process/project engineering, technology transfer, scale-up, and technical services. Your expertise will be crucial in developing methods for upgrading operational techniques, improving yield, efficiency, and cost-effectiveness of processes, and training Process Engineers on newly developed technologies. Join us at GFCL EV Products Limited and contribute to the continuous improvement and success of our technology transfer and commercialization processes.,

We are looking for R&D Project Managers for end to end Project Completion from Molecule / Noble Discovery molecule of CDMO Customers to Prototype Development, Tech Transfers, Tech Absorption and Industrialisation. Title: Senior Manager Projects - R&D Qualification: B.Tech / B.E - Chemical Engg. PMP Certification is desirable Experience: 12 Years to 20 Years Location : Pune Saturdays - 2 Offs Transport facility : Yes You should be working in R&D Units of Agro Chem / Pesticies / Crop Protection Chemical Mfg Companies in the business of CRAMS / CDMO for Customers / Global Clients. In this role, you will lead research and development projects focused on Crop Sciences / Crop Protection Chemical products, ensuring seamless technical transfers, efficient project execution, and alignment with client needs. Candidates working at Mfg locations managing Capex Projects are in-eligible. Key Role: Develop, implement, and monitor comprehensive project plans, timelines, milestones, and deliverables to ensure on-time and on-budget completion of R&D initiatives. Coordinate all Project-related activities for the Technical transfer of products from development to manufacturing, including Synthesis processes. Lead cross-functional project teams, including R&D, manufacturing, quality assurance, and regulatory affairs, to achieve optimal project outcomes and resolve any issues promptly. Evaluate Project planning scenarios, including milestone dates, decision points, and resource allocation to balance risks and efficiencies. Be Single Point of Contact for the Projects assigned for External Clients and R&D Scientist and Factory Team. Skills: Excellent Communication Skills. Good Interpersonal Skills. Should have good stakeholders management skills. Candidates working at Mfg locations managing Capex Projects are in-eligible.

Role & responsibilities Responsible for execution of Cost improvement projects (CIP) for the existing processes and products . To prepare the basic and detailed engineering for CAPEX projects. Preparation of qualification documents for CAPEX projects. Responsible for execution of Operational excellence (OE) activities at site. Trouble shooting of plant problems and de-bottle necking of processes. Support the respective department personnel during execution of new initiatives/modifications/ improvements in existing processes. Conducting HAZOP for any product/process/plant and preparation of HAZOP report. Preferred candidate profile B.Tech in Chemical Engineering with 2 to 4 years of work experience in Technical Service department (API Industry only) . Please share CVs to ramya_n@hikal.com with subject line as Application for Technical Service department .

Role & responsibilities Coordinate implementation of initiatives for continuous improvement journey Monitor improvement projects and support progress to adhere to project deliverables Identify and implement opportunities for improvement of capacity, yield, solvent recovery, safety, environment Debottleneck the capacities as per market demand Implement energy conservation initiatives Drive usage of analytical tools for continuous improvement through training and development Coodinate with R&D for new products scale up, lab demonstration, process troubleshooting Support engineering function for process equipment design parameters, material of construction, HAZOP, PSSR, automation Coordinate activities for internal and external assessments and audits Preferred candidate profile Candidates with 4-7 years of experience in process engineering with pharmaceutical | chemical industry Interested candidates can share their CV on honey_panchal@atul.co.in

Role & responsibilities Manage technology transfer activities from development to commercial manufacturing for OSD tablets. Oversee and execute process scale-up, process optimization, and validation to ensure smooth transition into commercial production. Maintain an in-depth knowledge of USFDA regulations for OSD products and ensure compliance with all regulatory requirements during tech transfer activities. Work closely with R&D, manufacturing, and quality teams to address any technical challenges during tech transfer. Preferred candidate profile Prefered candidates from OSD (manufacture Tablets , capsules,)background . USFDA experince is must Its a plant based role.

Role & responsibilities To execute activities related to R&D Process Development, along with a group comprising of Research Officers/ Research Assistants under guidance from the Project Leader/Group Leade Require to Plan and carry out Chemistry related experiments, recording the observation in Protocol Computer literacy etc. Job Description: Literature search with respect to assigned project and its documentation Experimentation (Process development, optimization and validation) Analysis, interpretation (HPLC, IR, NMR, Mass and CHN) and documentation of data General Laboratory Management etc. Scale-up and Technology transfer activity Project related impurities synthesis.

Role & responsibilities Literature survey report preparation. Expertise in an API Synthesis. Organize for relevant patents and papers from literature Organize / order raw materials / chemicals from different vendors / plants Develop a most economical / eco friendly commercially viable technology at bench scale APIs by effective use of sustainability tool & Statistical (DOE) tools. Participating in cross-functional project teams and contributing to scientific strategies and goals. Presenting data and reports on project status at meetings. Contributing to the development of new peptide-based technologies. Adhering to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Troubleshooting and maintaining peptide synthesis equipment. Participating in optimization and automation improvements for enhancing peptide synthesis capacity. Maintaining a clean and organized laboratory environment. Strong proficiency in solid-phase peptide synthesis, analytical techniques (HPLC, LC-MS, NMR), and data analysis. Excellent communication, teamwork, and problem-solving skills are essential. Familiarity with laboratory safety protocols and regulatory guidelines is also important Daily experimental planning, execution, recording & data Compilation To meet EHS and compliance expectation Supporting/report preparation of Genotoxic & nitrosamine impurities To prepare reports such as safety, vendor qualification reports, Supporting/Preparation of Process development report, ACMI report Technology transfer and piloting of developed peptides RMC sheet preparation Competencies required Sound knowledge of organic chemistry, Spectroscopy, Drug Regulatory Affairs & Quality Assurance ICH Guidelines and basic IP understanding Good experimental hand & Scale-up knowledge Innovative thinking & excellent observance Note - API experience is mandatory. Interested candidate can share their profile on jasleen.kaur@tapi.com or connect on 8076954558.

Role & responsibilities 1. Pilot Plant Operations Management: Supervise and lead a team of technicians and operators to ensure efficient and safe operation of the pilot plant. Develop and implement standard operating procedures (SOPs) for various pilot plant processes and activities. Coordinate with cross-functional teams, including research and development, engineering, and analytical to ensure seamless integration and execution of pilot plant activities. Monitor and maintain equipment and instrumentation, ensuring their proper calibration and functionality. Troubleshoot and resolve operational issues to minimize downtime and optimize productivity. Ensure compliance with safety protocols, environmental regulations, and good manufacturing practices (GMP) during pilot plant operations. 2. Process Development and Optimization: Collaborate with R&D teams to design, develop, and scale-up new processes and technologies for pilot-scale production. Conduct experiments and trials to optimize process parameters, yields, and efficiencies. Analyze and interpret data generated from pilot plant experiments, identifying trends and recommending improvements. Work closely with engineers to evaluate and select appropriate equipment and technologies for pilot plant operations. Document and maintain comprehensive records of pilot plant activities, including process parameters, batch records, and deviations. 3. Project Management: Plan and execute pilot-scale production campaigns in accordance with project timelines and objectives. Coordinate with internal stakeholders to ensure timely availability of resources, materials, and utilities required for pilot plant operations. Monitor project progress and provide regular updates to management, highlighting any potential risks or deviations from planned schedules Collaborate with external vendors and contractors, as necessary, to procure equipment, supplies, and services for the pilot plant. 4. Training and Compliance: Train and mentor pilot plant staff on standard operating procedures, safety protocols, and quality standards. Ensure compliance with regulatory requirements, quality management systems, and company policies. Participate in audits and inspections, addressing any findings and implementing corrective actions. Stay updated with industry trends, technological advancements, and best practices related to pilot plant operations Preferred candidate profile Should possesses strong knowledge of chemical processes, unit operations, and equipment commonly used in pilot-scale manufacturing Familiar with process optimization techniques, statistical analysis, and experimental design Excellent leadership and team management skills, with the ability to motivate and inspire a diverse group of individuals Strong project management abilities, including the capability to prioritize tasks, manage resources, and meet deadlines Effective communication skills, both verbal and written, with the ability to interact with cross-functional teams, senior management, and external stakeholders Attention to detail, analytical thinking, and problem-solving skills Takes personal responsibility to make things happen and continuously raise the bar. Displays a high degree of emotional maturity and awareness of own impact. Defines and leads change initiatives for own work area Continuously raises the teams performance to best in class levels and creates a culture of high accountability

As an Assistant General Manager (AGM) Formulation Development specializing in Injectable dosage forms, you will be responsible for the development, scale-up, and validation of both simple and complex formulations for Injectable products. Your primary focus will be on creating dosage forms compliant with regulations in the US, EU, India, Canada, Brazil, and other markets. Your key responsibilities will include: - Developing Injectable dosage forms for various global markets - Scaling up and transferring technology for Injectable products across different regions - Designing formulation strategies and overseeing the drug product development roadmap - Reviewing stability data of products under development and during validation batches - Handling regulatory queries and conducting studies as necessary - Coordinating with internal departments and external vendors for drug product development - Troubleshooting product and process failures, particularly for US, EU, and other markets - Providing technical guidance to subordinates and ensuring compliance with laboratory practices and safety regulations - Following Good Documentation Practices and Data Integrity requirements during GxP operations - Ensuring understanding and adherence to Data Integrity requirements and consequences - Reviewing data for compliance with Data Integrity requirements in the context of job responsibilities Your role will be crucial in ensuring the successful development and validation of Injectable dosage forms for multiple markets, requiring strong technical expertise, regulatory knowledge, and attention to detail.,

Role & responsibilities Review of Technology data package and preparation of Gap analysis document. Preparation of technology transfer protocol and report. Co-ordination with FD for smooth Tech Transfer. Monitoring of validation batches at production site. Perform Feasibility trials, Product evaluation trials to understand critical process parameter for smooth transfer and process understanding. Review of MPCR and protocol. Planning for Execution of Process design, Process qualification batch. Coordination with Production, Quality assurance, Quality control, Engineering, Regulatory Affairs, SCM and warehouse for the TT activities. Should be part of handling deviation, change control and failure investigations. Process manufacturing parameters for Qualification batches Vs Commercial batches. Preparation and reviewing of intended batch documents for regulatory submission. Trouble shooting of existing products and process improvement to increase output or to reduce processing time or to improve the quality of products. Preferred candidate profile required from OSD pharmaceutical Executive - TT: Exp required: 04 to 06 years Dy. Manager: Exp required: 09 to 12 Years Candidate should be willing to relocate/work in Nanjangud, Mysuru Plant.

Roles and Responsibilities Lead process development activities for hormone manufacturing processes, focusing on scale up and technology transfer. Develop and implement new technologies to enhance capacity and improve efficiency in existing processes. Collaborate with cross-functional teams to identify areas for improvement and optimize processing conditions. Ensure compliance with regulatory requirements during all stages of product development. Provide technical support to production teams to resolve issues related to process operations. Desired Candidate Profile 8-12 years of experience in pharmaceutical industry, preferably in hormonal manufacturing or similar field. B.Tech/B.E. degree in Chemical Engineering from a recognized institution. Strong understanding of chemical engineering principles, including mass transfer kinetics, heat transfer, and fluid mechanics. Experience with process development methodologies such as PFDs (Process Flow Diagrams), P&IDs (Piping & Instrumentation Diagrams), and SOPs (Standard Operating Procedures).

KEY FUNCTIONS / RESPONSIBILITIES Project initiation activities:- To understand project timelines and required activities for the timely execution. To perform literature search required for idea generation form (IGF) upon receiving IGF. To review DMF received from suppliers. To prepare product feasibility based on IGF received. To create the item codes for material and procure material and Reference Listed Drug (RLD). To assist AD lab for Q1 Q2 estimation of RLD. To draft tentative specification for API, RM and finished good. To plan laboratory trials and stability batches. To finalize proposed manufacturing process. To initiate filter validation process with the filter supplier. To handle Bead mill and high pressure homogenise . Documentation:- To prepare tech transfer documents including MFR, BOM, Process flowchart, Critical process parameters and critical quality activities. To review product specifications, manufacturing documents. To prepare documents for trial batches. To prepare product development report. To prepare and review SOPs and prepare response for internal audits. To review documents related to filter validation. Product Specification/ Tech Transfer/ Commercialization To organize and execute trial pre exhibit and exhibit batches at plant. To execute first three commercial batches at plant. To provide technical support for existing commercial batch. To perform investigation of failures during exhibit batches/ stability (Out of Specification). Innovation To come up with innovative and patentable formulations proposals. To come up with novel ideas which can reduce workload or expenses. Train, mentor and supervise the team To mentor RAs in planning the project activities in minute and actionable details. Help RAs in carrying out literature search. Help RAs in carrying out procurement of RLD, API and excipients. Plan and execute Knowledge sharing session for compatibility studies, reverse engineering, laboratory batches planning, filter compatibility, process optimization and recent updates in the field to emphasize importance of timeline adherence to team member

As a Manager-II in the MSTG department at Sun Pharmaceutical Industries Ltd, your primary responsibility will be to provide support for the execution and monitoring of trial, scale up, exhibit process qualification batches. You will be involved in preparing and reviewing new product documents such as material requirement sheet, master formula card, bill of material, master formula, risk assessment reports, sampling protocol, reports, exhibit batch manufacturing record, and exhibit protocols. Additionally, you will be required to prepare regulatory responses and share process knowledge with cross-functional departments through presentations for smooth technology transfer. You will play a key role in reviewing and evaluating product history and process parameters for technical remediation and improvement of product robustness. Your duties will also include preparing and submitting investigation reports for OOS, OOT, and any failure during exhibit/validation/commercial batch manufacturing and stability testing. Furthermore, you will be responsible for tracking activities related to change control, CAPA, planned deviations, unplanned deviations, and more. Your role will involve preparing and reviewing product containment approaches, risk assessment reports for new products, elemental impurities, Nitrosamine impurities, and residual solvent. You will also be tasked with arranging placebos for quality control testing, change part development, and evaluating the feasibility of products. Statistical evaluation for process assessment, preparation and review of standard operating procedures, training schedules, conducting training sessions, and participating in regulatory audits to support the plant will also be part of your responsibilities. Overall, as a Manager-II in the MSTG department, you will be at the forefront of ensuring the quality and compliance of processes and procedures while contributing to the continuous improvement and development of new products within the organization.,

Job Title: Dy Manager R&D-Technology Transfer Location : Mumbai Location Industry: Pharma Industry Experience: Minimum 5.to 10 years . Able to scale up technology from R&D to Kilo scale/ pilot scale/ commercial scale Coordination with R&D team for generating negative study data, concluding to optimize process parameters interested candidates can share cv to hr3@sarthee.com or call at 9033033650

Responsible for scale up technology from R&D to Kilo scale/ pilot scale/ commercial scale Coordination with R&D team for generating negative study data, concluding to optimize process parameters Observe R&D demo batches & preparation of demo batches report Identify & propose ideas to improve process efficiency, effective utilization for unit process & operations Preparation of BFD, PFD, P&ID, mass balance, energy balance sheets Monitor process optimization & validation batches at pilot/ commercial scale at different manufacturing sites Support the external job work activity to achieve desired yield and quality Coordination with cross functional teams to implement process through scale-up & capacity enhancement Preparation of optimization & validation campaign reports after completion of projects

l Interaction with R&D department for new product development l Equipment mapping for kilo lab and kilo lab to pilot plant. l Responsible for preparing BPCR,PCOCR l Responsible for lab demonstration in R&D l Study of new product in R&D and plan batch in pilot scale l Planning for raw materials for batch trial. l Enquiry floating of equipment and technical clearance of equipment. l Responsible for scale up activities of new projects as well as cost reduction of product and waste reduction. l Able to lead subordinate technology transfer process engineer team l Planning and resource management for continuously pilot plant operation. l Equipment selection, Process mapping, Time cycle calculation, Volume calculations for new product . l Responsible for material balance and energy balance of product. l Utility calculation,hydraulic calculation and cost estimation of new products l Identify and analyze bottlenecks,implement best practice and continuous improvement for process optimization. l Optimize resource utilization,reduce waste for process efficiency. l Capacity calculation capacity enhancement for any new or existing products. l Plant development, Plant validation batches report preparation. l Detailed workout for equipment modification along with detailed job list & PFD for scale up purpose

Synthesis of Compounds and Process Scale up To ensure that the process parameters are maintained well within the limits All SOPs and safety procedures are followed during the Operation, and abnormality is reported back. Required Candidate profile Halogenation – Chlorination / Bromination / Fluorination Nitration Methylation Oxidation Redox reactions High Pressure reactions Exposure to Distillation processes – simple, fractional, etc.