121 Organic Synthesis Jobs - Page 5

JOB DESCRIPTION Jubilant Bhartia Group . About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared) in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology & In-vitro ADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - Trainee research Associate/ A0 Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities Synthesis, purification and characterization of chemical intermediates. Deliver small to large quantities of novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Excellent knowledge of basic organic chemistry with mechanism. Good knowledge of Name Reactions & functional group transformation. Good knowledge of molarity, normality, equivalency. Practical experience in thin-layer chromatography, column purification and extraction. Good understanding of NMR, IR and mass spectrometry. Interest to adapt and knowledge of laboratory safety practices. Enthusiasm to work in a dynamic research environment. Good Soft & Scientific Communication skills. Person Profile Qualification: - M.Sc. in Chemistry/Organic Chemistry/Pharmaceutical Chemistry or related field or M. Pharma (Specialized in Organic Synthesis) with 0-1 years project experience. Experience: - 0-1 year of exp. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Synthetic experience from Gram to kilogram scale Experience in handling moisture and light sensitive reagents API’s Analysis and characterization of molecule using techniques Structural interpretation of intermediates and finished products

: Medicinal chemistry; Research and development; Literature search; Scifinder / Reaxys; Design and synthesis; combiflash/Biotage; C-C coupling etc Qualifications MSC - Organic Chemistry.

Carry out the assigned Lean projects / transformations independently with zero conflicts by utilizing change management and project management skills Own, manage and track local Lean implementation plan (both short term during the Lean project but also long-term for continuous improvement) Ensure appropriate local resources are involved and trained during the Lean project and ensure sustenance Support in managing performance management infrastructure, namely the definition, tracking and reporting of KPIs, adequate structure of meetings and performance dialogues and definition and implementation of corrective action Coach/ train local Lean teams in Lean methodology and toolset following the Lean Academy curriculum Independently manage IDEA generation program from generation until implementation and ensure sustenance Qualifications Bachelors/Post Graduates in science (Good knowledge in lab processes involved in drug discovery & development is a must)Lean certification from a reputed institute8+ Years

Conduct multi-step organic synthesis for pharma intermediates, APIs, and agro actives. Execute and monitor reactions, purify products, and characterize them using TLC, MP, IR, NMR, HPLC, and GC. Maintain lab notebooks and document experimental procedures and results accurately. Ensure safe handling of chemicals, solvents, and hazardous reagents, adhering to lab safety protocols. Support process optimization and scale-up trials from gram to kilogram scale. Keep up-to-date with technical developments and best practices in synthetic chemistry. Qualifications Candidates to be from Pharma or Agro CDMO background. Strong fundamentals in organic chemistry and reaction mechanisms. Hands-on experience in synthesis and basic analytical techniques (NMR, HPLC, GC preferred). Understanding of pharma and agro sector regulatory standards is a plus.

Skills Description Proficiency Level (General Awareness; Working Knowledge; Functional Expert, Mastery ) Functional Skills Organic Chemistry, Purification skills, Inert Reactions, Named Reactions Ability to self-design synthetic schemes, plan and order chemicals and deliver the targets in the stipulated time-line. Excellent trouble-shooting skills Responsible for laboratory maintenance on day to day basis. Functional Expert Behavioral Skills Strong communication skills are essential so as to individually procure chemicals, taking care of laboratory maintenance. Working Knowledge

Skills Description Proficiency Level (General Awareness; Working Knowledge; Functional Expert, Mastery ) Functional Skills Organic Chemistry, Purification skills, Inert Reactions, Named Reactions Ability to self-design synthetic schemes, plan and order chemicals and deliver the targets in the stipulated time-line. Excellent trouble-shooting skills Responsible for laboratory maintenance on day to day basis. Functional Expert Behavioral Skills Strong communication skills are essential so as to individually procure chemicals, taking care of laboratory maintenance. Working Knowledge

We are seeking a highly skilled R&D, Group Leader with extensive experience in the Api industry. Individual will lead a team of chemists from R&D. Candidate should have experience in New Product Development , with experience in producing cost-effective, for the synthesis of reliable APIs and intermediates. Education: PhD - Organic Chemistry with around 10-15 years of experience in API Companies. Location: Hyderabad Job Description: 1. To lead a team of chemists from R&D. 2. To develop and produce cost-effective, non-infringing, safe and eco-friendly technologies for the synthesis of reliable APIs and intermediates. 3. Creative capabilities in the areas of organic chemistry in designing and conducting multi step organic synthesis that is very much attractive from commercial aspects. 4. To Identifying and select API molecules based on developing non-infringing process for API molecules. 5. Support in transformations in synthetic organic chemistry aimed at target molecule from R&D scale to plant scale. 6. Conduct research and design experiments to develop and optimize synthetic routes for API molecules. 7. Perform literature searches for identified API molecules to determine synthesis routes, polymorphs, and analytical methods. 8. Conduct experimental trials to assess feasibility and optimize designed synthetic routes for API molecules. 9. Strongly self-motivated, believing in team work and efficient problem solver, having good skills for development of subordinate potentials. 10. Exhibit Good Laboratory Practice. 11. Efficient handling of High pressure, Hazardous, Highly moisture sensitive and other specialized reactions. 12. API- cost effective process development. 13. Impurity impact on process, identification & synthesis. 14. Development of new API molecules and technology transfer of the same. Documentation: *Record all experiments in the laboratory notebook (LNB) and maintain corresponding analytical data in organized folders * Design synthetic routes for the synthesis and isolation of impurities and reference standards. * Ensure all documentation meets Good Manufacturing Practices (GMP) and regulatory standards. Safety and Compliance: • Adhere to all safety protocols and ensure a safe working environment in the laboratory. • Develop non-infringing synthetic processes based on literature, raw material availability, and polymorph studies. • Stay up-to-date with industry trends, regulatory guidelines, and advancements in chemical synthesis and analytical techniques. Interested candidates share resume on anuverma@sauravchemicals.com Contact and what's app on 9988339860

Job Title: Sr. Research Assistant Summary: Pursue new silicone polymer, oligomer or silane materials development efforts and analytical characterization in close collaboration with BU and execute in alignment with project goals Evolve as an impactful team player with good organizational citizenship and use project management skills appropriately. Responsibilities Include: EH&S: Learn & adhere to safe work practices in lab; Exhibit & promote pro-active safe behaviors in lab activities. Responsible for synthesis and development of novel silicone-based polymers, oligomers or silane materials for varied applications. Work inclusively in close collaboration with BU s/global stakeholders across multiple functions. Work collaboratively in a team setting & work with project leaders to execute project plans for timely positive progress - Technical problem-solving aptitude is required. Required to effectively communicate the results within CRD and with global partners. Qualifications: The following are required for the role Masters in Chemistry With 1-2 years of experience in organic chemistry/polymer chemistry or equivalent Experience in handling complex polymer/organic synthesis procedures in a safe & efficient manner Knowledge & expertise in synthetic chemistries and standard characterization techniques (NMR, GC, GPC etc). Use of basic statistical tools to provide clear understanding to experimental results. Strong safety ethics and knowledge/experience to safely lead lab research methods What We Offer: At Momentive, we value your well-being and offer competitive total rewards and development programs. Our inclusive culture fosters a strong sense of belonging and provides diverse career opportunities to help you unleash your full potential. Together, through innovative problem-solving and collaboration, we strive to create sustainable solutions that make a meaningful impact. Join our Momentive team to open a bright future. #BePartoftheSolution About Us: Momentive is a premier global advanced materials company with a cutting-edge focus on silicones and specialty products. We deliver solutions designed to help propel our customer s products forward products that have a profound impact on all aspects of life, around the clock and from living rooms to outer space. With every innovation, Momentive creates a more sustainable future. Our vast product portfolio is made up of advanced silicones and specialty solutions that play an essential role in driving performance across a multitude of industries, including agriculture, automotive, aerospace, electronics, energy, healthcare, personal care, consumer products, building and construction, and more. Momentive believes a diverse workforce empowers our people, strengthens our business, and contributes to a sustainable world. We are proud to be an equal opportunity employer . Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by law. To be considered for this position candidates are required to submit an application for employment and be of legal working age as defined by local law . An offer may be conditioned upon the successful completion of pre-employment conditions, as applicable, and subject to applicable laws and regulations . Note to third parties: Momentive is not seeking or accepting any unsolicited assistance from search and selection firms or employment agencies at this time.

Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensure safe operations and compliance to company s integrity quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals. Govern and Review safety metrics from time to time. Core Purpose of the Role: Personnel handling this profile will be responsible for conducting reactions and delivering final compounds within a fast turnaround time, meeting the specific requirements of both the project and Syngene. The candidate should be capable of independently designing the synthetic scheme for any target and solve chemistry problems. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene. Role Accountabilities: Expected to design a synthetic scheme for any given target and to be proactive in identifying rate limiting steps along with the mitigation strategy. The candidate should be we'll versed in using literature search engines and predictive synthesis tools Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipment s Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. The candidate should be capable of meeting Syngene s productivity expectations (# of compounds/month, # of steps/month and productivity index of around 1.5) without compromising on safety and quality. The candidate should be capable of synthesizing the final compounds at a faster turnaround time. The candidate should have excellent analytical interpretation and purification skills. Ensure that they know the SDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms. Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety. Attend all mandatory trainings and update training records as and when trainings are completed. Always ensure confidentiality. Skills and Capabilities: Should have deeper knowledge with concepts of organic synthesis and reaction mechanisms. Should be capable of designing synthetic schemes and troubleshooting synthesis problems independently. Should be excellent in purification and analytical interpretation skills. Familiar with operations of relevant apparatus - instrument / equipment. Education: M.Sc. in general or organic chemistry

Role & responsibilities: Creating and Preparation of reports. Data Analysis and presentation. Software (Power point, Side presentation. Q R Code creations. Computer Skills. Good verbal and written communication skills and Proficiency with computer knowledge. Good Knowledge in Chemical and Toxicology. Preferred candidate profile: 1. The Incumbent should be M. Sc. in Chemistry (Organic/Physical/Analytical) from a reputed university/ Institute with excellent academic background. 2. 3 to 6 years good working experience in Regulatory Research Associates in Public/ private limited company preferably in Agrochemical manufacturing industry, making technical grade Agrochemicals/ Intermediates. Perks and benefits: Negotiable

Role & responsibilities: Creating and Preparation of reports. Data Analysis and presentation. Software (Power point, Side presentation. Q R Code creations. Computer Skills. Good verbal and written communication skills and Proficiency with computer knowledge. Good Knowledge in Chemical and Toxicology. Preferred candidate profile: 1. The Incumbent should be B. Sc. Chemistry / Computers from a reputed university/ Institute with excellent academic background. 2. 0 to 3 years good working experience in Regulatory Associates in Public/ private limited company preferably in Agrochemical manufacturing industry, making technical grade Agrochemicals/ Intermediates. Perks and benefits: Negotiable

Job Area: Engineering Group, Engineering Group > Hardware Engineering General Summary: As a leading technology innovator, Qualcomm pushes the boundaries of what's possible to enable next-generation experiences and drives digital transformation to help create a smarter, connected future for all. As a Qualcomm Hardware Engineer, you will plan, design, optimize, verify, and test electronic systems, bring-up yield, circuits, mechanical systems, Digital/Analog/RF/optical systems, equipment and packaging, test systems, FPGA, and/or DSP systems that launch cutting-edge, world class products. Qualcomm Hardware Engineers collaborate with cross-functional teams to develop solutions and meet performance requirements. Minimum Qualifications: Bachelor's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 3+ years of Hardware Engineering or related work experience. OR Master's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 2+ years of Hardware Engineering or related work experience. OR PhD in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 1+ year of Hardware Engineering or related work experience. Key Technical skills requirement: Candidate should have deep and sound understating of: Memory basic design understating for different architectures Memory measurement parameters Memory timing/power characterization and compiler engine building with all accuracy parameters involved Memory power views All the LVF/different forms of variation parameter Memory lib w.r.t. parameters/arcs/SDF conditions/variation parameters/QA steps/different formats Different Simulator tools Should have thorough understanding of release process to customers Knowledge of scripting languages such as Shell, Perl Good working knowledge of MS excel, PPT Mentoring skills to Juniors Applicants Qualcomm is an equal opportunity employer. If you are an individual with a disability and need an accommodation during the application/hiring process, rest assured that Qualcomm is committed to providing an accessible process. You may e-mail disability-accomodations@qualcomm.com or call Qualcomm's toll-free number found here. Upon request, Qualcomm will provide reasonable accommodations to support individuals with disabilities to be able participate in the hiring process. Qualcomm is also committed to making our workplace accessible for individuals with disabilities. (Keep in mind that this email address is used to provide reasonable accommodations for individuals with disabilities. We will not respond here to requests for updates on applications or resume inquiries). Qualcomm expects its employees to abide by all applicable policies and procedures, including but not limited to security and other requirements regarding protection of Company confidential information and other confidential and/or proprietary information, to the extent those requirements are permissible under applicable law. To all Staffing and Recruiting Agencies Please do not forward resumes to our jobs alias, Qualcomm employees or any other company location. Qualcomm is not responsible for any fees related to unsolicited resumes/applications. If you would like more information about this role, please contact Qualcomm Careers.

Position: Junior Scientist / Scientist Synthetic R & D Looking for candidates with 3+yrs of experience as a chemist or scientist in Synthetic R & D. Total Experience: 3-6yrs Qualification : M Sc Organic Chemistry / General Chemistry Location: Bangalore (Peenya) Roles & Responsibilities: Carry out assigned research to meet assigned project, setup, operate and maintain laboratory instruments and equipments, method development for synthesis of target compounds, perform small scale laboratory experimentation and purification to achieve high purity. Responsible for operation process, sampling and isolation process. Writing a technical report and documentation. Analysing and characterization of products. Validating the process on bulk scale. Demonstrating the process at a production scale. Knowledge of chemistry including the safe and disposal of chemicals, science skills and verbal communication skills.

Role & responsibilities We are seeking a qualified individual with strong expertise in organic chemistry, including in-depth knowledge of chemical reactions and mechanisms. The role involves: Distillation of organic solvents and purification of organic compounds using column chromatography, vacuum distillation, and crystallization. Scaling up chemical reactions from gram to kilogram scale. Conducting experiments for assigned projects and maintaining accurate records of observations in the lab notebook. Proficiency in using online resources, including chemistry-related searches, to support research and project work. Operation and maintenance of laboratory equipment such as round-bottom flasks (RBF), TLC chambers, pH meters (calibration and use), rotary evaporators, Buchner filters, microfilters, vacuum systems, and tray dryers. Candidates should demonstrate hands-on experience and attention to detail in laboratory practices. Preferred candidate profile:- API/CRO- R&D Qualifications:- M.sc Organic Chemistry/Industrial Chemistry / M. Pharma (Medicinal Chemistry)

We are looking for a meticulous Assistant Manager R&D to spearhead API development initiatives at Glochem Industries. As Assistant Manager, you will play a crucial role in executing complex organic syntheses, optimizing reaction conditions, and assisting in the development of scalable and environmentally friendly synthetic routes for API manufacturing. Your responsibilities will span from meticulous documentation of experimental procedures and results to collaborating with cross-functional teams, including analytical, kilo lab, and pilot plant teams, for sample analysis and process scale-up. The ideal candidate will have a strong foundation in organic chemistry, a deep understanding of API manufacturing processes, and familiarity with pharmaceutical industry regulations. You will also contribute to technology transfer activities, troubleshoot synthetic issues, and ensure compliance with safety protocols. This role demands a proactive approach to staying updated on recent literature, participating in team discussions, and supporting the preparation of technical reports and regulatory documentation. Your expertise will directly influence the efficiency and quality of our API development pipeline, ensuring Glochem Industries maintains its position as a leader in the pharmaceutical industry. Job Details: Industry: Pharmaceuticals Department: Research & Development Role: Assistant Manager R&D Location: Hyderabad Compensation: 6-10 LPA Experience: 5-10 years Employment Type: Full-time Qualification: Master’s or PhD in Organic Chemistry or related field Responsibilities: Organic Synthesis and API Development Execute multi-step organic syntheses for API development, adhering to established protocols and under the guidance of senior scientists. Optimize reaction conditions to enhance yield, purity, and cost-effectiveness of API synthesis. Develop scalable and environmentally friendly synthetic routes for API manufacturing, considering green chemistry principles and Glochem Industries' sustainability goals. Troubleshoot synthetic issues during development, employing analytical techniques and literature review to identify and resolve problems. Ensure compliance with chemical safety procedures and handle hazardous chemicals responsibly, following GLP guidelines. Assist in the preparation of development summaries and technical reports, documenting key findings and experimental data for API projects. Research and Development Conduct literature searches and stay abreast of the latest advancements in organic chemistry and API development to identify innovative solutions. Design and execute experiments to investigate new synthetic methodologies and optimize existing processes for API production. Collaborate with cross-functional teams to identify and evaluate potential new API candidates for development. Contribute to the development of intellectual property, including patent applications, related to novel synthetic routes and API formulations. Analyze and interpret experimental data to draw conclusions and make recommendations for future research directions. Present research findings at internal meetings and contribute to the preparation of scientific publications and presentations. Project Management Assist in the planning and execution of API development projects, ensuring adherence to timelines and budgets. Track project progress and identify potential roadblocks, proactively proposing solutions to mitigate risks. Coordinate with internal and external stakeholders to ensure effective communication and collaboration throughout the project lifecycle. Contribute to the preparation of project reports and presentations, summarizing key findings and progress updates for management review. Participate in project team meetings and contribute to the development of project strategies and objectives. Manage laboratory resources and equipment to ensure efficient operation and support project activities. Compliance & Safety Ensure strict adherence to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) guidelines in all aspects of API development. Maintain accurate and complete documentation of all experimental procedures, data, and results in accordance with regulatory requirements. Participate in internal audits and inspections to ensure compliance with company policies and regulatory standards. Implement and maintain a strong safety culture within the laboratory, promoting safe work practices and adherence to safety protocols. Conduct risk assessments for all experimental procedures and implement appropriate control measures to minimize hazards. Ensure proper handling, storage, and disposal of hazardous chemicals and waste materials in accordance with environmental regulations. General Expectations and Past Experiences: Master’s or PhD in Organic Chemistry with 5-10 years' API development experience in the pharmaceutical industry, focusing on organic synthesis and process chemistry. Independently execute and troubleshoot multi-step organic syntheses, optimizing reaction conditions for yield, purity, and scalability. Utilize NMR, HPLC, GC-MS, and LC-MS for sample analysis, characterization, and impurity profiling to support API development and process optimization. Maintain a strong understanding of FDA, ICH, and GMP guidelines to ensure regulatory compliance in R&D activities. Contribute to DMF submissions and other regulatory documents, ensuring accuracy and completeness. Participate in experiment design and execution for process development, optimization, and validation of APIs. Contribute to identifying and evaluating new technologies and synthetic methodologies to enhance API development capabilities.

Proud to be recognized as one of Forbes Americas Best Startups! Also proud to be recognized as a Most Loved Workplace! Enveda is looking for a Director, Medicinal Chemistry to join our team in Hyderabad, India The contribution you will make: We are looking for a Director, Medicinal Chemistry with a demonstrated track record ofdelivery of optimized leads and clinical candidates for advancing them into human clinical trials. You will lead medicinal chemistry activities for two or more projects in parallel. You will be involved in identifying pre-leads, design and optimization of leads for potency, selectivity and druggability and also strong IP generation. You will recruit PhD and M. Sc. synthetic chemists and mentor them as medicinal chemists and manage their performance and improve their productivity. You will collaborate with your peers in Medicinal Chemistry and work as a team to increase delivery of compounds to the Clinical Pipeline of Enveda. You will also collaborate with Senior Leaders in other functional departments such as ADME, Analytical Sciences and Pharmacology and deliver high value molecules to Enveda. As a member of the broader Drug Discovery team, you will report to the VP, Discovery Chemistry. You get to collaborate on Medicinal Chemistry of Lead Generation and Lead Optimization of Pipeline Projects. Understand Structure Activity Relationships and Structure Property Relationships of various projects. Collaborate with Medicinal Chemistry, Pharmacology, Analytical, ADME, Tox, IP, Site and Global Leadership. Develop appropriate flow schemes with relevant in vitro, in vivo, ADME/PK and tox studies. Appropriate allocation of resources for maximum cost effectiveness. Work effectively with Project ManagementMake presentations of your projects at various Enveda forums. You work with the site safety head and emphasize the importance of safe practices in the chemistry laboratories Who will thrive in this role? Doctor of Philosophy in Synthetic Organic Chemistry15-20 years of post-PhD experience in Medicinal ChemistryProven track record of delivery of leads and clinical candidates to the pharmaceutical industry. Management and mentoring of synthetic chemists. Good understanding of intellectual property of medicinally valuable compounds with respect to composition of matter, method of use and chemical processes. Strong understanding of safety practices in organic synthesis laboratories. If you dont meet all of the requirements listed here, we still encourage you to apply. No job description is perfect, and we might find an even more suitable opportunity that matches your experience. What to expect in the interview process: HR Screen (30 minutes) Hiring Manager Interview (45 minutes) Work Sample Interview (60 minutes)T echnical Interview (60 minutes) Enveda Culture Interview (45 minutes) Some of the total rewards of working here Culture: Enveda lives for people Healthcare: Medical insurance premium for coverage of the employee, spouse, and kids is fully sponsored by the company. The premium for coverage of dependent parents is partially sponsored by the company (at 50%). PTO: Block leaves (that we encourage and celebrate) and company-wide weeklong break to recharge in addition to 8 observed holidays. Work-Life Harmony Come join us! Our employees are the lifeblood of our work and our inspiration to press on. Together weve built a special place here a drug discovery platform thats unique in the world with an incredible team collaborating in a creative, transformative culture. Our mission is to bring hope to patients everywhere. Our progress towards that goal would not be possible without talented people like you. Employee Promise Using our imagination and dedication, we are working to improve human health and give hope to patients everywhere. Our work together is empowering, trustable and collaborative, enabling you to do your best work. Envedas values Curiosity : Learn and challenge. Agency : Own and initiate. Journey : Love the process. Charity : Take care of each other. Unity : We are one Enveda. We value your uniqueness One of lifes gifts is to interact with a variety of people. Each of us has a unique story that shapes how we view the world, and solve problems. Learning from each other enhances our collective wisdom while achieving better outcomes at a faster clip. People from all kinds of backgrounds can succeed in all kinds of roles. Our work environment appreciates the contributions of every person. Working together is how we produce results that illuminate our Purpose - To Deliver Hope To Every Patient. Unity is a company value because success depends on trusting, working relationships that respect the commonality and differences of people. At Enveda we are building a place where every person can do the best work of their lifetime. Enveda is an equal opportunity employer. We do not discriminate on the basis of characteristics protected by federal, state or local laws. *Please note jobs may be taken down from our website, this does not mean they have been filled. This is to maintain our candidate experience for current applicants. If you are in the interview process and would like to request a copy of the job description, reach out to your recruiting contact.

1) Expertise in identification techniques using Mass, NMR, HPLC, GC, and IR 2) Expertise in handling of various Cryogenic, Pyrophoric or Hazardous Chemicals. 3) Ability to work on new molecules. 4) Ability to handle multi step synthesis. 5) Calibration of equipment related to downstream processing. 6) Responsible for conducting experiments. 7) Drive continuous improvement by leveraging Process Intensification technologies including flow chemistry to reduce cost, reduce waste, improve yield. 8) Assess and manage process risks arising from scale or process changes. 9) Improve Process safety by training plant personnel and working on safety improvement projects. 10) Competency to deliver on time bound projects.

As an Assistant Manager - Payroll,?you will be supporting the end-to-end payroll related activities while ensuring you are adhering to the policies and processes. Your primary responsibilities include:? Process payroll data in accordance with legal, IBM and customer requirements related to personal data protection Ensure the timeliness of payroll processing (sending inputs to payroll services providers, approving payrolls) Ensure the timeliness of payroll payments processing (requesting uploads and payments releases, uploading payroll payments into the bank system, monitoring the rejected payments) Carry out the validation of payroll inputs and the reconciliation of output files and properly handle any discovered errors/discrepancies? Monitor execution of compliance activities if required Perform any activities related to electronic payslip handling Communicate any risks to the?payroll process or deadlines in accordance with escalation paths Interact with employees, clients, payroll stakeholders or third-party providers to process payroll data and ensure the correct and timely pay Report the status of the?payroll cycle in a timely and accurate manner Support year-end processes or any other country-specific processes not related to the?monthly payroll cycle Initiate and actively support any continuous improvement activities or other process and/or tool improvements using the existing change management channels Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise Graduate or postgraduate with 6-8 years of experience in payroll operations for any International IT / ITES Company Good communication skills in English both oral & written Strong knowledge of MS Excel and MS Word Ability to pre-empt potential issues and reprioritize work to meet ever-changing needs of customers both internal and external; proactively follows up with key customers on resolution and action plans Ability to think through complex issues and situations and develop robust, well-thought-out solutions that meet the needs of the business Effectively Works with Others - Works well with internal customers and external suppliers and can positively influence others in problem-solving and work process improvements Excellent Customer Service skills – ability to communicate to all people at all levels within the organization. Proven experience in People management will be an added advantage. Must have the ability to resolve difficult customer service issues

Title: Group Leader - Personal Care Level: AGM Qualification: M.Sc in Organic Chemistry, Ph.D. is desirable. Experience: In Fine Chemical / Surfactants Industry for use in Cosmetics / Personal Care products as Raw Materials / Ingredients 15 years minimum to 22 years. 4-5 Team members will report to this role. Working : Alternate Saturday off. Industry: Fine Chemicals / Surfactants Chemicals Mfg for Cosmetics / Personal Care Key Responsibilities include: Assessment of the given Molecule w.r.t. Literature Search , Route Proposition, Cost of Raw Material Contribution Calculation (RMC) Synthesis, execution planning & scheduling of Chemicals as your assigned project. Planning & execution of activities like Vendor Qualification, Generation of specifications for RMs & KRMs Liaising with Procurement to achieve milestones for lab development activity Ensure availability of all required resources for your Projects Lead & troubleshoot the validation of the developed processes in pilot & commercial plant scale.

Role & responsibilities Improve delivery efficiency and quality through delivery management Ensure seamless execution of project through effective planning Build Lasting client relationship Ensure safety at work through enforcement of best lab management practices Maintain records, date integrity and IP confedentiality Ability to Literature search, conduct experiments and monitor reactions with the aid of minimum supervision. Adherence to online documentation, quality standards, safety standards & delivery timelines Provide necessary support to kilo lab/manufacturing team. Ensuring full adherence to safety & quality SOPs Document the reactions executed, research findings/observations accurately in ELNB to ensure data integrity. Maintain strict IP Confidentiality and adhere to all policies. Preferred candidate profile PHD (Organic Chemistry) with 0-4 years of relevant experience