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software engineer ii

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research scientist

scientist ii bioassay

US Pharmacopeia

<div>
 
 Description
 
 
 
 At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
 
 
 USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds&mdash;regardless of background&mdash;to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
 
 
 
 Brief Job Overview
 
 
 
 This is a hands-on, non-supervisory position in USP-India's Biologics laboratory. In this position, the scientist will spend 80-100% of the time in laboratory and will perform bioassays and binding for various biologics product class such as recombinant proteins and mAbs, perform vaccine and cell and gene therapy (CGT) functional characterization assays, and viral assays. Scientist will be responsible for hands-on execution of projects which can be collaborative testing of reference standards, characterization of biological products, method development and validation for development of standards (Documentary Standards, Physical Reference Standard &amp; Performance Standards). Responsible for supporting activities related to India Biologics laboratory.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
 
 
 Additionally, USP&rsquo;s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
 
 
 <ul>
 <li>
 Proficient in in vitro cell based relative potency.
 </li>
 <li>
 Proficient in handling cell lines and primary cells. Experienced in functional activity and immunogenicity assays.
 </li>
 <li>
 Experienced in method qualification and validation, protocol, and report writing.
 </li>
 <li>
 Plans and executes research projects under supervision.
 </li>
 <li>
 Works with cross-functional teams within the organization to solve/support both technical and
 
 
 </li>
 </ul>
 process-related issues.
 
 
 <ul>
 <li>
 Keeps abreast of current trends and developments in related scientific field.
 </li>
 <li>
 Seeks out innovative ways to apply knowledge or skills to improve protocols and results
 </li>
 <li>
 Assists team lead in planning, implementing, and evaluating laboratory procedures/systems
 </li>
 <li>
 Supports in departmental trainings as applicable.
 </li>
 <li>
 Attends scientific seminars and conferences
 </li>
 <li>
 Supports lab management activities
 </li>
 <li>
 Follows GLP and QMS practices. Recommend improvement to systems and all other supporting
 
 
 </li>
 </ul>
 activities as assigned by the team lead. Participates in internal and external audits.
 
 
 <ul>
 <li>
 Aligns with USP's mission, and complies with USP's guidelines and other requirements
 </li>
 <li>
 Performs other duties as assigned.
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 
 
 MSc. in Biochemistry, or related Biological Science field with 3-6 years of Industrial experience in bio pharmaceutical product development and quality testing, relative potency assays, mAb functional assays, expertise in flow cytometry, and primary cell culture. Able to analyze and interpret data using appropriate statistical software/methods and calculation for relative potency determination.
 
 
 <ul>
 <li>
 An equivalent combination of education and experience may be substituted. Laboratory experience must include expertise developing and validating assays, and QMS knowledge and experience.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 <ul>
 <li>
 Working experience in the biotechnology/biopharmaceutical industry strongly preferred.
 </li>
 <li>
 Demonstrated research, technical, and analytical skills, as well as the ability to take highly technical scientific information and make recommendations.
 </li>
 <li>
 Ability to learn new technologies and strong computer, scientific, and organizational skills.
 </li>
 <li>
 Good written and verbal communication skills, time management skills as well as interpersonal skills.
 </li>
 <li>
 Individual must possess the ability to handle multiple priorities in fast-paced environment.
 </li>
 <li>
 Experience with reference materials development is a plus.
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 Benefits
 
 
 
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
 
 
 Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Scientist II, Bioassay

MetLife

<div>
 
 Requirements
 
 
 
 
 Description and Requirements
 
 
 
 
 GOSC- GG10- Data Scientist (IC)
 
 
 
 
 Position Title:
 
 
 
 Senior Data Scientist (IC)
 
 
 
 Function, Responsibility Level:
 
 
 
 
 Reports to (Responsibility Level):
 
 
 
 
 GG13 Director Data science or
 
 
 
 
 GG12 Lead Data Scientist
 
 
 
 
 Supervises:
 
 
 
 
 Location:
 
 
 
 Hyderabad/Noida
 
 
 
 Global Grade: 10
 
 
 
 
 Cost Center (85 series):
 
 
 
 ####
 
 
 
 Complexity:
 
 
 
 
 PID/s Load Mapping:
 
 
 
 
 Position Summary
 
 
 
 Continuing with the tradition of innovation, MetLife, as part of its Data and Analytics function, has established a Data and Analytics (DnA) center in India. The setup of DnA center is a key multi-year strategic initiative focused on scaling business solutions using AI, data science, data governance, data engineering, business intelligence, agile project management capabilities, enabling more cost-effective analytics operating model and increasing AI maturity across the MetLife global community.
 
 
 
 Role Value Proposition:
 
 
 
 We are looking for you: high performing data and analytics professional - driven by passion and purpose, to drive quality standards and support end-to-end development of actionable, high-impact AI solutions for MetLife&rsquo;s enterprise functions and lines of businesses across markets.
 
 
 This position requires hands-on experience of developing an end-to-end Machine Learning/AI solution that can be leveraged for maximum business impact through on prem /cloud in both real time and batch mode depending upon business requirements. The role would collaborate with multiple stakeholders under the guidance of Lead/Director Data scientists to develop robust, stable, and scalable advanced analytics/machine learning solutions leveraging new age methodologies/techniques. Superior problem-solving ability, curiosity, strong coding skills and attention to detail are the key success factors.
 
 
 
 Job Responsibilities
 
 
 
 <ul>
 <li>
 Hands on development and implementation of AI/ generative AI models &amp; algorithms to solve complex problems and drive innovation across organization.
 </li>
 <li>
 Collaborate with Lead Data Scientist/AI product owner to translate given business problem into analytical use-cases with defined outcomes.
 </li>
 <li>
 Perform data exploration, machine learning models development &amp; active collaboration with cross functional teams
 </li>
 <li>
 Contribute to the implementation of AI solutions to deliver business impact with focus on value, success criteria alignment, scalability, and operationalization.
 </li>
 <li>
 Drive best practices throughout development process, efficient coding and publish learnings/feedback for continuous learning.
 </li>
 <li>
 Drive innovation within teams, by enhancing existing solutions and designing new ones.
 
 
 
 </li>
 </ul>
 
 Knowledge, Skills, And Abilities
 
 
 
 
 Education
 
 
 
 Bachelor&rsquo;s/master&rsquo;s degree in an information technology/computer science or relevant domain
 
 
 
 Experience
 
 
 
 
 Technology Skills
 
 
 
 <ul>
 <li>
 3-5 years of hands-on experience in Analytics, data science or similar function
 </li>
 <li>
 Strong hands-on proficiency in any of Data Science technologies i.e., Python, PySpark,
 
 
 
 </li>
 </ul>
 , R &amp; have experience in machine learning libraries &amp; frameworks such as
 
 
 TensorFlow, PyTorch, or Keras.
 
 
 <ul>
 <li>
 Strong hands-on expertise in traditional as well as modern statistical &amp; ML techniques like regression, support vector machines, Regularization, Boosting, Random Forests &amp; other ensemble methods.
 </li>
 <li>
 Good Understanding of NLP models using: Nltk, spacy, Word 2 Vec , BERT etc.
 </li>
 <li>
 Experience in technologies like Azure, AWS, and advanced analytics concepts like
 
 
 
 </li>
 </ul>
 Simulation, Deep Learning etc. are considered as a plus.
 
 
 <ul>
 <li>
 Ability to meet deadlines for product deliverables in a timely, proactive, and
 
 
 
 </li>
 </ul>
 entrepreneurial manner.
 
 
 
 General Management skills:
 
 
 
 <ul>
 <li>
 Analytical and problem-solving skills to ideate.
 </li>
 <li>
 Excellent written and verbal communication skills; ability to discuss technical issues with peers, business stakeholders and senior management.
 </li>
 <li>
 Strong conceptual and creative problem-solving skills; ability to learn new and complex concepts quickly.
 
 
 
 </li>
 </ul>
 
 Working Relationships
 
 
 
 
 Internal Contacts
 
 
 (And purpose of relationship):
 
 
 
 MetLife GTO Engineering, Digital Office and Global Data and analytics
 
 
 Business
 
 
 GOSC Leadership
 
 
 
 External Contacts
 
 
 
 (And purpose of relationship) &ndash; If Applicable
 
 
 Vendors
 
 
 Consultants
 
 
 
 About MetLife
 
 
 
 Recognized on Fortune magazine's list of the "World's Most Admired Companies" and Fortune World&rsquo;s 25 Best Workplaces&trade;, MetLife, through its subsidiaries and affiliates, is one of the world&rsquo;s leading financial services companies; providing insurance, annuities, employee benefits and asset management to individual and institutional customers. With operations in more than 40 markets, we hold leading positions in the United States, Latin America, Asia, Europe, and the Middle East.
 
 
 Our purpose is simple - to help our colleagues, customers, communities, and the world at large create a more confident future. United by purpose and guided by our core values - Win Together, Do the Right Thing, Deliver Impact Over Activity, and Think Ahead - we&rsquo;re inspired to transform the next century in financial services. At MetLife, it&rsquo;s #AllTogetherPossible . Join us!
</div>

Data Scientist - I

PI Health Sciences Ltd

<div>
 
 
 Job Title: Research Scientist / Senior Research Scientist &ndash; Process R&amp;D
 
 
 
 
 Department:
 
 R&amp;D &ndash; Process Development
 
 
 
 Industry:
 
 CDMO / API
 
 
 
 
 
 
 Purpose of the Role:
 
 
 
 To lead and execute the development, optimization, and scale-up of robust, cost-effective, and regulatory-compliant chemical processes for Active Pharmaceutical Ingredients (APIs) and intermediates, ensuring smooth technology transfer from lab to kilo lab and manufacturing.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 1. Strategic Responsibilities
 
 
 <ul>
 <li>
 Drive innovation by designing synthetic routes that align with project timelines and regulatory requirements.
 </li>
 <li>
 Contribute to technology differentiation strategies that enhance the CDMO&rsquo;s scientific credibility and client value proposition.
 </li>
 <li>
 Collaborate with cross-functional teams (Analytical, QA/QC, and Regulatory) to support integrated drug development solutions.
 </li>
 </ul>
 
 
 2. Operational Responsibilities
 
 
 <ul>
 <li>
 Perform route scouting and literature searches, and develop robust and scalable chemical processes using QbD principles.
 </li>
 <li>
 Conduct laboratory experiments for reaction optimization, impurity profiling, and process safety assessment.
 </li>
 <li>
 Prepare and review technical reports, SOPs, and technology transfer documents.
 </li>
 <li>
 Ensure compliance with GMP/GLP and EHS standards during lab-scale and pilot-scale operations.
 </li>
 <li>
 Participate in troubleshooting during scale-up or commercial production batches and provide technical support during client audits.
 </li>
 </ul>
 
 
 3. Financial Responsibilities
 
 
 <ul>
 <li>
 Optimize process economics by reducing cycle time, yield improvement, and minimizing raw material costs.
 </li>
 <li>
 Support cost estimation activities during project proposals or client RFQs by providing technical insights.
 </li>
 </ul>
 
 
 4. People &amp; Collaboration Responsibilities
 
 
 <ul>
 <li>
 Guide junior team members on experimental planning, data interpretation, and documentation best practices.
 </li>
 <li>
 Promote a culture of safety, learning, and innovation within the team.
 </li>
 <li>
 Work closely with program management and business development to align project goals with customer expectations.
 </li>
 </ul>
 
 
 
 
 
 Qualifications &amp; Experience
 
 
 <ul>
 <li>
 M.Sc. (Organic Chemistry) / PhD
 </li>
 <li>
 3&ndash;7 years of experience in Process R&amp;D, preferably in CDMO organizations
 </li>
 <li>
 Hands-on expertise in synthesis, scale-up, impurity profiling, and technology transfer
 </li>
 <li>
 Familiarity with analytical techniques (HPLC, GC, NMR) and regulatory documentation
 </li>
 </ul>
 
 
</div>

Research Scientist

ProPharma

<div>
 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality &amp; compliance, pharmacovigilance, medical information, and R&amp;D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners&rsquo; most high-profile drug and device programs.
 
 
 
 Job Summary
 
 
 
 The Pharmacovigilance (PV) Scientist supports the activities in the Benefit Risk group by ensuring that day-to-day operational activities are completed. The PV Safety Scientist is expected to be professional and diligent and liaise with the director and management group members within the team on any issues, as well as coordinate the work with the senior PV Scientists. The PV Safety Scientist is also expected to lead by example and ensures quality standards are upheld within the company.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Authoring of Aggregate reports (PSURs/PBRERs, PADERs/Annual Reports/ ACO/ DSUR) for submission to local and other Health Authorities.
 </li>
 <li>
 Authoring of Risk Management Plans (RMPs) as a part of regular Pharmacovigilance activities.
 </li>
 <li>
 Authoring of Signal Management Reports.
 </li>
 <li>
 Performing literature search and validity check for the aggregate reports.
 </li>
 <li>
 Reconciliation of relevant process trackers.
 </li>
 <li>
 Extraction and validation of data (RSI, Sales, previous reports, RMP, signals).
 </li>
 <li>
 Generation of Line Listings (LL) from safety database
 </li>
 <li>
 </li>
 <li>
 Providing reliable support for high priority Ad-hoc activities.
 
 
 </li>
 </ul>
 
 Necessary Skills And Abilities.
 
 
 
 <ul>
 <li>
 Analytical and problem-solving skills.
 </li>
 <li>
 Sound organizational skills
 </li>
 <li>
 Able to work within a team in an open and professional manner
 </li>
 <li>
 Excellent attention to detail and focus on quality
 </li>
 <li>
 Understanding of ICH-GCP, FDA, EMA and other relevant Global regulations related to PV
 </li>
 <li>
 Demonstrable ability to analyze and quantify large volumes of data in a concise and scientific manner, in keeping with regulatory deadlines.
 </li>
 <li>
 Awareness of global culture and willingness to work in a matrix environment
 </li>
 <li>
 Knowledge in other pharmacovigilance processes, ability to author/update SOPs or WIs, to identify and author deviations/CAPAs."
 </li>
 <li>
 Ensuring that deliverables to the clients comply with the relevant regulatory requirements and are sent to the client within agreed timelines.
 </li>
 <li>
 Capability to make concise, accurate and relevant synopses of medical text and data, and the ability to write unambiguous medical text
 </li>
 <li>
 Computer proficiency, IT skills, expertise and an ability to work with web based applications, and familiarity with the Windows Operating system and the MS Office suite (Word/Excel/Power Point)
 
 
 </li>
 </ul>
 Educational requirements
 
 
 <ul>
 <li>
 Bachelor/master&rsquo;s degree in pharmacy, Nursing, Life Science, or other health-related field, or equivalent qualification/work experience
 
 
 </li>
 </ul>
 
 Experience Requirements
 
 
 
 <ul>
 <li>
 2+ years&rsquo; experience in Pharmacovigilance with a focus on medical writing and/or literature search and/or signal detection
 </li>
 <li>
 Experiences in contributing to the compilation of metrics and participating in discussions about quality internally and with Clients
 </li>
 <li>
 Experience in literature screening activities and/or experiences in authoring and reviewing aggregate reports
 
 
 </li>
 </ul>
 We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
 
 
 ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
</div>

Pharmacovigilance Safety Scientist

Golden Opportunities

<div>
 
 Job Description
 
 
 
 Define, build, and lead a team of Data Scientists and Data analysts Discover areas in operations that can be automated through machine learning Demonstrate through technical knowledge on Statistical modeling, Probability and Decision theory, Operations Research techniques and other quantitative modeling techniques Understand the business reality behind large sets of data and develop meaningful solutions comprising of analytical solutions Work closely with internal stakeholders and align them with respect to your focus area Innovate by adapting new modeling techniques and procedures Implementing and operating stable, scalable data flow solutions from production systems into end-user facing applications/reports.
 
 
 
 Skills Required
 
 
 
 RoleData Scientist
 
 
 Industry TypeIT/ Computers - Software]
 
 
 Functional AreaIT-Software
 
 
 Required Education
 
 
 Employment TypeFull Time, Permanent
 
 
 Key Skills
 
 
 <ul>
 <li>
 DATA SCIENCE
 </li>
 <li>
 MACHINE LEARNING
 
 
 </li>
 </ul>
 Other Information
 
 
 Job CodeGO/JC/1384/2025
 
 
 Recruiter NameRamya V
</div>

Data Scientist - GO/JC/1384/2025

NxtWave

<div>
 
 Job Title:
 
 Full Stack Software Development Engineer &ndash; II (SDE-II)
 
 
 
 Department:
 
 Engineering
 
 
 
 Location:
 
 Hyderabad (Work from Office)
 
 
 
 Employment Type:
 
 Full-time
 
 
 
 🏢 About NxtWave
 
 
 
 
 NxtWave
 
 is one of India&rsquo;s
 
 fastest-growing EdTech startups
 
 , revolutionizing the way India learns technology.
 
 
 Through our
 
 CCBP 4.0 programs
 
 , we empower youth from diverse educational backgrounds to become
 
 highly skilled software professionals
 
 equipped for the 21st-century job market.
 
 
 Founded by
 
 Rahul Attuluri (Ex-Amazon, IIIT Hyderabad)
 
 ,
 
 Sashank Reddy (IIT Bombay)
 
 , and
 
 Anupam Pedarla (IIT Kharagpur)
 
 , NxtWave has raised
 
 ₹275 crore
 
 led by
 
 Greater Pacific Capital
 
 , alongside
 
 Orios Ventures
 
 ,
 
 Better Capital
 
 , and marquee angel investors.
 
 
 As an official
 
 partner of NSDC (Ministry of Skill Development &amp; Entrepreneurship, Govt. of India)
 
 and recognized by
 
 NASSCOM
 
 and
 
 Startup India
 
 , NxtWave is shaping the next generation of tech talent at scale.
 
 
 🌐 Know more about NxtWave
 
 
 📰
 
 Featured in:
 
 Economic Times | CNBC | YourStory | VCCircle
 
 
 
 🚀 Why NxtWave
 
 
 
 As a
 
 Full Stack SDE-II at NxtWave
 
 , you will:
 
 
 <ul>
 <li>
 Build applications at scale and release them quickly to thousands of NxtWave learners &mdash; sometimes within weeks.
 </li>
 <li>
 Take complete ownership of the features you design, working closely with product and UX teams.
 </li>
 <li>
 Thrive in a fast-paced, empowering culture that promotes autonomy, experimentation, and innovation.
 </li>
 <li>
 Fail fast, learn faster: Freedom to try, fail, learn, and improve continuously.
 </li>
 <li>
 Gain first-hand experience in scaling systems and products used by millions.
 </li>
 <li>
 Work in a world-class developer environment, applying best practices in clean code architecture, testing, and CI/CD.
 
 
 </li>
 </ul>
 
 💼 Key Responsibilities
 
 
 
 
 End-to-End Engineering Ownership
 
 
 
 <ul>
 <li>
 Lead design and delivery of complex, full-stack features across frontend, backend, and data layers.
 </li>
 <li>
 Make strategic architectural decisions on frameworks, data models, and performance optimization patterns.
 </li>
 <li>
 Review and approve pull requests, ensuring adherence to clean coding principles and SOLID design patterns.
 
 
 </li>
 </ul>
 
 Frontend &amp; Backend Development
 
 
 
 <ul>
 <li>
 Build and maintain shared UI component libraries and backend microservices for scalable reuse.
 </li>
 <li>
 Implement responsive, accessible, and SEO-optimized UIs following WCAG standards.
 </li>
 <li>
 Design and integrate RESTful and GraphQL APIs with robust validation and security layers.
 
 
 </li>
 </ul>
 
 Performance, Security &amp; Scalability
 
 
 
 <ul>
 <li>
 Identify and eliminate bottlenecks in browser rendering, server throughput, and database queries.
 </li>
 <li>
 Ensure secure code implementation (OAuth2/JWT, XSS/CSRF protection).
 </li>
 <li>
 Manage caching, indexing, and asynchronous processing for high-performance systems.
 
 
 </li>
 </ul>
 
 DevOps, CI/CD &amp; Testing
 
 
 
 <ul>
 <li>
 Own CI/CD pipelines &mdash; automating builds, testing, deployments, and rollbacks.
 </li>
 <li>
 Define and enforce comprehensive testing strategies: unit, integration, and end-to-end.
 </li>
 <li>
 Instrument services with metrics, logging, and observability for better reliability.
 
 
 </li>
 </ul>
 
 Leadership &amp; Collaboration
 
 
 
 <ul>
 <li>
 Partner with Product, UX, and Operations to translate business goals into technical roadmaps.
 </li>
 <li>
 Facilitate sprint planning, estimation, and retrospectives for predictable delivery.
 </li>
 <li>
 Mentor and guide SDE-I engineers and interns, fostering a culture of learning and excellence.
 
 
 </li>
 </ul>
 
 🧠 Qualifications &amp; Skills
 
 
 
 
 Technical Expertise
 
 
 
 <ul>
 <li>
 Experience: 3&ndash;5 years in designing, building, and deploying full-stack production applications.
 </li>
 <li>
 Frontend: React (preferred) or Angular/Vue with TypeScript and modern CSS frameworks.
 </li>
 <li>
 Backend: Node.js (Express/NestJS), Python (Django/FastAPI), or Java (Spring Boot).
 </li>
 <li>
 Databases: MySQL/PostgreSQL with indexing and optimization; NoSQL (Elasticsearch/DynamoDB) and Redis caching.
 </li>
 <li>
 DevOps: Hands-on experience with Docker and AWS services (EC2, Lambda, S3, API Gateway).
 </li>
 <li>
 Testing: Unit/Integration (Jest, pytest) and E2E (Cypress, Playwright).
 </li>
 <li>
 Performance: Strong understanding of frontend profiling (Lighthouse) and backend tracing tools.
 
 
 </li>
 </ul>
 
 Additional Strengths
 
 
 
 <ul>
 <li>
 Sound understanding of secure coding principles and compliance frameworks.
 </li>
 <li>
 Experience reviewing PRs and providing constructive technical feedback.
 </li>
 <li>
 Strong communication skills to simplify complex technical ideas for non-technical stakeholders.
 
 
 </li>
 </ul>
 
 🌟 What We Value
 
 
 
 <ul>
 <li>
 A problem-solving mindset with creativity and analytical thinking.
 </li>
 <li>
 The attitude to own outcomes and deliver excellence.
 </li>
 <li>
 Collaboration and humility &mdash; being flexible, friendly, and team-oriented.
 </li>
 <li>
 A learning-driven mindset, embracing challenges and continuous growth.
 </li>
 <li>
 Open-mindedness to feedback and constant improvement.
 
 
 </li>
 </ul>
 
 📍 Location
 
 
 
 <ul>
 <li>
 Work Location: NxtWave Headquarters, Hyderabad
 </li>
 <li>
 Work Mode: On-site
 
 
 </li>
 </ul>
 
 ✨ Why This Role Matters
 
 
 
 As a
 
 Full Stack SDE-II
 
 at NxtWave, you won&rsquo;t just build software &mdash; you&rsquo;ll shape the infrastructure and experiences that empower
 
 hundreds of thousands of learners
 
 to build their futures.
 
 
 This is your opportunity to grow fast, lead impactful projects, and work in a company redefining tech education in India.
</div>

Software Development Engineer - II

<div>
 
 Description
 
 
 
 
 Who is USP?
 
 
 
 The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide.
 
 
 At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare.
 
 
 USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work&mdash;an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.
 
 
 
 Brief Job Overview
 
 
 
 The role is engaged in the synthesis and delivery of USP Reference Standard candidate materials and API impurities through design and development of cost-effective synthetic routes. Candidate should carry literature search using scientific databases and work on planning and execution of synthesis of target molecules in mg to multigram/KG scale. Candidate should ensure the completion of assigned tasks as per timelines, prepare project reports, communicate with the team and update on the project progress. Candidate should be adherent to quality management systems (QMS) and lab safety practices.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments.
 
 
 
 The Scientist II Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Carry out literature search related to assigned projects using various scientific data base.
 </li>
 <li>
 Design synthetic routes for the target molecules and prepare project proposals with tentative cost estimates
 </li>
 <li>
 Procure key raw materials and reagents required for the project
 </li>
 <li>
 Perform the reactions in small as well as large scale in the lab for the synthesis of target compounds
 </li>
 <li>
 Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems.
 </li>
 <li>
 Troubleshooting synthesis and purification issues
 </li>
 <li>
 Contributing effectively towards more challenging and complex projects through innovative methodologies
 </li>
 <li>
 Ensuring the availability of chemicals and equipment required for the projects and forward the purchase requisitions
 </li>
 <li>
 Interpretation of analytical data of synthesized compounds by IR, NMR, Mass Spectra, Elemental analysis etc.
 </li>
 <li>
 Produce quality materials as per customer requirement
 </li>
 <li>
 Packaging of synthesized compounds
 </li>
 <li>
 Plan, execute and complete the projects as per the timelines
 </li>
 <li>
 Document all experiments conducted as per QMS guidelines.
 </li>
 <li>
 Responsible to ensure the calibrations of the equipment as per the schedule
 </li>
 <li>
 Periodic check of the assigned equipment to ensure its working condition
 </li>
 <li>
 Work on any other assigned tasks/ lab management activities.
 </li>
 <li>
 Conversant with lab safety norms and strictly follow them.
 </li>
 <li>
 Communicate within the team and cross functional teams
 </li>
 <li>
 Learn and practice Diversity, Equity, Inclusion &amp; Belonging culture.
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 
 
 <ul>
 <li>
 M Sc (Organic Chemistry) from a reputed university with minimum 3-6 years of industrial experience in CDMO/CRO/ API Process R&amp;D
 </li>
 <li>
 Strong background in synthetic organic chemistry, Interpretation of spectral data of compounds based on IR, NMR, HPLC, Mass, Elemental analysis and other analysis.
 </li>
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 Ability to independently search literature, design, optimize and develop synthetic processes for any given target molecules/APIs.
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 Hands on experience in process development of diverse chemical class of APIs/ NCEs on lab scale.
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 Excellent troubleshooting skills in synthesis and purification of target compounds.
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 Should possess good verbal and written communication skills.
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 Should possess good organizational, communication, and interpersonal skills.
 
 
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 </ul>
 
 Additional Desired Preferences
 
 
 
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 Extensive knowledge of a wide range of organic reactions, and hands-on experience in handling various sensitive chemicals/reagents.
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 Should have exposure to GMP/GLP environment and documentation procedures. Have good practical, documentation &amp; presentation skills.
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 Attention to detail, strategic thinking and problem-solving skills.
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 Demonstrated ability to work both independently and as a member of a team with a passion for quality
 
 
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 </ul>
 
 Supervisory Responsibilities
 
 
 
 No
 
 
 
 Benefits
 
 
 
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
 
 
 Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
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Scientist II, Synthetics Laboratory

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