399 Spectroscopy Jobs - Page 11

A Trainee Analytical Chemist assists in the analysis of substances to determine their composition and properties. This role involves conducting experiments, analyzing data, and preparing samples under the guidance of senior chemists. They learn to use various analytical techniques and instruments to support research, quality control, or other scientific applications. Here's a more detailed breakdown:Key Responsibilities: Sample Preparation: Preparing samples for analysis by weighing, dissolving, diluting, or otherwise modifying them according to established procedures. Running Experiments: Performing a variety of analytical tests using techniques like spectroscopy, chromatography, or titration, and accurately recording the results. Data Analysis: Analyzing the data obtained from experiments, including calculations and interpretation of results. Maintaining Laboratory Equipment: Ensuring the cleanliness and proper functioning of laboratory equipment, including reporting any malfunctions. Following Procedures: Adhering to strict laboratory safety protocols and standard operating procedures. Essential Skills and Qualifications:. Laboratory Skills: Proficiency in basic laboratory techniques, such as solution preparation, weighing, and handling chemicals. Analytical Skills: Ability to analyze data, interpret results, and draw conclusions. Problem-Solving Skills: Ability to troubleshoot and solve problems that may arise during experiments. Communication Skills: Good written and verbal communication skills for reporting results and collaborating with others. Teamwork: Ability to work effectively as part of a team. Safety Awareness: A strong understanding of laboratory safety procedures and regulations. Job Type: Full-time Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Food provided Health insurance Schedule: Day shift Rotational shift Supplemental Pay: Yearly bonus Work Location: In person

Job Description Job Title: Assistant Manager - Research & Development About The Function Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo’s 30,000+ people work in Supply Chain and Manufacturing. It’s an intricate and sophisticated operation that’s the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We’re committed to realising our ‘Society 2030: Spirit of Progress’ goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we’ll help you to thrive in our inclusive culture. About The Role This role is responsible for executing and managing analytical R&D projects related to alcoholic beverages. It includes conducting precise chemical and instrumental analysis of raw materials, intermediates, and finished liquids in alignment with defined test methods, Good Laboratory Practices (GLP), and ISO 17025 requirements. The position also supports senior analysts in innovation and research initiatives and contributes to technical capability building across stakeholders through training and knowledge sharing. Role Responsibilities Key Technical Responsibilities: Conduct and support analytical R&D projects for product and process development Perform chemical analysis on raw materials, intermediates, and finished liquids using validated methods Ensure compliance with GLP and ISO 17025 in all laboratory operations Assist in method development, verification, and validation Train internal teams and stakeholders on analytical techniques and data interpretation Core Technical Competencies Instrumental Techniques: Proficient operation and data interpretation of: GC-FID / GC-ECD/GC-MS – For volatile compounds, congeners, fusel oils HPLC– For organic acids, polyphenols, flavor-active compounds UV-Vis Spectroscopy – For color, % transmittance, phenolic profiling Strong hands-on experience in general laboratory instrumentation: pH meter, Conductivity meter, Turbidity meter, etc. Classical Wet Chemistry Techniques Titration for acidity, sulfur content, etc. Alcohol content analysis using pycnometer, hydrometer, or digital density meter Analytical Methodology & Validation Sound knowledge of: Method development, verification, and validation Instrument qualification (IQ/OQ/PQ) Calibration and measurement uncertainty Determining LOD/LOQ Chemometric tools and application of statistical techniques (e.g., ANOVA, control charts) Data Handling & Reporting Understanding of data analytics and statistical tools for research applications Clear, structured reporting and presentation of analytical findings Accurate and timely documentation of results as per regulatory and internal standards Leadership & Behavioral Expectations Organizational Impact: Understands role priorities and delivers as per direction from manager. Supports team-level goals and process improvements. Decision-Making & Problem Solving: Anticipates analytical challenges and recommends practical, data-based solutions. Integrates technical knowledge with insights to improve outcomes. Communication & Collaboration: Clearly articulates scientific findings in verbal and written form. Engages cross-functional teams through knowledge sharing and training initiatives. Self-Management & Ownership: Independently plans workload and seeks guidance when needed. Demonstrates accountability, precision, and curiosity in laboratory work. Experience / Skills Required Education: PhD or MSc in Analytical Science / Chemistry / Organic Chemistry Experience: Minimum 5 years of experience in chemical and instrumental analysis in the food and beverage or allied industries Flexible Working Statement: Flexibility is key to our success. From part-time and compressed hours to different locations, our people work flexibly in ways to suit them. Talk to us about what flexibility means to you so that you’re supported from day one. Diversity statement: Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this. We embrace diversity in the broadest possible sense. This means that you’ll be welcomed and celebrated for who you are just by being you. You’ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more. Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world. Feel inspired? Then this may be the opportunity for you. If you require a reasonable adjustment, please ensure that you capture this information when you submit your application. Worker Type Regular Primary Location: Bangalore Technical Centre Additional Locations : Job Posting Start Date 2025-07-01

Functional or Technical skills JOB DESCRIPTION Job Role : Analytical Chemistry-Analyst (NPD) Department : Analytical - BGRC Job Location : Bangalore About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures 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: This role involves method development, method validation, method transfer and R&D stability studies by using laboratory instruments like Ultra performance liquid chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectrophotometer, Polarimeter, Particulate matter analysis using Malvern, PAMAS, HIAC and other relevant instrumentation techniques. etc. Role Accountabilities: Must have strong hands-on experience in development and validation of Assay & related substances methods for drug substance/drug product. Must have experience in handling HPLC, UPLC (Empower-3 software), GC, UV Visible spectrophotometer balances, Potentiometer, and stability chambers, Particulate matter analysis techniques. Shall have experience on Good documentation/laboratory practices such as ALCOA+. Experience in calibration and qualification of various analytical instruments HPLC, UPLC, GC, and other QC laboratory instruments Shall prepare and review the raw data sheets, instrument operating procedures, and standard operating procedures Shall have good experience in handling of QMS (such as incidents, Out of Specifications, Deviations, and Change control). Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards / Chemicals / Reagents / Consumables / Spares etc., required for the projects Shall adhere to the procedure of GxP/Safety and as per the procedure defined in the internal standard operation procedure Shall operate the MS office (word, excel, ppt), outlook, and other essential tools required for routine activity Must possess good communication and e-mail etiquettes. Behavioural Skills Good Interpersonal skills Self-time management Good team player Good communication skills Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience 0-6 years Skills and Capabilities: Hands-on HPLC, UPLC/UHPLC, CG, UV-visible spectrophotometer, Potentiometer, Particulate matter analysis techniques and QC other analytical instruments Theoretical knowledge in Chromatography and spectroscopy technique Good documentation/laboratory practices such as ALCOA+. Able to follow work instructions and perform the tasks under the supervision of the Team leader Preparation and Maintenance of all the documents Good knowledge of MS-office (word, excel, ppt) Education M. Pharm/ M. Tech/ M.Sc. / B.Tech., B.Sc. (Analytical chemistry/Chemistry) Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Job Title: Chemist / Analytical Chemist / QC Manager Location: Palakkad Salary: Up to ₹40,000 per month (based on experience and designation) Job Description: We are looking for a dedicated and experienced Chemist , who can be considered for roles ranging from Analytical Chemist to QC Manager , based on their skills and experience. The ideal candidate will be responsible for conducting quality control tests, analytical testing, and ensuring compliance with industry standards. Key Responsibilities: Perform chemical analysis and laboratory tests on raw materials, in-process samples, and finished products. Maintain and calibrate laboratory instruments and equipment. Prepare and maintain accurate documentation of test results and procedures. Ensure all activities comply with safety, environmental, and quality standards. Review and approve quality control reports (for senior-level roles). Guide and supervise junior chemists or lab technicians (for QC Manager role). Coordinate with the production team for quality improvements and issue resolutions. Requirements: Bachelor’s or Master’s degree in Chemistry or related field. 2+ years of experience in a similar role in a manufacturing or pharmaceutical industry. Strong knowledge of analytical techniques such as HPLC, GC, UV-Vis Spectroscopy, etc. Experience with documentation and quality systems (GMP/GLP preferred). Leadership and team-handling experience is a plus (required for QC Manager role). Designation Offered: Will be finalized based on the candidate's profile — Chemist / Analytical Chemist / QC Manager. Interested candidates can send their updated resume to mdjinitha@gmail.com Job Type: Full-time Schedule: Day shift Work Location: In person

Please call 9947350555 more details Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. Male candidate can apply Using chromatography, spectroscopy, and spectrophotometry techniques. Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. Conferring with scientists and engineers to analyze, interpret, and develop tests. Introducing heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Writing technical papers and reports, and preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and purchasing new laboratory supplies. Evaluating and ensuring compliance with laboratory safety procedures and standards. Job Type: Full-time Pay: ₹16,500.00 - ₹18,000.00 per month Benefits: Health insurance Provident Fund Schedule: Rotational shift Education: Bachelor's (Preferred) Language: Malayalam (Preferred) Work Location: In person Speak with the employer +91 9947350555

UPLC Knowledge must Pharma Company Exp Required Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials Required Candidate profile Experience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC.

Role Overview We are hiring a Product Manager – Analytical to manage a strategic portfolio of advanced instrumentation, including: Horiba – Particle Size Analyzers, Raman Spectroscopy, and Optical Spectroscopy Nicoya – Surface Plasmon Resonance (SPR) platforms for biomolecular interaction studies AES – iCIEF systems for charge heterogeneity and protein characterization The Product Manager will focus on portfolio strategy, business development, and sales enablement, working closely with our Field Application Scientists (FAS) for technical execution. ⸻ Key Responsibilities Own the business strategy and growth plan for Horiba, Nicoya, and AES product lines. Support the sales team in lead generation, customer segmentation, and pricing strategy. Collaborate with FAS for demos, installations, and technical discussions. Build relationships with key biopharma and research customers across India. Coordinate with global principals for training, updates, and commercial alignment. Monitor market trends and competitor activity to guide positioning and differentiation. Plan and execute marketing initiatives including webinars, workshops, and industry events. Work cross-functionally with service, logistics, and regulatory teams. ⸻ Candidate Profile Bachelor’s or Master’s in Life Sciences, Biophysics, Chemistry, or related field. 3–6 years of experience with scientific instrumentation (biopharma or analytical focus preferred). Strong understanding of analytical platforms used in biologics characterization. Excellent communication, commercial thinking, and stakeholder management skills. Willingness to travel across India. Job Type: Full-time Work Location: In person

QC chemist For Agro chemical Industry In Saykha, Bharuch, Gujarat Job Title : Chemist Department : Quality Assurance & Quality Control Experience Required : 06-08 years (Agrochemical or Chemical Industry Experience Must) JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 1 Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. (qualitative and quantitative chemical and collect/physical analysis of raw materials, finished products and/or stability samples) 2 Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. 3 Using chromatography, spectroscopy, and spectrometer techniques. 4 Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. 5 Conferring with scientists and engineers to analyze, interpret, and develop tests. 6 Writing and preparing standards and specifications for processes, tests, and products. 7 Maintaining laboratory instruments, troubleshooting malfunctions. 8 ensuring compliance with laboratory safety procedures and standards. 9 Strong problem-solving, critical thinking, and analytical skills. 10 Experience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC. Experience 3 - 8 Years Industry Manufacturing Production Quality Qualification B.Sc, M.Sc Key Skills Pharmaceutical QC Chemist Bharuch Agro Chemical MSC Chemistry GC-MS Agrochemical Chemical Test Procedures UPLC Chromatography Finished Products LCMS Quality Control

About the team: The AI Core team is a small and nimble team focused on AI innovation, experimental modelling, and scientific validation. Its mission is to build highly efficient, adaptable and efficacious large models for multiple general-purpose applications in chemical metrology. To stay aligned with the mission, the team follows advancements in AI, including next-generation deep learning architectures, autonomous agents, large-scale optimization algorithms, reinforcement learning methodologies, and innovative data simulation techniques. Machine Learning Scientist The Machine Learning Scientist is critical to the AI Core team by creating AI models from the ground up and steering model development through every stage, leading to the fulfilment of the research objective. Responsibilities: Experiment with advanced architectures like CNNs, RNNs, transformers, autoencoders etc. appropriate for the research objective Develop training strategies (e.g., self-supervised learning, few-shot learning) - Optimize loss functions and metrics for performance, manage hyperparameter tuning - Optimize training pipelines and debug training failures - Develop reproducible training/evaluation pipelines. Skills: Expertise in PyTorch/TensorFlow or other frameworks Strong Python skills (NumPy, SciPy, scikit-learn) and GPU acceleration (CUDA, cuDNN) Experience with ML experiment tracking (W&B, MLflow etc.) Experience with RL frameworks (Stable Baselines3, Ray RLlib) Passion: Building AI agents with superior capabilities Qualifications: Bachelor's or Master's degree in Data Science, Computer Science, or a related technical field. 8+ years of experience in machine learning and deep learning Prior roles within AI research teams Background in chemometrics, spectroscopy, or analytical chemistry, desirable Advantage: Networks involving very large matrix operations About Picarro: We are the world's leader in timely, trusted, and actionable data using enhanced optical spectroscopy. Our solutions are used in a wide variety of applications, including natural gas leak detection, ethylene oxide emissions monitoring, semiconductor fabrication, pharmaceutical, petrochemical, atmospheric science, air quality, greenhouse gas measurements, food safety, hydrology, ecology, and more. Our software and hardware are designed and manufactured in Santa Clara, California and are used in over 90 countries worldwide based on over 65 patents related to cavity ring-down spectroscopy (CRDS) technology and are unparalleled in their precision, ease of use, and reliability. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, gender identity, social orientation, nor on the basis of disability. Posted positions are not open to third party recruiters/agencies and unsolicited resume submissions will be considered free referrals. If you are an individual with a disability and require reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Picarro, Inc. at disabilityassistance@picarro.com for assistance.

Department :- Quality Assurance & Quality Control Experience Required :- 06-08 years (Agrochemical or Chemical Industry Experience Must) JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 1 Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. (qualitative and quantitative chemical and collect/physical analysis of raw materials, finished products and/or stability samples) 2 Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. 3 Using chromatography, spectroscopy, and spectrophotometry techniques. 4 Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. 5 Conferring with scientists and engineers to analyze, interpret, and develop tests. 6 Writing and preparing standards and specifications for processes, tests, and products. 7 Maintaining laboratory instruments, troubleshooting malfunctions. 8 ensuring compliance with laboratory safety procedures and standards. 9 Strong problem-solving, critical thinking, and analytical skills. 10 Experience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC

Job Title: Research Associate API R&D Experience: 2-3 Years Qualification: MSc in Organic Chemistry Job Location: R & D, Mahape, Navi-Mumbai . Job Description: We are seeking a motivated and skilled Research Associate to join our API R&D team . The ideal candidate will have 2-3 years of experience in Active Pharmaceutical Ingredient (API) research and development, with a strong educational background in chemistry. Key Responsibilities: Conduct experiments for the development of APIs , including synthesis , optimization, and process development. Perform literature searches and study patents to design and develop cost-effective, scalable, and efficient synthetic routes. Optimize reaction parameters such as yield, purity, and productivity while adhering to project timelines. Work on process validation and transfer from the laboratory to pilot and production scale. Prepare and maintain accurate documentation, including laboratory notebooks, development reports, and other required records. Collaborate with cross-functional teams, including Analytical, Quality, and Regulatory departments, to ensure project alignment. Ensure compliance with GMP and safety protocols in all laboratory activities. Stay updated on advancements in API R&D and integrate innovative techniques into projects. Key Skills and Competencies: Strong knowledge of organic synthesis and process development. Experience with API manufacturing processes and regulatory requirements . Proficiency in analytical techniques such as HPLC, GC, and spectroscopy (NMR, IR, MS). Good problem-solving skills and attention to detail. Strong documentation and reporting skills. Ability to work independently and in a team environment. Preferred Skills: Experience in handling scale-up operations and technology transfer. Familiarity with regulatory guidelines such as ICH, FDA and EMEA.

Job Summary: The R&D Chemist is responsible for conducting research, developing new chemical products, and improving existing formulations. This role involves working in a laboratory setting, performing experiments, analyzing data, and ensuring that products meet the required quality, safety, and performance standards. The R&D Chemist will collaborate with cross-functional teams to drive innovation and support the companys product development initiatives. Key Responsibilities: Research & Development: Conduct experiments to develop new chemical products or improve existing formulations. Perform research on the properties, composition, and reactions of substances to develop new processes or materials. Develop formulations for chemical products, ensuring that they meet performance, quality, and safety standards. Innovate new product ideas and applications based on market trends, customer needs, and emerging technologies. Analyze experimental data, interpret results, and make recommendations for further research or product optimization. Laboratory Work: Perform laboratory experiments using chemical techniques, including synthesis, purification, and characterization of chemical compounds. Maintain accurate records of experimental procedures, results, and observations in laboratory notebooks. Operate and maintain laboratory equipment, ensuring accurate and reliable results. Ensure that all laboratory work complies with safety regulations and standard operating procedures (SOPs). Product Testing & Analysis: Conduct tests to evaluate the performance, stability, and safety of chemical products. Use analytical techniques such as chromatography, spectroscopy, and titration to measure the chemical properties of substances. Interpret test results and adjust formulations to optimize product performance or resolve issues. Work closely with quality control and production teams to ensure that products meet required standards before commercialization. Collaboration & Cross-functional Support: Collaborate with the production, quality assurance, and regulatory teams to ensure that new formulations are scalable for manufacturing. Support the technical sales team by providing expertise on the chemical properties and applications of products. Liaise with suppliers and external research institutions to source materials or gather information for product development. Documentation & Reporting: Prepare detailed reports on research findings, product development progress, and experimental results. Document all research and development activities, ensuring that accurate records are maintained for regulatory and patent purposes. Present research findings and new product ideas to senior management and other departments. Assist in preparing technical documentation for new product launches or regulatory submissions. Regulatory Compliance & Safety: Ensure that all R&D activities comply with relevant regulatory standards and industry guidelines. Follow proper safety protocols in the laboratory, ensuring safe handling, storage, and disposal of chemicals. Stay up-to-date with changes in chemical regulations and industry trends to ensure that products are compliant. Continuous Improvement & Innovation: Stay informed about advancements in chemical research, materials science, and industry technologies. Participate in training and development programs to enhance knowledge of new methods, tools, and techniques. Propose new ideas and improvements for products, processes, and materials to keep the company at the forefront of innovation. Qualifications: Bachelors degree in Chemistry, Chemical Engineering, or a related field. 3+ years of experience in an R&D or laboratory environment, preferably in the chemical, pharmaceutical, or materials industries. Strong knowledge of chemical synthesis, formulations, and analytical methods. Experience with laboratory techniques such as chromatography, spectroscopy, and titration. Excellent problem-solving skills and attention to detail. Proficiency in using laboratory equipment and software for data analysis. Ability to work independently and as part of a team in a dynamic, fast-paced environment. Preferred Qualifications: Masters degree or PhD in Chemistry or related discipline. Experience in product development in industries such as coatings, adhesives, polymers, or specialty chemicals. Familiarity with regulatory standards (e.g., REACH, OSHA, GHS) and industry-specific guidelines. Knowledge of Good Laboratory Practices (GLP) and ISO standards. Strong project management and communication skills.

Job Description : Carry out Experiments for process feasibility and optimization. Impurity Synthesis and their Characterization using NMR and Mass Techniques, following proposed ROS. Writing LNB / ELNB and proper documentation. Scale-up of Intermediates and products in Lab in the given timeline. Learning and updating Job related knowledge, like process development, Quality, and regulatory aspects. Carryout Experiments to support Plant for trouble shooting in ongoing products to address OOS and OOT issues. Adhering to SOPs / Guidelines, Safety Norms in Lab and maintain cleanliness of work area. Supporting senior colleagues in Development & Optimization activities. Maintaining personal hygiene, safety, and discipline in the workplace.

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description We are looking for an energetic and forward-thinking professional in the Advanced Characterization Team who brings enthusiasm, adaptability, and a results-driven mindset. The ideal candidate will possess excellent problem-solving skills, strong communication abilities, and a proactive approach to challenges, contributing positively to team goals and driving continuous improvement within a fast-paced, evolving work environment. He/she will be responsible for designing, planning and performing microstructure-based analysis using suitable Solid State Characterization Techniques as per required project timeline. Morphology Identification and Structural understanding of Drug Substances, Reverse Engineering, Delamination Study, Particulate Matter Analysis, Particle Size Distribution, Globule Size Distribution, Identification of Crystalline and Non-Crystalline Particles, Core Size, Layer Thickness by high-end microscopy and spectroscopy techniques. Method Development and Method Validation for assigned projects as per agreed stipulated timeline. Sameness data generation and reporting. Repot preparation as per agency/customers and legal requirements. Take part in innovative method/protocal development using Image and data analytics. Transfer of the developed analytical methods to Q.C., explain the critical parameters involved & troubleshoot when required to facilitate smooth product scale up. Maintain GLP (good laboratory practices) & GDP (good documentation practices) in the analytical laboratory to adhere to SOPs & compliance. Capable to perform analysis with minimal guidance as per cGMP and cGLP practices. Addressing plant investigations (majorly exterior matter characterization), regulatory queries and litigation queries related to various microscopy techniques. Maintenance of the instruments and coordination with vendor during breakdown. Qualifications M Pharm/MSc in general science, pharmaceutical or analytical chemistry. Team player with good interpersonal skills & communication skill. Experience in pharmaceutical development and workflow. Additional Information Experience: 3 to 6 Years

Seeking a skilled chemist experienced in laboratory-level synthesis and characterisation of Advanced Nano Materials . The role involves working with materials such as: -Zinc Oxide -Titanium Dioxide -Aluminium Oxide -Carbon Nanotubes Sol-gel method, wet chemical synthesis, and nanoparticle handling is important. The candidate should be familiar with characterization techniques such as XRD, SEM, TEM, FTIR, and UV-Vis spectroscopy. Prior experience in nanomaterials research or applications will be an added advantage.

About ThinkBio.Ai ThinkBio.Ai is revolutionizing the biopharmaceutical and healthcare fields with AI-powered resources. Our five specialized teams clinical, science, AI, software, and managed services work together to develop AI-based solutions that are deployed horizontally (data platforms and workflow tools) and vertically (clinical focus areas such as oncology, autoimmune diseases, and cardiology). Our mission is to help our clients find answers to their toughest questions and to accelerate the application of scientific breakthroughs in the clinic. Position Summary: We are seeking a highly motivated individual with expertise in structural biology to join our team as a Postdoctoral Fellow or Scientist, depending on experience level. The position will involve applying structural biology techniques to understand protein-protein interactions, drug-target binding, and disease mechanisms, integrating these insights into computational models. The successful candidate will have a PhD in structural biology, biophysics, biochemistry, or a related field, with a deep understanding of macromolecular structure and function. Fresh PhD graduates will be hired as Postdoctoral Fellows for a two-year term, while candidates with at least two years of postdoctoral fellowship or industry experience will be considered for a Scientist position. : Apply deep domain knowledge in structural biology to characterize macromolecular complexes and understand their roles in disease pathways. Integrate structural insights with multi-omics data (genomics, transcriptomics, proteomics, and metabolomics) to understand molecular mechanisms of disease. Utilize and develop computational tools for structural modeling, molecular dynamics simulations, and ligand docking to complement experimental data. Stay up to date with the latest advancements in structural biology, biophysics, and computational methods to incorporate cutting-edge research into disease modeling efforts. Collaboration & Project Management: Work closely with cross-functional teams, including disease domain experts, computational scientists, and clinicians to enhance translational research efforts. Work with the Scientific Manager to help in project planning, execution, and reporting, ensuring alignment with research objectives. Communicate findings effectively through reports, presentations, and discussions with internal teams and external collaborators. Publish research findings in high-impact, peer-reviewed journals. Present work at scientific conferences, symposia, and internal research meetings. Contribute to grant applications and funding proposals where relevant. Qualifications & Experience: PhD in structural biology, biophysics, biochemistry, or a closely related field. Strong expertise in at least one major structural biology technique (e.g., X-ray crystallography, cryo-electron microscopy (cryo-EM), NMR spectroscopy). Solid understanding of protein structure-function relationships, macromolecular interactions, and their relevance to disease biology. Experience in experimental design, data collection, data processing, and structure determination. Excellent verbal and written communication skills, with the ability to convey complex structural biology concepts clearly. Preferred: Experience with computational structural biology tools (e.g., Rosetta, AlphaFold, molecular dynamics software). Previous experience working in a multidisciplinary research environment. Familiarity with AI/ML approaches in structural biology or drug discovery. Other Considerations: Fresh PhD graduates will be hired as Postdoctoral Fellows for a two-year term with an opportunity for promotion to Scientist based on performance. Candidates with at least two years of postdoctoral experience in structural biology in either academia or industry will be hired as Scientists with opportunities for career advancement. Why Join Us? Work at the cutting edge of structural biology and disease research. Contribute to groundbreaking disease modeling and molecular insights. Collaborate with leading experts in multiple disease domains. Competitive salary, benefits, and career development opportunities. Application Instructions: Interested candidates should submit a cover letter and CV to careers@thinkbioai.com .

University: Delft University of Technology (TU Delft) Country: Netherlands Deadline: 2025-07-22 Fields: Chemical Engineering, Chemistry, Materials Science, Environmental Engineering, Process Engineering Delft University of Technology (TU Delft) invites applications for a postdoctoral position focused on heterogeneous catalysis and high-pressure instrumentation for the catalytic transformation of CO₂ into sustainable aviation fuel (SAF). The successful candidate will join a multidisciplinary team to design and develop advanced reactor–catalyst systems, contributing to the decarbonization of air transport through innovative process engineering. Responsibilities Include – Designing and operating novel high-pressure flow/batch reactor systems. – Developing and synthesizing tailored catalyst materials for targeted hydrocarbon production. – Integrating system components and evaluating process performance under relevant operating conditions. – Conducting comprehensive process analysis to establish a scalable CO₂-to-SAF platform. Requirements – PhD in Chemical Engineering, Chemistry, Materials Science, or a closely related discipline. – Hands-on experience with high-pressure reactor operation and catalyst synthesis. – Proven experience in process development and optimization for gas-phase reaction systems. – Familiarity with analytical techniques for gas and liquid product analysis. – Expertise in material characterization methods (e.g., XRD, surface area analysis, spectroscopy, microscopy). – Strong problem-solving skills and ability to optimize complex reaction processes. – Excellent verbal and written communication skills in English, with a demonstrated publication record. – Ability to work independently and as part of a multidisciplinary team. Application Procedure Interested candidates are invited to apply by 22 July 2025. Please submit your CV and a motivational letter via the application portal at: https://careers.tudelft.nl/job/Delft-Postdoc-in-Heterogeneous-Catalysis-and-High-Pressure-Instrumentation-for-CO%E2%82%82-to-SAF-2628-CD/823591702/ Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee!

JOB TITLE : Laboratory Analyst DEPARTMENT: CPS QSE Function BASE LOCATION: CPS Plant (Sanand) Job Summary Key roles and responsibilities of this position Provides analytical support to operating unit w.r.t.chemical analysis & Microbiology analysis using internal/external valid & official test methods and international literatures. Provides analytical support to operating unit which mainly includes working in chemical lab as well as in waste water treatment plant (ETP/STP) for water analysis Ensures all the analytical testing programs are executed in accordance with Company and ISO/IEC 17025 requirements. Effective implementation of quality control procedures to ensure products and manufacturing processes are in compliance with Company policies, procedures, practices and standards. Key Duties/Responsibilities Quality Execution- 60% Test and analyse ingredients, intermediates and finished products to ensure compliance with the Company specifications. Perform organoleptic tests & Sensory evaluations of Ingredients and Finshed product beverage bases. Analysis of Ingredients and Finished products using a range of modern techniques like high performance liquid chromatography and spectroscopy. Raw water/process water, Waste water (ETP/STP) sampling and analysis of consent parameters on daily basis. Managing chemical inventory, instrument calibration and analytical data for audit purpose. Also analyse waste water data to indicate improvement opportunities. Responsible to making sure that data is accurately recorded and reported in accordance to company guidelines. Conduct capability a study for testing equipment’s & laboratory processes in accordance with Company as well as ISO/IEC 17025 requirements. Ensure Calibration & preventive maintenance of laboratory instruments is carried out as per schedule and complies with the requirements of ISO/IEC 17025. Participation in internal/external proficiency testing programs in accordance with ISO17025. Identify, classify, and maintain documentation and sensitive information consistent with record handling and retention requirements. Conduct Periodic review of laboratory equipment’s, lab processes to ensure operational fitness in accordance with Company and ISO/IEC requirements. Prepare sampling and testing plan for ingredients, intermediate, finished products, or other materials in order to perform analyses (e.g., chemical, physical, sensory). Genrate data, perform data evaluation and trend analysis to support and risk assessments. Play active role in Laboratory global Network teams and deliver the objectives. Provide support to other parts of the laboratory as require. Management system knowledge of ISO 14001 & ISO 9001 , ISO 17025. Quality Assurance - 40% Ensure products are manufactured as per Company guidelines. Compliance of manufacturing processes with the Company’s quality and food safety requirements. Maintaining ETP/STP/WTP records, conducting trend analysis, graphical representation of results, and communicating the necessary data and record retention in accordance with Company policy and Legal requirements (MPCB Consent). Ensure compliance to quality, food safety and Environmental, safety & Loss Prevention program requirements when conducting analytical/microbiology work and discarding materials (reagents, samples, etc.) to minimize any risks identified. Maintaining appropriate records, communicating the necessary data and record retention in accordance with Company policy and requirements of ISO 9001, ISO/IEC 17025, ISO 22000 and PAS 220. Implement GLP requirements and Laboratory Safety programs. Implement formal corrective actions to avoid issues recurrence. Participate in root cause analysis sessions to solve non-conformances. Perform data audits in order to ensure accuracy of data and analytical processes which may include database queries, statistical process control, correlation studies, notebook review, and/or traceability exercises Participate in the laboratory quality system activities such as internal audits, writing standard operating procedures, and documentation review Record data from analyses or experiments in a computer, log book, or laboratory notebook Organization Impact/Influence This position works with Laboratory Manager and QA Manager and provides support for testing and release of ingredients and finished products and to comply the Laboratory operation requirements as per TCCC and ISO/IEC 17025 Accreditation requirements. The job scope will also involve the interactions with internal and external stake holders as below. Internal Interactions Leadership team, all QA ,Manufacturing and warehouse staff to communicate the decisions related to Quality matters, Material disposition and reporting. Process control and manufacturing team on initiatives to create and achieve Zero defect product quality mind-set. Involve with Laboratory and Quality team to conduct Analytical test method validation and implementation of quality control test procedures. Warehouse and logistics team on incoming ingredient and packaging material identification and disposition activities External Interactions Global CPS Lab community for Laboratory initiatives, receive analytical testing support, problem solving , sharing and implementing of best practises as per company requirements. IQD/APTC/EASC and third party laboratories to coordinate for testing and release. Supplier and vendors: Calibration & Maintenance and Third party service support. Supervisory Responsibilities Coordinate with admin and plant associates to monitor and implement GLP and GMP activities. Coordinate and Supervise Visitor /contractor activities related activities to ensure compliance as per Company requirement. Related Job Requirements/Qualifications Minimum 3-4 years in Quality control /Laboratory in Food / health care or Pharma company as Analyst or similar positions. Good Knowledge of qualitative and quantitative chemical analysis, environment analysis. Knowledge of using advanced analytical instruments, trouble shooting and data interpretation. Through knowledge of Microbiology testing of Treated water, raw water, Commercial sterility of Finished products & Testing of pulp and fruit Juices. Must be proficient and capable to handle and lead problem solving of issues related to microbiological contaminations and testing. Knowledge chemistry to understand composition, structure and properties of ingredients and finished products. Exposure on principles and techniques of basic food science and their application to the beverage industry. Should have experience in analytical processes using instruments such as GC, LC, IC, AA, FTNIR, Particle size analysis, PCR & Rapid microbiology. Should be familiar with accreditation and certification programs such as ISO17025, 9001, FSSC 22000. Good Knowledge of laboratory information management system, SAP functionalities including quality module. Conduct review of scientific or other literature and able to apply develop and implement new analytical test methods. Systematic thinking and problem solving ability. Educational/Skill Requirements M. Sc. Chemistry / Biochemistry/ Analytical Chemistry deg.in food science or equivalent. Language: Good written and oral communication skills in English. Good IT and presentation skills- Microsoft Excel, Power point and Word, Power BI. Experience of LIMS and SAP and system database. Cultural Diversity Able to interact in English and local language internally and externally. No ethnic or cultural differences faced in this job Judgment And Decision Making Key decision maker in determining whether actions are necessary to address quality issues identified as part of analytical monitoring program. Working Conditions Laboratory environment. Use of chemicals and standards under good laboratory practices, Microbiology testing as per microbiology standard requirement & GLP norms. Highly unlikely, it is possible that, this position is subject to hazards and risks associated with normal chemical testing laboratory such as noise, heat stress and hazardous chemical / ingredient exposure conditions. Travel Requirements This position will be primarily based in Gujrat, India with minimum travelling (maximum 5% of work time under normal conditions). Trips include occasional visits or training at other concentrate plants, bottling operations and training centers. Skills Data Compilation; Testing Methods (Inactive); Quality Control (QC); Communication; Recordkeeping; Data Entry; Laboratory Testing; Researching Annual Incentive Reference Value Percentage:8 Annual Incentive reference value is a market-based competitive value for your role. It falls in the middle of the range for your role, indicating performance at target.

Job Title: Laboratory Chemist- Special Process Job Description: The Laboratory Chemist will be responsible for conducting chemical analyses and tests to ensure the quality and compliance of surface treatment processes used in aerospace applications. The role involves developing, optimizing, and monitoring chemical processes and materials to enhance performance and safety. The chemist will work closely with engineering and production teams to troubleshoot issues and improve methodology. Responsibilities include preparing lab samples, performing experiments, documenting results, and ensuring adherence to industry regulations and standards. Additionally, the Laboratory Chemist will be tasked with maintaining laboratory equipment, managing inventory of chemicals, and training junior staff. Key Responsibilities: - Conduct chemical analyses and experiments to develop and optimize surface treatment processes. - Analyze and interpret results, preparing comprehensive reports and documentation. - Collaborate with production and engineering teams to resolve technical issues and improve product quality. - Ensure compliance with safety regulations and environmental standards in laboratory practices. - Maintain laboratory equipment and chemical inventories, ensuring proper storage and handling of hazardous materials. - Perform routine and non-routine testing, and develop standard operating procedures (SOPs) for laboratory operations. - Train and mentor junior lab staff on best practices and safety protocols. Skills and Tools Required: - Bachelors or Masters degree in Chemistry, Chemical Engineering, or a related field. - Strong understanding of Laboratory testings, Periodic testings, chemical analysis techniques, including spectroscopy and titration. - Experience with surface treatment processes such as anodizing, plating, and Paint coatings is preferred. - Familiarity with standards in the aerospace industry, such as ASTM,AMS, ISO,NADCAP and Major Primes. - Proficiency in using laboratory software for data analysis and reporting. - Strong attention to detail and critical thinking skills for problem-solving. - Excellent communication and teamwork abilities to collaborate effectively with cross-functional teams. - Adept at multitasking and managing time efficiently in a high-paced environment. - Knowledge of safety protocols and hazard management in a laboratory setting.

Walk In Drive For Quality Control In Formulation Division @ Corporate Office Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-28-06-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Job Title: Service Engineer Department: Customer Support Location: Delhi About Inkarp Instruments Services Inkarp Instruments is a trusted name in delivering high-quality laboratory, analytical, scientific, and research instrumentation across various sectors including healthcare, pharmaceuticals, academia, and industrial R&D. With a focus on excellence in service and technical support, we aim to empower scientific progress through precision and reliability. Job Summary We are seeking a motivated and skilled Service Engineer to join our Technical Services team. The role involves installation, calibration, maintenance, troubleshooting, and repair of a wide range of laboratory, analytical, and scientific instruments. The position also includes execution and management of Annual Maintenance Contracts (AMC), ensuring high standards of service and customer satisfaction. Key Responsibilities  Installation & Commissioning: Set up and install scientific instruments at customer sites, ensuring full operational readiness.  Preventive & Corrective Maintenance: Perform scheduled maintenance and attend breakdown calls for instruments under warranty or AMC.  Troubleshooting & Repairs: Diagnose and resolve technical issues efficiently, both remotely and on-site.  AMC Execution: o Carry out service activities for instruments under AMC contracts, including scheduled visits, preventive checks, and emergency support. o Maintain and update AMC service logs, renewal status, and customer communication. o Coordinate with the service coordinator/manager to ensure timely and complete AMC delivery.  Calibration & Validation: Conduct calibration and support IQ/OQ/PQ documentation as per industry and regulatory requirements.  Customer Support: Provide technical assistance and training to end-users for optimal instrument operation and longevity.  Documentation: Maintain accurate and timely service reports, AMC logs, and instrument history records.  Sales Support (Optional): Identify opportunities for AMC renewals, spares, and upgrades during service visits and communicate with the sales team.  Compliance: Ensure all service activities are carried out in line with safety, quality, and regulatory standards. Required Qualifications & Skills  Education: Diploma / B.E. / B.Tech in Electronics, Instrumentation, Biomedical Engineering, or related field.  Experience: 1–5 years in servicing laboratory or scientific instruments, including AMC execution.  Technical Skills: Strong technical troubleshooting, hands-on maintenance, and documentation skills; knowledge of electrical, mechanical, and software systems related to lab instruments.  Soft Skills: Good communication, interpersonal skills, customer focus, and ability to work independently.  Travel: Willingness to travel extensively to customer sites as needed. Preferred Qualifications  Familiarity with AMC management practices and reporting.  Experience with instruments from global OEMs in spectroscopy, chromatography, microscopy, etc.  Understanding of service CRM systems and ERP tools.  Knowledge of quality standards like ISO, GLP, GMP, NABL. What We Offer  Competitive compensation and travel allowances.  Opportunities for professional growth and training.  Exposure to advanced lab and analytical technologies.  Supportive work environment with a focus on service excellence.

University: Istituto Italiano di Tecnologia (IIT) and Politecnico di Milano Country: Italy Deadline: 2025-09-10 Fields: Physics, Materials Science, Electrical Engineering, Nanotechnology, Optical Engineering The Istituto Italiano di Tecnologia (IIT) and Politecnico di Milano invite applications for Postdoctoral and PhD positions in the field of Nano-Optics. These positions are part of an internationally recognized research group led by Professor Antonio Ambrosio, focusing on advanced topics such as structured light, 2D materials, metasurfaces, and light–matter interactions at the nanoscale. Available Positions Postdoctoral Position – Research focus: Nano-Optics Innovation through Metasurfaces and Light Structuring – Responsibilities: Design and fabrication of metasurfaces, investigation of ultrafast optical control, and study of polaritonic responses in van der Waals materials – Location: IIT – CNST, Milan – Application deadline: 2025-09-10 – Application link: https://lnkd.in/dqQhSGxC PhD Position #1 – Research focus: Tailoring Light–Matter Interactions via Structured Light – Responsibilities: Study of complex optical beams and their interaction with anisotropic and 2D materials, unveiling novel photonic phenomena – Required skills: Optical setup design, metasurface fabrication, FDTD simulations – Location: Politecnico di Milano – PhD in Physics – Application link: https://lnkd.in/dA–_WZJ PhD Position #2 – Research focus: Light–Matter Interaction at the Nanoscale in 2D Materials – Responsibilities: Engineering and imaging of polaritons in van der Waals materials using advanced nano-imaging and nano-spectroscopy techniques – Required skills: 2D materials synthesis, nano-optics, numerical modeling – Location: Politecnico di Milano – PhD in Physics – Application link: https://lnkd.in/dA–_WZJ Requirements – A strong academic background in physics, materials science, electrical engineering, nanotechnology, or a related field – Relevant laboratory and/or computational skills as described per position – Motivation and ability to work in an interdisciplinary, international environment Additional Information – International applicants are encouraged to apply – Support is available for relocation and research stays abroad – These positions were advertised by Professor Antonio Ambrosio on LinkedIn For further details and to submit your application, please refer to the respective links above. Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register

Job Description Roles and Responsibilities: Lab Business set up as per testing requests, tender & contracts with customers, Marketing as per Testing facility available in lab, Man power adjustment, Authorisation of SOP, Method Development & Method Validation, Standard Regulation comply with as per norms, Training program arrangement-Plan & impart Technical & Quality related Training to the staffs, evaluate & maintain, Authorisation of Test Reports, Take action for the purchase of consumables, spares of Instruments, chemicals, CRMs, Standards etc., Monitoring & supervising overall activity of the designed lab Experience/ Knowledge Have proper knowledge of water/ waste water/ Textile & Dye/ Chemicals analysis for wet lab Parameters, Spectroscopy parameters, heavy Metals & alloys analysis/ Chromatography testing. Have skills for method development, verification & validation. Have management skills for lab development. Have proper complete knowledge for analytical Instrument like; GC/GC-MS/HPLC/LC-MS/ICP/UVVIS etc. handling/ Calibration/ trouble shooting. Have proper documentation knowledge for Quality standard document

Company Description BacAlt is dedicated to converting post-harvest waste into value-added biopolymers applicable in various industries such as textile, skincare, wound care, and agriculture. Our innovative approach addresses sustainability by transforming waste into useful products. Located in Bengaluru, BacAlt strives to contribute to a more sustainable future by leveraging cutting-edge technology and research. Job Title : Analytical Scientist C Department : R&D Department Reporting to : Head of Polymer Science Location : Bangalore Qualification : Master's degree in Analytical Chemistry with 3-4 years of industrial experience. Experience in Pharmaceutical industry desirable. Job Type : Full-Time Salary Range. : 4.8 - 7.2 LPA Key Responsibilities · Develop and validate analytical methods for various instruments, including: HPLC, GC, GC-MS, IR, UV-Visible Spectroscopy, Particle Size Analyser, Dynamic light scattering, Kinematic & Dynamic Viscosity Measurement, Dissolution and Disintegration Testing. · Responsible for wet analysis in lab such as LOD, Karl fisher, bloom testing, kinematic viscosity, moisture analyser, calibration of balance, titration method and plan out other testing methods as well after discussion with head of dept. · Plan out stability study of raw materials, intermediates as well as finished products with desired temperature and humidity conditions. · Conduct testing as per established protocols and procedures for formulations, Active Pharmaceutical Ingredients (APIs), and excipients. · Possess comprehensive knowledge of instrumental analysis, method development, sample preparation, and interpretation of results clearly and concisely. · Record and report experimental data, ensuring accuracy and compliance with standard operating procedures (SOPs) and Good Laboratory Practices (GLP). · Assist in laboratory and equipment maintenance adhering to GMP requirements. · To initiate an incident, deviation, change control, out of specification (OOS), out of trend (OOT), out of change (OOC) or corrective and preventive action (CAPA) in consultation with the department head. · Strong analytical and problem-solving abilities to address complex issues in analytical chemistry. · Adherence to safe laboratory practices and waste disposal protocols in line with company policies. Behavioural Attributes · Demonstrates personal commitment to the team and values individual differences to support shared goals. · Self-disciplined to drive assigned experiments and achieve desired results. · Aptitude to learn and grow, building a better understanding of analytical chemistry work, SOPs, protocols, and GLP processes. · Willingness to take on tasks beyond the listed responsibilities as per team requirements. . Ability to work effectively within a team, demonstrating flexibility and resourcefulness to meet targets with minimal supervision. Ensure all laboratory activities comply with BacAlt Biosciences internal policies and procedures.

Role - Peptide Characterization/Advance Characterization Using HRMS/LC-HRMS/LC/MS Level - Team Lead Position at Mid / Senior level role Key Responsibility: Handing LC-HRMS, Characterization of Peptides for Small molecules, API in Analytical R&D Job Profile:- Leading Characterization of peptides and small molecules with Liquid Chromatography and High-resolution mass spectrometry (LC-HRMS, LC-MS/MS) for structural elucidation, impurities profiling. Managing a team of Peptide / Protein characterization (HRMS) Method development and impurity profiling of Peptides/Proteins and Impurities characterization using HRMS. Spectroscopy (UV-Visible, Circular Dichroism, Spectrofluorometer), Capillary Electrophoresis, and analytical method development, method validation. Impurities profiling & characterization of peptides impurities, small molecules with LC-HRMS and tandem mass spectrometry . Knowledge of liquid chromatography, ionization, mass spectrometry fundamentals, general analytical chemistry is must for characterization of small and large molecules. Method development and method validation for characterization of peptides on spectroscopy (UV-Visible, CD, Fluorescence, etc) and capillary electrophoresis instruments. Qualifications PhD in Analytical chemistry or Analytical Method development with relevant experience. 9 - 20 years experience in High-resolution mass spectrometry (LC-HRMS, LC-MS/MS) etc. Strong Expertise in LC-HRMS method development is an imp criteria. Strong organizational, critical thinking and communications skills. Attention to detail and good judgement. Candidate with relevant exp can share profiles on rashmi.gupta@biocon.com Kindly mention below details while sharin g CV:- Current CTC? Have you handled LC-HRMS ? if yes, how much exp you have? Are you handling Advance Characterisation/ Peptide Characterisation ? Are you PhD or not? Notice Period? Ready to work in Bangalore (onsite) ? (5 Days working)