116 Spectroscopy Jobs

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)

Role Description This is a full-time on-site role for a Postdoctoral Fellow (upto 3 years) in Cancer Biology or Solution NMR Spectroscopy based in Kharagpur. The Postdoctoral Fellow will be responsible for conducting research in their specialized area, collaborating with other researchers, writing papers, and presenting findings at conferences. Qualifications Strong background in Cancer Biology or Solution NMR Spectroscopy Experience in conducting research and writing scientific papers Ability to work collaboratively in a team Excellent analytical and problem-solving skills PhD in a relevant field (Cancer Biology, Biochemistry, Biophysics, etc.) Experience with lab techniques and equipment related to the field Strong communication and presentation skills

Position: Subject Matter Expert (Chemistry) Role Type: Solution Author Employment Type: Contract-Based Location: Remote Shift Timing: Early Morning Shift – 4:00 AM to 1:00 PM (IST) Note: Fresh graduates are welcome to apply. If you are currently employed full-time elsewhere, please do not apply. This role demands full dedication and consistent availability. Only apply if you are actively seeking new opportunities or pursuing higher education, and can commit to working 8 hours each day. Overview: Endeavor Academy, a reputed EdTech service provider, is hiring Chemistry Subject Matter Experts for early morning shifts. The SME will be responsible for authoring detailed, high-quality academic solutions, resolving student queries, and contributing to assessment content across various subfields of chemistry. Key Responsibilities: Solution Authoring Create clear, accurate, and step-by-step solutions to academic problems from topics such as: Physical Chemistry (Thermodynamics, Equilibrium, Kinetics, Electrochemistry) Organic Chemistry (Nomenclature, Mechanisms, Reactions, Functional Groups) Inorganic Chemistry (Periodic Table, Chemical Bonding, Coordination Compounds) Analytical Chemistry (Titrations, Spectroscopy, Chromatography) Ensure academic alignment with prescribed curricula and content standards. Doubt Resolution Respond to academic doubts and queries posted by students via the platform. Deliver concept-driven, easy-to-understand responses within expected timelines. Assessment Support Create and review assessment questions and solutions. Grade and provide feedback on student responses where required. Portal Interaction Utilize the designated platform for submission and progress tracking. Ensure quality, formatting, and timely submission of solutions. Content Accuracy Maintain high accuracy in all academic content. Revise or update existing content as per academic changes or feedback. Qualifications: Bachelor’s or Master’s degree in Chemistry or related fields. Strong command over core chemistry concepts across disciplines. Good written English communication skills. Prior experience in teaching, tutoring, or content creation is a plus. Key Skills & Attributes: High attention to detail and accuracy. Strong problem-solving and analytical skills. Time management and ability to meet tight deadlines. Passion for education and simplifying complex topics. Why Join Us? Competitive compensation based on content quality and volume. Remote working opportunity with a fixed early morning shift. Be part of a dynamic team making an impact in digital education. Continuous learning and professional development. Application Process: Interested candidates should submit their updated resume and any sample academic content (if available) to hr@endeavoracademy.co.in Shortlisted candidates may be required to complete a subject-specific test as part of the selection process.

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 Bachelor's 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.

Analytical R&D Analyst I - TAPI Job Details | Teva Pharmaceuticals Find a Career With Purpose at Teva Search by Postal Code Area of Interest Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Analytical R&D Analyst I - TAPI Jun 18, 2025 Greater Noida, India, 201306 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industrys broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you ll spend your day Excellent communication and with hands on experience. Having working experience of analytical method development/ validation for HPLC/GC test methods, from different markets. Troubleshooting/OOS investigations during validations. Having a good knowledge of HPLC, IR, UV, KF Titrator, Halogen Moisture analyzer, Polarimeter and wet analysis Having good knowledge of HPLC trouble shooting. Sound knowledge of Organic Chemistry & Spectroscopy. Having a good knowledge of HPLC Method development of API/RM/KSM and SM using various detector like Mass, IR, CAD, ELSD, UV-PDA and UV. Structure elucidation and Identification and characterization of APIs, known and unknown impurities and intermediates by various spectroscopy techniques. Data interpretation by NMR, Mass Spectrometer, DSC, TGA & FTIR Having a sound knowledge of Analytical method validation. Hands on experience of various Analytical Instruments-Coulometer, FT-IR, UV, Karl Fisher, Halogen Moisture Analyzer etc., sound knowledge of Organic Chemistry & Spectroscopy. Your experience and qualifications MSc (Organic chemistry/Analytical chemistry) 4- 7 years Already Working @TEVA? Teva s Equal Employment Opportunity Commitment

Morepen Proprietary Drug Research Pvt Ltd (MPDRPL) , a leading pharmaceutical research and development organization, is seeking a talented and motivated Medicinal Chemist to join our innovative team. With a commitment to excellence and the advancement of healthcare, we are dedicated to discovering and developing breakthrough therapeutic solutions that improve patient outcomes worldwide. Roles & Responsibilities : Design and synthesize novel small molecule compounds with potential therapeutic applications Conduct structure-activity relationship (SAR) studies to optimize lead compounds for potency, selectivity, and drug-like properties Perform multi-step organic synthesis of pharmaceutical intermediates and active pharmaceutical ingredients (APIs) Analyze and interpret analytical data (NMR, MS, HPLC) to confirm compound identity and purity Maintain detailed laboratory notebooks and prepare comprehensive reports on synthetic methods and compound characterization Stay current with scientific literature and emerging trends in medicinal chemistry and drug discovery Support patent applications and intellectual property documentation Ensure compliance with laboratory safety protocols and MPDRPL Environmental Health Safety (EHS) guidelines Knowledge & Experience : Master's degree (M.Sc.) or Bachelor's degree (B.Sc.) in Organic Chemistry, Medicinal Chemistry, or related field 1-4 years of hands-on experience in medicinal chemistry, pharmaceutical research, or related chemical synthesis roles Strong foundation in organic synthesis, reaction mechanisms, and synthetic methodology Experience with modern analytical techniques including NMR spectroscopy, mass spectrometry, and chromatography Knowledge of structure-activity relationships (SAR) and drug design principles Familiarity with chemical databases, literature searching, and computational chemistry tools Understanding of pharmaceutical development processes and regulatory requirements Excellent problem-solving skills and ability to work independently as well as in team environments Strong communication skills and ability to present scientific data effectively Preferred Qualifications: Experience with parallel synthesis and library design Knowledge of ADMET properties and their optimization Familiarity with fragment-based drug discovery approaches Experience with process chemistry and scale-up activities Publications in peer-reviewed journals or patent applications Why Join us: Opportunity to work on cutting-edge drug discovery projects with significant therapeutic potential Access to state-of-the-art laboratory facilities and advanced analytical instrumentation Collaborative research environment with opportunities for professional growth and skill development Competitive compensation package with performance-based incentives Comprehensive benefits including health insurance, retirement plans, and professional development support Mentorship opportunities with senior scientists and exposure to diverse therapeutic areas Contribution to meaningful research that directly impacts patient health and well-being Application Process: To apply, please submit your resume and a cover letter highlighting your relevant experience and research interests to jobs@morepenpdr.com We are an equal opportunity employer committed to fostering an inclusive and diverse workplace environment.

GeneTech- ATS GeneTech Private Limited is looking for Biochemist to join our dynamic team and embark on a rewarding career journey Research: Conduct laboratory experiments and studies to investigate biochemical processes, including metabolism, cellular signaling, and genetic expression Analysis: Analyze and interpret data from experiments, using various techniques such as spectroscopy, chromatography, and molecular biology methods Hypothesis Testing: Develop and test hypotheses to understand the molecular and chemical basis of biological phenomena Publication: Prepare and publish research findings in scientific journals, contributing to the advancement of knowledge in the field Teaching and Education: Educate and mentor students and junior researchers in biochemistry, often in an academic or research institution Collaboration: Collaborate with other scientists, researchers, and interdisciplinary teams to address complex biological questions Instrumentation: Use and maintain laboratory equipment and instruments to carry out experiments effectively

The Process Development Scientist-I with some supervision from the Chemical Development Lead focuses on the route scouting and Chemical Process Development of Bayers' existing and pipeline crop protective agents Collaborates with all internal and external functional teams The job holders ensure all the experimental work is done following the highest safety standards and document the generated data in the Electronic Lab Notebook The applicant will have an excellent practical and theoretical understanding of synthetic organic chemistry or a relevant technology and can design and execute high-quality, thoughtful experimentation while making significant contributions both independently and as a member of a team The candidate will work within an interdisciplinary and cross-divisional team in the Crop Protection Innovation organization, TASKS AND RESPONSIBILITIES: Conduct process chemistry research as an individual contributor, which includes, but is not limited to, research on inventing new synthetic routes and associated manufacturing processes that turn the molecules into agrochemical solutions Conduct experiments for route scouting, process optimization, safety evaluation, high throughput screening and chemo/biocatalytic reaction discovery and optimization Invent synthetic routes and develop safe, robust, and cost-effective processes to manufacture Crop Protection Agents developing the synthetic routes Contribute to the Chemical Development Process by conducting laboratory experiments by own hand and providing experimental results, technical updates, documentation, data interpretation, recommendations for process optimization, etc With the help of the Process Engineer optimize unit operations Investigate optimization, generate safety and process engineering data required for scale-up of chemical reactions This is a highly practical role where you will be working in the R&D laboratories to generate new synthetic routes and assist in the design, planning and execution of multi-step experimental studies guided by risk assessment to deliver safe, efficient, robust manufacturing processes, Collaborate within project teams by working closely with analytical chemists, process engineers, pilot plant team and project managers within the Crop Protection Innovation organization, Staying up to date with the latest advancements in chemistry and technologies Find opportunities to use these technologies in solving process development challenges Follow all company, site and laboratory Environmental, Health and Safety (EHS)-related protocols, processes, guidelines and SOPs Actively participate in EHS discussions with peers and management for continuous improvement of EHS practices, KEY WORKING RELATIONS: Internal Crop Protection Innovation Team Analytical Chemist from Pilot Plant Team AIM Production Team AIM Analytical team at Vapi External Coordinate with various vendors and engineers for instrument installation/maintenance activities

Our purpose at Avient Corporation is to be an innovator of materials solutions that help our customers succeed, while enabling a sustainable world. Innovation goes far beyond materials science; it s powered by the passion, creativity, and diverse expertise of 9,000 professionals worldwide. Whether you re a finance wizard, a tech enthusiast, an operational powerhouse, an HR changemaker, or a trailblazer in materials development, you ll find your place at Avient. Join our global team and help shape the future with sustainable solutions that transform possibilities into realities. Your unique perspective could be the key to our next breakthrough! Job Summary We are seeking an experienced R&D Engineer/Chemist from a polymer & colour sciences background interested in advancing their career within Avient s Corporate Technology Group. The R&D scientist is responsible for identifying and innovating new technologies for color matching techniques, devices, and color rendering. In addition, the scientist must possess a good understanding of pigment/dye chemistries and their suitability for applications with engineering polymers. Successful candidates will be creative and impactful within a team environment. Essential Functions Conduct work in a safe, respectful and ethical manner Drive innovation that enriches Avient s intellectual property portfolio Take responsibility for colour and spectroscopy expertise as a core member of colour system digitization project Evaluate, connect, correlate, and maintain data in current colour system and digital platform Refine, aggregate, and organize current colorant database Interact with data scientists, data analysts and IT to drive development of colour matching interface Conduct test on new equipment for implementation of digital platform Write work instruction and organize training for colour, device, digital platform, interfaces, etc. Coach and train commercial and technical teams to use device & digital platform, and trouble shoot Work with cross business unit and collaborate with colour specialists within Avient Other duties as based on need at time #LI-GM1 Education and Experience MSc (PhD Preferred) in Colour Science, Organic Chemistry, or Polymer Science Possess significant experience in color matching for plastics resins and in management of colorant database Good understanding of masterbatch production process, including mixing, extrusion and palletization. Strong knowledge of regulatory requirements for plastics resins by applications and industries Strong skills in the scientific method and use of design of experiments for data-driven research Experience analytical characterization techniques for rheological, mechanical and, thermal properties of polymers Experience with quality control methods, part & product approval processes and engagement with OEMs & customers is desirable. Additional Qualifications Use of statistical software (StatEase, Minitab, SigmaPro or similar) for executing DOEs Strong competencies in using Microsoft Word for documentation and report writing Strong competencies in use of Microsoft Excel, PowerPoint and Project Greenbelt (or higher) in Six Sigma DMAIC or Lean Six Sigma for continuous improvement We believe that all of our global employees are leaders and that the six most important behaviors for driving our strategy and culture are the same no matter if an employee is a leader of self, a leader of others, or a leader of the business.By playing to win, acting customer centric, driving innovation and profitable growth, collaborating seamlessly across Avient, and motivating and inspiring and developing others and yourself you will accelerate your ability to achieve Avient s strategic goals, to meet our customer needs, and to accomplish your career goals. At Avient, we believe a wide variety of thoughts, ideas and backgrounds gives us the creativity to be successful in a rapidly changing world. In support of this, we stress equality of opportunity for all qualified individuals in accordance with applicable laws. Decisions on hiring, promotion, development, compensation or advancement are based solely on a person s qualifications, abilities, experience and performance. Avient is an equal opportunity employer. We maintain a policy of non-discrimination in providing equal employment to all qualified employees and candidates regardless of race, sex, sexual orientation, gender identity, age, color, religion, national origin, disability, genetic information, protected veteran s status, or other legally protected classification in accordance with applicable federal, state and local law. If you need an accommodation because of a disability to complete an online application, please contact the Avient.

Conduct chemical analysis of plant materials to identify active compounds and assess their properties. Research and develop new plant-derived chemicals. Use advanced analytical techniques (e.g., chromatography, spectroscopy, and mass spectrometry) to separate, identify, and quantify chemical components of plant samples. Conduct experiments to synthesize plant-based chemicals and assess their effectiveness in various applications. Ensure compliance with regulatory standards in product development and testing. Collaborate with other scientists, researchers, and engineers to optimize the extraction and formulation of plant-derived chemicals. Prepare detailed reports and presentations on research findings and experimental results. Maintain accurate lab records, including data, protocols, and experimental results. Job Type: Full-time Pay: ₹22,000.00 - ₹35,338.77 per month Benefits: Health insurance Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Apply now » Analytical R&D Analyst I - TAPI Date: Jun 18, 2025 Location: Greater Noida, India, 201306 Company: Teva Pharmaceuticals Job Id: 62433 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day Excellent communication and with hands on experience. Having working experience of analytical method development/ validation for HPLC/GC test methods, from different markets. Troubleshooting/OOS investigations during validations. Having a good knowledge of HPLC, IR, UV, KF Titrator, Halogen Moisture analyzer, Polarimeter and wet analysis Having good knowledge of HPLC trouble shooting. Sound knowledge of Organic Chemistry & Spectroscopy. Having a good knowledge of HPLC Method development of API/RM/KSM and SM using various detector like Mass, IR, CAD, ELSD, UV-PDA and UV. Structure elucidation and Identification and characterization of APIs, known and unknown impurities and intermediates by various spectroscopy techniques. Data interpretation by NMR, Mass Spectrometer, DSC, TGA & FTIR Having a sound knowledge of Analytical method validation. Hands on experience of various Analytical Instruments-Coulometer, FT-IR, UV, Karl Fisher, Halogen Moisture Analyzer etc., >sound knowledge of Organic Chemistry & Spectroscopy. Your experience and qualifications MSc (Organic chemistry/Analytical chemistry) 4- 7 years Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

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 1-6 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.

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Excellent communication and with hands on experience. Having working experience of analytical method development/ validation for HPLC/GC test methods, from different markets. Troubleshooting/OOS investigations during validations. Having a good knowledge of HPLC, IR, UV, KF Titrator, Halogen Moisture analyzer, Polarimeter and wet analysis Having good knowledge of HPLC trouble shooting. Sound knowledge of Organic Chemistry & Spectroscopy. Having a good knowledge of HPLC Method development of API/RM/KSM and SM using various detector like Mass, IR, CAD, ELSD, UV-PDA and UV. Structure elucidation and Identification and characterization of APIs, known and unknown impurities and intermediates by various spectroscopy techniques. Data interpretation by NMR, Mass Spectrometer, DSC, TGA & FTIR Having a sound knowledge of Analytical method validation. Hands on experience of various Analytical Instruments-Coulometer, FT-IR, UV, Karl Fisher, Halogen Moisture Analyzer etc., >sound knowledge of Organic Chemistry & Spectroscopy. Your Experience And Qualifications MSc (Organic chemistry/Analytical chemistry) 4- 7 years Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws. Show more Show less

We are looking for a meticulous and detail-oriented Trainee/Chemist to contribute to our quality control and assurance processes at Synnat Pharma Private Limited, a leading API manufacturer. This role is crucial in ensuring that our raw materials, in-process materials, and finished products meet stringent quality standards. The ideal candidate will possess a foundational understanding of Good Laboratory Practices (GLP) and GMP guidelines, applying these principles to meticulously execute sampling procedures and conduct thorough data analysis. As a Trainee/Chemist, you will collaborate with cross-functional teams, contributing to the maintenance of laboratory standards and adherence to compliance requirements. Your contributions will be instrumental in upholding the integrity of our manufacturing processes and ensuring the delivery of high-quality pharmaceutical products. This is an excellent opportunity for a motivated individual to gain hands-on experience in the pharmaceutical industry and develop a strong foundation in quality control and assurance. Job Details: Industry: Active Pharmaceutical Ingredient (API) Manufacturer Department: Quality Control / Quality Assurance Role: Trainee / Chemist Location: Visakhapatnam Compensation: 1.5 – 2.0 LPA Experience: 0 – 1 year Qualification: Bachelor's or Master's degree in Chemistry, Pharmacy, or a related field Responsibilities: Raw Material Sampling and Analysis Perform sampling of raw materials as per defined procedures, ensuring representative collection. Conduct visual inspections to detect contamination or degradation. Prepare samples using wet chemistry and instrumental techniques. Accurately record sampling activities in laboratory notebooks/e-systems. Compare results to pre-defined specifications and escalate deviations. Maintain hygiene and safety standards in the sampling area. In-Process and Finished Product Sampling Collect in-process material samples during manufacturing as per sampling plans. Conduct routine testing to monitor key process parameters. Sample finished API products before QC release. Document sampling with detailed reports (sample ID, date, process stage). Collaborate with production and QA to address discrepancies. Ensure all activities align with GMP and regulatory norms. Laboratory Operations and Compliance Follow GLP principles to ensure traceability and data integrity. Maintain detailed records for analyses, calibrations, and maintenance. Prepare and standardize reagents as per lab SOPs. Assist during audits and promptly address observations. Adhere to lab safety protocols and use PPE consistently. Support method development and validation activities. Data Analysis and Reporting Analyze data from techniques like chromatography, spectroscopy, and titrimetry. Interpret results, identify trends, and flag potential issues. Prepare summary reports including tables, graphs, and conclusions. Review and verify analytical data for accuracy. Share test results with QA, Production, and Regulatory teams. Maintain secure and accessible databases for analytical data. General Expectations and Past Experiences: Possess a Bachelor's or Master’s degree in Chemistry, Pharmacy, or a related scientific field. Foundational understanding of GLP and GMP principles. Skilled in wet chemistry and basic analytical techniques. Strong analytical and observational skills to interpret data. Effective communication and ability to work in team environments. Proficient in MS Office (Excel, Word, PowerPoint) for reporting. Highly detail-oriented, quality-focused, and eager to learn. Show more Show less

Our purpose at Avient Corporation is to be an innovator of materials solutions that help our customers succeed, while enabling a sustainable world. Innovation goes far beyond materials science; it’s powered by the passion, creativity, and diverse expertise of 9,000 professionals worldwide. Whether you’re a finance wizard, a tech enthusiast, an operational powerhouse, an HR changemaker, or a trailblazer in materials development, you’ll find your place at Avient. Join our global team and help shape the future with sustainable solutions that transform possibilities into realities. Your unique perspective could be the key to our next breakthrough! Job Summary We are seeking an experienced R&D Engineer/Chemist from a polymer & colour sciences background interested in advancing their career within Avient’s Corporate Technology Group. The R&D scientist is responsible for identifying and innovating new technologies for color matching techniques, devices, and color rendering. In addition, the scientist must possess a good understanding of pigment/dye chemistries and their suitability for applications with engineering polymers. Successful candidates will be creative and impactful within a team environment. Essential Functions Conduct work in a safe, respectful and ethical manner Drive innovation that enriches Avient’s intellectual property portfolio Take responsibility for colour and spectroscopy expertise as a core member of colour system digitization project Evaluate, connect, correlate, and maintain data in current colour system and digital platform Refine, aggregate, and organize current colorant database Interact with data scientists, data analysts and IT to drive development of colour matching interface Conduct test on new equipment for implementation of digital platform Write work instruction and organize training for colour, device, digital platform, interfaces, etc. Coach and train commercial and technical teams to use device & digital platform, and trouble shoot Work with cross business unit and collaborate with colour specialists within Avient Other duties as based on need at time Education And Experience MSc (PhD Preferred) in Colour Science, Organic Chemistry, or Polymer Science Possess significant experience in color matching for plastics resins and in management of colorant database Good understanding of masterbatch production process, including mixing, extrusion and palletization. Strong knowledge of regulatory requirements for plastics resins by applications and industries Strong skills in the scientific method and use of design of experiments for data-driven research Experience analytical characterization techniques for rheological, mechanical and, thermal properties of polymers Experience with quality control methods, part & product approval processes and engagement with OEMs & customers is desirable. Additional Qualifications Use of statistical software (StatEase, Minitab, SigmaPro or similar) for executing DOEs Strong competencies in using Microsoft Word for documentation and report writing Strong competencies in use of Microsoft Excel, PowerPoint and Project Greenbelt (or higher) in Six Sigma DMAIC or Lean Six Sigma for continuous improvement We believe that all of our global employees are leaders and that the six most important behaviors for driving our strategy and culture are the same no matter if an employee is a leader of self, a leader of others, or a leader of the business.By playing to win, acting customer centric, driving innovation and profitable growth, collaborating seamlessly across Avient, and motivating and inspiring and developing others and yourself you will accelerate your ability to achieve Avient’s strategic goals, to meet our customer needs, and to accomplish your career goals. At Avient, we believe a wide variety of thoughts, ideas and backgrounds gives us the creativity to be successful in a rapidly changing world. In support of this, we stress equality of opportunity for all qualified individuals in accordance with applicable laws. Decisions on hiring, promotion, development, compensation or advancement are based solely on a person’s qualifications, abilities, experience and performance. Avient is an equal opportunity employer. We maintain a policy of non-discrimination in providing equal employment to all qualified employees and candidates regardless of race, sex, sexual orientation, gender identity, age, color, religion, national origin, disability, genetic information, protected veteran’s status, or other legally protected classification in accordance with applicable federal, state and local law. If you need an accommodation because of a disability to complete an online application, please contact the Avient. Show more Show less

This Job is based in Australia One of Australia’s leading research & teaching universities Vibrant campus life with a strong sense of community & inclusion Enjoy a career that makes a difference by collaborating & learning from the best At UNSW, we pride ourselves on being a workplace where the best people come to do their best work. The School of Materials Science and Engineering is one of the top ranked Materials programs in the Asia- Pacific regions and strongly positioned in every facet of materials science and engineering. It offers undergraduate programs in Materials Science and Engineering (Honours), as well as a number of combined degree programs with Chemical Engineering, Biomedical Engineering and Commerce. The Postdoctoral Fellow is expected to contribute towards the research effort of UNSW and the School of Materials Science and Engineering and to develop their research expertise through the pursuit of defined projects relevant to their particular field of research. This position will carry out research in an industry sponsored project over four years, requiring skills in high-temperature materials, process metallurgy, materials selection, and materials characterisation. This project will be conducted in collaboration with a key industry partner and other researchers and academics based at UNSW, Monash and Deakin. As part of the School’s academic staff, the Postdoctoral Fellow will also be expected to contribute to lab management and engagement and leadership in the institution. About The Role $110K - $117K plus 17% superannuation and annual leave loading Fixed Term – 4 years Full-time (35 hours per week) The role of Postdoctoral Fellow reports to Professor Sophie Primig and has no direct reports. The Postdoctoral Fellow will also work closely with Professor Jianqiang Zhang and Emeritus Professor David Young. Specific Responsibilities For This Role Include Develop understanding of Aluminium process metallurgy from bauxite, via alumina to Aluminium products. Develop new sustainable processing routes for bauxite and alumina in collaboration with our industry partner. Carry out experimental work on high temperature materials in our process and physical metallurgy labs (e.g., isothermal and cyclic thermal treatments under steam or controlled gas atmospheres, scale growth kinetics, direct reduction, arc melting etc.). Prepare microscopy samples using various metallography techniques. Carry out advanced microscopy including state-of-the-art methods of scanning electron microscopy, X-ray diffraction and related. Carry out FactSage simulations to underpin experimental results. Address materials selection problems based on literature surveys and using the Ansys Granta materials selection software. Closely collaborate with industrial partners, researchers and academics at UNSW, Monash and Deakin. Prepare presentations and progress reports for our industrial partner. Prepare publications for submission to leading journals and conferences of the field. Liaise with the related School academic and technical staff on research progress, lab management and leadership. Other duties as assigned in consultation with the supervisor. Align with and actively demonstrate the Code of Conduct and Values. Cooperate with all health and safety policies and procedures of the university and take all reasonable care to ensure that your actions or omissions do not impact on the health and safety of yourself or others. About The Successful Applicant To be successful in this role you will have: A PhD in Materials Science and Engineering or a related discipline and/or relevant work experience. Strong track record of research in Process Metallurgy, with particular focus on high temperature materials, phase transformations, characterisation techniques, and basic computational skills. Experience in advanced characterisation techniques (scanning electron microscopy, X-ray diffraction). Knowledge of those techniques and willingness to gain skills in other related techniques (e.g., energy dispersive spectroscopy). Experience in hot corrosion testing. Demonstrated experience in computational tools such as FactSage. Experience or interests in applied research at the interface of science, engineering and technology. Excellent interpersonal skills and the ability to work in a team environment, with industrial partners and with academic collaborators. Excellent written and verbal communication skills. Demonstrated ability to present research findings as evidenced by presentations at conferences and other venues. Strong organisational skills including the ability to prioritise a range of tasks and meet deadlines. An understanding of and commitment to UNSW’s aims, objectives and values in action, together with relevant policies and guidelines. Knowledge of health and safety responsibilities and commitment to attending relevant health and safety training. You should systematically address the selection criteria listed within the position description in your application. Please apply online - applications will not be accepted if sent to the contact listed. Contact : Sophie Primig E: s.primig@unsw.edu.au Applications close: July 2nd, 2025 Find Out More About Working At UNSW At Www.unsw.edu.au UNSW is committed to equity diversity and inclusion. Applications from women, people of culturally and linguistically diverse backgrounds, those living with disabilities, members of the LGBTIQ+ community; and people of Aboriginal and Torres Strait Islander descent, are encouraged. UNSW provides workplace adjustments for people with disability, and access to flexible work options for eligible staff. The University reserves the right not to proceed with any appointment. Show more Show less

Job Title: Assistant Manager - Quality Control Validation Company: SAVA Healthcare is amongst the fastest emerging pharmaceutical company in India with global reach to customers in Canada, Ukraine and the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur and in near future in Indore holds various accreditations and produces wide variety of dosage forms across therapeutic categories. Our GMP compliant, State of Art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel and Ointment formulations with dedicated manufacturing sections supported by In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and manpower of 500+ employees engaged across locations. Job Location: Surendranagar Plant, Gujarat Job Summary The Senior Executive / Assistant Manager - QC Validation will be responsible for ensuring the quality and compliance of our manufacturing processes and products through rigorous validation protocols. This role is pivotal in maintaining our commitment to producing safe and effective pharmaceuticals. Key Responsibilities Validation Protocol Development: Develop and implement validation protocols (IQ/OQ/PQ) for equipment, systems, processes, and methods in the QC laboratory. Execution of Validation Activities: Conduct validation studies, including risk assessments, to ensure compliance with regulatory requirements and company standards. Documentation: Prepare and review validation documents, including protocols, reports, standard operating procedures (SOPs), and work instructions. Compliance: Ensure all validation activities comply with GMP, FDA, EMA, and other relevant regulatory guidelines. Audit Support: Support internal and external audits by providing validation documentation and responding to audit findings related to QC validation. Continuous Improvement: Identify opportunities for continuous improvement in validation processes and implement best practices. Training: Train QC staff on validation procedures and ensure adherence to validation standards and practices. Cross-functional Collaboration: Work closely with QA, manufacturing, and R&D teams to ensure successful validation activities and integration of new products/processes into production. Qualifications Education: Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field. Experience: Minimum of 5 years of experience in QC validation within the pharmaceutical industry. Knowledge: In-depth knowledge of validation principles, GMP, FDA, EMA regulations, and industry standards. Technical Skills: Proficiency in analytical techniques and instrumentation, such as HPLC, GC, spectroscopy, and microbiological methods. Documentation Skills: Strong experience in writing and reviewing technical documents. Attention to Detail: High level of accuracy and attention to detail. Problem-solving: Excellent analytical and problem-solving skills. Communication: Strong verbal and written communication skills. Teamwork: Ability to work effectively in a team environment and collaborate with cross-functional teams. Preferred Qualifications Certification in Quality Assurance or Validation from a recognized institution. Experience with statistical analysis and validation software. Familiarity with Lean Six Sigma methodologies. Working Conditions Primarily office-based with regular interaction in laboratory and manufacturing environments. May require occasional travel for audits, training, and conferences. Show more Show less

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 Show more Show less

Key Responsibilities: 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.

Assistant Professor (Physics) Academic Level 10 Sri Sathya Sai Institute of Higher Learning (SSSIHL) Assistant Professor (Physics) Academic Level 10 Department of Physics, Prashanti Nilayam Campus Advertisement No: SSSIHL/24-25/PHY/ACA/040 15 June 2025 Full-time (Men applicants) Salary: Basic: 57,700 + Dearness Allowance (DA) & House Rent Allowance (HRA) as per Institute rules Higher qualifications and relevant experience will be considered ESSENTIAL QUALIFICATIONS & EXPERIENCE Ph.D. in Physics (Preferred area: Lasers, Fiber Optics, Optics & Photonics) Master s degree in Physics (Specialization in Photonics preferable) Good academic performance in relevant fields from a recognized University/Institute Must have cleared UGC NET/CSIR NET/SLET/SET Proficiency in English and ability to mentor students effectively Commitment to SSSIHL s code of conduct and values-based integral education system KEY RESPONSIBILITIES Teaching and Academic Leadership Undergraduate-level fundamental Physics courses and Physics laboratory courses Postgraduate level courses in Fiber Optics, Nonlinear Optics, Ultrafast Optics, Semiconductor device physics & Technology / Embedded systems Tech. level courses like Optical Communications, Optical Networks, Optoelectronics, and Signal processing Knowledge of Programming (C / C++ / Python), automation, and basic electronics Enable experiential learning Research and Innovation Research focus in Photonics, Nonlinear Optics, Ultrafast Fiber Lasers, Laser Spectroscopy Use of Data analytics and AI in physics research in areas like (but not limited to) Optical Communications, Photonics Student Engagement and Mentorship Participation in curricular, co-curricular activities Guidance for student projects HOW TO APPLY SSSIHL/24-25/PHY/ACA/040 STEP 2 Attach your detailed resume (must include details of Ph.D. qualification, NET/SLET/SET or other national level exams passed, teaching/professional experience, roles, and responsibilities in chronological order, list of research publications published in reputed UGC CARE journals and conference presentations & proceedings, list of research projects, significant achievements/recognitions, post-docs and research students guided, Areas of expertise and courses taught at UG/PG level, and at least two references (academic and/or professional) STEP 3 Scanned copies of all certificates/documents related to your educational qualifications and professional experience Applicants desiring to apply for more than one position should submit separate applications for each. SSSIHL reserves the right to reject application forms that are incomplete and not as per specified requirements. SSSIHL reserves the right to call only the requisite number of candidates for an in-person demo and/or interview after shortlisting based on the candidate s suitability for the vacant position. There will be no personal communication with candidates other than those shortlisted for the interview. All applicants are required to ensure that all the information submitted (Resume, Annexure form,and documents) is accurate and correct for scrutiny If any application is found to contain information that is inaccurate or false either during the employment process or after the appointment of the candidate, SSSIHL reserves the right to reject the application at any stage or take stringent action on the employee as deemed suitable.

Job Description :- Department : Quality Control Location : Medivisual Healthworld Industry : Pharmaceutical & Cosmetic Manufacturing Experience : 3-4 years is relevent experience. Qualification : B.Sc. (Pharma) / M.Sc. (Pharma) or equivalent in relevant scientific discipline. Responsibility :- Perform testing of raw materials, in-process, and finished products (tablets, syrups, skin care products, etc.) Ensure quality checks are conducted as per laid SOPs and regulatory standards Make independent quality decisions (accept/reject) based on control parameters Maintain and update all test records, reports, and logbooks in compliance with regulatory norms Ensure compliance with legal, safety, and quality standards Key Skills Required : Hands-on experience in HPLC / GLC Karl Fischer Titration Technique Analysis using pH Meter, UV-Vis Spectroscopy, IR Spectroscopy Good knowledge of cGMP & GLP practices Product Range : Tablets, Syrups, Ointments, Creams, and other cosmetic & skin care products . Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹30,000.00 per month Schedule: Day shift Work Location: In person

Qualification: B.Sc. (Chemistry) Passed Out Year: 2020 To 2024 Department: R&D Work Location: Nakkapalli. Roles & Responsibilities: 1. Candidates need to work in R&D Operations. 2. Need to attend his duties in rotational shifts. 3. Basic understanding of chemical and production processes. 4. Executing the production processes as per Standard Operating Procedures (SOPs). 5. Ensure and maintain to work with Good Manufacturing Practices 6. Operate and monitor production equipment's such as reactors, centrifuges, dryers and filtration process. 7. Should follow safety and personal protective equipment (PPE), while working in operational areas.

TestRight is the fastest-growing startup in the dairy deep tech sector. Our breakthrough IoT product, MBscan, revolutionizes the industry by automating the Methylene Blue Reduction Test (MBRT)—a century-old manual process. Having a solid technical team in spectroscopy, MBscan is based on a novel patent-pending tech. We are looking for a candidate with the following skillsets: - Soldering : Both throughhole + SMD - Screwdriver fitting - Quality Control - Machine Assembly - PCB Repair Job Type: Full-time Pay: ₹14,000.00 - ₹16,000.00 per month Schedule: Day shift Experience: total work: 1 year (Required) Work Location: In person

Key Responsibilities: 1. Conduct chemical analyses using various techniques such as chromatography, spectroscopy, and titration. 2. Develop, validate, and implement new analytical methods. 3. Operate and maintain laboratory equipment, including instrumentation and software. 4. Collaborate with cross-functional teams to design and execute experiments. 5. Analyze and interpret data, preparing reports and presentations as needed. 6. Ensure compliance with laboratory safety protocols and regulations. Location: Kandla, Near Gandhidham, Gujarat Regards Team HR Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹45,000.00 per month Benefits: Health insurance Life insurance Provident Fund Schedule: Day shift Fixed shift Morning shift Supplemental Pay: Performance bonus Yearly bonus Experience: Lab Chemist: 3 years (Required) Work Location: In person