399 Spectroscopy Jobs - Page 8

Directly Apply On ARAI Career Site: https://www.araiindia.com/pages/career-with-arai ARAI, Pune is a premier Automotive Research Institute, with the Ministry of Heavy Industries, involved in R&D, Homologation, Testing & Certification, Calibration & Skill Development services to Automotive and Allied industries globally. We are looking for the following position for our Fatigue and Materials Centre of Excellence (FMCE) Department Designation: Research Engineer (Battery Material & Electrical Testing) – 01 No. (ARAI Contract) Location: ARAI- Homologation and Technology Centre, Chakan Candidates should have M.Tech or M.Sc. in Materials Science, Electrochemistry or Electrical Engineering. Candidate poses necessary skills and experience should apply for the position. Job Description: Battery pack disassembly, module separation & Cell component separation in Glove box Material Characterization using Scanning Electron Microscope (SEM-EDS), X-Ray diffraction (XRD), Computed Tomography (CT), Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) Characterization using Electrochemical Impedance Spectroscopy (EIS), Cyclic Voltammetry (CV) and Galvanostatic charge-discharge (GCD) Document research findings, data interpretation & prepare technical reports. Evaluate battery management system (BMS) data to assess health and safety parameters. Required Skill: Understanding of lithium-ion battery cell architecture (cathode, anode, separator, electrolyte). Hands-On electrochemical characterization methods: cyclic voltammetry, EIS, Galvanostatic charge-discharge and knowledge of interpreting dQ/dV and dV/dQ plots. Hands-On analytical characterization using Scanning Electron Microscope (SEM-EDS), X-Ray diffraction (XRD), Computed Tomography (CT), Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), Raman Spectroscopy, Gas Chromatography-Mass Spectrometry (GSMC) & FTIR. Ability to interpret battery degradation mechanisms such as SEI layer growth, lithium plating, electrode cracking & Gas pocket formation. Awareness of standards and regulations for battery testing (e.g., IS, IEC, UL). Proficiency in data analysis using Python/MATLAB/Excel for trend analysis or predictive modelling Educational Background: M.Tech or M.Sc. in Materials Science, Electrochemistry or Electrical Engineering. Strong foundation in battery technology and energy storage systems. Experience in R&D or testing in battery performance and degradation is highly preferred. Experience: should have Min 1 + years of experience relevant to this job description This vacancy is on ARAI contract i.e. on ARAI Payroll for 1 year. Last Date of Application: 9th August 2025 Directly Apply On ARAI Career Site: https://www.araiindia.com/pages/career-with-arai

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. About The Role Reckitt Research and Development (Gurugram, Haryana, India) is seeking a self-motivated, experienced analytical chemist to join our team in the role of Senior Associate in the Germ Protection Analytical Research & Development team. The successful candidate will be active scientist in the lab and a people leader of other analytical chemists. The role plays a key role in product development of Germ Protection brands including Dettol, Harpic, and Lizol brands. Your responsibilities Contribute to the development of new products and technologies, conducting studies to understand product functionality and efficacy. Lead the development and validation of new methods for product launch and claim support. Utilize a wide range of Analytical techniques, including chromatography (LC and GC), mass spectrometry, and spectroscopy to provide efficient and robust analysis. Support the advancement of analytical capabilities through identification of new technologies and methodologies. Conduct studies in a timely manner and concisely communicate results to a variety of audiences. Prepare scientific reports, technical documents, SOPs, and protocols for internal or external publication/presentation. Serve as manager for chemists within the Analytical team Manage multiple projects within established timelines and concisely communicate results to a variety of audiences. Prepare scientific reports, technical documents, standard operating procedures, and test protocols. The experience we're looking for PhD plus 5 years, MS plus 8 years, or BS in chemistry or related field plus 10 years of relevant work experience in an R&D analytical laboratory setting Knowledge of a wide range of analytical techniques such as LC, GC, FTIR, and wet chemistry techniques Advanced knowledge in liquid chromatography is preferred. Strong communication skills (both written and verbal). Results-oriented and self-motivating, seeking information from others to accomplish objectives. Intellectual curiosity and proven problem-solving skills. Ability to work well independently and in a cross-functional team environment while remaining flexible to changing project priorities. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

Educational Qualification & Work Experience Preferred Qualification M.Pharm / M.Sc. Preferred Years Of Experience 0 to 2 years Experience Profile Required We are seeking a highly motivated scientist to join our dynamic research team. The ideal candidate will hold M.Pharm / M.Sc (Chemistry) and possess extensive basic knowledge on modern analytical techniques. The incumbent preferred to have proficiency in handling of analytical techniques such as Spectroscopy (UV-Vis, FT-IR), Chromatography (HPLC) and other instruments (Potentiometric titrator, KF), etc. and have adequate interpretation skills. Job Role Key Responsibilities: Analysis of raw material, In-Process and finished products. Generation of analytical data with respect to accuracy and adequacy. Preparation of reference, working and Impurity standards. To ensure timely completion of assigned Training Modules and Skill Evaluation. Ensure the availability of all the consumables like chemicals, columns, Standards etc. before and during experimental activities. Maintain and adhere to safety and quality culture. Participate in Lab activities necessary to maintain compliance in the lab. Job Description - Responsibilities & Duties Knowledge on Method development /Stability analysis Expertise in Handling Spectroscopy (UV-Vis, FT-IR), Chromatography (HPLC) and other instruments (Potentiometric titrator, KF) Basic knowledge of cGMP, GLP and GDP procedures etc. Understanding of development activities and processes in pharmaceutical industry. Actively listens, shares information in a clear, concise and impartial manner. Actively contributes to achieving team Goals Maintain accurate records of research activities and results. Safety: To follow appropriate safety practices in the workplace. Participate in routine safety training and maintain current knowledge on safety related corporate and site policies. Enforce safety requirements as they relate to job function. Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Research and Development

Role Summary: As a Senior FrontEnd Developer, you will lead the development of the client-side of our web applications. Your primary responsibility will be to translate both company and customer requirements into functional and engaging interactive applications You will work closely with stakeholders to create mockups and prototypes, effectively incorporating feedback to enhance user experience. We expect you to be a tech-savvy professional with a keen curiosity about new digital technologies. You should aspire to merge usability with visually appealing digital solutions. You Will: Develop new user-facing features and enhance the user experience using ReactJS. Build reusable code and libraries for future use. Ensure the technical feasibility of UI/UX designs. Optimize applications for maximum speed and scalability. Assure that all user input is validated before submitting to the back-end. Collaborate with other team members and stakeholders. Test the interface under different browsers and screen sizes to ensure cross-browser compatibility and responsiveness. Provide high-quality graphics and visual elements. Get feedback from, and build solutions for users and stakeholders. Help back-end developers with coding and troubleshooting. Stay up-to-date on emerging technologies. Must-Have Qualifications: Bachelor's degree in computer science, Engineering, or a related field. 8+ years of work experience as a Frontend Developer. Proficient understanding of web markup, including HTML5 and CSS. Strong knowledge of client-side scripting and JavaScript frameworks, including jQuery, Angular, Reach, or Vue.js. Good understanding of asynchronous request handling, partial page updates, and AJAX. Proficient understanding of code versioning tools, such as Git. Good problem-solving skills. Excellent verbal communication skills. Good interpersonal skills. Experience working in an agile-based methodology. Nice to Have: Experience with Docker/Kubernetes. Experience collaborating with remote teams across time zones. About Picarro: We are the world's leader in timely, trusted, and actionable data using enhanced optical spectroscopy. Our solutions are used in various 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. They are used in over 90 countries worldwide based on over 65 patents related to cavity ring-down spectroscopy (CRDS) technology. They are unparalleled in their precision, ease of use, and reliability. At Picarro, we are committed to fostering a diverse and inclusive workplace. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, national origin, protected veteran status, gender identity, social orientation, or disability. Posted positions are not open to third-party recruiters/agencies, and unsolicited resume submissions will be considered free referrals.

Picarro is seeking an exceptional QA Lead to lead a global team of engineers focused on functional testing and test automation. This role requires a hands-on leader who can guide and mentor the team, drive testing strategies, and contribute directly to the automation of software testing processes. Key Responsibilities Lead and manage a distributed team of 3–6 QA Engineers. Collaborate with product owners and development teams to understand requirements and translate them into detailed test cases. Conduct risk assessments and develop comprehensive test plans using a test-tracking system. Execute test cases, log defects, and work closely with developers to ensure prompt resolution. Develop and implement automation strategies for both existing and new features. Design, develop, and maintain automated test suites. Ensure consistent test coverage across platforms including Linux, Windows, and embedded systems. Must-Have Qualifications 9+ years of experience in functional and manual testing with strong skills in test case design and execution. Minimum of 5 years of hands-on experience in automating UI and backend applications, particularly in Python. Proficiency in testing across Linux/Windows environments and embedded devices. Solid programming experience in Python or another major language. Strong knowledge of automation frameworks and tools such as Selenium, RestAssured, TestNG, etc. Thorough understanding of SDLC and STLC processes. Proficiency with tools like JIRA for test management and defect tracking. Experience with API testing tools such as Postman or SoapUI. Working knowledge of SQL and ability to write queries for backend validation. Excellent analytical and problem-solving skills with a high attention to detail. Strong communication and collaboration skills, with the ability to work across global teams. Nice-to-Have Qualifications Bachelor's degree in Computer Science or a related field. 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.

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description We are seeking a skilled and detail-oriented Analytical R&D Analyst with a strong foundation in organic chemistry and spectroscopy. The ideal candidate will bring hands-on experience in analytical method development and validation, along with expertise in operating a wide range of analytical instruments. This role supports API development and impurity profiling, while ensuring compliance with global regulatory standards. Key Responsibilities Analytical Method Development & Validation Develop and validate HPLC/GC test methods for diverse regulatory markets Perform troubleshooting and support OOS investigations during validations Conduct trace analysis, related substances testing, and carryover evaluations Prepare protocols and reports in line with data integrity and GMP guidelines Instrument Operation & Maintenance Handle routine operation and calibration of HPLC, IR, UV, Karl Fischer Titrator, Halogen Moisture Analyzer, Polarimeter, and wet lab techniques Operate advanced detection systems such as UV-PDA, ELSD, CAD, IR, and Mass detectors Manage routine troubleshooting and preventive maintenance of analytical instruments Spectroscopic Characterization & Data Interpretation Perform structure elucidation and characterization of APIs and impurities using spectroscopy Interpret analytical data using NMR, MS, DSC, TGA, and FTIR techniques Support identification of known/unknown impurities and intermediates Documentation & Compliance Maintain lab notebooks, calibration records, and validation documents Ensure compliance with GLP, GMP, and safety protocols during lab operations Work collaboratively with cross-functional teams including QA, QC, RA, and manufacturing Qualifications The ideal candidate will have: M.Sc. in Organic / Analytical Chemistry. 4 to 7 years of experience in a relevant field Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Job Title: ADL Officer/Executive Location: Changodar , Ahmedabad, Gujarat, India Department: Analytical Development Laboratory (ADL) Employment Type: Full-Time We are seeking a dedicated and detail-oriented Associate to join our Analytical Development Laboratory (ADL) team. The successful candidate will play a pivotal role in developing, validating, and executing analytical methods to ensure the quality and compliance of our pharmaceutical products. Key Responsibilities Method Development & Validation : Develop, optimize, and validate analytical methods for raw materials, intermediates, and finished products using techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy, adhering to ICH guidelines. Routine Analysis : Conduct routine quality control tests on pharmaceutical products to ensure compliance with company and regulatory standards. Analyze raw materials, in-process samples, and finished products for various physical and chemical parameters. Documentation : Maintain accurate and detailed laboratory records, including test results, equipment logs, and validation documents. Prepare and review standard operating procedures (SOPs) and analytical method documents. Regulatory Compliance : Ensure all activities comply with GMP (Good Manufacturing Practice) and GLP (Good Laboratory Practice) regulations. Support regulatory audits and inspections by preparing necessary documentation and reports. Equipment Calibration & Maintenance : Ensure proper calibration and maintenance of laboratory equipment. Troubleshoot analytical instruments and coordinate repairs as needed. Team Collaboration : Collaborate closely with formulation, R&D, and production teams to support product development and troubleshooting. Engage with cross-functional teams on various projects. Qualifications & Skills Bachelor's or Master's degree in Science (Chemistry, Biochemistry) or Pharmacy. Proficiency in analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy. Familiarity with regulatory guidelines (e.g., ICH, FDA, EMEA). Strong attention to detail and excellent organizational skills. Effective communication and teamwork abilities. Freshers & Experienced both can apply. Why Join Us? Be part of a dynamic team committed to excellence in pharmaceutical industry. We offer opportunities for professional growth, continuous learning, and the chance to make a meaningful impact on healthcare. Job Types: Full-time, Permanent, Fresher Pay: ₹21,000.00 - ₹35,000.00 per month Benefits: Commuter assistance Life insurance Provident Fund Education: Bachelor's (Required) Experience: pharmaceutical: 2 years (Required) Analytical chemistry: 1 year (Preferred) Work Location: In person

This position is no longer available. University: IRCELYON / CNRS (Université Claude Bernard Lyon 1) Country: France Deadline: Not specified Fields: Chemistry, Chemical Engineering, Materials Science, Environmental Science, Renewable Energy PhD Position – Solar Valorization of Biomass via Photoelectrochemistry IRCELYON / CNRS in Villeurbanne (Lyon), France, invites applications for a fully-funded, 3-year PhD position as part of the ANR SOLBIOPEC project, in collaboration with INL Lyon and CEA Saclay. Project Overview The project focuses on the development of photoelectrochemical (PEC) devices to convert biomass-derived compounds (such as furfural and HMF) into high-value chemicals, including furfuryl alcohol, 2-methylfuran (biofuel), and FDCA (bioplastic precursor). Research activities will involve the integration of advanced III-V photocathodes, oxide photoanodes (WO₃/BiVO₄), and operando spectroscopy techniques (Raman, XPS, FT-IR, XAS). The successful candidate will have access to synchrotron facilities (SOLEIL, ESRF, MAX IV). The ultimate objective is to develop a functional PEC demonstrator for rural biorefinery applications. Candidate Requirements Master’s degree in Chemistry or Chemical Engineering. Solid theoretical background in electrochemistry. Experience with analytical techniques (NMR, XRD, GC, HPLC) is desirable. Demonstrated interest in solar energy, green chemistry, and sustainable materials. Position Details Location: IRCELYON, CNRS – Lyon, France Start Date: October 2025 Salary: Approximately 1700 €/month Duration: 36 months Also See Postdoctoral Opportunity in Exsolution-Based Electrode Design for High-Temperature… Two Ph.D. Positions in Advanced Material Recovery and Printing Technologies at… PhD Opportunity in Digital Twin Development for Climate-Resilient Railway Infrastructure at… Fully Funded PhD Position in Advanced Water-In-Salt Electrolytes for Aqueous Batteries PhD Opportunity in Organic Chemistry – Exploring Prebiotic Peptide Synthesis via the Lossen… Application Procedure Interested candidates should send a CV and cover letter to mathieu.prevot@ircelyon.univ-lyon1.fr For further information, please visit: www.ircelyon.univ-lyon1.fr This position offers a unique opportunity to engage in interdisciplinary research at the intersection of renewable energy, electrochemistry, and biomass valorization, with access to world-class laboratories and research infrastructure in France. 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

This position is no longer available. University: Max-Born-Institute Country: Germany Deadline: Open until filled Fields: Physics, Materials Science, Physical Chemistry, Photonics, Electrical Engineering The Max-Born-Institute (MBI) is seeking applications for a PhD position in the area of ultrafast magnetization dynamics probed by laser-generated extreme ultraviolet radiation. This research aims to experimentally investigate the fundamental mechanisms of ultrafast magnetization reversal in thin magnetic films, a phenomenon with significant implications for both data storage technologies and solid-state physics research. The successful candidate will join a team utilizing advanced high harmonic generation techniques to perform ultrafast, element-selective spectroscopy on magnetic thin film systems. The laboratory is equipped with a state-of-the-art, high-power laser system capable of sub-10 femtosecond pulse durations. The position offers a stimulating research environment with opportunities for national and international collaboration, as well as theoretical support via in-house ab-initio electronic structure calculations. The candidate will also be part of the Graduate School of the Collaborative Research Center “Ultrafast Spin Dynamics.” Requirements – Master of Science or Diploma degree in Physics (or closely related field) with above average grades – Strong motivation and ability to work effectively in a team environment – Hands-on experience in optical laboratory work – Beneficial experience includes: ultrashort laser pulses, soft x-rays, vacuum technology, and data analysis software (e.g., Matlab, Python) Offer – Fully funded 3-year PhD program – Salary according to the German TVöD scheme (75%) – Equal opportunity employer with a focus on supporting women and individuals with disabilities – Family-friendly work environment certified by audit berufundfamilie Application Process Applications should include a cover letter, curriculum vitae, certificates, and a description of previous professional activities. Please submit your application electronically via the MBI online recruiting platform: https://mbi-berlin.de/career. The position is open until filled. Also See Master Thesis Opportunity in Ultrafast Photonics at Helmut Schmidt University PhD Opportunity in Time-Resolved NAP-XPS for Photocatalyst Dynamics at University of Lille Fully Funded PhD and Postdoctoral Opportunities in Catalysis Research at TU Delft Postdoctoral Position in Time-Resolved Electron Microscopy for Light-Energy Conversion in… PhD Opportunity in Formal Analysis and Control of Multi-Agent Cyber-Physical Systems at… For further information, please contact Dr. Clemens von Korff Schmising (korff@mbi-berlin.de) or Prof. Stefan Eisebitt (eisebitt@mbi-berlin.de). 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 Title: ADL Officer/Executive Location: Changodar , Ahmedabad, Gujarat, India Department: Analytical Development Laboratory (ADL) Employment Type: Full-Time We are seeking a dedicated and detail-oriented Associate to join our Analytical Development Laboratory (ADL) team. The successful candidate will play a pivotal role in developing, validating, and executing analytical methods to ensure the quality and compliance of our pharmaceutical products. Key Responsibilities Method Development & Validation : Develop, optimize, and validate analytical methods for raw materials, intermediates, and finished products using techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy, adhering to ICH guidelines. Routine Analysis : Conduct routine quality control tests on pharmaceutical products to ensure compliance with company and regulatory standards. Analyze raw materials, in-process samples, and finished products for various physical and chemical parameters. Documentation : Maintain accurate and detailed laboratory records, including test results, equipment logs, and validation documents. Prepare and review standard operating procedures (SOPs) and analytical method documents. Regulatory Compliance : Ensure all activities comply with GMP (Good Manufacturing Practice) and GLP (Good Laboratory Practice) regulations. Support regulatory audits and inspections by preparing necessary documentation and reports. Equipment Calibration & Maintenance : Ensure proper calibration and maintenance of laboratory equipment. Troubleshoot analytical instruments and coordinate repairs as needed. Team Collaboration : Collaborate closely with formulation, R&D, and production teams to support product development and troubleshooting. Engage with cross-functional teams on various projects. Qualifications & Skills Bachelor's or Master's degree in Science (Chemistry, Biochemistry) or Pharmacy. Proficiency in analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy. Familiarity with regulatory guidelines (e.g., ICH, FDA, EMEA). Strong attention to detail and excellent organizational skills. Effective communication and teamwork abilities. Freshers & Experienced both can apply. Why Join Us? Be part of a dynamic team committed to excellence in pharmaceutical industry. We offer opportunities for professional growth, continuous learning, and the chance to make a meaningful impact on healthcare. Job Types: Full-time, Permanent, Fresher Pay: ₹21,000.00 - ₹35,000.00 per month Benefits: Commuter assistance Life insurance Provident Fund Education: Bachelor's (Required) Experience: pharmaceutical: 2 years (Required) Analytical chemistry: 1 year (Preferred) Work Location: In person

Key Responsibilities: Assist in the formulation and testing of new products or materials. Conduct laboratory experiments according to established protocols and safety standards. Analyze samples using techniques such as titration, spectroscopy, chromatography, or other analytical methods. Maintain accurate and detailed records of experiments, results, and observations. Prepare chemical solutions and reagents as required for experiments. Calibrate, clean, and maintain laboratory equipment s. Support scale-up trials and process optimization efforts. Ensure compliance with internal safety, health, and environmental policies. Collaborate with cross-functional teams including production, quality control, and regulatory. Qualifications: Bachelor s degree in Chemistry, Chemical Engineering, or a related field. 1 to 3 years of experience in a laboratory or R&D environment (freshers, internship or training experience is also preferred). Knowledge of laboratory practices, chemical handling, and safety procedures. Familiarity with analytical instruments and lab software is a plus. Strong attention to detail, analytical thinking, and documentation skills. Willingness to learn and take direction in a fast-paced research environment. Working Conditions: Laboratory environment; exposure to chemicals and lab equipment. Use of personal protective equipment (PPE) is mandatory. May involve standing for extended periods and handling hazardous materials. Key Skills : Titration Spectroscopy Calibrate

Job Description :- Department : Quality Control Location : Derabassi Industry : Pharmaceutical & Cosmetic Manufacturing Experience : 3-4 years is relevent experience. Qualification Preferred- 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 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

Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Job Description Thermo Fisher Scientific is a global leader in science services, with $40 billion in revenue annually. Our goal is to help customers improve health and safety worldwide. We offer diverse technologies, easy ordering, and pharmaceutical services through renowned brands. Visit www.thermofisher.com for details. Responsibilities Responsible for performing the routine/preventive maintenance, servicing, and breakdown repairs on GC/GCMS/HPLC instruments in Gujarat & MP (Central Region). Support the GC/GCMS new installation commissioning and field solving at customer sites and to provide remote support to the clients as needed. Delivering demonstrations to ensure the customers are educated on safe and effective equipment use. Provide complete detailed service reports on a regular basis as soon as service visits are completed. Understanding customer needs and concerns, Providing a high level of customer service. Ensure that customers receive first-class service and support in line with service agreements. Perform to designated goals of turn-around-time, response time, repair rate and customer expectations. Actively support to achieving the CAS and business goals. Take ownership for customer satisfaction for services performed. Work in accordance to all relevant certification, regulatory requirements and safety norms by company and customers at site. Travel as per advise by the reporting manager to provide customer service. Education: Bachelor’s degree in Instrumentation, Electronics Field. Years of Experience: Minimum of 7 to 8 years of experience in the field of gas chromatography and mass spectrometry instrument services. Knowledge, Skills, Abilities: Gas chromatography & Mass Spectroscopy and special Gas chromatography analyzer hands on experience in relevant Industries & Processes. To maintain a professional and positive approach whilst being committed to things we value of integrity, intensity, innovation and involvement. Including: Exceeding customer service level expectations (external & internal) Working to agreed target days, A focus to finding solutions. Working within quality and company policy guidelines, Maintaining a professional appearance at all times Competency: Effective interpersonal, communication and listening skills., problem solving, customer centric approach Handling the complicated situations Experienced in Microsoft applications including Microsoft office. Strong analytical skills, Interpersonal skills with an ability to handle time efficiently and meet agreed timelines.

Job Description You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise. Officer - Quality Control Company: Ahlcon Parenterals IN Ltd Job Posting Location: IN-Bhiwadi Functional Area: Quality Working Model: Onsite Requisition ID: 6517 Are you a Officer Quality Control professional passionate about analytical chemistry, instrumentation, and raw material analysis? Join our QC team at Ahlcon Parenterals, a B. Braun company, where your skills in analytical techniques and regulatory compliance will play a vital role in ensuring the quality and safety of incoming raw materials used in sterile manufacturing. Your key responsibilities: Chemical analysis of raw materials Instrument experience - Ultraviolet-Visible Spectroscopy (UV-Vis) , Infrared Spectroscopy (IR), Polarimeters , Potentiometers , total organic carbon (TOC) analysers, atomic absorption spectrophotometry (AAS) What you will bring to the team: Strong knowledge of analytical chemistry and instrumental techniques. Ability to work independently and as part of a cross-functional team. Problem-solving mindset and readiness to learn and adapt. B.Pharm / M.Sc. qualification with 2–3 years of experience in QC analysis of raw materials in the pharmaceutical industry. What sets B. Braun apart? Ahlcon Parenterals (India) Limited is a B. Braun group company, located at Bhiwadi, Rajasthan. We are a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic and export markets. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision - to protect and improve the health of people around the world. What can we offer you? Convenient transport and subsidized canteen services. Mediclaim and Life Insurance. Learning programs and workshops to drive your development. Mental Wellness Support with counselling and mindfulness sessions. Paternity & Birthday Leave for life’s special moments. Fun activities and team building events. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on social media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube

Job Description : Literature search, understanding of Quality by design, design of experiments, US-FDA product specific guidance, EMA guidelines, ICH guidelines, Statistical tools required in product development. Exposure of different software’s and tools required for QBD and DOE. Prototype formulation design to Lab scale development, process optimization using DOE and modern approach. Understating of complex APIs, Polymers, lipids and peptides APIs, Impurities. Characterization of complex formulations by advance techniques and interpretation of data. Understanding of DSC, AFM, DLS, SEM, TEM, Cryo-TEM, Raman-Spectroscopy, NMR, PXRD, SAXS, Zeta Sizer. Should be experience in Lab scale, scale up and technology transfer of complex process for exhibit/validation at GMP sites, optimization of critical process parameters at large scales. Should be experience in preparations and review of protocols, reports and Product development reports, Manufacturing Formulation Records, BMRs, Products Specifications. Should be experience in Product development as per the regulatory requirements of US-FDA, MHRA, and EMA. Different filling stages to approval process. Regulatory queries handling, preparation of justification. Should be experience in Product development by QbD approach (QTPP, CQA, CMA, CPP), Risk assessment by FMEA. Should be experience in Team handling and experiment design, planning, data interpretation, complex analytical methods. Should be experience in GLP/GMP compliance requirements, Different SOPS of Development Lab. Understanding of Pre-clinical studies, Bio equivalence studies, clinical studies (phases) Skills & Qualification : Microspheres Depot, Liposomes, Nanoparticles, Emulsion, Lyophilized injection - Minimum 07-12 years of experience required - M.Pharm (Pharmaceutics/Pharmaceutical Technology), Ph.D. (Preferred)

Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Thermo Fisher Scientific is a global leader in science services, with $40 billion in revenue annually. Our goal is to help customers improve health and safety worldwide. We offer diverse technologies, easy ordering, and pharmaceutical services through renowned brands. Visit www.thermofisher.com for details. Responsibilities Responsible for performing the routine/preventive maintenance, servicing, and breakdown repairs on GC/GCMS/HPLC instruments in Gujarat & MP (Central Region). Support the GC/GCMS new installation commissioning and field solving at customer sites and to provide remote support to the clients as needed. Delivering demonstrations to ensure the customers are educated on safe and effective equipment use. Provide complete detailed service reports on a regular basis as soon as service visits are completed. Understanding customer needs and concerns, Providing a high level of customer service. Ensure that customers receive first-class service and support in line with service agreements. Perform to designated goals of turn-around-time, response time, repair rate and customer expectations. Actively support to achieving the CAS and business goals. Take ownership for customer satisfaction for services performed. Work in accordance to all relevant certification, regulatory requirements and safety norms by company and customers at site. Travel as per advise by the reporting manager to provide customer service. Education: Bachelor’s degree in Instrumentation, Electronics Field. Years of Experience: Minimum of 7 to 8 years of experience in the field of gas chromatography and mass spectrometry instrument services. Knowledge, Skills, Abilities: Gas chromatography & Mass Spectroscopy and special Gas chromatography analyzer hands on experience in relevant Industries & Processes. To maintain a professional and positive approach whilst being committed to things we value of integrity, intensity, innovation and involvement. Including: Exceeding customer service level expectations (external & internal) Working to agreed target days, A focus to finding solutions. Working within quality and company policy guidelines, Maintaining a professional appearance at all times Competency: Effective interpersonal, communication and listening skills., problem solving, customer centric approach Handling the complicated situations Experienced in Microsoft applications including Microsoft office. Strong analytical skills, Interpersonal skills with an ability to handle time efficiently and meet agreed timelines.

Are you a Officer Quality Control professional passionate about analytical chemistry, instrumentation, and raw material analysis? Join our QC team at Ahlcon Parenterals, a B. Braun company, where your skills in analytical techniques and regulatory compliance will play a vital role in ensuring the quality and safety of incoming raw materials used in sterile manufacturing. Your key responsibilities: Chemical analysis of raw materials Instrument experience - Ultraviolet-Visible Spectroscopy (UV-Vis) , Infrared Spectroscopy (IR), Polarimeters , Potentiometers , total organic carbon (TOC) analysers, atomic absorption spectrophotometry (AAS) What you will bring to the team: Strong knowledge of analytical chemistry and instrumental techniques. Ability to work independently and as part of a cross-functional team. Problem-solving mindset and readiness to learn and adapt. B.Pharm / M.Sc. qualification with 2–3 years of experience in QC analysis of raw materials in the pharmaceutical industry. What sets B. Braun apart? Ahlcon Parenterals (India) Limited is a B. Braun group company, located at Bhiwadi, Rajasthan. We are a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic and export markets. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision - to protect and improve the health of people around the world. What can we offer you? Convenient transport and subsidized canteen services. Mediclaim and Life Insurance. Learning programs and workshops to drive your development. Mental Wellness Support with counselling and mindfulness sessions. Paternity & Birthday Leave for life’s special moments. Fun activities and team building events. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on social media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube

Job Description You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise. Officer - Quality Control Company: Ahlcon Parenterals IN Ltd Job Posting Location: IN-Bhiwadi Functional Area: Quality Working Model: Onsite Requisition ID: 6517 Are you a Officer Quality Control professional passionate about analytical chemistry, instrumentation, and raw material analysis? Join our QC team at Ahlcon Parenterals, a B. Braun company, where your skills in analytical techniques and regulatory compliance will play a vital role in ensuring the quality and safety of incoming raw materials used in sterile manufacturing. Your key responsibilities: Chemical analysis of raw materials Instrument experience - Ultraviolet-Visible Spectroscopy (UV-Vis) , Infrared Spectroscopy (IR), Polarimeters , Potentiometers , total organic carbon (TOC) analysers, atomic absorption spectrophotometry (AAS) What you will bring to the team: Strong knowledge of analytical chemistry and instrumental techniques. Ability to work independently and as part of a cross-functional team. Problem-solving mindset and readiness to learn and adapt. B.Pharm / M.Sc. qualification with 2–3 years of experience in QC analysis of raw materials in the pharmaceutical industry. What sets B. Braun apart? Ahlcon Parenterals (India) Limited is a B. Braun group company, located at Bhiwadi, Rajasthan. We are a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic and export markets. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision - to protect and improve the health of people around the world. What can we offer you? Convenient transport and subsidized canteen services. Mediclaim and Life Insurance. Learning programs and workshops to drive your development. Mental Wellness Support with counselling and mindfulness sessions. Paternity & Birthday Leave for life’s special moments. Fun activities and team building events. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on social media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube

The Application Engineer will play a pivotal role in driving the adoption and success of IAS’ NIR Technology products within the agriculture market in India, with a primary focus on the Indian grains and oilseeds industry. This position requires a dynamic individual with deep technical knowledge, excellent communication skills, and a strong support to our Field Sales Engineers promote IAS products across India. Job Responsibilities: · Implement strategic support and modelling plans to effectively promote IAS products to Channel partners, Resellers and End customers in India. · Support in tender specification preparation and represent IAS in technical paper presentations at seminars, forums, and conferences. · Collaborate with Channel Partners’ Field Sales Engineers to execute these plans and achieve sales targets. · Provide application and technical support for Field Sales Engineers and their prospective customers. · Proactively engage with customers and end-users to understand their needs, provide modelling solutions, and ensure customer satisfaction. · Conduct site visits and perform fieldwork outside the office as assigned. · Provide presentations, demonstrations, and technical support to customers and in events (such as trade expos, Workshops and Seminars) when necessary. · Build and maintain strong relationships with end-users to foster long-term partnerships. · Provide frontline and after-sales service responses and support to customers, coordinating with HQ for unresolved issues. · Prepare and deliver schedules and reports on a regular update to the reporting manager, including detailed daily updates during the initial phase of the role. Requirements: Educational Background · Bachelor’s degree or higher in Chemical Engineering, Food Technology, Analytical Chemistry, Biotechnology, Agriculture, or related sciences Professional Experience · Minimum 2 years of experience with NIR, FTIR, or similar spectroscopy-based instruments · Hands-on experience in calibration development is a must Skills & Attributes · Strong understanding of agri-food/feed matrices and quality parameters · Excellent communication skills in English and Hindi; knowledge of regional languages is a plus · Proficient in Statistics, MS Excel and PowerPoint · Self-driven, proactive, and able to work independently and as part of a cross-functional team · Willing to travel extensively (up to 75% of each calendar month) to customer site all over India. · Strong sense of responsibility, good communication and interpersonal skill, able to work individually and in team. · Immediate availability is highly preferred. Benefits: · Opportunities for overseas travel

QC Lab Chemist with 1 to 7 years of experience Preferably from Metal Industry or LEAD Industry Work Location – Manali (Chennai) Educational Qualification – BSC Chemistry / MSC Chemistry Should have experience in LEAD base analysis Handling spectroscopy AAS, OES Spectro etc. Handling Pollution control equipment Interested candidate please share your resume through WhatsApp (7092549951/ 9578306766) Regards HR Department Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Commuter assistance Leave encashment Work Location: In person

Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Job Description Thermo Fisher Scientific is a global leader in science services, with $40 billion in revenue annually. Our goal is to help customers improve health and safety worldwide. We offer diverse technologies, easy ordering, and pharmaceutical services through renowned brands. Visit www.thermofisher.com for details. Responsibilities Responsible for performing the routine/preventive maintenance, servicing, and breakdown repairs on GC/GCMS/HPLC instruments in Gujarat & MP (Central Region). Support the GC/GCMS new installation commissioning and field solving at customer sites and to provide remote support to the clients as needed. Delivering demonstrations to ensure the customers are educated on safe and effective equipment use. Provide complete detailed service reports on a regular basis as soon as service visits are completed. Understanding customer needs and concerns, Providing a high level of customer service. Ensure that customers receive first-class service and support in line with service agreements. Perform to designated goals of turn-around-time, response time, repair rate and customer expectations. Actively support to achieving the CAS and business goals. Take ownership for customer satisfaction for services performed. Work in accordance to all relevant certification, regulatory requirements and safety norms by company and customers at site. Travel as per advise by the reporting manager to provide customer service. Education: Bachelor’s degree in Instrumentation, Electronics Field. Years of Experience: Minimum of 7 to 8 years of experience in the field of gas chromatography and mass spectrometry instrument services. Knowledge, Skills, Abilities: Gas chromatography & Mass Spectroscopy and special Gas chromatography analyzer hands on experience in relevant Industries & Processes. To maintain a professional and positive approach whilst being committed to things we value of integrity, intensity, innovation and involvement. Including: Exceeding customer service level expectations (external & internal) Working to agreed target days, A focus to finding solutions. Working within quality and company policy guidelines, Maintaining a professional appearance at all times Competency: Effective interpersonal, communication and listening skills., problem solving, customer centric approach Handling the complicated situations Experienced in Microsoft applications including Microsoft office. Strong analytical skills, Interpersonal skills with an ability to handle time efficiently and meet agreed timelines.

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 Work Location: In person

Dear Candidates, Please note, we will be able to respond to only those candidates, whose cvs are shortlisted. We respect your valuable time for applying. Location: Gandhinagar, Gujarat (On-site) Job Title: Quality Control (QC) Engineer - Pharmaceutical Filtration Unit Position Details • Department: Quality Control • Reporting To: Senior QC Engineer • Experience Required: 3–5 years • Employment Type: Full-time • Working Days: 6 days/week • Compensation: ₹6 – ₹6.5 LPA Industry Preference (Mandatory) Applicants must have prior work experience in at least one of the following regulated manufacturing sectors: • Sterile/Injectables Manufacturing • Medical Devices Manufacturing • Medicinal Equipment Manufacturing Contact - madhurib@corporatecomrade.com Position Overview We are looking for a proactive and detail-driven Quality Control (QC) Engineer with 3–5 years of experience in Sterile/Injectables, Medical Devices, or Medicinal Equipment manufacturing environments. This role is critical to ensuring consistent product quality through comprehensive analytical testing and adherence to stringent regulatory standards. The ideal candidate will have hands-on expertise in chemical analysis, pharmacopeial testing, and GMP-compliant documentation, especially within a sterile or cleanroom environment. Key Responsibilities • Conduct routine testing of raw materials, in-process samples, and finished products in accordance with pharmacopeial guidelines (IP/BP/USP/Ph. Eur.). • Perform detailed Pharma Copea Testing including identification, assay, dissolution, impurity profiling, and other analytical parameters. • Execute general wet chemistry procedures along with pH and conductivity testing. • Operate and calibrate analytical instruments including IR Spectroscopy, STIR, and related chemical analysis equipment. • Ensure strict compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal Standard Operating Procedures (SOPs). • Maintain complete and accurate documentation including test reports, calibration records, instrument logs, and change control records. • Support investigations related to Out of Specification (OOS) and Out of Trend (OOT) results, including root cause analysis and CAPA. • Liaise with Quality Assurance (QA), Production, and R&D teams for resolution of analytical issues and technical support. • Prepare for and participate in internal and external audits, ensuring full laboratory compliance and readiness. • Manage sample collection, labeling, storage, and contribute to stability studies where applicable. Candidate Requirements Educational Qualification (Preferred): • B.Sc / M.Sc in Chemistry • B.Pharm / M.Pharm with a focus on Pharmaceutical Chemistry Experience: • 3–5 years of relevant experience in a pharmaceutical or regulated manufacturing environment • Must have worked in Sterile, Injectables, Medical Devices, or Medical Equipment manufacturing Technical Skills: • In-depth knowledge of pharmacopeial testing methods and documentation practices • Hands-on experience with IR Spectroscopy, STIR, pH meters, and conductivity meters • Familiarity with analytical method validation and instrument calibration • Strong understanding of Data Integrity, GDP (Good Documentation Practices), and compliance in regulated cleanroom settings

Design and execute experiments related to the formulation development of oral solid dosage forms using HME techniques. Operate and maintain HME equipment including twin-screw extruders, feeders, and associated downstream processing units (milling, compaction, etc.). Conduct pre-formulation studies, including excipient compatibility and thermal analysis (DSC, TGA). Perform process optimization and scale-up studies for HME-based formulations. Prepare solid dispersions, amorphous systems, and evaluate physical and chemical stability. Perform solid-state characterization using tools such as XRPD, FTIR, Raman spectroscopy, and microscopy.

About the Company Bioscan Research is a MedTech company developing advanced diagnostic and monitoring solutions for brain injuries and trauma care. Our flagship device, CEREBO, is a non-invasive, handheld system leveraging near-infrared spectroscopy and machine learning to detect intracranial injuries such as bleeds and edema. As we expand into regulated markets including the United States and Europe, we are seeking an experienced QA/RA Manager to lead quality and regulatory functions across the organization. Role Summary The QA/RA Manager will be responsible for implementing and maintaining the Quality Management System (QMS) in alignment with international medical device standards, as well as leading regulatory affairs activities required for product approvals and ongoing compliance. This role requires close collaboration with cross-functional teams including R&D, Clinical, Manufacturing, and Leadership. Key Responsibilities Quality Assurance (QA): Lead the implementation, maintenance, and continuous improvement of the QMS in compliance with ISO 13485, 21 CFR 820, and other applicable standards Oversee documentation control, change management, non-conformances, CAPA, internal audits, and employee training programs Ensure design control, risk management, process validation, and device history records are maintained accurately and consistently Coordinate management reviews, supplier qualification, and audit readiness activities Own and maintain key documents such as QSPs, SOPs, and the Device Master Record Regulatory Affairs (RA): Prepare and manage regulatory submissions including US FDA 510(k), CE marking under MDR, CDSCO registration, and other international requirements Monitor and interpret global regulatory changes and integrate them into internal processes and product development lifecycles Maintain the Essential Principles Checklist, GSPR documentation, and support compliance with labeling, UDI, and PMS requirements Coordinate with external consultants, testing laboratories, and notified bodies as needed Support post-market surveillance activities and field safety corrective action procedures Candidate Profile Bachelor’s or Master’s degree in Biomedical Engineering, Life Sciences, Quality Management, or related field Minimum of 2-5 years of relevant experience in a QA/RA role within a medical device company Strong knowledge of ISO 13485, IEC 62304, ISO 14971, 21 CFR 820, EU MDR, and applicable national regulatory frameworks Demonstrated experience in leading or supporting regulatory submissions and quality audits Strong documentation, communication, and analytical skills Ability to work independently and cross-functionally in a dynamic, high-growth environment Experience with hardware, embedded firmware, or connected health systems is preferred