227 Spectroscopy Jobs - Page 2

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

Location: Gandhinagar, Gujarat (On-site) Job Title: Quality Control (QC) Engineer - Cleanroom 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 Position Overview We are looking for a proactive and detail-driven Quality Control (QC) Engineer with 3–5 years of experience in (Cleanroom), 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 Application Process Eligible candidates who meet the above criteria are invited to send their updated CV to hr2@gopani.com . Subject Line: Application for QC Engineer – Sterile/Medical Devices Industries We Operate In Plastics Manufacturing Pharmaceutical Manufacturing Medical Equipment Manufacturing Even if a candidate matched the 70% of the JD can be considered for the role.

Job Description Job Description: R&D Assistant Manager – Online Gas Chromatography Req No : 101677 An excellent career opportunity is currently available for a R&D Assistant Manager – Online Gas Chromatography at Honeywell India Technology Center in Gurugram. This position seek to work in a highly dynamic work environment dealing with characterization & evaluation of complex molecules through online Gas Chromatography technique. The role will be accountable for managing a small group of scientists along with guiding them for troubleshooting actionable & resolving technical challenges. Responsibilities Position responsibilities Lead activity of online GC lab, develop online methods & configuration to support smooth data generation through pilot plant operation. Lead & Develop team member & help to resolve complex problem & ensure high quality data output. Strategies & advance planning for online GC & NIR to achieve zero downtime. Strong co-ordination with operation team & synergies with priority as per project plan. Follows HS&E policies and guidelines and ensures that pilot plant and laboratory operations are conducted in accordance with HS&E procedures. Identify/highlight opportunities for continuous improvement through automation, use of advanced scientific principles and process efficiencies. Drive initiatives for continuous improvement and innovation. Managing spares & consumables through inventory control & procurement follow up. Qualifications You Must Have MSc in pure chemistry / organic Chemistry or bachelor’s in engineering degree. Doctoral degree is optional. 8-12 Years of enriched hands-on experience over Gas chromatography instrument, especially on hardware part including configuration, installation, maintenance & troubleshooting. At least 5 years’ experience of managing a small technical group in similar industries. Knowledge on software like chemlaunch, Chemstation & open lab Chromatography data system is must. Adequate know how on process safety & Lab safety. Strong understanding of online Chromatography & spectroscopy. Experience in developing, set up & quick troubleshooting for online analyzer. We Value Basic knowledge on LAN, Server configuration, remote operation will be added advantage. Self-motivated & have Passion for Analytical / Separation & Spectroscopy science related to Refining, Petrochemical, Gas processing industry. Knowledge of Six Sigma concepts and their application in managing risk and uncertainty. Excellent interpersonal and communication skills. Dedication to continuous learning and professional development. Demonstrate ability to lead or work on multi-disciplinary teams across different time zones and cultures. Innovative mindset and proactive approach to identifying opportunities for improvement. The position required highly flexible mindset & hands on engagement with instrument(75%) along with supervisory skill set (25%) or vice versa as on required. About Us Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments – powered by our Honeywell Forge software – that help make the world smarter, safer and more sustainable.

Description Brief Job Overview This is a hands-on, non-supervisory scientific position the Global Biologics department. The incumbent is responsible for providing support for the development of USP documentary standards and reference standards for biological products such as peptides, Oligonucleotides, protein, carbohydrates, Complex Biologics, Vaccines, Antibiotics, and advanced therapies. The incumbent will provide quality and technical review of scientific documents for accuracy, clarity and compliance, manage and track reference standard stability program and organize efforts for continuous process improvements. The incumbent will also focus on supporting the reference standard suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports for confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in time-bound manner. How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. The Sr. Scientist -I (RSS-Review) has the following responsibilities: Roles and Responsibilities Performs technical and quality reviews of documents to ensure a high level of document quality and compliance before QA review Manages and tracks efforts for continuous process improvements. Develops and reviews SOP’s, Operation Manuals, and training documents. Assists in investigations of quality related issues resulting from customer complaints to include root cause analysis, corrective action identification, action planning, and implementation monitoring. Supports the day to day operation of the reference standard stability program. Works with internal stakeholders to develop new and innovative standards for analytical analysis of biological products. Communicates and maintains working relationships with cross functional USP departments regarding assigned projects Supports day to day operations of the RS Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure CSU testing is completed as per protocol and in timely manner. Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use. Compiles, assess current and historical stability testing data and prepare stability trend reports in a time-bound manner. Support the maintenance and updation of various databases documenting laboratory data and program determinations on suitability and Stability interval updates. Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Supporting Quality Assurance and Reference Standard Evaluation in the investigation of unexpected stability testing results Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps. Prepare, present and discuss regular work updates with Team Lead and other team members Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: PhD. degree in Biochemistry/Biology/Pharmacy, or a related field Minimum of 7 to 10 years, or Masters degree in Biochemistry/Biology/Pharmacy or a related field with 11 to13 years of years of commensurate industrial experience. Demonstrated experience in Techical review of analytical documents in Quality Assurance. Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc. Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development. Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays. Excellent technical writing, presentation and oral communication skills are required. Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders. Additional Desired Preferences Knowledge of USP products and services is highly desirable. Operates collaboratively at all levels of the organization in a highly technical environment. Must be able to work in a fast-paced environment and respond to shifting priorities. Well-developed interpersonal, negotiation, conflict-resolution and listening skills. Must possess the ability to multi-task and to work effectively with a team. Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality. Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred. Supervisory Responsibilities No Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide. At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.

Expereince- 3 to 8 Compulsory experience in pharma/ medical equipments/ sterile injectibles industry  Perform day-to-day testing of raw materials, in-process samples, and finished products in accordance with pharmacopeial standards (IP/BP/USP/Ph. Eur.).  Conduct comprehensive Pharma Copea Testing including identification, assay, dissolution, impurity profiling, and other critical parameters.  Carry out general wet chemistry tests along with pH method and conductivity testing.  Operate and maintain laboratory instruments such as IR Spectroscopy, STIR, and other analytical tools.  Ensure strict compliance with GMP/GLP guidelines, regulatory norms, and internal Standard Operating Procedures (SOPs).  Prepare and maintain accurate documentation including test reports, calibration records, instrument usage logs, and change controls.  Participate in investigations for Out of Specification (OOS) and Out of Trend (OOT) results, and support the implementation of corrective and preventive actions (CAPA).  Coordinate with Quality Assurance (QA), Production, and R&D teams for technical clarifications and analytical issue resolutions.  Participate in internal and external audits, ensuring laboratory readiness and compliance at all times.  Manage sample collection, proper labeling, storage, and contribute to stability studies as required. Candidate Requirement Job Type: Full-time Pay: ₹300,000.00 - ₹600,000.00 per year Application Question(s): Experience in pharma/ medical equipments/ sterile/ injectibles industry Work Location: In person

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice. Process Development Scientist I POSITION PURPOSE: 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 WHO YOU ARE: M.Sc/M.Pharm in Organic Chemistry with more than 8 year’s experience or Fresh PhD or PostDoc in Organic Chemistry in designing and performing experiments in a laboratory setting to meet project timelines and objectives. Experience in independent planning and execution of experiments for multistep synthesis of complex organic molecules. Experience in independent interpretation of data from experiments and using it to make conclusions/decisions regarding the direction of future experimentation Comprehensive and state-of-the-art knowledge of modern synthetic methodologies as well as a basic understanding of organic reaction mechanisms and retrosynthesis. Strong understanding of small molecule analysis including chromatographic and spectroscopic techniques and structure elucidation by NMR and Mass Spectroscopy is required Embraces ambitious goals and drives progress with urgency. Consistently seeking opportunities to acquire knowledge, develop skills, and share insights. Possesses a strong willingness to learn and grow through challenging experiences, actively engaging in giving and receiving constructive feedback to foster continuous improvement. Effectively interacts with diverse teams across functions, cultivating strong working relationships with both internal and external collaborators to enhance overall performance Ability to work in the shifts Ever feel burnt out by bureaucracy? Us too. That’s why we’re changing the way we work— for higher productivity, faster innovation, and better results. We call it Dynamic Shared Ownership (DSO). Learn more about what DSO will mean for you in your new role here https://www.bayer.com/en/strategy/strategy Bayer does not charge any fees whatsoever for recruitment process. Please do not entertain such demand for payment by any individuals / entities in connection with recruitment with any Bayer Group entity(ies) worldwide under any pretext. Please don’t rely upon any unsolicited email from email addresses not ending with domain name “bayer.com” or job advertisements referring you to an email address that does not end with “bayer.com”. YOUR APPLICATION Bayer is an equal opportunity employer that strongly values fairness and respect at work. We welcome applications from all individuals, regardless of race, religion, gender, age, physical characteristics, disability, sexual orientation etc. We are committed to treating all applicants fairly and avoiding discrimination. Location: India : Gujarat : Vapi Division: Crop Science Reference Code: 833702 Contact Us 022-25311234

University: Delft University of Technology Country: Netherlands Deadline: 2025-09-01 Fields: Chemistry, Chemical Engineering, Materials Science, Computational Chemistry, Physical Chemistry Are you driven to advance the frontiers of catalysis research and eager to develop innovative solutions for sustainable chemical processes? If you are seeking to deepen your expertise in molecular catalysts, reaction mechanisms, and computational chemistry, the ISE group at Delft University of Technology (TU Delft) offers a unique opportunity to contribute to groundbreaking research in this dynamic field. At TU Delft, fully funded PhD and Postdoctoral positions are now open in the ISE group under the supervision of Dr. Evgeny Pidko. These positions focus on the development of reactivity theories, mechanistic understanding, and new design strategies for robust and sustainable molecular hydrogenation catalysts. The research aims to explore the life cycle of molecular catalysts, including their dynamics, deactivation, and performance optimization, using state-of-the-art computational modeling, chemistry automation, kinetic studies, and operando spectroscopy. About The University Or Research Institute Delft University of Technology (TU Delft), located in the Netherlands, is internationally recognized as a leading institution in science, engineering, and technology. TU Delft fosters a vibrant academic environment that emphasizes interdisciplinary collaboration, innovation, and excellence in research. The university is renowned for its commitment to sustainable solutions and offers world-class facilities, making it an ideal place for ambitious researchers to thrive. The ISE group, led by Dr. Evgeny Pidko, is at the forefront of catalysis research, integrating advanced experimental and computational techniques to address pressing challenges in molecular chemistry and sustainable catalysis. Research Topic and Significance The primary focus of these positions is the study of reactivity theories and mechanisms of catalytic reactions, with an emphasis on the design of more robust and sustainable molecular hydrogenation catalysts. Hydrogenation reactions are central to numerous industrial processes, from the synthesis of fine chemicals to large-scale energy applications. However, the stability and efficiency of molecular catalysts remain significant challenges. By investigating the dynamics, deactivation pathways, and performance tuning of these catalysts, the research seeks to provide novel insights and practical strategies for the development of next-generation catalytic systems. This work is highly relevant in today’s context, where sustainable chemical processes are critical for addressing global energy and environmental issues. Project Details The Available Positions Are Part Of The ISE Group At TU Delft, Led By Dr. Evgeny Pidko. The Group’s Research Encompasses Both Experimental And Computational Approaches To Catalysis. The Projects Will Involve – In-depth investigation of molecular hydrogenation catalyst dynamics and deactivation mechanisms. – Performance tuning using computational modeling, chemistry automation, kinetic studies, and operando spectroscopy (including FTIR, UV-Vis, NMR). – Development of new design strategies for catalysts through data-driven and mechanistic approaches. There Are Two Specific Positions Available Postdoc: Catalyst Dynamics & Reaction Mechanisms – Focused on organometallic chemistry, homogeneous catalysis, reaction mechanisms, and advanced spectroscopy. – Emphasizes experimental innovation, lab automation, and chemical kinetics. PhD: Catalysis Theory & In Silico Catalyst Design – Centered on computational chemistry, quantum chemistry, and computational catalysis. – Involves coding, automation, and data-driven catalyst design, with a strong interest in catalytic conversion fundamentals and reaction network analysis. Candidate Profile For The Postdoctoral Position The ideal candidates for these positions will have a strong academic background and a passion for advancing catalysis research. Specific requirements include: – A PhD in organometallic chemistry or homogeneous catalysis. – Expertise in organometallic chemistry, homogeneous catalysis, reaction mechanisms, and operando spectroscopy (FTIR, UV-Vis, NMR). – Strong affinity with lab automation, coding, chemical kinetics, and experimental innovation. For The PhD Position – An MSc in computational chemistry, physical chemistry, or a related field. – Experience with quantum chemistry and computational catalysis. – Affinity with coding and automation. – Strong interest in the fundamentals of catalytic conversion, reaction network analysis, or data-driven catalyst design. Applicants should be motivated, innovative, and eager to work collaboratively in an interdisciplinary environment. Application Process Description The application deadline for both positions is September 1, 2025. For detailed descriptions and to apply, please visit the following links: – Postdoc Position: https://lnkd.in/dzKYNXD9 – PhD Position: https://lnkd.in/dCFcZJ5H For any questions, interested candidates are encouraged to contact Prof. Evgeny Pidko directly at E.A.Pidko[at]tudelft[dot]nl. Conclusion If you are passionate about catalysis and aspire to contribute to transformative research in molecular chemistry, these fully funded PhD and Postdoctoral positions at TU Delft offer an outstanding platform to advance your career. We encourage all eligible and motivated candidates to apply and to explore similar opportunities in the field. Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee! Also See Postdoctoral Researcher in Life Cycle Assessment (LCA) of Bio-Based Processes and Products… Postdoctoral Opportunity in Applied Planning and Scheduling Under Uncertainty for Offshore… PhD Position in Catalysis with Supported Metal Phosphides at Max-Planck-Institut für Kohlenforschung Fully Funded PhD Scholarships in Carbon Capture, Utilisation, and Storage (CCUS) at Edith… Two Postdoctoral Positions in Biofabrication at the MERLN Institute, Maastricht University

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.

As an enthusiastic salesperson, you will be responsible for client acquisition, relationship management, and promoting analytical services through technical sales, presentations, and industry networking. Your role will involve leveraging your life sciences background, strong communication skills, and willingness to travel extensively to achieve sales targets and provide market insights. In terms of client acquisition and relationship management, you will be required to identify and engage potential clients, build and nurture long-term relationships with clients and key decision-makers, as well as understand client needs and recommend appropriate analytical solutions. For technical sales and promotion, you will need to effectively communicate the technical capabilities of analytical services, conduct presentations and consultative discussions with customers, and attend industry conferences, exhibitions, and other networking events to promote analytical services. To achieve sales targets, you will develop and execute territory-wise sales strategies, track and meet sales targets, provide sales forecasts and performance reports to management, and collaborate with internal teams for timely proposals and service delivery. In terms of CRM and market insights, you will maintain up-to-date records in the CRM system, accurate records of client communications and sales progress, monitor market trends, competitor activities, and emerging customer needs, and provide feedback to the technical team for continuous service improvement. Your role will also involve extensive travel across India to meet clients, assess projects, and build market presence. Ensuring regular field visits and follow-ups with leads and existing clients, as well as providing post-sale support to ensure client satisfaction and repeat business will be crucial aspects of your responsibilities. The ideal candidate for this position would have an M.Sc. in Chemistry, Biotechnology, Biochemistry, Pharma, or related life science discipline, along with at least 3 years of sales experience in analytical services, CRO/CDMO, life sciences, or pharma/biopharma sector. A solid understanding of analytical techniques, proficiency in using CRM tools, excellent communication, negotiation, and presentation skills, and willingness to travel extensively across India are essential requirements for this role. Experience working with GLP/NABL certified labs, familiarity with regulatory requirements, a strong service ethos, go-getter attitude, and a knack for closing deals would be considered advantageous.,

MEDI ANALYTIKA IS RECOGNIZED AS THE LARGEST INSTRUMENTATION COMPANY IN INDIA HAVING TIE UPS WITH 50+ WORLD LEADING INSTRUMENTATION COMPANIES FROM USA - CANADA - UK - EUROPE - JAPAN - REPUBLIC OF KOREA - ISRAEL. Our existing clients include all major universities, research institutions, hospitals, pharmaceutical / CROs, food processing companies, chemical industries and other industries. Role & responsibilities : As a service engineer, you will have to visit our clients spread all over India to install and also provide after sales service support.

Description At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities. Brief Job Overview This is a hands-on, non-supervisory scientific position the Global Biologics department. The incumbent is responsible for providing support for the development of USP documentary standards and reference standards for biological products such as peptides, Oligonucleotides, protein, carbohydrates, Complex Biologics, Vaccines, Antibiotics, and advanced therapies. The incumbent will provide quality and technical review of scientific documents for accuracy, clarity and compliance, manage and track reference standard stability program and organize efforts for continuous process improvements. The incumbent will also focus on supporting the reference standard suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports for confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in time-bound manner. How will YOU create impact here at USP? In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments. The Sr. Scientist -I (RSS-Review) Has The Following Responsibilities Roles and Responsibilities Performs technical and quality reviews of documents to ensure a high level of document quality and compliance before QA review Manages and tracks efforts for continuous process improvements. Develops and reviews SOP’s, Operation Manuals, and training documents. Assists in investigations of quality related issues resulting from customer complaints to include root cause analysis, corrective action identification, action planning, and implementation monitoring. Supports the day to day operation of the reference standard stability program. Works with internal stakeholders to develop new and innovative standards for analytical analysis of biological products. Communicates and maintains working relationships with cross functional USP departments regarding assigned projects Supports day to day operations of the RS Stability (CSU) program covering the USP Biologics RS catalog inventory. Reviews RS testing history and drafts test protocols for CSU studies and submits to labs based on designated testing requirements and schedules. Liaisons and Assists laboratories to ensure CSU testing is completed as per protocol and in timely manner. Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use. Compiles, assess current and historical stability testing data and prepare stability trend reports in a time-bound manner. Support the maintenance and updation of various databases documenting laboratory data and program determinations on suitability and Stability interval updates. Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Supporting Quality Assurance and Reference Standard Evaluation in the investigation of unexpected stability testing results Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps. Prepare, present and discuss regular work updates with Team Lead and other team members Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience PhD. degree in Biochemistry/Biology/Pharmacy, or a related field Minimum of 7 to 10 years, or Masters degree in Biochemistry/Biology/Pharmacy or a related field with 11 to13 years of years of commensurate industrial experience. Demonstrated experience in Techical review of analytical documents in Quality Assurance. Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc. Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development. Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays. Excellent technical writing, presentation and oral communication skills are required. Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders. Additional Desired Preferences Knowledge of USP products and services is highly desirable. Operates collaboratively at all levels of the organization in a highly technical environment. Must be able to work in a fast-paced environment and respond to shifting priorities. Well-developed interpersonal, negotiation, conflict-resolution and listening skills. Must possess the ability to multi-task and to work effectively with a team. Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality. Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred. Supervisory Responsibilities No Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time

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 Are you passionate about chemistry and impurity profiling? Join our state-of-the-art Global R&D Centre and help advance tomorrow’s therapies through cutting-edge spectroscopy and LC-MS expertise. Shape innovation, impact quality, and grow with a team that values collaboration and scientific excellence. 🔬 Key Responsibilities 🧪 Impurity Identification & Characterization Perform identification, structure elucidation, and characterization of APIs, known and unknown impurities, and intermediates using advanced spectroscopy techniques Lead the quantification and characterization of Nitrosamine impurities using LC-MS and related methods Develop and validate methods for genotoxic impurity quantitation using LC-MS 📄 Documentation & Compliance Prepare detailed characterization reports in alignment with regulatory standards Ensure all analytical activities meet compliance and quality requirements 🤝 Cross-Functional Collaboration Independently drive analytical initiatives and collaborate effectively with cross-functional teams including R&D, QA, and Regulatory Affairs ⚙️ Instrumentation Expertise Maintain hands-on expertise in operating advanced analytical instruments, including: Mass Spectrometers (Qualitative & Quantitative) Q-TOF and Triple Quadrupole MS systems FT-IR, UV-Vis Spectroscopy, and other analytical platforms 🧬 Scientific Knowledge & Data Interpretation Apply strong theoretical and practical knowledge in organic chemistry, spectroscopy, and analytical data interpretation to support research and development goals 🌟 Skills & Attributes Excellent communication and documentation skills Strong analytical thinking with ability to interpret complex data Self-motivated with a proactive approach to problem-solving Capable of working independently and managing deliverables in a dynamic research setting Qualifications We’re looking for candidates with a strong academic background and hands-on industry experience in chemistry and impurity profiling. The ideal candidate will have: M.Sc. in Organic/Analytical Chemistry with a minimum of 4-6 years of relevant industrial experience OR Ph.D. in Chemistry with at least 2-3 years of experience in Impurity Profiling. 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!

Company Description Sinsil International Pvt Ltd supplies Scientific Research Equipment to over 10,000 customers across India, including Educational Institutes, Colleges, and Industries. With 7 branches and 25 years of service, we provide a wide range of equipment in fields such as Photovoltaics, Spectroscopy, Electrochemistry, Fuel Cells, Thin Film Metrology, Nanoscience/MEMS, Remote Sensing/Hyperspectral, Battery Charge/Discharge, and Power Processing Systems. We also offer comprehensive after-sales service for the equipment we supply. Role Description This is a full-time on-site role for a Sales and Service Engineer located in Kolkata. The role involves day-to-day responsibilities such as troubleshooting, providing field service, technical support, maintenance, and repair of scientific research equipment. The Sales and Service Engineer will interact with clients to ensure their equipment is functioning optimally and address any technical issues promptly. Qualifications Skills in Troubleshooting and Maintenance & Repair Experience in Field Service and Technical Support Excellent Communication skills Ability to work independently and assess clients' technical needs Knowledge of scientific research equipment and relevant technical expertise in the fields mentioned Generate AMC/Service revenue suggesting new accessories/Systems to existing client Experience of installing new systems Bachelor's degree in Engineering or related technical field is preferred Strong customer service orientation