216 Spectroscopy Jobs - Page 2

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

IT Full-Time Job ID: DGC00921 Chennai, Tamil Nadu 1-4 Yrs ₹1.8 - ₹05 Yearly Job Description Conduct laboratory experiments and studies to investigate biochemical processes, including metabolism, cellular signaling, and genetic expression. Analysis : Analyze and interpret data from experiments, using various techniques such as spectroscopy, chromatography, and molecular biology methods. Hypothesis Testing : Develop and test hypotheses to understand the molecular and chemical basis of biological phenomena. Publication : Prepare and publish research findings in scientific journals, contributing to the advancement of knowledge in the field. Teaching and Education : Educate and mentor students and junior researchers in biochemistry, often in an academic or research institution. Collaboration : Collaborate with other scientists, researchers, and interdisciplinary teams to address complex biological questions. Instrumentation : Use and maintain laboratory equipment and instruments to carry out experiments effectively.

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.,

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

This Job is based in Australia One of Australia’s leading research & teaching universities Vibrant campus life with a strong sense of community & inclusion Enjoy a career that makes a difference by collaborating & learning from the best At UNSW, we pride ourselves on being a workplace where the best people come to do their best work. The DNA Nanotech Lab at UNSW Sydney is recruiting a postdoctoral researcher to join a team working at the interface of supramolecular chemistry, DNA nanotechnology, and biomaterials science. The successful candidate will build functional, responsive systems from the bottom up using DNA and RNA self-assembly, under the supervision of Dr. Felix Rizzuto. This is a hands-on research role with significant intellectual freedom. The appointee will design and execute programs that leverage the chemistry of small and light-activated molecules for non-equilibrium DNA systems; characterise materials using advanced imaging (AFM, TEM), fluorescence spectroscopy, and biostructural tools; and collaborate with a diverse team of students and researchers across chemistry, biology, and materials science. Opportunities exist for the fellow to supervise students, collaborate with industry partners on translational research, contribute to grant development, and establish new lines of inquiry within the group’s broader mission. For more info on the group, see https://www.rizzutogroup.org/.. About The Role $113K - $121K plus 17% Superannuation and annual leave loading Fixed Term – 2 years Full-time (35 hours per week) The role reports to Scientia Senior Lecturer Dr. Felix Rizzuto and has no direct reports. About Us UNSW isn’t like other places you’ve worked. Yes, we’re a large organisation with a diverse and talented community; a community doing extraordinary things. But what makes us different isn’t only what we do, it’s how we do it. Together, we are driven to be thoughtful, practical, and purposeful in all we do. If you want a career where you can thrive, be challenged, and do meaningful work, you’re in the right place. The School of Chemistry is internationally recognised for its excellence in research and teaching. Our mission is to nurture students to become leaders who will generate societal, economic, and environmental benefits. The School is one of the largest and most prestigious schools in Australia for thriving research programs. Our School’s QS ranking for 2025 is #49 globally and the highest in Australia. For further information on the School go to https://www.unsw.edu.au/science/our-schools/chemistry Specific Responsibilities For This Role Include Contribute independently or as a team member in collaborative research with a focus to enhance the quality of research outcomes in the discipline area. Conduct research (as per the norms of the discipline) and/or enable research teams to create scholarly output that is recognised by peers. Undertake specific research project/s under the guidance of a research leader and contribute to development of research activities. Support the dissemination of research outcomes through appropriate channels and outlets. Undertake discipline-appropriate research activities, e.g. surveys, literature reviews, data gathering and/or recording of results using appropriate research methods. Participate in and/or present at conferences and/or workshops relevant to the project as required. Assist with the supervision of research students in the research area where required. Align with and actively demonstrate the Code of Conduct and Values. Cooperate with all health and safety policies and procedures of the university and take all reasonable care to ensure that your actions or omissions do not impact on the health and safety of yourself or others. About The Successful Applicant (Selection Criteria) To Be Successful In This Role You Will Have A PhD in Chemistry, Biotechnology, Nanotechnology, or a related discipline. Strong prior experience in DNA nanoscience and/or DNA origami synthesis and characterisation. Previous experience with non-academic and industry projects is desirable. Demonstrated expertise in supramolecular chemistry, computational modelling, and/or biochemistry is desirable. Demonstrated ability to undertake high quality academic research and conduct independent research with limited supervision. Evidence of supervision or mentoring of students. Demonstrated track record of publications and conference presentations relative to opportunity. Evidence of highly developed interpersonal skills, ability to work in a team, collaborate across disciplines and build effective relationships. An understanding of and commitment to UNSW’s aims, objectives and values in action, together with relevant policies and guidelines. Knowledge of health and safety responsibilities and commitment to attending relevant health and safety training. You should systematically address the selection criteria listed above in your application. Please apply online - applications will not be accepted if sent to the contact listed. Contact : Felix Rizzuto E: f.rizzuto@unsw.edu.au Applications close: August 12th, 2025 Find Out More About Working At UNSW At Www.unsw.edu.au UNSW is committed to equity diversity and inclusion. Applications from women, people of culturally and linguistically diverse backgrounds, those living with disabilities, members of the LGBTIQ+ community; and people of Aboriginal and Torres Strait Islander descent, are encouraged. UNSW provides workplace adjustments for people with disability, and access to flexible work options for eligible staff. The University reserves the right not to proceed with any appointment.

As a Chemical Laboratory Technician, you will be responsible for preparing test solutions, compounds, and reagents for conducting tests and coordinating test procedures. You will be tasked with determining the chemical and physical properties, compositions, structures, relationships, and reactions of both organic and inorganic compounds. Utilizing chromatography, spectroscopy, and spectrophotometry techniques will be a key aspect of your role. Your duties will also include the development, improvement, and customization of products, equipment, formulas, processes, and analytical methods. Collaboration with scientists and engineers to analyze, interpret, and develop tests will be essential. Additionally, you will introduce heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Furthermore, you will be responsible for writing technical papers and reports, as well as preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and procuring new laboratory supplies will also fall under your purview. Evaluating and ensuring compliance with laboratory safety procedures and standards will be a critical part of your responsibilities. This is a full-time, permanent position with benefits such as health insurance and Provident Fund. The work schedule includes day and morning shifts, with additional perks like performance bonuses and yearly bonuses. The work location is in person.,

As a Metallurgical Engineer, you will be responsible for developing and formulating metallic raw materials for dies and precision tools. You will analyze and recommend alloy compositions to ensure mechanical strength, wear resistance, and corrosion performance standards are met. Collaborating with R&D and production teams, you will work on new die/tool material innovations. Conducting metallurgical failure analysis, you will suggest improvements in tool performance and durability. Additionally, you will evaluate and manage heat treatment processes, coating, and surface finishing techniques while ensuring quality compliance with ISO and industry standards for metallurgy. Working closely with vendors/suppliers, you will verify that material specs are met for procurement. To qualify for this role, you should hold a B.E./B.Tech/M.Tech in Metallurgical Engineering or Materials Science and have at least 3 years of experience in tool/die metallurgy or a related manufacturing environment. A strong knowledge of steel grades, tool steels, powder metallurgy, and heat treatment is essential. Hands-on experience with spectroscopy, microstructure analysis (SEM/EDX), and hardness testing is required. Excellent analytical, problem-solving, and cross-functional communication skills will be beneficial in this position.,

Please call 9947350555 more details Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. Candidate will be qualified MSc chemistry . This job will prefer male candidate. Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. Using chromatography, spectroscopy, and spectrophotometry techniques. Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. Conferring with scientists and engineers to analyze, interpret, and develop tests. Introducing heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Writing technical papers and reports, and preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and purchasing new laboratory supplies. Evaluating and ensuring compliance with laboratory safety Job Type: Full-time Pay: ₹16,500.00 - ₹17,000.00 per month Benefits: Food provided Health insurance Provident Fund Schedule: Rotational shift Education: Master's (Preferred) Language: Malayalam (Preferred) Work Location: In person Speak with the employer +91 9947350555

Job description Job Title: Junior-Level Analyst – HPLC, UV, Dissolution, Assay, RS, and Method Validation Company: KMS Healthcare Pvt. Ltd. Department: Quality Control / Analytical R&D Experience: 0-1 years in pharmaceutical analysis Job Summary: We are seeking an experienced Analyst with expertise in HPLC, UV-Vis spectroscopy, dissolution testing, assay, related substances (RS), and method validation as per ICH guidelines . The candidate will be responsible for conducting analytical testing, preparing protocols/reports, and ensuring compliance with regulatory standards. Key Responsibilities: 1. Analytical Testing & Instrumentation; 2. Method Validation & Transfer; 3. Documentation & Compliance; 4. Cross-Functional Collaboration: Qualifications & Skills: Education: Bio Technology/ M.Sc./B.Pharm/M.Pharm in Chemistry/Pharmaceutical Sciences. Experience: 0-1 years in pharmaceutical QC/ADL labs HPLC/UPLC (Method development/validation preferred). Soft Skills: Detail-oriented, problem-solving, teamwork. Preferred: Experience in oral solid dosages (tablets/capsules) . Career growth in analytical development/validation. Job Type: Full-time Location: Walk-In-Interview: Door No.6, Kamarajar St, East Tambaram, Selaiyur, Chennai, Tamil Nadu 600059 . Timing Interview Schedule: 12 pm to 4pm Job Type: Full-time Pay: ₹12,000.00 - ₹18,000.00 per month Day shift Morning shift Work Location: In person Expected Start Date: 21/07/2025 Job Type: Full-time Pay: ₹12,000.00 - ₹18,000.00 per month Schedule: Day shift Morning shift Work Location: In person Expected Start Date: 21/07/2025

Job description Job Title: Junior-Level Analyst – HPLC, UV, Dissolution, Assay, RS, and Method Validation Company: KMS Healthcare Pvt. Ltd. Department: Quality Control / Analytical R&D Experience: 0-1 years in pharmaceutical analysis Job Summary: We are seeking an experienced Analyst with expertise in HPLC, UV-Vis spectroscopy, dissolution testing, assay, related substances (RS), and method validation as per ICH guidelines . The candidate will be responsible for conducting analytical testing, preparing protocols/reports, and ensuring compliance with regulatory standards. Key Responsibilities: 1. Analytical Testing & Instrumentation; 2. Method Validation & Transfer; 3. Documentation & Compliance; 4. Cross-Functional Collaboration: Qualifications & Skills: Education: Bio Technology/ M.Sc./B.Pharm/M.Pharm in Chemistry/Pharmaceutical Sciences. Experience: 0-1 years in pharmaceutical QC/ADL labs HPLC/UPLC (Method development/validation preferred). Soft Skills: Detail-oriented, problem-solving, teamwork. Preferred: Experience in oral solid dosages (tablets/capsules) . Career growth in analytical development/validation. Job Type: Full-time Location: Walk-In-Interview: Door No.6, Kamarajar St, East Tambaram, Selaiyur, Chennai, Tamil Nadu 600059 . Timing Interview Schedule: 12 pm to 4pm Job Type: Full-time Pay: ₹12,000.00 - ₹18,000.00 per month Day shift Morning shift Work Location: In person Expected Start Date: 21/07/2025 Job Type: Full-time Pay: ₹12,000.00 - ₹18,000.00 per month Schedule: Day shift Morning shift Work Location: In person Expected Start Date: 21/07/2025

Assistant Professor, Associate Professor, and Professor Desired Skillset: Applicants should preferably hold a Ph.D. in the relevant subject from reputed Institutions. Should have sufficient experience in Teaching, Industry & Research with reputed Institutions. Should have research papers published in International / National Journals. Should have books published and Scholars awarded / currently working for. Applicants with patents registered / consultancy works carried out will be given preference. Exposure in handling high-value funded projects will be an added advantage Preferred Qualifications: Ph.D. in relevant streams with good academic records Areas of Specialization: Expertise in revealing the mechanistic basics of chromatin modification. Structure determination of macromolecular complexes by Cryo-EM/ NMR spectroscopy. X-ray crystallography and related biochemical. Biophysical and cellular characterizations. Responsibilities: Academics: Classroom presentation Laboratory Instructions Development Learning of Resource Materials & Laboratory Development Student Assessment & Evaluation including Examination work of University. Participation in Co-curricular & extracurricular activities Student s guidance, counseling & helping in their personal, ethical, moral, and overall character development Keeping abreast of new knowledge and skills, help to generate new knowledge and help dissemination of such knowledge through books, publications, seminars, handouts, etc Continuing Education Activities Self-development through upgrading qualifications, Experience & Professional activities Research Consultancy: Research development activities & Research guidance Industry sponsored projects Providing consultancy and testing services Promotion of industry-institution interaction and R & D Academic / Administration: Academic and Administrative management of the institution Policy planning, monitoring & evaluation, and promotional activities; both at the department level and institution level Design and development of a new programme. Preparing projects for funding in areas of R&D work, laboratory development, modernization, expansion, etc Administration both at departmental & institutional levels Development, administration, and management at Institutional levels Monitoring and evaluation of academic and research activities Participation in policy planning at the Regional / National level for the Development of Technical Education Helping mobilization of resources for the Institution Develop, update and maintain MIS Plan and implement Staff Development activities, conduct Performance Appraisal Maintain Accountability Extension / Industrial Connectivity Interaction with Industry and Society Participation in Community services Providing R&D support and consultancy services to Industry and other user agencies Providing non-formal modes of education for the benefit of the Community Promotion of Entrepreneurship and Job rotation Dissemination of knowledge Providing Technical support in areas of social relevance Apart from the above duties, any other relevant work is assigned by the Dean of the respective schools

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

QA Engineer Location: Bangalore, India Job Term: Full-Time The Opportunity: Picarro is building the next generation of integrated solutions that incorporate various analytical instrumentation, such as our state-of-the-art laser-based gas sensors. These systems are adapted for numerous different industries to deliver trusted, actionable data to end users, allowing them to make critical operational decisions in their facilities based on unambiguous information that we provide. We seek an accomplished QA Engineer to enhance current capabilities in manual and automation testing. Our ideal candidates are familiar with the requirements associated with commercial grade applications that comply with established coding standards, design patterns, and technical specifications. Our culture encourages you to create innovative solutions and gives you the opportunity to work with some of the best and brightest in the industry. Job Summary: This position requires a passionate QA Engineer to design automated tests by creating scripts that run testing functions automatically as well as run tests manually. This includes participating with the development team to understand functionality, design test strategy and scenarios, determine the priority for test scenarios and create execution plans to implement these scenarios. Our ideal candidates are familiar with the software development life cycle (SDLC) based on Agile Scrum. Our culture encourages you to create innovative solutions and gives you the opportunity to work with some of the best and brightest in the industry. Responsibilities: Responsible for test design, implementation, and execution of manual, automated, functional, system integration, reliability, security, and performance testing. Responsible for development and maintenance of test automation frameworks and development and execution of test scripts Integrate automation to the CI/CD setup and operationalize automated smoke tests and daily automated runs to product releases Coordinating and supporting the planning and execution of QA/testing activities Coordinating activities across onshore and offshore resources Minimum Qualifications: A bachelor's degree in computer science, software engineering, computer engineering, or a related major is required 8 years of experience as QA Engineer Experience with Cloud, On-premises Hands-on knowledge of CI/CD, Container Orchestration (Docker, Kubernetes), Monitoring/Alerting, Security best practices, automated deployments, version control, merging, branching etc. Experience in tools and technologies like browser testing, selenium, TestNG, cucumber, python, GitHub, Jira, VM server, Kubernetes, Docker Experience working with Agile/Scrum Excellent communication/presentation skills Team player; flexible, dependable, and adaptable The right attitude, good work ethics and integrity Aspiration: Hunger to learn and contribute to solutions Initiator, self-starter & problem solver About Picarro: Picarro, Inc. is the world's leading producer of greenhouse gas and optical stable isotope instruments, which are used in a wide variety of scientific and industrial applications, including: atmospheric science, air quality, greenhouse gas measurements, gas leak detection, food safety, hydrology, ecology and more. The company's products are all designed and manufactured at Picarro's Santa Clara, California headquarters and exported to countries worldwide. Picarro's products are based on dozens of patents related to cavity ring-down spectroscopy (CRDS) technology. Picarro's solutions are unparalleled in their precision, ease of use, portability, and reliability. Honors awarded to the Company include the World Economic Forum of Technology Innovation Pioneer, IHS CERA Energy Innovation Pioneer, the U.S. Department of Energy Small Business of the Year, the TiE50 Winner and the Red Herring Global 100 Winner. Key investors include Benchmark Capital Partners, Greylock Management Corporation, Duff, Ackerman & Goodrich, Stanford University, Focus Ventures, Mingxin China Growth Ltd., Ntt finance and Weston Presidio Capital. 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 part recruiters/agencies and unsolicited resume submissions will be considered free referrals.

Job Title: Middle-Level Analyst – HPLC, UV, Dissolution, Assay, RS, and Method Validation Company: KMS Healthcare Pvt. Ltd. Department: Quality Control / Analytical R&D Experience: 3-7 years in pharmaceutical analysis Job Summary: We are seeking an experienced Analyst with expertise in HPLC, UV-Vis spectroscopy, dissolution testing, assay, related substances (RS), and method validation as per ICH guidelines . The candidate will be responsible for conducting analytical testing, preparing protocols/reports, and ensuring compliance with regulatory standards. Key Responsibilities:1. Analytical Testing & Instrumentation: Perform routine and non-routine analysis using HPLC, UV-Vis, dissolution apparatus , and other lab instruments. Conduct assay, related substances (RS), dissolution, and stability testing as per pharmacopeial methods (USP/EP/BP/IP). Troubleshoot and maintain analytical instruments (HPLC, UV spectrophotometer, dissolution apparatus). 2. Method Validation & Transfer: Prepare and execute method validation/verification protocols (Accuracy, Precision, Linearity, Specificity, LOD/LOQ, Robustness) as per ICH Q2(R1) . Support method transfer activities between labs or sites. 3. Documentation & Compliance: Prepare analytical reports, validation protocols, and reports in compliance with GMP/GLP . Review and ensure data integrity (ALCOA+ principles). Follow SOPs, pharmacopeial guidelines (USP/EP), and ICH requirements . 4. Regulatory & Audits: Support regulatory submissions (ANDAs, DMFs) with analytical data. Participate in internal/external audits (FDA, WHO, MHRA). 5. Cross-Functional Collaboration: Work with QA, R&D, and production teams for investigations (OOS/OOT, deviations). Train junior analysts on analytical techniques and compliance. Qualifications & Skills: Education: Bio Technology/ M.Sc./B.Pharm/M.Pharm in Chemistry/Pharmaceutical Sciences. Experience: 3-7 years in pharmaceutical QC/ADL labs , with hands-on experience in: HPLC/UPLC (Method development/validation preferred). UV-Vis spectroscopy, dissolution testing (Apparatus I/II). Assay, RS, forced degradation studies. Regulatory Knowledge: ICH, USFDA, GMP, GLP. Software: Empower, LabSolutions, Dissolution software. Soft Skills: Detail-oriented, problem-solving, teamwork. Preferred: Experience in oral solid dosages (tablets/capsules) . Knowledge of impurity profiling, stability studies (ICH Q1A). Why Join Us? Opportunity to work in a GMP-compliant lab with advanced instrumentation. Career growth in analytical development/validation. Exposure to global regulatory standards. Job Type: Full-time Location: Door No.6, Kamarajar St, East Tambaram, Selaiyur, Chennai, Tamil Nadu 600059 Job . Job Type: Full-time Pay: ₹30,000.00 - ₹60,000.00 per month Schedule: Day shift Morning shift Work Location: In person Expected Start Date: 25/07/2025

Hello Connection Greetings from Nexus...!!! We are urgently looking for Electrical Engineer for one of the Govt. Research Services Industry Location: Vadodara, Gujarat Experience: 3-8 yrs Qualification: BE / B.Tech in Electrical Engineering (First Class) Job Description : 1. HV equipment Diagnostics testing. 2. Analysis of condition monitoring data & preparation of report. 3. Special tests execution (i.e, ELCID, RSO, PD detection by AE & Dielectric spectroscopy etc) 4. Preparation of project proposal for R&D activity related to electrical diagnostic 5. Coordination for quality related activity. Technical Competencies/ Skills Required: 1. Knowledge of various diagnostic kits like c/ tandelta, SFRA, RSO kit, PD, etc 2. Hands on knowledge on ISO:17025. 3. Experience in various techniques for Diagnostics of switchyard equipment’s like Transformer, CT/PT, bushings, surge arrestors & rotating machines etc. 4. Hands on experience at site for Condition Monitoring testing 5. Experience in R&D project work If you are looking for job change share your updated CV on nexusgroup.hr3@gmail.com Feel free to Connect HR Specialist Riya 9925248488 Job Type: Full-time Pay: ₹500,000.00 - ₹900,000.00 per year Schedule: Day shift Experience: HV equipment Diagnostics testing: 4 years (Preferred) R&D project work: 4 years (Preferred) ISO :17025 related activity: 4 years (Preferred) Work Location: In person