35 Mass Spectrometry Jobs

Intas Pharmaceuticals is a renowned multinational pharmaceutical company known for its significant presence in multiple countries and its expertise in top-ranking therapeutic segments such as CNS, Cardio, Diabeto, and Oncology. With cutting-edge research and manufacturing facilities in India, the UK, Mexico, and Greece, Intas focuses on the development of cost-effective Biosimilars and plasma-derived therapeutics. The company's core values include a dedication to innovation, customer satisfaction, and social responsibility. As a Research Scientist specializing in Mass Spectrometry at Intas Pharmaceuticals in Ahmedabad, you will be responsible for conducting research, analyzing mass spectrometry data, formulating analytical methods, and collaborating with diverse teams to support the biopharma and plasma fractionation units of the company. To excel in this role, you should have a solid background with 4-8 years of experience in Mass Spectrometry, Analytical Chemistry, and Research Methodologies. Proficiency in biopharmaceuticals, oncology, and plasma-derived therapeutics is essential. Additionally, you must possess expertise in data analysis, method development, and quality control processes. A thorough understanding of EU-GMP and WHO-GMP guidelines is crucial for ensuring compliance with industry standards. Strong problem-solving abilities and effective collaboration skills are key attributes required for this position. Ideally, you should hold a Master's or Ph.D. degree in Chemistry, Biochemistry, or a related field to meet the educational qualifications necessary for this role. If you are passionate about advancing pharmaceutical research, driving innovation, and contributing to the development of life-saving therapeutics, this opportunity at Intas Pharmaceuticals could be the ideal fit for you.,

You should have 3 - 4 years of experience and hold a qualification of M.Sc in Chemistry. As a Lab Technician, your responsibilities will include: - Performing routine lab tasks following standard operating procedures for sample preparation using standard techniques. - Conducting chemical solutions, standards, and dilutions as per the defined procedures. - Evaluating data and reporting/uploading it into the data reporting system. - Reporting any unusual test occurrences to the department manager and adhering to laboratory QA/QC practices. - Maintaining general housekeeping in the work area/department. - Conducting instrument maintenance, including Gas Chromatography / Mass Spectrometry, and troubleshooting as necessary. - Assisting other laboratory technicians in different departments based on workload requirements. - Ensuring instruments are running optimally to meet clients" needs by uploading calibration curves and data. - Collaborating with the department manager to enhance efficiency, reduce downtime, and costs. - Updating Standard Operating Procedures (SOPs) and working towards continuous improvement of methods, instruments, and protocols to meet benchmarks. You will work closely with the department manager to achieve operational excellence and deliver high-quality results to meet the organization's objectives.,

Key Responsibilities: Perform aseptic handling for various upstream operations. Prepare media and feeds for shake flask experiments and bioreactor batches. Handle shake flasks for clone selection, media optimization, and feed strategy development. Prepare and maintain bioreactors at different scales (1L, 5L, 20L). Execute upstream batches in small-scale and large-scale bioreactors. Conduct in-process sample analysis including cell count, viability, and metabolite levels (glucose, lactate, ammonia, glutamine, etc.). Draft and maintain Standard Operating Procedures (SOPs) for instruments and processes. Participate in shift duties for continuous batch monitoring and process support. Collaborate effectively within a team environment to ensure smooth upstream operations.

We are Reckitt Home to the worlds 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 were 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 Reckitts 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 Reckitts pay for performance philosophy. We recognise that in real life, great people dont always tick all the boxes. Thats why we hire for potential as well as experience. Even if you dont 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.

You should be fluent in Application Development and have experience in developing applications for compound and biomolecule analysis. Your expertise in Mass Spectrometry will be crucial, as you will be skilled in using mass spectrometry for detection and analysis. Additionally, you should be well-versed in instrument handling and operation, understanding mass spectrometry instrumentation and its operational workflows. Proficiency in sample pre-processing techniques is required for accurate analysis, along with a strong ability in quantification and spectral data interpretation. You should also be skilled in method troubleshooting and validation, capable of identifying issues and ensuring method consistency and compliance through process and method validation. The key requirements for this role include a postgraduate or PhD in Analytical Chemistry with specialization in Mass Spec or Physics. The job location for this position is Bangalore. For more information or to apply, please contact us at career@bigtec.co.in or hr@bigtec.co.in.,

You will be joining Reckitt, home to some of the world's most beloved hygiene, health, and nutrition brands. Our purpose is to protect, heal, and nurture in our continuous efforts towards a cleaner, healthier world. As a global team, we are united by this purpose, striving to ensure that access to top-quality hygiene, wellness, and nourishment is a fundamental right for all. As a Senior Associate in the Germ Protection Analytical Research & Development team at Reckitt Research and Development in Gurugram, Haryana, India, you will play a crucial role in the product development of Germ Protection brands like Dettol, Harpic, and Lizol. We are looking for a self-motivated and experienced analytical chemist who can actively contribute to the team as a scientist in the lab and as a leader to other analytical chemists. Your responsibilities will include contributing to the development of new products and technologies, conducting studies to enhance product functionality and efficacy, leading the development and validation of new methods for product launch and claim support, and utilizing various analytical techniques such as chromatography (LC and GC), mass spectrometry, and spectroscopy for efficient and robust analysis. Additionally, you will be expected to support the enhancement of analytical capabilities by identifying new technologies and methodologies, manage multiple projects within established timelines, and effectively communicate results to diverse audiences through scientific reports, technical documents, SOPs, and protocols. The ideal candidate should possess a PhD with 5 years, MS with 8 years, or BS in chemistry or related field with 10 years of relevant work experience in an R&D analytical laboratory setting. Knowledge of a wide range of analytical techniques including LC, GC, FTIR, and wet chemistry techniques is required, with advanced knowledge in liquid chromatography being preferred. Strong communication skills, both written and verbal, along with being results-oriented, self-motivated, and having a problem-solving attitude are essential. You should also showcase intellectual curiosity and the ability to work independently as well as in a cross-functional team environment while being adaptable to changing project priorities. At Reckitt, we offer an environment that values equality and encourages personal and professional growth. Join us in our mission to create a cleaner, healthier world for all.,

Summary 400! This is the number of associates in Global Analytical R&D, across 4 countries, working tirelessly on innovative and patient centric medicines. As part of this group, you design, plan and/or perform scientific/technical studies. By bridging the analytical science to the clinical performance, you will drive the transformation of our molecules into medicines that improve and extend patient s lives. The position is based in the Genome Valley, Hyderabad, within the Technical Research and Development Organization (TRD) of Global Drug Development (GDD). About the Role Major accountabilities: Design, plan and interpret scientific experiments for projects at different clinical phases of drug substance and drug product development with minimal guidance. Well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports. Provide scientific guidance to the laboratory associates Write, review and/or approve analytical documentation in timely and high-quality manner, such as releases, analytical batch records, method validations, stability, technical reports, SOP s etc. ensuring compliance with Novartis and health authorities guidelines Helping to define the overall analytical control strategy Contribution to scientific exchange groups within Novartis Report and present scientific/technical results internally and contribute to publications, presentations, and patents Manage interactions and contribute to a high level of collaboration with internal and external stakeholders. Adhere to Quality metrics, Compliance and Good Documentation Practices following ALCOA+ principles, GLP, OQM, HSE, ISEC and Novartis guidelines. Should be a Team player by adding value in collaborating with other teams to support project deliverables within agreed timelines, mentoring new joiners, active participation in project meetings / networks / meetings and contributing to team goals while meeting individual objectives. Ability to perform investigations, guide team members, communicate proactively and clearly to global stakeholders and handle multiple priorities. Provide input into CMC documents to support regulatory submission and respond to HA queries. Role Requirements PhD in analytical chemistry or equivalent and a minimum 6 years experience or M. Pharma/M. Sc with a minimum of 12 years experience in the pharmaceutical industry in analytical research and development Experience in leading analytical activities in NCE across different phases of drug development, including complex injectables, parenteral, oligonucleotides/ peptides. Strong experience in various chromatography techniques is a pre-requisite. Experience in mass spectrometry applied to biological molecules would be an asset Profound expertise in liquid chromatography separation techniques such as (RP, IEX and HILIC) is a must Experience in Late phase method validation is an asset Good knowledge of software and computer tools such as Office package, LIMS, chromatography data-evaluation software (e.g. Chromeleon) etc. GMP experience in analytical laboratory Successfully demonstrated expertise in a specific scientific/technical area Good presentation skills and scientific/technical writing skills. Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

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.,

As the Lead Specialist GOE CAL at dsm-firmenich in Mumbai, you play a crucial role in bridging the gap between taste, texture, and health through innovative ingredients and solutions. Diversity, Equity & Inclusion is at the core of our values, ensuring equal access to opportunities, a sense of belonging, and authenticity celebrated across the organization. Your responsibilities include planning and conducting analytical techniques such as GC-MS, LC-MS for flavors, perfumes, and natural products, contributing to method development and the team's technical growth. You will manage analytical instruments, lab operations, ensure SOP compliance, accurate documentation, and collaborate closely with cross-functional teams to provide effective analytical support. Utilizing your expertise in gas chromatography and mass spectrometry, you will conduct volatile compound analysis, prepare analytical reports, and serve as a subject matter expert in analytical/flavor chemistry. Your problem-solving mindset, drive for innovation, and strong sense of ownership will be essential in delivering meaningful results and collaborating within diverse teams. We offer a supportive and empowering environment that encourages personal growth, a crucial role in projects, and the opportunity to build your brand. If you hold an MSc. with 5+ years or Ph.D. with 2+ years of experience in analytical chemistry, possess hands-on experience in method development, and demonstrate knowledge of ISO 17025:2017 standards, we invite you to apply online via our career portal. Join our global and collaborative team at dsm-firmenich, where innovating in nutrition, health, and beauty is at the heart of what we do. With a diverse workforce and a commitment to progress, we aim to create essential solutions for life, desirable products for consumers, and a more sustainable future for the planet.,

Long Description 1. Perform characterization of peptides , nucleic acids-based (oligonucleotides) or other injectable drug products using High Resolution Mass Spectrometry (LC-HRMS) . Experience with QToF/Orbitrap instruments and Ion Mobility will be preferred. Additional experience in Fluorescence, particle size analysis (DLS), and other relevant techniques (e. g. SEC-MALS) are desirable. 2. Analyze and interpret LC-MS and MS/MS data for impurity profiling and characterization. Solve problems and implement new research methods through literature search, coordinate with cross-functional teams (formulation, QA, QC, regulatory, etc. ), application specialists, etc. to complete analytical tasks. 3. Prepare, review and share LC-MS data and documentation (SOP, STP, Test Reports, etc. ) in a timely manner for regulatory submissions. Follow good laboratory practices (GLP) , manage samples (collection, storage, and disposal), deviations and incidences as per established procedures. 4. Undertake routine maintenance & calibration of the analytical instruments, troubleshoot equipment malfunction often in coordination with service engineers, etc. Assist in the maintenance of the laboratory, inventory of R&D consumables, & other lab management activities from time to time Competencies Education Masters in Pharmacy or Applied Chemistry Doctorate in Pharmaceutical Technology or Analytical Chemistry Work Experience 5 - 7 years (with MPharm) or NIL (with PhD)

Looking Chemist for Metals and Minerals testing for world's leading testing & Certification company,NABL , 17025 lab having experience in ICP OES Job Summary: Provide expertise in chemical analysis and research to contribute to the development and improvement of products and processes. Conduct experiments, analyze results, and interpret data to draw conclusions and make recommendations. Ensure compliance with regulatory standards and safety protocols. Key Responsibilities: Perform chemical synthesis, purification, and characterization of compounds. Use analytical techniques such as spectroscopy, chromatography, and mass spectrometry for qualitative and quantitative analysis. Document experimental procedures, results, and findings accurately. Collaborate with multidisciplinary teams to achieve project goals. Stay current with scientific literature and advancements in the field. Maintain laboratory equipment and ensure proper calibration and operation.

Role & responsibilities Manager technical is the In-charge of Analytical Division. He/She shall report to the SBU-head about all the activities in the Analytical Division. He/She shall look after all the operations of the Division under the guidance/ supervision of SBU-Head. He/She shall be responsible for the standardization and validation of the test methods. He/She shall be responsible for ensuring the availability of the reference material / working reference standard. He/She shall be responsible for assigning the jobs to the analyst as per their calibre. He/She shall be responsible for checking the calculation part and reporting of the results before sending for authorized signatory. He/She shall be responsible for the smooth operations of the equipments/Instruments. He/ She shall be responsible for signing the test certificate / test reports. He/ She shall be responsible for verifying the outside calibration certificates. He/She shall be responsible for the supervision of technical staff working under him/ her. He/She shall be responsible for filling the change control, deviation control, OOS, CAPA raised by technical department. He/She shall be responsible for the preparing / reviewing the scope as per requirements. He/She shall ensure that the glassware used in his / her section should be duly calibrated or verified as required. He/She shall be responsible for the qualification and calibration of new instruments/ equipment. He/She shall be responsible for the maintaining overall quality as per ISO/IEC 17025. He/She shall be responsible for all the relevant works of VP- Technical/GM Operation in his absence.

Role & responsibilities Preferred candidate profile

Job Title: Lead Specialist - GOE CAL (Experience in Metal & Pesticide Analysis) Location: Mumbai, India Work Type: On-site At dsm-firmenich we strive to achieve a world where you don t have to choose between taste, texture, or health - and can enjoy it all. Our innovative ingredients, expertise, and solutions bridge the gap between the delicious, the nutritious, and the sustainable. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your Key Responsibilities Perform GC-MS and LC-MS analysis of flavors, perfumes, aroma chemicals, and natural products. Manage and maintain lab instruments, SOPs, documentation, and inventories to ensure ISO17025:2017 compliance. Develop and validate analytical methods and contribute to team knowledge sharing. Collaborate with cross-functional teams including Creation, Application, QA, and regional/global counterparts. Prepare, review, and communicate analytical reports using internal tools and databases. Lead coordination of analytical support from global or external resources and provide subject-matter expertise. We bring A team of diverse employees who aren t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you re empowered to grow and share your ideas. You Bring MSc (+5 years) or PhD (+2 years) in Analytical Chemistry or related fields. Hands-on experience with GC-MS and LC-MS techniques in commercial/research labs. Strong skills in mass spectrometry and analytical method development. Familiarity with ISO17025:2017 and exposure to metal & pesticide analysis. High level of ownership and drive for results in a cross-functional environment. Strong communication skills with the ability to collaborate and influence across teams. The application process: Interested in this position? Please apply on-line by uploading your resume in English via our career portal. For . We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate : theres a place for everyone at dsm-firmenich. Dsm-firmenich is an Equal Opportunity and Affirmative Action Employer. dsm-firmenich people are as diverse as our customers. For us that includes a commitment to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicants race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know. About dsm-firmenich As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the worlds growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than 12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people.

Your Key Responsibilities Perform GC-MS and LC-MS analysis of flavors, perfumes, aroma chemicals, and natural products. Manage and maintain lab instruments, SOPs, documentation, and inventories to ensure ISO17025:2017 compliance. Develop and validate analytical methods and contribute to team knowledge sharing. Collaborate with cross-functional teams including Creation, Application, QA, and regional/global counterparts. Prepare, review, and communicate analytical reports using internal tools and databases. Lead coordination of analytical support from global or external resources and provide subject-matter expertise. We bring A team of diverse employees who aren t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you re empowered to grow and share your ideas. You Bring MSc (+5 years) or PhD (+2 years) in Analytical Chemistry or related fields. Hands-on experience with GC-MS and LC-MS techniques in commercial/research labs. Strong skills in mass spectrometry and analytical method development. Familiarity with ISO17025:2017 and exposure to metal & pesticide analysis. High level of ownership and drive for results in a cross-functional environment. Strong communication skills with the ability to collaborate and influence across teams.

Role & responsibilities :- 1) Knowing HPLC/ GC, Dissolution, UV, FT-IR, Potentiometer Troubleshooting, Calibration, Method Validation and Method Development. 2) Perform the analysis individually for In process and stability samples as per plan. 3) Follow Good manufacturing practices, Good laboratory practices and Good documentation practices in ADL. 4) Method Development of new products for test like Cleaning, Assay, Residual solvent, Dissolution & organic impurities. 5) Preparation, storage and usage of Volumetric / Reagent / Standard / Indicator solution. 6) Perform the calibration and verification of all instrument / equipment as per calibration scheduled. Preferred candidate profile :- Post-Graduation in M.Sc. Analytical Chemistry, Organic Chemistry From the Pharma Background Industry. Knowing GCMS, LCMS is added advantage Perks and benefits :- As per the company Policy

Job Description : Experience in operation and calibration of (HRMS/qTOF). Experience on Intact Mass Analysis, peptide Mapping, Impurity profiling, unknown impurity structure identification, sequencing of Peptides, biosimilars and small molecules. Independent Data analysis of characterization experiments. Experience in impurity profiling of GLP1 analog peptide API and formulation products. Preparation of summary reports, SOPs, Protocols and Reports Transportation & Canteen Facilities Available

Hi Everyone We Are hiring for Senior Analyst with the below information: Sr.Analyst with 5-6 years exp in food testing labs Good hands on experience in handling either LCMSMS or GCMSMS Antibiotics and pesticides samples preparation Method validations as per SANTE and EU 808/2021 guidelines If Any Interested candidate can Reach out to : lavanya.m@intertek.com/ Whats app 9205065847

#hiring. Know anyone who might be interested? Veeda Lifesciences (Veeda Clinical Research) is seeking a passionate "Characterization Specialist" Experience: with 3 to 6 yrs Location: Bangalore Interested candidates can share an updated CV to mahendra.t3705@veedalifesciences.com JOB DESCRIPTION: Role & responsibilities: Experiments Execution of planned experiments/studies using physico-chemical methods. Develop advanced LC-MS-based methodologies for the characterization of protein and peptide products. Design and implement integrated analytical strategies by combining chromatography and mass spectrometry techniques. These strategies aim to qualitatively and quantitatively assess product-related variants and impurities. This includes the development of innovative sample preparation methods, with a focus on LC-MS, CEX-MS, and SEC-MS, native MS, HDX as well as the characterization of innovator product batches sourced from various geographical regions to establish a comprehensive quality target profile. Lead the development of sophisticated analytical workflows, including multi-attribute methods for post-translational modifications (PTMs), sequence variant analysis, profiling of host cell proteins (HCPs), disulfide bond analysis and shuffling, cell culture metabolite analysis, and glycan profiling. Data Generation Sample preparation, data acquisition, data analysis/processing of HPLC/UPLC/LCMS/HRMS/CE based experiments/studies. Preferably on Thermo/Waters/Sciex platforms. Interpretations Scientific interpretations of processed data (manual/software-driven). Reporting Reporting of scientific data into suitable/approved report formats. Data Integrity Adherence to data integrity principles (ALOCA++) and quality compliance, as applicable. Documentation Preparation and up-keep of documents such as standard operating procedures, instrument/equipment related documents on qualification/validation, as applicable. Instrumentation Co-ordinate for maintaining the operational status of respective instrument/equipment with vendors/OEM. Ad-hoc Studies Execute ad-hoc studies/experiments/activities based on organizational needs/priorities. Knowledge Upskill with advancements in physico-chemical and/or structural characterization through literature surveys/webinars/conferences/symposiums. Conferences Participate in scientific meetings/interactions and present scientific data in form of posters/oral presentations/publications.

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr Shyam S Bhartia and Mr Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services Jubilant Bhartia Group has four flagships CompaniesJubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited Currently the group has a global workforce of around 43,000 employees About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research servicesfrom target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)in partnership with leading worldwide healthcare companies With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology,in-vivo,in-vitromodels and translational sciences Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the worlds leading pharmaceutical, biotech companies, academic institutions and research foundations Find out more about us at www jubilantbiosys com The Position Organization : Jubilant Biosys Designation & Level: Senior Research Associate (SRA-1/ SRA-2) (S3/S4) Location: Greater Noida Department: Synthesis Key Responsibilities Synthesis, purification, and characterization of novel intermediates Deliver small to large quantities of by novel chemical entities for drug discovery Work collaboratively in a team to drive chemistry projects forward Responsible for safe conduct of reactions Excellent knowledge in basic and advance organic chemistry Good knowledge in functional group conversion and multiple step synthesis Basic knowledge retrosynthetic analysis (desirable) Good expertise in handling pyrophoric reactions Good knowledge of TLC, column purification, extraction Excellence in analysing NMR, IR and Mass Spectrometry data Always adhere to safe laboratory practices Enthusiasm to work in a dynamic research environment Always stretch when project challenge increases Good knowledge in computer (MS-word/Excel/Power point) and structure drawing (Chem Draw/ISIS) and recording in electronic lab notebook Good communication and presentation skill Good in literature search using Sci Finder Person Profile Qualification: - Sc in Organic Chemistry or related field/ M Experience: (below are Sample points) 5-10 years of industry experiences with any leading CRO organization Jubilant is an equal opportunity employer All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances

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

Roles and Responsibilities Develop analytical methods for biochemistry samples using GC-MS, LCMS, and other relevant techniques. Conduct method validation, optimization, and transfer to ensure accuracy and reliability of results. Collaborate with cross-functional teams to resolve method-related issues and improve overall efficiency. Maintain accurate records of experiments, data analysis, and reporting in accordance with regulatory requirements. Stay up-to-date with industry developments in mass spectrometry technologies and apply this knowledge to improve laboratory operations. Desired Candidate Profile 2-7 years of experience in Analytical Method Development & Validation (GC-MS & LCMS). MS/M.Sc(Science) degree in Bio-Chemistry or Chemistry from a recognized university. Strong understanding of chromatography principles, including HPLC/UPLC systems. Proficiency in developing analytical methods for biochemistry samples using various instruments such as GC-MS/MS.

Work Schedule Standard Office Hours (40/wk) Environmental Conditions Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description About Chromatography & Mass Spectrometry Division! The Chromatography and Mass Spectrometry business creates innovative instruments, consumables, and software solutions for analytical sciences. Roles and Responsibilities: Support Thermo Fisher customers through technical service, installation, operation, training, and repair of specialized analytical equipment like HPLC and CAD (Aerosol detector). Undertake product installation on client premises and demonstrate features related to 21 CFR compliance. Provide training and technical advice on instrument use, both in person and by phone, sharing Dos and Don ts for optimum performance of the system. Investigate difficulties and solve faults arising from operation or utilization. Rectify problems, suggest solutions, or arrange for repairs to be made. Provide a vital link between customers and Sales and Marketing. Ensure effective service is provided to the customer by maintaining communication between the customer and the company. Monitor repairs in terms of the organization s service/warranty cover and make suggestions for product improvements. Carry out planned maintenance calls and perform regular customer visits. Make recommendations about spare parts requirements and assist with monitoring equipment. Achieve assigned spares and service revenue targets by promoting PM kits, instrument upgrades, and software upgrades. Extensive traveling within the territory is required, with potential travel outside the territory if needed. Knowledge, Skills, and Abilities: Bachelor of Technology (Biotechnology/Electronics). 4 to 5 experience in analytical equipment like HPLC and CAD (Aerosol detector). Proficient in written and verbal communication. Interpersonal skills needed for a role that involves interacting with various individuals within and outside the company. Ability to prioritize service requests and produce clear and concise documentation. Self-motivated and proactive in technical and support approaches. Work closely with customers to understand their pain areas and act as a consultant between the organization and the customer, helping both achieve regional commercial goals. Build good rapport with customers and educate them about the procurement of PM kits annually, reducing system downtime.

Technical and people leadership of sample analysis activities carried out at the Innovation Centre, Supervise and provide support to Analytical Scientist team, Responsibility for the reporting and dissemination of sample analysis results to internal and external stakeholders as necessary, To perform as proactive liaison with the R&D and Innovation Centre faculty team to ensure planned work can proceed to schedule, To coordinate with key stakeholders to ensure successful project deliveries, To develop enhanced analytical methods used for sample characterization, Contribute to the progression of CCSL s IP portfolio, To develop and present various standard and ad-hoc reports for a variety of audiences, Ensuring the smooth operation of analytical suite. This role will be based on site 5 days a week in the office Masters degree in Chemical Engineering, Chemistry, Analytical Chemistry or Materials Science (or related), PhD preferable. 5+ years of analytical laboratory research experience necessary. Strong demo

Immunology innate immune mechanisms in disease pathogenesis Metabolomics, particularly in the context of aging and metabolic disorders Organoid-Based Cell and Developmental Biology Genomics Informatics Lipid Trafficking Department hosts state-of-the-art research facilities in genomics, mass spectrometry, drug screening, flow cytometry, Drosophila biology, protein expression and characterization, in vivo & in vitro biosafety laboratories and an advanced imaging facility. Additionally, they are home to two major research centers: the Center for Integrative and Translational Research, which support preclinical models of health and disease and the Center of Excellence in Epigenetics. These are further strengthened by university-wide initiatives such as the SNU-Dassault Systems Center that facilitates computational biology studies. Selected candidates will be expected to establish and maintain an independent, externally funded research program, actively engage in undergraduate and graduate teaching, and contribute to the development of interdisciplinary courses and initiatives in collaboration with other departments across the university. Qualification Faculty appointments are open at all levels from Assistant to Full Professor based on the candidate s qualifications, experience, and alignment with the department s strategic vision. Applicants must hold a Ph.D. in the Sciences and have completed a productive postdoctoral tenure that clearly demonstrates strong potential for an internationally recognized and impactful research career.