341 Method Development Jobs - Page 4

Detailed Job Role Conduct biochemical tests and research to support drug development and quality control processes. KRA (Key Responsibility Areas) Experiment design, sample analysis, data recording, method development KPI (Key Performance Indicators) Experiment accuracy, validation rate, milestone achievement, innovation outputs Job description Department: Research & Development / Quality Control Reports To: Senior Scientist / R&D Manager Job Purpose / Summary: To conduct biochemical tests, research, and analysis to support drug development and quality control processes, ensuring accurate data generation, method validation, and compliance with scientific standards. Key Responsibilities & Duties (KRA): Experiment Design & Execution : Plan and perform biochemical experiments for drug discovery and quality testing. Sample Analysis : Conduct biochemical and molecular assays on samples using standard laboratory techniques. Data Recording & Documentation : Accurately record experimental results, maintain lab notebooks, and prepare reports. Method Development : Support in developing, validating, and optimizing biochemical test methods. Collaboration : Work closely with R&D, quality, and cross-functional teams to achieve project goals. Compliance : Adhere to laboratory safety protocols, GLP/GMP, and organizational quality standards. Key Performance Indicators (KPI): Accuracy of Experimental Results (%) Method Validation & Success Rate Milestone Achievement (Projects/Timelines met) Number of Innovation Outputs (e.g., new techniques, process improvements) Compliance with Safety & Documentation Standards Education Required B.Sc / M.Sc (Biochemistry/Life Sciences)

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation DQA Department Development Quality Assurance / Formulation Quality Assurance R&D: Handling of QMS documents and Ensure the SOP compliance Review of Formulation Analytical Development Documents & Formulation Product Development Documents. Method Validation and Transfer Protocols and Reports Product development with QbD approach Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs. Review of FRD activities (LNBs, BDRs, PDRs, MFRs and MPR) SOPs and Guidelines Preparation and Review and Approval of SOPs. Responsible for conducting Internal Audits/External Audits for Cross functional Departments in Formulation Division and External Division. Conducting and Coordinating Employee Trainings. Responsible for Review and Approval of Vendor Qualification Should have experience in IPQA and Analytical QA (OSD/Injectable) Ref to Friends or colleagues. Please share update resume: careers@biophore.com Total Exp: Current CTC: Exp CTC : Notice Period: Current Designation:

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation AR&D Department . Position : Research Analyst or Sr Research Analyst Experience : 3 - 8 Yrs Job Description: Responsible for Analytical Method Development activities solid orals and injectables Responsible for Responsible for Planning and Monitoring of Method development activities and Regular Analysis for solid orals and Injectables. Responsible for Routine and Stability analysis activities for solid orals and injectables. Responsible for the Review of documents generated in Method development activity. Responsible for the Preparation and Review of Tentative method of analysis and Method development Reports. Responsible for the review of Routine samples documents, Preformulations documents for the Solid oral products and Parental products. Responsible for the Review of Calibrations documents (i.e Dissolution, HPLC, UV and balance). Knowledge on ICH guidelines and all Regulatory guidelines Ref to Friends or colleagues Please share resume: careers@biophore.com at below mentioned address (Interview Date 29-08-2025-30-08-2025) Biophore India Pharmaceuticals Pvt Ltd. Plot# 231, IDA Phase -II, Pashamylaram, Biophore Road, Patancheru (M), Hyderabad. Sangareddy District Telangana 502307

As a Quality Control Analyst in the chemical industry at Gait Naurish (I) Ltd. located in Sector 155, Noida, Uttar Pradesh, you will be responsible for ensuring that all incoming raw materials, in-process samples, and finished products meet predefined quality and regulatory standards. With a minimum of 1 year of experience in a chemical/QC laboratory environment, you will play a crucial role in conducting various analytical tests and maintaining high-quality standards. Your key responsibilities will include performing analytical testing such as chromatographic analyses using GC and HPLC, moisture determination via Karl Fischer titration, and TLC for qualitative assessments. Additionally, you will assist in developing, optimizing, and validating new analytical methods following ICH and USP guidelines, while also supporting quality assurance by preparing analytical reports, investigating nonconformities, and participating in audits to ensure compliance with GLP/GMP standards. To excel in this role, you should hold a Bachelor's or Master's degree in Chemistry, Analytical Chemistry, or a related discipline, along with at least 1 year of hands-on experience in a QC/analytical laboratory within the fine chemicals, pharmaceutical, or related industry. Technical expertise in GC, HPLC, Karl Fischer titration, and TLC techniques is essential, along with proficiency in chromatographic software and LIMS. Your soft skills should include attention to detail, analytical mindset, problem-solving ability, strong communication skills, and the ability to work independently and collaboratively in a fast-paced environment. At Gait Naurish (I) Ltd., we offer a competitive salary, performance-based incentives, comprehensive health insurance, professional development opportunities, and a collaborative work culture in a cutting-edge R&D and manufacturing environment. If you are interested in this full-time position, please send your CV and a cover letter to hrm@fnni.in with the subject line "Quality Analyst Chemist - Sector 155, Noida". Join us to be part of a dynamic team dedicated to quality and innovation in the chemical industry.,

Works closely with the Lead Scientist to develop and refine pouch formulations, Focuses on ingredient optimization, flavor blending, and pilot-scale testing Supports transition from lab to production. Required Candidate profile M. Pharma with 8+ years of experience in oral formulations and operations in pharmaceuticals.

Oversee all R&D initiatives for nicotine pouches and related oral dosage innovations Leads formulation strategy, raw material research, stability studies, and new product concepts acts as the technical head for regulatory submissions and IP. Required Candidate profile Experience in pharma and oral drug delivery products.

As a Quality Assurance & Analytical Chemist at FMC, you will be part of a team dedicated to providing innovative solutions for agriculture, contributing to the productivity and resilience of farmers" land. With a focus on science and technology, you will play a vital role in developing new herbicide, insecticide, and fungicide active ingredients, product formulations, and pioneering technologies that benefit both farmers and the environment. Your responsibilities will include: - Ensuring laboratory safety and industrial hygiene protocols are followed at all times. - Developing, validating, and implementing qualitative and quantitative analysis methods to meet business needs. - Conducting routine and non-routine analysis to support project quality and timing requirements. - Collecting data, generating summaries, and preparing reports. - Collaborating with tech leaders to investigate quality incidents and implement corrective actions. - Operating and maintaining various analytical instruments (HPLC, GC, IC, MS, Titrator, FTIR) to provide accurate data. - Collaborating with chemists and engineers to provide analytical results and structure determinations. - Managing the quality of active ingredients and intermediates with contract manufacturers. - Supporting changes in processes, equipment, and materials through QAR coordination. - Reviewing MOA and analytical Teck pack for improvement suggestions. - Performing other tasks as assigned by the line manager. The ideal candidate will have: - A Master's degree or above in chemistry/biochemistry or equivalent experience. - 10+ years of experience with a minimum of 8 years in analytical development/quality control. - Proficiency in method development and troubleshooting with various lab instruments/techniques. - A track record of delivering quality results on time. - Strong interpersonal skills, problem-solving abilities, and communication skills. - Familiarity with computer software packages from different instrument manufacturers. If you are a motivated leader with a technical background and a commitment to safety and efficiency, we invite you to apply for this role and become a valuable part of our team at FMC.,

As an M. Sc Analytical Chemistry professional with 2-4 years of experience in method development and validation in Analytical Development Laboratory (ADL), you will be responsible for ensuring the accuracy and reliability of analytical methods used in the testing of chemical substances. Your expertise in chemical analysis will be crucial in supporting research and development efforts within the organization. You should have a strong foundation in analytical chemistry principles and techniques, as well as hands-on experience in method development and validation. Your attention to detail and problem-solving skills will be essential in identifying and resolving any issues that may arise during the analytical process. A background in the chemical industry is a must for this role, as it will provide you with the necessary knowledge and understanding of the various chemical compounds and processes involved in method development and validation. Additionally, you must be prepared to work in shifts to support the operational needs of the laboratory and ensure continuous testing and analysis of samples. Your dedication to quality and precision in analytical work, coupled with your ability to adapt to changing priorities and work effectively in a team environment, will make you a valuable asset to the ADL team.,

Responsibilities Collaborate with clients to understand their business requirements and translate them into cloud-based solutions, Design and architect scalable, reliable, and secure cloud solutions on platforms such as Amazon Web Services (AWS), Microsoft Azure, or Google Cloud Platform (GCP), Conduct cloud assessments and provide recommendations on cloud migration strategies, including lift-and-shift, re-platforming, or refactoring, Develop architecture blueprints, diagrams, and documentation that clearly articulate the proposed solutions, Work closely with development teams to ensure cloud architecture best practices are followed throughout the software development lifecycle, Assist in the evaluation and selection of cloud services, tools, and frameworks to meet project requirements, Implement and configure cloud services, infrastructure, and networking components as required, Ensure security and compliance of cloud solutions by implementing appropriate security controls and following industry best practices, Collaborate with operations teams to optimize cloud resource utilization, monitor performance, and troubleshoot issues, Stay up to date with the latest cloud technologies, trends, and best practices, and share knowledge with the team and clients, Candidate requirements: Bachelors degree in computer science, Information Technology, or a related field, Proven experience as a Cloud Solution Architect or a similar role, with a deep understanding of cloud technologies and architectures, Strong knowledge of cloud platforms such as AWS, Azure, or GCP, including their core services and capabilities, Experience designing and implementing scalable, reliable, and secure cloud solutions, Familiarity with cloud migration strategies and patterns, Knowledge of cloud security principles and best practices, Proficiency in infrastructure-as-code (IaC) tools and techniques, such as Terraform or CloudFormation, Strong problem-solving and analytical skills, with the ability to understand complex requirements and propose appropriate cloud solutions, Excellent communication and presentation skills, with the ability to effectively communicate technical concepts to both technical and non-technical stakeholders, Relevant certifications such as AWS Certified Solutions Architect, Microsoft Certified: Azure Solutions Architect, or Google Cloud Certified Professional Cloud Architect, Experience with DevOps practices and CI/CD pipelines is a plus

Walk-In Drive For API Plant Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Saturday 30-08-2025. Requirement for Executive / Senior Executive - API Plant AR&D - API Analytical Research & Development(AR&D) HPLC,GC API QC Experience also Consider High performance liquid chromatography (HPLC) & GC HPLC with Software lab solu. UV-VIS Spectrometer GC with Software lab solution PH-Meter Moisture Analyser Karl Fischer titrator Micro- Weighter Balance API QC Experience also Consider Responsible for an Analytical team involved in Method development, Method Transfer and Validation for various stages of drug development. Method Validation of analytical methods as per internal and country specific regulatory guidelines and execution through proper protocols. Compliance of Good Laboratory Practice in the lab Responsible for providing support to technical issues related to R&D to file the Drug Master files. Effective method development ensures that laboratory resources are optimized, while methods meet the objectives required at each stage of drug development. Responsible for ensuring delivery time-lines and adherence to quality and standards and customer Relationship management. Facilitating scientific and technical discussions with team members and external collaborators to resolve issues and communicating conclusions from stability studies. Interview Date : Saturday 30-08-2025 Department : Plant Analytical Research & Development(API AR&D) HPLC,GC API QC Experience also Consider Experience : 1 to 6 Years Qualification : M.Sc Position: Executive / Senior Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details :Venue Details : MSN Laboratories Pvt. Ltd, R&D Centre, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana

We are seeking an experienced Asst. QC Head to lead our QC department. The candidate should have extensive knowledge of instruments like HPLC, GC along with sound background of validation, stability monitoring and regulatory compliance.

Job Description : Job Title: Assistant Manager - Research & Development About the Function: Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo's 30,000+ people work in Supply Chain and Manufacturing. It's an intricate and sophisticated operation that's the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We're committed to realising our Society 2030: Spirit of Progress goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we'll help you to thrive in our inclusive culture. About the role: This role is responsible for executing and managing analytical R&D projects related to alcoholic beverages. It includes conducting precise chemical and instrumental analysis of raw materials, intermediates, and finished liquids in alignment with defined test methods, Good Laboratory Practices (GLP), and ISO 17025 requirements. The position also supports senior analysts in innovation and research initiatives and contributes to technical capability building across stakeholders through training and knowledge sharing. Role Responsibilities: Key Technical Responsibilities: Conduct and support analytical R&D projects for product and process development Perform chemical analysis on raw materials, intermediates, and finished liquids using validated methods Ensure compliance with GLP and ISO 17025 in all laboratory operations Assist in method development, verification, and validation Train internal teams and stakeholders on analytical techniques and data interpretation Core Technical Competencies: Instrumental Techniques: Proficient operation and data interpretation of: GC-FID / GC-ECD/GC-MS - For volatile compounds, congeners, fusel oils HPLC- For organic acids, polyphenols, flavor-active compounds UV-Vis Spectroscopy - For color, % transmittance, phenolic profiling Strong hands-on experience in general laboratory instrumentation: pH meter, Conductivity meter, Turbidity meter, etc. Classical Wet Chemistry Techniques: Titration for acidity, sulfur content, etc. Alcohol content analysis using pycnometer, hydrometer, or digital density meter Analytical Methodology & Validation: Sound knowledge of: Method development, verification, and validation Instrument qualification (IQ/OQ/PQ) Calibration and measurement uncertainty Determining LOD/LOQ Chemometric tools and application of statistical techniques (e.g., ANOVA, control charts) Data Handling & Reporting: Understanding of data analytics and statistical tools for research applications Clear, structured reporting and presentation of analytical findings Accurate and timely documentation of results as per regulatory and internal standards Leadership & Behavioral Expectations: Organizational Impact: Understands role priorities and delivers as per direction from manager. Supports team-level goals and process improvements. Decision-Making & Problem Solving: Anticipates analytical challenges and recommends practical, data-based solutions. Integrates technical knowledge with insights to improve outcomes. Communication & Collaboration: Clearly articulates scientific findings in verbal and written form. Engages cross-functional teams through knowledge sharing and training initiatives. Self-Management & Ownership: Independently plans workload and seeks guidance when needed. Demonstrates accountability, precision, and curiosity in laboratory work. Experience / skills required: Education: PhD or MSc in Analytical Science / Chemistry / Organic Chemistry Experience: Minimum 5 years of experience in chemical and instrumental analysis in the food and beverage or allied industries Flexible Working Statement: Flexibility is key to our success. From part-time and compressed hours to different locations, our people work flexibly in ways to suit them. Talk to us about what flexibility means to you so that you're supported from day one. Diversity statement: Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this. We embrace diversity in the broadest possible sense. This means that you'll be welcomed and celebrated for who you are just by being you. You'll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more. Ourambitionistocreatethebestperforming,mosttrustedandrespectedconsumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world. Feel inspired Then this may be the opportunity for you. Worker Type : Regular Primary Location: Bangalore Technical Centre Additional Locations : Job Posting Start Date : 2025-07-01

Role Overview: This role involves routine calibration and in-vitro studies for respiratory products, supporting characterization work in coordination with the development team. Role & responsibilities Performing daily calibration activities in the lab Performing in vitro studies of all respiratory products Helping development group for characterization studies (has to travel at plant and Sinnar R&D) as per requirement Attend all training and maintain proper training file Prepare instrument/equipment SOP Preferred candidate profile Education : M. Pharm in Analytical Chemistry. Experience: 1 -5 years of relevant experience Analytical development of Respiratory portfolio. Knowledge & Skills : Maintaining good lab practises in the lab. Testing of all respiratory products. Familiar with all ICH Guidelines. Experience of facing US FDA and other regulatory bodies compliance. Knowledge of Empower software Perform HPLC and GC analysis as per requirement Interested candidates with relevant experience can apply.

We are seeking a skilled Analyst with hands-on experience in FTIR/Disso/UV/KF/HPLC techniques(Multiple requirements). The candidate should be well versed with Method Development, Method Validation and routine analysis. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) If interested please share profiles on nilesh.kadam@geochem.net.in No walk-in interviews on 27-Aug-25

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Senior Chemist-Residues Analysis of Pesticide residues in Food and Feed samples. Operation and Maintenance of LC-MS/MS and GC-MS/MS. Reference standards maintenance. Calibration of LC-MS/MS and GC-MS/MS. Recording and maintenance of temperature and humidity sheets. Calibration of Maintenance of micropipettes and analytical balances. Preparation of standard stock and working solutions. Qualifications M.Sc Chemistry Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Maintenance and use of GC FID To test and analyze proximate parameters like UV parameters, Analysis of Fatty acids Maintaining samples before and after analysis Maintaining the CRM Method verification & validation SOP preparation Interpretation of the results. Qualifications 6-8 years experience of working in food testing laboratory. Proficient in analytical techniques of wet chemistry, proximate analysis, watr analysis, Allergen testing, Meaurement of Uncertanity calculation. Greaduate Bsc/Msc in Chemistry Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Analysis of Pesticide residues in Food and Feed samples. Operation and Maintenance of LC-MS/MS and GC-MS/MS. Reference standards maintenance. Calibration of LC-MS/MS and GC-MS/MS. Recording and maintenance of temperature and humidity sheets. Calibration of Maintenance of micropipettes and analytical balances. Preparation of standard stock and working solutions. Qualifications 4-6 years experience of working in food testing laboratory. Proficient in analytical techniques of instrumental chemistry. Proficient in handling GC/MS-MS, Should be proficient in Method validation. Graduate in B.Sc/M.Sc chemistry Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

JOB DESCRIPTION SUMMARY OF ROLE R&D Analytical Officer - Selfcare working across various NPD Projects. Responsible for but not limited to alternate RM vendors qualification, analytical method development, analytical method transfer and analytical method validation. Stability testing and review and approval of analytical and chromatographic data for non-commercial product release for various NPD projects. Writing analytical method development, analytical method transfer and analytical method validation, stability protocols, reports, other scientific justification documents and conducting stability studies and laboratory work including interpretation and reporting of results for projects as required. Hands on skill for Analytical method development & validations on HPLC/UPLC, GC, Dissolution, UV, IR, KF, Empower (CDS), Viscometer, ICP-MS/OES, Malvern particle sizer other ancillary instruments. Role is based in Gurgaon, India. Person will report to R&D Senior Analytical Associate, also be expected to be self-starting as well as able to work within strong team. Role required travel to EMO/outsourcing labs as well. RESPONSIBILITIES Functional Utilize technical expertise to develop new analytical methods and method validations. Partner with key functions – Quality, supply, regulatory, Medical to define and uphold product quality standards and continuously improve to achieve “right first time” practice in working area by following documented procedures and good documentation practice. To support, stability studies and method development and method validation for the various NPD Projects, manufacturing/analysis of lab samples for evaluation, etc. Responsible for test method preparation/updating (RM & FG) as and when required. Responsible to guide new joiners during experimental and laboratory work. To support the outsourcing of analytical activities for R&D Category Selfcare projects. To maintain EHS standards as per site policy. Working on QMS tools and SAP to support the R&D Category Selfcare projects. To be responsible for calibration of laboratory instruments, working standard qualification and another lab support as when required. To be responsible for enabling compliance in shared lab. To be responsible for the maintenance of laboratory equipment, working space, lab consumables and inventory and ensure with other colleagues, that the required safety measures are in place. To be flexible and positive to the changes in priorities at short notice. Need to take part in team meetings to report on project progress and contribute positively to problem solving. Calibration of various instruments and working standard preparation as and when required. To be flexible for travel across various EMO & outsourcing labs for analytical method development, analytical method transfer and analytical method validation. Stability testing and review and approval of analytical and chromatographic data Cross Functional To liaise with regulatory team on projects as required. To liaise with supply, QA, QC, RA and Supply Technical as required for projects. Others Good communication and written skills in Business (English) language and good presentation and decision-making skills. EXPERIENCE/QUALIFICATION Minimum 3+ years of experience in Analytical research & development for Drug and Ayurvedic formulation like - Solid, Semisolid and Liquid oral & Topical. Minimum M. Pharmacy/M.Sc. in Analytical chemistry

LC-MS/MS expert for a NABL-accredited lab to perform high-precision analysis of pesticide, mycotoxin, antibiotic residues in food and water samples. Expertise in method development, validation, troubleshooting ability, data accuracy are essential. Required Candidate profile Must have thorough expertise in LC-MS/MS and complete understanding of NABL/ISO 17025 regulations. Candidate is expected to independently handle, operate, and maintain LC-MS/MS instrumentation. Perks and benefits Best in the industry.

Your new role challenging and future- oriented: The department are responsible for the thermodynamics and gas-turbine performance from the conceptual design stage through development, manufacturing, testing, fleet analysis and service upgrades for the entire gas turbine portfolio. This team has ownership of the performance models for customer negotiations and is also responsible for customer and factory gas turbine performance testing. The team continuously develops, maintains and improves our internal gas turbine performance related tools and methods to increase the competitiveness of the Siemens Energy portfolio and improve productivity. The role will support both existing and new customers through analysis, bid support, evaluation of fleet and tuning of engines. We value that you are driven and customer oriented. You share knowledge and encourage others to grow. Working with colleagues across the world, it is important that you communicate well and enjoy working in a team. We value diversity and see many benefits with having a team with different backgrounds and experiences. We dont need superheroes, just super minds: Mechanical/Aerospace Engineer graduate/Post graduate from recognized college/university More than 6 years of gas turbine experience in research, design, development and technical support with concentration in thermodynamic analysis, performance testing and/or fleet support Strong knowledge of gas turbine engine thermodynamics. Experience in gas turbine performance prediction and R&D. Experience in gas turbine engine testing. Experience in gas turbine engine diagnostics. Candidate must be capable of interpreting data and results Candidate must be detailoriented, analytical and organized Candidate must be assertive, selfmotivated, and results oriented Candidate must be capable of working on complex issues and offer solutions Strong knowledge in Tools & Methods Development Strong programming skills with expertise in VBA, C# & Phyton Capable of leveraging programming knowledge to enhance processes and develop efficient solutions. Committed to continuous learning and improving technical proficiency across various programming languages and tools. Additional Preferred Experience/Skill: Excellent verbal and written communications skills, including good presentation skills. Demonstrated ability to successfully manage a task/project to satisfy technical, budget, and schedule requirements. Quality and customer-oriented mindset. Must be proactive and highly motivated. Self-Reliant and Fast leaner. Intercultural experience/sensitivity. Promotes a culture of inclusion where everyone feels respected and valued. Puts our customers first and has their success as key objective. Acts as an owner of our company, with a passion to win and deliver exceptional results through continuous improvement. Collaborates across organizations and acts in the companys best interest to deliver better solutions. Communicates openly and honestly without compromise, shares successes and failures. Eager to learn and to understand. Can easily work independent as well as in team. Proficient in English language

Role & responsibilities Perform quality control testing of oncology products (raw materials, intermediates, and finished products) using validated analytical methods. Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometer, Dissolution Apparatus, FTIR, and other relevant equipment. Conduct stability testing as per ICH guidelines and prepare stability reports. Review and document analytical results in compliance with GDP and cGMP requirements. Identify and investigate deviations, OOS (Out of Specification) and OOT (Out of Trend) results, and implement corrective and preventive actions (CAPA). Support method validation, method transfer, and analytical troubleshooting. Ensure adherence to EHS (Environment, Health, and Safety) policies during laboratory operations. Maintain proper documentation, records, and ensure audit readiness for regulatory inspections (USFDA, MHRA, WHO, etc.). Collaborate with cross-functional teams to resolve quality issues and improve processes.

Role & responsibilities Develop, optimize, and validate analytical methods (HPLC, UPLC, GC, LC-MS, dissolution, etc.) for oncology drug substances and drug products. Perform characterization, stability testing, and release testing of clinical and commercial oncology formulations. Prepare analytical documentation including method validation protocols, reports, SOPs, and regulatory submission documents as per ICH and FDA/EMA guidelines. Support formulation development teams by providing analytical insights for process development, scale-up, and tech transfer activities. Conduct forced degradation and impurity profiling studies for oncology drug candidates. Ensure all analytical work is compliant with GLP/GMP and applicable regulatory requirements. Troubleshoot analytical challenges and provide technical guidance to junior team members. Interface with QA, Regulatory Affairs, Formulation Development, and Manufacturing teams to ensure seamless project execution.

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Planning/performing and reporting of acute toxicology studies Assist in preparation of SOP"™s, Protocols and Reports Participate in GLP / AAALAC related activities Literature search Maintenance of animal house and relevant documents as per GLP and AAALAC norms. To Assist and work along with SD and TC in Planning, initiation and conduct studies. Test item administration, dose formulation preparation and blood collection. Assistance in data collection, compilation and verification. Participate in GLP inspections and ensure relevant regulatory compliance guidelines. Support in interpretation and reporting of study data. Assist in report preparation and coordination of activities. Assist in archiving of all study related materials. Skills Required: Understanding of the agrochemical and pharmaceutical R&D process Behavioral Competencies: Good in oral / written communication skills. If you're interested in applying or learning more, send your updated resume to [email protected] with the subject line "Research Scientist/Senior Research Scientist - Acute "“ Toxicology - Bangalore". Qualifications Qualification M.Sc. in Zoology/Biosciences Additional Information Specialization Toxicology Department Acute "“ Toxicology Experience (years) 2 to 8 only

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Leadership role to manage team size of 10+ scientists (Ph.D. and M.Sc.) Extensive knowledge in E&L Extractable and Leachable experience in CCS as per USP monograph and medical devices as per ISO guidelines Managing multiple instruments (LC-MSMS, GC-MSMS, ICP-MS, IC etc.) Method development experience in LC-MSMS, GC-MSMS and ICPMS instrument Preparation and Implementation of SOP"™s related to E& L , general laboratory processes and best guidance. Good knowledge of 21 CFR part 11, Data Integrity principals, good documentation practices in cGMP lab Monitor and management of day-to-day laboratory activities Extensive knowledge of preparation, reviewing and approval capability for standard operating procedure (SOP) and COA Sound knowledge of structural elucidation and interpretation using analytical techniques such as NMR, IR, HPLC, GC, LC-MS etc. Resolving the team conflicts and provide training to the team for development and empowers team members Provide scientific and leadership direction to team members Good knowledge of laboratory safety and be a strong promoter of SHE activities in the lab. Skills Required: For M.Sc, 16-18 years of Discovery Analytical R&D experience and for PhD, 14-16 years of experience in CRO environment Excellent technical, problem-solving, writing, influencing and communication skills Strong leadership with excellent interpersonal skills, proven success of analytical projects and managing cross functional teams Demonstrative communication skills and confident in conveying information to internal/ external customers Skill for resolving the team conflicts and provide training to the team for development and empowers team members Behavioral Competencies: Excellent oral / written communication skills and flexibility to work in a dynamic environment Excellent in Knowledge sharing at all levels Qualifications Qualification M.Sc./PhD/Postdoc Additional Information Specialization Analytical Chemistry /Organic Chemistry, Department E&L Experience (years) 16 - 20

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. : Medicinal chemistry; Research and development; Literature search; Scifinder / Reaxys; Design and synthesis; combiflash/Biotage; C-C coupling etc Qualifications MSC - Organic Chemistry.