341 Method Development Jobs - Page 3

You will be responsible for maintaining quality results, ensuring regulatory compliance, and improving existing systems to prevent non-conformance. This includes operating, calibrating, and maintaining various instruments such as HPLC, Dissolution, Analytical Balance, UV Spectrophotometer, Viscometer, GC, etc. You will also be required to record and maintain online entries in the instrument usage log book and follow good laboratory and documentation practices. Your responsibilities will also include performing analysis as per test request forms, following correct test procedures for analytical validations/verifications, routine analysis, and stability studies. Basic knowledge of method development and validation, as well as experience in drug product analysis, will be advantageous. To be considered for this role, you should have an M.Sc. in Organic/Analytical Chemistry and be able to join as soon as possible. A good technical knowledge and understanding of the mentioned instruments and procedures will be required to excel in this position. If you meet the qualifications and are looking to contribute to a dynamic team focused on maintaining high quality and compliance standards, we encourage you to drop your resume at recruitment@cironpharma.com or contact (EXT-250).,

Perform IVRT studies for topical and transdermal products Conduct in IVPT using human /animal skin in Franz diffusion cells. Develop methods for topical dosage forms for content/assay and RS estimation.

Dear Candidate, We are Inviting Applications for the positions in our Analytical Research & Development department. Job Description : Position Name: Research Chemist/Senior Research Chemist/Research Associate Experience: 1 to 5 years Qualification: M.Sc Analytical Chemistry/Organic Chemistry/M.pharm Work location: Uppal/Mallapur Key Skills and Competencies: High-Performance Liquid Chromatography (HPLC) Key Skills and Competencies: Operation and Maintenance : Proficiency in operating HPLC systems (e.g., Agilent, Waters, Shimadzu) and performing routine maintenance, calibration, and troubleshooting of equipment issues like pressure fluctuations or detector errors. Method Development and Validation : Ability to develop and optimize HPLC methods for analyzing small molecules, impurities, or degradation products, adhering to ICH guidelines (e.g., ICH Q2 for validation). Data Analysis : Expertise in interpreting chromatograms, quantifying analytes, and using software like Empower or ChemStation for data processing and reporting. Sample Preparation : Skilled in preparing samples (e.g., dissolution, extraction) for pharmaceutical or chemical analysis, ensuring reproducibility and accuracy. Regulatory Compliance : Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) for documentation, method validation, and audit readiness. Troubleshooting : Ability to diagnose and resolve issues such as peak tailing, baseline drift, or column degradation. Experience Level (1-5 Years) : 1-2 years: Basic operation, routine analysis, and data interpretation under supervision. 3-5 years: Independent method development, validation, and troubleshooting with familiarity in handling complex matrices. Prep HPLC Key Skills and Competencies Operation and Maintenance Hands-on experience with Preparative HPLC systems (e.g., Agilent, Waters, Shimadzu, GE KTA). Proficiency in system setup, gradient programming, scale-up from analytical to preparative runs. Routine maintenance and calibration of pumps, fraction collectors, and detectors. Troubleshooting common issues such as pressure fluctuations, air bubbles, or pump leakage. Purification & Method Development Strong background in method development and optimization for preparative HPLC to isolate target compounds (APIs, impurities, natural products, metabolites, peptides). Experience in scaling up analytical methods to preparative scale while ensuring recovery, purity, and yield requirements. Knowledge of different stationary phases (C18, C8, size-exclusion, chiral) and selection of appropriate mobile phases. Sample Preparation & Fraction Collection Skilled in preparing crude samples (reaction mixtures, fermentation broths, plant extracts) for scalable purification. Competence in managing fraction collection strategies , solvent recovery, and sample lyophilization/drying. Ensuring high-quality isolation of compounds with reproducibility. Data Analysis & Reporting Ability to interpret chromatograms , verify purity and recovery using both analytical HPLC/UPLC and complementary techniques (LC-MS, NMR). Proficiency in software like ChemStation, Empower, Unicorn, or equivalent for processing preparative runs and reporting results. Documentation of purification workflows in compliance with client and regulatory requirements. Regulatory Compliance & CRO Environment Knowledge of Good Laboratory Practices (GLP) and CRO industry requirements for method documentation, record-keeping, and reproducibility. Familiarity with client-driven project timelines and requirements. Experience preparing project reports, tech-transfer documents, and audit-ready records. Troubleshooting & Continuous Improvement Expertise in diagnosing issues like sample overload, poor recovery, carry-over, baseline instability, or column degradation. Ability to suggest process improvements for higher throughput and purity levels. Experience Level (Typical Range: 1-5 Years) 1-2 years: Basic operation of preparative HPLC systems. Performing routine purification runs under supervision. Basic troubleshooting and hands-on sample preparation. 3-5 years: Independent purification and method development for wide compound classes. Competent in scale-up from analytical to preparative levels. Handling of challenging crude matrices and optimization of recovery/yield. Active participation in client projects , troubleshooting, and mentoring junior team members. Interested candidates can contact 6309995773 or share their profiles to saivardhan.kothuri@chemvedals.com

Job Summary We are seeking a dynamic and experienced Analytical Scientist in Advanced Characterization Structural Elucidation Team (ACT-SEL) for utilizing sophisticated analytical techniques and instruments to investigate the composition, structure, and properties of substances at a molecular and atomic level. To Support Structural Elucidation across all modalities and mechanism elucidation into Research & Development and to study release of drugs substance and structure of unknown Impurities through various method development and validation techniques. Roles & Responsibilities You will be responsible to employ advanced analytical techniques such as Gas Chromatography with Mass Detector( GCMS/MS), Inductively coupled Plasma Mass Spectrometry (ICPMS) , Inductively coupled Optical emission spectroscopy (ICP-OES), Atomic Absorption Spectroscopy (AAS), Ion Chromatography (IC) and other specialized techniques to analyse and characterize materials. You will be responsible to design and execution of experiments and the analysis of data. Also find the critical parameters and develop innovative solutions to complex problems in pharmaceutical research and development You will be responsible to deduce the chemical structure and composition of complex molecules, compounds, and materials, elucidating their atomic and molecular arrangements using advanced analytical methods. You will be responsible to develop and optimize analytical methods and protocols to facilitate the accurate and efficient characterization of diverse materials, ensuring the reliability and reproducibility of results. You will be responsible to perform comprehensive data analysis and interpretation of experimental results, employing statistical tools and software to extract meaningful insights into the structure, composition, and properties of the materials under investigation. You will be responsible to actively contribute to research projects aimed at developing novel methods for the characterization and elucidation of complex structures and stay updated with the latest advancements in analytical techniques and technologies You will be responsible to Collaborate with cross-functional teams, including chemists, material scientists, and engineers, to provide analytical support and contribute insights to research and development projects. Effectively communicate findings and recommendations to the team and stakeholders. You will be responsible to ensure adherence to quality control standards and regulatory requirements in all analytical processes, maintaining high standards of accuracy, precision, and reliability in data generation and analysis. You will be responsible to troubleshoot instrument-related issues and perform routine maintenance and calibration of analytical equipment to guarantee the accuracy and performance of instruments used in structural elucidation. You will be responsible to maintain comprehensive records of all experimental procedures, results, and observations. Prepare detailed reports and presentations summarizing analytical findings, methodologies, and conclusions for internal and external stakeholders. You will be responsible to adhere to strict safety protocols and guidelines while handling hazardous materials and operating complex analytical instruments. Ensure compliance with all relevant safety regulations and best laboratory practices. Qualification Educational qualification: MS in Pharmaceutical Analysis/Post Graduation in Pharma/Physics Minimum work experience: 3-8 years of experience Skills & attributes: Technical Skills Hands on experience on Elemental analysis techniques such as Inductively coupled Plasma Mass Spectrometry (ICPMS) , Inductively coupled Optical emission spectroscopy (ICP-OES), Atomic Absorption Spectroscopy (AAS). Through understanding on ICHQ3D studies, Delamination studies, Extractable & Leachable studies and its analytical methods. Understanding and experience on Gas chromatography with Mass Detector(GC-MS/MS) for method development and method validations for Nitrosamines analysis. Expertise in method development and validation of Ion Chromatography (IC) methods in critical projects. Experience in Instrument Calibration & trouble shooting. Familiar with Current Good Laboratory Practices (CGLP). Behavioural Skills Excellent communication and interpersonal skills. Ability to work with cross functional teams. Strong analytical and problem-solving abilities. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Hiring for Assistant Manager / Manager in Analytical Method Development (Formulations) - Solid orals for Regulated Market. Experience : 10 to 15 years into analytical method development Qualification : M.Sc . / M.Pharma Your responsibilities will include: - Supervising a team of 6 to 8 members for method development and routine testing. - Providing guidance and mentorship to analysts through practical training in analytical method development. - Conducting SOP training and certifying analysts for new team members. - Planning daily activities and allocating work for team members. - Monitoring routine analysis and troubleshooting issues. - Assisting in critical troubleshooting and on-site investigations. - Reviewing raw data, LNB, and filing routine analysis reports.

Dear All, We are seeking a highly motivated and talented Analytical R&D Scientist( Topicals ) to join our innovative team. The ideal candidate will have a strong foundation in Analytical development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 4-7 Years Job Responsibilities: 1. To ensure scientifically strong justification for the analytical tasks taken up. 2. To follow the departmental SOPs. 3. To ensure the error free and online documentation. 4. To ensure only calibrated instrument /equipment's are used for analysis. 5. To coordinate with supervisor and lead development of methods for IVRT, IVPT, ex-vivo, assay by UV/HPLC and RS by HPLC. 6. To coordinate with supervisor in developing the methods for residual solvents and other volatile components by GC. 7. To perform analysis of development samples for IVRT, IVPT, ex-vivo, Assay by UV/HPLC and RS by HPLC as per test method. 8. Perform validation of test procedures like IVRT, IVPT, ex-vivo, Assay, Related substances, residual solvents, Residue and Chiral purity etc., 9. To ensure the instruments/equipment are cleaned after completing the analysis and columns are washed to ensure maximum life. 10. Receipt, storage and management of samples/standards. 11. Labeling of standards, chemicals and reagents. 12. Receipt of logbooks and SOPs from QA. 13. To ensure GLP compliance in laboratory. 14. Supporting the installation of instruments and equipment's. 15. To ensure the reference, working standards and impurities are maintained as per GLP. 16. To ensure timely archival of completed files and LNB. 17. Assist and/or perform analysis of development samples for in-process and finished product parameters as per Analytical Test Method/Standard Test Procedure. 18. Coordinate and assist with timely completion of Instrument calibration and preventive maintenance. 19. To participate in formulation development trails. Note: Interested candidates can share their resumes to raghuveera.vutla@aizant.com and Immediate joiners are more preferable

* 10–15 years of exp. in CRO industry with strong expertise in LC-MS, HPLC/Prep. method development for NCE molecules at an analytical scale. * Lead, train & mentor young scientists. https://o2h.recruitee.com/o/senior-principal-scientist-prep-hplc

You must have experience in analytical development or handling of oligonucleotides method development. Additionally, you should possess experience in characterization techniques related to oligonucleotides. In this role, you will be responsible for providing routine analysis support to the process development team for various projects. It is essential that you have good documentation skills in line with laboratory GMP practices and the ability to understand and adhere to current Good Manufacturing Practices. Your duties will include ensuring compliance with all quality audits, maintaining data integrity, and following ALCOA++ Principles. You will also be required to prepare and review method development reports, method validation protocols, and reports. Experience in method qualification activities is necessary for this position. As part of your responsibilities, you will work with the instruments assigned for analysis and be involved in their calibration. Collaboration with DQA/Plant QC for method transfer will also be expected. Any additional experience in characterization techniques of oligonucleotides and peptides will be considered advantageous. It is preferable that you have experience in amino acids analysis, SEC-MALS, DLS, CE, and other related techniques. Interpretation of characterization data is a crucial aspect of this role, and you should be capable of performing this task effectively.,

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.

Roles and Responsibilities Conduct research analysis for formulation development, including method development, calibration, and assaying of samples using HPLC techniques. Develop and validate new methods for analyzing pharmaceutical products to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to troubleshoot issues related to product quality and stability. Maintain accurate records of experimental data, results, and conclusions in accordance with Good Laboratory Practices (GLP). Stay up-to-date with industry developments in analytical chemistry and implement best practices in the laboratory setting. Desired Candidate Profile 3-5 years of experience in a similar role within the pharmaceutical or life sciences industry. Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution. Strong understanding of analytical chemistry principles, including chromatography (HPLC), spectroscopy, and electrophoresis. Experience working with various types of instruments such as UV-Vis Spectrometer, Polarimeter, FTIR etc.

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 7 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Support R&D/formulations: experiment planning, DoE, scale-up/tech transfer, method/cleaning validation, and dossier documentation aligned to global registration needs. Additional info: Bachelors degree in relevant field (B.E / B.Tech / B.Sc / M.Sc) Good interpersonal and communication skills Willingness to relocate API Pharmaceutical Industry experience preferred Must demonstrate strong ownership, attention to detail, and the ability to work in a fast-paced, inspection-ready environment. Familiarity with ICH, WHO TRS, ISPE, and data integrity principles is expected; hands-on with spreadsheets/ERP/LIMS is a plus.

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 06-09-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to interact with cross - functional and cross - cultural teams. Previous experience of running analytical techniques such as HPLC, Dissolution, KF, IC with the ability to extract and prep various samples in a variety of forms. As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team. Note : Formulation Quality Control Candidates also eligible. Interview Date : 06-09-2025 Department : Formulation Analytical Research & Development(FAR&D) Experience : 1 to 6 Years Qualification : M. Pharmacy / M.Sc. / B Pharm Position: Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details MSN Laboratories, R&D Center,Pashamylaram, Hyderabad

"Opportunity for M.Pharm professionals in Formulation Development (R&D) to work on sterile and non-sterile dosage forms (ANDA/ROW/US-OTC) with leading pharmaceutical projects in Mumbai.

To perform calibration of the analytical instruments as per calibration schedule and follow the standard practices c-GLP during lab experiments. You will be responsible for cleaning verification method development and validation, API method evaluation and verification, as well as API solubility study assessment. Additionally, you will be involved in working standard qualification, method development for drug product formulation, routine analysis of development samples and lab stability samples, and method verification of different analytical methods. Your role will also include reporting of analytical data and submitting it for review and release, developmental release of raw material and packaging material, and preparation of test procedures for routine development analysis. You will be expected to follow in-house compliance systems, maintain hygienic conditions in the respective department, ensure the use of personal protective equipment, attend EHS training, and manage waste disposal according to EHS requirements. Effective communication is key as you will be required to liaise with formulators for analysis and data submission, CRA for project-specific technical documents/queries, suppliers/vendors for instrument maintenance and inquiries about columns/chemicals, and outside analytical labs for specific analysis. Following GxP (GMP, GDP, GLP) for all processes is essential in this role. Qualifications: - M. Pharmacy/M.Sc/Ph.D Required Skills: - Method development - Data review About Us: In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth while adhering to ethical and values-driven practices. We base our employment decisions on merit considering qualifications, skills, performance, and achievements, ensuring equal opportunities for all applicants and employees in personnel matters. About The Team: Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) that offers end-to-end development and manufacturing solutions across the drug lifecycle. Through a globally integrated network of facilities in North America, Europe, and Asia, we provide a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Job Identification: 7889 Job Category: Analytical Development Posting Date: 03/14/2025, 04:17 AM Degree Level: Master's Degree Job Schedule: Full time Location: Plot No:-19, PHARMEZ, Sarkhej-Bawala NH-8A, Ahmedabad, Gujarat, 362001, IN,

You will be a Quality Assurance & Analytical Chemist at FMC, where your primary responsibility will be to provide daily analysis support by developing, validating, and applying various modern analytical technologies and approaches for the development and commercialization of agricultural products. You will ensure that FMC quality standards and good laboratory practices are implemented at the Toller site by conducting cross-checks and on-site audits as per business needs. Your role will involve knowing, understanding, and practicing all aspects of laboratory safety and industrial hygiene protocols, developing, validating, and implementing methods for qualitative and quantitative analysis, conducting routine and non-routine analysis, collecting data, generating summaries and reports, supporting investigations of quality incidents, and operating and maintaining various analytical instrumentation. You will work closely with synthetic chemists and engineers to provide structure determinations and analytical results as requested, manage the quality of active ingredients and intermediates with contract manufacturers, review MOA and analytical Teck pack, and perform other tasks assigned by the line manager. To be successful in this role, you should have a Master's degree or above in chemistry/biochemistry or equivalent experience, along with 10+ years of experience and a minimum of 8 years in analytical development/quality control positions. You should have experience with method development and troubleshooting using various lab instruments/techniques and a track record of delivering quality results on time. Strong interpersonal, problem-solving, and troubleshooting skills are essential, along with good written and oral communication and coordination capabilities with different stakeholders. Familiarity with computers and software packages from various instrument manufacturers is also desirable. If you are a motivated leader with a strong technical background and a passion for safety and efficiency, we invite you to apply for this dynamic role and become a part of our team at FMC.,

Role & responsibilities Perform the calibration and preventive maintenance of the instruments as per the respective schedules. Analysis of raw material / finished products / stability samples / Dissolution profiling for R&D/ Plant support. Analytical Method Development /Verification Assay, Related substances, Dissolution etc . Perform the determination of KF factor, Daily verification of Balances, pH meter, Milli-Q water system, Hot Air Oven, Refrigerator temperature monitoring. Develop/ optimize the analytical methods by Chemical/ instrument analysis Verify/ validate the analytical methods by Chemical/ instrument analysis Preparation / Revision of Specification and Method of analysis for Raw materials / Finished Product / Inactive / Excipients etc Appropriate documentation of results and calculations, preparation of SOPs, specifications and test methods. Interpret results, evaluate data, draw relevant conclusions and give timely feedback to concerned Departments. Analytical Technology transfer of analytical methods by Chemical/ instrument analysis Perform the Impurity standard/ working standard/ primary reference standards. Receiving and filling controlled copy of specifications / method of analysis / SOP / STP etc Operation of various software like Oasis LIMS, Q Edge TMS, Chromeleon etc Preferred candidate profile Qualification: B. Pharm / M.Pharm / M. Sc Experience: Minimum 2 years in HPLC Analysis Development and Validation Perks and benefits Mediclaim

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Please see the following position summary: Client Name: CDMO Partner for Ophthalmic & Derma products for global markets. Position: Officer / Sr. Officer - IVRT R&D Markets: USA, Canada & ROW Products: Topical Formulations & Ophthalmic Preparations Location: Mumbai Job Profile: To carry out analysis as per work planning or based on the organizational requirement. To follow and perform all required activities in IVRT department as per Standard Operating Procedure (SOP). To follow and maintain quality service in IVRT department by enforcing periodical Quality Management system i.e. Good Laboratory Practices, Good Documentation Practices etc., while working. To perform operation and calibration of instruments and equipments as per respective SOP of instrument and equipment. To co-ordinate and support for work wherever applicable with the internal department of R&D centre, visitor, external vendors etc. To perform IVRT method development, IVRT method validation and IVRT comparison study, Analytical method development, method validation and method transfer for the project assigned by team lead / Management. To execute and complete the project work related to IVRT analysis within stipulated timeline as per organizational requirement. To prepare and review documents like Standard Operating Procedure, protocols and reports etc. related to IVRT Department. To be involve in preparation and review of Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) documents (wherever applicable) for the instruments and equipments which is to be install in IVRT department. To attend the training but not limited to SOP, protocol training, safety training organized by internal department of R&D centre or external party. To follow all safety precautions while working in IVRT department and other departments of R&D centre. To upkeep of IVRT laboratory for all time audit readiness and to participate in audit work wherever required as per organizational requirement. To support in training and involve in analyst qualification work for the new joined employee in IVRT department. To follow all rules and regulations set up by the organization during work tenure. Desired Profile: M.Sc / M.Pharm (Pharmaceutical / Pharmaceutical Analysis / related discipline) with 4 to 6 years of experience in IVRT R&D for Regulated markets especially for topical and ophthalmic preparations to the pharmaceutical industries. Prior experience in IVRT method development and validation is essential. Familiarity with USFDA, Health Canada & ROW guidelines for topical dosage forms & Ophthalmic Preparations. Must have good experience in IVRT R&D as per SOP. Ensure Good Laboratory & Good Documentation Practices in IVRT department. Expertise to perform IVRT method development, IVRT method validation Should have experienced to prepare & review documents related to IVRT department. Good knowledge of preparation & review documents of Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) documents in IVRT department. Must have good Audit experience in IVRT laboratory. Strong documentation, technical writing, and regulatory compliance knowledge. Good problem-solving, analytical thinking, and team collaboration skills. Recruiter Details: BEST - FIT Recruitment Riders G-7, Amrit Complex, Opp: Mahavir Jain Vidhyalaya & Jain Derasar, R.V. Desai Road, Near Goyagate Circle, Vadodara-390001, Gujarat, India Mobile: 09722052906, 09722042906 E-Mail: career@bfrr.in Website: www.bestfitrecruitment.co.in

As an Analytical Chemist at our leading Contract Research Organization (CRO), you will have the opportunity to assist in conducting analytical testing of samples using instruments such as HPLC, GC, LC-MS/MS, and UV Spectrophotometer under supervision. You will play a crucial role in preparing reagents, solutions, and standards following Standard Operating Procedures (SOPs) with precision and attention to detail. Your responsibility will include accurately recording and maintaining raw data, logs, and reports in compliance with GLP/GMP standards. By ensuring proper documentation, you will play a pivotal role in meeting regulatory and internal audit requirements. You will provide essential support in method development and validation for pharmaceuticals and biologics. Under the guidance of senior analysts, you will contribute to stability studies and impurity profiling, gaining valuable hands-on experience in the field. Learning and assisting in calibrating and maintaining analytical instruments will be part of your routine tasks. Following preventive maintenance schedules diligently and promptly reporting any malfunctions will be essential in ensuring the smooth functioning of instruments. Adhering to GLP, GMP, and regulatory guidelines while performing your assigned tasks will be crucial. Your active participation in audits and commitment to maintaining compliance with safety and quality standards will be highly valued. You will have the opportunity to enhance your proficiency in analytical techniques through active participation in training sessions. Staying informed about new methodologies, instruments, and advancements in the field will be key to your professional development. We are looking for candidates with a background in M.Sc. (Analytical Chemistry, Organic Chemistry, or related field), M.Pharm, or B.Pharm with practical academic experience. A basic understanding of analytical techniques and foundational knowledge of instruments like HPLC, LC-MS, or GC is desirable. Familiarity with GLP and GMP guidelines will be an advantage. Strong analytical and critical thinking abilities, effective communication and teamwork skills, and enthusiasm for learning and adapting to new challenges are essential soft skills we are seeking in potential candidates. Joining us will provide you with the opportunity to kickstart your career in a structured training environment, tailored to help freshers transition into a professional analytical setting. You will gain hands-on experience with advanced analytical instruments and methodologies, along with clear career progression paths and professional development programs.,

As an R&D Executive at PTC - MORAIYA, your primary responsibility will be to perform analysis of Drug Product and Drug Substances for various test parameters according to the product development requirements. You will be involved in the method development of Drug Product and method verification of Raw Materials. Conducting literature searches for method development and impurity profile of drug products will also be a key part of your role. Additionally, you will be responsible for compiling analytical results and preparing Method Development Reports. Ensuring adherence to Good Laboratory Practices (GLP) in the analytical laboratory is crucial to maintain quality standards. Your contributions in these areas will play a vital role in the overall research and development process at PTC - MORAIYA.,

Division Department Sub Department 1 Job Purpose Part of the TA COE responsible to manage and support global leadership hiring through extensive market research, candidate sourcing, preliminary screening and support the end-to-end recruitment process, ensuring a seamless experience for both candidates and internal stakeholders Also support enablers in global leadership hiring like compliance & governance, liaisoning with cross functional teams and other operational requisites of the role Key Accountabilities (1/6) Market Research/Mapping for key leadership roles including global talent trends Independently c onduct deep-dive research on global leadership talent landscape including proactive mapping, Analyze talent data to generate insightful heatmaps to recommend potential talent for senior management, Regular upkeep of the market/talent mapping data Identify and evaluate new global search partners for niche and hard-to-fill roles Key Accountabilities (2/6) External vendor Management Track performance metrics of global search partners working with Cipla to enable future engagements, Collaborate with legal, tax, and finance to ensure contractual and regulatory payment alignment, Track and manage vendor budgets and SLAs across regions, Manage contracts for retained search partners globally Manage service agreements and SLAs with external vendor partners Multicurrency invoice process management Key Accountabilities (3/6) Pre & Post selection Process Management ? Till Onboarding Independently onboard senior leaders joining the organization with exceptional candidate experience and closing monitoring induction programs, Drive the candidate recruitment lifecycle on available digital platforms, ensuring 100% adherence to system compliances, Provide white glove pre and post onboarding support to senior hires, including relocation and integration, Ensure system compliance on digital hiring platforms, Key Accountabilities (4/6) Recruitment Data, Hiring Report Accuracy & hygiene of data related to global leadership hiring Generate reports on recruitment metrics and candidate progress with insights and making it available to relevant stakeholders on timely basis Preparing executive hiring decks for senior management, Track and report TA budget utilization and ROI on leadership hiring, Ensure data hygiene and audit readiness for all global leadership hiring records, Key Accountabilities (5/6) Recruitment Administration & Governance Travel & accommodation for domestic & international candidates during the hiring process, Planning and coordinating internal connects of senior leaders hired Liaisoning with Admin and Travel team Ensure governance in recruitment process (reference checks, pre-employment medicals etc) Special Projects & Initiatives Support talent acquisition/ external partner events Collaborate with cross-functional teams on strategic hiring initiatives, Drive continuous improvement initiatives in leadership hiring processes, Key Accountabilities (6/6) Candidate sourcing, pipeline management, screening & interviews Hiring for Global Leadership roles across functions Source and engage passive leadership talent through strategic channels (e g , LinkedIn, alumni networks, referrals) with focus on diversity & inclusion, Recruitment through cost effective sources with reduce time to hire , Independent management of few positions with minimal supervision, Build and maintain relationships with potential candidates Conduct initial candidate screenings to ensure quality resumes are recommended for further process Drive candidate experience excellence across all touchpoints including end to end interviews , Major Challenges High quality talent requirement in cost effective manner Maintaining active talent pipeline for prospects Handling multicultural external & internal stakeholders Key Interactions (1/2) HRBP Department & Functional SPOCS Policy & Rewards Team Finance & Travel Team Legal & Admin Team Key Interactions (2/2) Potential Candidate Pool Search Partners Global Background verification Agencies Other vendor Partners (Enablers) Dimensions (1/2) ~30 leadership positions globally Market mapping for 20+ roles (Inclusive of desk searches) Cost Effective hiring & mapping globally to the tune of INR 5 Cr (gross) TAT Target ? 80% of the positions to be closed within agreed SLA Dimensions (2/2) Key Decisions (1/2) Sourcing Channel Market research depth and candidate recommendation Key Decisions (2/2) Use of available source channels and or innovate unique ones As per role requirement and hiring brief Education Qualification Graduate with Masters degree in Business Administration or equivalent Relevant Work Experience 5-6 years of experience with flair for Talent Acquisition

Your Team Responsibilities MSCI is seeking a dynamic and results-driven Business Finance professional to join our Technology & Data function in Mumbai This is a high-impact role that supports the largest function within MSCI, driving strategic financial planning, investment governance, and business transformation initiatives The ideal candidate will be an agile finance partner who brings analytical rigor, commercial acumen, and stakeholder management expertise to help shape and deliver the financial strategy Your Key Responsibilities Expense & P&L Management: Manage EBIT expenses for the Technology & Data function, ensuring alignment with organizational goals, Financial Planning & Analysis: Lead budgeting, forecasting, and in-depth variance analysis to provide insights and recommend corrective actions, Capital Budgeting: Implement a disciplined capital budget allocation framework, ensuring effective prioritization and ROI tracking, Cost Optimization: Drive cost reduction strategies and operational efficiencies across the Technology & Data organization, Transformation & Analytics: Champion business transformation by leveraging AI tools, Power BI dashboards, and other analytical platforms, Your Skills And Experience That Will Help You Excel CA / CMA / MBA (Finance) or equivalent qualification from a reputed institution, 36 yearsof relevant experience in financial planning & analysis, business partnering, or technology finance roles, Strong understanding of capital budgeting, investment governance, automations and cost optimization methodologies, Proven experience working in a global matrix organization with senior leadership exposure, Proficient in financial modelling, Excel, PowerPoint, and data visualization tools e g Power BI, Experience with ERP systems is a plus, Strong analytical, communication, and stakeholder management skills, Exposure to AI and digital transformation initiatives will be advantageous, About MSCI What we offer you Transparent compensation schemes and comprehensive employee benefits, tailored to your location, ensuring your financial security, health, and overall wellbeing, Flexible working arrangements, advanced technology, and collaborative workspaces, A culture of high performance and innovation where we experiment with new ideas and take responsibility for achieving results, A global network of talented colleagues, who inspire, support, and share their expertise to innovate and deliver for our clients, Global Orientation program to kickstart your journey, followed by access to our Learning@MSCI platform, LinkedIn Learning Pro and tailored learning opportunities for ongoing skills development, Multi-directional career paths that offer professional growth and development through new challenges, internal mobility and expanded roles, We actively nurture an environment that builds a sense of inclusion belonging and connection, including eight Employee Resource Groups All Abilities, Asian Support Network, Black Leadership Network, Climate Action Network, Hola! MSCI, Pride & Allies, Women in Tech, and Womens Leadership Forum, At MSCI we are passionate about what we do, and we are inspired by our purpose to power better investment decisions Youll be part of an industry-leading network of creative, curious, and entrepreneurial pioneers This is a space where you can challenge yourself, set new standards and perform beyond expectations for yourself, our clients, and our industry, MSCI is a leading provider of critical decision support tools and services for the global investment community With over 50 years of expertise in research, data, and technology, we power better investment decisions by enabling clients to understand and analyze key drivers of risk and return and confidently build more effective portfolios We create industry-leading research-enhanced solutions that clients use to gain insight into and improve transparency across the investment process, MSCI Inc is an equal opportunity employer It is the policy of the firm to ensure equal employment opportunity without discrimination or harassment on the basis of race, color, religion, creed, age, sex, gender, gender identity, sexual orientation, national origin, citizenship, disability, marital and civil partnership/union status, pregnancy (including unlawful discrimination on the basis of a legally protected parental leave), veteran status, or any other characteristic protected by law MSCI is also committed to working with and providing reasonable accommodations to individuals with disabilities If you are an individual with a disability and would like to request a reasonable accommodation for any part of the application process, please email Disability Assistance@msci and indicate the specifics of the assistance needed Please note, this e-mail is intended only for individuals who are requesting a reasonable workplace accommodation; it is not intended for other inquiries, To all recruitment agencies MSCI does not accept unsolicited CVs/Resumes Please do not forward CVs/Resumes to any MSCI employee, location, or website MSCI is not responsible for any fees related to unsolicited CVs/Resumes, Note on recruitment scams We are aware of recruitment scams where fraudsters impersonating MSCI personnel may try and elicit personal information from job seekers Read our full note on careers msci

Job Description Designation : Water Testing Trainee Section : Training Qualification : Ph D / M Tech / M Sc / B Tech / B Sc, Experience : Fresher Employment Type : Short Term / Long Term Location : Gurugram, Haryana Responsibility Adherence to Safety Protocols: Strictly follow all laboratory safety guidelines and protocols to prevent accidents and ensure the well-being of all participants, Active Participation: Engage actively in all training sessions, discussions, and practical exercises Complete all assigned tasks and projects on time, Respect for Equipment and Facilities: Handle all laboratory equipment and materials with care Report any damages or malfunctions to the instructor immediately, Collaboration and Teamwork: Work collaboratively with fellow participants, sharing knowledge and supporting each others learning, Integrity and Accuracy: Maintain a high standard of integrity in all testing procedures and documentation Ensure that all results are accurate and reliable, Requirements Skills, Knowledge And Abilities Commitment to the Program: Participants must demonstrate a commitment to the training program by attending all scheduled sessions, completing all assignments, and actively participating in practical exercises A signed commitment agreement may be required before the start of the program, Health and Safety Compliance: Participants must comply with health and safety regulations, including wearing appropriate personal protective equipment (PPE) and adhering to all safety protocols A medical clearance or proof of immunizations may be required for certain training programs, Get in Touch Email at trainings@farelabs

Role & responsibilities Experience in operation and trouble shooting of process in plant. Isolation and purification of different organic compound using column chromatographic and crystallization techniques. Optimize the process parameters, what-if studies, holding studies etc. for scale up. Investigation of OOS/OOT and stability related issues. Handled various reagents like NaH, NaBH4, Br2, BHA, n-BuLi,TMSCl, TFA,PPA, Raney Nickel, Pd/carbon & also hazardous chemicals like POCl3, SOCl2 etc. Reactions performed like Hydrogenation,Brominaion,Oxidation,Reduction and condensation. Handling of Moisture sensitive reactions. Study and understand the project requirements, identifying and collection of suitable literature. Support lab manager to prepare weekly technical reports and other project related technical documents (impurity profile tables,Plant batch data,developmental reports) Executing assigned reactions of project. • Looking after the Safety equipments management and maintaining it as per regulatory requirement in R&D lab. • Study the MSDS of each chemical using in every new project and make arrangement of Safety equipments accordingly. Handled HPLC system of Agilent technologies Ezichrome (A.04.07) and version Open Lab cds2.4 • Good in Thin layer chromatography & Column chromatography. Preferred candidate profile Perks and benefits

Roles and Responsibilities Develop new APIs through organic synthesis, method development, and optimization. Conduct literature reviews to stay updated on latest research trends and technologies. Ensure compliance with GMP guidelines during API manufacturing processes. Collaborate with cross-functional teams for product development, scale-up, and commercialization. Perform impurity analysis using techniques like NMR, DSC, etc. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Ph.D/Doctorate in Chemical Sciences from a recognized university. Strong expertise in areas such as API synthesis, organic chemistry, method development/validation/transfer/methodology. 9-14 years of experience in Research & Development (R&D) or related field. Key Responsibilities Literature Review & Route Identification Perform comprehensive literature and patent searches (SciFinder, Reaxys, PubChem, etc.). Identify and evaluate synthetic routes for APIs, intermediates, and impurities. Synthetic Research & Development Plan and perform multi-step organic synthesis experiments. Develop and optimize cost-effective and robust synthetic processes. Work on impurity profiling and synthesis of known/unknown impurities (including nitrosamines/nitroamines). Process Optimization & Scale-Up Support Optimize reaction parameters for higher yield, purity, and reproducibility. Support process development, kilo-lab trials, and technology transfer. Address scale-up challenges in collaboration with process R&D teams. Analytical Collaboration Interpret analytical data (HPLC, LC-MS, NMR, IR) for structure confirmation. Work with Analytical R&D to characterize intermediates, APIs, and impurities. Documentation & Compliance Maintain accurate lab notebooks, experiment records, and reports. Prepare technical documents for DMFs, ANDAs, and regulatory submissions. Ensure GLP, GMP, EHS, and data integrity compliance. Teamwork & Leadership (For Sr. Executive Level) Independently lead assigned projects with minimal supervision. Mentor and guide junior chemists/trainees in lab activities. Provide technical support for regulatory/customer queries.

Detailed Job Role Perform microbial testing of materials and products, prevent contamination, and maintain laboratory standards. KRA (Key Responsibility Areas) Sample testing, contamination investigation, report maintenance KPI (Key Performance Indicators) Test volume, contamination rate, report accuracy, corrective action closure Job Summary: We are seeking a detail-oriented Microbiologist to perform microbial testing, prevent contamination, and ensure adherence to laboratory standards. The ideal candidate will support quality control and research initiatives by generating accurate and timely data. Key Responsibilities: Conduct microbial testing of raw materials, in-process samples, and finished products. Monitor laboratory environments to prevent contamination. Investigate and resolve contamination issues. Maintain accurate laboratory records, test results, and reports. Ensure compliance with laboratory protocols, safety guidelines, and regulatory standards. Support method development and validation as needed. Key Performance Indicators (KPIs): Volume of tests performed Rate of contamination or non-conformance Accuracy and timeliness of laboratory reports Closure of corrective and preventive actions (CAPA) Skills & Competencies: Strong knowledge of microbiological techniques and laboratory procedures Attention to detail and analytical skills Knowledge of quality standards and regulatory requirements (GLP, GMP) Good documentation and reporting skills Ability to work independently and in a team environment