523 Method Development Jobs - Page 10

You will be joining a company committed to delivering high-quality pharmaceutical products and services, with a mission to enhance the quality of life through innovative healthcare solutions. The culture at Zydus revolves around collaboration, integrity, and excellence. As the ADL - Analytical Development Laboratory Executive/Senior Executive, your primary responsibility will involve method development, verification, and validation to ensure compliance with Pharmacopeial standards. You will also support various analytical activities within the department. Your key responsibilities will include method development, verification, and validation for Pharmacopeial standards, DMF updations, and ot...

The job involves carrying out the complete maintenance of all instruments such as HPLC, pH meter, weighing balances, etc. It includes method development for non-pharmacopoeial and pharmacopoeial analysis of raw materials, formulations of pharmaceutical, ayurvedic, and food products. Regular analysis of raw materials, finished products, and intermediates of JP, JSRF, JIPL, and outsourced products is also part of the job description. Additionally, the analysis of stability samples of JP products, JSRF products, and outsourced products is required. The responsibilities also include maintaining spares required for the HVAC system and utility equipment, as well as carrying out validation and cali...

The job involves preparing and analyzing samples from various sources in order to provide information on compounds or quantities of compounds present. This includes using analytical techniques and instrumentation such as gas chromatography (GC), high performance liquid chromatography (HPLC), and spectroscopy (ultraviolet) to investigate chemical compositions. Additionally, wet analysis will be performed. The responsibilities also include interpreting data, reviewing and evaluating experiments and analyses, and presenting scientific results to relevant teams. The role requires the development of new HPLC and GC methods, as well as collaborating with cross-functional teams. Staying up to date ...

You will be responsible for performing microbiological analysis, media inventory, and culture maintenance. This includes executing microbiological method development, method validation, and method verification. In addition, you will be required to perform qualification and calibration of instruments and equipment. It is essential to ensure concurrent documentation of analysis to maintain accurate records. Furthermore, you will be responsible for water sampling and testing to ensure compliance with regulatory standards. Your attention to detail and precision in executing these tasks will be crucial for the successful completion of your responsibilities.,

Role & responsibilities Method development : HPLC/GC Stability study Wet chemistry analysis (UV, IR, SOR, Titration...etc) Reaction monitor Routine support GLP awareness

Job Summary: We are seeking a motivated and detail-oriented fresher to join our Analytical Chemistry team focused on small molecule analysis. The role involves working with advanced analytical instruments and supporting the development, validation, and quality testing of small molecule compounds in a pharmaceutical or chemical environment. Key Responsibilities: Assist in the analysis of small molecules using techniques such as NMR, HPLC, GC, UV, IR, and dissolution testing Prepare analytical test reports and maintain laboratory documentation in compliance with GLP/GMP guidelines Support method development and routine analysis under supervision Calibrate and maintain analytical instruments ac...

Job Summary: The Lab Technician is responsible for performing routine and specialized laboratory tests, preparing samples, maintaining lab equipment, and ensuring the accuracy and reliability of test results. This role supports research, development, quality control, or clinical analysis activities within the laboratory. Key Responsibilities: Collect, prepare, and analyze samples according to standard operating procedures (SOPs). Perform routine laboratory tests and record results accurately. Calibrate, maintain, and clean laboratory equipment and instruments. Maintain laboratory inventory, including reagents, supplies, and equipment. Ensure adherence to safety protocols and maintain a clean...

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 devel...

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 Valida...

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( GCM...

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 inve...

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 supe...

* 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...

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...

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 ...

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 improv...

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...

"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 pa...

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, con...

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 Ra...

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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 sup...