518 Method Development Jobs

Job description: Related to the analysis of nitrosamine impurities such as NDMA (N-nitrosodimethylamine) and NDPA (N-nitrosodipropylamine) typically focus on analytical method development and validation, LCMS Analyst / Scientist Analytical Method Development & Validation by LCMS. Preparation of Protocols and Reports. Method Development and Validation by LCMS (nitrosamine) Develops and validates reproducible and appropriate analytical methods as needed respecting the GMP practices; Participates in analytical troubleshooting; Writes methods, validation protocols, validation reports and investigation reports; Performs analyses; Participates in drafting SOP/ working instructions. Required Candid...

We are looking for a skilled Senior Data Engineer with 4 to 7 years of experience to join our team, focusing on PowerBI development. The ideal candidate will have a strong background in data engineering and excellent technical skills. Roles and Responsibility Design, develop, and implement data models and architectures to support business intelligence solutions. Develop and maintain complex data visualizations using PowerBI. Collaborate with cross-functional teams to identify and prioritize project requirements. Ensure data quality, integrity, and security by implementing robust data governance policies. Optimize data performance and scalability through advanced analytics techniques. Provide...

Read and understand various in vivo study protocols Good knowledge of various in vivo animal models employed in DMPK arena Handling of laboratory animals (mice, rats, guinea pigs, rabbits, hamsters etc.) Conduct various in vivo ADME studies (IV and PO studies, excretion studies etc.) Ability to administer compound via various routes in rodents (IV, PO, IP, SC, tropical, intravitreal etc.). Should be adept at conducting IV studies employing infusion pumps Should be able good at rodent cannulations (jugular, carotid, femoral) and conduct studies in these animals Maintain required documentation for animal ethics committee purpose Conducting simple pre-formulation work for day-to-day PK studies....

- Literature search & compilation, generating chemistry new approaches & simplification areas. - Experimentation, Documentation of hard copy & SAP entry. - Bounding of expt. Data sheets & analytical observations, Submission of Lab documents. Required Candidate profile - 5+ years of experience as Research Scientist. - Excellent analytical & Interpersonal skills.

Desing, Planning, development, and implementation of innovative, safe, and cost-effective construction methods for High Rise Towers. CMPC Lead shall supports project team and the CMPC leadership in preparing method statements, site logisitcs, analysing risks, coordinating with design functions, and applying engineering solutions for the efficient and faster execution of projects. Prepare comprehensive logistics plans for site mobilisation, equipment positioning, resource flow, and material handling. Design enabling works to support the smooth initiation and execution of major project components Identify opportunities to reduce cost or construction time through alternative methodologies. Assi...

JOB DETAILS 1 Taking ownership of business research assignments entrusted and work closely with the team to produce impeccable quality outputs 2 Conduct secondary/ primary research based on tactical and strategic information needed to fulfil client requirements 3 Analyzing information, providing insights and writing reports with logical structure and flow 4 Ability to take responsibility of assigned tasks and work with minimum guidance 5 Interact regularly with team lead/ project manager and other team members Skills Set: 6 Excellent written and verbal communication skills 7 Experience in Business Intelligence/ Competitive Intelligence/ Market Intelligence functions 8 Strong interpersonal, t...

About the Role We are currently seeking a data-driven and detail-oriented Program Intern to join Leap. This role will involve critical thinking, problem-solving, and analytical thinking to drive operational improvements and support strategic initiatives. The charter for this role will include: Work closely with the founder/senior leaders to turn ideas into validated experiments. Dive into industry trends, discover competitor insights while also working on user research. Build a hypothesis to solve the different problem statements, execute, validate and scale the results Align with stakeholders across the org to drive the actionables; be a driving force in cross-functional teams Present findi...

Conduct laboratory tests and analyze results with high accuracy and attention to detail. Maintain and calibrate laboratory equipment to ensure proper functioning. Prepare and maintain accurate records of test results and patient information. Required Candidate profile Minimum 2 years of experience in a laboratory setting, preferably in a hospital or medical services setting. Strong knowledge of laboratory procedures and protocols.Excellent analytical skills

As an Analytical Scientist in the Analytical Development New Product Development (NPD) department of a Global Pharmaceutical MNC based in Bangalore, your role will involve the following responsibilities: - Conduct analytical testing for solid oral formulations including tablets, capsules, ODTs, softgels, and ER/DR formulations. - Develop and validate methods for assay, related substances (RS), dissolution, and stability following ICH guidelines. - Troubleshoot analytical issues, manage Out of Specification (OOS) and Out of Trend (OOT) results, and support Root Cause Analysis (RCA). - Operate and troubleshoot a variety of instruments such as HPLC, UPLC, GC-MS, LC-MS/MS, UV, IR, and XRD. - Sup...

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department Masters degree level in Chemistry,M pharmacy & B pharmacy 2023,24,25 passed outs. 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Bio-analytical: Role and responsibility: In process quality control of ongoing studies. Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling. Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles. Checking of the con...

Responsibilities: Experience in Method Validation. Experience in Stability Study. Experience of review Electronic data review and backup systems. Expert in Qualification of analytical instruments like HPLC, GC, AAS, FTIR, UV etc. Expert in Calibration of analytical instruments like HPLC, GC, AAS, FTIR, UV etc. Must have minimum 3+ years of experience as a Reviewer. Must have an experience of reviewing all types of QC software. Must be familiar with cGMP/GLP practices and ICH and FDA Guidelines. Required Skills Must be excellent in written and spoken English; net savvy and adept at computer skills. Logical thinking. Organizing. Good in communication. Required Qualification: - B.Sc/M.Sc - Chem...

Regular Batch Analysis by using LCMS. Preparation and analysis of method validation, method transfer, method verification and method development protocols and reports. Experience in GTI & NDSRI by LCMS

Manager - Quality Control (Formulations) 10 to 15 years of experience in Pharmaceutical Industry especially in Formulations Unit. Should have experience in successfully handling Quality Audits. Thorough knowledge in all types of Analytical instruments, analytical methods, HPLC, Method validation and method development etc., Should possess profound knowledge and skills in OSD/Formulations products. Total Quality Management (TQM), preparation and successful implementation of SOP's. Should lead a team in QC department and responsible for TQM. Sound working knowledge in MS Office and computer skills. Responsible for day-to-day and periodical MIS reports. Coordination with Production, QA and othe...

Conducting Regular Analysis by HPLC Method Validation Method Development

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.

Role & responsibilities Job Description: Lead and manage the ADL team, providing guidance, mentorship, and performance management. Develop, validate, and transfer analytical methods for drug substances, intermediates, and raw materials as per current guideline. Optimize methods for accuracy, precision, and efficiency. Prepare validation protocols, conduct experiments, and generate validation reports. Ensure adherence to regulatory guidelines and standards (e.g., ICH, GMP). Possess in-depth knowledge of analytical techniques (e.g., HPLC, GC-HS, , IR, UV, etc) and support to regulatory query response. Troubleshoot analytical issues and identify root causes. Collaborate with R&D, Regulatory, an...

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 manag...

The successful candidate will be responsible for designing, developing, and optimizing OSD formulations, ensuring product quality, stability, and performance. Interested candidates please sent your resumes to email id: jones.naveen@insta-pill.com Food allowance Health insurance Office cab/shuttle Provident fund

Walk- In - Drive Method Validation/ FML AQA- MSN Laboratories, Formulation Unit - V, RK Puram, Hyderabad on Saturday 15-11-2025. ASRD Responsibilities : 1) Execution of Analytical Method validations for drug products for various markets. 2) Execution of DPDM Method validations for drug products. 3) Analytical method transfers to the Quality control labs. 4) Performing the calibrations of the analytical instruments. 5) Preparation & review of Analytical Method validations protocols and reports. 6) Responsible for cGLP, documentation and implementation of departmental quality systems. AQA Responsibilities : 1. Preparation and Review of AQA SOPs. 2. Review of validation protocols & reports. 3. ...

Job Description: As an Application Engineer for LCMS, you will play a crucial role in supporting the sales and customer success teams by providing technical expertise and application support for our Liquid Chromatography Mass Spectrometry products. You will work closely with customers to understand their analytical needs, provide demonstrations of our LCMS solutions, and offer guidance on method development and optimization. This role requires a combination of scientific knowledge, technical proficiency, and strong communication skills to ensure customer satisfaction and drive business growth. Key Responsibilities: Customer Engagement: Collaborate with the sales team to engage with customers...

As a Quality Assurance & Analytical Chemist at FMC, you will be part of a team dedicated to providing innovative solutions for agriculture and the planet. Your role will involve utilizing your knowledge and experience to provide daily analysis support, develop, validate, and apply modern analytical technologies, and ensure quality standards are met at the Toller site. You will be expected to work collaboratively with the team, adapt to changes, and meet project quality and timing needs. **Key Responsibilities:** - Know, understand, and practice all aspects of laboratory safety and industrial hygiene protocols. - Develop, validate, and implement methods for qualitative and quantitative analys...

As a Quality Assurance & Analytical Chemist at FMC, you will play a crucial role in providing daily analysis support by developing, validating, and applying modern analytical technologies for the development and commercialization of agricultural products. Your responsibilities will include: - Knowing, understanding, and practicing all aspects of laboratory safety and industrial hygiene protocols. - Developing, validating, and implementing methods for qualitative and quantitative analysis to meet business needs. - Conducting routine and non-routine analysis of process technical data to ensure project quality and timing needs are met. - Collecting data, generating summaries, and reports. - Sup...

We are looking for a highly skilled and experienced professional to join our team as a Scientist - I at Narsee Monjee Institute of Management Studies (NMIMS). The ideal candidate will have 2-5 years of experience in the field. Roles and Responsibility Conduct experiments and collect data to test hypotheses and validate results. Analyze and interpret complex data sets to draw meaningful conclusions. Develop and implement new methods and techniques to enhance research efficiency. Collaborate with cross-functional teams to achieve project goals. Design and execute experiments to test new products and services. Prepare and present reports on experimental findings and recommendations. Job Require...

Walk-In Drive For API Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Saturday 01-10-2025. Requirement for Executive / Senior Executive - API AR&D - API Analytical Research & Development(AR&D) HPLC,LCMS,GC,GCMS,PXRD High performance liquid chromatography HPLC,GC,GCMS,PXRD HPLC with Software lab solu. UV-VIS Spectrometer GC with Software lab solution PH-Meter Moisture Analyser Karl Fischer titrator Micro- Weighter Balance 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...

Job Responsibilities: 1. Review of Analytical Method Validations/ Verifications protocol/ reports 2. Review of Analytical Method Transfer protocol/ reports 3. Review & release of Reference standard characterization data 4. Review of R&D data and Lab note book for regulatory submission 5. Review of Instrument/Equipment Qualification & Calibration reports 6. Review of CSV (Software Qualification) documents (Protocol &Reports) 7. Review of DS & DP STPs (Reference standard, Raw Material, Intermediate, In process, Semi finished & Finished product). 8. Preparation, Review & training of CQA SOP (Related to R&D Labs) 9. Review of SOPs for R & D function (Analytical Research Laboratory, DDRL (Pilot L...