746 Method Validation Jobs - Page 14

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.,

As a Scientist C in the GCMSMS & LCMSMS section at our laboratory located in Gurugram, Haryana, you will be responsible for creating a conducive working environment and ensuring harmonious inter-laboratory working conditions. Your primary duties will include working in compliance with ISO17025 documentation, conducting environment monitoring of Food & chemical laboratories, maintaining log books, and standardizing titrimetric solutions. You will play a crucial role in facing technical audits conducted by regulatory bodies such as NABL, BIS, APEDA, AGMARK, FSSAI, MOEF, EIC, and CPCB, as well as customers. Your responsibilities will also involve calibration, uncertainty calculation, preparing ...

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...

We are looking for skilled Analysts with expertise in HPLC and GC techniques for immediate joining. The candidate will conduct analytical testing to ensure pharmaceutical product quality, develop and validate analytical methods, and contribute to continuous laboratory improvement initiatives. Key Responsibilities: Perform analytical testing using HPLC, GC, UV-Vis, ICP-MS, and LC-MS techniques to assess product quality and purity. Develop, validate, and optimize analytical methods in compliance with cGMP guidelines. Collaborate with cross-functional teams to troubleshoot and resolve method validation and analytical issues. Maintain detailed and accurate records of test results, instrument cal...

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...

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). ...

JOB DESCRIPTION Designation: Method validation Expert Job Location: Bangalore Department: Analytical Method Validation and Special Instrumentation About Syngene About Syngene At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and ...

Analytical Method Development of Assay, Related Substances, Residual Solvents & Dissolution Test Methods with Literature Search & Report. Analytical Method Validation. Troubleshooting in Method Development and Validation. Analysis of In-process Development Trail Batches & Stability Batches. Cleaning Method Development & Validation. Excipients Compatibility Study. Preparation of Analytical Method Development Reports, Stability Reports. Preparation of Standard Testing Procedures, Standard Operating Procedures.

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...

Aquachem Industries Private Limited is looking for QC Chemist to join our dynamic team and embark on a rewarding career journey Chemical Analysis: Conduct chemical and physical testing on raw materials, in-process samples, and finished products to assess their quality and compliance with specifications Instrument Operation: Operate and maintain laboratory equipment and instruments, such as HPLC, GC, UV-Vis spectrophotometers, and other analytical instruments Data Analysis: Analyze and interpret test results, ensuring accuracy and consistency in data reporting Quality Control: Implement and maintain quality control standards and procedures to ensure that products meet regulatory and quality r...

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

Roles and Responsibility Manage daily operations of the centre, ensuring efficient workflow and high-quality patient care. Supervise staff members, providing guidance and training to ensure excellent customer service. Coordinate with various departments to ensure seamless communication and collaboration. Implement new policies and procedures to improve quality and efficiency. Maintain accurate records and reports, ensuring compliance with regulatory requirements. Foster a positive work environment, promoting teamwork and employee development. Job Requirements Minimum 4 years of experience in a similar role, preferably in the biotechnology or pharmaceutical industry. Strong knowledge of clini...

* 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 should possess a B. Pharmacy/M. Pharmacy (Pharmaceutical Analysis and Quality Assurance) or M. Sc. in Chemistry or equivalent with 5 to 8 years of experience in formulation pharmaceutical industries in the quality control department. In this role, you will be responsible for handling day-to-day activities related to sampling, testing, and release of active ingredients, inactive ingredients, packaging materials, in-process and finished products, stability samples. Your primary responsibilities include ensuring that all activities within the quality control section meet current applicable cGMP guidelines and regulatory expectations. You will be accountable for ensuring timely sampling, ana...

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...

Hikal Ltd is looking for Officer to join our dynamic team and embark on a rewarding career journey The Senior Officer plays a crucial role in the organization, responsible for overseeing and executing various tasks and projects to ensure the smooth functioning of operations This role requires strong leadership, analytical skills, and the ability to collaborate effectively with team members and stakeholders Key Responsibilities: Leadership:Provide leadership and guidance to team members, fostering a positive work environment Lead by example, demonstrating professionalism, integrity, and dedication to the organization's goals and values Project Management:Manage and coordinate projects from in...

Position Department: Synthesis Reason for the Vacant: New Position in Each Department Educational Qualification: Ph.D. (Chemistry), MSc (Chemistry, Applied Chemistry)/ M. pharm Mandatory Skills: Column chromatography, Name reaction, Documentation, general chemistry, Scale up activity, computer skill Desirable Skills: Development, of Unknown Compounds& API, Column Chromatography, literature search, Documentation. Other Specifications: LC Mass, NMR Interpretation, IR, Name Reaction, critical condition analysis Documentation.

Position Department: Synthesis Reason for the Vacant: New Position in Each Department Educational Qualification: Ph.D. (Chemistry), MSc (Chemistry, Applied Chemistry)/ M. pharm Mandatory Skills: Column chromatography, Name reaction, Documentation, general chemistry, Scale up activity, computer skill Desirable Skills: Development, of Unknown Compounds& API, Column Chromatography, literature search, Documentation. Other Specifications: LC Mass, NMR Interpretation, IR, Name Reaction, critical condition analysis Documentation.

The ideal candidate brings 1-7 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) Lead microbiology practices including EM, MLT, sterility assur...

Executive for Micro R&D 1 Post based in Amritsar. The ideal candidate brings 6 - 8 yrs exp. 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). Lead...

Assistant Manager based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 8-10 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)...

Sr. Executive / Executive based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 5-8 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/...

The ideal candidate brings 10- 15 yrs exp 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) Lead microbiology practices including EM, MLT, sterility ...

Job Overview: We are seeking a Lab Attendant to support our Chemical R&D team. The ideal candidate should have average to above-average knowledge of chemistry, willingness to learn, and passable communication skills. Key Responsibilities: Assist in routine lab operations, sample preparation, and testing. Maintain cleanliness, safety, and order in the lab. Support researchers with experiments and basic chemical handling. Ensure proper storage, labeling, and disposal of chemicals. Record and update experimental data as directed. Requirements: B.Sc. / M.Sc. in Chemistry (preferred). 01 year of experience in a lab environment. Basic understanding of chemical processes and lab practices. Ability ...

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...