746 Method Validation Jobs - Page 8

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Maintenance and use of GC FID To test and analyze proximate parameters like UV parameters, Analysis of Fatty acids Maintaining samples before and after analysis Maintaining the CRM Method verification & validation...

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Responsible to develop, implement and be responsible for the production plan for their respective departments. To deliver timely and accurate analysis of samples to meet customer commitments. Be responsible for re...

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Senior Chemist-Residues Analysis of Pesticide residues in Food and Feed samples. Operation and Maintenance of LC-MS/MS and GC-MS/MS. Reference standards maintenance. Calibration of LC-MS/MS and GC-MS/MS. Recording...

1. Researching and adding tests and technologies in AVM Labs for in-house or OST menu. 2. Building scientific knowledge

Testing Raw Materials, In-process Samples and Finished Products - Wet analysis HPLC Method Development Quality Audits Record keeping and COA preparation Support troubleshooting of quality deviations Calibrate and maintain laboratory instruments

Role & responsibilities Implement norms for safety culture and 5S in laboratory Provide support and execute analytical method development and validation Coordinate for analytical testing and reporting Execute calibration of various analytical instruments as per schedule Adhere to ADL department policies and SOPs Comply with statutory and regulatory requirements Experience: MSc : 10 to 15 years PhD : 2 to 4 years Eligibility Individuals who have cleared 10th and 12th in first attempt (50% and above) MSc (50% and above), with no academic gap. Interested candidates can share their CV to juhi_bhavsar@atul.co.in or call on 81605 01583

As the leader of the DQA department, your role is to ensure the implementation of CGMP rules and regulations in Research & Development. Your responsibilities include: - Reviewing the Lab validation Protocol and Report of CRD. - Reviewing the Process Development report for DMF filing. - Reviewing the Specification and STP of Key Raw Material, In-Process, Intermediate stage, and Finished Product. - Reviewing the Method Development Report, Method Validation Protocol/Report, Method Transfer Protocol of ADL. - Reviewing the stability protocol and Report. - Preparing SOP, Formats / Annexures, Log books, and ensuring RA and GLP Compliance. - Interacting and communicating with R&D, ARD, QA, and Regu...

You will be responsible for the execution of analytical method optimization/development, validation/verification of analytical test methods related to Compendia, In-house developed methods, Site transfer methods, Regulatory queries, Method Life Cycle Management (MLCM) studies, Supplier Driven Changes (SDC), and other procedural updations. This includes the preparation of method validation/verification protocols and reports. Your key responsibilities will include: - Executing method optimization/development studies. - Validating/verifying in-house methods, Compendia, SDC, MLCM, and Cleaning Analytical methods while adhering to regulatory procedures. - Preparing Method verification/Method tran...

You will be working as a Senior Executive - AQA at Jubilant Pharmova Limited located in Nanjangud, Mysore. Your role will involve the following key responsibilities: - Responsibility for analytical compliance in accordance with current regulatory guidelines, monograph requirements, customer needs, and internal procedures. - Reviewing laboratory metrics to identify areas for improvement in laboratory compliance and ensuring right first-time laboratory performance. - Reviewing and approving laboratory Quality Management System (QMS) documents such as Out of Specification (OOS), Out of Trend (OOT), Deviation, Change management, Incidents, Action items, Corrective and Preventive Actions (CAPA), ...

Position: R&D Executive-API synthesis Company: Titan Pharmaplus Pvt. Ltd Qualification: MSc-Organic Chemistry Experience: 6-10 years Location: Mahad, Raigad And R&d Navi Mumbai Job description: Synthesize APIs/intermediates/impurities Literature search, selection of cost effective synthesis route Good knowledge of Purification & characterization techniques Data evaluation, characterization report preparation & submission in time Expertise to work from gram to kilo scale Roshani Patil/ Vaibhavi Behere: 022-67857000 Share cv on: recruitment@titanpharma.com, roshani.p@titanpharma.com, vaibhavi.b@titanpharma.com

Job Title: Microbiologist (Quality Control) Biopesticides & Biofertilizers Location: Panoli, Ankleshwar, Gujarat, India Employment Type: Full-Time Position Summary We are seeking a skilled and detail-oriented Microbiologist to join our Quality Control (QC) team. The ideal candidate should have a minimum of 1-2 years of experience in microbiological quality control, with a strong understanding of the Fertilizer Control Order (FCO) and Central Insecticides Board (CIB) regulations. This role involves ensuring that our biopesticide and biofertilizer products meet the highest standards of safety, efficacy, and regulatory compliance. Key Responsibilities Microbiological Testing : Conduct routine a...

B.Sc./M.Sc. with 1–4 years in QC (API). Hands-on with HPLC, GC, UV, and wet analysis. Experienced in raw material, in-process, and finished product testing. Strong in GMP, documentation, and analytical techniques. Required Candidate profile B.Sc./M.Sc. with 1–4 years’ QC experience in API. Proficient in HPLC, GC, wet lab testing, and GMP documentation. Detail-oriented, accurate, and skilled in analytical methods. Perks and benefits GMP GLP plant| Growth| Safety| Compliance| Perks

Experience in Operation and calibration of LCMS /GC Method development and validation of Genotoxic impurities/ nitroso amine impurities/NDSRIs in pharmaceutical products/ substances by LC-MS/MS. Development of MS compatible methods for the HPLC RS methods for the identification of unknown peaks by LC-MS Development of MS compatible methods for the identification of degradation impurities and unknown impurities

Responsibilities: * Develop analytical methods using ADL principles * Validate methods according to industry standards * Collaborate with cross-functional teams on method implementation Annual bonus Provident fund

As an Officer-Microbiology at Actylis in Ahmedabad, your role involves performing sampling and analysis of finished products, monitoring and recording day-to-day activities as per GDP guidelines, and ensuring clean, hygienic, and safe work environment. You will be responsible for microbial testing in accordance with USP, EP, IP, or customer guidelines, as well as participating in required inspection and monitoring programs. Additionally, you will have opportunities for personal growth. Key Responsibilities: - Ensure calibration and maintain microbiology lab equipment - Perform microbial testing in accordance with USP, EP, IP, or customer guidelines, including microbial parameters in water, p...

Who We Are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Ho...

Company Description At TAPI, we're not just a companywe're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide. Our strength lies in our peoplea team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that t...

Sample processing Sample analysis Method Development Method Validation Working experience on LCMS Required Candidate profile Must have worked in Bioanalytical Department with Pharma AND / OR CRO

Roles and Responsibilities : Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Team management. Desired Candidate Profile : Bachelor's degree in pharmacy (B.Pharma) or Ma...

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of ho...

Main Accountabilities Routine analysis & Stability Analysis (assay, RS, dissolution, water content etc.) of R&D formulation projects (solid & liquid orals, injectables) Daily calibration of pH meters, balances etc. Stability sample management (loading & withdrawal as per stability plan) Preparation of Stability Reports & other protocol based study reports for assigned projects, as applicable Hands-on experience of analytical instrumental techniques (HPLC with chromatographic software etc.) Assisting analytical method development/validation/method transfer activities, as per need Supporting other assigned lab responsibilities for GLP compliance Performance Indicators: Timely execution of assi...

Kindly read the below details and then apply Immediate Hiring !!!! Location: Cuddalore, Tamil Nadu Interview Mode: Level1 : Virtual (Mircosoft Teams) Level 2 : Face to Face Role & responsibilities QC Analyst (IC/HPLC) Experience: Minimum 5-8 years in core area (IC/HPLC and wet analysis) Educational qualification: Only Postgraduate in Chemistry/equivalent Work background: Only Pharma (API/Formulation/excipients) Key responsibilities: 1. Hands on experience on Ion Chromatography is most preferable. 2. Responsible for independently handling IC/HPLC analysis. 3. Qualification and troubleshooting of HPLC instruments. 4. Shall have handled software including Chromoleon 5. Shall have good knowledge...

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of ho...

Work Flexibility: Hybrid What you will do - This role intends to recruit a talent who will seat on the divisional team and will have responsibilities for making testing efforts and goals a success working with local and global test lab Drive consistency in terms divisional procedures, be an active contributor in making development/verification testing a success. Responsible for sign off on key deliverable from testing/test lab perspective. Example: protocols, reports etc Ensure continual improvement in capability building , quality, delivering higher value services. Learn and contribute In making overall R&D process efficient by bringing predictability in terms of plan, execution, budgeting ...

1. Amino acid validation. 2. In-Process and finished products analysis. 3. Product development product analysis. 4. Documentation. 5. Responsible for method process Share resume to hrd@stedmanpharma.com, Call 7904827192/9786920463 Perks and benefits Canteen and other welfare benefits.