8 Method Validations Jobs

About Intertek JOB DESCRIPTION Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices and over 46,000 people in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification solutions for our customers operations and supply chains. Intertek Total Quality Assurance expertise, delivered consistently with precision, pace and passion, enabling our customers to power ahead safely. True to the spirit of our founders, we lead the industry with unparallel ATIC services. The spirit ignited by our co-founder Thomas Alva Edison who gave one of the biggest inventions to the world ...

You will be responsible for overseeing the quality control activities in the Intermediates and API manufacturing unit. Your role will involve the following key responsibilities: - Handling all the wet lab & Analytical labs equipments including HPLC, GC, UV, IR, TLC, MR, Muffle Furnace, and others. - Demonstrating a strong knowledge in Stability Studies. - Preparing Method Validations and conducting Equipments Calibrations as per standard operating procedures. - Managing the QC staff by assigning and overseeing their Roles & Responsibilities. - Being available for 8-hour shifts, with a willingness to manage duty extensions during emergencies. - Revising and implementing Standard Operating Pro...

Responsibilities: Testing Key Actions: Sample analysis & Method Validations under the guidance of Section In-Charge Understanding the complete requirement of the method before initiating the analysis Maintenance of all logbooks of equipment being used in section Working reference standard preparation Maintenance of records for working reference standards with their logbooks under the supervision of Section In-Charge Glassware calibration Intermediate checks of equipment under the supervision of Section In-Charge Specific responsibility of the assigned instrument (AAS/ICP-MS, GCMS-MS, LCMS-MS, IRMS) Calculating uncertainty of measurement for different parameters Responsible for calibration, m...

As a Quality Control professional at PPL Digwal, your role will involve performing chemical and instrumentation analysis for various stages of production to ensure compliance with GMP and safety standards. You will be responsible for allotting work to the chemists, calibrating instruments, maintaining documentation, managing stock levels of standards and chemicals, and ensuring timely analysis and release of products. Key Responsibilities: - Perform chemical and instrumentation analysis for in-process, raw materials, intermediates, and finished products to meet production schedules. - Allocate work to chemists within the QC department. - Conduct instrument calibrations according to the sched...

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. ...

You will be joining the Quality Control - Analytical team at Dr. Reddys Laboratories Ltd. where your primary responsibility will be to conduct analysis of Biosimilar products including drug substance, drug products, in-process samples, and stability samples. Your role will involve ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety. To excel in this role, you will be required to perform various chromatography techniques like RP-HPLC, Glycan, SEC, IEX, and pep map for Biosimilar Molecules. Method validations on RP-HPLC, Glycan, SEC, IEX, and pep map will also be part of your responsibilities. Adhering to GMP practices, good d...

Purpose of Position To carry out the Microbiological sampling and analysis of water, food and environmental samples as per the relevant national & international standards / method validations / SOPs and lab accreditation scope. The position performs in line with the Bureau Veritas Quality Assurance System, including the BV Code of Ethics, the BV Group policy, NABL, BIS, and EIC and other applicable guidelines. Major Responsibilities Perform the microbiological sampling and sample collection across the India. To carry out the microbiological analysis after getting trained. To carry out the assigned day to day tasks such as sampling and analysis as per the work plan To assist the microbiologis...

Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPL. Responsible for performing the instrumentation like ICP-MS and LC-MS analysis for In-process, raw materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule. Responsible for performing the analytical method developments, analytical method validations, analytical method transfers and analytical method verifications by ICP-MS and LC-MS/MS. Responsible to prepare and review the protocols, work sheets and reports for metho...