8 Chromatographic Analysis Jobs

Role Overview: As a Scientist-II at USP, you will be working in the Reference Standard Laboratory in a non-supervisory position. Your main responsibilities will include performing required tests for projects, maintaining a GLP environment in the laboratory, and collaborating with teams for efficient laboratory operations. You will utilize your technical expertise and knowledge of pharmaceutical analysis to ensure accurate testing and contribute to the overall success of the projects. Key Responsibilities: - Execute all testing and analyze data with excellence and minimal errors. - Support Verification, GPH, PQM, stability, and other departmental teams with testing when required. - Manage sam...

Perform chromatographic analyses and tests, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. Required Candidate profile Follow safety protocols and guidelines to ensure a safe working environment in the chromatography laboratory. Handle and dispose of hazardous chemicals and waste materials

QC officer -04 Qc Executive - 01 Analytical QA - 01 Perform chromatographic analyses and tests, including HPLC, Gas Chromatography (GC),Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. LIMS, Docs IQ Required Candidate profile We are looking for Male candidate due to work in rotation shift ( First/Second/Night) preferred B.Sc./MSc chemist & required experience of pharma formulation Sterile/Non Sterile product.

Role & responsibilities Preparation and review of analytical method validation and method verification protocols and reports. Execution of analytical methods as per approved protocols. Coordination with cross-functional departments (QA, ADL, Production, etc.) for analytical method validation activities. Ensure compliance with Good Laboratory Practices (GLP) and Safety Guidelines in all laboratory operations. Ensure all laboratory activities are performed as per existing Standard Operating Procedures (SOPs) . Provide technical guidance and training to team members on SOPs and analytical techniques. Support the QA team by ensuring timely availability of audited and reviewed validation document...

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...

QC officer -04 Qc Executive - 01 Perform chromatographic analyses and tests, including HPLC, Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. LIMS knowledge preferred. Required Candidate profile We are looking for Male candidate due to work in rotation shift ( First/Second/Night) preferred B.Sc./MSc chemist & required experience of pharma formulation Sterile/Non Sterile product.

Perform chromatographic analyses and tests, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. Required Candidate profile Stay informed about industry trends,advancements in chromatographic technology,regulatory changes related to chromatographic analysis,quality control. Participate in continuing education/training

We are seeking a meticulous and experienced Executive/Sr. Executive to spearhead chromatographic analysis and data review at Synnat Pharma Private Limited, a rapidly growing API manufacturer. In this pivotal role, you will be responsible for ensuring the accuracy, reliability, and compliance of analytical data generated within our QC laboratory. Your expertise will be crucial in adhering to stringent regulatory standards, including ICH guidelines and pharmacopeial requirements, while contributing to the overall quality and integrity of our pharmaceutical products. The ideal candidate will possess a strong understanding of HPLC and GC systems, coupled with proficiency in Empower CDS and a dee...