4349 Hplc Jobs

Core Responsibilities - Defines the day-to-day duties of this role 1. Assists sales account managers and product specialists to meet or exceed sales quota by providing sales and customers with technical/scientific expertise, primarily in the areas of application and technical support. 2. May be client or product oriented. 3. Contributes to sales account planning. 4. Participates actively in the sales process from deal qualification to deal closure. 5. Owns the deal s technical closure. 6. Responsible for meeting sales targets and for supporting sales organizations to meet targets. 7. Is knowledgeable of competition and able to identify lockout specifications (identify Agilents competitive ad...

M.Pharma/Phd - Phytochemistry, pharmacognosy, Nataral Products Chemistry 5 - 7 Years 8 - 10 LPA Location - Thane West Phytochemical Expertise product Development Extraction System Design Quality Control prepare Regulatory Documents

Responsibilities: * Analytical skills in using instruments such as HPLC, GC, UV is mandatory. * Experience in validation and calibration activities required. * Ensure compliance with industry standards through method validation and regular testing.

Role & responsibilities QA/QC: Supervise quality control testing (HPLC, GC, etc.) Ensure all products meet quality and regulatory standards Handle audits, documentation, OOS, OOT, and CAPA Maintain SOPs and ensure GMP/GLP compliance Guide and train QA/QC team HPLC & GC handling, Wet Analysis, Documentation Audit, OOS, OOT, CAPA R&D: Lead product and process development projects Manage lab trials, scale-up, and technology transfer Support innovation and improvement in formulations Coordinate with production and regulatory teams Preferred candidate profile 3 to 5 years Experience and Masters in Oil Technology/M.Sc. Organic/Analytical Chemistry Preferred Qualifications: Prior experience in the ...

Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Job: R&D (Synthesis) R & D (ADL) - Agrochemical

1) Analysis of Intermediates / Finished goods / Stability on HPLC/GC-LAS & GC-HSS. 2) Operation and Maintenance of HPLC & GC-ALS & GC-HSS (Empower-3 Software) 3) Basic understanding of laboratory practices, analytical techniques, GMP/GLP concepts, and willingness to learn quality systems. 4) Attention to detail, good communication, ability to follow SOPs. 5) Willingness to learn, ability to work in a team, and flexibility to work in shifts. This is a walk-in post. Even then candidates are encouraged to share their resumes in advance at talenthire-unit4@metroapi.com with the subject line Profile for Quality Control This will help our team connect with you beforehand and guide you about the po...

Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA

Role & responsibilities Should have knowledge of - QC CFR Compliant instruments like HPLC, GC, KF, IR, UV etc. - Wet Lab Testing, FG Testing etc. - Maintaining of documents of testing as per USFDA guidelines. - Instrumentation validation process - Willing to come in Shift duty.

Walk-In @ MBL - Bhiwadi on 28th Dec 25, Sunday Q.A. - 9 Post, Exp. 2 - 8 Yrs (CQA, IPQA & Documentation) Q.C. - 9 Post, Exp. 2 - 7 Yrs (Exp. in HPLC/GC/AAS/FTIR/UV/Dissolution test) Maintenance - 10 Post, Exp. 1 - 8 Yrs (Fitter/ Electrician/ HVAC) Required Candidate profile Candidate must have Pharma Exp. Ready to Relocate Bhiwadi, Rajasthan, ROW & EU Plant Experience Prefer Mob: 7240001632 hrd@medicamen.com admin-ho@medicamen.com Perks and benefits Salary based on Pharma Experience & Knowledge

We are hiring from Quality executive designation : Quality executive Work location: Bangalore Jd: Job Title: Area Quality Control (QC) Executive Location: [Bangalore] Department: f& v quality executive Job Summary: The Area QC Executive is responsible for overseeing quality control operations across 35 designated stores. This role involves conducting daily store visits, ensuring adherence to quality standards, analyzing complaints and write-offs, and implementing corrective actions to enhance product quality and customer satisfaction. Key Responsibilities: • Conduct daily visits to assigned stores to monitor and evaluate quality control processes. • Ensure compliance with FIFO protocols and ...

Wet Lab Experience GC & HPLC Analysis, Sampling Experience

Role Summary The Quality Control Manager will oversee laboratory operations and ensure the quality of raw materials, in-process products, and finished goods through effective inspection, testing, and analytical evaluation. The role requires strong expertise in lipid technology , advanced analytical instruments, and team leadership to maintain product integrity, regulatory compliance, and efficient QC operations. Key Responsibilities Oversee QC inspection and testing of raw materials, in-process samples, finished products, and by-products. Perform, review, and interpret analytical testing related to lipids, fats, and oils , including quality parameters such as FFA, peroxide value, anisidine v...

Should be capable of handling instruments like HPLC , GC and other instrument like IR, UV, Potentiometer etc Should be familiar with the review mechanism of audit trails of application softwares used in chromatography and other stand alone instruments Should having the knowledge of GLP and GMP practices

Job Title: Lead Agentic AI Architect - Pharma AI Experience: 12+ Years Location: Any Job Summary We are looking for a Lead Agentic AI Architect with strong expertise in Generative AI, agentic AI systems, and Azure cloud architecture, focused on building compliant AI solutions for pharmaceutical workflows and regulatory processes. Key Responsibilities Design and build Azure-native agentic AI solutions for HPLC method validation, protocol generation, and pharma workflows. Lead hands-on development using Claude Code for rapid AI prototyping and implementation. Develop advanced RAG systems and intelligent document processing pipelines using LangGraph, LangMem, and LlamaIndex. Establish LLM evalu...

Job Title: Quality Control Manager Pharma Industry: Pharmaceuticals Functional Area: Quality Control Role Category: Quality Control Manager Job Location: Sterling Healthcare Ltd., Talegaon, Pune Employment Type: Full-Time Experience Required: 5– 10 Years Job Description Sterling Healthcare Ltd. is seeking an experienced Quality Control Manager to lead and manage Quality Control laboratory operations in a pharmaceutical manufacturing environment. The role is responsible for ensuring product quality, regulatory compliance, and adherence to GMP and global quality standards . Key Responsibilities Manage and oversee day-to-day operations of the Quality Control laboratory Ensure testing of raw mat...

Key Responsibility area /Activities Documentation & Review of analytical data (RM, PM, SFG, FG, Stability,Hold time, PV, CV, WS, Water, Volumetric solutions,Calibration etc.,) hard copy and as well as electronic data (LabWare LIMS, Empower and other instrument software). Verification of instrument usage logbook and e-Logbook Review of certificate of analysis. Online review of electronic data and documents. To review / Approve instrument methods created on Empower and other standalone instruments. To review the electronic data in LabWare LIMS. To review the audit trail of computerized systems Review of Stability Study Records and summary reports. Handling of Issuance, retrieval, destruction o...

Job Responsibilities of the Microbiology Section head: 1. Laboratory Operations: Planning and Execution: Plan, manage and oversee all day-to-day analytical activities within the Microbiology Laboratory. This includes scheduling, resource allocation (personnel and equipment) and ensuring efficient workflow to meet production and quality deadlines. Sample Control and Reporting: Allocate incoming samples to qualified microbiologists for various microbiological analysis, ensuring proper documentation and traceability. Oversee the entire batch release process from analysis through to the final reporting of microbiological test results, ensuring timely and accurate delivery of data. LIMS Data Mana...

JD: Perform analysis of RM/PM, in-process, and finished products as per STP/Specifications. Operate analytical instruments such as HPLC, GC, UV, IR, KF, Dissolution, and related systems. Ensure documentation as per ALCOA+ principles and maintain data integrity. Execute method validation, method transfer, and stability sample analysis as applicable. Handle laboratory incidents, OOS/OOT results, and deviation investigations as per SOP. Maintain qualification/calibration status of instruments and adhere to lab safety standards. Support regulatory inspections, internal audits, and continuous improvement activities Skills: Strong knowledge of HPLC, GC, Dissolution, and Analytical Techniques Good ...

Job Description Key Responsibilities: Having a Knowledge of Instrument operation like HPLC, GC, UV, IR, Karl Fischer, Auto Titrator Good knowledge of LIMS and Documentation having Experience of working with 21 CFR compliance, and CGMP environment. Ready for shift duty and good communication skill Qualifications Qualification: M.Sc / B.Pharm / M.Pharm Designation: Officer/Sr. Officer Analyst IP-FP-ST_ HPLC Analyst Job for Automation

Job Location: Daman & Dahej Qualification:- M.Sc. (Chemistry)/ B. Pharma/ M. Pharma Experience:- 2-7 Years in (API or Solid Oral or formulation) Required Candidate profile * 2- 7 years of experience into LCMS, HPLC, GC & Wet Chemical sections, Analytical Validation, Finished Goods, Raw Material, Stability & GLP

Roles and Responsibilities Conduct analytical testing of bulk drugs, APIs, and finished products using HPLC and other relevant methods. Ensure compliance with cGMP guidelines and regulatory requirements for quality control laboratories. Develop and maintain SOPs for laboratory operations, instrument calibration, and data validation. Collaborate with cross-functional teams to resolve issues related to product release decisions based on test results. Participate in continuous improvement initiatives to enhance laboratory efficiency and effectiveness. Desired Candidate Profile 4-6 years of experience in Analytical Quality Assurance (AQA) or similar role in pharmaceutical industry. Bachelor's de...

Role Overview: As a Quality Control Analyst at Sisco Research Laboratories Pvt. Ltd. (SRL), you will be responsible for conducting quality analysis and documentation of raw materials, finished products, and formulations. Your role will also involve supporting audit activities and maintaining all relevant QC documentation in compliance with regulatory and company standards. Key Responsibilities: - Perform chemical analysis of raw materials, intermediates, and finished products as per approved specifications and SOPs. - Maintain accurate documentation of analytical data, reports, and test results. - Ensure compliance with quality standards and regulatory requirements (ISO, GMP, etc.). - Conduc...

Role & responsibilities Daily routine analysis on HPLC Quality Control testing using HPLC, GC, and other instruments Work in FP, IP, RM and PM Preferred candidate profile Worked in API plants. Ready to Relocate to working location.

Walkin drive for QC and Production for EU Approved Pharma API Co at Dombivli office Job location: Boisar Tarapur Interview Date: 21st December 2025 (Sunday) Time: 9.30 am to 4 pm QC: QC officer & Executive Experience - 3 to 8 yrs Production: officer, Executive, Assistant Manager Experience - 3 to 12 yrs Call us on For QC : 8779376464 For Production: 7678074456 Mail Id - shweta.d.chatur@gmail.com

Position 3- Officer QA Location - MEPL U II Qualification Diploma , B.E. Electrical Required Experience 4 to 5 Year Total requirement- 1