391 Ftir Jobs - Page 5

This Position reports to: TMC- (Trade and Transportation) Manager What we believe in At ABB, we are dedicated to addressing global challenges. Our core values: care, courage, curiosity, and collaboration - combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to empower everyone to create sustainable solutions. That's our story. Make it your story. Your role and responsibilities In this role, you will have the opportunity to manage Trade & Compliances processes, and look after the custom operation, Trade Advisory, Trade Compliance, Trade & Transport, follow with the Freight forwarders & shipping lines, ensure the material delivery. The work model...

Employment Mode : Contract to Hire Offshore OT Analyst Roles and Responsibilities: Good experience working in the Cyber security domain with a minimum of 5 years in the Industrial automation and controls space Strong understanding of various components in the ICS ecosystem, common security issues faced and best practices to be followed from a security standpoint Strong understanding of Industrial control operations and protocols Sound knowledge of the ICS cybersecurity framework IEC 62443 Good understanding of concepts like Industry 4.0, Cyber Physical Systems, Digital Twin Preferable to have hands-on experience working at a Manufacturing plant Demonstrable credentials in the Industrial cont...

As a Scientist in this role, your primary responsibilities will include: - Executing experiments for analytical method development, qualification, and transfer - Conducting in-process and stability sample testing, biosimilarity analysis, and new high throughput formats of testing using chromatography (HPLC/UPLC), electrophoresis/capillary electrophoresis, UV spectrophotometer, Solo-VPE, and other high-end analytical tools - Analyzing samples in GC, Atomic absorption spectroscopy (AAS), Charged Aerosol Detector (CAD), and glycan analysis - Planning experiments sequentially and logically - Accurately recording experiment details in electronic laboratory notebook following good documentation pr...

Role & responsibilities Strong knowledge of TQM, ISO-IMS Standards. Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis, FTIR, etc. Chemistry knowledge, Chemical analysis and Pesticide-Tech & Various formulation sample test procedure and regulation. Good knowledge of Operational Excellence methodologies such as 5S, TPM, FMEA, and related tools. Preferred candidate profile Strong knowledge of TQM, ISO-IMS Standards. Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis, FTIR, etc. Chemistry knowledge, Chemical analysis and Pesticide-Tech & Various formulation sample test procedure and regulation. Good knowledge of Operational Excellence methodologies su...

Company Name Gangwal healthcare Job Title Quality Control Manager Job Location: Maharashtra Description Job Summary: We are seeking an experienced and detail-oriented Quality Control professional with strong expertise in Nutraceutical products testing, nutritional profiling, and regulatory compliance. The ideal candidate will ensure all raw materials, in-process samples, and finished goods meet internal quality standards, statutory requirements, and international regulations. Key Responsibilities Testing & Analysis Perform qualitative and quantitative analysis of nutraceutical and food products. Conduct nutritional profile testing including macronutrients, micronutrients, vitamins, and miner...

We are seeking a skilled Analyst with hands-on experience in FTIR/Disso/UV/KF/HPLC techniques(Multiple requirements). The candidate should be well versed with Method Development, Method Validation and routine analysis. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) Walk-in interview 22-Sept to 26-Sept 9.30am to 5pm on 27-Sept-25(Saturday) from 9.30am to 3pm

As a Validation Specialist at our company, your primary responsibility will be to plan, execute, and document analytical method validation activities for raw materials, in-process samples, finished products, and cleaning validation. This will involve assessing various parameters like accuracy, precision, specificity, linearity, robustness, LOD/LOQ, and others. You will also review and approve validation protocols and reports to ensure compliance with ICH Q2(R1), USP, and other regulatory standards, maintaining adherence to GMP, GLP, and cGMP guidelines. Your role will require collaboration with R&D, QA, and Production teams to facilitate seamless tech transfer and validation support. Trouble...

Home The University Job Opportunities and Working At Swansea Current Vacancies Research Officer in Antihydrogen Physics Back to list Research Officer in Antihydrogen Physics Related pages Current Vacancies Benefits & Rewards Equality Diversity & Inclusion Information for Applicants Information for for colleagues from around the world Our reward and benefits, and ways of working enable those who join us to have enriching careers, matched by an excellent work-life balance, About The Role The group is a leading member of the ALPHA collaboration with responsibility for positrons, antihydrogen synthesis, laser-spectroscopy and frequency metrology Recent research highlights include the first laser...

On-site assessment and selection of target trainees and hospitals to ensure the selections result in optimal quantity and quality of trainees and Phaco conversion rates for the Phaco Development Program. Onsite (Operating Room) and wet lab instruction and consultation of trainees in the entire process of converting from ECCE and SICS to Phaco. This includes working with designated outside-Alcon consultants (course instructors and on-site proctors) to ensure effective trainee Phaco conversion rates and high quality surgical results Demonstrate product and procedural excellence to best technical model and coach trainees and affiliated personnel how to achieve optimal surgical and patient resul...

Key Responsibilities: Manage field information related to defective parts and quality concerns Handle defective parts recovery and dispatch for the domestic market Coordinate with DHL for part recovery and logistics for the export market Prepare executive summaries and monthly KPI reports using PowerPoint Maintain concern and defect data in Power BI for tracking and analysis Monitor bill settlements and payments related to parts handling and recovery Coordinate with MSIL for part-related queries, including FTIR replies Perform regular follow-up and coordination with stakeholders to ensure timely closure of quality concerns Support other related tasks as assigned by the department

Job Description: We are looking for a motivated and detail-oriented Research Associate to join our Analytical R&D team within the Peptide Synthesis division. The selected candidate will support the development and execution of analytical methods for peptide characterization, working closely with cross-functional teams in R&D and Quality. Key Responsibilities: Assist in developing and performing analytical methods (e.g., HPLC, UPLC, UV, FTIR, KF, LC-MS) for the characterization and quality assessment of peptides Conduct routine testing of raw materials, intermediates, and final peptide products Support method validation, transfer, and troubleshooting under the guidance of senior scientists Do...

Role Overview: As a member of the Corporate Quality Control department in the Pharmaceutical & Life Sciences industry, your primary responsibility will be to perform the analysis of raw materials, intermediates, and finished products of Active Pharmaceutical Ingredients (APIs). You will operate and maintain analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, Melting Point Apparatus, among others. Key Responsibilities: - Perform analysis of raw materials, intermediates, and finished products of APIs according to approved specifications and SOPs. - Review and verify analytical data, ensuring proper documentation in compliance with cGMP and GLP guidelines. - Prep...

Role Overview: As a Research Scientist in this role, you will be responsible for synthesizing and immobilizing photocatalysts for solar hydrogen production. You will conduct material characterization using techniques such as XRD, SEM, TEM, FTIR, UV-Vis, etc., and analyze the related data through Python coding, theory, and simulations. Your primary duties will involve designing and executing experiments focused on solar-driven water splitting. You will be tasked with optimizing reaction conditions and analyzing performance metrics to enhance efficiency. Furthermore, you will leverage your programming skills in Python, Artificial Intelligence (AI), and Machine Learning (ML) for data processing...

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:-1 to 5 Years Skills :- HPLC | GC | Dissolution | IP/FP | Stability (OSD & Injectables) | USFDA | Regulatory approvals Division :- Formulation Interview Date:-20-09-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur | MSNF-IV, Mekaguda | MSNF-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Car...

Good knowledge of QC processes and GMP compliance. Skills: MS Office proficiency and strong communication skills. Responsible for quality testing, documentation, and ensuring product compliance with industry standards. Required Candidate profile Experience: 5-6 years in Pharma/API Education: B.Sc / M.Sc in Chemistry Must have hands-on experience with HPLC.

Designation : Junior Analyst / Analyst / Senior Analyst Department : Residue / N&W Location : Hyderabad Qualification : M.Sc. (Organic Chemistry/Chemistry/Analytical chemistry) Experience : 1 - 5 Years Industry : CRO & Testing Laboratory Roles and Responsibilities: Analysis of Pesticide residues of Food and Agriculture products as per SOPs, IS, AOAC, FSSAI. Method development, validation and report preparation. Operation and Calibration of equipment i.e., LC-MS/MS, GC-MS/MS, Analysis of Pesticide residues in Water samples. Analysis of Antibiotics in Aqua & Marine products, Feed, Milk & Milk products. Analysis of Pesticide Residues in Fruits and vegetables, Milk & Milk products, Feed & Feed P...

Review overall QC documents, Prepare training modules as required and provide training to QC staff, Approve COAs for water analysis from the microbiology dpt, Required Candidate profile Propose new Standard Operating Procedures (SOPs) and analytical instruments, HPLC/UHPLC/GC/UV/FTIR, and stability data, Approve new equipment qualification (DQ/IQ/OQ/PQ).

Job Summary We are seeking a highly skilled Analytical Scientist in to join our Research and Development team for Injectable Division for developing and validating analytical methods for injectable products, ensuring compliance with the regulatory requirements, conducting literature reviews, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. This role demands a strong understanding of analytical principles, excellent documentation skills, and the ability to work effectively in a collaborative team environment. scaling up for manufacturing of batches, coordinating manufacturing readiness, ov...

As a Quality Control (QC) Officer in the pharmaceutical (Formulation) industry located at Waghodia GIDC, Vadodara, your main responsibilities will include: - Performing quality checks on raw materials, in-process materials, and finished products. - Carrying out lab testing using instruments like HPLC, GC, UV, FTIR, etc. - Ensuring all work complies with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other regulatory requirements. - Identifying and reporting any issues like defects, deviations, or non-conformities. - Maintaining accurate records, including test reports and documentation. - Working closely with production and QA teams to address and resolve quality-re...

We are a reputed organization based at Ahmedabad and having business of sales and services of Milk testing instruments Pan India. Please visit our website https://www.Indifoss.com/ for more details. We are hiring for the position - Sr. Sales Executive/Sales Executive Deputed Location (from where candidate will operate): Kolkata Territory offered to Handle: EAST Region Experience Required: 2 5 Years Qualification: Any Science Graduate with instrument sales experience Prospecting leads and contacting them to pitch in Dairy & Cattle Feed Industries Setting up meetings with the prospective clients Presenting product/ service demonstrations to the client Participate in conferences, exhibitions, a...

- M.Sc / B. Pharm / M.Pharm - 03-05 years experience in pharmaceutical manufacturing machine maintenance 1. Sampling and Testing of raw material 2. Testing of Finished product & semi finished products 3. Knowledge of HPLC/ GC Empower software 4. Knowledge of Operation of instruments like Dissolution/ FTIR / HPLC / GC / Polarimeter 5. Knowledge about basic QMS in QC like Incidence / OOS etc.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials.

Key Responsibilities Develop and implement quality control systems: Creating procedures and policies to ensure products and services meet defined quality standards. Monitor and analyze quality data: Tracking data to identify trends, defects, and areas for improvement in quality processes. Manage quality teams: Supervising and advising quality assurance personnel and quality inspection teams. Ensure compliance: Making sure the organization adheres to relevant industry standards and regulatory requirements. Implement corrective and preventive actions: Identifying issues and implementing solutions, as well as proactively preventing potential errors. Lead continuous improvement: Driving initiati...