1437 Gc Jobs - Page 18

About The Role : Job Title Transactional FX Specialist Corporate TitleAssociate LocationMumbai, India Role Description Transactional FX is a high-profile joint venture between the Corporate Bank (CB) and Investment Bank (IB). Transactional FX team is responsible for delivering one of the fastest growing revenue streams in CB & IB by providing market leading FX workflow solutions to clients. Transactional FX leverages the firms position as a market leader in CB and offers variety of standard and bespoke FX solutions to solve for clients FX workflow needs. What well offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy, Best in class leave policy. Gender...

Responsible for managing hospital pharmacy operations including medicine dispensing, inventory control, regulatory compliance, and staff supervision. Ensures patient safety through accurate drug handling and counseling. Key Responsibilities: Oversee daily pharmacy operations and prescription validation. Manage stock, procurement, expiry control, and vendor coordination. Ensure compliance with NABH/Drug Control guidelines and maintain records. Supervise, train, and schedule pharmacy staff. Provide patient counseling on medication use and side effects. Monitor billing, control wastage, and support audits. Preferred candidate profile Strong knowledge of drugs, dosage, and interactions. Inventor...

EXPRIENCE: 14 - 20 Years EDUCATIONS: M.SC/B.SC/B.PHARMA DESIGNATIONS: DGM-QC PREFRIED PROFILES: Having a minimum of 5 years experience in a USFDA-approved plant as a QC Team Lead." JOB RESPONSIBILITIES: 1. OVERALL TO PLAN & CONTROL QC AND QC MICRO SHOP FLOOR OPERATION ACTIVITIES IN SYSTEMATIC WAYS & IN TIMELY MANNER TO ASCERTAIN AND ALIGN PRODUCTION SAMPLES GET ANALYSED TO SUBMIT REPORTS. 2. TO WORK COHESIVELY WITH CROSS FUNCTION TEAM TO ACHIEVE COMMON GOAL OF ORGANIZATION. 3. ALL TIME READINESS IN COMPLAINT MODE FOR AUDIT ACROSS QC AREAS. 4. TO ATTEND MANAGEMENT REVIEW MEETINGS WITH COMPLETE PROGRESS OF QC STATUS. 5. TO MAINTAIN DATA INTEGRITY IN THE LAB. 6. TO PROVIDE SAFE WORK ENVIRONMENT...

Job Purpose and Impact The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver im...

i. Experienced in independent instrumental analysis of raw material, in process samples, finished product and stability samples of pharmaceutical products. ii. Well versed in analysis of Tablets, capsules, liquids samples, for common test as Assay, Related substances, Dissolution and preservative content analysis as per controlled specification and method of analysis. iii. Should able to operate, calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR etc. iv. Experience of Empower, Lab solution software shall be recommended. v. Exposure to perform AMV or development shall be preferred. vi. Aware about on line & good documentation practices. vii. Should have know...

Analysis of samples by using HPLC (Open Lab Solutions).Wet Analysis by using IR, UV, pH, etc.Quality Control Documentation. Responsibilities: Conducting Laboratory Experiments: Plan and execute a variety of chemical experiments, including synthesis, analysis, and characterization. Operate and maintain laboratory equipment such as spectrophotometers, chromatographs, and titrators. Collect and record experimental data accurately and meticulously. Data Analysis and Interpretation: Analyze experimental data using statistical and other relevant methods. Interpret results, draw conclusions, and prepare technical reports and presentations. Identify and troubleshoot problems encountered during exper...

Hands-on experience in - Perform the Analytical Method Validation by HPLC/GC Preparation and review of AMV Protocol and Reports Operations and calibration of the instruments like HPLC, GC etc. Preferred candidate - Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV

Job Description : Hands-on experience in -Perform the Analytical Method Validation by HPLC/GC Preparation and review of AMV Protocol and Reports operations and calibration of the instruments like HPLC, GC etc. Preferred candidate -Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV. Organisational Entity Zuventus Healthcare Ltd. Vertical ZHL Sikkim Factory Department Quality Control Continent Asia Country India Zone East Location Type S01-ZHL Factory

Perform chemical analysis using instruments like GC, HPLC, GCMS, and KF Titrator Troubleshoot and calibrate laboratory equipment as per standard protocols Maintain and update documentation in compliance with NABL and ISO standards Ensure adherence to Good Laboratory Practices (GLP) Prepare and standardize reagents and solutions used for analysis Maintain accurate records of test results and equipment calibration Conduct stability and quality tests on raw materials and finished products Coordinate with cross-functional teams to ensure product quality Assist in internal and external audits as required

As an ARD Chemist / Scientist at the Udaipur location, you will be a key member of the ARD team, responsible for method development and validation, impurity profiling, and instrumental analysis to support Synthesis R&D and quality operations. - Developing and validating HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples. - Developing HPLC methods suitable for Analytical Method Validation (AMV) and transfer to QC. - Performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry. - Ensuring that all analytical instruments are maintained in optimal working condition through regula...

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...

Job Description Core Responsibilities - Defines the day to day duties of this role 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. May be client or product oriented. Contributes to sales account planning. Participates actively in the sales process from deal qualification to deal closure. Owns the deals technical closure. Responsible for meeting sales targets and for supporting sales organizations to meet targets. Is knowledgeable of competition and able to identify lockout specifications (identify Agilent&aposs competitive adv...

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.

Urgent Hiring QC Executive (OSD / Formulations) | Immediate Joiners / 1 Month NP Preferred Location: Karkapatla, Hyderabad Industry: Pharmaceuticals (Tablets & Capsules OSD) Shift & Timings: Day Shift | 6 Days Working | only MALES Role Overview: We are looking for a QC Executive with hands-on experience in OSD/Formulations (Tablets & Capsules). The role involves ensuring quality compliance in production processes and maintaining strict adherence to industry standards. Key Responsibilities: Conduct quality control tests for OSD formulations (tablets & capsules). Review and analyze in-process and finished product samples. Ensure compliance with regulatory standards and SOPs. Maintain accurate ...

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...

Role & responsibilities Sampling and analysis of Raw Materials, In-process samples, Finished Products , and Stability samples as per SOP and test methods. Preparation and standardization of volumetric solutions, reagents , and reference standards . Performing routine chemical, instrumental (HPLC, GC, UV, FTIR), and microbiological testing (for applicable roles). Equipment/instrument calibration and maintenance logs. Participation in method validation , stability studies, and process validation activities. Adherence to Good Laboratory Practices (GLP) and regulatory standards. Supporting internal and external regulatory audits (like USFDA, WHO-GMP). Reporting deviations, OOS results, and non-c...

Position Summary: Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activities in a saf...

A QC Officer performs visual inspections, tests, and measurements on raw materials, in-process products, and finished goods. This is done to identify any defects or deviations from the quality standards and specifications. Required Candidate profile Previous experience in a quality control, quality assurance, or manufacturing environment is highly valued. A strong understanding of quality control principles, testing methods

Field Service Engineer We are seeking a highly skilled and experienced Field Service Engineer to join our team on a contract basis. This role requires a minimum of 0 years and a maximum of 3 years of experience in the Pharma/Healthcare/Lifesciences industry, providing on-site technical support and maintenance in Bangalore, karnataka ,India.Tasks Provide on-site technical support and maintenance for gas chromatography and liquid chromatography equipment. Troubleshoot and resolve equipment malfunctions. Perform preventative maintenance and calibration procedures. Maintain accurate records of service activities and equipment performance. Collaborate with internal teams to ensure timely resoluti...

GC, HPLC, UV, Malvern, LCMS | SOPs, MSDS, COA | 5S, NABL, GLP, IMS | Reports | Impurity Profiling Inventory, AMC, CMC & LIMS management. Monthly/Yearly report preparation. Audit exposure

Maintain H1B petitions including annual H-1B CAP, extensions of current visas and transfer petitions for new employees. Prepare in-house documents and petitions for other visas including but not limited to F-1, L1, and dependent visas (H4, L2 etc). Have ability to lead immigration process from start to finish, working with non-immigrant & immigrant Visa applications and processes (H1-B, H-4, L-1, TN, and EB non-immigrant petitions, RFE, etc.), EAD renewals of employees and dependents. Maintain Public Access Files ensuring compliance, documentation and execution of immigration policies and procedures. Experience of handling FDNS site visits, PAF, DOL audits. Consultation: Assessing employees ...

QC Officer with strong expertise in HPLC, GC, UV-Vis, Karl Fischer, SAP, COA, Calibration, SOP preparation, and QMS compliance. Candidates with experience in pharma/chemical QC operations and knowledge of GMP, GLP, ICH & ISO/IEC 17025:2017 Required Candidate profile Skills: HPLC, GC, UV-Vis, Karl Fischer, SAP, COA, Calibration, SOP, QMS Preferred Industry: Chemical / Pharma API

Job Title: Bench Sales Recruiter (0-1 Year Experience) Job Type: Full-time Location: [Sri Devi Complex, 2nd Floor, Y.V.R Street, 56-11-13A, MG Rd, near Sweet Magic, Vijayawada, Andhra Pradesh 520010, Onsite] Job Description: We are looking for an enthusiastic and motivated Bench Sales Recruiter (Entry Level) to join our US Staffing team. This role is ideal for freshers or candidates with up to 1 year of experience who are eager to build a career in US IT Recruitment and Bench Sales. The recruiter will be responsible for marketing our bench consultants, identifying job opportunities, and coordinating with vendors and clients. Key Responsibilities: Market and place bench consultants (OPT, CPT,...

As a Quality Control Officer at FMC, your primary responsibility will be to ensure that all products meet the laydown quality specification. This will involve conducting tests, analyzing results, and documenting quality data. You will work closely with production teams to identify issues and implement corrective actions to ensure compliance with company and regulatory standards. Key Responsibilities: - Hands-on experience of handling HPLC, GC, and other instruments and troubleshooting any issues that may arise. - Strong analytical and problem-solving skills to effectively assess and inspect incoming raw materials, in-process items, and finished products as per specifications. - Perform regul...