385 Gc Jobs - Page 9

Location: Onsite Type: Full-time Experience: 1- 3 years in US IT Bench Sales Job Summary: We are seeking a dynamic and results-driven Bench Sales Recruiter with experience in US IT staffing. The ideal candidate will be responsible for marketing our bench candidates (consultants) to staffing vendors, implementation partners, and direct clients across the United States. Key Responsibilities: Proactively market bench consultants (H1B, GC, OPT, CPT, and US Citizens) to vendors and clients. Maintain strong relationships with existing vendors and build new ones. Submit qualified resumes, coordinate interviews, and follow up with vendors/clients. Negotiate rates and close deals efficiently. Work closely with consultants during the marketing process and provide interview coaching and guidance. Maintain records of submissions, interview schedules, and placements. Monitor and ensure timely placement of candidates. Use job portals (Dice, Monster, CareerBuilder, Indeed) and social media (LinkedIn, etc.) for lead generation and networking. Requirements: Proven 13 years of experience in Bench Sales in US IT staffing. Strong knowledge of US Tax Terms (W2, 1099, C2C) and work visa classifications. Hands-on experience working with OPT, CPT, H1B, GC, and Citizens. Familiarity with marketing technologies: Job Portals, LinkedIn, email campaigns. Excellent communication and interpersonal skills. Ability to multitask, prioritize, and meet deadlines in a fast-paced environment.

Position: QC Executive Location: Derma Unit, Karakhadi Role & responsibilities Analysis of In-process, Intermediates, Raw material, Packing material, Finished products, Stability study, Hold time study, Process validation, Cleaning samples, Vendor development and any analysis allocated by team leader and release with proper documentation.. Responsible for ensuring the quality and purity of pharmaceutical products using High-Performance Liquid Chromatography (HPLC) techniques Prepare samples for HPLC analysis according to established SOPs and specifications. Analyze HPLC data, interpret results, and generate reports documenting test results and deviations. Ensuring analysis is performed compliance to GLP. Ensuring analysis raw data is documented on-line. Initiation, Completion and filing of Daily analysis reports. Ensuring any abnormal results, incidents, deviations, discrepancies are reported immediately to the reporting Section Head. Ensuring all relevant log entries are made for every activity wherever applicable. Supervise compliance to all cGMP, GxP or any other regulatory requirements including EHS requirements. Report any quality concerns or suggestions for improvements to Department Head. Execute and supervise all tasks and activities as per the applicable SOPs and company policy. To maintain the safety norms while working in lab. (e.g. Wear goggles, PPE, Disposal of sample/media as per procedure etc). Ensuring analysis is performed as per valid procedures and by using calibrated instruments / Standards. Ensuring self-discipline with respect to wearing aprons, attendance and personnel hygiene and inter relations. To perform Labware LIMS related activities. Any other assignment given by the Section Head or Department Head.

compliance with GMP and quality policie Approve RM/PM vendors and conduct regular quality audit validation, qualification, and batch release. GMP training $ support factory-wide implementation. Manage change control, deviation, and QMS execution.

Overall technical & operational activities of entire laboratories and coordination with the all Lab HODs related samples & test report reviewing and reporting results of performed analysis and timely deliver with accurate result and provide guidance to the customer if required and also negotiation with chemical & Instrument suppliers. Good Knowledge of latest instruments such as LCMSMS, HPLC, GC, GCMS, GC-HS, ICP-MS, ICP-OES etc. Coordination with QA team for implementing and maintaining the QMS as per ISO/IEC 17025:2017. Documentation for the upcoming audit for the bodies such as NABL, MoEF, CPCB, BIS, FDA, FSSAI, GLP, Ministry of Ayush, CDSCO etc. And proper closure of client complaint & NCs. Maintain TAT with accuracy as per quality system as well as client requirement. Conducting internal audits and provides training to the laboratory staff and Participation in regulatory meetings. Business development activities for testing samples of food and agriculture, pharmaceuticals, environmental parameters and footwear products. Build and maintain relationships with customers and Schedule regular follow-ups. and check-ins to ensure client satisfaction and identify new opportunities.

Job summary We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performing the PM. To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP. To attend the breakdown's and close notification or order of the instrument /equipment after the Completion of breakdown maintenance. To be a part of investigating the incidence related to instrument Responsible for the maintaining of required spares for all instruments in warehouse. To get the quotations for the required spares and services for the maintenance of the instruments. To generate the purchase requisitions for the required spares and services. To perform the PM in the given frequency within the given period. Adhering to the allotted shift schedule with right time. If any changes prior permission shall be taken from Group leader. Qualification Educational qualification: An B.Tech. or any Degree in Instrumentation, Mechanical, Electronics, Electrical. Required Work experience : 3 to 6 years Skills & attributes: Technical Skills • Hands-on Experience on maintenance of Waters HPLC (Arc, e2695), Agilent HPLC (1200, 1260 Infinity), Agilent GC-HSS (7890, 8890, 7897, G1888), Dissolution Testers (Electrolab, Sotax), Metrohm Titrators. • Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). • Basic knowledge in SAP usage Behavioural skills • Prioritizes effective communication and demonstrates a performance-oriented mind-set. • Effective verbal and written communication skills. • Performance-oriented approach, consistently striving for high standards. • Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Quality Control Formulations For more details, please visit our career website at https://careers.drreddys.com/#!/

Role & responsibilities Handling of Analytical Instruments like HPLC, Gas Chromatography, Dissolution, UV, pH and conductivity meter, Analytical Balances, etc. along with software. Analytical method development by HPLC & GC (Liquid Oral Dosage forms) Knowledge about ICH guidelines for Analytical method development and Validation by HPLC& GC. Calibration of HPLC, GC, Dissolution test apparatus, pH meter, KF Potentiometry and Balances. Analysis of Regular and stability samples. Preparation and Review of STP, Protocols and Analytical Reports. Following inhouse systems and Procedure to ensure the cGMP practices and regulatory requirements (US market) Preferred candidate profile Analytical method development using HPLC and GC for Liquid Orals , Topicals, Semi solids (US market). Experience in Nasal sprays will be added advantage. Analytical method development, routine and stability analysis using HPLC/GC instruments. Interested candidates may send CV to karthik.bonam@zolon.com

Role & responsibilities Handling of Analytical Instruments like HPLC, Gas Chromatography, Dissolution, UV, pH and conductivity meter, Analytical Balances, etc. along with software. Analytical method development by HPLC & GC (Liquid Oral Dosage forms) Knowledge about ICH guidelines for Analytical method development and Validation by HPLC& GC. Calibration of HPLC, GC, Dissolution test apparatus, pH meter, KF Potentiometry and Balances. Analysis of Regular and stability samples. Preparation and Review of STP, Protocols and Analytical Reports. Following inhouse systems and Procedure to ensure the cGMP practices and regulatory requirements (US market) Preferred candidate profile Analytical method development using HPLC and GC for Liquid Orals , Topicals, Semi solids (US market). Experience in Nasal sprays will be added advantage. Analytical method development, routine and stability analysis using HPLC/GC instruments. Interested candidates may send CV to karthik.bonam@zolon.com

Role & responsibilities 1. Planning and analysis of Related substances, Dissolution and Assay by HPLC & UV. 2. Planning and analysis of Residual solvents and purity by GC. 3. Operation and calibration of HPLC, Dissolution, GC, pH meter, analytical balance & UV systems as per SOP. 4. Review the all analytical data. 5. Integration and Review of chromatograms, spectrums, analytical data and analytical reports of stability samples, Raw material, Finished and In-process samples. 6. Fill and verify the Equipment and column log books. 7. Execute documents review and close monitoring. 8. Verify the Equipment calibrations and update as per schedule. 9. Verification of glassware cleaning before use. 10. Analysis of Method Verification, Method Validation and Method Transfers by HPLC, UV, Dissolution and GC with documentation. 11. To update inventory record for chemicals, reagents, and solvents and indent as per requirement. 12. Verification of integrity of the chromatograms and calculations in raw data sheets compare with SP&TP. 13. Verify the column performance and maintenance. 14. Prepare and paste the tags with relevant details (on Mobile phase bottles, instruments, reagents, Test solutions and chemicals). 15. Handover the documents to in-charge after completion of his/her shift duties. 16. Room temperature record maintenance. 17. Maintain the external service reports instrument wise. 18. To update the usage record of working standards & Reference standards. 19. Inform immediately to In-charge whenever any abnormality is found. 20. Handover the work to the next shift person after completion of shift activity. 21. In the absence of his superior, shall be responsible for his activities. 22. Maintain the GLP, GSP in the work area. 23. If any instrument / equipment breakdown maintain the document recording and follow as per SOP. 24. Perform the analysis of vendor samples, working standard evaluation and stability samples. 25. Raise the OOS, OOT, Incidents, Deviations and support to investigation. 26. Raise the change control whenever required and Reporting to Instrumentation In-charge. 27. SP&TPS preparation and SOPS Preparations.

Roles and Responsibilities Conduct quality control testing of OSD products using HPLC, GC, and other relevant instruments. Ensure compliance with GLP guidelines and maintain accurate records in LIMS system. Review batch manufacturing records (BMRs) and perform audits as required. Implement QMS procedures to ensure product quality and regulatory compliance. Collaborate with cross-functional teams to resolve quality issues.

Interview 7th April for Pharma Companies for BSc Chemistry - Freshers - Company, Dahej Contact Urvi Madam on 9712914207 & Visit Our Office Share with yr friends Golden opportunity to Start career for Fresher Candidates.

Key Responsibilities: Analytical Testing: Conduct routine and non-routine testing of raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis Spectroscopy, FTIR, and microbiological methods. Documentation: Prepare, review, and maintain accurate laboratory records, test reports, and validation documentation in compliance with Good Laboratory Practices (GLP) and regulatory requirements. Quality Assurance: Collaborate with Quality Assurance (QA) to ensure compliance with cGMP (current Good Manufacturing Practices) and regulatory guidelines (FDA, EMA, etc.). Equipment Calibration: Perform calibration, maintenance, and troubleshooting of laboratory equipment. Deviation Management: Investigate deviations, out-of-specification (OOS) results, and implement corrective and preventive actions (CAPA). Method Validation: Assist in the validation and transfer of analytical methods to ensure accuracy, precision, and reproducibility Contact : Kanagavel M | +91 8072654123.

We're hiring a Chemist and Formulator with 4+ years of experience in pesticides. Proficiency in HPLC, GC, and lab equipment is required. Responsibilities: * Formulate pesticides. * Operate HPLC, GC, and other lab equipment.

Job description Job Title: OPT Recruiter Experience: 3 TO 6+ years Job Responsibilities: Source and recruit candidates from OPT, Green Card holders, H1s, H1 transfers, and US citizens for positions across various domains. Build and maintain a strong pipeline of qualified candidates for both contract and full-time roles. Engage with candidates for screening, interviewing, and evaluation. Work closely with account managers and clients to understand job requirements and present suitable candidates. Maintain detailed candidate databases and reports on recruiting activities. Ensure compliance with US immigration laws and client specifications during the recruitment process. Skills and Qualifications: Proven experience in US IT recruiting, with a focus on sourcing candidates for OPT, GC, H1s, and H1 transfers. Strong understanding of the US staffing process and legal employment regulations. Ability to handle high-volume recruiting while delivering quality candidates. Excellent communication, negotiation, and interpersonal skills.

Roles and Responsibilities: 1 . Analysis of In-process, Intermediates, Raw material, Packing material, Finished products, Stability study, Hold time study, Process validation, Cleaning samples, Vendor development and any analysis allocated by team leader and release with proper documentation.. 2. Ensuring analysis is performed compliance to GLP. 3. Ensuring analysis raw data is documented on-line. 4. Initiation, Completion and filing of Daily analysis reports. 5. Ensuring any abnormal results, incidents, deviations, discrepancies are reported immediately to the reporting Section Head. 6. Ensuring all relevant log entries are made for every activity wherever applicable. 7. Supervise compliance to all cGMP, GxP or any other regulatory requirements including EHS requirements. 8. Report any quality concerns or suggestions for improvements to Department Head. 9. Execute and supervise all tasks and activities as per the applicable SOPs and company policy. 10. To maintain the safety norms while working in lab. (e.g. Wear goggles, PPE, Disposal of sample/media as per procedure etc). 11. Ensuring analysis is performed as per valid procedures and by using calibrated instruments / Standards. 12. Ensuring self-discipline with respect to wearing aprons, attendance and personnel hygiene and inter relations. 13. To perform Labware LIMS related activities. 14. Any other assignment given by the Section Head or Department Head.

Hands on skill and Knowledge of LCMS, HPLC, UHPLC, GC, GCMS, Wet chemical Understanding of analytical chemistry, discussion with synthesis, plant, PE laboratory analysis of samples in time., Ensure that laboratory work is carried out in a safe manner Required Candidate profile Analytical Research & analytical method development for organic molecules. Method validation. Method transfer. Stability studies. GLP. GDP, Building Problem Solving, Customer Centricity, Analysis

Walk-In Drive For API Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Saturday 05-04-2025. Requirement for Executive / Senior Executive - API AR&D - API Analytical Research & Development(AR&D) HPLC,LCMS,GC,GCMS,GCHS High performance liquid chromatography HPLC,LCMS,GCMS HPLC with Software lab solu. UV-VIS Spectrometer GC with Software lab solution PH-Meter Moisture Analyser Karl Fischer titrator Micro- Weighter Balance Responsible for an Analytical team involved in Method development, Method Transfer and Validation for various stages of drug development. Method Validation of analytical methods as per internal and country specific regulatory guidelines and execution through proper protocols. Compliance of Good Laboratory Practice in the lab Responsible for providing support to technical issues related to R&D to file the Drug Master files. Effective method development ensures that laboratory resources are optimized, while methods meet the objectives required at each stage of drug development. Responsible for ensuring delivery time-lines and adherence to quality and standards and customer Relationship management. Facilitating scientific and technical discussions with team members and external collaborators to resolve issues and communicating conclusions from stability studies. Interview Date : Saturday 05-04-2025 Department : Analytical Research & Development(API AR&D) HPLC AND GC Experience : 2 to 8 Years Qualification : M.Sc Position: Executive / Senior Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details :Venue Details : MSN Laboratories Pvt. Ltd, R&D Centre, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana Saturday 05-04-2025

Interview For QA & QC on 08-04-2025 For API Pharma Company in Jhagadia & Baroda Location Qualification : Bsc / Msc Chemistry/ B.pharma/M.Pharma Experience : 1 to 5 Year CTC : Up to 5.0 LPA Required Candidate profile Send CV on sdpbharuch@gmail.com with Subject: QA QC MNC & call on 7600033423 knowledge of GC & HPLC Instrument Share with Your Friends & Colleagues Free Jobs Placement

We are seeking a driven and dynamic Account Manager (Bench Sales) to join our expanding team in Hyderabad, Pune, Bhopal, Noida . In this role, you will play a pivotal role in our sales efforts, focusing on identifying and engaging with qualified IT consultants who are currently on the bench. Job Details: Position: Account Manager - Bench Sales Mode: Work from Office_Hyderabad, Pune, Bhopal, Noida Office hours: 7:00 pm 4:00 am (IST) Location: Hyderabad, Pune, Bhopal, Noida(Onsite) Responsibilities: Utilize various sourcing techniques to identify suitable requirements to place IT consultants. Build and maintain strong relationships with consultants, understanding their skills, preferences, and career aspirations. Actively promote consultants to our client base, showcasing their expertise and suitability for available positions. Negotiate contract terms, rates, and other aspects of the placement process with both consultants and clients. Collaborate closely with recruiters and account managers to facilitate smooth transitions for consultants into new roles. Must have experience working with Tier 1 vendors, Implementation partners, MSP, and VMS clients Build upon existing business and obtain referrals Provide ongoing support and guidance to consultants throughout the placement process, addressing any concerns or issues that may arise. Stay abreast of industry trends, market developments, and competitive landscape to inform sales strategies and tactics. Must have basic knowledge on the H1b visa transfer process and US immigration law Qualifications: Bachelor's degree in Business Administration, Marketing, or a related field (preferred). Proven track record of success in sales, with a focus on the IT staffing industry. Solid understanding of IT roles, technologies, and industry trends. Excellent communication skills, both verbal and written, with the ability to effectively engage with consultants and clients. Strong negotiation skills, with the ability to secure favorable terms and agreements. Important Link: Kindly make sure to go through the company link, and URL for a detailed understanding of the organization - www.compunnel.com To proceed, kindly share your updated CV via email at tarun.oommen@compunnel.com or WhatsApp at 8233937578

Job Title: Bench Sales Recruiter Exp : Freshers and 1 - 5 years Experience In Bench Sale's.. Qualification: Graduation (Any Graduate) Interview Timings: 7:00pm to 10pm * Location : Somajiguda Hyderabad (Onsite only - No WFH) * Shift Timings: 6:30 pm to 3:30 am IST We are Looking for an aggressive Bench Sales Recruiter with good communication skills and 1-5 years exp. It should be well versed in the US IT Recruitment process & provide staffing needs based on the client requirements. Experience in the US IT Staffing market. Connect with candidates, discuss in detail about the profile, and start marketing. Roles & Responsibilities: Involved in marketing profiles of H1B, OPT, CPT, TN, GC, USC. Responsibility for marketing IT Bench Consultants (H1B, US Citizen, TN, GC, OPT and CPT) with prime vendors or Direct Client Conducting initial candidate screenings and interviews Negotiating pay rates and terms of employment with candidates Building and maintaining a network of potential consultants Collaborating with internal teams to meet client staffing needs Providing regular updates to candidates on the status of their applications Requirements and Skills: Proven experience as a Bench Sales Recruiter or similar role Must be well versed with US Tax terms like W2, Corp2Corp & 1099, etc. Strong negotiation and communication skills Strong hands-on knowledge in marketing H1B and H1B transfers Knowledge of IT industry trends and technologies Attention to detail and the ability to work in a fast-paced environment Contact Person: Sai Narasa Reddy(HR) Contact Number: 7036191310 Email id: hrindia@cloudninetek.com

Ensure quality standards compliance, test RM,IP,FP, stability & WS qualification. Calibrate instruments, validate methods, prepare specifications. Expertise in HPLC, GC. Handle GLP, OOS, deviation, CAPA & ensure audit compliance.

Roles and Responsibilities Conduct analytical testing using various instruments such as GC, HPLC, XRD, LIMS, Empower3, and other relevant equipment. Develop and validate new methods for biochemistry tests to ensure accuracy and reliability. Collaborate with cross-functional teams to resolve issues related to test results or instrument malfunctions. Maintain accurate records of test data, instrument calibration, and maintenance schedules. Participate in continuous improvement initiatives to optimize laboratory processes. Desired Candidate Profile 2-7 years of experience in a similar role within the pharmaceutical industry. MSC or B. pharm or M pharm Strong understanding of biochemistry principles and techniques including chromatography (HPLC), spectroscopy (GC), microscopy (XRD), mass spectrometry (LIMS). Proficiency with analytical instruments such as LIMS software for data management. API Experience will not be considered

Role & responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Preferred candidate profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Division :- Formulation Interview Date:- 05-04-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 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 Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Skills Customer Management Sales customer service Micro Banking Description Assistant Branch Manager will assist the Branch Manager in providing leadership to the bank through efficient daily operations in all areas of banking service Schedules and supervises customer service representatives, head teller, tellers, safety deposit clerk, and financial service managers in daily tasks and operations, Conducts performance evaluations that are timely and constructive, Assists manager in efforts to reach profit, performance, and customer service goals, Oversees banking services, especially customer service, to ensure excellence; contacts or assists customers and prospective customers Reviews and manages staffing procedures, ensuring that staff assignments and responsibilities are reasonable, and that salary structure is equitable, Performs other related duties as assigned.

Walk-In Drive - API- Quality Walk-in Interviews for API - Quality Roles based out of Kurkumbh (Job location) on 06 & 07 April, '2025 (Sunday& Monday), from 1000hrs. to 1600 hrs. at Kurkumbh, Maharashtra We have the below openings: API - Quality Control : M.Sc. (Analytical / Organic Chemistry) with 2-5 years experience with Expertise in handling RM, intermediates & Finished products in API manufacturing. Handling HPLC, GC, LCMS, ICPMS. Knowledge of Particle Size Analyzer/LCMS /GCMS preferred API - Quality Assurance: M.Sc. (Organic Chemistry) BE/B Tech (Chemical Engineering) with 2-5 years of experience with Must have experience only in API. Experience in API Inprocess QA, API line clearance , QMS, APQR, Process & Cleaning validations will be desirable. Experience of API production as well as QA will be preferred.