30 Icp Jobs - Page 2

Job Title : Chemist (Metal Mining) Location : KSA (Gulf) Experience : 3+ Years Work Schedule (Duty hrs) : 10 Hrs Job Overview : We are seeking a skilled Chemist to join our team in the metal mining industry. In this role, you will conduct chemical analyses and oversee quality control processes to ensure raw materials and finished products meet regulatory and internal standards. Your primary responsibilities will include performing laboratory tests, analyzing results, and supporting the overall quality assurance of our mining operations. Key Responsibilities : Conduct chemical tests and analyses on raw materials, in-process samples, and finished products to ensure compliance with industry standards and regulatory requirements. Operate, calibrate, and maintain laboratory equipment, including ICP-OES, AAS, titrators, and pH meters. Prepare and standardize chemical reagents, solutions, and test samples. Follow Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLP) to maintain quality assurance. Perform troubleshooting and routine maintenance of laboratory instruments; support method validation and instrument calibration processes. Apply specialized techniques such as Cyanide Leaching and Fire Assay methods in metallurgical analysis. Maintain detailed and accurate records of quality inspections, test results, and any deviations from standards Qualifications : Bachelors or Masters degree in Chemistry. Strong understanding of NABL ISO/IEC 17025 standards for laboratory quality and competence. Proficiency in MS Office and laboratory information management systems (LIMS).

Role & responsibilities Preferred candidate profile

We are seeking a skilled Analyst with hands-on experience in HPLC or GC or ICP techniques. The candidate should be well versed with Method Development, Method Validation and Method Transfer. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) If interested please share profiles on nilesh.kadam@geochem.net.in or any more information call on 9870476784

At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Performing analytical method validations and related documentation, as well as analysis of RM, PM, Intermediates, API, and Finished products. Key Responsibilities: Performing Chromatographic and Non-chromatographic analysis for Drug substances, Drug products, Intermediates, Excipients, etc ). Conduct the analysis on qualified techniques per the approved specification / protocol / procedures , interpret the data from analytical instruments, report the results, and promptly submit the completed documents for review within the established window. Recording of analytical observations/findings, reporting of data and results in observation data sheets, forms, logbooks, LIMS, and ELN application software, and support in preparing stability summary reports and review of final documents. Responsible for timely intimation/investigation of any events or deviations to the Department Head, QA function, supporting the related investigations to the clients, and timely closure. Instrument calibration as per schedule, hot water flushing of HPLC, and general preventive checks for laboratory instruments. Perform validation activities and method transfers for multiple client projects. Actively participate in client and regulatory audits. Ensure to follow cGMP and GDP. Preparing the certificate of analysis for standards and impurities and Reports for Analytical Method Validation and Analytical Method Transfer. Support in performing Qualification and Calibration of assigned Instruments and Equipment. Create/prepare documents, master data, and static data in LIMS, ELN, and LMS software as applicable. Outsourcing of sample testing is based on requirements and updating in respective logbooks. Coordination with engineering & maintenance and external vendors for preventive maintenance and calibration activity. Support in preparation of instruments URS, DQ, and IOP. Supported preparing standard operating procedures and uploading data in LIMS and other relevant activities per departmental requirements. Use of required safety PPE while sampling, analyzing, and working in the Laboratory. Individuals working in the GMP environment are responsible for documenting/recording the activities contemporaneously and accurately as per good documentation practices. Ensure safety compliance as per Syngene policy and EHSS requirements. Taking any other jobs by the Head QC/Group Leader/Designee. To ensure safety compliance as per Syngene policy and EHSS requirements. Educational Qualification: M Sc / M Pharma (Analytical/General chemistry) Technical/Functional Skills: Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA, etc... Being well-versed in the Chromeleon data management application and LIMS will be advantageous. Experience: 3- 6 years

Job Description: RESPONSIBILITIES. Timeliness and accuracy to meet turnaround time and that the daily test result is produced accurately and precisely. Information from the clients is kept as strictly confidential and never revealed to the third party Compliance to testing and environmental QA/QC procedures All analytical equipment, apparatus etc are to be appropriately maintained and calibrated as per the required schedule. Root-cause of all non-conformities or customer complaints are investigated and identified and appropriate corrective and preventive actions are taken. To go on client site for any environment analysis with required instruments. Responsible for effective implementation and maintenance of MS ISO/IEC 17025/14000 standards as well as Intertek group quality System & Adhering to Intertek Lab safety procedures Coach and ensure up-gradation of competency level in of the lab technician Train, supervise and monitor junior staff with assigned test methods and procedures To treat the Testing Program seriously and make sure the result obtained is most accurate and precise and as per environmental standards. To ensure all the standard methods used are up to date or the latest version. To ensure all controlled environmental quality procedures, test methods and document are kept confidentially and restricted within Intertek premise Ensure Good Housekeeping and Good Laboratory practice in the laboratory Expertise at : Minimum 1+ years of Experience in Crude oil/Liquid Hydrocarbon/ Produced Water/ Gas testing. Should possess good hands-on experience on modern analytical techniques like IC, UV-VIS, & IR spectrometer ICP for water & Oil & gas chromatography for gas analysis. Should possess through knowledge on calibration and maintenance of modern laboratory equipments. Should possess through knowledge on sampling procedure for oil & gas samples as per standard methods like ASTM IP etc. Should posses good communication skills for day-to-day activities. Should comply with HSE requirements of company while on duty. All the personnel requirements shall possess multi skills for the present operations and shall be ready carry out multidisciplinary tasks if required. Excellent condition of physical fitness. Should have proficiency in MS word, Excel, PPT and SAP etc. Managing inward and outgoing transmittals of documents. Candidate must be Full time Graduate in Chemistry from UGC. If Any Interested Candidate can Rech out to lavanya.m@intertek.com.