237 Instrument Calibration Jobs

Date: 2 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Dedicated Centre Job Description Designation: Research Associate (9-I) or Senior Research Associate (9-II) Job Location: Bangalore Department: BBRC PD ARD GMP About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngenes clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240- a strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation. Job Purpose (1-2 Lines): Analytical Research and Development working on Analytical GMP testing (AGT), and Syngene BMS Laboratory (SBL) stability programs Key Responsibilities Testing of samples (drug substance and drug product for release testing and stability) using chromatographic, dissolution, and wet analytical techniques under a GMP environment following cGMP practices Analysis of API clinical campaign samples manufactured in Syngene pilot plant Qualification or requalification of API reference standards. Performing instrument calibration and qualification Performing method validation, and method transfers Troubleshooting HPLC, dissolution apparatus and other analytical instruments in the lab Deliver analytical results within the established windows and as per applicable guidelines Compliance & implementation of quality systems Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety Electronic lab notebook documentation Miscellaneous lab responsibilities Educational Qualifications: M.Sc. Chemistry for 9-I; M.Sc. Chemistry or M. Pharm for 9-II; Technical/Functional Skills The candidate should have a good educational and theoretical, analytical chemistry background Good knowledge of analytical techniques The candidate should understand instrument calibration, qualification, method validation, and analytical testing Good understanding of documentation as per GxP requirements (electronic notebook) The candidate should have good proficiency in MS office tools Experience in stability samples testing and good knowledge of ICH guidelines & cGMP regulatory requirements Must have worked in a cGMP-regulated environment, exposure to regulatory inspections like US FDA, MHRA, etc. is preferred. Experience: 1-2 years with M.Sc. for 9-I ; 3-5 years with M.Sc. or 1-2 years with M. Pharm for 9-II Behavioral Skills Strong commitment toward work and a high level of dedication, enthusiasm, and motivation Good speaking-listening-writing skills, attention to detail, proactive self-starter Ability to work successfully in a dynamic environment Should be able to work in a team and flexible for working in shifts. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Show more Show less

Job Description: As an Instrumentation Designer, you will be responsible for handling various tasks related to control systems design, instrument calibration, data acquisition, and instrument datasheets. Your role will involve activities such as print review, cable schedule, cable drum schedule, bulk MTO, wiring diagrams, interconnection schedule, cable block diagram, IO database management, and installation details. It is important to note that 3D modeling or 2D drafting skills are not required for this position. The ideal candidate should have a minimum of 3 to 10 years of experience in the Oil and Gas or Chemical Industry. A qualification of BE/Diploma in Instrument Engineering is required for this role. The duration of the project is expected to be six months to one year with a possibility of extension based on project requirements. Key Responsibilities: - Prepare, maintain, and update instrument datasheets in the specified formats. - Review and provide feedback on post-order vendor documents to ensure compliance with project specifications. - Participate in meetings with vendors to address comments and obtain document approval. - Perform instrument installation engineering activities including junction box grouping, cable scheduling, and bulk MTO. - Update the instrument database with information from various engineering documents such as P&ID, GAD, wiring diagrams, and cause & effect diagrams. This position is based in Vadodara, Mumbai, Bangalore, or Chennai with a preference for early joiners. If you meet the qualifications and are interested in this opportunity, please send your updated resume to petroengineeringconsultant@gmail.com. In the email subject, kindly mention "Instrument Engineer for Vadodara/Mumbai/Bangalore/Chennai" followed by your preferred location.,

The responsibilities for this role include reviewing raw and finished product specifications, ensuring good laboratory practices in the Quality Control department, reviewing audit trial records, analyzing analytical records, reviewing instrument calibration and equipment qualification documents related to QC, validating analytical methods, verifying samples, handling reserve sample room, ensuring analyst qualification, reviewing working standards, managing deviations, change control, OOT, OOS, laboratory incidents, investigations, and annual trends, coordinating CAPA implementation verification and closure, reviewing instrument and equipment preventive maintenance, monitoring and recording temperature and humidity in the laboratory area, and managing document control. The ideal candidate should possess skills in audit trial, OOT, deviation handling, OOS, backup and restoration data management, sample handling, instrument maintenance, quality assurance, instrument calibration, laboratory practice, laboratory incidents management, change control, method edit forms, working standards review, analytical records analysis, quality control, document management, equipment qualification, stability protocols, analyst qualification, analytical method validation, CAPA implementation, and temperature monitoring.,

Responsibilities: * Ensure compliance with ISO 9001 standards through electrical panel inspections, wiring inspections, instrument calibration, and non-conformance reporting.

Responsibilities: * Ensure compliance with NABL standards during calibrations * Maintain accurate records of instrument data and reports * Collaborate with cross-functional teams on equipment maintenance schedules Health insurance Annual bonus Provident fund

Field Calibration Engineer Must travel 80 to 90 kms up and down daily Must have bike will provide bike and petrol allowance ECE, EEE, Physics

Division Manufacturing Department Active Pharmaceutical Ingredient Sub Department 1 Engineering - API Job Purpose The incumbent is a team member of Unit Engineering Maintenance & Reliability Team and carries overall responsibility to: 1.Execute the maintenance activities in the plant & ensure the minimum Instrumentation & Automation breakdown with maximum efficiency by following safety & GMP Standards 2.Support EM & R Senior Instrumentation Engineer in carrying out Functional EM&R Planning, Detailed Scheduling and Execution of CMP to- ensure continuity of availability of plant & equipment at optimal cost; achieve standard capacity; ensure overall plant & equipment integrity & reliability - in compliance with Cipla Policies, Standards & Procedures; Reporting of EM&R MIS, Incidents & Deviations @ SOP; Instrumentation Engineer is responsible for executing maintenance tasks as assigned by Senior Engineer for his function in the Manufacturing & Packing Area. Where outsourced, 3rd Party Instrumentation Engineer is accountable for the Service Floor / Technical Floor maintenance execution Key Accountabilities (1/6) I. Shift Maintenance Activity: Execute maintenance activities in a shift by managing available resources to achieve shift maintenance plan. ¢ Execute assigned tasks as per planned Instrumentation & Automation maintenance activity to meet maintenance targets for a shift ¢ Cater to machine maintenance requirements of Unit as a responsible member of the team with overall ownership of Unit Operations. ¢ Increase the efficiency of area by ensuring better utilization of equipment and by reducing downtime in manufacturing area ¢ Prepare and submit Instrumentation shift engineer report to ensure smooth shift handover II. Comprehensive Maintenance Plan Execution: Give inputs for preparing & adhere to unique planner for planned preventive maintenance & instrument calibrations for effective maintenance and adherence to standards. ¢ Schedule shift activities in line with the CMP including PM, Calibration, and condition monitoring activities. ¢ Execute planned Instrumentation & Automation maintenance and update related documentation o Preventive Maintenance o Calibration o Condition Monitoring o Planned Corrective Actions ¢ Follow good Engineering practices during planned preventive activity. ¢ Perform validation, qualification and calibration as per schedule and update output of all activities in the systems ¢ Prepare new documents and update existing documents as per GMP requirement ¢ Update Metrics on Schedule compliance III. Breakdown Maintenance: Handle breakdown maintenance to avoid recurrence and maintain continuous process operations ¢ Execute Instrumentation & Automation breakdown work expeditiously but safely and in compliance with cGMP. ¢ Receipt and tracking the job card for the break down activity ¢ Maintain critical Instrumentation & Automation spares inventory of all machines to reduce resolution time Key Accountabilities (2/6) IV. Efficient Equipment Operation: Operate the equipment efficiently without error and deviation as per SOP to meet shift targets ¢ Operate an equipment only when trained and authorized to do it. ¢ Perform unit operations as per SOP & unit processes as per work instructions ¢ Maintain equipment, facility and block premises as per SOP for audit readiness. Ensure equipment, facility and block premises are maintained as per regulatory compliance ¢ Ensure all operations are performed as per GMP & Safety norms by reviewing all processes and documents for compliance ¢ Maintain system integrity by updating documentations and deviations on CipDox while performing operations V. New Technology / Capex: Use new technologies initiated by Management while adhering to CAPEX and OPEX targets to improve Machine/system performance ¢ Implement new technologies in the plant initiated by management ¢ Attend planned trainings and incorporate the learnings on the floor for improving machine performance ¢ Implement and close ideas generated through internal audits / Idea generation sessions ¢ Monitor present energy use of the plants to identify and report areas for energy conservation ¢ Implement Energy Conservation activities to improve the equipment efficiency, reduce error and reduce production cost ¢ Identify areas of improvement in instrumentation functoin for waste & work simplification ¢ Manage activities to operate within budget and to reduce operating expenses ¢ Verification of the contract invoices and making of the job orders as per estimates VI. Spares Management: Perform Material and Spare management and issue Consumables, spares, materials, log books etc. to avoid delays due to unavailability of materials ¢ Issue required Instrumentation & Automation materials (spares and consumables) to the contractors from stores and make SAP entries for the receipts and issuance ¢ Maintain the inventory of critical spares and consumables by tracking consumption and monitoring of stocks ¢ Assess log book requirements, raise the request to QA and issue them within required timelines ¢ Classify the unused / spare / usable scrap materials or components and reuse the same where ever possible Key Accountabilities (3/6) VII. EHS Compliance: maintain high level of Safety during maintenance to avoid major breakdown and report accidents/ incidences ¢ Complete preplacement Safety Training before starting the work in any area. ¢ Monitor safe operations of the machine as per SOP and timely report any safety deviations ¢ Maintain proper procedures for safety permits in plant Ensure safety systems and procedures followed by the operators in the shift ¢ Issue work permits to contractual staff after verifying the safety aspects, monitoring and communicating safety hazards and safety near miss to the concern. ¢ Ensure availability and usage of PPEs in the shift by coordinating with EHS department for requirements and shift schedule; Ensure usage and maintenance of PPEs by self & other workmen during shifts ¢ Report any safety incident to the Shift In charge as well as the Senior Engineer for the following o Near Miss o Safety Incident o Work Place Inspection o Unsafe Act o Unsafe Condition ¢ Attend safety meetings and ensure implementation of actions planned during departmental safety meeting at shop floor ¢ Ensure compliances to safety training targets by monthly reconciling attendance records VIII. cGMP Compliance: Execute and update online documentation to meet cGMP requirements ¢ Complete preplacement cGMP Training before starting the work in any area. ¢ Monitor cGMP compliance in the impact domain and report any incident / cGMP deviation to the Shift In charge as well as the Senior Engineer. ¢ Maintain online instrumentation documentation and timely entries in all documents in cGMP environment and their supporting documents ¢ Check documentation before submission to ensure data integrity. In case of any deficiency or errors in documents and rectify them as per SOP ¢ Conduct training related to cGMP, equipment operation, safety and housekeeping for workmen ¢ Optimize the use of resources in housekeeping; Ensure good housekeeping and sanitisation as per the guidelines ¢ Operate software such as SAP, CipDox and QMS as required and basis training & certification. ¢ Execute CAPA as guided by the Instrumentation Senior Engineer. ¢ Prepare and maintain engineering documents wrt cGMP and Good Engineering Practices Key Accountabilities (4/6) IX. Continuous Improvements: Provide suggestions for optimization of processes to manufacture quality product ¢ Propose and implement new idea to enhance production, optimise the use of consumable goods and maximum utilization of resources ¢ Provide new ideas and simplify processes to reduce process cycle time and achieve new targets ¢ Participate in internal audits / Idea generation sessions to improve on deficiencies to verify GEP and GMP. ¢ Implement action plans for improving on deficiencies observed through internal / external audits X. [E] Self Development on functional & leadership aspects ¢ Keep self-updated on regulatory guidelines and product regulatory requirements of all markets to which product manufactured by the Site is exported. ¢ Undergo training on Functional & Leadership capability building as per guidance from HR function and the Global Operations Team. Key Accountabilities (5/6) Key Accountabilities (6/6) Major Challenges CapEx and OpEx Adherence to the budget Cost vs performance trade off in equipment Ageing Asset leading to escalating OpEx Cost Challenges around capability & competence of personnel and service providers Key Interactions (1/2) Internal ¢ Central Engineering for technical standards and guidance ¢ EHS for safe operations and near-misses ¢ Site head & Unit heads for Proposals, breakdowns and developments ¢ Indirect purchase for Spares, scope, insurance and new vendors ¢ Central purchase for provide Technical inputs and clarifications for CAPEX ¢ Global Leadership Team Guidance & Updates in TLT, Focus Calls & Reviews ¢ Corporate Affairs & Legal Team Guidance & Updates on Compliance matters External ¢ OEMs for projects , automations, alternate vendor development , quality issues and maintenance ¢ Facility maintenance contractors for Improve maintenance and quality standards ¢ Industry Bodies Connect on external benchmarking & information on technology evolution ¢ Statutory Bodies Connect for Regulatory compliance Key Interactions (2/2) Dimensions (1/2) Direct Reports: 0, Team Size 9-12 Unit Maintenance + Utility Budget: 15-20 CR [ Functional ~ 33% of this] Capex Budget: Sustenance 10 CR [ Functional ~ 33% of this] Revenue of Goa I: 300-400 CR Current Replacement value of Assets Maintained: Net Block > 50 CR; CRV > 200 CR Dimensions (2/2) Key Decisions (1/2) Decisions ¢ Spends within Approved Budget Capex & Opx ¢ Maintenance & Reliability Strategies ¢ Engineering & Project Vendors & service Providers as per EA ¢ Technology for Manufacturing ¢ Resource Conservation initiatives ¢ Capability Programs Recommendations ¢ Opex & Project costs Proposal ¢ New vendor addition ¢ Facility audits ¢ Hiring consultants ¢ New equipment & Technology Key Decisions (2/2) Education Qualification BE / B Tech (Mechanical / Electrical / Instrumentation) Relevant Work Experience 2-5 years of experience in manufacturing (Maintenance and Projects). Ability to implement new techniques, deep understanding of manufacturing process, planning and organizational skills, prioritization multi-tasking, understanding of financial concepts Good technical knowledge of Pharma / API machinery and utility requirements Good knowledge and experience in execution of green field / brown field project Knowledge of GMP and various regulatory requirements Good leadership skills and experience in industrial automation

You should have a Degree in Electrical Engineering with a minimum of 10+ years of experience or a Diploma with 12+ years of experience. As an RCM, you will be responsible for various project activities such as starting and ending projects as per requirements, planning manpower and store management, preparing detailed bill of quantities and estimates, designing earthing systems and lightning protection, supervising site activities, executing work as per client design and maintaining quality standards. Additionally, you will be involved in installation, testing, and commissioning of various electrical equipment, coordinating with clients, contractors, and subcontractors, preparing progress reports, and ensuring compliance with project specifications and company procedures. Your role will also include coordinating with stores for material inspection and issue, working on permits, billing, material issues, and gate entry passes, raising requests for site modification drawings and documents, conducting tests, inspections, and calibrations, and ensuring compliance with safety practices and procedures. You will be responsible for commissioning systems, troubleshooting problems, managing maintenance activities, inventory control, and coordinating audits. Additionally, you will be required to follow maintenance schedules, ensure compliance with company's ISO quality procedures, and participate in meetings with various stakeholders to discuss site changes and requirements. This is a full-time position that requires in-person work at the specified location.,

We are looking for a skilled professional with expertise in Oracle Exadata to join our team at Habilelabs Pvt. Ltd., an IT Services & Consulting company located in [location to be specified]. The ideal candidate will have 15 years of experience. Roles and Responsibility Design, implement, and manage Oracle Exadata solutions for clients. Collaborate with cross-functional teams to identify business requirements and develop technical solutions. Develop and maintain documentation of Oracle Exadata implementations and configurations. Provide training and support to end-users on Oracle Exadata applications. Troubleshoot and resolve issues related to Oracle Exadata performance tuning and optimization. Work closely with the development team to ensure seamless integration of Oracle Exadata with other systems. Job Requirements Strong understanding of Oracle Exadata architecture and its components. Experience with Oracle Exadata installation, configuration, and management. Knowledge of database concepts and data modeling techniques. Familiarity with programming languages such as Java or Python is desirable. Excellent problem-solving skills and attention to detail. Ability to work effectively in a team environment and communicate complex technical ideas clearly.

We have an opening for the position of Mechanical Engineer and are looking to hire three candidates in total. Specifically, we need two engineers to join our production team and one engineer to focus on quality assurance and quality control (QA/QC) activities. If you are passionate about mechanical engineering and are in search of a rewarding opportunity, we encourage you to apply!

Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong understanding of instrument calibration procedures under cGMP regulations. Proficiency in maintaining IQ, OQ, PQ documentation for laboratory equipment.

Why you might be excited about us We are on a mission to build the fastest diagnostic lab in India. We have a bunch of Talented folks who relentlessly work towards bringing a WOW customer experience. Rated currently at 4.9. Our team has a wide range of experience .Folks at OH have worked earlier with companies like flipkart,Practo, Unacademy, Swiggy, Metropolis, Licious, cure.fit etc. and we are excited to learn from you too. We care for your career & growth and hence we will help you to shape a career you are excited about. We work hard and we party harder. Our People NPS is >90% and Glassdoor rating is 4.9. Competitive Pay What will you get to do Perform a wide range of diagnostic tests in the areas of Biochemistry, Clinical Pathology, and Hematology, using manual and automated machines. Prepare patient samples for analysis, ensuring proper labeling and adherence to standard operating procedures (SOPs). Operate and maintain automated laboratory instruments, troubleshoot any technical issues, and perform routine maintenance as required. Conduct calibration and quality control checks on laboratory equipment to ensure accurate and reliable test results. Analyze and interpret test results, record findings accurately, and prepare detailed reports for review by medical professionals. Adhere to safety protocols and maintain a clean and organized work environment to prevent cross-contamination and ensure a safe working environment. Collaborate with other laboratory staff and healthcare professionals to ensure efficient workflow and timely delivery of test results. Assist in the development and implementation of new testing methods and protocols, as required by the company. Keep abreast of the latest advancements in laboratory techniques, equipment, and relevant scientific research. Participate in continuing education programs and training sessions to maintain proficiency in laboratory practices. Adhere to company policies, guidelines, and ethical standards in all laboratory activities. Skills we are looking for Bachelors degree in Biochemistry, Clinical Pathology, Hematology, or a related field. Proven experience of 6 - 10 years as a Senior Lab Technician in a diagnostic laboratory, with a focus on Biochemistry, Clinical Pathology, and Hematology. In-depth knowledge and hands-on experience with both manual and automated laboratory instruments used in diagnostic testing. Familiarity with laboratory safety protocols and quality control procedures. Strong analytical skills with the ability to interpret complex data and troubleshoot technical issues. Detail-oriented and organized approach to work, ensuring accuracy and precision in test results. Excellent communication skills, both written and verbal, to report findings and collaborate with team members effectively. Ability to work independently and as part of a team in a fast-paced and dynamic environment. Flexibility to work various shifts, including weekends and holidays, as required by the companys operational needs. Prior experience in a diagnostic company or healthcare setting will be an advantage.

You are being hired as a fresher for the role of Quality Executive to support the quality control team in inspection and documentation work. Your main responsibilities will include assisting in inward, in-process, and final inspections, supporting Pre-Dispatch Inspection (PDI) activities, learning to use basic measuring tools like Vernier and micrometer, checking assembly quality, maintaining machine history cards, preparing inspection reports, supporting instrument calibration tracking, reporting quality issues to the supervisor, following quality control procedures and safety rules, and coordinating with other teams for basic quality tasks. You are required to have a Diploma (DME) or BE in Mechanical Engineering, basic knowledge of mechanical components and machines, willingness to learn quality inspection processes, familiarity with basic measuring tools (Vernier, micrometer, etc.), ability to read simple mechanical drawings (preferred), basic computer skills (MS Excel, Word), good observation and attention to detail, strong communication and teamwork skills, discipline, punctuality, and responsibility, and an interest in documentation and report preparation.,

Responsibilities: * Conduct lab tests on instruments * Ensure compliance with industry standards * Maintain accurate records and reports * Collaborate with cross-functional teams * Perform instrument calibrations

JOB DESCRIPTION Designation: Senior Research Associate (9-II) Job Location: Bangalore Department: BBRC PD ARD CDAS Facing Analytical About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240- a strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation. Job Purpose (1-2 Lines): Analytical Research and Development enabling Chemical Development and API Supply Key Responsibilities: Routine analysis of in-process and isolated samples for early intermediates and APIs using chromatographic and wet analytical techniques Method qualification and instrument calibrations Electronic lab notebook documentation Miscellaneous lab responsibilities Educational Qualifications: M.Pharm Technical/Functional Skills: The candidate should have a good educational and theoretical, analytical chemistry background Good knowledge of analytical techniques The candidate should understand instrument calibration, method qualification, and routine analysis Good understanding of documentation as per GxP requirements (electronic notebook) The candidate should have good proficiency in MS office tools Experience: 0-2 years Behavioral Skills: Strong commitment toward work and a high level of dedication, enthusiasm, and motivation Good speaking-listening-writing skills, attention to detail, proactive self-starter Ability to work successfully in a dynamic environment Should be able to work in a team and flexible for working in shifts. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Responsibilities: * Perform preventative maintenance on analytical instruments * Conduct field instrumentation checks * Maintain electrical instrumentation * Calibrate equipment according to schedule Health insurance Accidental insurance Gratuity Provident fund

Experience in Calibration like, temperature, RH, pressure, sound & Lux. Should be able to prepare the report generation. Should have experience in NABL Lab (approved). Having experience SOP preparation & Calibration reports schedule updation.

Essential Qualification : Diploma in Instrumentation Desirable Qualification : B.E (Instrumentation),BSc/MSc (Physics) Essential Role & responsibilities : Minimum 2 years hands on experience in M & V Calibration Laboratory. Minimum Age : 23 years

As a Jr. Scientific Officer in the Department of Chemistry at Ashoka University, located in Sonipat, you will be responsible for managing and operating the Field Emission Scanning Electron Microscope (FESEM) in the advanced materials characterization facility. Your primary duties will include sample preparation, instrument calibration, image acquisition, routine maintenance, and providing support to users from research and industrial backgrounds. The Department of Chemistry at Ashoka University is known for its interdisciplinary approach to learning and research in the chemical sciences. Offering rigorous undergraduate and Ph.D. programs, the department focuses on integrating chemistry with physics, biology, and computational sciences. Research areas include sustainable chemistry, nanoscience, materials, chemical biology, theoretical, and computational chemistry. The department is equipped with state-of-the-art laboratory facilities and modern instrumentation, fostering collaboration with industry and academic institutions. Your role will involve operating the FESEM for high-resolution imaging and elemental analysis, preparing samples using various techniques, conducting routine calibration and maintenance, interpreting imaging data, and collaborating with researchers and engineers to meet project-specific needs. Additionally, you will be responsible for training students and staff in FESEM operation, ensuring compliance with safety and quality standards, maintaining detailed experiment logs, managing inventory and supplies, and promoting FESEM services to external partners. In summary, as a Jr. Scientific Officer in the Department of Chemistry at Ashoka University, you will play a crucial role in supporting cutting-edge research, facilitating collaboration, and promoting the use of advanced imaging technology for scientific advancement.,

Execute Instrumentation Maintenance Selection and specification of instruments based on Continues process requirements. Calibration, installation, testing, and commissioning of instruments. PLC system configuration, troubleshooting, and maintenance Required Candidate profile Coordination with vendors and cross-functional teams (electrical, mechanical, process). Ensure compliance with industry standards and safety regulations. Maintain documentation

Perform analysis using GC, HPLC, UV, KF & wet methods. Ensure GLP, timely reporting, data review, instrument calibration & method validation. Handle OOS, guide juniors & coordinate with QA/production for batch release. Ensure SOP/ISO compliance.

Location: Tirunelveli,Thoothukudi Industry: Industrial / Manufacturing / Utilities / Oil & Gas Key Responsibilities: Install, calibrate, maintain, and troubleshoot instrumentation systems and equipment (e.g. pressure, flow, temperature, and level sensors). Read and interpret technical diagrams and P&ID drawings. Perform routine inspection and preventive maintenance of instruments and control systems. Support shutdown, turnaround, and project execution activities. Coordinate with electrical and mechanical teams for integrated system functioning. Maintain documentation and report service/repair logs. Required Skills & Qualifications: ITI / Diploma in Instrumentation or related field. Minimum 48 years of experience in industrial instrumentation. Hands-on experience with PLCs, DCS, and field transmitters. Familiar with safety protocols and industrial standards. Preferred: Experience in industries like oil & gas, power plants, or manufacturing units. Knowledge of calibration tools and multimeters.

1) Preparation of solutions for lab procedures 2) Laboratory record keeping as per quality SOP 3) Cleaning and maintaining laboratory equipment and instruments. 4) Testing of raw material (non-ferrous metal) and FG (non-ferrous metal oxide) Required Candidate profile BSc (Chemistry/ General) (minimum) with 1 year of minimum experience in analytical chemistry and lab testing. We prefer people who have worked in manufacturing units.

Role Overview Responsible for qualification & calibration of Microbiology instruments and equipment as per procedures with QMS. Illustrative Responsibilities Ensure that qualification & calibration activities are planned and executed within time frame defined by the procedure and equipments are released on time as per the pre-defined schedule. Responsible for coordinating with lab supervisors / system owners for handling of any non-conformances or escalations Handling of QMS related activities like, Change control, CAPA and Deviation with its effectiveness check. Responsible for quality compliance activities for laboratory instruments qualification and calibration. Summarize, review, and report the analytical Instruments qualification and calibration for further approval. Ensure a disciplined work environment to provide expertise to subordinates colleagues in the proper performance of laboratory procedures. Ensure on time GDP in technical function with right first time (RFT) approach. Responsible for ensuring team compliance to EHS, Quality & Business policies Any other work given by management from time to time. Quality & Compliance Responsible for following GMP/GLP/ GDP/EHS policies by self as well as the team Required skills Technical expertise in Microbiology instruments qualification, calibration, protocol preparation and QMS. Build cohesive team valuing team spirit Able to handle biosafety cabinet, LAF, glass bead sterilizer, water bath, Autoclave, refrigerator, Incubator, Balance & pH meter etc. Clear thoughts and effective and crisp communication. Job requirement M.Sc – specializing in Microbiology/Biotech with proven experience of min. 2-3 yrs. in Instrument qualification and calibration. Awareness of analytical instruments qualification and calibration, protocol preparation, CAPA, Investigations, Deviations (QMS) Good Knowledge of ICH guidelines and different global regulatory authorities. Job Location - Mulund

Job Summary Plan, organize and carry out inspection of items / material received from the suppliers and in house machining. Carry out in process inspection as required. Record the result of inspection in report format. Record NCRs, if any and follow up the actions. Primary Responsibilities Follow the daily inspection activity Plan defined by supervisor. Verify the goods receipt / Work order, QITP and PO (Where required). Select the required inspection tools and verify the calibration validity date Inspect and verify the items as per drawing, Work order requirement as per the procedure Record the inspection results in respective format Update the status of inspection on ERP / Work order. Record NCRs in NCR Portal, if any Move the material along with all reports to next stage. Comply with all NOV Company and HSE policies and procedures. Communicate with all related department employees Identify the items as required. Suggest for the improvements through CAR / PAR Take active part in audits. Facility/Group Specific Responsibilities Inspection of items as per drawings and work orders. Verify the calibration date of inspection tools, prior to inspection. Work as per procedure / WI First article and in-process inspection as required as per procedure. Record all inspection results in respective format Update WO status in ERP / on WO Welding inspection shall be carried out as per procedure Verify PWHT reports per WI / Procedure Record and communicate NCRs through mail Raise scrap note for scrap items All NCR / Scrap items need to be moved to designated area Education & Experience Qualifications BE/Diploma in Mechanical Engineering Minimum 3 years / 5 Years of experience in inspection Must be proficient with computer basics Strong knowledge of all measuring instruments and GD&T Must be able to communicate in English. Knowledge of ASTM, NDE and Welding from Oil & Gas preferred. Knowledge of CMM preferred. Job Requirements Inspection Behavioural & Technical Competencies Good behaviour Measuring Instrument, GD&T and Instrument calibration