545 Lab Testing Jobs

Dear Candidate We have immediate vacancies for the post of Chemist, Microbiologist, Production, Quality Assurance, Quality Control, Regulatory Affairs, R & D, Research Associate, Lab Asst. Qualification : BSc / MSc Chemistry / Microbiology / Biotechnology / M Pharma Freshers and Experienced Salary : 4 Lakhs Per Annum to 9 LPA Contact Mr Vasanth Managing Director 7259549756 / 8722187029 Karnataka Information Solution No.6, Basement Floor, ASVNV Bhavan, Opp State Bank Of India, K.G Road, Majestic, Bangalore - 09 PH : 080 - 22260106.

As a team member responsible for managing Project Management Activities, you will be involved in the planning and execution of development and homologation test requirements. Your key responsibilities will include executing testing activities as per the established plan and conducting thorough root cause analysis to identify underlying issues. You will also be involved in crash model development and will collaborate closely with the CAE and design teams to validate and implement results, ensuring effective communication and coordination throughout the process. In addition to your technical/functional competencies, which include experience in Vehicle Component Safety (Lab Testing) and proficiency in conducting lab testing for various vehicle components related to safety, you should have specific expertise in tests such as seat belt anchorage, head form impact, bumper, and interior fitting tests. Your awareness of passive safety regulations and homologation requirements for passenger vehicles, including knowledge of standards such as IS 15139, IS 15904, IS 15223, UNR14, R12, R21, will be crucial in this role. Moreover, practical experience using UG (Unigraphics) software, a popular CAD/CAM/CAE tool in the automotive industry, will be beneficial. On the behavioral front, traits such as being a team player, possessing good analytical and presentation skills, strong decision-making abilities, and the capacity for future planning and conceptualization thinking are essential. As a Project Management Specialist in the test domain, you are expected not only to have technical expertise but also to be a team player who demonstrates strong analytical and presentation skills. Your decision-making abilities should be excellent, and you should possess future planning and conceptualization thinking skills to contribute to the long-term success of model development activities. To qualify for this role, you should have an educational background of BE/B.Tech/M.Tech.,

The Medical Assistant at Phelps Health plays a crucial role in providing patient care under the delegation of the clinic LPN/RN, physician, or mid-level provider. As a Medical Assistant, you will need to demonstrate a high level of professionalism, excellent customer service skills, organizational skills, attention to detail, ability to multitask efficiently, critical thinking skills, and work effectively in a fast-paced environment. Your responsibilities will include following established hospital policies to ensure patient safety, interacting directly with patients in the clinic, routing phone messages and patient communications to the appropriate personnel, acting as a liaison between physician/APP and patients, assisting with medication renewals and administration, performing point-of-care lab testing, scheduling appointments and procedures, monitoring supply inventory, and educating patients about My Chart. To qualify for this position, you must have completed an accredited Medical Assistant or Medical Specialist program or have an equivalent amount of working experience. A high school diploma is required. While one year of Medical Assistant experience is preferred, it is not mandatory. Certification as a Registered Medical Assistant (RMA) or a Certified Medical Assistant (CMA) through an approved accrediting organization is preferred, along with American Heart Association Basic Life Support certification. This role requires considerable mental concentration, lifting up to 35 lbs, and constant walking. You will be exposed to infectious diseases and may have to deal with hostile individuals at times. However, physical discomfort is minimal. If you are looking for a challenging yet rewarding opportunity to make a difference in healthcare, Phelps Health offers a supportive team, attractive benefits, and opportunities for growth. Join us in our mission to provide top-quality care to our community by applying now.,

As a Food Safety Specialist at Sodexo, your primary responsibility will be to ensure the deployment of a Zero Harm mindset within frontline employees. You will be in charge of implementing Safety improvement plans at the site/account and confirming the deployment of Sodexo Safety Net and Client Safety initiatives. Additionally, you will be responsible for overseeing the overall upkeep, food hygiene, and safety standards of the location, monitoring activities throughout the food chain to uphold food safety standards. You will need to conduct Risk Assessments to identify potential risks related to the working environment, machinery, or equipment, and suggest preventive measures to the site manager. It will be your duty to prepare Risk Assessments & Risk Registers, update them post-incident or new scope additions, and train frontline staff in hazard identification and reporting. Furthermore, you will be required to prepare and update the Legal Register, ensuring all legal compliance is in place and escalating in case of non-compliances. Your role will involve conducting safety walks and Safety Observations, reporting them in the Salus system, and tracking for closure. You will also create awareness on Nearmiss reporting, report Nearmiss incidents in Salus, and manage Incident Management by informing regional HSE & region Head, investigating incidents, preparing Root Cause Analysis (RCA), and ensuring all corrective actions are implemented at the site. In addition to the above responsibilities, you will need to ensure adherence to various HSE practices such as Time-temperature, FIFO, Sorting Process, Thawing, salt & Turmeric processes, CCPs, Deep Cleaning, Pest Control, PPM of Equipment, Electrical Safety, Global engineering practices, and HSMS processes. Monitoring that all required checklists and records are maintained, conducting HSE trainings, safety campaigns, calibrations, self-inspections, and safety declarations will also be part of your duties. To qualify for this role, you should have a Graduate/Postgraduate degree in Food Science or related field, along with a minimum of 4-5 years of experience in Food Safety and Health and Safety Systems Management. Possessing certifications like Certified Lead auditor ISO22000/HACCP/ISO 9001/ISO45001 and Advance Diploma in Food Safety would be advantageous. As a Food Safety Specialist, it is crucial to possess strong business acumen, client obsession, financial understanding, and a range of behavioral competencies including optimizing work processes, driving results, effective communication, collaboration, and managing ambiguity. Your ability to make good decisions, exhibit courage, and resilience will be key to succeeding in this role. If you are passionate about ensuring food safety standards and promoting a culture of safety in the workplace, we invite you to apply for the Food Safety Specialist position at Sodexo by sending your application to sona.bhardwaj@sodexo.com.,

Lab Technician jobs in Canada / Australia / New Zealand Call & Whatsapp - 8800897895 Receive, label and analyze samples (blood, toxic, tissue etc.) Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organize and store all chemicals substances, fluids and compressed gases according to safety instructions Record all data and results in specified forms (paper and electronic) with accuracy and responsibility Maintain equipment and assist in ordering laboratory supplies Ensure that all safety guidelines are followed strictly at all times and maintain a clean and orderly environment

Job Description: As a valued member of our company's lab Operations team, you will be responsible for a variety of key roles and responsibilities. Your primary tasks will include working with instrumentation such as Pressure and Temperature sensors, as well as possessing knowledge of soldering techniques. Additionally, you will need to have a good understanding of Electrical Panels, particularly 230V and 420V systems, and be skilled in instrumentation wiring and panel wiring for pressure sensors. It will be essential for you to be able to interpret panel drawings and schematic layouts accurately. Your commitment to safety will be crucial, including knowledge of safety protocols like LOTO and HIRA. Understanding I/O modules and basic calibration principles will also be part of your daily duties. You will collaborate closely with engineers, technicians, lab and test operations personnel, and product validation teams. Proficiency in basic computer operations, Windows operating systems, and Microsoft Office will be advantageous. Additionally, you will conduct lab testing activities and set up equipment while ensuring adherence to 5S practices in the work area. Requirements: To excel in this role, you should possess a minimum of 2 to 4 years of experience in a relevant field. A degree in Mechanical Engineering or a related discipline, such as a B.E. or Diploma, will be required to demonstrate your qualifications for this position.,

The Senior Manager - Feed Stock in the Petrochemical Industry role requires 8 to 10 years of experience. The position is based in Bharuch, Gujarat, with a work schedule of 6 days a week for 8 hours each day. The salary range for this role is 15 to 25 LPA, and the notice period is immediate to 45 days. Candidates applying for this role must have a basic education level of Diploma, Graduate, B.Tech, BE, ME, M.Sc., or M.Tech in Science (Chemistry) or Technology/Engineering (Chemical Engineering, Petroleum Engineering and Technology, Oil Technology). For Bachelor's or Master's degree holders, 8 to 10 years of relevant industry experience is required, while Ph.D. degree holders should have 3 to 5 years of relevant industry experience. The ideal candidate should have a minimum of 7 years of experience as a researcher in the petrochemical field and currently be performing the role of a Scientist. Expertise in Crude Oil is essential, along with a background that includes starting a career as a chemist in a Lab and experience in oil testing. A strong understanding of oil components, properties, sources, as well as geopolitical knowledge related to oil origins is highly desirable.,

Career Category Quality Job Description Sr Associate QC QC Systems Templating Role Name: Sr Associate QC Department Name: Quality Control Role GCF: 4 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today. ABOUT THE ROLE Role Description: Let s change the world. Amgen is hiring for a Senior Associate to support the Electronic Lab Notebook (ELN) and consumable inventory system infrastructure in the Quality Control (QC) network. This candidate will primarily work a shift-based schedule to enable the business in delivering Amgen s mission to serve patients. The candidate may need to work outside of his/her routine workday to support business needs. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN ), and provide remote support from AIN to Amgen sites across multiple time zones globally. Roles & Responsibilities: This position will be responsible for creating, revising, peer-reviewing and qualifying template s for analytical method executions in ELN which includes ELN interfaces with other systems such as LIMS, Empower, and Chromeleon . Creation and revision of consumable templates, and supplementary master data will also be in the scope of responsibility. In addition, this position will collaborate with the US-based Master Data Group (MDG) and will also be involved in ELN template administration / registration activities , ensuring tasks align with procedures, best practices, and service level agreements for QC standardization. Coordination with site representatives and other ELN template builders and qua l ifiers is required to convert QC source documents into ELN templates accurately . Coordination with members within the team at AIN on the same shift and members of the team at AIN on different shifts will be critical in ensuring deliverables are met in accordance with schedule. To effectively provide support, candidates must demonstrate proficiency in virtual communication tools and have experience managing remote collaborations. Secondary responsibilities may include cross-training in to LIMS, Empower, and Chromeleo n . The following are some examples of tasks for the position Creation a n d revision of ELN templates Peer reviewing templates built by colleagues Qualification of ELN templates Creation and revision of consumable templates Collaboration with method subject matter experts , template builders and template qualifiers throughout the QC network Ensuring training is up to date Additional r espon s ibilities may involve: Providing performance metrics Driving global QC system alignment Understanding prioritization of requests with the QC network Basic Qualifications and Experience: Masters degree with 3-6 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience Functional Skills: QC lab testing experience Proficiency in ELN a pplications Knowledge of Data Integrity Requirements for QC systems Microsoft Office proficiency Familiarity with Good Manufacturing Practices Soft Skills: Excellent English verbal and written communication skills Problem-solving and troubleshooting abilities Independence in delivering right first time EQUAL OPPORTUNITY STATEMENT We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation . .

Qualified phlebotomist with 1 year experience for home and lab collection. DMLT CERTIFICATE OR DIPLOMA Required Candidate profile Blood sample collection fluent in sales and patient management Perks and benefits Increment and commission on sales

Job Summary: We are looking for a diligent and detail-oriented Lab Assistant to support our laboratory operations in a chemical manufacturing environment. The ideal candidate will assist in conducting tests, maintaining lab equipment, and ensuring quality standards are met. Key Responsibilities: Assist in preparing and setting up laboratory experiments and tests. Collect, prepare, and analyse samples as per standard procedures. Maintain cleanliness and organisation of laboratory tools and equipment. Record and document test results accurately in lab reports. Support in calibration and maintenance of laboratory instruments. Follow safety protocols and handle chemicals with care. Assist senior technicians or scientists in routine lab activities. Ensure compliance with environmental and safety regulations. Manage inventory of lab supplies and chemicals. Report any equipment malfunctions or safety hazards to supervisors.

Experience of heat treatment shop Through hardening, case hardening, induction hardening&carbonitriding manufacturing process.Individually perform Vickers, metallography inspection testing forCutting, policing &Ht parts Rockwell hardness, micro micro

Career Category Quality Job Description Associate QC QC Systems Templating Role Name: Associate QC Department Name: Quality Control Role GCF: 3 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today. ABOUT THE ROLE Role Description: Let s change the world. Amgen is hiring for a n Associate to support the Electronic Lab Notebook (ELN) and consumable inventory system infrastructure in the Quality Control (QC) network. This candidate will primarily work a shift-based schedule to enable the business in delivering Amgen s mission to serve patients. The candidate may need to work outside of his/her routine workday to support business needs. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN) and provide remote support from AIN to Amgen sites across multiple time zones globally. Roles & Responsibilities: This position will be responsible for the creation , revision and qualification of template s for analytical method executions in ELN . C reation and revision of consumable templates will also be in the scope of responsibility . The Associate will ensu re assigned tasks are carried out according to the correct procedures, best practices, and service level agreements for QC standardization. Coordination with members within the team at AIN on the same shift and members of the team at AIN on different shifts will be critical in ensuring deliverables are met in accordance with schedule. To effectively provide support, candidates must demonstrate proficiency in virtual communication tools and have experience interacting in remote collaborations. The following are some examples of tasks for the position Creation a n d revision of ELN templates Qualification of ELN templates Creation and revision of consumable templates Understand and follow established instructions to complete assigned deliverables within expectations Collaboration with AIN team members to support the QC network needs Ensuring training is up to date Additional r espon s ibilities may involve: Assistance in providing performance metrics Basic Qualifications and Experience: Master s degree with 1-3 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience. Functional Skills: QC lab testing experience Exposure to ELN a pplications Microsoft Office proficiency Familiarity with Good Manufacturing Practices and Good Documentation Practices Soft Skills: Excellent English verbal and written communication skills Ability to learn quickly with attention to detail Delivering results right first time within a team environment EQUAL OPPORTUNITY STATEMENT We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation . .

Job responsibilities 1. Updating the Quality record as per approved (FQP) field quality plan, approved material, ensuring that Quality of executed work. 2. Maintain the Standard Field Quality Plan (SFQP) approved by client of various activities at project. 3. Update Client modification to QA/QC program, method, material sources etc. 4. Preparation & review of Quality Assurance Manual Ensuring construction best practice and procedure. 5. Mix Design preparation and review of PCC & RCC work quality. 6. Batching plant erection, calibration as per IS:4925 and proper control of Batching plant as per requirement of Mix & specification 7. Participation in quality review meeting with Employer. 8. Material testing (Coarse and fine aggregate, steel, cement, soil) as per FQP & IS Code and Test Record maintain properly. 9. Water Supply pipeline quality Inspection.. 10. Responsible for Quality of work & client satisfaction. Testing of materials with relevant IS code or according to clients requirement. 11. Awareness and knowledge of IS codes if amendments. Training for Quality assurance team 12. Conduct training with all Site engineer and officials for quality of work. 13. Daily review of lab equipment and document files. 14. Site & store visit for better material handling & control site deviation. 15. Identify potential errors in the process or standard and design improvements that could create a more efficient and effective execution of project. Candidates having experience in Water supply and irrigation projects will be considered.

Dear Candidates Greetings from Z-Tech Solutions - Chennai Urgent Requirement for Design Engineers for Design Job (Traiing Cum Placement within Short span of 15 to 30 days)- Chennai Qualification : B.E / B.Tech/ Diploma ( Mech, Automobile) Passed out : 2019,2020,2021,2022, 2023 & 2024 Note : Passed Out 2025 not included Experience : 0 to 1 yr exp Salary ranges : 2.4LPA to 3.6LPA Required Key skills : Autocad Solidworks Catia V5 Position - Design Engineers Role : Permanent job Company Type : Own Equipment Manufacturing Company Required Other benefits : Free Food & Transport will be provided based on company norms Working hours : 8 hours Job location : Chennai Note : We Required immediate joiners only Intrested candidates should contact this number : Contact Rekha - +91 9884082586 Interested Candidates kindly share your Updated Resume through this whatsapp number : +91 98840 82586 HR Rekha - 98840 82586 NOTE : WE PREFER ONLY SOUTH INDIAN CANDIDATES Chennai Coimbatore Tuticorin Madurai Tirunelveli Trichy Erode Dindigul Sivagangi Kanyakumari Kerala Cuddalore Kumbakonam Theni Salem Thanks&Regards, Z Tech solutions

Job Title: Lab Manager Location: Pushpalata D Y Patil Hospital and Research Centre, Ambi Talegaon Department: Laboratory Employment Type: Full-Time Job Summary: The Lab Manager is responsible for overseeing and managing the daily operations of the medical laboratory. This includes supervision of lab personnel, ensuring the accuracy and quality of diagnostic tests, equipment maintenance, inventory control, and adherence to accreditation and safety standards. Key Responsibilities: Manage the overall functioning of the laboratory, including testing, reporting, and timely sample processing. Supervise and coordinate work schedules for lab technicians, assistants, and phlebotomists. Ensure high standards of test accuracy, quality assurance, and report turnaround time. Maintain inventory of reagents, consumables, and laboratory equipment; ensure timely procurement. Implement and monitor IQC (Internal Quality Control) and EQAS (External Quality Assurance Schemes) . Oversee calibration, maintenance, and performance checks of laboratory instruments. Ensure full compliance with NABL / hospital quality protocols . Develop, update, and enforce Standard Operating Procedures (SOPs). Conduct staff training, competency evaluations, and support skill development. Ensure proper biomedical waste disposal and infection control measures. Coordinate with clinicians and departments to address test-related queries and improve lab-clinical interface. Support audit processes and ensure documentation for inspections and accreditations. Qualifications: M.Sc. in Medical Laboratory Technology /MBA or related field Minimum 8+ years of experience , with at least 2 - 3 years in a supervisory/managerial role Key Skills: Strong leadership and team management skills In-depth knowledge of clinical laboratory operations and quality standards Proficiency with Laboratory Information Systems (LIS) Excellent communication, documentation, and problem-solving skills

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Responsibilities: * Perform tests for raw materials and concrete * Prepare and revise mix designs for different grades of concrete * Coordinate with plant and site teams for quality related issues * Ensure compliance with industry standards House rent allowance

Responsibilities: * Perform tests for raw materials and concrete * Prepare and revise mix designs for different grades of concrete * Coordinate with plant and site teams for quality related issues * Ensure compliance with industry standards House rent allowance

About Native: Urban Company stands as a trailblazer in the realm of home solutions, crafting innovative products to enrich the lives of our customers. From our position as the foremost provider of professional home services in India and Asia, we have ventured into the realm of smart home products under the ' NATIVE by UC ' brand. In 2023, we launched our own RO Water Purifier. With our 8+ years of experience in servicing water purifiers, we brought great innovations and delightful features to guarantee 2 years of unconditional warranty! Committed to excellence, we strive to deliver unmatched customer experiences, echoing the standards set by industry giants like Apple. Join our dynamic team and be a part of reshaping the future of home living with our innovative products. Currently, our product portfolio includes residential smart water purifiers and smart door locks . Role Summary: As an R&D Engineer, you will support the development and testing of water purifiers and filtration systems. You will design testing protocols , run experiments , and develop high-impact solutions . This is a hands-on, execution-heavy role with high ownership , giving you the opportunity to define and shape the R&D function within our organization. This role involves managing day-to-day lab operations, conducting tests, setting up and maintaining test rigs, and providing insights for product performance improvement. You will be actively involved in lab testing, benchmarking, and supporting compliance with BIS/NSF standards, working closely with cross-functional teams to contribute to the product development process. Key Responsibilities: Oversee and manage daily laboratory operations, including setup, calibration, and maintenance of testing equipment. Conduct water quality, performance, and durability tests for water purifiers, filters, and components. Design and assemble test setups for various R&D experiments and validation activities. Analyze test results and provide technical insights for product improvement as part of the R&D team . Support benchmarking of competitor products to derive insights for innovation and enhancement. Assist in modifying components for improved performance, cost optimization, or localization. Work with electrical and electronic components such as solenoids, pumps, sensors, and control units. Support development and validation of new test methods, SOPs, and documentation as per BIS/NSF standards (e.g., IS 16240, IS 10500). Maintain accurate records of tests, observations, and analysis for reporting and compliance. Coordinate with external labs for specialized testing and validations. Ensure adherence to lab safety protocols and maintain a well-organized lab environment. Visit field sites for R&D activities if required. Required Skills & Experience: B.E./B.Tech in Mechanical/Electrical/Electronics/Chemical Engineering OR B.Sc./M.Sc. in Chemistry, Environmental Science, or related fields. 25 years of relevant experience in lab testing for water purifiers or similar appliances. Good understanding of water purification technologies (RO, UV, UF, Carbon filters). Hands-on experience with electrical/electronic components (solenoids, pumps, sensors). Familiarity with BIS/NSF standards for water quality and purifier testing. Ability to design and execute test setups for R&D evaluation. Strong analytical, troubleshooting, and problem-solving skills. Proficiency in documentation and record-keeping. Collaborative mindset for working with cross-functional teams. Why Join Native? Be part of an innovation-driven organization shaping the future of water purification. Work with cutting-edge technologies and contribute to impactful R&D projects. Collaborative, growth-oriented work culture with opportunities for skill development . Work-life balance with a dynamic and supportive team.

Desired Candidate Profile 2-7 years of experience in Lab Asistant Strong knowledge of lab management, lab testing, and project management principles. Ability to work independently with minimal supervision while maintaining high standards of quality control.

Role summary Responsible for leading the planning, execution and supervision of prototype testing, product evaluation and type testing qualifications to support design validation and innovation. Technical skills Knowledge of testing standards, Report documentation, Product validation and testing, Safety, Capacity planning, Manufacturing processes Requirements Good knowledge of design fundamentals Exposure to and knowledge of pressure testing and elevated / low temperature testing Knowledge of prototype testing and evaluation methods Ability to create test set-ups to handle valve testing Safety in material handling and testing Knowledge of valve basics is preferred Ability to interact with other functions like Purchase, Production, Quality Control Ability to liaise with external inspectors for offering of valve testing and external labs Handling trouble shooting and root cause analysis Ability to handle testing instruments and gauges for testing Plan for maintaining and upgrading lab infrastructure, instruments and testing tools Ability to create reports and presentations and be able to interact with Sales and service teams Should be a good team player, able to guide and train his team members Should have good oral and written communication skills Exposure to software MS Office, AutoCAD, Creo software

Our Client a reputed 60Yrs Chemical Company needs - Post : QC In-Charge Location :Palghar Experience : Min 15 years of experience in QC. Qualification : M.Sc. Chemistry / B.Tech in Chemical or related field Salary : 15 LPA Job Profile: Should have thorough experience in laboratory of chemical manufacturing unit. Operation/calibration of analytical instrument. Analysis of raw material. Water analysis. Lead the QC team and manage all quality control activities across the plant. Ensure timely and accurate testing of raw materials, in-process, and finished products. Coordinate with production, QA, and R&D teams to ensure consistent quality. Ensure calibration, maintenance, and proper functioning of QC instruments. Skills: Strong knowledge of chemical analysis and lab/QC techniques. Leadership and team management. Root cause analysis and problem-solving. Documentation and report writing. Attention to detail and quality mindset. Email CV with current salary and notice period to resume@jobspothr.com All job updates on www.jobspothr.com Call 99877 06721 / 83697 08611 after mailing CV Good Luck !

formulate and develop solvent water based , uv inks for flexo gravure printing process. lab testing, pigment dispersion, color matching and rheological adjustments. work with ,production, quality department ink performance on foils, films and paper

p style="text-align:justify"> Oakridge Gachibowli is a premium international day school in India. We have the proud privilege of being the pioneers of IB schooling in South India and one of the largest providers of IB education in India. We have 150+ IB-trained teachers with years of experience, helping us consistently achieve outstanding results and seeing our students go on to study at some of the world s leading universities. Oakridge offers IB, CBSE, and Cambridge curricula, and is recognized as one of the best schools in Hyderabad, India. . Job Description Please write the Job Description. Job Responsibilities

Role & responsibilities Experience in Ci & SG grade, Experience in Spectro meter operating, Micro structure analysis, Tensile Testing, and hardness testing standards Preferred candidate profile