6425 Calibration Jobs - Page 48

Job details Employment Type : Full-Time Location : Pune, Maharashtra, India Job Category : Field Operations Job Number : WD30246551 Job Description Build your best future with the Johnson Controls team As a global leader in smart, healthy and sustainable buildings, our mission is to reimagine the performance of buildings to serve people, places and the planet. Join a winning team that enables you to build your best future! Our teams are uniquely positioned to support a multitude of industries across the globe. You will have the opportunity to develop yourself through meaningful work projects and learning opportunities. We strive to provide our employees with an experience, focused on supporting their physical, financial, and emotional wellbeing. Become a member of the Johnson Controls family and thrive in an empowering company culture where your voice and ideas will be heard – your next great opportunity is just a few clicks away! What we offer: Competitive salary Paid vacation/holidays/sick time Comprehensive benefits package including 401K, pension, medical, dental, and vision care On the job/cross training opportunities Encouraging and collaborative team environment Dedication to safety through our Zero Harm policy What we are looking for: Hands on experience in ELV, Security and Mechanical system project (CCTV/Fire Alarm/Access control/Public Address system/GSS/VESDA/ RSS/WLD) Key Responsibilities: Develop and implement project-specific QAQC plans and procedures. Conduct inspections and tests of materials, processes, and products to ensure compliance with project specifications and industry standard. Review and approve construction or production procedures, work instructions, and quality documentation. Monitor and report on quality performance metrics, non-conformities, and corrective/preventive actions. Coordinate with engineering, procurement, and construction teams to ensure quality objectives are met. Maintain proper documentation, including test reports, inspection records, material certificates, and calibration logs. Interface with clients, consultants, and third-party inspectors regarding quality-related matters. Ensure compliance with health, safety, and environmental (HSE) regulations and company policies. Participate in internal and external quality audits. Provide quality training and awareness to staff and subcontractors as needed. Strong communication and Project Management skills. Should be aware of various standards applicable to Building security system installation in Data centre.

Industrial Equipment / Machinery Full-Time Job ID: DGC00959 Chennai, Tamil Nadu 0-2 Yrs ₹1.5 - ₹2.5 Yearly Job description Well dressed and being a professional is a basic requirement Prepare an introduction about yourself; Learning attitude and respect for all Graduate with a clear passed out Degree & good communication skills are essentials E Graduate in Mech, Auto, Mechatronics, EEE, ECE, ICE or equivalent, with a clear Degree certificate Freshers can apply; 1 or 2 years of experience in NABL Accredited Calibration Lab is an added advantage. High level of commitment and professionalism in work conduct. You should be willing to work on a job rotation in all our departments Core of the job is into Technical Calibration & Testing at our 20+ Labs Remember to carry a photo copy of all your credentials, ID copies, educational certificates for verification

TITLE : Maintenance Engineer DEPARTMENT : Maintenance REPORTING TO : Maintenance Head QUALIFICATIONS: Diploma/Degree Mechanical 4+6 years of experience in Injection Molding maintenance department in any industry. Job Location Ambernath RESPONSIBILITIES: Responsible for handling team of maintenance and authorized for teams daily work schedule. Responsible for determining the preventive maintenance schedule for Injection molding Machines. Periodical inspection of entire utility system. Responsible for the preventive maintenance activities to be conducted on time and as per schedule. Responsible for all maintenance activities of machinery and Utilities and their Corrective & Preventive Maintenance, Predictive Maintenance, planning for Spares Procurement etc. To train departmental Personnel for effective maintenance. To implement quality system in department. To coordinate with the Quality Assurance Manager for calibration of equipment To co-ordinate the validation activities of equipment and utilities.

As a candidate for the position at Piramal Enterprises Limited located in Dhar, Madhya Pradesh, you will have the opportunity to contribute towards becoming one of the top three global Contract Manufacturing and research organizations while aiming to be the most preferred supplier in the chosen space. Your role will involve supporting the Strategic Business Unit (SBU) in achieving its vision by ensuring the timely availability of high-quality products at a competitive price, developing efficient systems and processes, maximizing resource utilization, and enhancing capabilities to adapt to the changing environment. Your responsibilities will include implementing GLP/GMP requirements, calibrating laboratory equipment, qualifying secondary reference standards, standardizing and preparing solutions/reagents/indicators, reviewing laboratory chemicals, procuring and maintaining lab chemicals and glassware, allocating work to workmen, training them, and maintaining records related to temperature, humidity, glassware cleaning, and calibration. To excel in this role, you should have a minimum of a Graduate/Post Graduate degree with a chemistry background, preferably with a technical background. Additionally, you are expected to have about 3 years of experience in manufacturing operations. It is essential to possess technical expertise in GLP and demonstrate skills in time management, planning, and a good understanding of laboratory operations. If you are technically experienced, detail-oriented, and have a passion for contributing to a dynamic manufacturing environment, we encourage you to apply for this full-time position at Piramal Enterprises Limited.,

You will be joining Synopsys, a company at the forefront of technological innovations that are shaping the way we live and connect in the Era of Pervasive Intelligence. Synopsys leads in TCAD, chip design, verification, and IP integration, enabling the development of high-performance silicon chips and software content. As part of this dynamic environment, you will have the opportunity to contribute to continuous technological innovation. As a highly skilled and knowledgeable professional with a deep passion for semiconductor physics and technology, you should hold a PhD or MS degree in Electrical Engineering, Physics, or Materials Sciences. Your expertise in semiconductor devices and process technologies, along with a profound understanding of semiconductor manufacturing processes and process modeling, will be instrumental in your role. Your ability to analyze and interpret experimental test/characterization data, coupled with excellent presentation and communication skills, will facilitate effective interaction across teams and organizational levels. In this role, you will be responsible for conducting TCAD calibration projects for advanced logic and memory technologies, providing consulting services to customers to enhance the value of TCAD, and collaborating with R&D, sales, marketing, and customers to drive product development and acceptance. Additionally, you will manage customer projects from definition to execution and follow-up. Your contributions will have a significant impact on improving the quality and functionality of TCAD tools, driving the successful adoption of TCAD products in customer projects, and contributing to product development through feedback and collaborative efforts with R&D teams. By fostering strong customer relationships, you will enhance Synopsys" market position as a leader in semiconductor technology and simulation tools. To excel in this role, you should possess a PhD degree in Electrical Engineering, Physics, Materials Sciences, or a related field, along with 5+ years of industry or research experience. Advanced knowledge and experience in semiconductor process technology, device design based on Silicon, and hands-on experience with TCAD simulation tools are essential. A strong understanding of semiconductor devices physics and proficiency in Python scripting would be advantageous. As a collaborative team player with a "help others succeed" mentality, you should be detail-oriented with strong problem-solving abilities, adaptable to fast-paced environments, proactive, self-motivated, and passionate about continuous learning and improvement. Your ability to interact effectively at both engineering and management levels within customer organizations will be key to your success. You will be part of the Product Application Engineering team within TCAD R&D, working on market-leading solutions and services for TCAD and EDA. Your role will involve driving the successful adoption of technologies and platforms at a diverse set of customers and partners across various market segments.,

This position is being hired to focus on quality aspects essential for the automation and service business. As the Quality Manager, you will oversee and ensure compliance with quality requirements and standards across both Automation and Service Business. Your responsibilities will include managing, establishing, and maintaining quality methodologies and systems to drive customer quality improvements and ensure compliance with regulatory requirements. You will be responsible for overseeing the Quality Management System (QMS), including standards such as ISO 9001:2008, ATEX, MID, BIS, and other regulatory requirements, supporting operations at both the Coimbatore and Mumbai locations. Your key responsibilities will involve driving quality standards across the organization, ensuring adherence to policies and procedures, validating quality processes by establishing product specifications and quality attributes, maintaining PPM levels within specified targets, preparing quality documentation and reports, and responding to customer complaints with containment actions, full analysis, and implementing countermeasures. The ideal candidate for this role will have a total experience of 11-13 years, a Bachelor's degree in Mechanical Engineering, and a Post-Graduation in MBA (Operations Management) or M.Tech (Quality Management). Mandatory certifications required include Six Sigma Green or Black belt and ISO or TS 16949 auditor. Other preferred courses/certifications include ATEX & UL Certifications. To be successful in this role, you should have knowledge and experience in tools like PPAP, 5S, FMEA, Calibration, 8D, 7QC tools, Standard Work, DM, MRB, Policy Deployment, and Visual Management. Strong analytical skills, communication skills, a commitment to continuous improvement, the ability to lead individuals and teams, proficiency in MS Office applications, knowledge of SAP QM Module, and familiarity with computers and cameras are essential. Six sigma green belt/black belt will be an added advantage for this profile. Gilbarco Veeder-Root, a Vontier company, is the worldwide technology leader for retail and commercial fueling operations, offering integrated solutions from the forecourt to the convenience store and head office. Vontier is a global industrial technology company uniting productivity, automation, and multi-energy technologies to meet the needs of a rapidly evolving mobility ecosystem. At Vontier, you will have the opportunity to drive meaningful change, contribute to a sustainable future, and thrive both personally and professionally. Join our community at Vontier, where your contributions matter, your innovation is valued, and together, we enable the way the world moves towards a brighter future.,

Engineer-Lab is responsible for assigning and carrying out tests as per the job priority given by Lab Manager and / or as per daily procedure Preparation of test report for all samples tested in the department Assistance in preparation and updating of technical procedures. Responsibility of making available appropriate resources for lab operations. Monitoring equipment maintenance, calibration and testing schedules. Monitoring environmental conditions. Maintenance of standard reference materials and records. Review and update work instructions from time to time Carry out internal calibration under guidance of Technical manager. Preparation of Measurement of uncertainty document with the help of Technical Manager. Maintain the documentation required as per NABL criteria. Ensure implementation of QMS in the area of responsibility corporate standards (e.g. Code of Ethics, BV Values, corporate identity, policies, procedures) Experience required 0 years to 5 years

As an Instrument Technician in the Oil & Gas industry based in Abu Dhabi, your main responsibility will be to handle the installation, calibration, testing, maintenance, and repair of field instrumentation and control systems. These tasks are crucial to guaranteeing the safe, reliable, and efficient operation of plant facilities while ensuring compliance with site standards and procedures. Your key responsibilities will include installing, maintaining, and calibrating various field instruments such as pressure, temperature, level, and flow transmitters, switches, control valves, analyzers, and gauges. You will need to proficiently read and interpret P&IDs, loop diagrams, hook-up drawings, and instrument datasheets to execute correct installation and maintenance activities. Performing routine preventive maintenance and inspection of instrumentation equipment according to the maintenance schedule will also be part of your daily tasks. It will be your duty to conduct calibration and functional testing using the appropriate calibration equipment and accurately document the results. Additionally, you will be responsible for troubleshooting and rectifying faults in instrumentation loops and control systems to ensure smooth operation. Moreover, you will play a role in loop checking, pre-commissioning, and commissioning activities with the guidance of supervisors or engineers. This is a full-time position that follows a day shift schedule and requires your physical presence at the work location.,

As an assembler of medical devices and equipment, your primary responsibility will be to follow detailed work instructions, blueprints, or engineering drawings to assemble the units accurately. You will also be required to conduct testing and calibration of the assembled units to ensure their functionality and compliance with specifications. This is a full-time, permanent position suitable for fresher candidates. The work schedule will be during the day shift from Monday to Friday with morning shifts. Additionally, weekend availability may be required. The work location for this position is in person.,

As an experienced SMT Maintenance Technician, you will be responsible for performing daily preventive maintenance on SMT machines such as pick-and-place, reflow ovens, screen printers (e.g., DEK, MPM), and AOI machines. Your primary goal will be to troubleshoot and repair machine faults efficiently to minimize downtime and ensure continuous production. Monitoring machine performance is crucial, and you will need to recommend improvements or upgrades as necessary. It will be your responsibility to calibrate SMT machines and tools according to the manufacturer's specifications, ensuring optimal functionality. In addition to maintenance tasks, you will be required to maintain accurate maintenance logs and service reports, supporting the process engineering team with machine setup, changeovers, and fine-tuning. Compliance with ESD, safety, and cleanroom procedures during maintenance tasks is essential. Providing technical support during NPI (New Product Introduction) and prototype builds, as well as managing spare parts inventory for SMT equipment, will also be part of your role. Training production operators on basic machine handling and minor troubleshooting will contribute to the smooth operation of the manufacturing process. To qualify for this position, you should hold a diploma or degree in Electronics, Electrical, or a related field, along with a minimum of 2-5 years of experience in SMT equipment maintenance in an EMS environment. Strong knowledge of SMT production processes and equipment, hands-on experience with equipment from manufacturers like Fuji, Yamaha, Panasonic, Juki, ASM, etc., and the ability to read and interpret electrical schematics and mechanical drawings are required. Familiarity with reflow profiling and soldering standards (e.g., IPC-A-610), basic PC skills (Windows OS, MS Office), good communication, and problem-solving skills are also essential. The role may require you to work in shifts and under pressure. This is a full-time, permanent position located in Gurugram, Haryana. The job offers benefits such as Provident Fund, and the schedule includes day shift, fixed shift, and morning shift options. Performance bonuses may also be provided based on your contributions. Ideally, you should have at least 2 years of experience in SMT maintenance to be considered for this role. If you meet these requirements and are looking for a challenging opportunity to contribute to a dynamic manufacturing environment, we encourage you to apply.,

You will be working as a Thermo-Aerodynamics- Attribute Engineer, responsible for defining and delivering vehicle-level attributes related to performance, fuel/energy efficiency, and driveability. Your role is crucial in ensuring that the vehicle meets customer expectations and competitive benchmarks in dynamic performance and real-world usability. Your key responsibilities will include defining attribute targets for vehicle performance (acceleration, top speed), energy/fuel efficiency, and driveability (throttle response, shift quality, NVH). You will lead cross-functional teams involving powertrain, chassis, calibration, and software to deliver attribute performance. Additionally, you will be responsible for developing and executing test plans for the validation of PED attributes in simulation, lab, and real-world environments. Benchmarking competitor vehicles and analyzing market trends to inform target setting will also be a part of your role. To achieve these goals, you will utilize data analytics and modeling tools to predict and optimize attribute performance. You will also be expected to support vehicle tuning and calibration activities to meet attribute goals. Regularly presenting attribute status updates will be another aspect of your responsibilities.,

You will be working as a Laser Cutting Machine Operator at GKMR Industries Private Limited, a company specializing in manufacturing durable, secure, and energy-efficient steel doors and windows for residential and commercial construction projects. Your role will involve setting up and operating laser cutting machines to create high-quality products. You will be based in Prathipadu and will play a crucial part in ensuring precision and quality control throughout the production process. Your responsibilities will include reading and interpreting blueprints, loading materials into the machine, adjusting machine settings, performing maintenance tasks, and ensuring that all products adhere to strict safety and quality standards. The ideal candidate for this role should have experience in operating and maintaining laser cutting machines, the ability to interpret technical drawings and blueprints, proficiency in machine setup, calibration, and troubleshooting, a keen eye for detail, and a strong commitment to quality control. Knowledge of safety protocols and regulatory compliance in manufacturing is essential, as is the ability to work both independently and as part of a team. A high school diploma or equivalent is required, and a technical certification would be considered a plus.,

As a Team Member in Chemical Research & Development at the Research & Development department, specifically in the Peptide Synthesis sub-department, your primary role is to perform chemical synthesis of molecules. This involves process development, process validation, and transferring the processes to production units. Your responsibilities include conducting literature searches, collecting MSDS, performing lab experiments, documenting experimental results, and interpreting spectral data. You will also be responsible for maintaining various documents such as patents, literature, and analytical reports. Collaborating with analytical chemists and DQA on analytical results and methods is an essential part of the role. To ensure the smooth functioning of the lab, you will need to account for chemical usage, availability of raw materials, and perform calibration of lab equipment like weighing balance, pH meter, and driers. Keeping track of regular solvents, reagents, and managing effluent generation from lab experiments are also part of your duties. In addition, you will be required to perform Manual Solid Phase Peptide Synthesis of Peptides on various scales, ranging from medium to commercial scale with minimal supervision. This includes purification of solid phase products, CGMP activities, synthesis of impurities, and degradation impurity standards for analytical method development and validation. Safety awareness and implementation are crucial aspects of this role, and you must strictly adhere to Good Laboratory Practices and Laboratory Safety Norms. Continuous learning and staying updated with industry trends are essential for success in this position. To qualify for this role, you should have an M.Sc. in Organic Chemistry and a minimum of 2 years of experience in the R&D Department of an API manufacturing company. Preferred qualifications include 6 years of experience and knowledge of Process R&D and scale-up processes. In terms of competencies, you should have a strong understanding of coupling reagents, documentation, GLP, safety compliances, plant scale-up, solid phase synthesis, solution phase synthesis, and purification. Behavioral competencies such as results orientation, customer centricity, collaboration & teamwork, problem-solving, planning, and communication are also essential for this role. Continuous learning and professional development are encouraged to excel in this position.,

Rockwell Automation is a global technology leader focused on helping the world’s manufacturers be more productive, sustainable, and agile. With more than 28,000 employees who make the world better every day, we know we have something special. Behind our customers - amazing companies that help feed the world, provide life-saving medicine on a global scale, and focus on clean water and green mobility - our people are energized problem solvers that take pride in how the work we do changes the world for the better. We welcome all makers, forward thinkers, and problem solvers who are looking for a place to do their best work. And if that’s you we would love to have you join us! Summary Job Description Perform the set-up, calibration, testing and troubleshooting of circuits, components, instruments and mechanical assemblies. Determine and may develop test specifications, methods and procedures from blueprints, drawings and diagrams. Test and troubleshoot assemblies and final systems. May complete rework on assemblies or systems as a result of testing. Prepare technical reports summarising findings and recommending solutions to technical problems. May help with the selection and set-up of specialised test equipment. You will report to the Team Lead, Sr. Sourcing You will work in Onsite work mode based in our Chennai plant in Kancheepuram, India. Your Responsibilities Read and understand documentation about product-assembly (e.g., work order information, schematics, one-line diagrams). Understand existing assembly processes and assist MEs in developing or improving new processes. Identify electrical schematic errors, device interferences and other simple problems and submit preliminary solutions to the ME. Understand existing assembly processes and proficiency the use of multiple tools (pneumatic/electric/torque tools) Simple troubleshooting for the product under testing. (Based on electrical schematics, wiring diagrams) Do the operation to testing devices (e.g., transformers, circuit breakers, relays, PLC terminal blocks). Feedback to engineers on problems occurring in the assembly process, including and not limited to engineering issues, material issues, and documentation issues. Implement standardised pre- and post-shift 5S and safety maintenance. Do the training for new employees after mastering assembly skills and complete relevant product skill certifications Implementation and follow-up of drawing updates, OCN, TECN. The Essentials - You Will Have Graduate of technical school or university, and electrical automation or mechatronics Low-voltage electrician's licence (must-have) Conscientious working attitude, motivation and flexibility in work The Preferred - You Might Also Have Minimum of 1 years and above of independent working experience in assembly or wiring of power distribution cabinets. Read and write simple English What We Offer Our benefits package includes … Comprehensive mindfulness programs with a premium membership to Calm Company volunteer and donation matching program – Your volunteer hours or personal cash donations to an eligible charity can be matched with a charitable donation. Employee Assistance Program Personalized wellbeing programs through our OnTrack program On-demand digital course library for professional development and other local benefits! At Rockwell Automation we are dedicated to building a diverse, inclusive and authentic workplace, so if you're excited about this role but your experience doesn't align perfectly with every qualification in the job description, we encourage you to apply anyway. You may be just the right person for this or other roles. ,

Job No. TECH 06 Department Support Staff and Tech Location Mumbai Work Experience 0 - 7 Years Qualification B. Sc or BPMT (Neurophysiology) Description Perform routine and complex EEG procedures to obtain data for use in the diagnosis of clinic disorders of the nervous system. To get the tracings reported by Neurologist. To assist with scheduling patients for EEG / EMG. Maintaining the equipment in the department, ensuring that a test run of the machine with calibration is conducted as and when required. Receiving the patients and checking for completeness of their papers, preparation for the test and collecting their previous investigation reports. To ensure that all equipments are in optimum working condition. To maintain inventory of required equipment and supplies. To maintain patient registers. Assisting in EEG / EMG monitoring in the OT. Conducting EEG’s in ICU, ICCU & PICU. To maintain professional conduct, good communication skills, and confidentiality in the care of patients. To be part of Quality Improvement Initiative & protocols of the organization. Apply Now

Job No. TECH 03 Department Support Staff and Tech Location Mumbai Work Experience 0 - 5 Years Qualification BSc with MLT from FDA approved institute Description Receiving and processing of specimens including quality control specimens. Interpretation & reporting of result as deemed necessary and dispatching reports to report Dispatch area. Archiving and Discard of specimen as per protocol. Assists to maintain inventory of supplies and equipment for laboratory use; document and perform cleaning, maintenance and calibration on laboratory equipment. Maintain quality control programs and perform various quality control procedures to maintain compliance with internal and external regulations. Report to the consultant regarding malfunction of equipment and take proactive steps to attend to the same Assists in maintaining, filing, archiving and destroying records and documents as per guidelines. Assists in stock checking, Inventory Control and Indent. To achieve harmony in the department. Learn new techniques in field of transfusion Medicine. Assist the Technical Supervisor / Consultant Transfusion Medicine in the smooth running of DTM. Keep all the records updated and authenticated by the Consultant Transfusion Medicine at all times. Keep track of Reagents that have crossed the expiry limits and ensure that they are discarded appropriately. Participates in continuous monitoring for compliance of Quality Assurance, Laboratory Safety and Accreditation related activities. Follow the Health and safety guidelines. Co-ordinate with the Technical Supervisor and keep the blood bank in readiness for an adult by the FDA at all times. Assisting the Consultant in daily Blood Bank related activities as per her directives. Apply Now

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Executive / Manager 2 Date: Jul 24, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Key Responsibilities: Analytical Method Development & Validation Develop and validate robust HPLC methods for characterization and quantification of biological products (e.g., monoclonal antibodies, recombinant proteins). Perform method optimization, robustness studies, and transfer protocols as per ICH guidelines. Routine & Stability Testing Conduct analysis of in-process, release, and stability samples using: HPLC/UPLC Capillary and Gel Electrophoresis UV spectrophotometric methods Host Cell DNA quantification (e.g., qPCR-based methods) HCP ELISA and other immunoassays Instrument Operation & Maintenance Perform routine maintenance, calibration, and troubleshooting of analytical instruments including HPLC, electrophoresis systems, spectrophotometers, and ELISA readers. Ensure timely qualification and performance verification of instruments. Documentation & Compliance Prepare and review SOPs, STPs, protocols, reports, and analytical records in compliance with regulatory requirements. Maintain accurate and complete documentation in laboratory notebooks and electronic systems. Quality & Regulatory Compliance Participate in internal and external audits, and support regulatory submissions with analytical data. Cross-functional Collaboration Work closely with R&D, Quality Control, and Regulatory Affairs teams to support product development and lifecycle management. Provide technical support during investigations, deviations, and CAPAs. Training & Development Train junior analysts and new team members on analytical techniques and laboratory practices. Stay updated with advancements in analytical technologies and regulatory expectations. Qualifications & Experience: M.Sc. / M.Tech / M.Pharm in Biotechnology, Biochemistry, or related life sciences discipline. 4–8 years of relevant experience in analytical development or QC of biopharmaceuticals. Hands-on experience with HPLC method development and ELISA based techniques. Familiarity with regulatory guidelines (ICH, FDA, EMA) and quality systems. Key Skills: Strong analytical and problem-solving skills Attention to detail and data integrity Excellent documentation and communication abilities Proficiency in software tools like Empower, Chromeleon, SoftMax Pro, etc. Ability to manage multiple projects and meet deadlines Apply Now » Apply Now Start applying with LinkedIn Please wait...

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr. Manager Batch Certification Date: Jul 24, 2025 Location: Dadra - Quality Assurance Company: Sun Pharmaceutical Industries Ltd Job Title: Sr. Manager – Batch Certification Business Unit: Global Quality & Compliance Job Grade G9B Location : Dadra At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Position Summary : Manage overall batch certification review of QC lab records, certificates of analysis/compliance and all related supporting documentation (i.e. documentation review, SOP compliance, laboratory application data reviews, instrument preventive maintenance/calibration/qualification/validation as per good manufacturing practices/good documentation requirements and ALCOA++ principles). The incumbent will assure individual compliance with all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures. Key Responsibilities : Lead the review of all QC records related to Batch certification program. Review Deviations, CAPAs, OOS/OOT investigations. Ensure that all activities are compliant with Standard Operating Procedure, STP and GP etc. Review initiated CAPA records related to QC investigations for completeness and adequacy. Review and approval of qualification, analytical method transfer, validation protocol and reports for accuracy, completeness and traceability as well as adherence to the Protocol/procedures. Training of QC and QA teams. Work in partnership with Quality Control and Quality Assurance. Follow the EHS policy, laboratory procedures and maintain the compliance to cGMP requirements. Travel Estimate Job Requirements Educational Qualification B.Pharm / M.Pharm Experience Tenure : 15 to 17 Yrs Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s). Apply Now » Apply Now Start applying with LinkedIn Please wait...

Title: Instrumentation and Automation Engineer Qualification: B.E in Electrical & Instrumentation Primary Responsibilities: 1. To attend /or supervise all jobs related to Instrumentation Engineering activities in site. 2. Timely execution of all calibrations of equipments/instruments as per schedule coordination with user. 3. To attend emergency breakdowns of all plant wide machines round the clock as and when required. 4. Maintain the Spare parts of all critical Instruments in site. 5. Timely execution and completion of Validation activities to be done in site. 6. Execution of all In-house Projects in instrumentation and automation in site. 7. Maintain the calibration logs, area /equipment logbooks, preventive maintenance schedule of all the activities. Audit readiness Secondary Responsibilities: 1. Preparation and Review of all documents related to engineering. Timely execution and completion of Performance verification of the equipments. Interested candidates can share your resume to [ Careers@curateqbio.com, hasumitha.chitti@curateqbio.com] with relevant subject line.

Responsibilities: Design, install, calibrate & maintain instrumentation systems on site. Ensure compliance with safety standards during boiler operations. Collaborate with maintenance team for equipment troubleshooting.

Flowserve is a world-leading manufacturer and aftermarket service provider of comprehensive flow control systems. Join a company whose people are committed to building a more sustainable future to make the world better for everyone. With 16,000+ employees in 50+ countries, we combine our global reach with local presence. Our team challenges themselves to approach each situation with ingenuity and creativity to help provide our customers with the most innovative flow control products and services. We support 10,000+ customers worldwide, creating products to meet the needs of our customers who are supplying energy, fresh water, pharmaceuticals and other essentials to consumers, businesses and governments globally. We invite you to put your talents and career in motion at Flowserve. Company Overview: If a culture of excellence, innovation and ownership is what you’re searching for, consider putting your experience in motion at Flowserve. As an individual contributor, or as a leader of people, your enterprise mindset will ensure Flowserve’s position as the global standard in comprehensive flow control solutions. Here, your opportunity for professional development and industry leading rewards will be supported by our foundational commitments to the values of people first, integrity and safety. Thinking beyond opportunity and reward, at Flowserve, we are inspired by working together to create extraordinary flow control solutions to make the world better for everyone! Role Summary: Establish and maintain Welding activities and Documentation both at In-House and at Sub-contract weld shops. Preparation of WPS/PQR/WPQ, Welding Procedure, Formats to meet the Standard / Organizational / Customer requirement, Training of Welders, Implementation of QMS and other product standards / specifications at weld shop. Attending Customer queries, Development of new welding sources, supporting for new product development, Ensure calibration and validation. Responsibilities: Ensure required, Hold, Witness, Monitor & Document review points are met as per ITP / QAP. Quality Documentation requirements and GRN closure on Time Conformance to check list, ITP, Customer specifications, work Instructions and procedures. Release of Product after welding (stage) inspection. Conformance of providing Qualitative & Quantitative data, for COPQ. Ensuring safety discipline at work center as per EMS and OHSAS. Coordinate with production in order to plan and execute inbound and production checks. Manage relations with customers or third-party inspectors. Participate in external supplier quality testing and audits. Participate in Continuous Improvement Process (CIP) events. Monitor product portfolio KPIs and drive effective root cause corrective actions where appropriate to address gaps to agreed targets. Manage customer witness inspections. Maintain and analyze data to provide information or identify problems for management and stakeholders on the state of a process or product quality. Create awareness in the Leadership community regarding what opportunities have been discovered or developed and how to realize them. Collaborate with the department or other company departments to clarify / resolve issues techniques related to Welding Quality. Other duties as assigned. Requirements: B E with 7 to 10 years experience in Welding. Knowledge on Welding & Heat treatments – Process, Procedure & Documents, Consumables, Equipment and accessories, welding defects, Inspection and testing, Heat treatment process. Knowledge on ERP System-SAP. Vision evaluation fitness. Proficiency in Microsoft Office -Excel,Word,Power Point. Preferred Experience / Skills: Certification on " American Welding Soceity Certified Welding Engineer ". Certification on NDT Level II – RT, MT, PT, VT. Excellent verbal and written communication skills. Req ID : R-10977 Job Family Group : Engineering Job Family : EN Quality Engineering EOE including Disability/Protected Veterans. Flowserve will also not discriminate against an applicant or employee for inquiring about, discussing or disclosing their pay or, in certain circumstances, the pay of their co-workers. Pay Transparency Nondiscrimination Provision If you are a qualified individual with a disability or a disabled veteran, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access flowservecareers.com as result of your disability. You can request a reasonable accommodation by sending an email to employment@flowserve.com. In order to quickly respond to your request, please use the words "Accommodation Request" as your subject line of your email. For more information, read the Accessibility Process.

Key Responsibilities: Analytical Method Development & Validation Develop and validate robust HPLC methods for characterization and quantification of biological products (e.g., monoclonal antibodies, recombinant proteins). Perform method optimization, robustness studies, and transfer protocols as per ICH guidelines. Routine & Stability Testing Conduct analysis of in-process, release, and stability samples using: HPLC/UPLC Capillary and Gel Electrophoresis UV spectrophotometric methods Host Cell DNA quantification (e.g., qPCR-based methods) HCP ELISA and other immunoassays Instrument Operation & Maintenance Perform routine maintenance, calibration, and troubleshooting of analytical instruments including HPLC, electrophoresis systems, spectrophotometers, and ELISA readers. Ensure timely qualification and performance verification of instruments. Documentation & Compliance Prepare and review SOPs, STPs, protocols, reports, and analytical records in compliance with regulatory requirements. Maintain accurate and complete documentation in laboratory notebooks and electronic systems. Quality & Regulatory Compliance Participate in internal and external audits, and support regulatory submissions with analytical data. Cross-functional Collaboration Work closely with R&D, Quality Control, and Regulatory Affairs teams to support product development and lifecycle management. Provide technical support during investigations, deviations, and CAPAs. Training & Development Train junior analysts and new team members on analytical techniques and laboratory practices. Stay updated with advancements in analytical technologies and regulatory expectations. Qualifications & Experience M.Sc. / M.Tech / M.Pharm in Biotechnology, Biochemistry, or related life sciences discipline. 4–8 years of relevant experience in analytical development or QC of biopharmaceuticals. Hands-on experience with HPLC method development and ELISA based techniques. Familiarity with regulatory guidelines (ICH, FDA, EMA) and quality systems. Key Skills Strong analytical and problem-solving skills Attention to detail and data integrity Excellent documentation and communication abilities Proficiency in software tools like Empower, Chromeleon, SoftMax Pro, etc. Ability to manage multiple projects and meet deadlines

Safran est un groupe international de haute technologie opérant dans les domaines de l'aéronautique (propulsion, équipements et intérieurs), de l'espace et de la défense. Sa mission : contribuer durablement à un monde plus sûr, où le transport aérien devient toujours plus respectueux de l'environnement, plus confortable et plus accessible. Implanté sur tous les continents, le Groupe emploie 100 000 collaborateurs pour un chiffre d'affaires de 27,3 milliards d'euros en 2024, et occupe, seul ou en partenariat, des positions de premier plan mondial ou européen sur ses marchés. Safran est la 2ème entreprise du secteur aéronautique et défense du classement « World's Best Companies 2024 » du magazine TIME. Safran Aircraft Engines conçoit, produit et commercialise, seul ou en coopération, des moteurs aéronautiques civils et militaires aux meilleurs niveaux de performance, fiabilité et respect de l'environnement. La société est notamment, à travers CFM International*, le leader mondial de la propulsion d'avions commerciaux courts et moyen-courriers. * CFM International est une société commune 50/50 de Safran Aircraft Engines et GE Aerospace. Descriptif mission Maintain workplace cleanliness and discipline as per 5S principles. Adhere to all safety and EHS (Environmental, Health & Safety) regulations. Understand customer and process-specific quality standards and requirements. Perform degreasing and part cleaning as per FPI process specifications. Handle parts and equipment safely to avoid contamination or damage. Support in identifying process improvement opportunities related to Quality, Cost, and Productivity (QCP). Assist in the upkeep and maintenance of equipment and tooling. Support documentation by completing production logs, inspection records, and electronic forms accurately. Operate and monitor equipment when necessary and verify equipment calibration. Ensure readiness of work area and documentation for audits at any time. Participate in continuous improvement initiatives and cross-functional team discussions. Support procedural development and hands-on training for new personnel as required. Technical Knowledge Strong understanding of engineering drawings and basic GD&T. Strong understanding of Basic Material Science. Familiarity with manufacturing processes turning, milling, drilling, grinding. Basic knowledge of mechanical measurements and inspection techniques. Awareness of Lean Manufacturing, 5S, and basic quality tools. Digital Skills Working knowledge of MS Excel, Word, and PowerPoint for basic reporting. Soft Skills Good communication and interpersonal skills. Team player with a strong work ethic and willingness to learn. Attention to detail and safety-conscious behavior. Flexible to work in shifts and extended hours if required. Additional Preferences (Not Mandatory) Exposure to special processes (e.g., thermal spray, FPI, shot peening, coating). Participation in diploma projects related to manufacturing or process improvement. Basic understanding of quality standards like ISO 9001 or AS9100 (if Aerospace-related).

Safran est un groupe international de haute technologie opérant dans les domaines de l'aéronautique (propulsion, équipements et intérieurs), de l'espace et de la défense. Sa mission : contribuer durablement à un monde plus sûr, où le transport aérien devient toujours plus respectueux de l'environnement, plus confortable et plus accessible. Implanté sur tous les continents, le Groupe emploie 100 000 collaborateurs pour un chiffre d'affaires de 27,3 milliards d'euros en 2024, et occupe, seul ou en partenariat, des positions de premier plan mondial ou européen sur ses marchés. Safran est la 2ème entreprise du secteur aéronautique et défense du classement « World's Best Companies 2024 » du magazine TIME. Safran Aircraft Engines conçoit, produit et commercialise, seul ou en coopération, des moteurs aéronautiques civils et militaires aux meilleurs niveaux de performance, fiabilité et respect de l'environnement. La société est notamment, à travers CFM International*, le leader mondial de la propulsion d'avions commerciaux courts et moyen-courriers. * CFM International est une société commune 50/50 de Safran Aircraft Engines et GE Aerospace. Descriptif mission Maintain workplace cleanliness and discipline as per 5S principles. Adhere to all safety and EHS (Environmental, Health & Safety) regulations. Understand customer and process-specific quality standards and requirements. Perform degreasing and part cleaning as per FPI process specifications. Handle parts and equipment safely to avoid contamination or damage. Support in identifying process improvement opportunities related to Quality, Cost, and Productivity (QCP). Assist in the upkeep and maintenance of equipment and tooling. Support documentation by completing production logs, inspection records, and electronic forms accurately. Operate and monitor equipment when necessary and verify equipment calibration. Ensure readiness of work area and documentation for audits at any time. Participate in continuous improvement initiatives and cross-functional team discussions. Support procedural development and hands-on training for new personnel as required. Technical Knowledge Strong understanding of engineering drawings and basic GD&T. Strong understanding of Basic Material Science. Familiarity with manufacturing processes turning, milling, drilling, grinding. Basic knowledge of mechanical measurements and inspection techniques. Awareness of Lean Manufacturing, 5S, and basic quality tools. Digital Skills Working knowledge of MS Excel, Word, and PowerPoint for basic reporting. Soft Skills Good communication and interpersonal skills. Team player with a strong work ethic and willingness to learn. Attention to detail and safety-conscious behavior. Flexible to work in shifts and extended hours if required. Additional Preferences (Not Mandatory) Exposure to special processes (e.g., thermal spray, FPI, shot peening, coating). Participation in diploma projects related to manufacturing or process improvement. Basic understanding of quality standards like ISO 9001 or AS9100 (if Aerospace-related).

Roles And Responsibilities Installation of Cinema Audio equipment Troubleshooting and Calibration of Professional Audio equipment Repairing & servicing professional Audio Equipments Crimping and soldering Cables as per the requirements provided by various department Training field engineers & end user Helping sales team on pre sales calls for closing the deal on tech front Preparing Cables & connectors for installation (soldering Connectors & Crimping) Maintain customer Database Prerequisite Candidate Must have basic knowledge about Audio Equipment & PCB repairing ITI / Diploma from relevant field with Minimum 0-2 year experience Knowledge in computer Hardware and Networking is also an added advantage Ready to travel across India Location: Chennai (Guindy) Powered by JazzHR 12157rYN2s