4890 Calibration Jobs - Page 17

Position: Test Engineer Location: Sonipat, Haryana Experience: 1–2 Years Industry: Geotechnical / Civil Testing / Engineering Consultancy Employment Type: Full-Time About KSR GTRS KSR-Geotechnical Testing and Research Solutions (KSR GTRS) is a NABL-accredited laboratory (Certificate No. TC-14802) committed to excellence in soil and rock testing, geophysical and seismic investigations, geological and geotechnical field studies, as well as advanced kinematic analysis and numerical modelling. With state-of-the-art facilities and esteemed leadership under Dr. Rao, the organization plays a pivotal role in national infrastructure projects including the Chenab Bridge and Silkyara Tunnel investigations. Role Summary We are seeking a motivated and meticulous Test Engineer to join our research-driven testing laboratory. This role offers a unique opportunity to engage in cutting-edge geotechnical analysis while contributing to mission-critical civil engineering projects. Key Responsibilities Conduct laboratory testing of soil and rock samples using NABL-compliant protocols Assist in laboratory activities Record, interpret, and report test results with accuracy and clarity Understand material behavior and contribute to characterization studies Ensure calibration and maintenance of lab equipment Collaborate effectively across multidisciplinary teams Uphold documentation standards and contribute to quality control systems Desired Skills & Qualifications Bachelor’s degree in Civil / Diploma or equivalent 1–2 years of hands-on experience in soil and rock testing preferred Strong adaptability and eagerness to learn emerging methods Familiarity with IS codes, testing protocols, and lab workflows Ability to work both independently and collaboratively Effective communication skills and a solution-oriented mindset Why Join KSR GTRS? Be part of an acclaimed NABL-accredited lab Collaborate with renowned geotechnical experts Contribute to nationally significant infrastructure projects Gain exposure to advanced testing and modelling techniques Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹27,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Application Question(s): Current Salary: Expected Salary: Work Location: In person Speak with the employer +91 9254988200 Expected Start Date: 21/07/2025

Location: Greater Noida Qualifications: B.E./B.Tech. in ECE, EE, Mechatronics, Robotics, or similar streams Should have done at least one hands-on project related to drones, robotics, or embedded systems Curious, self-driven, and ready to learn with the team Skills Required: Familiarity with ESCs, BLDC motors , and sensors like RPM or current sensors Familiarity with KK Flight Controller or other RC-based FCs Proficient in Embedded C/C++ for microcontrollers (Arduino, STM32, ESP32) Basic knowledge of IMU/accelerometers (MPU6050 or similar) Experience with servo/stepper motor control Knowledge of accelerometer/compass calibration procedures for drones (especially in ArduPilot/Pixhawk/KK ecosystem) Hands-on with 3D mechanical design (Fusion 360, SolidWorks, or similar) Embedded programming skills (Arduino/ESP32) Good understanding of rotation matrices , coordinate systems, and orientation control

Job Title: Technical Service Engineer Location: Bhopal, Indore Experience: 3-6 years Job Overview: We’re hiring a Service Engineer to install, maintain, and service lab equipment at client sites. Candidates with a background in Electronics, Biomedical, or Instrumentation Engineering and a customer-focused mindset are ideal. This is a travel-based role with hands-on troubleshooting responsibilities. Key Responsibilities: Install, commission, and validate laboratory instruments at customer locations Perform routine maintenance, calibration, and repair of equipment Troubleshoot and resolve technical issues both on-site and remotely Deliver product training and technical guidance to end users Maintain accurate documentation of service activities, reports, and compliance records Ensure adherence to lab safety protocols and company quality standards Coordinate with logistics, support, and product teams for smooth service delivery Build and maintain strong client relationships through effective communication and support Manage service schedules, travel plans, and timely response to service calls Required Skills & Qualifications: Diploma or Bachelor's degree in Electronics, Biomedical, Instrumentation, or related field 3-6 years of field experience in servicing laboratory/medical/diagnostic equipment Strong technical knowledge of lab instruments and troubleshooting methods Excellent communication and customer service skills Proficiency in MS Office and service reporting tools Willingness to travel extensively for on-site support Knowledge of lab safety norms and standards

About The Company (Industry & Sector) An advanced-technology scale-up at the crossroads of Quantum Computing, Artificial Intelligence and Semiconductor Engineering . The hardware division designs full-stack enterprise quantum computers—spanning superconducting processors, cryogenic control electronics and RF instrumentation—to unlock breakthroughs across life-sciences, finance, transportation and space. Role & Responsibilities Design and execute quantum-device experiments—from cryogenic fixture design to automated data acquisition—for superconducting-qubit characterisation. Develop and refine protocols to measure coherence times, gate fidelities, and perform quantum-state / process tomography, feeding results back into device design. Maintain, troubleshoot and optimise cryogenic measurement stacks and microwave-RF chains to guarantee low-noise, high-throughput data collection. Implement data pipelines in Python / MATLAB that process raw traces into actionable metrics and dashboards for cross-functional teams. Collaborate with quantum-processor, control-electronics and theory groups to correlate empirical results with simulations and accelerate design-of-experiments cycles. Document methodologies, publish findings and help shape the roadmap for next-generation, fault-tolerant quantum processors. Skills & Qualifications Must-Have MSc / MTech / PhD in Physics, Electrical Engineering, Materials Science or related field with quantum focus. Hands-on experience designing cryogenic or microwave testbeds and performing quantum measurements on superconducting qubits or similar platforms. Proven ability to measure and analyse device parameters (T₁/T₂, gate fidelity, tomography). Solid understanding of circuit QED and error-correction concepts relevant to superconducting hardware. Proficiency in Python (NumPy/Pandas/Matplotlib) or MATLAB for data analysis and instrument control. Strong problem-solving, communication and teamwork skills; comfortable in fast-paced R&D settings. Preferred Track record of peer-reviewed publications or conference presentations in quantum technology. Experience writing DoE-driven analysis reports that steer experimentation plans. Familiarity with cold-atom or spin-qubit platforms, autonomous calibration routines, or GPU-accelerated simulators. Knowledge of error-mitigation / bosonic-code techniques and their experimental implementation. Exposure to clean-room fabrication workflows and materials studies for superconducting devices. Contributions to open-source quantum-measurement tooling or instrument-control libraries. Skills: hamiltonian engineering,coherence times measurement,quantum-state tomography,ldpc codes,surface codes,gate fidelity measurement,python-based quantum platforms,circuit qed,automated data acquisition,numerical tool-chains,fault-tolerant architectures,superconducting-qubit error-correction schemes,computational modelling of quantum circuits,data processing in matlab,quantum device characterization,problem-solving,experimental protocols,matlab,error-mitigation techniques,quantum-software stacks,cryogenic fixture design,collaboration,quantum computing,artificial intelligence,data processing in python,quantum error-correction codes,quantum-process tomography,teamwork,python,error-correction concepts,quantum-state & process tomography,communication,qubit-control schemes,semiconductor,peer-reviewed publications,dynamical decoupling,numerical methods

The Instrument Technician is responsible for the installation, calibration, maintenance, troubleshooting, and repair of instrumentation and control systems in Water Treatment Plants (WTP), Wastewater Treatment Plants (WWTP), and Multiple Effect Evaporator (MEE) plants. The technician ensures that all process instruments function efficiently and comply with operational and safety standards to support continuous plant operations

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 Electrical & Power est l'un des leaders mondiaux des systèmes électriques aéronautiques. La société est un acteur clé dans le domaine de l'électrification des équipements et de la propulsion électrique et hybride. Elle compte 14 000 collaborateurs répartis dans 13 pays. Mission description As per JD As per JD - Good analytical skills and knowledge on tools and machinery

Position Manager – Engineering and Projects Job Title Job Grade: G10 Function Engineering & Projects Sub-function Plant Maintenance Manager’s Job Title Skip Level Manager’s Title: Function Head Title Location: Ranipool (Sikkim-2) No. of Direct Reports (if any) Areas of Responsibility To ensure Preventive Maintenance of all Utility system and Process machineries done as per schedule in SAP & ensure record is maintained. To review SAP order MEMO. To ensure uninterrupted supply of all utilities in process. To ensure all the break-downs are attended promptly & minimize the impact on production loss. To perform job assigned by the Reporting Manager time to time. To ensure Calibration activity are performed at site with respect to approved schedule. To ensure QMS related activities are performed within TCD. Handling & Closing of Audit observation on Time. Deputation and analysis of Work Vs Manpower of area and monitoring Project work Vs Actual Progress. Coordination with cross functional Team & others. To ensure the Compliance of cGMP & EHS are followed by the Team while doing operation & Maintenance activities. To ensure list of critical spares are prepared & all the stocks of spares are available. To ensure that in order to minimize break down RCA (Root Cause Analysis) are being carried out & necessary actions are taken to minimize it. To approve the PR and GIM. To review and approve Documents in EDMS. To Review, Approve activities in Track wise system and evaluate the impact of multi- sites changes. To understand all relevant SOP & ensure that the procedure is carried out as per SOP. To ensure the use of all PPEs by Team during carrying out all maintenance activities. To propose and initiate the development work for new system/ equipment. To ensure day to day problems are resolved. To ensure the discipline and punctuality among the colleagues / subordinates / workman are maintained. Travel Estimate Job Scope Internal Interactions (within the organization) External Interactions (outside the organization) Geographical Scope Financial Accountability (cost/revenue with exclusive authority) Job Requirements Educational Qualification Electronic or Electrical Engineering / Instrumental Engineering Specific Certification Plant Maintanance Skills Experience 12 to 15 years of work experience. 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).

Job Description: Conduct routine quality control tests on raw materials, in-process products, and finished goods. Analyze test results and maintain accurate records of all quality control activities. Ensure compliance with internal and external quality standards and regulations. Familiarity with regulatory standards and laboratory accreditation processes. (e.g., ISO, GMP). Collaborate with production and R&D teams to troubleshoot quality issues and implement corrective actions. Assist in the development and validation of new testing methods and protocols. Monitor and report on quality metrics and trends, recommending improvements as necessary. Maintain laboratory equipment and ensure proper calibration and maintenance. Participate in internal and external audits related to quality control. Provide training and support to staff on quality control procedures. Strong knowledge of quality control methodologies and laboratory practices. Proficient in using laboratory instruments and software for data analysis. Excellent attention to detail and problem-solving skills. Strong communication and teamwork abilities Education: : B.Sc / M. Sc (Chemistry) Role: Chemist – Quality Control Industry Type: Ion exchange Resins, Chemicals, Water Treatment, Wastewater Treatment Functional Area: Quality Checks, Conducting tests, Running Test Cycles, etc Job Types: Full-time, Permanent, Fresher Pay: From ₹150,000.00 per year Benefits: Health insurance Ability to commute/relocate: Sanand, Gujarat: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: Quality control: 1 year (Required) Compliance management: 1 year (Required) Laboratory Testing: 1 year (Required) Chemist: 1 year (Required) Work Location: In person

We're Hiring: Innovative Diploma Electrical Engineer (Arduino & Interactive Tech) Urbanmistrii is seeking a dynamic and technically skilled Diploma Electrical Engineer to join our team in New Delhi. If you thrive on bringing creative concepts to life through electronics, coding, and immersive installations, this is your opportunity! Location: New Delhi Employment Type: Full-time Salary: ₹18,000 – ₹25,000/month Experience: 0–5 years About Urbanmistrii: At Urbanmistrii, we specialize in transforming spaces and experiences with cutting-edge digital art and smart installations. We're where creativity meets technology, and we're looking for someone excited to push those boundaries with us. The Role: This position is perfect for a hands-on engineer eager to experiment with microcontrollers, sensors, and lighting, turning imaginative designs into tangible, interactive realities. You'll be instrumental in developing smart environments, digital artworks, and bespoke interactive features. Key Responsibilities: Develop & Program: Design, program, and debug Arduino (and similar microcontroller) setups for intricate interactive lighting, motion, and sensor-based installations. Circuit Design & Wiring: Precisely design and implement digital and analog wiring for various components including sensors, addressable LEDs, relays, stepper/servo motors, and custom control systems. Installation Support: Provide critical electrical and technical support for on-site setup, calibration, and commissioning of complex interior and art installations. Interdisciplinary Collaboration: Work closely with a diverse team of designers, architects, and artists, translating their artistic visions into functional technological solutions. Troubleshooting & Optimization: Diagnose and resolve electrical, wiring, and programming issues efficiently on-site to ensure seamless project delivery. What You Bring: Educational Foundation: Diploma in Electrical or Electronics Engineering. Microcontroller Proficiency: Solid practical understanding and hands-on experience with Arduino programming, including basic C/C++ development. Digital Electronics Experience: Proven experience working with digital sensors, relays, various types of LEDs, and motor controls (stepper/servo). Technical Acumen: Ability to accurately read, interpret, and implement electrical wiring diagrams and circuit schematics. Creative Drive: A genuine passion for creative technology, experimental electronics, and transforming ideas into interactive experiences. On-site Adaptability: Comfortable and willing to work on-site across the Delhi-NCR region as required by projects. Bonus Points (Good to Have): Familiarity with Raspberry Pi or ESP-based microcontroller systems. Prior experience in developing projects for exhibitions, museums, or digital art installations. Ignite Your Passion: If you're energized by the possibilities of wires, code, and transforming ambitious creative concepts into stunning, working installations, then we want to connect with you! Ready to innovate? Email your application to: mail@urbanmistrii.com

Job Role : Sr.Manager - Production (QMS) Location : Paonta Sahib Qualification : B.Pharm / M.Pharm Experience : 15 to 18 Yrs Job Responsibilities To ensure continuous improvement in achievement of productivity, manufacturing yields & quality norms; Launch of new products 100% in time. Quality: Demonstrate compliance to established Manufacturing Operations and Quality Standards. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. Strive for reduction in Out of Specification, Deviations, reduce Market complaints. Document Integrity: To support compliance of practices to established procedures and Good Manufacturing Practice standards. To approve the SOPs & format, batch records relating to production operations and to ensure their strict implementation. Cost: Overhead recovery, and manufacturing efficiency to be maintained. Cascading Sun Values and culture to the root level. People Development: Develop Talent pipelines for level II, III & IV key jobs. Monitoring and control of the manufacturing environment; Process validation and calibration of analytical apparatus; Designation and monitoring of storage conditions for materials and products; compliance with GMP requirements. To ensure the qualification and maintenance of department, premises and equipment. To ensure that the appropriate validations are done. Retention of records; Performance and evaluation of in-process controls; Training, including the application and principles of QA; To design and implement the policies, systems and procedures as required for the efficient management of the shop floor.

Job Role : Production Head Job Grade : General Manager (G7) Location : Paonta Job Responsibilities To ensure delivery of products in time, of desired quality and quantity at optimum cost. Commit to Demand & Supply to commit as per Key Performance Indicator targets. To ensure continuous improvement in achievement of productivity, manufacturing yields & quality norms; Launch of new products 100% in time. Quality: Demonstrate compliance to established Manufacturing Operations and Quality Standards. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. Strive for reduction in Out of Specification, Deviations, reduce Market complaints. Document Integrity: To support compliance of practices to established procedures and Good Manufacturing Practice standards. To approve the SOPs & format, batch records relating to production operations and to ensure their strict implementation. Cost: Overhead recovery, and manufacturing efficiency to be maintained. Cascading Sun Values and culture to the root level. People Development: Develop Talent pipelines for level Il, Ill & IV key jobs. Monitoring and control of the manufacturing environment; Process validation and calibration of analytical apparatus; Designation and monitoring of storage conditions for materials and products; compliance with GMP requirements; To ensure the qualification and maintenance of department, premises and equipment. To ensure that the appropriate validations are done. Retention of records; Performance and evaluation of in-process controls; Training, including the application and principles of QA; To design and implement the policies, systems and procedures as required for the efficient management of the shop floor. To co-ordinate with other departments to control costs to meet the business goal. To plan for budgetary expenses and control them. To enhance the productivity by working on different projects.

Job Summary The position is responsible for heading the Quality Assurance function in NOSD Parenteral Block at Sun Pharma laboratories Limited, Guwahati Responsible to set the team goals and objectives for the NOSD Quality at Guwahati site in alignment with goals of Cluster Quality and other business function(s). Responsible to collaborate and support to functional heads of QA, QC, Microbiology, Production, IT, Regulatory Affairs and commercial department to align organizational goal and business strategies for achieving overall quality. Responsible for providing guidance to ensure achievement of targeted completion of tasks and execution of team. Responsible for facilitate harmonization and consistent implementation or Quality Systems and procedures (Pertaining to parenteral), in alignment with Global Quality Policies, Standards and applicable SOPs. Essential Job Functions: Primary Responsibility: Review and monitoring of Quality operations at Parenteral Block. To execute, monitor, review, and approval of Quality management systems i.e. Change control, Deviation, and CAPA management as per requirements. To review and approve Standard Operating Procedure etc. To ensure the compliance of documentation at various stages of the process i.e. (Manufacturing, Filtration, Filling, Visual Inspection, Labelling and Packing operations). To review, approve the Master and executed BMR, BPR, Validation, Qualification and other GMP documents. To evaluate and monitor the Aseptic process simulation (Media Fill) activities with respect to the APS planner, Trending of intervention protocol & reports. To facilitate harmonization and consistent implementation of the quality systems and procedures at the site in alignment with corporate quality policies /procedures. To review, update, respond to GQS/Regulatory audit observations within the stipulated time frame. To participate in the review & approval of investigation in case of Non- conformance events i.e. Process Deviation, OOS, OOT & Product Quality Complaint. To ensure release, approval, or rejection of Raw Material, Packing Material, Intermediate, Finished products as per approved specifications. To ensure completion and implementation of CAPA as per established procedure and follow up to verify the effectiveness of CAPA. Responsible for the batch disposition (Batch release or reject). To ensure compliance of electronic systems such as manufacturing equipment/instruments etc. To ensure equipment /instrument, qualification/calibration and prevent maintenance are performed as per approved planner. To ensure that processing and storage area are qualified as per the approved procedure and GMP requirements. To impart training to the plant personnel as per requirement and ensure the effectiveness. To be part of self-inspection and or quality audits that regulatory appraises the effectiveness and applicability of the quality system as per schedule. To ensure and perform work as per established approved procedure, regulatory norms and its compliance as per the current regulatory requirement. Facilitate/support the implementation of new initiatives of Corporate functions at site. Secondary Responsibility Specific emerging projects as applicable. Perform any other responsibility assigned by the Quality Head/Management.

Job Description Position: QA Sterile Manager Department: Quality Assurance Designation: Manager - I Education Qualification: M.Sc. in Biotechnology / Microbiology / Chemistry Total years of Experience: 10+ Years Job Role: Management of Quality Assurance functions of Manufacturing Block – P. Responsibilities Ensure that manufacturing and packing of the batch is executed and records are completed and reviewed in accordance with established SOPs and cGMP regulations. Conduct certification of batch production records for compliance and stage-wise completion. To release / reject the Batch after complete review of batch and related quality documentation. Tracking and monitoring of QMS system. Ensure logical closure of deviations and investigations of related product before release. Conduct thorough investigations along with production for any complaints / deviations/ OOS / stability failure for products manufactured at the site and logical / timely closure of Complaints. To ensure contamination controls implemented and followed at site as per contamination controls strategy (CCS) and respective procedures. Work directly with planning, QC, other QA functions, and Regulatory Affairs to ensure Batches are released to meet supply chain requirements. Participate in self-audits of facility and equipment in partnership with Manufacturing and Engineering to ensure readiness for operations. Participate in Aseptic simulation (Media Fill) activity, Monitoring and Implementation for PENEM DF. Identify continuous improvement opportunities to improve compliance, process clarity, and operational efficiency. Review and approve master batch production records (Manufacturing / packing) and SOPs. Review and approve equipment qualification & process validation protocols and reports for accuracy, completeness, and traceability as well as adherence to protocol / procedures. Review and approve Annual Product Review (APR) reports for the products as per the schedule. Stability sample management of finished goods. Management of control sample pertaining to collection, review, storage and destruction. Management of line clearance, in-process check, coding approval and water sampling. Review and approval of IPQA instrument calibration record. Management of IPQA activities for Block-Penem. Review and approve artwork of Packaging material, STP and Specification. Provides appropriate training and development to support staff to meet their respective job responsibilities. Work in partnership with Manufacturing, Engineering, and QC to increase knowledge and understanding of cGMPs and improve practices and procedures. Review activities related to the Microbiology Laboratory. Review activities related to the beta-lactam containment monitoring. Compliance with Quality Policy of the organization. Improvement of System and procedures, Quality of products manufactured and delivered.

Job Description Position : Microbiology Head Reports to: Quality Head Department: Quality Grade: G8 Functional Area: QC - Microbiology Location: Dewas Position Summary Manage overall site microbiology department wrt sampling, testing, planning, qualifications, media fill program ( for sterile manufacturing),compliance and upgrades of facilities and procedures. Conduct effective review of team and portfolio, provide direction and guidance to the team and develop team competence with the objective of ensuring the quality of products released with adherence to GMP norms and timelines The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, Standard and Procedures. Key Responsibilities Provide leadership and direction to achieve all quality goals. Manage & Organize timely microbiological sampling, testing and release of raw materials, finished product, commercial stability, Exhibit stability, miscellaneous samples. Manage & Organize timely Microbiological sampling, testing and release of water and Utility samples. Manage & Organize timely Microbial Environmental Monitoring of passive air/active air/ Compressed air/equipment surfaces /personnel monitoring & Drain points of manufacturing blocks, warehouses & Microbiology lab etc. Monitoring effectiveness of the disinfectants used at the site and make appropriate timely change to the ineffective proved disinfectants. Manage & Organize timely handling & maintenance of microbial cultures. Isolation & identification of microbial isolates from various sources. Manage & Organize timely laboratory investigation of out of specification results /Out of trends/Out of limit, root cause analysis and Risk assessment and Health hazard evaluation of identified microorganisms. Participate in internal, external and/or regulatory inspections of Microbiology operations at the site. Learn from external regulatory audit observations and implement Global CAPA and local CQA observations CAPA in micro lab Ensure trend and annual summary reports of water/microbial environmental monitoring/Microbial isolates etc. Ensure calibration, validation and qualification of laboratory equipment/instrument. Ensure timely availability of laboratory Chemicals, media/ stationary/ gloves and Consumable. Ensure consistency in Microbiology lab operations and drive continuous improvements in laboratory performance. Ensure compliance to cGMPs and applicable safety standards in the Microbiology laboratory. Train microbiologist about the microbiological techniques, aseptic practices, critical quality management skills, including decision-making, handling of quality exceptions, staff development, personnel and planning, etc. Managing people on a day-do-day basis. Preparation of annual capex & revenue budget for microbiology section. Ensure adherence to approved budget work plan. Oversee that the cost of testing is controlled in microbiology lab. Liaison with Corporate Micro team to implement microbial risk assessment program and work to mitigate effective CAPA’s to prevent failures. Minimum Education/Experience Requirements Microbiology Graduateor Equivalent Minimum 15years With Microbiology Work Experience Preferred REQUIRED SUCCESS ATTRIBUTE Knowledge Of GxP’s, CGMP And Other Regulatory Requirements. Compliance Collaboration Accountability Customer service orientation Planning and prioritization Secondary Success Attributes Attention to detail People connect Emotional control Effective communication Problem solving Roles

Job Description Position: Engineering Penem Head Department: Engineering and Projects Designation: Senior Manager – II Total Years of Experience: 15+ Years Education Qualification: B.E. in Electronics Job Role: Accountable for Engineering and Maintenance related activities for Block P (Sterile), Block F (OSD), Supporting Facilities (Micro/Stability, QC, Warehouse and Export Warehouse) and External area. Site Projects, Process Control System (PCS) Validation and Support to IT Compliance. Responsibilities Overall responsible and accountable for engineering and maintenance related activities of Block P (Sterile), Block F (OSD), Supporting Facilities (Micro/Stability, QC, Warehouse and Export Warehouse). Overall responsible and accountable for upkeep of external facility of site. Maintain the expense (Power/ Fuel/ Water/ Spares/ R&M) within the budget. Review and effectively implementation of Preventive Maintenance, Facility Maintenance and Calibration System. Promptly attend the maintenance related work of equipment’s/ system/ Facility to minimize the losses. Analysis of plant breakdowns, and initiate corrective measures for prevention, maintain MTTR within the specified limit. Maintain the HVAC; maintain the environmental condition in the manufacturing area as per specifications. Site Project and Site upkeep project management. Prepare Monthly Engineering Update for SGO. Spare requirement assessment and procurement initiation. Continuous evaluation/ maintenance of engineering equipment/ facility. Engineering drawing management. Vendor bill approval, GRN Verification. Ensure compliance to engineering regulatory requirement in the manufacturing. Ensure implementation and Compliance of SOPs. Ensure data integrity visibility at workplace. Extend support in qualification and Validation. Manage the Process Control System Validation activities at site. Provide support to IT Compliance. CAPA, Deviation and Change Control Management of Engineering Department. Maintain the safe working condition in the area and compliance to EHS SOPs. CSP development and assessment. Provide support to Scrap Management. Educating and trained to all the engineering persons including engineering CSPs for compliance. To ensure contamination control are available and followed at site as per Contamination Control Strategy (CCS) and respective procedures. People Development – Knowledge sharing with team to improve the technical competency level. Time to time guidance to subordinate for proper planning and excel the individual and team performance. Motivate the team and develop team spirit among the departmental people. SME Management, represent engineering department during various inspections.

Job Description: As a Field Service Engineer at AguaClan, you will be responsible for the installation, maintenance, troubleshooting, and repair of our water purification systems at customer locations. You will play a key role in ensuring the highest standards of service and customer satisfaction, ensuring the optimal performance of our products. Key Responsibilities: Installation & Commissioning: Install and commission water purification systems at customer sites, ensuring adherence to quality and safety standards. Maintenance & Troubleshooting: Conduct routine maintenance checks and troubleshoot any issues with water purifiers. Perform necessary repairs and system upgrades. Customer Support: Provide on-site technical support to customers, addressing their concerns and resolving any technical issues related to water purifiers in a timely manner. Product Testing & Calibration: Perform testing, calibration, and quality checks on equipment to ensure proper functionality and optimal performance. Documentation & Reporting: Maintain accurate service reports, job logs, and documentation of repairs or replacements performed. Submit detailed reports to the management on a regular basis. Training & Guidance: Educate customers on product operation, maintenance practices, and safety procedures. Provide hands-on training to clients as required. Inventory Management: Keep track of inventory and spare parts for the systems to ensure availability when required. Manage stock efficiently to avoid delays in servicing. Upgrades & Recommendations: Identify and recommend system upgrades or additional services based on customer needs and requirements. Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Health insurance Provident Fund Ability to commute/relocate: Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): What is your Current Salary (Per Month)? What is your Expected Salary (Per Month)? What is your notice period? Experience: Total: 1 year (Required) Field service: 1 year (Required) Work Location: In person

Exciting Opportunity for Physical Verification Engineers ! Elevate your career with Digicomm Semiconductor Private Limited and take the next leap in your professional journey. Join us for unparalleled growth and development. Responsibilities:- Design Rule Checking (DRC): Run DRC checks using industry-standard tools to identify violations of manufacturing design rules. Collaborate with layout designers to resolve DRC issues. Layout vs. Schematic (LVS) Verification: Perform LVS checks to ensure that the physical layout accurately matches the schematic and that there are no electrical connectivity discrepancies. Electrical Rule Checking (ERC): Verify that the layout adheres to electrical constraints and requirements, such as voltage and current limitations, ensuring that the IC functions as intended. Design for Manufacturing (DFM): Collaborate with design and manufacturing teams to optimize the layout for the semiconductor fabrication process. Address lithography and process variation concerns. Process Technology Calibration: Calibrate layout extraction tools and parameters to match the specific process technology used for fabrication. Resolution Enhancement Techniques (RET): Implement RET techniques to improve the printability of layout patterns during the photolithography process. Fill Insertion: Insert fill cells into the layout to improve planarity and reduce manufacturing-related issues, such as wafer warping and stress. Multi-Patterning and Advanced Nodes: Deal with challenges specific to advanced process nodes, including multi-patterning, coloring, and metal stack variations. Hotspot Analysis: Identify and address potential hotspot areas that may lead to manufacturing defects or yield issues. Post-Processing Simulation: Perform post-processing simulations to verify that the layout is compatible with the manufacturing process and does not introduce unwanted parasitics. Process Integration Checks: Collaborate with process integration teams to ensure the smooth integration of the design with the semiconductor fabrication process. Documentation: Maintain detailed documentation of verification processes, methodologies, and results. Qualifications:- BTECH/MTECH Experience:- The Engineers with 5+ years of Experience Location:- Bangalore/ Noida

Characterization of RLD pack samples. Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement. Identification of new packaging material & new vendor development for packaging materials. Mold development for primary packaging material & secondary packaging material & its validation. Support to Regulatory team on ANDA’s/NDA’s filling for regulated market. Coordination with NPI & planning team for launch of ANDA’s/NDA’s. Preparation & revision of packaging material specification. Preparation & review of MPC, FMEA, TA, DHF & AFMEA. Preparation & review of Development Study protocol & report & execute the study. Performing functional test as per regulatory requirement. Coordination with Cross functional team like (FDD/RA/Plant/Marketing/PMO) for completion of task. Participating in FAT of machines. Support to plant for validation, trouble shooting and market complaints. SOP preparation, periodic review and packaging lab equipment handling/maintain calibration records. Preparation of Packaging documentation (Pack Style, Justification Report etc. as per Product/Regulatory) as required. Handling of primary and secondary packaging material in storage area & maintaining the PM quantity for stability packaging at R&D.

Development & Qualification of multiplex based cytokine release assay and Elispot/ flow cytometry based T cell assays to measure the innate and adaptive Immunogenicity of synthetic peptide products Job Responsibilities Manage the study sample analysis for pipeline products, preparation of study schedule, design of experiments, trouble shooting, data analysis and review of reports. Isolation of PBMC from whole blood and maintenance of commercial cell lines. Coordinate with internal and external stakeholders for reagent procurement, blood collection, instrument installation and calibration. Statistical analysis of data using software. Preparation/ review of standard operating procedures (SOP), method development reports (MDR), sample analysis report (SAR) and analytical test procedures (ATP). Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations. Responsible for the operation and maintenance of the Flow Cytometry, Multiplex, ELISPOT and other instruments and statistical software. Managing of chemicals, consumables & critical reagents inventory. Performing calibration of instruments and equipment. Troubleshooting instrument performance and equipment issues. Draft responses for regulatory queries and facilitate internal and external audits.

Key Responsibilities The candidate is expected to develop LC-MS based methods for protein and peptide product characterization. The candidate is expected to qualify the methods for intended purpose for all pipeline products. The candidate is expected to design and implement integrated strategies, linking appropriate chromatography and mass spectrometry tools, to perform a qualitative and quantitative assessment of product related variants and impurities. Develop and apply novel sample preparation with emphasis on LC-MS, CEX-MS, SEC-MS Characterization of innovator product batches sourced from different geographical region and preparation of quality target profile. Responsible for designing advance workflows such as multi-attribute methods for PTMs, sequence variants, qualitative and quantitative profiling of HCPs, Disulfide shuffling and bond analysis, cell culture metabolite analysis, glycan analysis etc. Preparation and review of method development reports (MDR) and analytical test procedures (ATP). Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations. The candidate is responsible for the operation and maintenance of the MS instruments To manage chemicals,consumables & critical reagents inventory. Performs calibration of instruments and equipment. Troubleshoots instrument performance and equipment issues. Responsible for managing the regulatory queries. The candidate is expected to draft the technical content for regulatory dossier. Educational Qualification M.SC./M.Tech in Biochemistry / Life Sciences / Biotechnology. Technical/functional Skills Sound knowledge of analytical method development, qualification and structural and functional characterization of therapeutic proteins. Experience of biosimilarity assessment of biologics for regulated market is desirable. Experience of analytical development for monoclonal antibodies and fusion proteins and peptide is highly desirable.

Key Responsibilities The candidate is expected to develop LC-MS based methods for protein and peptide product characterization. The candidate is expected to qualify the methods for intended purpose for all pipeline products. The candidate is expected to design and implement integrated strategies, linking appropriate chromatography and mass spectrometry tools, to perform a qualitative and quantitative assessment of product related variants and impurities. Develop and apply novel sample preparation with emphasis on LC-MS, CEX-MS, SEC-MS Characterization of innovator product batches sourced from different geographical region and preparation of quality target profile. Responsible for designing advance workflows such as multi-attribute methods for PTMs, sequence variants, qualitative and quantitative profiling of HCPs, Disulfide shuffling and bond analysis, cell culture metabolite analysis, glycan analysis etc. Preparation and review of method development reports (MDR) and analytical test procedures (ATP). Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations. The candidate is responsible for the operation and maintenance of the MS instruments To manage chemicals, consumables & critical reagents inventory. Performs calibration of instruments and equipment. Troubleshoots instrument performance and equipment issues. Responsible for managing the regulatory queries. The candidate is expected to draft the technical content for regulatory dossier.

Position: Site QA Head Reports to: Site Quality Head Department: Quality Location: Halol Position Summary Manage overall quality assurance oversight and site activities wrt to quality systems: documentation review and SOP update, in-process quality assurance, sampling and batch release, preventive maintenance/calibration/qualification/validation, internal audit, compliance, quality oversight of electronic systems, budget, and continuous improvement of quality systems, RA support, monitoring of pest control, retention sample management as per Good Manufacturing Practices requirements. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures. Key Responsibilities Responsible for defining operational strategy and road map for quality assurance management at site. Define site quality assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at site. Provide strong leadership and expertise to ensure achievement of all Quality Assurance accountabilities at site. Identify and implement solution for improving existing site quality assurance systems and processes. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. Ensure that performance issues are managed in a consistent and timely manner. Develop site quality assurance revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams. Responsible for executing Quality Management Reviews at site, monitor individual Performance and set improvement areas. Responsible for ensuring market complaints, failures, deviations are investigated and corrective and preventive actions are implemented as per set timeline. Responsible for ensuring compliance to regulatory requirements on product, process and release procedures. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. Responsible for ensuring smooth collaboration with all Sun Pharma sites and leveraging synergies. Review & tracking of quality assurance metrics e.g. deviation, change control, OOS/OOT, CAPA effectiveness, market complaints with site manufacturing / QC Management and driving them down. Ensure processes for supply chain management / Global Material Sourcing for vendor selection is followed for vendor selection, qualification and monitor vendor quality performance Provide inputs to manufacturing, R&D and PDL work processes to ensure Quality by Design. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and QA systems at the site. Facilitate internal and regulatory agency audits, ensuring that findings from site audits are understood, assessed and addressed site wide in a comprehensive manner. Monitor industry trends/issues faced internally and identify scope for improving Site quality assurance management and processes. Responsible for fulfilling all training requirements of quality assurance employees. Ensure the quality policies, standards and procedures for computerized systems are implemented and adhered at site. Ensure all GxP computerized systems are validated in compliance with the quality policies, standards and procedures and are maintained in validated state throughout the lifecycle with adequate security and controls to ensure data security. Review and approve the documents as per quality procedures. Work in partnership with the site cross functions and corporate functions for implementation of new initiatives. Minimum Education/Experience Requirements B.Pharm / M.Pharm 17 to 18 Yrs ( with QA experience in - OSD)

Job Description Candidate should have sound knowledge about upstream process development (Cell culture and Fermentation). Hands on experience of shake flask studies including sample analysis and documentation. Experience in handling and operation of cell culture and microbial related experiments in bioreactor including sample analysis and documentation. Aseptic handling of seed inoculum and its maintenance Independently handle media and feed preparation for conducting studies. Should be able to trouble shoot in case of any deviation from process/parameter. Good documentation practice. Should be able to perform cell culture (IPQC) analysis. Preparation of SOP, Support for Equipment qualification, Calibration pertaining to Upstream process as per laid down procedures Ensure quality compliance in Biotechnology Upstream laboratory as per Quality standards requirements

Position Senior Manager - QE Job Grade G9B - Senior Manager 2 Function Engineering & Projects Location: Central or South India (Greenfield Project) Job Summary QE (Quality Engineer) Lead's responsibilities encompass leading a QE team, defining quality standards, developing testing strategies, and ensuring software quality throughout the development lifecycle. Areas of Responsibility To aware about the process like vial washing, depyrogenation, filtration, filling, manufacturing, lyophilizer, component washing and sterilization,terminal sterilization, isolators, CIP SIP skid, leak test, X ray inspection, VHP, clean utility like Clean steam, compressed air, PW and WFI generation system, AHU, FFM, To handle the designing and qualification activity of Utility like Pure steam generation and distribution system, Purified water and WFI generation and distribution system, Nitrogen and compressed air generation and distribution system, AHU, FFM, LAF, area, cold storage etc To handle preparation, review and execution of qualification protocol of new equipment like, User requirement specification, Design qualification, Installation qualification, operational qualification, performance qualification and Computer system validation and qualification To prepare and execution of schedule requalification protocol of equipment’s and utility. To prepare new standard operating procedure for qualification activity and also review SOP of process equipment’s. To handle communication with vendor and procurement team on design parts of new equipment’s. Issuance, retrieval and storage of qualification documents. Exposure of regulatory auditors like USFDA, EU, ANVISA, CANADA etc. To handle the designing and qualification activity of process equipment’s like vial washing, tunnel sterilizer, filling machine, capping machine, Lyophilizer loading and unloading system, Lyophilizer, filtration skid, and isolators, VHP passbox, manufacturing skid, suspension manufacturing skid, CIP SIP skid for manufacturing and filtration equipment’s, dispensing isolators, manufacturing isolators, pH meter, DO meter, integrity tester, Autoclave, Terminal sterilizer, ultrasonication machine, GMP washer, external washing machine, leak test and X ray inspection machine, packing equipment’s etc. To handle indenting to procurement of accessories and equipment’s required for qualification activity of above equipment’s and area. To prepare schedule for qualification activity, calibration activity, updation of status label of qualification activity etc. To handle the QMS documents like change control, CAPA, risk assessment, deviation etc. To handle the QMS documents like change control, CAPA, risk assessment, deviation etc. To ensure compliance to cGMP and documentation for various qualification activities. Ensure proper planning and execution of the qualification activity in accordance with the plan and allocation of man power. Travel Estimate Medium Job Requirements Educational Qualification B. Pharmacy, M. Pharmacy Skills Technical Skills/Competencies (Software packages, experience with specific machines etc.) Excellent communication skills, strong collaborator, problem solving, interdepartmental coordination, team leadership. Experience (15 to 17 Years of experience in relevant field in Pharmaceutical Industry.)

Minimum 5+ years of relevant experience in SAP PP/ QM and well-versed in S4 HANA/ ECC with good analytical skills along with domain experience in manufacturing industry Experience in Implementation and Support Projects. In-depth knowledge in the below areas: Master Data - Bill of materials, Work centers/ Resources, Routings/ Recipe, Production versions, Inspection Plan, Master inspection, Characteristics, Catalogues and Code groups Material Requirement Planning - Configuration and Integration with, Procurement, Sales and Distribution, New strategy definition Production Order Execution - Order confirmation, Goods issue, Goods receipt and Back flushing Quality Management - Quality in Procurement, Quality in Production, In process inspection, Calibration and Quality in Sales Should have experience in writing Functional Specification, co-ordination with ABAP team, testing of new functionalities. Must have experience in SAP PP-QM integration with third party tool A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to get to the heart of customer issues, diagnose problem areas, design innovative solutions and facilitate deployment resulting in client delight. You will develop a proposal by owning parts of the proposal document and by giving inputs in solution design based on areas of expertise. You will plan the activities of configuration, configure the product as per the design, conduct conference room pilots and will assist in resolving any queries related to requirements and solution design You will conduct solution/product demonstrations, POC/Proof of Technology workshops and prepare effort estimates which suit the customer budgetary requirements and are in line with organization’s financial guidelines Actively lead small projects and contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Ability to develop value-creating strategies and models that enable clients to innovate, drive growth and increase their business profitability Good knowledge on software configuration management systems Awareness of latest technologies and Industry trends Logical thinking and problem solving skills along with an ability to collaborate Understanding of the financial processes for various types of projects and the various pricing models available Ability to assess the current processes, identify improvement areas and suggest the technology solutions One or two industry domain knowledge Client Interfacing skills Project and Team management