37 Isolators Jobs

Key Responsibilities: Promote and sell containment equipment and solutions including isolators, RABS, glove boxes, sampling/dispensing booths, and other high-containment systems for HPAPI and potent compound handling. Identify key prospects in pharmaceutical, biotech, chemical, and API manufacturing sectors, and develop strong customer relationships. Collaborate closely with the regional sales teams to qualify leads, conduct site visits, deliver technical presentations, and secure orders. Understand client-specific containment requirements and recommend suitable solutions in collaboration with engineering and applications teams. Lead the techno-commercial discussions and drive projects through the sales cyclefrom inquiry to order finalization. Maintain a strong understanding of containment trends, regulatory requirements (such as OEB/OEL classifications), and evolving customer needs. Participate in industry exhibitions, seminars, and technical conferences to represent the company and generate new business leads. Provide market intelligence, sales forecasts, and strategic inputs to support business planning and growth initiatives. Preferred candidate profile Familiarity with high-potency manufacturing environments and exposure control strategies. Understanding of pharmaceutical process flow and integration of containment equipment in production setups. Prior experience dealing with EH&S teams, engineering consultants, and validation teams is advantageous

About Company Job Description • Installation, Operation, maintenance, troubleshooting and commissioning of 66 / 33 KV GIS and above switchyard with all associated equipment’s i.e. CB, CT, PT, LA, Isolator, CVT, Protection relays, CRP Panel, RTCC panel,25MVA Transformer, SCADA, SAS and battery charger Panel with battery. • Testing, Commissioning, relay setting, troubleshooting of Protection relays, PLC and SCADA system. • Fault analysis of various electrical faults in electrical system. • Operation and maintenance of 33KV, 11 KV HT switchgear panel, Fast bust transfer system,11KV Motor, 33/11KV & 33/0.400 KV Transformers, NGR, PCC, MCC Panel, AMF Panel, Synchronization Panel, LT motors and VFD drives. • Operation, maintenance, commissioning and troubleshooting of DG and UPS system. • Operation, maintenance, commissioning and troubleshooting of Large utility System, i.e. Air compressors, HVAC, PEN, PUW, PEX, N2 generation plant and other associated equipment’s with Electrical system. • 7.Effective operation and maintenance for HT/LT Electrical System. • Spare and Inventory management for electrical System in SAP/ERP system. • Training to Sub ordinates. • IMS implementation with preparation of SOP, Work instruction, maintenance schedule, 5S etc. • 11.Preparation & Monitoring of Energy reports with cost saving analysis. • 12. Implement safety culture within department and organization. • 13.Hands on experience of Erection, testing commissioning and operation and maintenance of Power distribution & Utility electrical System including SCADA and SAS.

The ideal candidate for this position should hold a B.E./BSc/ Diploma in Electronics with 1-4 years of experience. This role is specifically for males and involves designing SMPS, DC-DC Converters, AC-DC Converters, Inverters, and UPS. The responsibilities include day-to-day tasks such as tracking new and old designs, designing schematics, and working on Power-based circuits from requirements to testing and debugging. The candidate should have expertise in power devices like Thyristors, MosFETs, IGBTs, interface circuitry, and troubleshooting noise and other issues. Preferred candidates will have experience in 3PH, 1PH design and operation in Power circuits. Desirable skills include experience in PCB layouts, type testing of units, and proficiency in using test equipment like DMMs, DSOs, etc. While travel is not a regular requirement for this role, occasional travel may be necessary for debugging or project trials on site.,

Role & responsibilities Responsible for executing hormonal API production activities as per cGMP guidelines. Must have hands-on experience in operating isolators and handling high-potent compounds safely. Ensure compliance with SOPs, batch records, and maintain clean-room discipline. Should be familiar with equipment operation, in-process checks, and documentation practices

Role & responsibilities Responsible for executing hormonal API production activities as per cGMP guidelines. Must have hands-on experience in operating isolators and handling high-potent compounds safely. Ensure compliance with SOPs, batch records, and maintain clean-room discipline. Should be familiar with equipment operation, in-process checks, and documentation practices

The Jhagadia Float Glass manufacturing unit of Saint-Gobain India Pvt Ltd Glass Business is a strategic investment of Saint-Gobain in western India, acquired in 2011 from erstwhile Ms. Sezal Architectural Glass. Situated in Central Gujarat in Jhagadia of Bharuch District, this state-of-the-art float glass plant spans across 150 acres. It has the capacity to produce 550 MT of clear glass per day, known for its high quality benchmark standard within India and globally, producing clear glass with less than 650 ppm of Iron. Saint-Gobain Jhagadia takes pride in setting a benchmark for its TVC campaign of Clear Glass of 654 PPM. The campus also houses an in-house Sand Beneficiation plant capable of producing 600 tons of treated sand per day. Over the past decade, Jhagadia glass site has positioned itself uniquely to attract future investments of Saint-Gobain in India. Accolades for Jhagadia: - HR Excellence award from CII in 2017, 2018 & 2019 - WCM Silver Award in 2020, ranking 3rd globally among Glass Plants and 3rd in the SG Plant in India region - Emerald Award for CO2 reduction, a Saint-Gobain Global recognition - An HPR certification from Xcel Catlin - Fostering innovation as culture for Industry 4.0 projects Key Role Responsibilities: - Operation and Maintenance of various equipment including switchyard, switchgears, transformers, motors, cranes, battery systems, PLCs, and more - Maintenance and operation knowledge in gensets, electrical panels, transformers, isolators, and lightning arrestors - Troubleshooting of various machines, circuit theory, and earthing concepts - Expertise in control systems, automation systems, VFD, PLC applications, encoders, feedback sensors, and power systems - Energy calculations and efficiency improvements Required Qualifications: - Diploma in Electrical Engineering from reputed Engineering Institutions with a good academic record - 3-5 years of experience in Manufacturing, Process, or Engineering Industry Required Skills and Attributes: - Ability to deploy functional knowledge effectively - Detail-oriented with strong analytical skills - Team player with multi-cultural compatibility The candidate must be willing to relocate to Bharuch/Ankleshwar and should be comfortable with working in shifts.,

You will be responsible for performing commissioning and qualification of Pharmaceutical equipment, specifically systems for Oral Solid Dosage, Injectables, and Fill/Finish. This includes a variety of equipments such as RMG, CoMil, Tablet press, Coating Machine, blister packing machine, Vial Filling Line, PFS Line, Isolators (Negative & Positive), RABs (Open and Closed), GL Reactors, Dryer, Nutsche Filters, Centrifuges, Lyophilizers, etc. Your responsibilities will include developing CQMP, VMP, FRA, cGMP review sheet, interdependencies, System boundary, URS, SCA/SLIA, CLIA, DQR, SRA/QRA, SAT protocol, commissioning protocol, IQ protocol, OQ protocol, PQ protocol, process validation, and cleaning validation protocol. You will execute Commissioning, qualification, and validation activities for Pharma Process Equipments for API, Fill/Finish, and OSD. Additionally, you will review, analyze, and interpret system performance data, handle deviations/discrepancies, conduct investigations, CAPA, and ensure promotion of cGMP and regulatory compliance in assigned projects. Furthermore, you will exercise good judgment in selecting methods and techniques for obtaining solutions, maintain GDP, ALCOA practices, and have hands-on experience with Pharma Process Equipments. Drafting equipment operation SOPs will also be a part of your role. Qualifications & Other Requirements: - BS/MS in Engineering (Chemical, Pharma). - 4-10 years of experience in validation, quality systems, operations, engineering, or a combination thereof. - Experience in multiple GMP validation disciplines with advanced technical knowledge. - Knowledge of Validation Lifecycle approach, international regulatory requirements, and standards. - Experience with Documentum or Maximo is a plus. - Strong verbal and written communication skills, excellent organizational and time utilization skills. - Ability to work independently and within project teams. - Industry experience related to cGMP drug manufacturing, validation, and chemical process design. - Strong computer knowledge including Microsoft Office products.,

Responsibilities: * Testing, relay/protection systems using switchgear, LV switchgear, MCCBs, circuit breakers, isolators, PTs & CTs. * Perform relay testing and protection relay commissioning. Provident fund Annual bonus Travel allowance Accidental insurance

Role & responsibilities Jr. Operator / Operator / Sr. Operator Vial washing, Depyrogenation, HPHV Steam Sterilizer, Production related activities Experience: 0 - 6 years Qualification ITI/Diploma/B.Sc/Equivalent Officer / Executive Production plan, filling activities, cGMP, SOP, Preventive maintenance, Lyophilizer, Aseptic Media fills, HPHV, Handling Filter integrities, DQ, IQ, PQ, OQ. Experience: 0 - 6 years Qualification B. Pharmacy / M. Pharmacy Asst. Manager / Manager QMS, SOPs, cGMP, DQ,IQ ,PQ, OQ Preventive Maintenance, filling activities, Training plan schedules. Experience 9-15 Years Qualification B. Pharmacy / M Pharmacy Preferred candidate profile Preferrable Injectable / Biological Production Experience

Job Area: Engineering Group, Engineering Group > Software Test Engineering General Summary: This position involves hands on testing for sensors, sensor related features and seamless context exchange between Qualcomm products integrating Qualcomm Sensing Hub. Qualcomm Sensing Hub enables extremely low power context detection and awareness by fusing information from different sensors and radios. The role is an individual contributor as part of an international sensor test team. Daily tasks will include hands-on testing, verification, and calibration of embedded HW integrating sensors, verification and testing of algorithms fusing sensor and radio data, testing features and communication across devices and development and maintenance of automated test cases. Job Function Responsibilities This position involves hands on testing for sensors, sensor related features and seamless context exchange between Qualcomm products integrating Qualcomm Sensing Hub. Qualcomm Sensing Hub enables extremely low power context detection and awareness by fusing information from different sensors and radios. The role is an individual contributor as part of an international sensor test team. Daily tasks will include hands-on testing, verification, and calibration of embedded HW integrating sensors, verification and testing of algorithms fusing sensor and radio data, testing features and communication across devices and development and maintenance of automated test cases. The following defines the main responsibilities: Testing Qualcomm Sensing Hub features for Qualcomm products. Test planning, test case development and execution. This includes hands-on testing with various mobile/handheld products both in lab and in the field. Developing test automation modules for the overall sensor automation framework using C# and Python. Verification and calibration of sensors in embedded HW. Testing communication and information sharing between devices embedding Qualcomm Sensing Hub. Test case automation and maintenance. Triaging issues observed during testing and isolating them into different test framework components, SW modules in embedded target SW or HW itself. Driving the resolution of the observed issues across the sensor and other QCT technology and target teams. Supporting test, SW development and system teams in analysis and debugging of observed issues in embedded targets. Interacting in a global team environment with various test architecture, power, SW, system, test, and test framework teams. Desire to understand in detail the Qualcomm Sensing Hub related SW and HW architectures and embedded SW designs from HLOS all the way down to sensor driver level across various target devices. Skills/Experience A minimum of 1-4 years of Work experience with testing embedded systems and developing automated test cases / automation frameworks for them. Proficiency in C and/or C++. Prior experience with developing and/or debugging embedded code. Prior experience with Android application programming. Previous programming experience with Java, Python, etc. Detail oriented, thorough, and analytical approach required with excellent communication skills. Ability to time-share and prioritize between multiple tasks is crucial. Proven team player that can drive bugs into resolutions across multiple global teams. Excellent understanding of debugging and isolating issues in embedded devices. Basic understanding of different radios (like cellular modem, WiFi, Bluetooth, location), audio and camera features in mobile phone. Familiar with oscilloscope and comfortable working with Qualcomm HW protolab to expose necessarily signals for testing and debugging purposes. Capable to validate and debug simple HW reworks exposing interrupt signals etc. Good understanding of test methodology and test processes, including requirements collection, test plan development, test execution and error tracking. Minimum Qualifications: Bachelor's degree in Engineering, Information Systems, Computer Science, or related field. Preferred Qualifications Previous experience with standard Qualcomm test automation framework and tools (Axiom, QXDM, QDSS, QMITestPro, Crashscope, Trace32) and Qualcomm DIAG implementation. Previous exposure to Sensors (inertial, pressure, magnetic, ambient light, proximity, capacitive, physiological) and associated test equipment beneficial. Previous testing experience with Linux Embedded, Linux Android and Windows mobile devices. Basic understanding of modem, WiFi, BT, audio, camera and location technologies and related test procedures and equipment.

Formulation/ Vaccine/ Sterile Drug Product Manufacturing Qualification requirement: M.Sc/B.Sc (Life Science) B.Pharm/M.Pharm Diploma / ITI (Experience in aseptic operation) Fresher's & Experienced (1 5 Years) Formulation Filling (Vials , BFS, PFS) Vial Washing, Depyrogenation Sealing & Capping Sterile aseptic operation C- Rabs, O-Rabs, Isolator Autoclave operation SOP/BMR/QMS

handle electrical installations, maintenance, and repairs for residential and commercial building projects. Responsibilities include wiring, circuit installation, lighting systems, load distribution, ensuring compliance with safety codes. Required Candidate profile experience in building construction , knowledge of electrical drawings and equipment. (HR- 8810366146)

JD- 1) Oversees the electrical Installation, Commissioning and Maintenance of the Substation, Power Plant. 2) Testing of Transformer, Relay, Circuit Breaker, Motor, Panel etc. 3) Complete power distribution system of industrial installation Required Candidate profile Criteria:- Diploma/ B-tech Electrical Engineer, 0-1 Years experience, Candidate should ready to relocation across India Post- 10 No. CALL:- Namrata- 8910291069 Arijit- 9748042221 Benchmark Global

As a Low Voltage Switchgear Sales executive you will cover Karnataka and Tamilnadu Regions potential customers and contribute to achieving monthly & yearly business plans.

Dear Aspirant , Greetings From Eugia Pharma Specialties Limited (Aurobindo Group)!!!! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit. Department : Quality Assurance (IPQA) No. of Vacancies : 30 Education Qualification : B. Pharmacy / M Pharmacy Experience : 2-5 Years Designation : Executive Required Skills : Aseptic Area Monitoring / Environmental Monitoring / Aseptic behavior / Media Fill / Gowning Practices / Sterility Assurance/ In Process checks in Injectable Work Location : Eugia Unit -3, Pashamylaram Walk In Details: Date : 29.06.2025 Time : 09 AM - 02 PM Venue : Aurobindo Pharma Limited - Unit - 3 Sy. No. 313, Bachupally, Hyderabad, Telangana 500090 Google Map : https://maps.app.goo.gl/qoL8vZ6EwDm5GcWb8 Contact : Mr Prabhakar / Ms Rama

Role & responsibilities Jr. Operator / Operator / Sr. Operator Vial washing, Depyrogenation, HPHV Steam Sterilizer, Production related activities Experience: 1 - 6 years Qualification ITI/Diploma/B.Sc/Equivalent Officer / Executive Production plan, filling activities, cGMP, SOP, Preventive maintenance, Lyophilizer, Aseptic Media fills, HPHV, Handling Filter integrities, DQ, IQ, PQ, OQ. Experience: 1 - 6 years Qualification B. Pharmacy / M. Pharmacy Asst. Manager / Manager QMS, SOPs, cGMP, DQ,IQ ,PQ, OQ Preventive Maintenance, filling activities, Training plan schedules. Experience 9-15 Years Qualification B. Pharmacy / M Pharmacy Preferred candidate profile Preferrable Injectable / Biological Production Experience

Job Summary: Decbectochem is looking for an experienced Fabrication Head to lead our fabrication division. The ideal candidate will bring expertise in fabrication, quality assurance, lean manufacturing, and safety management. This role requires a leader who can optimize fabrication processes, ensure high-quality standards, and drive continuous improvement in manufacturing efficiency. Key Responsibilities: 1. Fabrication & Production Management Lead the fabrication team in manufacturing high-performance industrial products. Optimize processes using lean manufacturing techniques like 5S, Kaizen, JIT Production, and DMAIC. Improve production efficiency while ensuring cost-effective operations. Implement Industry 4.0 practices to enhance automation and digital transformation. 2. Quality Assurance & Compliance Ensure all fabrication work meets company and industry standards. Implement strict quality control measures to minimize defects and rework. Maintain compliance with safety regulations, environmental standards, and company policies. 3. Safety & Training Maintain zero-accident safety practices, ensuring a safe working environment. Conduct safety training sessions (minimum 60 hours per quarter). Implement best practices in workplace safety, including GEMBA walks and POSH compliance. 4. Leadership & Team Management Lead, mentor, and train the fabrication team to improve efficiency and quality. Foster a collaborative work culture, reducing conflicts and enhancing team morale. Manage workforce planning, task delegation, and performance reviews. 5. Process Optimization & Cost Management Reduce fabrication cycle times and minimize material waste. Implement SAP-based production planning (PP Module, QM Basic) for better workflow. Coordinate with procurement teams to ensure timely availability of raw materials. Key Requirements: Education & Experience: B.Tech in Mechanical Engineering or a related field. 6+ years of experience in fabrication, quality control, and manufacturing. Experience with heavy fabrication (pressure vessels, heat exchangers, structural components, etc.). Skills & Competencies: Expertise in fabrication techniques, welding, and inspection methods. Strong knowledge of Lean Manufacturing tools and process improvements. Excellent people management and conflict resolution skills. Proficiency in fabrication software and tools such as AutoCAD, SolidWorks, etc. Strong understanding of safety regulations and quality control procedures. Effective communication and decision-making abilities. Why Join Us? Lead a dynamic and growing fabrication team. Opportunity to implement innovative manufacturing technologies. Work in a safety-first and quality-driven environment. Competitive salary and benefits package. How to Apply: Interested candidates can send their resumes to pravin.shinde@decbectochem.com / harshali.jala@decbectochem.com

Role & responsibilities Job summary We are looking for an individual to perform filling/washing and sterilization operations within GMP (Good Manufacturing Practices), regulatory, and organizational guidelines. The objective is to produce products within defined volumes and timelines, ensuring compliance with quality standards, GMP, and regulatory requirements as per schedule. " Roles & Responsibilities Perform filling, washing, sterilization operations as per the day plan, executing batch production records. Participate in filling area line clearance activities and perform machine cleaning operations. Handle material dispensing and issuance from the warehouse. Issue discrepancies, work with cross-functional departments to close discrepancies, and implement appropriate corrective actions. Compliance with GMP, safety standards, and SOPs (Standard Operating Procedure) for designated manufacturing equipment. Maintain records in machine operation log books. Maintain manufacturing equipment to ensure correct functionality and calibration compliance. Actively engage in validation and qualification activities for all manufacturing area machines. Promote safety awareness and improvements, engage in continuous improvement activities, and adhere to the company's safety rules. Report all unsafe matters, near misses, and accidents. Preferred candidate profile Educational qualification and work experience Educational qualification: A Diploma or B.Pharm. Minimum work experience: 4 to 6 years of experience in batch formulation operations Skills & attributes Technical Skills Proficiency in comprehending and overseeing sterile and fill finish operations in pharmaceutical manufacturing, demonstrating familiarity with the processes involved. Practical experience and hands-on knowledge in executing sterile and fill finish operations, showcasing the ability to actively participate in and manage these critical manufacturing processes. Practical expertise in equipment validation, process validation, and cleaning validation, demonstrating the ability to validate and ensure the reliability of manufacturing equipment and processes. Behavioral skills Effective listening skills, ensuring a comprehensive understanding of information. A keen eye for detail, ensuring accuracy and precision in tasks. Awareness and sensitivity to deadlines, ensuring timely completion of tasks. Analytical skills and the ability to troubleshoot, enabling effective problem-solving. Strong interpersonal skills and the ability to work well in a team, fostering collaboration and positive team dynamics. Location: Pydibhimavaram Dr Reddy's Formulations Limited(DFL-02) Injectable Facility, Aseptic Manufacturing Hiring For : Filling,Compounding,Autoclave,Lyo Operators, PM(Preventive Maintenance),Documentation, MS Office

Formulation/ Vaccine Drug Product Qualification: M.Sc / B.Sc (Micro, Virology, Biochemical) / B.Tech / Diploma Autoclave operation Formulation Filling (Vials , BFS, PFS) Vial Washing, Depyrogenation C- Rabs, O-Rabs, Isolator Sterile aseptic operation Sealing & Capping BMR/ QMS

We are hiring for- Role: Chassis Design Engineer Experience: 8-12 Years Location- Pune Qualification: BE / M-Tech: Mechanical / Automobile Roles & Responsibilities: Design and Development: Create and develop suspension isolators for Engine/HV battery installation, aggregate mounts and related components to minimize vibrations and noise. Design and Development: Chassis aggregates mainly Casting parts and sheet metal parts for the mounting of battery, Engine and other aggregates etc. Design / solution identification as per requirement and align within cross functional department, also interaction with development partners Problem-Solving: Strong problem-solving skills to troubleshoot and resolve issues that may arise during the design, installation, and operation of isolators Must Have: Suspension Isolator Technology: In-depth knowledge of rubber technology, including design principles, operational procedures, and maintenance protocols, Suspension Isolator Dynamics Mechanical Design and Engineering: Proficiency in mechanical design and engineering to create robust and reliable suspension isolator systems for High voltage battery, Engine and other aggregate mounting. Project Coordination: Ability to manage and coordinate activities with cross-functional teams and suppliers for serial changes and within projects. Manufacturing Processes: Understanding of manufacturing processes such as rubber, sheet metal, casting, and machining. CATIA V5 R20: Hands-on experience in CATIA V5 R20 for model preparation using modules like part design, SMD, GSD, assembly, and drawings. Design Documentation: Capability to perform design documentation in PLM and generate Bill of Materials. GD&T: Good knowledge of Geometric Dimensioning and Tolerancing (GD&T) and ability to perform tolerance stack-up analysis. Interpersonal Skills: Strong interpersonal, communication, and presentation skills. Team player. Responsibility and Decision-Making: Willingness to take responsibility and make decisions. Cross-Functional Teamwork: Ability to work in cross-functional teams to support project teams. International Travel: Flexibility for international travel Good to Have: PLM Systems: Knowledge or working experience in PLM systems such as Windchill or OAS. CATIA V5 Simulation: Knowledge of CATIA V5 Simulation Module GAS/GPS.' -- Muugddha Vanjarii 7822804824 mugdha.vanjari@sunbrilotechnologies.com

Should have hands-on experience with Siemens PLC. Should know industrial protocols like TCP IP, Ethernet IP, Modbus TCP IP, Profibus, DNP, RS-485, RS-232. knowledge of Relay, isolators. Required Candidate profile has strong technical skills, has good communication skills. has strong exposure in the Siemens PLC, Relay, isolators etc.

Responsibilities: * Conduct relay testing on panels & breakers. * Test power transformers, circuit breakers, switchgear. * Ensure LT/HT switchgear functionality at switchyards. * Commission transformers, isolators, CTs/PTs. Food allowance Travel allowance Provident fund Annual bonus Life insurance House rent allowance

Biological E. Limited (BE) invites both experienced professionals and fresh diploma holders, as well as graduates and self-driven individuals, to join its Specialty Injectables Business located in Shamirpet, Hyderabad. The available positions are listed below: Injectables QUALITY ASSURANCE : Designation : Executive & Senior Executive Qualification : B. Pharm / M. Pharm / M.Sc. Experience : 3-9 Years Role : IPQA (In process QA Injectables) PRODUCTION PHARMA: Designation : Officer & Senior Officer Qualification : Diploma / B. Sc. Experience : 2-6 Years Role : Filling/Autoclave/Compounding/Lyo PRODUCTION PHARMA: Designation : Executive & Senior Executive Qualification : M. Pharmacy / B. Pharmacy/M.Sc Experience : 2-10 Years Role : Filling/Autoclave/Compounding/Lyo Quality Control: Designation : Executive Qualification : B. Pharm / M.Sc. Experience : 3-6 Years (Injectables) Role : RM/FG/Stability Microbiology: Designation : Executive Qualification : M.Sc (Microbiology/Biotechnology) Experience : 3-6 Years Role : Testing /EM Interested Candidates may Walk-in with an updated Resume, latest increment letter, and payslips for the last 3 months on Sunday, Jun 22, 2025 from 09:00 am to 01:00 pm at Hotel Grace Majestic, Beside Mathany Saldanha Administrative Complex, Ambaji Road, Fatorda, Margao - Goa 403602. Candidates with relevant pharmaceutical experience may walk-in for the interview.

Skilled in installation, maintenance, and troubleshooting of LT panels, MCC panels, DBs, and control panels, Welding machines, press brakes, shearing machines roll forming machines sensors compressors Galvanizing furnace control systems exhaust units

Qualification: BE / M-Tech: Mechanical / Automobile Experience Range: 8 to 12 Years Roles & Responsibilities: Design and Development: Create and develop suspension isolators for Engine/HV battery installation, aggregate mounts and related components to minimize vibrations and noise. Design and Development: Chassis aggregates mainly Casting parts and sheet metal parts for the mounting of battery, Engine and other aggregates etc. Design / solution identification as per requirement and align within cross functional department, also interaction with development partners Problem-Solving: Strong problem-solving skills to troubleshoot and resolve issues that may arise during the design, installation, and operation of isolators Must Have: Suspension Isolator Technology: In-depth knowledge of rubber technology, including design principles, operational procedures, and maintenance protocols, Suspension Isolator Dynamics Mechanical Design and Engineering: Proficiency in mechanical design and engineering to create robust and reliable suspension isolator systems for High voltage battery, Engine and other aggregate mounting. Project Coordination: Ability to manage and coordinate activities with cross-functional teams and suppliers for serial changes and within projects. Manufacturing Processes: Understanding of manufacturing processes such as rubber, sheet metal, casting, and machining. CATIA V5 R20: Hands-on experience in CATIA V5 R20 for model preparation using modules like part design, SMD, GSD, assembly, and drawings. Design Documentation: Capability to perform design documentation in PLM and generate Bill of Materials. GD&T: Good knowledge of Geometric Dimensioning and Tolerancing (GD&T) and ability to perform tolerance stack-up analysis. Interpersonal Skills: Strong interpersonal, communication, and presentation skills. Team player. Responsibility and Decision-Making: Willingness to take responsibility and make decisions. Cross-Functional Teamwork: Ability to work in cross-functional teams to support project teams. International Travel: Flexibility for international travel Good to Have: PLM Systems: Knowledge or working experience in PLM systems such as Windchill or OAS. CATIA V5 Simulation: Knowledge of CATIA V5 Simulation Module GAS/GPS.