Component Engineer Jobs

Required 7 to 10 years of experienced Candidate with mechanical Experience. Address: TEL Components Pvt Ltd (TEL / Client) has its manufacturing facility at Sy No. 308-327 Thimjepal Village Hosur Kelamangalam Denkanikotta Krishnagiri Tamil Nadu India 635113 Facility: TEL JASMINE PLANT HOSUR - HARD FM Qualification: Graduate Experience: 7 - 10 years Source: Sodexo India | Job Code: IJP548584

Need candidate with minimum of 4 years experience in core Address: TEL Components Pvt Ltd (TEL / Client) has its manufacturing facility at Sy No. 308-327 Thimjepal Village Hosur Kelamangalam Denkanikotta Krishnagiri Tamil Nadu India 635113 Facility: TEL JASMINE PLANT HOSUR - HARD FM Qualification: Diploma Experience: 4 - 6 years Source: Sodexo India | Job Code: IJP571489

Need candidate with minimum of 4 years experience in core Address: TEL Components Pvt Ltd (TEL / Client) has its manufacturing facility at Sy No. 308-327 Thimjepal Village Hosur Kelamangalam Denkanikotta Krishnagiri Tamil Nadu India 635113 Facility: TEL JASMINE PLANT HOSUR - HARD FM Qualification: Diploma Experience: 3 - 6 years Source: Sodexo India | Job Code: IJP571611

Need candidate with minimum of 4 years experience in core Address: TEL Components Pvt Ltd (TEL / Client) has its manufacturing facility at Sy No. 308-327 Thimjepal Village Hosur Kelamangalam Denkanikotta Krishnagiri Tamil Nadu India 635113 Facility: TEL JASMINE PLANT HOSUR - HARD FM Qualification: Diploma Experience: 3 - 6 years Source: Sodexo India | Job Code: IJP571612

Need candidate with minimum of 4 years experience in core Address: TEL Components Pvt Ltd (TEL / Client) has its manufacturing facility at Sy No. 308-327 Thimjepal Village Hosur Kelamangalam Denkanikotta Krishnagiri Tamil Nadu India 635113 Facility: TEL JASMINE PLANT HOSUR - HARD FM Qualification: Diploma Experience: 4 - 6 years Source: Sodexo India | Job Code: IJP571488

Superintendent - Mechanical Maintenance oversees the maintenance operations of dredging vessels and associated equipment, focusing on mechanical components like gearboxes and hydraulic systems to ensure fleet reliability and availability. Source: Adani Group | Job ID: 50900

The Lead - Incoming & NDT (QA Blade) manages quality assurance for incoming inspections and non-destructive testing (NDT) of blade components, ensuring compliance with design specifications and industry standards. This role oversees material validation, coordinates NDT processes, manages non-conformances, and maintains comprehensive quality records. The position involves leading and training QA teams, developing inspection protocols, and collaborating with cross-functional teams to enhance the overall quality and integrity of blade manufacturing. Source: Adani Group | Job ID: 28477

Responsible for electrical installation maintenance troubleshooting and repair of electrical systems wiring lighting power equipment control panels and related electrical components. Ensure preventive maintenance identify and rectify electrical faults follow safety procedures and maintain proper records of electrical work. Address: Verna Industrial Area Verna Facility: SIEMENS - IN-GOAV1 Qualification: Graduate Experience: 3 - 8 years Source: Sodexo India | Job Code: IJP569105

Responsible for electrical installation maintenance troubleshooting and repair of electrical systems wiring lighting power equipment control panels and related electrical components. Ensure preventive maintenance identify and rectify electrical faults follow safety procedures and maintain proper records of electrical work. Address: Verna Industrial Area Verna Facility: SIEMENS - IN-GOAV1 Qualification: Graduate Experience: 3 - 8 years Source: Sodexo India | Job Code: IJP569107

Work Flexibility: Onsite 3rd shift: Sunday - Thursday 10:00 pm - 6:30 am What You Will Do: Under general supervision, operate machinery and inspect machined components using precision measuring equipment while keeping accurate production records and maintenance logs Adhere to site specific quality systems and processes Identify and accurately record scrap, maintenance requests, and production documents Operate simple manufacturing equipment, demonstrate machining/mechanical aptitude, and learn new responsibilities and tasks as needed Train others on operational and/or documentation procedures as needed Identify and appropriately report safety concerns, production issues, and documentation errors. Assist execution of continuous improvement projects. Effectively collaborate with peers, functional departments, and visitors of Stryker What You Need: Preferred High School or GED 2+ Years of Manufacturing Experience Blueprint reading, measuring tools – calipers, micrometers, gauges $21.90 + $1.50 Shift Premium per hour plus bonus eligible + benefits. Travel Percentage: None Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate

Responsibilities: Manage the preparation and submission of new product registrations, post approval submission, and follow-up closely on queries and through approval Responsible for reviewing and writing CMC modules 2 and 3 Exposure to EU and CIS region in regulatory filings Herbal product development background Manage and coordinate product life cycle management Ensure regulatory compliance with local regulatory requirements Foster and maintain professional relationships with the health authorities Provide regulatory support including timely registration of new product and line extensions to support new product launches and tender applications when necessary Maintain regulatory work processes and tracking tools that improve performance levels and transparency Exposure in writing of Product Quality Review Promote regulatory intelligence in both local and regional initiatives Develop regulatory strategies, prepare regulatory applications, and support maintenance activities within relevant therapy areas Execution of regulatory strategies (local and regional) that are in line with the business plan Complete regulatory activities for a defined number of products to ensure all regulatory obligations and business objectives are met Ensure adherence to timelines and quality set parameters R eview of formulation, generation of ingredient list, and claims per set standards Compilation and review of labeling components per SOP Deliverables: CMC modules 2 and 3 Management of the preparation and submission of new product registrations, post approval submissions, and follow-up on queries through approval Review of CMC modules Execution of regulatory strategies (local and regional) that are in line with the business plan Compilation of PQR as per SOP – Summary report of variations submitted as per the specified period. Review of formulation, generation of ingredient list, and claims per set standards Compilation and review of labeling components per SOP Experien

Job Title Material Handler 2 Job Description The Material Handler 2 will assist group leads prepare the line for production; they will ensure the correct components have been issued for the work order based on the BOM. The Material Handler will keep the line supplied with components and remove waste from the line as needed. Your role: Assist the group lead manage the workflow within the assigned manufacturing cell to achieve the daily production objective. Supervise workflow, move full pallets of finished goods to the proper location and monitor inventory of components to insure the line has enough components to complete the order. Interface with warehouse personnel to ensure all components are correct and staged in the appropriate area to avoid delays in production. Maintain the all the materials needed to complete the work order and take appropriate action when it's not. You're the right fit if: You have a high school diploma, GED or equivalent. No experience required, preferably knowledgeable on any of the following manufacturing production e

Job Title Material Handler 2 Job Description The Material Handler 2 will assist group leads prepare the line for production; they will ensure the correct components have been issued for the work order based on the BOM. The Material Handler will keep the line supplied with components and remove waste from the line as needed. Your role: Assist the group lead manage the workflow within the assigned manufacturing cell to achieve the daily production objective. Supervise workflow, move full pallets of finished goods to the proper location and monitor inventory of components to insure the line has enough components to complete the order. Interface with warehouse personnel to ensure all components are correct and staged in the appropriate area to avoid delays in production. Maintain the all the materials needed to complete the work order and take appropriate action when it's not. You're the right fit if: You have a high school diploma, GED or equivalent. No experience required, preferably knowledgeable on any of the following manufacturing production e

Work Flexibility: Onsite Schedule: Monday - Friday, 4:45am-1:15pm OT Required: 2 Saturdays per month What you will do: Paints and uses powder operations to properly prepare components that may include sub-assemblies and all other related components to contribute to completion of a variety of products Unloads parts, part racks, and hooks from the line while visually inspecting completed parts Applies painting and/or powder process in accordance with product specifications Sets paint/powder equipment for proper tolerances, color and feed rate Responsible for work preparation, clean up, and quality assurance of own work and work area Committed to quality by striving for reliability and quality in our products, continuously searching for ways to enhance performance and meeting all training and documentation criteria Strives for operational excellence by promoting a team-based, product-focused organization, contributing to continuous improvement, participating in preventative maintenance and safety programs, striving for cost reduction, and committing to on-time, complete, and error-free shipments Meet work schedule and overtime requirements, including weekends Must be able to lift/push/pull 50&#43; lbs throughout shift What you need Preferred High School or GED Manufacturing Experience $23.90 Hourly plus bonus eligible &#43; benefits Travel Percentage: None <p style=

Natera is seeking an Associate Director to lead a team of Bioinformatics Scientists in our Women's Health and Organ Health research organization. You will oversee the scientific planning and execution of research and assay-development of diagnostic projects, and you will be responsible for creating production-ready pipeline components. You will manage your team and its professional growth, the research strategy behind new product development, and the handoff of research work into production. The role calls for deep experience in algorithm and assay development, NGS data processing across multiple modalities, and the full life cycle of diagnostic product research and development in a regulated (CLIA) setting. You will evaluate new technologies and NGS assays, implement methods to optimize performance, and help define the product profile from a bioinformatics perspective, with input from R&D, Product, and Laboratory Directors. Primary Responsibilities: Team Leadership and Development: Lead and mentor a team of Bioinformatics Scientists. Own their professional growth, their responsibilities, and the standard the team holds itself to. Research Strategy: Own the research strategy behind new product development, from scoping through execution, working with cross-functional stakeholders on what the team takes on and in what order. Assay Science: Lead bioinformatics analysis for assay development and optimization, and troubleshoot experiments alongside laboratory scientists. This spans multi-omic approaches including methylation and fragmentomics and other cell-free DNA (cfDNA) derived features. It also spans short-read and long-read sequencing and both hybrid-capture and amplicon target enrichment. Study Design and Data Quality: Partner with laboratory teams on study design at the research and feasibility stage, covering new technology assessment, optimization, and performance determination. Make sure the resulting data holds up before anyone builds on it. Analys