6102 Calibration Jobs - Page 3

Job Title: Healthcare Quality Excellence Assistant Manager – Voice Processes Basic Function The Quality Excellence Assistant Manager is responsible for ensuring smooth functioning of Quality Compliance, driving compliance and process improvement initiatives in the allocated business processes. Essential Functions Ensure timely onboarding and incubation of QCAs and QE AMs for assigned voice processes and ensure quality deliverables such as call monitoring, coaching/feedback, and reporting targets are met. Support the setup and stabilization of Quality Compliance for voice processes in coordination with Operations, Migrations, and Training teams. Ensure timely and accurate reporting of quality performance metrics, internal quality scores, and client SLA parameters such as accuracy, soft skills, and compliance scores. Conduct regular call calibration sessions (Gage R\&R) internally and with clients to align on quality expectations and minimize variance. Review calls and associated documentation to ensure adherence to quality standards (QSDs) and facilitate updates in quality control procedures as required. Drive compliance to internal guidelines and third-party certifications (like COPC, ISO) by partnering with Operations to close audit gaps. Collaborate closely with the Customer Experience (C-Sat/DSAT) team to analyze VOC insights and drive improvements in customer interaction quality. Identify process gaps and support continuous improvement initiatives, including participation in AIM, Lean, and Six Sigma projects in collaboration with GBs/BBs. Conduct refresher trainings and mentorship programs for QCAs and QE AMs on quality tools, root cause analysis, and communication best practices. Maintain close engagement with Operations to proactively address quality trends and identify improvement opportunities. Education Requirements Graduate in any stream, preferably with a background in Healthcare or Customer Service/Call Center Operations. Green Belt Trained (Mandatory); Green Belt / Black Belt Certified (Preferred) for external candidates. Primary Internal Interactions QCAs for assigning tasks and giving feedback. Ops AM / Manager and Quality Excellence AM/Manager / Sr. Manager Ops / Quality Excellence AVP

You will be responsible for designing, installing, and maintaining instrumentation and control systems. This includes calibrating sensors and instruments for accuracy and reliability, developing P&IDs and control logic, and collaborating with electrical and mechanical engineers to integrate systems. In addition, you will troubleshoot and repair instrumentation and control systems, implement SCADA, PLC, and DCS-based solutions, and ensure compliance with safety and environmental regulations. Your role will also involve supporting the commissioning and start-up of new installations and maintaining documentation such as manuals, calibration records, and datasheets. To qualify for this position, you should have a Bachelor's degree in Instrumentation Engineering and [2-5+] years of relevant industry experience. You are expected to have a strong understanding of sensors, transmitters, actuators, and controllers, as well as experience with PLCs (e.g., Siemens, Allen Bradley), SCADA, and DCS systems. This is a full-time position with benefits including Provident Fund. The work location is in person.,

Key Responsibilities Monitor and evaluate inbound and outbound calls for quality, accuracy, and adherence to company standards. Assess call recordings to identify strengths, improvement areas, and training needs for agents. Provide constructive feedback and actionable recommendations to team leaders and agents. Create and maintain call quality evaluation forms and scoring metrics tailored to the EdTech customer journey. Collaborate with training teams to design skill enhancement sessions based on quality assessment outcomes. Track and analyze call quality trends, preparing regular performance reports for management. Ensure compliance with internal policies, data security protocols, and regulatory requirements. Suggest process improvements to enhance customer satisfaction and increase learner conversions. Conduct calibration sessions with the QA team and supervisors to maintain scoring consistency. Strong analytical and listening skills. Knowledge of EdTech sales and support processes will be an added advantage.

Designation: Job Inspector Qualifications: ITI / Diploma Experience: 2 to 3 years Package: INR 2.0 to 2.5 Lakhs per annum Job Requirements: 1) Complete knowhow / understanding of all Measuring Instruments like Vernier Callipers, Micrometres, Dial Gauges, Height Gauges, Bore Gauges, and Pin Gauges etc. 2) Experience in Computerized VISION MEASURING SYSTEM preferable. 3) Understanding of technical drawings. 4) Knowledge of ISO/TS 16949 & QMS documents. 5) Ready to work in shifts. 6) Knowledge of SAP preferable. 7) Knowledge of Quality Tools preferable. 8) Experience in Inspections of Small or Micro Components. Job Responsibilities: 1) Inspects and approves incoming materials by confirming specifications, conducting visual and measurement tests, and rejecting and returning unacceptable materials. 2) Inspects in-process production by confirming specifications, conducting visual and measurement tests, communicating required adjustments to production supervisor. 3) Approves finished products by confirming specifications, conducting visual and measurement tests, returning products for re-work, and confirming re-work. 4) Documents inspection results by completing reports and logs, summarizes re-work and waste, and inputs data into quality database. 5) Keeps measurement equipment operating by following operating instructions and calibration requirements, and calling for repairs. 6) Maintains safe and healthy work environment by following standards and procedures, and complying with legal regulations. 7) Updates job knowledge by participating in educational opportunities and reading technical publications. 8) Accomplishes quality and organization mission by completing related results as needed.

Date: 31 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Manufacturing Services Job Description Designation: Junior Manager Level: 8- I Job Location: Bangalore The Company Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngenes 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. Key Result Areas Role-specific Functional Responsibilities: Ensure All Biopharmaceutical Development Lab Equipment are in state of GLP and Safety Compliance by rectifying equipment breakdowns, maintaining critical spares & consumables and carrying out equipment installations as per approved protocols. Attend breakdown of S1, S2 & S20 Equipment/ Instrument in lab and get it operational with support from instrument vendor and E&M team. Responsible for IQ, OQ, PQ for new instrument installation, calibration and maintain the supporting documents in coordination with DQA and E&M team. Responsible for the equipment requalification and completion of documents coordination with DQA and E&M team. Ensure that the S1, S2 & S20 Equipment/ Instrument calibration and equipment PM are completed before the due date in accordance with the Calibration and PM planner monthly in coordination with E&M. Responsible for Equipment/ Instrument discard procedure and ensure completion of discard process on time. Responsible for the initiation and completion of Equipment /Instrument QMS activities (Change control, Deviation and CAPA) before targeting closer date. Responsible for preparation of equipment related SOP/EOP/IOP and implementation in process. Responsible for calibration and completion of calibration documents of HPLC/UPLC and handling of breakdown of the equipment. Monitor & support sanitation & fumigation activities in lab with support from tech team, EHSS and E&M team Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Pls visit us at https://syngeneintl.com/ to know more about us and what we do. Show more Show less

Job Summary As a meticulous individual at Dr. Reddys Laboratories Ltd., you will be responsible for supporting wet analysis in pharmaceutical products to ensure precise identification and quantification. Your role will involve performing sample analysis, method development, validation, and equipment calibration, all crucial for maintaining accuracy, reliability, and adherence to safety and cGLP guidelines. Roles & Responsibilities Your primary responsibilities will include: - PM of analytical instruments - Calibration of thermal sensors - Following up with external vendors/Engineers for calibration and PM services - Raising deviations according to SOP procedures - Handling breakdowns of analytical instruments Qualifications To qualify for this position, you should have: - Educational qualification: An M.Sc or B.SC. degree in Chemistry, Analytical Chemistry, or a related field - Minimum work experience: 0 to 5 years Skills & Attributes Technical Skills: - Knowledge of calibration and performance verification of analytical instruments and equipment as per the master schedule - Proficiency in advanced instrumentation techniques - Experience in maintaining, preparing, and procuring laboratory standards, chemicals, and solvents following established procedures - Participation in equipment/instrument qualifications and change control mechanisms - Procurement expertise for laboratory requirements Behavioural Skills: - Attention to detail and commitment to ensuring compliance with QMS (Quality Management System) documents - Ability to respond to internal and external audits and participate in QMS-related activities - Strong organizational skills for LIMS (Lab Information Management System) related activities - Effective communication and collaboration skills for coordinating and implementing SOPs About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, our Global Manufacturing Organisation is dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With 19 state-of-the-art manufacturing plants across various locations, we are a leading force in the pharmaceutical industry. Benefits Offered At Dr. Reddys, we prioritize your career growth and professional development through personalized learning programs. Our benefits are on par with the best industry standards, including joining & relocation support, family support, learning and development opportunities, medical coverage, and life coverage. Our Work Culture Our employees at Dr. Reddys Laboratories are driven by the credo that "Good Health Cant Wait". We believe in healthcare solutions that empower patients to lead healthier lives. Our culture fosters empathy, dynamism, and teamwork, enabling individuals to make a difference while collectively striving for shared success. For more information, visit our career website at https://careers.drreddys.com/#!/,

Skill required: Trust & Safety - Quality Management Designation: Quality Auditing Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years Language - Ability: Marathi - Expert About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? Accenture is a trusted, innovative, comprehensive, and experienced partner to leading platform companies. The Trust and Safety offering within Accenture Operations helps keep the internet safe and helps platform companies accelerate, scale, and improve their businesses. You will be responsible for the quality assurance of Content Moderation whose role includes analyzing and reviewing user profiles, audio, videos, and text-based content and/or investigating, escalating and/or resolving issues that are reported by users or flagged by the system. Due to the nature of the role, the individual and you may be exposed to flashing lights or contrasting light and dark patterns. Content moderation is meaningful work that helps keep the internet safe. It may also be challenging, at times. In the context of this role, individuals may be directly or inadvertently exposed to potentially objectionable and sensitive content (e.g., graphic, violent, sexual, or egregious). Therefore, any role supporting content moderation needs strong resilience and coping skills. We care for the health and well-being of our people and provide the support and resources needed to perform their role responsibilities. Active participation in Accenture’s well-being support program, designed specifically for the Trust & Safety community, provides valuable skills to promote individual and collective well-being. What are we looking for? As a Quality Auditor, you will be: Responsible for Quality Audits ensuring service meets the client and org goals and standards of quality. Need to enforce the defined policy guidelines for all workflows assigned under the Content Moderation scope. Need to ensure timely quality insights are shared to drive process improvements. Should ensure timely feedback and individual performance development is tracked and reported. Should work with the core Operations Team and drive overall quality standards defined as per the process. Content Moderation Guidelines: In-depth understanding of content moderation guidelines and policies specific to the platform or industry. Digital Literacy: Familiarity with various types of online content, including text, images, videos, and audio. Attention to Detail: Keen eye for identifying inappropriate, offensive, or harmful content. Policy Interpretation: Ability to interpret and apply content moderation policies consistently and accurately. Decision Making: Skill in making well-informed and consistent content approval or rejection decisions. Risk Assessment: Capability to assess the potential risks associated with various types of content. Data Analysis: Basic data analysis skills to identify trends, patterns, and areas of improvement. Communication Skills: Excellent verbal and written communication skills to deliver engaging refresher sessions. Active listening skills to understand reviewer questions and concerns. Engage in client discussion for process improvement sessions. Quality Assurance: Knowledge of quality assurance processes and best practices for maintaining content standards. Proficient in MS Excel/PPT/Word and/or Google Sheets/Docs/Slides with advanced skills in creating reports. Data analysis Roles and Responsibilities: Assess the quality of analysts on the project. Meet volume and quality targets for all quality assurance audits. Develop and maintain knowledge of client and their business needs processes. Develop and maintain an understanding of client Service Level Agreements and the department s key performance requirements. Develop and maintain product, industry, and business and professional skills by participating in on-the-job and classroom training. Participate in process calibration sessions with clients and cross-vendor. Take accountability for effectively handling escalations. Identify root causes for business-related issues and recommend solutions to improve overall client satisfaction. Assist with monitoring and tracking incidents to ensure timely resolution. Deliver individual and group feedback, provide coaching sessions, motivating, and encouraging analysts to improve performance.

Skill required: Trust & Safety - Quality Management Designation: Quality Auditing Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years Language - Ability: Marathi - Expert About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? Accenture is a trusted, innovative, comprehensive, and experienced partner to leading platform companies. The Trust and Safety offering within Accenture Operations helps keep the internet safe and helps platform companies accelerate, scale, and improve their businesses. You will be responsible for the quality assurance of Content Moderation whose role includes analyzing and reviewing user profiles, audio, videos, and text-based content and/or investigating, escalating and/or resolving issues that are reported by users or flagged by the system. Due to the nature of the role, the individual and you may be exposed to flashing lights or contrasting light and dark patterns. Content moderation is meaningful work that helps keep the internet safe. It may also be challenging, at times. In the context of this role, individuals may be directly or inadvertently exposed to potentially objectionable and sensitive content (e.g., graphic, violent, sexual, or egregious). Therefore, any role supporting content moderation needs strong resilience and coping skills. We care for the health and well-being of our people and provide the support and resources needed to perform their role responsibilities. Active participation in Accenture’s well-being support program, designed specifically for the Trust & Safety community, provides valuable skills to promote individual and collective well-being. What are we looking for? As a Quality Auditor, you will be: Responsible for Quality Audits ensuring service meets the client and org goals and standards of quality. Need to enforce the defined policy guidelines for all workflows assigned under the Content Moderation scope. Need to ensure timely quality insights are shared to drive process improvements. Should ensure timely feedback and individual performance development is tracked and reported. Should work with the core Operations Team and drive overall quality standards defined as per the process. Content Moderation Guidelines: In-depth understanding of content moderation guidelines and policies specific to the platform or industry. Digital Literacy: Familiarity with various types of online content, including text, images, videos, and audio. Attention to Detail: Keen eye for identifying inappropriate, offensive, or harmful content. Policy Interpretation: Ability to interpret and apply content moderation policies consistently and accurately. Decision Making: Skill in making well-informed and consistent content approval or rejection decisions. Risk Assessment: Capability to assess the potential risks associated with various types of content. Data Analysis: Basic data analysis skills to identify trends, patterns, and areas of improvement. Communication Skills: Excellent verbal and written communication skills to deliver engaging refresher sessions. Active listening skills to understand reviewer questions and concerns. Engage in client discussion for process improvement sessions. Quality Assurance: Knowledge of quality assurance processes and best practices for maintaining content standards. Proficient in MS Excel/PPT/Word and/or Google Sheets/Docs/Slides with advanced skills in creating reports. Data analysis Roles and Responsibilities: Assess the quality of analysts on the project. Meet volume and quality targets for all quality assurance audits. Develop and maintain knowledge of client and their business needs processes. Develop and maintain an understanding of client Service Level Agreements and the department s key performance requirements. Develop and maintain product, industry, and business and professional skills by participating in on-the-job and classroom training. Participate in process calibration sessions with clients and cross-vendor. Take accountability for effectively handling escalations. Identify root causes for business-related issues and recommend solutions to improve overall client satisfaction. Assist with monitoring and tracking incidents to ensure timely resolution. Deliver individual and group feedback, provide coaching sessions, motivating, and encouraging analysts to improve performance.

Role Overview: As a Senior Testing Engineer at NTRI, you will play a crucial role in the execution, supervision, and documentation of electrical and mechanical tests on high-voltage equipment and materials. You will be responsible for ensuring that all testing activities meet national and international standards, particularly those required under NABL accreditation. This role is ideal for someone with strong technical expertise, practical hands-on experience, and a deep understanding of testing standards for electrical infrastructure products. Key Responsibilities 1. Testing & Execution: Plan, conduct, and supervise routine and type tests on electrical products (insulators, switchgear, etc) Interpret test standards (IS/IEC/BIS) and ensure accurate and compliant test procedures. Operate and maintain testing equipment. 2. Documentation & Reporting: Prepare detailed and accurate test reports for client submissions and internal records. Ensure all reports align with NABL, BIS, and ISO/IEC 17025 requirements. Review and validate results generated by junior engineers. 3. Quality & Compliance: Adhere to and enforce strict quality assurance and safety practices in the lab. Support the Quality Manager during audits and inspections. Contribute to root cause analysis and continuous improvement efforts. 4. Team Leadership & Mentoring: Train and mentor junior testing engineers and technicians. Assist in scheduling and resource planning for testing activities. Act as the technical point-of-contact during customer visits or inspections. 5. R&D & Expansion Support: Support the development of new testing procedures for expanding product scope. Collaborate with management on feasibility studies for additional accreditation scope. Required Qualifications: M.Tech/M.E./B.Tech/B.E. in Electrical Engineering 3–5 years of hands-on experience in a testing laboratory (preferably NABL-accredited) Familiarity with high-voltage, mechanical, and thermal testing methodologies Proficiency in technical documentation and reporting Strong communication and leadership skills Preferred: Candidates having strong working knowledge of IS, IEC, and BIS standards applicable to insulators, arrestors, and switchgear. Experience with ISO/IEC 17025 compliance and audits Prior experience in similar product testing NABL Lab. Familiarity with calibration procedures and measurement uncertainty

Location: Noida, UP Department: Quality Employment Type: Full-Time (6 days a week) CtC- 2.4- 3.6 lpa About Futwork Futwork is a modern workforce platform that helps businesses hire, train, and manage telecalling and remote sales agents at scale. With a focus on flexibility, speed, and quality, Futwork enables companies to quickly build distributed teams to handle outbound sales, lead generation, customer support, and other voice and non-voice based processes. By leveraging its tech-driven platform and pre-vetted talent pool, Futwork ensures businesses get trained and performance-ready agents who deliver measurable results. https://www.futwork.com/ Position Summary We are looking for a proactive and detail-oriented Quality Analyst to join our team in Noida. This position combines facilitating training programs with monitoring and improving process quality. The ideal candidate is skilled at engaging learners, ensuring compliance with process standards, and driving continuous improvement through constructive feedback and coaching. Key Responsibilities Quality Assurance Responsibilities: · Monitor calls/chats/emails as per defined sampling and quality parameters. · Evaluate agent performance against process guidelines, quality standards, and customer experience metrics. · Identify gaps, trends, and recurring issues and work with teams to implement corrective actions Share regular quality reports, feedback, and insights with stakeholders. · Participate in calibration sessions and contribute to standardizing quality assessment criteria. Qualifications & Skills ● Graduate in any discipline (Bachelor’s degree required; Master’s preferred). ● Minimum 2 years of experience in quality analysis (Document verification experience will be preferred) · Strong communication, facilitation, and feedback delivery skills. · Excellent observation, analytical, and reporting abilities. · Good understanding of quality frameworks, audit processes, and continuous improvement practices. · Proficiency in MS Office (Excel, PowerPoint, Word) and google docs, sheet; knowledge of QA tools or LMS is a plus. · Ability to manage priorities, work independently, and collaborate across teams. kindly mail your resume at ghazal@futwork.com.

Who are we? Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success. At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like: Brief Call : Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you! Interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities! Case study : Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc. As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience. We look forward to meeting you! Job Description About the Role Join our expert team to lead the commissioning of a Continuous Galvanizing Line (CGL) furnace project in India. As Furnace Commissioning Supervisor, you will coordinate and supervise all start-up activities, ensuring safe, reliable, and optimized operation of the galvanizing furnace. Key Responsibilities Safety & Compliance – Enforce safety regulations, conduct inspections, and ensure a zero-incident work environment. Installation & Pre-Commissioning – Oversee furnace installation, piping, controls wiring, and pre-commissioning checks. Start-Up & Testing – Lead furnace start-up, perform I/O tests, calibrate instruments, and validate automatic sequences. System Calibration – Adjust combustion parameters, pressure controls, and thermal cycles for peak efficiency and safety. Troubleshooting & Optimization – Diagnose issues, implement corrective actions, and fine-tune process settings. Documentation & Training – Record commissioning progress, update functional descriptions, and train client teams. Team Leadership – Guide and mentor on-site technicians, coordinate tasks, and maintain clear communication across stakeholders. Position Details Start Date: End of August Duration: 6–12 months (estimated) Location: India (work permit required) What You Bring 5–7 years’ experience commissioning industrial furnaces—CGL or CAL experience is a strong plus Proven skills in I/O testing, instrument calibration, and combustion control Deep understanding of industrial control/automation systems and thermal cycle optimization Excellent troubleshooting, problem-solving, and project-management abilities Strong leadership and teamwork skills; able to mentor and coordinate technicians Fluent English (written and spoken); additional language skills are a bonus Willingness to work on-site with travel as needed Proficiency with Microsoft Office and standard commissioning tools Why You’ll Love This Role Make an immediate impact by bringing critical industrial equipment online Work in a collaborative, safety-focused environment with a global team Gain hands-on experience with state-of-the-art galvanizing technology Develop your leadership skills by guiding and inspiring a talented field team Amaris Consulting is proud to be an equal opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Job Description Position: Junior Executive – Manufacturing (Production) Position Reports to: Associate Manager – Manufacturing Downline Reporting: Associate Executives & Operators Location: Jigani, Bangalore, India Job Responsibilities To achieve Daily / Shift targeted production at required quality levels at specified costs in conformance with procedures specified in the quality system by ensuring availability of manpower, machines, and materials. To deliver products on time to the internal customers as per the production plan duly tying up suitable manpower requirement in the Department. To be Responsible for achieve the shift KPI factors such as, Labour Productivity, Optimum utilization of Consumables, progress of improvement projects, RTY, stocks, etc., are closely monitored. To consistently achieve and maintain optimum levels in the prescribed and established quality standards in the manufacturing process and as a practice keep the scrap and wastage as per prescribed and established norms and Endeavor to constantly improve the quality further. To supervise timely delivery of processed materials to other departments for further process of the final product and thus avoid zero idle time in department and Endeavor to achieve optimum productivity. To focus on achieving the Quality, EMS and Health & Safety objectives applicable to the department. Prepare and submit the Shift / Daily reports. To maintain efficient workplace by practicing 1S. To identify non-conformances and implement corrective and preventive actions as per the procedure. To ensure that all Operators are trained in consultation with the Human Resource Department to achieve the required skill level and acquire as many multi-skills as possible and become proficient in eliminating losses. To disseminate the overall knowledge with the respect to the established process and systems for the Department across all the subordinates. To consistently counsel and motivate the subordinates in such a way that their motivational and morale levels are always high and inculcate positive discipline. To take counter measures to eliminate accidents due to unsafe conditions / acts, near miss that have been identified in the Department. To ensure calibration and validation of the equipment that are used in the Department are carried out as per the requirements for the process. Maintain Safe & Healthy work environment including safety of people, assets & properties of the company. Reporting of EHS activities /concerns /incidents /near miss and accidents. Ensure no injuries at workplace. To ensure that there is no adverse impact on the environment due to the activities of the department. To ensure compliance of GMP, SOPs and other systems / procedures of the company. To ensure that the requirements of ISO 9001, USFDA QSR-CFR Part 820, ISO 13485, ISO 14001, MDSAP and such other international standards are implemented and maintained. This job description is subject to change by the Management to suit changing requirements from time to time. Such other assignments the management may give from time to time, including orientation to Project Teams / Sub-Committees. To ensure that ERP system is properly followed in the department in a timely manner and to ensure data accuracy. Comply with and monitor work practices are according to Lifestyles values and Ethical Business Conduct Policy. About the Company LifeStyles has a history dating back to 1905 when Eric Ansell first started making condoms in Richmond Australia. Today LifeStyles is a Global leader in the sexual wellness sector, comprising a broad range of condoms, personal lubricants, and other related products and other products in over 60 countries. Owning a large portfolio of trademarks, LifeStyles manufactures and commercialises its products either under leading global non-latex condom brands SKYN® under its local heroes such as LifeStyles®, Manix®, Unimil®, and Blowtex® and Control®. Outside of branded products, the Company also supports universities, NGOs, and other organizations as part of a broader effort to promote sexual health and prevent the spread of STDs and STIs. LifeStyles owns and operates manufacturing facilities in Thailand, India and Spain, and it employs over 1,600 teammates globally. LifeStyles Healthcare was created on September 1, 2017, when the consortium of Humanwell Healthcare & CITIC Capital private equity purchased the Sexual Wellness division from Ansell. As of December 1, 2022, Lifestyles is owned by Linden Capital Partners , a Chicago-based private equity firm focused on the healthcare industry. This is an exciting time to join us. We combine century-long history with the opportunity of a new beginning as a stand-alone company - this means a new way of thinking, the opportunity to explore new horizons and the chance to make a mark in an exciting, fresh business. LifeStyles Healthcare is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We are empowered professionals, and we are committed to creating a team of the world’s “best of the best.” Our business foundation is strong, among our values are Integrity and Respect, our people are highly engaged, and we are excited about a new phase in the company history. We have a focus on safety and teamwork - and we want you to join us! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Discover more about us at: https://www.linkedin.com/company/lifestyles-healthcare/ Curious to know what does every day look like at LifeStyles? Find out by looking at employee testimonials: https://lifestylesglobal.com/careers Due to the high number of applications, we would like to inform you that only selected candidates will be contacted.

Required exp – 3+years Job Description Conduct daily routine maintenance and inspections of arcade to ensure they are in safe and operational condition. Perform repairs and troubleshoot mechanical, electrical, and technical issues in a timely and efficient manner. Diagnose and resolve problems related to engines, transmissions, braking systems, steering systems, and other components. Keep accurate records of maintenance activities, including service schedules, repairs, and parts inventory in a computerized format. Regularly inspect and maintain safety features such as seat belts, roll cages, and safety harnesses. Ensure compliance with safety regulations and industry standards. Perform engine tuning, carburettor adjustments, and fuel system maintenance. Maintain cleanliness and organization of the workshop and tools. Assist in track operations, including kart assembly, disassembly, and track setup. Train and guide junior technicians, providing them with necessary support and knowledge. Stay updated on the latest industry trends, technology advancements, and safety protocols related to go-kart maintenance and repair. Apply usage of digital equipment and applications to incorporate a smart working environment. Install new games as they arrive packed from manufacturer, 1st power up and setup Calibration and setting Trouble shoot and fix common problems Check power supply and operation Repair in case of breakdown, circuit board level Change spare parts and maintain part required list

About Us Mieux Display is a proud Make in India and GeM-registered manufacturer of advanced LED Video Walls. We deliver innovative, locally engineered solutions to elevate visual experiences. Role Summary You’ll handle the installation, configuration, and commissioning of various LED video walls—indoor and outdoor—including façade, wall-mounted, and pole setups. This includes all technical, calibration, and documentation tasks. Key Responsibilities: Install and align LED panels across diverse structures (facades, walls, poles). Set up LED controllers, manage power/data cabling, and handle signal routing. Calibrate brightness, color uniformity, pixel mapping, and create/display-ready file content. Troubleshoot on-site installation issues and ensure system performance. Review installation drawings and maintain documentation and safety compliance. Collaborate with project teams and support client handovers. Qualifications: Diploma / ITI / B.Tech in Electronics, Electrical, or AV Technology. 1–3 years of experience in LED video wall installations and maintenance, including façade and pole systems. Strong technical skills in LED display systems, controllers, calibration, and structured cabling. Why Mieux Display? Join a future-forward, Indian-made brand working on diverse, impactful LED installations with a clear and technically driven approach. Send us your CV at hr@mieuxdisplay.com

Job Title: Senior / Lead Robot Control Engineer – Surgical Robotics Location: Chennai Employment Type: Full-time Mandatory Primary Skills: C / C++ 11 and above, PLC, TwinCAT or EtherCAT. About the Role: We are seeking a skilled and detail-oriented Senior Robot Control Engineer to join our multidisciplinary team developing cutting-edge surgical robotic systems . This role involves designing, implementing, and validating real-time motion control software using TwinCAT, PLC programming (Structured Text), and C++ . You will work closely with mechanical, electrical, and systems engineers to deliver high-performance, safety-critical motion functionality for precision surgical applications. Key Responsibilities: Design and implement real-time motion control software using Beckhoff TwinCAT 3, Structured Text, and C++. Develop PLC logic for motor control, sensor integration, and actuator feedback. Collaborate on control system architecture to meet safety, precision, and performance requirements for surgical robotic arms. Integrate motion controllers, encoders, and servo drives into the system. Participate in system bring-up, debugging, calibration, and tuning of servo systems. Conduct software testing, documentation, and participate in formal reviews and validations for medical device regulatory compliance (e.g., IEC 62304). Work with cross-functional teams including mechanical, software, QA, and clinical application experts. Support development of safety-critical functions including emergency stop, limit switches, and fault handling logic. Required Qualifications: Bachelor's or Master’s degree in Electrical Engineering, Mechatronics, Computer Engineering, or related field. Minimum 3 to 10+ years of hands-on experience in motion control software development using: Beckhoff TwinCAT 3 PLC programming (IEC 61131-3 Structured Text) C++ (preferably in real-time or embedded systems) Experience with servo motors, encoders, motion profiling, PID tuning. Understanding of industrial fieldbuses such as EtherCAT. Familiarity with real-time operating systems and deterministic control. Strong debugging, documentation, and version control skills (e.g., Git). Preferred Qualifications Exposure to motor control algorithms (FOC, PID tuning, etc.). Experience with real-time industrial automation systems or robotics platforms. Familiarity with medical device standards such as IEC 60601 or ISO 13485 is a plus. Background in safety-critical or medical systems development. What You'll Gain: • Opportunity to shape real-world solutions that impact lives through precision healthcare. • Be part of a multidisciplinary and innovation-driven R&D team at the forefront of medical robotics. • Work in a culture that promotes creativity, technical excellence, and continuous learning.

Job Title: Senior Field Service Engineer Location: New Delhi, India Job Type: Full-Time Company Name : ASP India Private Limited Job Summary : We are seeking a skilled Senior Field Service Engineer to join our team in New Delhi. The ideal candidate will be responsible for the service, repair, and installation of products and solutions at customer sites in Kerala and nearby regions. This role involves performing electrical and mechanical testing, diagnosing system failures, and providing cost-effective solutions. The role will also handle customer support calls and escalate complex issues when necessary. Opportunities for developing new customer service and product agreements may also be part of the role. Leadership and Coordination : Act as a lead, coordinating the work of others and ensuring that team efforts are well-organized and productive. Key Responsibilities Service and Repair: Conduct on-site service, repair, and installation of products and IT solutions. Perform repair and testing as per maintenance contracts. Diagnose system failures and implement the most cost-effective solutions. Customer Support Respond to customer support calls within the assigned territory promptly. Address and resolve customer issues effectively, ensuring high levels of customer satisfaction. Develop and maintain positive relationships with customers. Technical Support Escalate complex issues to higher-level technical support or quality reporting systems. Provide detailed reports and documentation for issues escalated. Agreement Development Assist in the development of new customer service and product agreements as needed. Calibration And Repair For those assigned to in-house calibration or repair, perform these tasks at established company repair sites or service centers. Qualifications Education: Advanced Diploma / Bachelor’s degree in Engineering or a related field. Experience: 10+ years of experience in a similar role. Skills : Strong troubleshooting and diagnostic skills. Excellent customer service and communication skills. Ability to work independently and manage time effectively. Knowledge of IT solutions and products. Additional Requirements Willingness to travel within the assigned territory. Flexibility to work outside regular business hours if required. Company Overview: ASP is a leading provider of Sterilization solutions and services, committed to delivering high-quality infection prevention solutions and innovative solutions to our clients. We value our employees and provide a dynamic work environment that encourages growth and development. How to Apply: Interested candidates should apply with their resume. Fortive Corporation Overview Fortive’s essential technology makes the world stronger, safer, and smarter. We accelerate transformation across a broad range of applications including environmental, health and safety compliance, industrial condition monitoring, next-generation product design, and healthcare safety solutions. We are a global industrial technology innovator with a startup spirit. Our forward-looking companies lead the way in software-powered workflow solutions, data-driven intelligence, AI-powered automation, and other disruptive technologies. We’re a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to groundbreaking sustainability solutions. We are a diverse team 17,000 strong, united by a dynamic, inclusive culture and energized by limitless learning and growth. We use the proven Fortive Business System (FBS) to accelerate our positive impact. At Fortive, we believe in you. We believe in your potential—your ability to learn, grow, and make a difference. At Fortive, we believe in us. We believe in the power of people working together to solve problems no one could solve alone. At Fortive, we believe in growth. We’re honest about what’s working and what isn’t, and we never stop improving and innovating. Fortive: For you, for us, for growth. About Advanced Sterilization Products ASP is a leading global provider of innovative sterilization and disinfection solutions, and a pioneer of low-temperature hydrogen peroxide sterilization technology.ASP’s mission is to protect patients during their most critical moments. We support healthcare facilities in the fight to protect patients against hospital acquired infections, which are a leading cause of morbidity and mortality. ASP’s products, which are sold globally, include the STERRAD system for sterilizing instruments and the EVOTECH and ENDOCLENS systems for endoscope reprocessing and cleaning. We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at applyassistance@fortive.com. Bonus or Equity This position is also eligible for bonus as part of the total compensation package. ASP is a leading global provider of innovative sterilization and disinfection solutions, and a pioneer of low-temperature hydrogen peroxide sterilization technology.ASP’s mission is to protect patients during their most critical moments. We support healthcare facilities in the fight to protect patients against hospital acquired infections, which are a leading cause of morbidity and mortality. ASP’s products, which are sold globally, include the STERRAD system for sterilizing instruments and the EVOTECH and ENDOCLENS systems for endoscope reprocessing and cleaning. We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at applyassistance@fortive.com. This position is also eligible for bonus as part of the total compensation package.

Job Title Executive/Sr Executive – Biotechnology (Protein Characterization) Business Unit R&D1 Regulatory Affairs Job Grade G12A / G11B Location : Baroda At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Job Description The candidate is expected to develop HPLC based methods for protein and peptide products. The candidate is expected to develop CE based methods for protein and peptide products. Responsible for analytical method qualification for all pipeline products. Characterization of innovator product batches sourced from different geographical region and preparation of quality target profile. Analytical similarity assessment of in-house products. 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 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. T/TTechnical 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 peptide is highly desirable. Travel Estimate NA Job Requirements Educational Qualification M.Sc/M.Tech in Biology Experience Tenure : 2-6 years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Title Executive - Biotechnology Business Unit R&D1 Regulatory Affairs Job Grade G12A Location : Baroda At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key Role Development 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 Description Responsible for study sample analysis for all pipeline products. Isolation of PBMC from whole blood and maintenance of commercial cell lines. Data compilation, QC & Statistical analysis of data. Preparation of standard operating procedures (SOP), method development reports (MDR) 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. Management of chemicals, consumables & critical reagents inventory. Performing calibration of instruments and equipment. Troubleshooting instrument performance and equipment issues. Travel Estimate NA Job Requirements Educational Qualification M.Sc/M.Tech in Biotechnology or Biochemistry Experience Tenure : 2-6 years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Title: Senior Field Service Engineer Location: Kolkata, India Job Type: Full-Time Company Name : ASP India Private Limited Job Summary : We are seeking a skilled Senior Field Service Engineer to join our team in Kolkata. The ideal candidate will be responsible for the service, repair, and installation of products and solutions at customer sites in Kerala and nearby regions. This role involves performing electrical and mechanical testing, diagnosing system failures, and providing cost-effective solutions. The role will also handle customer support calls and escalate complex issues when necessary. Opportunities for developing new customer service and product agreements may also be part of the role. Leadership and Coordination : Act as a lead, coordinating the work of others and ensuring that team efforts are well-organized and productive. Key Responsibilities Service and Repair: Conduct on-site service, repair, and installation of products and IT solutions. Perform repair and testing as per maintenance contracts. Diagnose system failures and implement the most cost-effective solutions. Customer Support Respond to customer support calls within the assigned territory promptly. Address and resolve customer issues effectively, ensuring high levels of customer satisfaction. Develop and maintain positive relationships with customers. Technical Support Escalate complex issues to higher-level technical support or quality reporting systems. Provide detailed reports and documentation for issues escalated. Agreement Development Assist in the development of new customer service and product agreements as needed. Calibration And Repair For those assigned to in-house calibration or repair, perform these tasks at established company repair sites or service centers. Qualifications Education: Advanced Diploma / Bachelor’s degree in Engineering or a related field. Experience: 10+ years of experience in a similar role. Skills : Strong troubleshooting and diagnostic skills. Excellent customer service and communication skills. Ability to work independently and manage time effectively. Knowledge of IT solutions and products. Additional Requirements Willingness to travel within the assigned territory. Flexibility to work outside regular business hours if required. Company Overview: ASP is a leading provider of Sterilization solutions and services, committed to delivering high-quality infection prevention solutions and innovative solutions to our clients. We value our employees and provide a dynamic work environment that encourages growth and development. How to Apply: Interested candidates should apply with their resume. Fortive Corporation Overview Fortive’s essential technology makes the world stronger, safer, and smarter. We accelerate transformation across a broad range of applications including environmental, health and safety compliance, industrial condition monitoring, next-generation product design, and healthcare safety solutions. We are a global industrial technology innovator with a startup spirit. Our forward-looking companies lead the way in software-powered workflow solutions, data-driven intelligence, AI-powered automation, and other disruptive technologies. We’re a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to groundbreaking sustainability solutions. We are a diverse team 17,000 strong, united by a dynamic, inclusive culture and energized by limitless learning and growth. We use the proven Fortive Business System (FBS) to accelerate our positive impact. At Fortive, we believe in you. We believe in your potential—your ability to learn, grow, and make a difference. At Fortive, we believe in us. We believe in the power of people working together to solve problems no one could solve alone. At Fortive, we believe in growth. We’re honest about what’s working and what isn’t, and we never stop improving and innovating. Fortive: For you, for us, for growth. About Advanced Sterilization Products ASP is a leading global provider of innovative sterilization and disinfection solutions, and a pioneer of low-temperature hydrogen peroxide sterilization technology.ASP’s mission is to protect patients during their most critical moments. We support healthcare facilities in the fight to protect patients against hospital acquired infections, which are a leading cause of morbidity and mortality. ASP’s products, which are sold globally, include the STERRAD system for sterilizing instruments and the EVOTECH and ENDOCLENS systems for endoscope reprocessing and cleaning. We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at applyassistance@fortive.com. Bonus or Equity This position is also eligible for bonus as part of the total compensation package. ASP is a leading global provider of innovative sterilization and disinfection solutions, and a pioneer of low-temperature hydrogen peroxide sterilization technology.ASP’s mission is to protect patients during their most critical moments. We support healthcare facilities in the fight to protect patients against hospital acquired infections, which are a leading cause of morbidity and mortality. ASP’s products, which are sold globally, include the STERRAD system for sterilizing instruments and the EVOTECH and ENDOCLENS systems for endoscope reprocessing and cleaning. We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at applyassistance@fortive.com. This position is also eligible for bonus as part of the total compensation package.

Join an industry leader and make a positive change in the sustainable use of the world’s natural resources. Together, we will transform the business and drive the industry toward a greener future. At Metso, you will be supported by our inclusive culture and a network of colleagues from around the world. With us, you will embark on a personal growth journey and are encouraged to realize your potential. This is your invitation to rise above the possible. Job posting end date: Position Name: Senior Engineer Instrumentation & Control Job Objective: Engineering activities related to the Basic & Detail Engineering, Proposal Engineering and Procurement activities for Instrumentation and Automation packages of EPS / EPC jobs pertaining to Ferrous / Non-Ferrous Process Plants. Co-ordination with intra departments, overseas teams, consultants, vendors, and clients during the various stages of project. Job Description: Detail Engineering activities like Preparation of Technical Specification, Instrument list, P&I drawings, specification data sheets of all type of field instruments, Valves, Cable etc, Preparation of Cable Schedule, Junction Box Schedule, Loop wiring and panel wiring diagram. Capable of doing Hook up drawings, cable tray layout, air distribution drawings, Instrument and Junction Box location drawings, control room layout etc. Enquiry requisitions, technical clarifications & evaluation of bids, meeting with vendors, technical bid analysis, Technical Recommendation vendor data / drawing review / approval Sizing calculation checking of Flow Element like Orifice Plates, Magnetic flow meter Venturi Meters etc. Also familiar with software checking of Control Valve sizing. Preparation of I/O List, cause effect list automation BOQ, Automation System Architecture etc. Familiar with software like AutoCAD, Comos, SPI. Working knowledge of Instrumentation Standards & Safety Standard. Concept of Zone area / hazard classification Inspection and FAT of instrumentation and automation items. Engineering, Design and Project Execution for Instrumentation, DCS, PLC, based automation system of process plant. Supervision of Erection, Calibration, Pre-Commissioning, I/O Checking and Commissioning of DCS/PLC Based automation system of Process Plant. Requirements & Competences: Requirements and Competencies: Latest versions of Auto CAD. COMOS 9.2 Versions. Meridian Blue cello Conversant with Windows Environment and software packages such as MS Office, MS Excel, and day-to-day usage engineering software. Control Valve sizing software Flow meter sizing software Knowledge in relevant international codes and standards The ability to take lead role in a project team The ability to supervise engineering work Self-sufficient package handling Willingness of international and domestic travel Effective communication skills both verbally and in writing in English Bachelor or master’s degree in Electrical Engineering Minimum 10 years’ experience in plant engineering and supply of process instruments Experience in Ferrous / Non-Ferrous Process Plants Performance metrics: On time delivery of drawings / documents Quality of deliverables Cooperation with internal and external stakeholders Collaboration and stakeholders Project & Procurement Teams Engineering Disciplines Vendor / supplier Consultant Client How to join - Working at Metso - About Metso - Diversity and Inclusion - Meet our people Metso is an equal opportunity employer committed to fostering an inclusive and diverse workforce culture. All qualified applicants will receive consideration for employment without regard to race, religion, color, nationality, gender, gender identity, sexual orientation, age, status as a protected veteran or status as a qualified individual with a disability. Metso is a frontrunner in sustainable technologies, end-to-end solutions and services for the aggregates, minerals processing and metals refining industries globally. We improve our customers’ energy and water efficiency, increase their productivity, and reduce environmental risks with our product and service expertise. We are the partner for positive change. Metso is headquartered in Espoo, Finland. At the end of 2024 Metso had close to 17,000 employees in around 50 countries, and sales in 2024 were about EUR 4.9 billion. Metso is listed on the Nasdaq Helsinki. metso.com

Vestas is the world leader in wind technology and a Defining-force in the development of the wind power industry. Vestas’ core business comprises the development, manufacture, sale, marketing and maintenance of Wind Turbines. Come and Join us at Vestas! Region APC > Service APAC > Service Site - Taralakatti Customer Service Department handles Post-sales Service Operations to meet the contractual obligations with customers. Responsibilities Manage the entire inventory lifecycle, from receiving to delivery. Conduct receiving inspections and raise NCRs for any deviations. Use SAP and MS Office to handle transactions and create reports. Ensure timely delivery of materials using a pick-and-pack process. Perform scheduled stock counts to maintain accuracy. Monitor for expired and out-of-stock items, following the FIFO process. Ensure all necessary documents (DC, e-waybill) are present for outgoing materials. Manage the disposal of waste and the calibration of equipment (PPEs, MIs, lifting tools). Maintain all store-related documents according to IQMS standards. Supervise external laborers for loading and unloading tasks. Implement and maintain the 5S process for a clean and organized store. Qualification 3 to 5 years of experience in store processes Proficiency in English and Kannada is required (reading and writing) Knowledge of Hindi is a plus Competencies Solid understanding of store processes, including inventory management Proficiency with SAP, specifically the MM module and store-related transactions Effective communication, coordination, and reporting skills Basic computer skills and experience with online reporting systems Valid driver's license What We Offer Vestas provides an open, respectful, and global culture, an attractive compensation package, and long-term career development. We care and respect all employees and will offer: On the job training, an ideal platform for professional and personal development, Bonus Program &, etc. In return, we expect you to go the extra mile to achieve results. Additional Information The work location is in Taralakatti, Karnataka. Please note: We do amend or withdraw our jobs and reserve the right to do so at any time, including prior to the advertised closing date. Please be advised to apply on or before 20th August 2025. Learn more about Vestas at www.vestas.com and follow us on our social media channels. Our commitment to a fair hiring At Vestas, we evaluate all candidates solely on professional experience, education, and relevant skills. To support a fair recruitment process, please remove any photos, dates of birth or graduation dates, gender pronouns, marital status, or other personal details not relevant to the role, before submitting your CV. Please keep your CV focused on work and educational details, and the necessary information that we contact you (email and phone number). We train our hiring teams in inclusive evaluation and regularly review process outcomes to ensure fairness. DEIB Statement At Vestas, we recognise the value of diversity, equity, and inclusion in driving innovation and success. We strongly encourage individuals from all backgrounds to apply, particularly those who may hesitate due to their identity or feel they do not meet every criterion. As our CEO states, "Expertise and talent come in many forms, and a diverse workforce enhances our ability to think differently and solve the complex challenges of our industry". Your unique perspective is what will help us powering the solution for a sustainable, green energy future. BEWARE – RECRUITMENT FRAUD It has come to our attention that there are a number of fraudulent emails from people pretending to work for Vestas. Read more via this link, https://www.vestas.com/en/careers/our-recruitment-process About Vestas Vestas is the energy industry’s global partner on sustainable energy solutions. We are specialised in designing, manufacturing, installing, and servicing wind turbines, both onshore and offshore. Across the globe, we have installed more wind power than anyone else. We consider ourselves pioneers within the industry, as we continuously aim to design new solutions and technologies to create a more sustainable future for all of us. With more than 185 GW of wind power installed worldwide and 40+ years of experience in wind energy, we have an unmatched track record demonstrating our expertise within the field. With 30,000 employees globally, we are a diverse team united by a common goal: to power the solution – today, tomorrow, and far into the future. Vestas promotes a diverse workforce which embraces all social identities and is free of any discrimination. We commit to create and sustain an environment that acknowledges and harvests different experiences, skills, and perspectives. We also aim to give everyone equal access to opportunity. To learn more about our company and life at Vestas, we invite you to visit our website at www.vestas.com and follow us on our social media channels. We also encourage you to join our Talent Universe to receive notifications on new and relevant postings.

Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - RA / SRA (S1/S2/S3/S4) Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-8y in analytical chemistry (HPLC/LCMS/NMR or purification) Interaction with synthetic team and problem solving skills. Should be able to handle the respective instrument Knowledge of instrumental technique with its application Should be able to handle routine analysis independently on respective instrument. Experience in method development on HPLC/LCMS will be desirable but not necessary Maintenance, cleaning, documentation and calibration of analytical instruments. Maintain laboratory as safe working place. Person Profile Qualification: - M. Sc (Analytical Chemistry) Experience: - 2 years of relevant experience Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Job Title Officer / Sr. Officer Peptide Business Unit Global API Business Job Grade G12C / G12B Location : Ahmednagar / Ahilyanagar At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key Responsibilities To issue and receipt of raw materials for manufacturing of Peptide Products as per requirement. Charging of batches and carry out all operations related to process as per BMR and written procedures. To manufacture peptide products as per BMR and written procedures in Peptide plant Operations, Calibration, Cleaning and Maintenance of process equipment and recording their usage logs. Monitor Process and cleaning turn around time (TR) during synthesis and purification of Peptide products. Monitor process parameter and yield. Reduction in Solvent usage and reduction in down time of the instruments. Reduction in batch failures, batch hold ups and generation of waste. Travel Estimate Job Requirements Educational Qualification B.Sc (Chemistry) / M.Sc. (Organic Chemistry) Experience Tenure : 5 to 7 yrs experience in Peptide API manufacturing Units Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Title Officer / Sr. Officer Peptide Business Unit Global API Business Job Grade G12C / G12B Location : Ahmednagar / Ahilyanagar At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key Responsibilities To issue and receipt of raw materials for manufacturing of Peptide Products as per requirement. Charging of batches and carry out all operations related to process as per BMR and written procedures. To manufacture peptide products as per BMR and written procedures in Peptide plant Operations, Calibration, Cleaning and Maintenance of process equipment and recording their usage logs. Monitor Process and cleaning turn around time (TR) during synthesis and purification of Peptide products. Monitor process parameter and yield. Reduction in Solvent usage and reduction in down time of the instruments. Reduction in batch failures, batch hold ups and generation of waste. Travel Estimate Job Requirements Educational Qualification B.Sc (Chemistry) / M.Sc. (Organic Chemistry) Experience Tenure : 5 to 7 yrs experience in Peptide API manufacturing Units Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Description To follow the safety rules in the premises according to the company norms. To ensure aseptic area cleaning and fogging to coordinating with engineering department as per the schedule. To maintain online the BMRs and other log books in the respective area as per cGMP and SOP. Responsible for manufacturing and supervising of Media fill and Drug products batches as per BMR. Responsible to perform the in process checks during operation. Responsible for Dispensing, checking and receiving of the Raw Material from warehouse. Responsible for Area cleaning and Maintain the area properly for autoclave area. Responsible for operation and cleaning of area equipment present in the autoclave area like Pass boxes, Glove cleaning and integrity testers. Preparation, filtration and issuance of disinfectant and deactivation solutions to all the sections in the production area. Operation and cleaning of table mounted LAF and Ceiling mounted LAF and steam sterilizer and HPHV steam sterilizer Preparation of loads meant for Autoclaving like garments, disinfectant, filling, filtration, rubber stopper and seals for sterilization as per the validated load pattern. Responsible for Maintenance and cleaning of Component preparation and sterilization area (Autoclave area). To maintain the BMRs and other log books in the Component preparation and sterilization area (Autoclave area) as per cGMP and SOP. Monitoring of DP, RH and temperature in compounding and filtration area, autoclave area. Responsible for operation, calibration and cleaning of weighing balance, pH meter, DO meter and conductivity meter, Compounding isolator, Manufacturing and filtration vessels, Heating & cooling skid, Air shower. Table mounted LAF and ceiling mounted LAF, Filter integrity tester, Sonicator , TFF, Homogenizer, Lipid extruder, Fogger, Heating magnetic stirrer with thermometer, SART system, Strip chart recorder, HAWO pouch sealer. Responsible for the co-ordination with cross functional departments like QA, QC, warehouse Engineering, HR and administration for the day to day activities. Timely completion of SOPs training and on the job trainings related to autoclave area and filling area. Responsible for operation and cleaning of dynamic pass box in autoclave area and filling area. To carry out CIP & SIP of the vessels related to autoclave area and filling area. Responsible for timely completion of calibrations and validations activity in coordination with Engineering and QA related to autoclave area and filling area. Preparation and periodic revision of SOPs related to aseptic processing area. Responsible to perform the in process checks during filling. Qualifications Qualification - B Pharma, M Pharma About Us Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion. About The Team The Human Resources team partners with all aspects of the organization, driving success through the effective and innovative management of people for both current and future business needs. Key Roles That The Human Resources Team Performs Executive Role: Specialists in all aspects of people management. High-level input at strategic level into all key business decisions. Audit Role: Ensures all areas of the organization are compliant with legal requirements AND best practice employment policies and procedures. Facilitator Role: Close partnership to support, advise and extend the ability of all areas of the organization to meet their objectives through implementation of highly effective employment practices in areas such as Talent Acquisition, Learning and Development, Reward systems, Performance Management, Health and Wellbeing. Consultancy Role: Provide expert advice to the organization and it’s managers on any aspect of workforce management and employee relations and performance. Service Role: Ensure the organization is fully aware of and is equipped to deal with developments impacting employment matters, such as changes in legislation, changes in the characteristics of the labor market.