Job Description ▪ JOB DESCRIPTION ▪ Please refer to the methodology template JOB TITLE JOB FAMILY DATE Supplier Quality Development Engineer QUALITY 01/10/2024 MANAGER TITLE (solid line) FUNCTIONAL MANAGER TITLE (dotted line) Country Purchase Asia SQD Manager MISSION The Supplier Quality D evelopment Engineer is responsible to improve supplier performance by doing supplier quality continuous improvement activit ies , audits, review s and assessments together with other relevant functions in the organization to meet PO Quality targets. Lead and facilitate development of supplier assigned during development and production phases. The Senior SQDE are working experts for the Supplier Quality System who will train, and mentor new PSQEs and SQDE’s assigned Responsibilities & Activities Product Development Phase Lead and Facilitate development of suppliers to meet P O Automotive Systems Requirements Manual s to improve quality, cost, and delivery performance of suppliers through PO APQP process. Responsible of Quality and Process Supplier Evaluation for all suppliers and Supplier Onsite Process Approval (SOPA) on key suppliers as required Responsible for the timeliness approval of PPAP per project requirements . Management of Supplier rating system in conjunction with Purchasing Department and necessary systems to include monthly reporting of Supplier PPM Scores. To lead Supplier Quality Management Reviews (SMQR) Level II at division level and support at plant level as needed. Management of Level II Containment Procedures and implementation . Product Production Phase Responsible of transfer from Supplier Quality Development to Plant Supplier Quality at the beginning of each program production phase plus 6 months or as necessary Lead and Facilitate suppliers to meet PO Automotive Systems Requirements Manual to improve quality, cost, and delivery performance of suppliers. Monitor of Supplier Performance Quality Rating on a monthly basis and schedule follow up audits and reviews for assigned suppliers. Champion supplier PPM reductions including read across of common commodity issue (i.e. focus on poor performing suppliers, high PPM, SNCR’s, and Critical Issues for their assigned suppliers.) Lead Supplier Improvement Audits and Supplier Onsite Process Approval (SOPA) on supplie rs assigned until closure of all the actions. Train and mentor Plant Supplier Quality Engineers assigned Others Train and mentor Supplier Quality Engineers assigned Lead/Support New Projects for Supplier Quality assigned Facilitate continuous improvement activities at suppliers to implement performance improvement, (i.e. Kaizen, Six Sigma, VA/VE events). Maintain quality document central file (supplier performance records pertaining to quality, cost, and delivery rating, evaluations, containment activities, etc.) per supplier Support internal customers (Program Teams, Logistics, Commodity Buyers, QE, SQE) & mfg. plant supplier issues Must comply with all work rules, policies and procedures. Must comply with all safety rules and regulations. Other duties as assigned Integrated Management System (IMS) Within his/her scope of responsibility, he/she respects the standards and rules in terms of Quality, Safety and Environment contributing to the IMS process management and improvement. ORGANIZATION Country Purchase Manager SQE POSITION KEY INTERFACES (internal and/or external) Internal Suppliers Program Core team (especially Buyers and QE) Plant Quality (QM and PSQE) SQDE External Equipment & service supplier (Domestic and oversea supplier) POSITION BACK UP Fill in with back-up position titles only. Back-up should be indicated for positions in charge of customer orders treatment, supplier on-time delivery, quality, production capacity, shared loading (multi-part station), lead time, inventory level, preventive maintenance, and calibration are the ones to be provided with a back-up. NA KEY MEASURES & FINANCIAL ACCOUNTABILITY Indicate the Key Indicators used to measure the performance of the position and the financial metrics on which the role has got a direct or indirect impact (budget, sales, …) Supplier Scorecard (Quality) PPAP Approval On-time Quality SNCR Closure and Recovery Supplier Request for Change Approval Key Project Implementation Profile Requirements Personal Background Bachelor's degree required (Engineering, Science or Technical) Have worked within the Quality, Process Engineering AND Supplier Quality for >5 years (Mandatory) Experience in APQP and PPAP required Management or Leadership exposure. Skills & Abilities Good Coaching skills Strong problem solving, decision making and prioritization skills required Fluent in English Good verbal and written communication skills required Experience TS16949, process auditor or CQA certification ( preferred. ) Rigourous and a bility to collect, maintain and analyze data. Ability to read and understand measurements and scales. Microsoft Office computer skills, particularly in Word, Excel, Project and ERP (SAP-preferred) Ability to maintain working relationship with internal and external customers. Must be flexible, dependable, and creative. Proven ability in a team environment. Organized and a bility to work independently and meet deadlines. Maintain confidentiality at all times. Able to travel to all requir ed countries. To define the Soft Skills required for the job, please refer to PO General Competencies available on Topnet . Job Description Approval Manager name & title: Jyoti Yadav Country Purchase Manager HR Manager Name & Title Sunaina Vashist Country HR Manager EMPLOYEE ACKNOWLEDGEMENT (optional, depends on local legal requirements) Employee Name Annex : Plastic Omnium General Competencies 1/2 8 GENERAL COMPETENCIES IMPACTING THE QUALITY OF WORK AND INTERACTIONS AT WORK. EACH COMPETENCY IS ILLUSTRATED WITH 3 BEHAVIORS. Listening Is an attentive and patient listener Asks questions to better understand thoughts and feelings of others Respects divergent points of view / willing to re-evaluate own point of view/Openly receives feedback Enthusiasm Has a positive outlook of the future, despite difficulties or tough situations Understands needs and motivations of others Gives meaning and purpose to projects and work in general Team Spirit Puts the interest of the team before own interest Doesn't hold back information, provides others with the information they need for their jobs. Give feedback Despite divergences, relates and cooperates well with peers and colleagues. Perseverance Pursues everything with energy Doesn't give up easily, is resilient facing difficulties and failures Strives to do the best Risk taking Generates new ideas Challenges the status quo Creates and implements needed changes Networking Creates and participates in opportunities to know people that are important for his/her job and for the company Entertains professional relationships internally and externally, participates in professional networks and associations Knows who to contact to get advice, find solutions, influence decisions Decision making Develops solutions that address problems Makes decisions timely, doesn't procrastinate Is comfortable deciding under uncertainty Communication Delivers clear and easy to understand information Conveys ideas and information with enthusiasm and conviction Is comfortable communicating to different types of audiences, upwards and downwards Annex : Plastic Omnium General Competencies 2/2 3 KEY COMPETENCIES OF PEOPLE MANAGERS. EACH COMPETENCY IS ILLUSTRATED WITH 3 BEHAVIORS. Develops his/her collaborators in the above general competencies Supports team members in their professional development and helps them to build their career. Builds appropriate development plans. Anticipates and suggests options for mobility and succession planning in the PO Group. Motivates his/her collaborators Knows well the members of the team (functional or hierarchical), identify their competencies and capabilities in order to give them responsibilities that motivate them and supports the development of their performance. Attracts the best people Enthusiastic and realistic about her/his job and professional environment, knows how to trigger the willingness of current employees and potential candidates to join his/her team and/or Plastic Omnium. Scope of Application & Responsibilities SCOPE OF APPLICATION ☐ Fuel Systems ☐ SCR Systems ☒ All Products ☒ Others: All POAI sites and products ☒ Division HQ ☒ Plant ☒ Technical Center / Antenna ☒ Analysis center ☒ Research center ☒ SILS SCOPE OF DISTRIBUTION ☒ Internal only ☐ Restricted to: ……. ☐ Supplier ☐ OEM Document History Version Revision Description Date Contributors Process Owner/Leader Validation V01E01 Creation 25/03/2016 C. Diniz C. Maire V02E01 Update to reorganize data and to add the part “back-up position” needed for IATF compliance 21/11/2017 V. Lassalle C. Diversy V02E02 Update indications on position “back-up” 27/02/2018 V. Lassalle C. Diversy V03E01 Update Responsibilities on Integrated Management System Update Responsibility and Activity section Update indications on PO General Competencies 28/01/2020 M. Longhitano C. Diversy Show more Show less

QUALIFICATION: Bachelor degree in Electrical engineering, Instruments and related to oil and gas field. EXPERIENCE: 3- 5 YRS ABOVE IN PIPELINE PROJECTS AND CONSTRUCTION CURRENT JOB LOCATION : Jalpaiguri, West Bengal (WILLING TO RELOCATE CANDIDATE ONLY). Position Overview: We are seeking a skilled Electrical & Instrumentation (E&I) Inspector with extensive experience in glanding, commissioning, inspection, and verification of motors and transformers, as well as expertise in quality control within hazardous EX atmospheres. The E&I Inspector will play a pivotal role in ensuring the quality, safety, and compliance of electrical installations, particularly focused on motors, transformers, and EX-rated environments. The ideal candidate should possess a deep understanding of industry standards, safety protocols, and possess a proven track record of successful field experience. Key Responsibilities: Motor and Transformer Inspection: · Conduct thorough inspections of motors and transformers during various project phases, ensuring adherence to technical specifications, codes, and standards. · Verify proper connections, insulation, grounding, and wiring of motors and transformers. · Perform detailed tests and assessments to ensure the optimal functionality and efficiency of these critical components. EX Atmosphere Expertise: · Apply specialized knowledge of hazardous EX atmospheres to assess, inspect, and ensure the safety and compliance of electrical installations in such environments. · Verify the proper selection and installation of EX-rated equipment and materials. Commissioning and Testing: · Oversee commissioning processes, ensuring motors, transformers, and associated instrumentation are integrated and function as intended. · Conduct functional tests, performance evaluations, and calibration of equipment to confirm their proper operation. Quality Control and Assurance: · Implement rigorous quality control measures to ensure that motors, transformers, and related systems meet established standards and project requirements. · Identify defects, discrepancies, or deviations in the installation process and provide recommendations for corrective actions. Safety Compliance: · Enforce stringent safety protocols and guidelines in compliance with EX atmosphere requirements and industry best practices. · Identify potential hazards and risks associated with electrical installations in hazardous environments and collaborate on effective mitigation strategies. Documentation and Reporting: · Maintain detailed documentation of inspections, tests, findings, and corrective actions taken. · Generate comprehensive reports outlining inspection results, deviations, and recommendations. Field Expertise: · Leverage extensive field experience to make informed decisions, troubleshoot complex issues, and provide practical solutions in real-world scenarios. Collaboration and Communication: · Collaborate closely with cross-functional teams, including engineers, contractors, and project managers, to ensure effective coordination and communication throughout projects. Professional Development: · Stay current with the latest industry trends, technologies, and regulations related to E&I systems, EX atmospheres, and quality control. please send resume to email id:hr@mastekengineering.com contact number : 9597088826 , 9597088822 Job Type: Full-time Benefits: Health insurance Provident Fund Ability to commute/relocate: Jajpur, Orissa: Reliably commute or planning to relocate before starting work (Preferred) Experience: E & I: 3 years (Preferred) Willingness to travel: 75% (Preferred) Work Location: In person

QUALIFICATION: Bachelor degree in Electrical engineering, Instruments and related to oil and gas field. EXPERIENCE: 3- 5 YRS ABOVE IN PIPELINE PROJECTS AND CONSTRUCTION CURRENT JOB LOCATION : Jalpaiguri, West Bengal (WILLING TO RELOCATE CANDIDATE ONLY). Position Overview: We are seeking a skilled Electrical & Instrumentation (E&I) Inspector with extensive experience in glanding, commissioning, inspection, and verification of motors and transformers, as well as expertise in quality control within hazardous EX atmospheres. The E&I Inspector will play a pivotal role in ensuring the quality, safety, and compliance of electrical installations, particularly focused on motors, transformers, and EX-rated environments. The ideal candidate should possess a deep understanding of industry standards, safety protocols, and possess a proven track record of successful field experience. Key Responsibilities: Motor and Transformer Inspection: · Conduct thorough inspections of motors and transformers during various project phases, ensuring adherence to technical specifications, codes, and standards. · Verify proper connections, insulation, grounding, and wiring of motors and transformers. · Perform detailed tests and assessments to ensure the optimal functionality and efficiency of these critical components. EX Atmosphere Expertise: · Apply specialized knowledge of hazardous EX atmospheres to assess, inspect, and ensure the safety and compliance of electrical installations in such environments. · Verify the proper selection and installation of EX-rated equipment and materials. Commissioning and Testing: · Oversee commissioning processes, ensuring motors, transformers, and associated instrumentation are integrated and function as intended. · Conduct functional tests, performance evaluations, and calibration of equipment to confirm their proper operation. Quality Control and Assurance: · Implement rigorous quality control measures to ensure that motors, transformers, and related systems meet established standards and project requirements. · Identify defects, discrepancies, or deviations in the installation process and provide recommendations for corrective actions. Safety Compliance: · Enforce stringent safety protocols and guidelines in compliance with EX atmosphere requirements and industry best practices. · Identify potential hazards and risks associated with electrical installations in hazardous environments and collaborate on effective mitigation strategies. Documentation and Reporting: · Maintain detailed documentation of inspections, tests, findings, and corrective actions taken. · Generate comprehensive reports outlining inspection results, deviations, and recommendations. Field Expertise: · Leverage extensive field experience to make informed decisions, troubleshoot complex issues, and provide practical solutions in real-world scenarios. Collaboration and Communication: · Collaborate closely with cross-functional teams, including engineers, contractors, and project managers, to ensure effective coordination and communication throughout projects. Professional Development: · Stay current with the latest industry trends, technologies, and regulations related to E&I systems, EX atmospheres, and quality control. please send resume to email id:hr@mastekengineering.com contact number : 9597088826 , 9597088822 Job Type: Full-time Benefits: Food provided Health insurance Provident Fund Ability to commute/relocate: Haldia, West Bengal: Reliably commute or planning to relocate before starting work (Preferred) Experience: E & I: 3 years (Preferred) Willingness to travel: 75% (Preferred) Work Location: In person

Job Description Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible to perform the environment monitoring activities Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record. Qualifications Education: B.Sc./ M.Sc in Microbiology Total Experience 7-10 Year inexperience in Environmental Monitoring for sterile manufacturing plant Note: Candidates who want to apply for internal jobs, must have completed at least 2 years within existing role. Show more Show less

Chromatography System Service Engineer Educational Qualifications Required Qualifications for a Chromatography System Service Engineer Bachelor’s degree in electrical engineering, Instrumentation, Biochemical Engineering, or a related field. Experience 2 - 5+ years of experience in industries, control systems, or a related field. Experience working in industries such as manufacturing, pharmaceuticals, automotive, or food processing Technical Skills & Experience Hands-on experience in servicing, troubleshooting, and maintaining chromatography systems Strong understanding of chromatographic techniques Knowledge of analytical instruments, pumps, detectors, and fluidic systems. Proficiency in calibration and validation of chromatography equipment. Familiarity with GMP, GLP, and FDA regulations for pharmaceutical/biotech environments. Experience with software and automation systems used in chromatography. Soft Skills Strong problem-solving and analytical skills. Ability to work independently and as part of a team. Good communication skills for customer interaction and technical support. Willingness to travel for onsite service and support. About Sartorius Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide. We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment. Join our global team and become part of the solution. We are looking forward to receiving your application. www.sartorius.com/careers Show more Show less

Senior Manager HRBP About organization About Vymo Vymo is a San Francisco-based next-generation Sales productivity SaaS company with 7 global offices. We are funded by top tier VC firms like Emergence Capital and Sequoia Capital. Vymo is a category creator, an intelligent Personal Sales Assistant which captures sales activities automatically, learns from top performers, and predicts ‘next best actions’ contextually. What is the Personal Sales Assistant A game-changer! We thrive in the CRM space where every company is struggling to deliver meaningful engagement to their Sales teams and IT systems. Vymo was engineered with a mobile-first philosophy. The platform through AI/ML detects, predicts, and learns how to make Sales Representatives more productive through nudges and suggestions on a mobile device. Explore Vymo on https://vymo.com/ Organization Context & Job Summary : At Vymo we have embarked on a journey of building the organization to 100 X scale , this entails building scalable systems and processes across the organization. The Human Resource function plays a critical role in building these scalable systems and processes in line with the organization priorities . The talent management and strategic programs manager will play a pivotal role in the employee success team in building robust processes and systems in the field of Talent Management , Organizational development, Ma nagerial Capability Building , Succession Planning , HR Tech & Transformation Employment Type ; Permanent Location : Bangalore , Hybrid About the Role: The Human Resource function plays a critical role in building these scalable systems and processes in line with the organization priorities . The HRBP will be embedded within our tech, product, and support orgs to provide strategic HR partnership and hands-on support. You’ll work closely with leadership and managers to understand business priorities, champion employee experience, and deliver high-impact people programs—from org planning and performance management to eNPS action planning and employee development . Job Responsibilities Strategic Business Partnership Act as a strategic advisor and coach to functional leaders in Engineering, Product, and Customer Support. Translate business goals into aligned people strategies—supporting org design, workforce planning, and team capability building. Use data-driven insights to influence decision-making and identify people trends, risks, and opportunities. CoE Program Design & Implementation Collaborate with CoE teams (Talent Management, Rewards, OD) to shape and execute org-wide initiatives. Provide business lens/feedback into CoE programs to improve relevance and adoption. Co-design and pilot HR programs such as: Capability frameworks and skills mapping Leadership development interventions Employee engagement & culture transformation Diversity & inclusion programs Rewards benchmarking and role calibration Employee Experience & Engagement Own and drive the eNPS (Employee Net Promoter Score) cycle—partnering with People Ops on survey design, running quarterly or biannual pulse checks, and facilitating action planning workshops with leaders and teams. Conduct regular listening sessions, skip-level conversations, and real-time feedback loops to stay ahead of issues. Champion a culture of psychological safety, trust, and continuous improvement. Performance & Talent Management Lead the performance enablement cycle—goal setting, ongoing feedback, mid-year and annual reviews. Partner with managers to develop high-potential talent and succession plans. Identify learning needs and collaborate with the L&D team to roll out targeted interventions. People Ops & Compliance Collaborate with HR Ops to ensure smooth onboarding, offboarding, and internal mobility processes. Support fair and consistent application of HR policies, handle employee relations cases with care and clarity. Maintain HR data accuracy and leverage dashboards for ongoing org health tracking. What We're Looking For 6–8 years of HR experience, with at least 3+ years in a strategic HRBP role in a high-growth tech/product company. 1-2 years experience in HR CoE role will be a plus Ability to lead one or two member team Demonstrated experience supporting Engineering/Product/Support teams. Strong analytical and diagnostic skills—comfortable working with tools like Excel, dashboards, or survey platforms to draw insights. Hands-on experience running eNPS or engagement surveys , analyzing data, and facilitating cross-functional action planning. High emotional intelligence and a collaborative, problem-solving mindset. Solid understanding of employment laws and HR practices in your region (global exposure a plus). Thrive in fast-paced, dynamic environments with shifting priorities. Show more Show less

Job Title: Calibration Engineer (Experienced) Company: NCQC Laboratory LLP Location: Ahmedabad (Gujarat) Job Type: Full-Time Salary: Rs. 3 Lakh to 4 Lakh per annum (Negotiable) Other Benefits: Travel and food allowance for visiting client’s place About NCQC Laboratory LLP NCQC Laboratory LLP, NABL accredited calibration laboratory based in Ahmedabad, is a premier provider of high-precision calibration and testing services since more than 25 years. We specialize in delivering reliable, accurate, and cost-effective calibration solutions to meet industry standards. Our laboratory is equipped with state-of-the-art instruments and technology, allowing us to serve a broad range of industries, including manufacturing, construction, engineeringand pharmaceutical companies. We are currently looking for a skilled Calibration Engineer to join our team. In this role, you will be responsible for calibration of the instruments and equipment of our clientsto ensure they remain accurate and compliant with relevant calibration standards. Job Description As an experienced Calibration Engineer, you will work closely with internal teams and clients to perform the calibration of various instruments and measurement equipment. You will be responsible for ensuring that all calibration activities are carried out according to industry standards and regulations while providing technical expertise to guarantee precision and compliance. Key Responsibilities: Calibration of Instruments: Perform calibration of various measuring, monitoring and testing instruments, including pressure gauges, thermometers, flow meters, energy meters, weight scales, and other specialized equipment. Inspection & Maintenance: Inspect and maintain calibration equipment to ensure it meets the required performance standards and is functioning optimally. Documentation & Reporting: Maintain detailed records of calibration activities, including calibration certificates, logs, and reports. Ensure documentation is accurate and compliant with regulatory requirements. Troubleshooting: Identify, diagnose, and resolve any calibration-related issues with instruments and equipment, ensuring minimal downtime for clients. Compliance: Ensure all calibration activities adhere to international and industry standards (e.g., ISO/IEC 17025) and meet legal and regulatory requirements. Customer Support: Provide technical support and guidance to clients regarding calibration issues, and assist with equipment setup and usage to ensure ongoing accuracy. Continuous Improvement: Stay up to date with the latest trends and developments in calibration technology, techniques, and standards. Training: Assist in training junior/ fresh engineers or technicians on calibration procedures and best practices. Skills and Qualifications: Bachelor’s degree/ Diploma in Engineering(mechanical, electrical, Instrumentation) or a related field. Proven experience in a calibration role, preferably in a calibration laboratory or industrial environment. Knowledge of calibration procedures, standards (e.g., ISO 17025), and measurement techniques. Proficient in the use of calibration equipment and tools. Good computer knowledge and proficient in working with Word, Excel and basic computer programs. Strong troubleshooting and problem-solving skills. Detail-oriented with excellent organizational and record-keeping abilities. Ability to work independently and as part of a team. Strong communication skills to provide technical assistance to clients and colleagues. Familiarity with calibration software and data management systems is an advantage. Additional Information: Candidate must be a local resident of Ahmedabad or willing to relocate to Ahmedabad Travel may be required to perform on-site calibrations at client facilities. A valid driver’s license and access to a vehicle will be necessary for on-site work. Shift flexibility may be required depending on project deadlines or client needs. If you meet the above qualifications and are interested in joining a dynamic and innovative team, please apply/ submit your resume Job Types: Full-time, Permanent Pay: ₹250,000.00 - ₹400,000.00 per year Benefits: Food provided Health insurance Schedule: Day shift Work Location: In person

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job Summary We are seeking an experienced individual to lead our Utility ,HVAC & Water System team having good technical knowledge and hands on experience on the Operation & maintenance .The role involves reviewing engineering deliverables, guiding event investigations, proposing corrective actions, and ensuring compliance with audit standards. The ideal candidate will focus on minimizing downtime, generating energy-saving ideas, and prioritizing safety for people, equipment, and facilities. Roles & Responsibilities Good knowledge of operation & maintenance of Utility, HVAC & Water System. Implement & Enforce Safe Working Practices throughout the plant by adhering to all the Safety Standards developed by CSSM guided by (MSI) My safety Index. To ensure that Current Good Manufacturing Practices (cGMP) are being adhered during the Maintenance of Utility Equipment Such as water system, HVAC, Compressed Air, PSG, steam etc. To ensure that Engineering Excellence measures, Energy Conservation measures & other initiatives are driven effectively at the plant with the central Engineering team guidance. To ensure that equipment operations, maintenance activities and its documentation is carried out adhering to existing quality management system. To ensure that the Utility equipment adhere to latest MES (Minimum Engineering Standards) Check list, Good Engineering Practices. Co-ordinate with internal customers for routine operational and maintenance issues by providing feedback to the Engineering Head from time to time. To ensure that Preventive maintenance of the utility machinery is carried out as per the schedule & applicable SOP. To ensure that support is provided for all the utility Equipment Preventive Maintenance, Breakdown Maintenance & Qualification as & when required as per the situation demand. To ensure that Breakdowns are addressed in a systematic way through SAP & proper documentation is maintained. To perform various tasks related to QMS like initiation of incidents, performing root cause analysis, initiation of CAPAs and execution. Execution of new projects as per the given project schedule. Continuously monitoring & controlling electrical Power & fuel consumptions. Working towards implementation of new ideas for power & utility savings. All time readiness for all internal & external audits. Maintain all Utility,HVAC & Water System healthy & to be perform with efficiently to avoid any critical breakdown. Ensure compliance to GMP & Audit requirements. To Ensure validation of HVAC system as per schedule and SOP. To monitor utilities power consumption and ensure the power consumption is within allocated budget. To ensure spares management, control revenue and maintenance budget and to maintain optimum level of inventory. Implementation capacity expansion, simplification and energy saving projects. Ensure Revision of Exiting SOPs and Preparation of new SOPs Whenever Required. Responsible for initiation and closure s of change controls as and when Required. To ensure that Breakdown is addressed in a systematic way through SAP and proper documentation is maintained. To Review the RCA (Root Cause Analysis) and CAPA implementation, spares management to reduce the equipment down time. Having experience of TPM & Lean management and good knowledge of FMEA AM/PM & JH for utility equipments. Qualifications Educational qualification: B.E. or B.Tech Mechanical /Electrical Minimum work experience: 15 to 20 years of experience Skills & attributes: Technical Skills Good knowledge of operation & maintenance of Utility, HVAC & Water System. Implement & Enforce Safe Working Practices throughout the plant by adhering to all the Safety Standards developed by CSSM guided by (MSI) My safety Index. To ensure that Breakdown is addressed in a systematic way through SAP and proper documentation is maintained. To Review the RCA (Root Cause Analysis) and CAPA implementation, spares management to reduce the equipment down time. Having experience of TPM & Lean management and good knowledge of FMEA AM/PM & JH for utility equipments. Knowledge on budgeting, preventive maintenance & calibration scheduling and execution. Ability to handle project related to machine upgradation, installation and commissioning of new equipment, area modification. Basic knowledge on PLC (Programmable Logic Controller) and computerized system (SCADA – Supervisory Control and Data Acquisition). Strong knowledge of preventive and breakdown maintenance strategies. Experience in event investigation and CAPA implementation. Familiarity with audit compliance standards in the pharmaceutical industry. Behavioural Skills Strong communication skill to co-ordinate with vendors, cross function team and regulatory/internal audits and inspections. Leadership and team management skills to guide and lead the process engineering team effectively. Safety-conscious mind-set with a commitment to ensuring the safety of people, equipment, and facilities. Show more Show less

Do you want to work with a high growth women fashion tech company ? At Aimhire.io we are the exclusive recruiting partner to our client and we are hiring urgently. The Customer Support Manager will lead our customer support quality assurance and training initiatives. This role is critical to ensuring our customer support team delivers consistent, high-quality service and continuously improves through effective onboarding, ongoing trainings, and performance feedback. Key Responsibilities- Develop, refine, and implement quality standards and evaluation processes for customer support interactions (voice, email, chat, social). Monitor and evaluate agent interactions against internal standards and customer expectations. Conduct regular quality audits, root cause analyses, and calibration sessions with support leadership. Design and deliver comprehensive onboarding programs for new hires in the support team. Create and maintain up-to-date training materials, playbooks, SOPs, and knowledge base content. Develop and manage ongoing learning initiatives including soft skills, product knowledge, tools training, and process updates. Identify performance trends and work with stakeholders to close skill and knowledge gaps. Analyze metrics and customer feedback to recommend and implement process improvements. Stay up to date with industry trends and emerging tools to continuously improve training and QA methodologies. You Are The Right Fit, If You Have – 6-10 years of experience in Customer Support. Exceptional communication and interpersonal skills. Strong analytical abilities to interpret data and drive informed decisions. Proactive problem-solving mindset with a passion for continuous improvement. Ability to thrive in a dynamic, fast-paced startup environment. Deep understanding of customer needs and a commitment to delivering outstanding service. Leadership and people management skills to coach, motivate, and support a high-performing team Show more Show less

Key Responsibilities: Monitor and evaluate daily calls (live and recorded) for accuracy, quality, and compliance Provide actionable feedback and coaching to agents for performance improvement Prepare detailed QA reports and maintain quality audit logs Analyze trends in call performance and escalate recurring issues to the operations team Assist in the development of call scripts, QA scorecards, and training modules Work closely with the training and operations teams to implement quality improvement initiatives Ensure adherence to compliance, process protocols, and customer service standards Participate in calibration sessions to ensure alignment across QA and operations teams Skills & Qualifications: Bachelor’s degree or diploma in any field 6 months of experience in quality analysis within a call center or BPO Excellent listening, analytical, and report writing skills Strong understanding of call center metrics and quality monitoring tools Proficient in MS Office (especially Excel and PowerPoint) Knowledge of CRM and call recording software is a plus Ability to work independently and in a team with minimal supervision Strong verbal and written communication skills Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹22,000.00 per month Benefits: Leave encashment Paid sick time Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Yearly bonus Education: Bachelor's (Required) Experience: Call Quality BPO: 1 year (Required) Location: Noida Sector 16, Noida, Uttar Pradesh (Required) Work Location: In person Speak with the employer +91 8800828679

Summary: We are looking for fresh graduates to join our team as Calibration Engineers, responsible for performing precise lab calibration and equipment adjustment activities. This role is ideal for candidates passionate about quality, accuracy, and technical problem-solving in the field of instrumentation and engineering. Job Title: Calibration Engineer Qualification: Diploma, ITI, B.E. in Electronics & Communication, Instrumentation, Mechanical, Electrical, or B.Sc. in Physics. Note: Biomedical not eligible Key Role and Responsibilities: Perform lab calibration and adjustment of instruments and equipment as per defined procedures. Maintain detailed records of calibration activities including dates, results, and equipment condition. Assist customers with technical support related to calibration and equipment usage. Ensure compliance with relevant industry standards and regulatory requirements. Stay updated on advancements in calibration techniques and tools. Skills: Technical knowledge in electronics, instrumentation, mechanical, or electrical systems. Analytical thinking and keen attention to detail. Ability to follow procedures and maintain documentation. Good communication and customer interaction skills. Ability to work independently and manage time effectively. Required Skills: Basic knowledge of electronic, mechanical, thermal, or optical systems. Ability to manage multiple tasks in a fast-paced environment. Clear verbal and written communication skills. Willingness to learn and grow in a technical field. Desired Skills: Familiarity with ISO 17025 calibration standards. Prior lab or workshop exposure through projects or internships (preferred, not mandatory). Reporting To: Manager / Senior Calibration Engineer Job Types: Full-time, Permanent, Fresher Pay: ₹13,000.00 - ₹15,000.00 per month Benefits: Provident Fund Schedule: Day shift Fixed shift Monday to Friday Morning shift Location: Porur, Chennai, Tamil Nadu (Preferred) Work Location: In person

Job description Urgently looking for skilled Technicians to handle AMC of Integrated Gas & Fire Detection Systems at RIL, Hazira, Village Mora, P.O. Bhatha, Surat-Hazira Road, Surat - 394 510, Gujarat. Candidates residing in and around Hazira, Mora, Surat would be preferred. Should have 2-5 years hands on experience in Servicing, Calibration, Installation, Commissioning of Integrated Gas, Fire & Flame Detection System used in Oil & Gas Industry projects. Hands on experience in maintaining Fire & Gas detection systems used in Oil & Gas Industry projects desired. Experience in commissioning, maintaining/servicing/troubleshooting/repairing of Integrated Fire & Gas Detection Systems and Instrumentation Control Systems used in Oil & Gas, Indian Railways, Petrochemical, Power, Steel, Chemical, Pharma, Fertilizer plants etc would be an added advantage. Knowledge of handling PLC based F & G systems would be an added advantage. Readiness to travel at project sites for execution as and when required. Desired profile of the candidate: ITI \ NCTVT in Instrument Mechanic Trade passed with 2-4 years of relevant experience as above. Excellent communication, Trouble shooting skills desired. Excellent Team player and Proactive. Candidate residing in Hazira, Gujarat should apply. Job Type: Full-time Pay: ₹200,000.00 - ₹300,000.00 per year Schedule: Day shift Ability to commute/relocate: Mora, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Do you have hands on experience in maintaining, servicing, Installation, commissioning of Gas, Fire & Flame Detection System used in Oil and Gas industry projects? Education: Diploma (Preferred) Experience: Maint of Gas, Fire Detection Sys Oil & Gas industry project: 2 years (Preferred) Maintaining Gas & Fire Detection Systems projects: 1 year (Preferred) Language: English, Gujarati, Hindi (Preferred) Location: Mora, Gujarat (Preferred) Shift availability: Day Shift (Preferred) Willingness to travel: 50% (Preferred) Work Location: In person

Axalta has remained at the forefront of the coatings industry by continually investing in innovative solutions. We engineer technologies that protect customers’ products – whether they are battling heat, light, corrosion, abrasion, moisture, or chemicals – and add dimension and beauty with colorful finishes. We have a vast and ever-evolving portfolio of brands primed to play an important part in everything from modernizing infrastructure around the world to enabling the next generation of electric and autonomous vehicles. We are currently looking for a QC Officer and Legal Specialist to join us at our facility in Savli, Gujarat. Department: Quality General Job Purpose To ensure testing & approval of received samples of RM/PM and finish product as per defined Customer’s specification. To conduct the testing of paint samples as per defined national/international standard test-methods. To issue the test-reports to customers as per defined test-report format To participate in MSA & ILC study Work with production and MT team for the RCFA of Internal Quality Incidence by conducting Lab experiments. Actively Participate in RCFA of Customer Complaints by conducting Experiments in Lab. To ensure revalidation process of expired RMs and Finish goods. To train QC team members for critical Quality test parameters. Lead Real Time Release project. Co-ordinate with Technical team, MT and production team to achieve Lean – RTR target. Conduct audit as per ISO/IEC17025:2005 as per annual audit schedule Responsibilities To ensure Quality of incoming RM, PM, Intermediate and Finish goods : Work with technology and MT team on new RMs and Finish goods Inspection plan in SAP and specification cantering after three alignment batches. Ensure all RMS and Finish goods release as per specification Trend analysis of finished-goods test-results Ensure timely calibration of all QC lab equipment Final shade approval for all finished-goods shades Ensure availability of standard panels and NF samples Communicate all incoming material rejection analysis with sourcing team Complaints and QIR analysis: Retain sample analysis for complaints evaluation Conduct experiments for complaints and QIR analysis and to reproduce the defects Participate in RCFA meetings for complaints and QIR and assist QA for closure of complaints/QIR Follow-up with technical team and highlight any abnormality observed during QC testing Record and analyze all the non-conformity reported in testing. Calibration To ensure that all measuring equipment are timely calibrated from nationally/internationally accredited laboratory To coordinate with external calibration agency for timely calibration of equipment Key QC KPI 1. Customer complaint- Product & Service 2. IATF16949 :2016 Compliance 3. ISO/IEC 17025 :2017 Compliance 4. Laboratory Safety Education/Training Bachelor degree in Chemistry / Polymer / Paint technology / Chemical Professional Experience 2-5 years’ experience in chemical industry & paint manufacturing experience is strongly preferred. Strong knowledge and experience on QMS, quality system audit and process audit, IATF16949:2016 & ISO/IEC17025:2017 background is strongly preferred. Knowledge of quality tools such as FMEA, MSA, SPC, APQP, RCFA High attention to detail and accuracy Good communication skill Good command of English, both in oral and writing skills Ability to effectively use Microsoft office products. Axalta operates its business in two segments: Performance Coatings and Mobility Coatings, which serve four end markets, including Refinish, Industrial, Light Vehicle and Commercial Vehicle, across North America, EMEA, Latin America and Asia-Pacific. Our diverse global footprint allows us to deliver solutions in over 140+ countries and coat 30 million vehicles per year. We’ve recently set an exciting 2040 carbon neutrality goal, in addition to 10 other sustainability initiatives, and we take pride in working with our customers to optimize their businesses and achieve their goals. Our Company: Axalta has remained at the forefront of the coatings industry by continually investing in innovative solutions. We engineer technologies that protect customers’ products – whether they are battling heat, light, corrosion, abrasion, moisture, or chemicals – and add dimension and beauty with colorful finishes. We have a vast and ever-evolving portfolio of brands primed to play an important part in everything from modernizing infrastructure around the world to enabling the next generation of electric and autonomous vehicles. Axalta operates its business in two segments: Performance Coatings and Mobility Coatings, which serve four end markets, including Refinish, Industrial, Light Vehicle and Commercial Vehicle, across North America, EMEA, Latin America and Asia-Pacific. Our diverse global footprint allows us to deliver solutions in over 140+ countries and coat 30 million vehicles per year. We’ve recently set an exciting 2040 carbon neutrality goal, in addition to 10 other sustainability initiatives, and we take pride in working with our customers to optimize their businesses and achieve their goals. 7 - Operatives (EEO-1 Job Categories-United States of America)

IT Full-Time Job ID: DGC00632 Chennai, Tamil Nadu 1-4 Yrs ₹02 - ₹06 Yearly Job description Key Responsibilities: Assist in carrying out land surveys, topographic surveys, and layout markings at project sites. Operate surveying instruments such as Total Station, Auto Level, GPS, and Theodolite. Support the preparation of site layout drawings and alignment maps. Assist in verifying land boundaries and plot demarcations as per project drawings. Record and maintain field survey data, measurements, and calculations accurately. Support senior surveyor in coordinating with civil engineers and site supervisors. Ensure that all surveying work complies with quality and safety standards. Maintain calibration and proper functioning of survey equipment. Participate in regular site inspections and reporting activities. Requirements Skills & Competencies: Hands-on experience with Total Station, Auto Level, GPS devices, and relevant tools. Basic knowledge of construction layouts, civil drawings, and site measurements. Understanding of survey principles, land laws, and measurement techniques. Strong attention to detail and accuracy. Good physical fitness for on-site work and outdoor environments. Ability to work as part of a team and follow instructions precisely. Preferred Background:

About the Position About the position Hoganas in India is looking for an ambitious person in the Quality Assurance function based out of the plant in Ahilyanagar, Maharashtra. Your profile We are looking for someone who has an Engineering Degree with Materials, Metallurgy with a minimum experience of 4 years in the Quality function. The person should be versed with the following elements of Quality: Quality Control- Process and Product Deviation Control (“All 5 plants - Melting & Atomization, Annealing, Mixing, INSIP & SSP” & “Raw Materials”) MSA Plan and execution SPC monitoring and process control Round Robin Test (Global lab conformity test) Product Specific Investigation Inclusion Analysis & Cross Contamination of Iron and Iron Alloys – Metallography analysis to report submission DC Correlation for critical grades (Base Powder + Mixes) Sintering Furnace Calibration and Mapping XRF – Method development, Calibration, Troubleshooting Maintaining Automix System Product Specification creation in M3 & CRAM Procurement & Inventory Management for lab stocks through M3 Product related documentation Export documents to logistic Legal documents for Govt. requirements Declaration / Statements for customers Monitor & share 4M changes to customer Samples to customers Benefits The organisation is having a good work culture and has been certified as a Great Place to Work. It offers good policies, supportive work environment, exposure to global stakeholders and opportunity to grow and develop. Working at Höganäs We aim to offer a great and meaningful place to work where you can fulfil your potential and ambitions. We welcome all applicants and strive for diversity. We have a clear management philosophy, and just like us you believe that through collaboration and openness we develop as individuals and as a company. We see all employees, regardless of position, as leaders when we approach the challenges that the world - and we - face. Höganäs ambition is to lead the transformation to better meet the needs of tomorrow and become the preferred supplier of sustainable metal powder on a global scale – join us in our journey of sustainable change and towards net-zero climate emissions . More about Höganäs Höganäs is the world leader in the market for metal powders, with a yearly capacity of 500,000 tons. Höganäs’ vision is to inspire the industry to make more with less, and its ambition is to be the preferred supplier of sustainable metal powders. In close cooperation with customers, Höganäs develops tomorrow's solutions for automotive components, electrical motors, brazing, surface coating, and additive manufacturing. Höganäs operates 16 production centres across the globe and has a workforce of 2,400 employees. The turnover for 2022 was €1.15 billion. Höganäs, which was founded in 1797, is owned by Lindéngruppen and Wallenberg-owned FAM. Interested? You would need to apply under the link mentioned. We will be proceeding fast with the selection process and hence it is better that you apply at the earliest and not wait till the last date of application. Working at Höganäs We aim to offer a great and meaningful place to work where you can fulfill your potential and ambitions. We welcome all applicants and strive for diversity. We have a clear management philosophy, and just like us you believe that through collaboration and openness we develop as individuals and as a company. We see all employees, regardless of position, as leaders when we approach the challenges that the world - and we - face. Höganäs ambition is to lead the transformation to better meet the needs of tomorrow and become the preferred supplier of sustainable metal powder on a global scale – join us in our journey of sustainable change and towards net-zero climate emissions. More about Höganäs Höganäs is the world leader in the market for metal powders, with a yearly capacity of 500,000 tons. Höganäs vision is to inspire the industry to make more with less, and its ambition is to be the preferred supplier of sustainable metal powders. In close cooperation with customers, Höganäs develops tomorrow's solutions for automotive components, electrical motors, brazing, surface coating, and additive manufacturing. Höganäs operates 17 production centres across the globe and has a workforce of 2,400 employees. The turnover for 2024 was €1.034 biljons . Höganäs, which was founded in 1797, is owned by Lindéngruppen and Wallenberg owned FAM. Interested? Apply today!

Location: Pune - Maharashtra, India - Village Mhal Job Family: Manufacturing Worker Type Reference: Regular - Permanent Pay Rate Type: Salary Career Level: T2 Job ID: R-45511-2025 Description & Requirements Job Description Introduction: A Career at HARMAN Automotive We’re a global, multi-disciplinary team that’s putting the innovative power of technology to work and transforming tomorrow. At HARMAN Automotive, we give you the keys to fast-track your career. Engineer audio systems and integrated technology platforms that augment the driving experience. Combine ingenuity, in-depth research, and a spirit of collaboration with design and engineering excellence. Advance in-vehicle infotainment, safety, efficiency, and enjoyment. About the Role As a Test Engineer, you will play a pivotal role in ensuring the quality, performance, and functionality of our products through comprehensive testing procedures. You will be responsible for reviewing circuit designs, developing and optimizing test systems, analysing test data, and providing valuable insights to improve product reliability and performance. This role offers the opportunity to work with cutting-edge technology and contribute to the continuous improvement of engineering and manufacturing processes. You will collaborate closely with cross-functional teams, including engineering, manufacturing, and R&D, to ensure products meet the highest standards of excellence. What You Will Do Review circuit board designs to ensure they meet testability requirements. Provide support to manufacturing by conducting failure analysis, debugging test equipment, and minimizing intermittent failures and downtime. Generate test reports, analyse test data, and prepare documentation with recommendations. Regularly review test equipment designs, data, and RMA issues with the team. Possess advanced knowledge and expertise in TestStand and LabVIEW, including test system development. Demonstrate proficiency in vision development and image processing systems, including knowledge of vision systems like Cognex and Banner. Have experience in C++ development and executing logic. Possess hands-on experience with PXI controllers, PCI, and troubleshooting related systems. Have experience with RF testing and related logic, as well as knowledge of vision systems. Demonstrate a solid understanding of CAN and LIN protocols. Direct and guide engineering and technical personnel on the operation of test equipment and control apparatus. Coordinate engineering activities related to the development, procurement, installation, and calibration of testing instruments, equipment, and control devices to record and analyze test data. Optimize test conditions, sequences, and phases of operations. Oversee the operational, functional, and performance phases of tests. Conduct moderately complex engineering tests on both standard and custom devices. Analyze and interpret test data, preparing technical reports for both test engineering and management teams. Develop or utilize computer software and hardware for testing machinery and equipment. Perform semi-routine technique development and maintenance, adhering to established standards, including ISO and QS. What You Need to Be Successful Apply knowledge of electronic circuit analysis. Utilize programming skills in LabVIEW, TestStand, C#, and VB. Work with various communication protocols (e.g., CAN, LIN, MOST). Contribute to the development of test programs and software. Operate and maintain a variety of test instruments. Demonstrate electrical circuit analysis skills and the ability to read and interpret schematics. What Makes You Eligible Education: Bachelor’s degree in Manufacturing, Industrial, Electronics, Mechanical Engineering, or a related field. Experience: At least five years of experience in EMS electronic manufacturing as a Test Engineer. Strong communication skills and a proven ability to build and collaborate effectively within teams. Extensive experience in the testing domain. What We Offer Flexible work environment, depends on test requests, mostly we request to work from office for best test quality results, Access to employee discounts on world-class Harman and Samsung products (JBL, HARMAN Kardon, AKG, etc.) Extensive training opportunities through our own HARMAN University Competitive wellness benefits Tuition Reimbursement Access to HARMAN Campus Fitness Center and Cafeteria An inclusive and diverse work environment that fosters and encourages professional and personal development. You Belong Here HARMAN is committed to making every employee feel welcomed, valued, and empowered. No matter what role you play, we encourage you to share your ideas, voice your distinct perspective, and bring your whole self with you – all within a support-minded culture that celebrates what makes each of us unique. We also recognize that learning is a lifelong pursuit and want you to flourish. We proudly offer added opportunities for training, development, and continuing education, further empowering you to live the career you want. About HARMAN: Where Innovation Unleashes Next-Level Technology Ever since the 1920s, we’ve been amplifying the sense of sound. Today, that legacy endures, with integrated technology platforms that make the world smarter, safer, and more connected. Across automotive, lifestyle, and digital transformation solutions, we create innovative technologies that turn ordinary moments into extraordinary experiences. Our renowned automotive and lifestyle solutions can be found everywhere, from the music we play in our cars and homes to venues that feature today’s most sought-after performers, while our digital transformation solutions serve humanity by addressing the world’s ever-evolving needs and demands. Marketing our award-winning portfolio under 16 iconic brands, such as JBL, Mark Levinson, and Revel, we set ourselves apart by exceeding the highest engineering and design standards for our customers, our partners and each other. If you’re ready to innovate and do work that makes a lasting impact, join our talent community today! #LI-RD2 Important Notice: Recruitment Scams Please be aware that HARMAN recruiters will always communicate with you from an '@harman.com' email address. We will never ask for payments, banking, credit card, personal financial information or access to your LinkedIn/email account during the screening, interview, or recruitment process. If you are asked for such information or receive communication from an email address not ending in '@harman.com' about a job with HARMAN, please cease communication immediately and report the incident to us through: harmancareers@harman.com. HARMAN is proud to be an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Be the First to Apply Job Description Business: Piramal Pharma Solution Department: Quality Control Location: Pithampur Job Overview Perform testing on in-process samples, RM's, finished drug product, and stability study samples in support of production, packing release and regulatory filings. Reporting Structure: Reports to QC lab Supervisor Experience 3 - 6 years' experience in a cGMP laboratory setting Familiar with cGMP and FDA requirements Responsibilities Perform analytical testing and release of in-process material, bulk drug substance, finished drug product, and stability sample Sampling, inspection and testing of raw materials and packaging components upon receipt Responsible for Sampling of Bulk API and Bulk drums (API and Raw material) Perform Calibration and minor troubleshooting on select laboratory equipment including GC, UV/Vis, IR, Potentiometer, Refractometer, Karl Fischer, Density meter and ICP/MS (with appropriate training) Qualifications Bachelor’s Degree in Chemistry or closely related degree. About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Job Info Job Identification 8665 Job Category Quality Control Posting Date 06/04/2025, 06:39 PM Job Schedule Full time Locations Piramal Enterprises Limited, Plot # 67-70, Sector II, Dhar, Madhya Pradesh, 454775, IN Show more Show less

Trending Job Description Ensure testing & release of Finished Products / Raw materials/ Packaging materials as per cGMP in time. Approval of analytical method validation protocol, and report. Responsible for stability study of all existing products and new projects. Facing Internal audits and External Audits and ensure compliance. Control of operating expenses. Responsible to provide analytical cost of existing/new projects to Accounts. Ensure effective implementation of systems and procedures as per GMP, GLP, ISO 9001, ISO 14001 and other regulatory requirements. Review of work output and pending work. Responsible for Timely data back up of HPLC, GC and storage Responsible to maintain & updation of the calculation spreadsheets. Responsible to verify and checking of audit trail functioning of the HPLC and GC. Carry out OOS investigation along with HOD. Ensure effective implementation of SOPs, systems & procedures. Ensure entry of data in system. Set annual performance goals for Team, monitors performance and guide them to attain it. On job training as necessary to develop skills and improve productivity. Allocation of work as per the skills of persons & supervision. Training to new persons as per Procedure. Review of laboratory data. To ensure calibration & maintenance of laboratory equipment's. Qualifications B.Pharma/ M.Sc About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Job Info Job Identification 4154 Job Category Quality Control Posting Date 06/04/2025, 01:38 PM Apply Before 06/05/2025, 01:38 PM Degree Level Bachelor's Degree Job Schedule Full time Locations Piramal Enterprises Limited, Plot # 67-70, Sector II, Dhar, Madhya Pradesh, 454775, IN Show more Show less

Be the First to Apply Job Description Key Roles/Responsibilities: To ensure cGMP in Quality Control laboratory. Review of QC / QA documents. Review and approve OOS, OOT, Incident, deviation and QC laboratory data and stability summary sheet. To prepare QMS (OOS, OOT, Lab Incident and Quality Event) Trends as per said procedure. To review and ensure effective implementation of regulatory requirement, guidelines and pharmacopeia changes like IP,BP,USP,Ph.Eur,JP etc. To review of QC laboratory records on periodic basis. To impart training to QC Laboratory personnel on SOPs, on-job training, regulatory requirements and guidelines. To ensure compliance of Qualification and calibration planner for QC instruments. To review QC Laboratory records (Issuance and archival of the documents like Laboratory note Book, Chromatograms, COA etc.). To provide Quest data on monthly basis to concern person. To perform self-audit of QC laboratory on periodic basis. To take the responsibilities of the activity in absence of immediate superior. To review audit trail for QC Instruments. To assign/disable password for QC Biometric system. Ensure compliance to KRA’s and other such assignments. Analytical and Electronic data review of respective batches at the time of release. Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data Integrity awareness at site. Issuance and management of HPLC and GC column. Verification of admin audit trail along with IT person. To perform level-3 signoff for QC instruments wherever applicable. Qualifications B.Pharma/M.Pharma About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Job Info Job Identification 8746 Job Category Quality Assurance Posting Date 06/04/2025, 06:40 PM Job Schedule Full time Locations Piramal Enterprises Limited, Plot # 67-70, Sector II, Dhar, Madhya Pradesh, 454775, IN Show more Show less

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards About Company: Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers. Join Thermo Fisher Scientific and make a meaningful impact on the world as part of a collaborative team. As a Facility Engineer in the Bioprocess Design Center, you will be responsible for the operation, maintenance, and continuous improvement of our innovative Single-Use Biomanufacturing Facility. Your role will encompass ensuring efficient facility performance, compliance with regulatory standards, and support for biomanufacturing activities. You will collaborate with cross-functional teams to maintain the facility's infrastructure, utilities, and equipment while driving powerful solutions to improve efficiency and reliability. Responsibilities: Facility Operations and Maintenance Coordinate day-to-day operations of the facility, ensuring all infrastructure and utilities (HVAC, purified water systems, cleanrooms, etc.) meet operational requirements. Perform routine maintenance, inspections, and troubleshooting of facility systems to ensure efficient performance and compliance with industry standards. Support the installation, qualification, and validation of equipment and systems used in single-use biomanufacturing. Develop and implement preventive and predictive maintenance programs to minimize downtime and operational disruptions. Regulatory Compliance and Safety Ensure facility operations adhere to cGMP, OSHA, and other regulatory requirements. Conduct risk assessments and ensure compliance with environmental, health, and safety (EHS) standards. Maintain comprehensive documentation for audits, including maintenance logs, calibration records, and operational procedures. Support the preparation and execution of internal and external inspections and audits. Utility Management Manage critical utilities supporting the bioprocess design center, including steam systems, water purification systems, and air handling units. Monitor utility performance and implement measures to optimize energy efficiency and sustainability. Troubleshoot utility-related issues and coordinate repairs or upgrades with contractors and vendors. Project Management Lead facility improvement projects, including upgrades, expansions, and new system installations, to support evolving biomanufacturing needs. Develop project plans, timelines, and budgets, ensuring completion within scope and schedule. Collaborate with external vendors and contractors to procure and install equipment and materials as needed. Single-Use Technology Support Support the integration and operation of single-use systems within the facility, including bioreactors, filtration systems, and storage solutions. Ensure facility infrastructure is compatible with single-use technologies and flexible for future process changes. Collaborate with process development teams to address facility-related challenges associated with single-use biomanufacturing. Continuous Improvement Identify and implement innovative solutions to improve facility performance, reduce operational costs, and promote sustainability. Stay updated on the latest technologies and standard methodologies in facility engineering and biomanufacturing. Propose and complete projects that improve efficiency and reliability in facility operations. Experience: Bachelor’s or master’s degree in mechanical engineering, Electrical Engineering, Facilities Management, or a related field. 3+ years of experience in facility engineering or operations, preferably in the biopharmaceutical, biotechnology, or healthcare industries. Familiarity with single-use technologies and bioprocessing systems is highly desirable. Experience with cGMP facilities, cleanroom operations, and critical utility management. Strong knowledge of HVAC, purified water systems, cleanroom operations, and facility management systems. Proficiency with CMMS (Computerized Maintenance Management Systems) and facility monitoring tools. Strong analytical and problem-solving skills with a hands-on approach to troubleshooting. Excellent organizational and project management skills with the ability to handle numerous responsibilities. Effective communication and collaboration skills to work with cross-functional teams and external vendors. Certification in facility management (e.g., CFM, PMP) is a plus. Knowledge of automation systems, Building Management Systems (BMS), and environmental monitoring systems. Experience in sustainability initiatives, energy management, and green building practices. Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our +100,000 extraordinary minds have a unique story to tell. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status . Show more Show less

Company Description We suggest you enter details here. Role Description This is a full-time on-site role for an Instrumentation Technician at APP Pharmaceuticals located in Kerala, India. The Instrumentation Technician will be responsible for process control, troubleshooting, preventive maintenance, instrumentation, and calibration tasks on a daily basis. Qualifications Process Control and Troubleshooting skills Preventive Maintenance and Calibration skills Experience in instrumentation maintenance Ability to work effectively in a team Strong attention to detail and problem-solving skills Technical certification or Associate's degree in related field Show more Show less

Responsibility Ensure compliance to cGMP and safety standards in the QC laboratory Conduct calibration and cleaning of laboratory equipment and instruments as per SOP. Culture Media preparation and sterilization. To perform growth promotion test of culture media. Maintenance of microbial culture. Document analytical data and calculate results. Maintain laboratory equipment, inventory and supplies. Ensure integrity, accuracy and adequacy of the analysis performed. Follow GLP activities and ensure their compliance. Conduct microbiological sampling and testing of sample. Conduct environmental monitoring. Identification of microorganism through Vitek 2 system. Daily Laboratory Monitoring including Temperature/Humidity and Testo Printout. Management of issuance and archival of log books and formats. Maintenance of various documents and records in Microbiology Lab. To assist in validation/Qualification exercise and any other assignment given by Lab. In charge / Mgr. Quality Control from time to time. Show more Show less

Responsibility Ensure compliance to cGMP and safety standards in the QC laboratory Conduct calibration and cleaning of laboratory equipment and instruments as per SOP. Culture Media preparation and sterilization. To perform growth promotion test of culture media. Maintenance of microbial culture. Document analytical data and calculate results. Maintain laboratory equipment, inventory and supplies. Ensure integrity, accuracy and adequacy of the analysis performed. Follow GLP activities and ensure their compliance. Conduct microbiological sampling and testing of sample. Conduct environmental monitoring. Identification of microorganism through Vitek 2 system. Daily Laboratory Monitoring including Temperature/Humidity and Testo Printout. Management of issuance and archival of log books and formats. Maintenance of various documents and records in Microbiology Lab. To assist in validation/Qualification exercise and any other assignment given by Lab. In charge / Mgr. Quality Control from time to time. Show more Show less

Ensure compliance to cGMP for all operational activities. Monitor the formulated products against stipulated conditions mentioned in the Batch production record. Conduct certificate of batch production records for compliance and stage wise completion. Conduct line clearance during manufacturing and the packing activities. Conduct sampling activities during the manufacturing and the packing activities. Conduct qualification, PPV, PM and calibration of in-process instruments as per schedule. Swab and Rinse sampling activity for cleaning validation and verification studies. Initiate Deviation, Change Control and Investigations. Provide support to conduct investigations related to deviation, CAPA, OOS, OOT, and Market complaint handling. Issuance of Batch production records. Review & Verification of Bin for Documents / Labels Destruction as per SOP. Show more Show less

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. To carry out the sampling of all the materials according to Standard Operating Procedure (SOP). To ensure the status label on the material and transfer such material in the respective area. To ensure that all activities followed in accordance with the SOP. To perform the analysis as per the specification & standard test procedure and record the necessary results in respective documents for Raw Material/Packing material/In-process sample, Validation sample, finish products and other samples. To involved and support in investigation of failure of any material or product in case of any out of specification (OOS) or OOT or laboratory incident or non-conformity and take corrective and preventive actions. To prepare reagents and volumetric solution and standardize it. To check and verify standardization and preparation of reagents and volumetric solution. To raise and implement change control or document change request wherever necessary. To perform chemical analysis To assess the results of testing of Raw Material/Packing material/In-process sample, Validation sample, finish products and other sample to ensure alignment with standard operating procedure (SOP) and regulatory guidelines. To perform the calibration of analytical instruments. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices and Good Manufacturing Practices (GMP) inside Quality Control. To ensure availability the working & impurities standards as per various pharmacopoeias. To assist Supervisor in preparation of SOP and give suggestions to improve system performance. To check, verify and review the calibration of all the analysis instruments whether performed as per the schedule. To check completion of method transfer successfully in coordination with Analytical Development Lab (ADL) Department. To make entry into LIMS. To ensure recording of all the data related to the testing online, on day-to-day basis and ensure traceability of the same. To work for lab readiness for audit and ensure compliance in Laboratory. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice. Show more Show less