3028 Calibration Jobs - Page 7

About Kennametal With over 80 years as an industrial technology leader, Kennametal Inc. delivers productivity to customers through materials science, tooling and wear-resistant solutions. Customers across aerospace and defense, earthworks, energy, general engineering and transportation turn to Kennametal to help them manufacture with precision and efficiency. Every day approximately 8,700 employees are helping customers in nearly 100 countries stay competitive. Kennametal generated $2.1 billion in revenues in fiscal 2023. Learn more at www.kennametal.com . Follow @Kennametal: Twitter, Instagram, Facebook, LinkedIn and YouTube. Technical Process Operator I Shift: C Shift Friday - Sunday, 5am - 5pm Company Celebrating its 80th year as an industrial technology leader, Kennametal Inc. delivers productivity to customers through materials science, tooling and wear-resistant solutions. Customers across aerospace, earthworks, energy, general engineering and transportation turn to Kennametal to help them manufacture with precision and efficiency. Every day approximately 10,000 employees are helping customers in more than 60 countries stay competitive. Kennametal generated nearly $2.4 billion in revenues in fiscal 2018. Learn more at www.kennametal.com. Summary Kennametal has an immediate opening for a dependable Technical Process Operator to work at its newly modernized manufacturing site located in Solon, Ohio. Responsible for supporting the operation of one or more automated in-line agile manufacturing systems, to a predetermined schedule using robotics for monitoring and refreshing worn tooling, and work piece loading. T his is an outstanding opportunity to join a growing company that offers highly competitive pay, excellent benefits and generous paid time off. Positions are available for Monday-Thursday 10-hour evening shifts ($1.25/hour shift premium). Or get paid for 40-hours for only working 36-hours on our weekend shift, Friday-Sunday 12-hour shifts ($2.00/hour shift premium for days and $3.00/hour shift premium for nights). Typical Duties Of The Operator/Engineer Include The Following Be committed, following all company safety policies and procedures to ensure commitment to 100% safe work environment Diligently identifying improved methods and controls for safe area and site operation. Complying with OSHA guidance for robotics operation (OSHA 29 CFR 1910.333 and OSHA 29 CFR 1910.147) Working in a team environment safely, operating complex production equipment, manufacturing software and tools in the manufacturing and transfer of various products. Following of digital work instructions, blueprints, guidelines, diagrams and schematics to ensure product and customer specifications and tolerance levels are met. Interpreting dashboards and reporting tools. Automated Line support: Executing assigned equipment calibration. preventive maintenance and other TPM functions to ensure continuous line operation and a safe, efficient work area. Making assigned adjustments to existing equipment Monitoring meters, gauges, valves, flow ratios, temperatures, pressures, and related controls and guidelines to ensure adherence to production/process specifications. Reporting any malfunctions or abnormalities and makes minor adjustments and repairs to equipment. As development skill set and experience allows, set-up and operate in-line millturns, 5-axis CNC and/or grinders. Align and secure tooling, holding fixtures, cutting tools, attachments, accessories, or materials onto machines and in 5-S storage format. Work from and read blueprints as well as setting and checking work to various quality control gages. Troubleshooting, determining causes of operating errors. Perform inspection of machined products by selecting and setting up precision gaging to ensure external and internal quality specifications and requirements Communication, Teambuilding and Continuous Improvement. Providing continuous feedback for manufacturing process improvement Participating in team functions and discussions with an attitude of See it; Own it; Solve it; Do it. Confer with engineering, supervisory, or manufacturing personnel to exchange technical information. Complete all necessary documentation, electronic data entries and communications accurately and timely. Move all materials, either physically or mechanically, necessary to complete assignments Support the Lean Enterprise initiatives and continuously strive to improve customer satisfaction through improved quality, reduction in waste and improved productivity. Works within standard operating procedures and/or scientific methods. Works with a moderate degree of supervision. Requirements High School diploma or GED Journeyman machinist papers a + Preferred technical knowledge - apprenticeship/technical certifications/Associates degree or 2 or more years of hands-on experience with: CNC, Robotics, Manufacturing controls and systems. Strong Knowledge in manufacturing safety, technical manufacturing (Blueprint, machining math, written communications), business acumen, basic computer skills, PLC, HMI. Hands-on working knowledge of CNC, Robotics, Manufacturing controls and systems a plus Proven abilities in critical thinking capabilities for trouble shooting, problem solving, continuous and quality control. Interpersonal skills with good communication working in team environment. Advanced knowledge of blueprint reading and GD&T methods of dimensioning, as well as proper use and care of precision measurement tools Proficient in shop math, including geometry and conversions Trigonometry, highly desired. Efficiently and effectively receive verbal and written information Proficient in MS Office and HMI Systems Understand written instructions and be willing and able to communicate those instructions to others Read process instructions and drawings and recognize/attend to details Has working knowledge and skills to perform a defined set of analytical/scientific methods or operational processes. Applies experience and skills to complete assigned work within own area of expertise. Performs specialized technical tasks required to support operations (e.g., IT development, research support, skilled trade) Successful completion of the TITANS of CNC Academy Building Blocks Series is a plus Some daily and weekend ove Can lift 25 pounds with frequency. Can stand and move around on feet for entire shift. Flexibility for over/under shift coverage. Equal Opportunity Employer

Job Title: Arabic Language Expert – Call & Chat Quality Analyst Department: Quality Assurance / Operations Location: Mohali (WORK FROM OFFICE) Work Type: Full-time / Rotational Shifts Experience: 1–3 years (BPO/Customer Support/QA) Job Summary: We are looking for a proficient Arabic Language Expert to join our Quality team and support Call and Chat Audit Processes . The role requires auditing customer interactions in Arabic, ensuring adherence to quality standards, compliance, and providing feedback to improve agent performance and customer satisfaction. Key Responsibilities: Listen to and audit voice calls and chat transcripts in Arabic (and English if required) to evaluate the quality of service provided. Monitor interactions for process compliance, communication etiquette, product knowledge, and customer experience. Identify improvement areas and share actionable feedback with relevant stakeholders. Prepare quality reports, summaries, and trends based on audit outcomes. Work closely with trainers and operations team to ensure corrective and preventive actions are implemented. Participate in calibration sessions to align with client expectations and quality benchmarks. Assist in translating training material, SOPs, or internal communications between Arabic and English as needed. Support any client-facing requirements such as quality reviews or feedback sessions in Arabic. Requirements: Fluent in Arabic (both spoken and written) – Native or certified proficiency. Good command over English for internal communication and documentation. Previous experience in BPO, QA, or Customer Support roles preferred. Knowledge of quality audit parameters and customer service metrics (CSAT, FCR, etc.). Attention to detail with strong listening and analytical skills. Comfortable working in rotational shifts, including weekends if required. Familiarity with QA tools and CRM platforms is an added advantage. Preferred Qualifications: Bachelor's degree in any stream (Language, Communication, or related field preferred). Arabic language certification (like CEFR Level B2/C1 or equivalent) is a plus. Experience working with Middle East clients or Arabic-speaking customers. Note: Candidates with exposure to multicultural environments and customer-centric roles will be given preference.

#HiringAlert Job Title: SAP QM Consultant Location: Hyderabad, Pune, Company: Yash Technologies Job Description: Should have 6+ years of experience in QM - S/4 HANA Projects and Overview of PP. Good knowledge of integration of SAP QM with cross-business process like Procure to Pay (MM), Order to cash (SD), Plan to inventory (PP), Should have experience of working on minimum of 2 end-to-end implementations projects along with support and roll-out projects. Should be able to handle L3 Support, change management activities, and represent and drive a technical team in CAB meetings. Should have knowledge of Project lifecycles, methodologies, SLAs, ticketing tools, and Project documentation (FS/TS, estimates, etc.) Good exposure to Interfaces, enhancements …etc Exposure to multiple quality management processes and various Quality assurance (QA) & Quality control (QC) processes. like Inspection Lot, Quality Notification, and Master Inspection Characteristics. Inspection Planning, Dynamic Modification Rule, Source Inspection Follow-up actions, Quality notification action box Batch Management, Batch derivation Warehouse Quality Management, Inspection Types Basic understanding of BOM, Routing, Production Order & Processing. Exposure to Calibration Process. Why Join Us: Work on exciting SAP projects with the latest technologies Collaborative and innovative work environment Career growth and development opportunities If you are considering a job change, please share your resume with the following details Samiksha.mishra@yash.com for further discussion: Total Experience: SAP Experience: Current Company: Current CTC: Expected CTC: Current Location: Availability (Notice Period): . Best regards, Samiksha Dubey Talent Acquisition Team Yash Technologies

For servicing of products illustrated in www.remilabworld.com at customer place as per procedure of Company, and on every service visit has to work out with same customer for outstanding collection & receiving enquiries. Required Candidate profile Must have service experience in lab/healthcare of Electro-Mech, Electronic Circuit & refrigeration system like Deep Freezers or similar products displayed in http//www.remilabworld.com

Job Title Executive Assitant Job Description Job Title : Executive Assistant Leadership support Supporting Head of PIC, HR and Finance in their day-to-day operations/functions, such as, structuring and scheduling high profile meetings with various levels of stakeholders and providing necessary support in networking (internal and external). Managing their travel, expense report submissions and all required administrative tasks. (Arranging air/hotel/ground transportation while creating detailed travel itineraries) Management of calendar and scheduling requirements across multiple geographical time zones. Manage effective communication with Internal & External stakeholders/partners Plan, coordinate and ensure the schedules are followed and respected. Act in a way as a “gatekeeper” and “gateway”, creating win-win situation for direct access to the leader’s availability. Coordinate PIC LT level meetings Preparing agenda and ensuring meetings are coordinated efficiently Proactive planning and execution of the tasks assigned, follow-up of the task of PIC LT Meetings, Strategy, Quarterly meeting and ensuring continuous improvement. PIC wide events Co-ordinate and support Town Meetings, Team Lunch & Dinner, OBL etc. Coordinate preparation and calibration meetings for Town Halls, R&R etc Visitor Management Ensuring flawless planning and management of visitors to PIC. Publishing of the visitors’ travel schedule and actively managing their meetings with PIC Head, HR & Finance Plan and schedule PIC overview/strategy meetings with visitors and LT Coordinating with EA team for agenda, logistics & BU gemba walks Executive Admin Lead & Functional Leader Act as the functional leader for all PIC Executive assistants and help in creating a collaborative team culture to take the EA team to the next level of operational excellence Driving close collaboration with Business & Global EAs by building relationships throughout the teams and across the company. BCP – be an active contributor in coordinating and supporting the BCP core team. Continuous improvement of policies and processes for better output, increased productivity and quality Preferred Qualifications Bachelor’s degree Skill Required Excellent communication skills (written and oral) Ability to build strong relationships, and manage multiple projects effectively Must be able to work cooperatively with other employees and managers to get things done Strong organizational skills, time management skills, and ability to work under pressure Be an active team player Positive and proactive working attitude, and high ethical, integrity standards, and discretion in handling confidential information Ability to learn and apply new skills Ability to work under limited supervision; methodical and thorough with a focus to detail and completion of tasks. How We Work Together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. Learn more about our business. Discover our rich and exciting history. Learn more about our purpose. If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

We are seeking a dedicated and detail-oriented Quality Control Technician with hands-on experience in HDPE pipe testing , IS: 4984 compliance , BIS documentation , and MJP (Maharashtra Jeevan Pradhikaran) documentation . The ideal candidate should be well-versed in quality standards, product testing protocols, and government licensing procedures relevant to plastic piping products. Key Responsibilities: Conduct all quality control testing as per IS: 4984 standards for HDPE pipes. Maintain and update all records related to BIS certification , including test records, inspection registers, and surveillance audit documents. Prepare and submit MJP documentation as required for government tenders, approvals, and projects. Handle all documentation and compliance required for BIS licensing and renewal , including coordination with BIS officials. Operate and maintain lab testing equipment like Hydrostatic Pressure Test, Carbon Black Content Test, Density, Melt Flow Index, Reversion, and Tensile Strength. Ensure proper calibration of lab instruments and maintain calibration records. Participate in internal audits, surveillance audits, and third-party inspections. Support production and R&D teams in troubleshooting quality issues and implementing corrective actions. Ensure timely sampling, lab testing, and documentation for both in-house and external testing. Maintain a clean, organized, and safe laboratory environment. Key Skills & Competencies: Strong knowledge of IS: 4984 and relevant quality testing procedures. Hands-on experience in HDPE pipe testing . Familiarity with BIS online portal (Manakonline) and documentation requirements. Working knowledge of MJP documentation and related regulatory processes. Good understanding of quality management systems (QMS) and lab protocols. Proficiency in MS Office (Excel, Word) for report preparation. Attention to detail, good documentation skills, and ability to work independently. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift Supplemental Pay: Performance bonus Ability to commute/relocate: Akola, Maharashtra: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Required) Experience: Quality control: 1 year (Preferred) Work Location: In person

PharmaACE is a growing Global Healthcare Consulting Firm, headquartered in Princeton, New Jersey. Our expert teams of Business Analysts, based across the US, Canada, Europe, and India, provide Analytics and Business Solutions using our worldwide delivery models for a wide range of clients. Our clients include established, multinational BioPharma leaders and innovators, as well as entrepreneurial firms on the cutting edge of science. We have deep expertise in Forecasting, Business Analytics, Competitive Intelligence, Sales Analytics, and the Analytics Centre of Excellence Model. Our wealth of therapeutic area experience cuts across Oncology, Immuno- science, CNS, CV-Met, and Rare Diseases. We support our clients' needs in Primary Care, Specialty Care, and Hospital business units, and we have managed portfolios in the Biologics space, Branded Pharmaceuticals, Generics, APIs, Diagnostics, and Packaging & Delivery Systems. Brief Introduction: The Associate Consultant/Consultant - Forecasting is responsible for developing, delivering, and maintaining forecasts (patient-based, TRxbased, etc.) and business insights for PharmaACE’s clients. Responsibilities: Project Management: Play an integral role in executing analytics/consulting engagements through effective and efficient project management. Generate forecasts, analysis and actionable insights that lead to the achievement of strategic and financial goals for our clients. Manage and coordinate complex consulting engagements through strong client and people management, subject matter expertise, communication skills (both written and verbal), and the ability to draw conclusions and recommendations from a variety of evidence. Operate effectively as part of a global team, by participating and contributing to client discussions and proactively helping them with their decisions in creating and/or validating assumptions. Provide robust competitive assessments and insights that inform key decision-making processes for clients such as strategic brand planning, forecasting, and lifecycle management. Perform in-depth (secondary) market research and data analysis to derive understanding of the disease and patient segments based on client requirements. Analyse and integrate primary research and secondary data with other market knowledge to draw inferences and conclusions. Identify risks and opportunities for the business and support key decisions on business strategy with customer and market insights. Leverage all relevant data such as DRG/IQVIA to provide insights into forecast assumptions. Forge effective relationships with various stakeholders (both internal and external), e.g., teams running Market Research initiatives. Ensure effective delivery of work (models and presentations) to clients onsite or through video/teleconferences, through self and others in accordance with the project timelines and quality parameters. Convert Excel models into presentable reports and PowerPoint slides for effective utilization by clients, focusing on the storyboarding and narrative. Leadership: Will be responsible for overall leadership, talent development, skill advancement, and engagement and retention of talent in the team (in case acting in the capacity of a team lead). Foster learning mindset in the team to proactively develop research and story-telling skills, leveraging multiple sources of data to answer business questions. Develop new capabilities leveraging new sources of data and methods that include segment-level analysis, etc. Engage with internal and external stakeholders to build effective relationships to create win-win engagement models. Mentor/Guide team members who can benefit from your expertise and experience. Qualifications: Bachelors/Masters in Pharma / other life sciences background (Biotechnology, Bioinformatics, etc.) or bachelor’s in engineering / B. Tech or Master’s in Business Administration. 3-7 years of relevant forecasting and commercial analytics experience. Experience building financial models (e.g., market sizing, sales, and profit forecasts) using Microsoft Excel and other tools. In-depth expertise in developing, implementing, and managing holistic strategies for modelling (design, development, validation, calibration, documentation, approval, implementation, monitoring and reporting) in collaboration with life sciences teams. Broad experience in key functional areas of CI, analytics, and market research including the ability to understand and identify key business levers. Strong strategic skills including ability to see the big picture, along with conceptual and out-of-the-box thinking. Work experience in the US/European pharma industry is a plus. Ability to balance conflicting priorities. Proven people management skills Other Competencies: Entrepreneurial orientation. Excellent interpersonal and communication skills (written and verbal). Innovative and collaborative behavior, team player. Customer centricity and paying attention to details

The Opportunity Under close supervision, responsible for completing product quality checks. Conducts routine testing and analysis of production work. Quality checks are typically reviewed for accuracy. Documents quality control issues as needed. Essential Functions Responsible for Timely analysis of under test samples giving timely results Coordination with production for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO implementation Knowledge of calibration, standard preparation, standardization and relevant documentation. Handling knowledge of HPLC,GC and wet analysis Department Specific/On-going Functions Give timely reports to SAP for result recording. Fill and update all documents. Zero accidents in the Quality operations. Achieving batch wise timelines, quantity and quality. Will train & supervise the working of all operators working in his dept. Will monitor the waste generated during operation. Will be member of the Emergency response team and will guide & train other team members in case of Emergency. Maintain ISO 9001:2008 and ISO/IEC 17025:2005, SAP, and other Quality system into department. Will maintain the analytical records / log sheets as per GMP & ISO guidelines Education MINIMUM REQUIREMENTS: M. Sc. (Chemistry) Experience 3-4 years of experience in Quality including cGMP, ISO and regulatory Audits including Laboratory Safety Preferred Skills/Qualifications Knowledge of Quality Control in Fine Chemicals and pharmaceutical company. Experience of cGMP Skills/Competencies Willingness to learn Team Player Good communication skills Disclaimer The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd Party Non-solicitation Policy By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation

Seeking On-site Service Engineers to handle troubleshooting, installation, and servicing of air gauges and mechanical instruments. Must have strong technical understanding and hands-on skills in precision instruments. contact: 9840682273 (Vetrisree) Required Candidate profile Diploma/BE Mechanical Engineer with knowledge of air gauges & mechanical instruments. Skilled in troubleshooting, servicing & client handling. Freshers or 1–2 yrs experience preferred.

Job description Opening for Executive Production – Pharma Company Sain Medicaments Pvt Ltd – Hyderabad About the Company: Sain Medicaments Pvt Ltd is a leading pharmaceutical formulation company, proudly serving Human healthcare since 1970s, we have come a long way to make a mark in the healthcare industry which has ISO 22000:2005, WHO GMP, GLP certified manufacturing unit situated at HYDERABAD. Job Duties: Granulation / Compression Coating Packing Review of BMR Batch manufacturing and all Equipment Knowledge of Tablet Manufacturing Filling of BMR/BPR as per GDP. Preparation of SOPs. Ensuring adherence to CGMP/GDP practices. Filling of Equipment cleaning/operation, Area cleaning, Environment Pressure difference monitoring logbook. Monitoring of all manufacturing stages personally. Ensuring daily calibration/verification of weighing balance. Maintaining all inventories of spare parts, tablet toolings. Monitoring of preventive maintenance schedule with engineering team. Communicating with QA, Engineering, and QC for smooth work on shop- floor. Participating in QA training. Following company policies, SOP s as laid down by QA. Skills: Production Planning, Safety, Quality, GMP, Documentation, Continuous Improvement, Facilitation, Preventive Maintenance, Quality Assurance, Quality Control. Experience: 5 to 8 Years of experience in Production department for highly reputed Pharma company at Hyderabad Location Qualifications: M. Pharm / B. Pharm / M. Sc Chemistry. IndustryPharmaceuticals

Seeking On-site Service Engineers to handle troubleshooting, installation, and servicing of AIR GAUGES AND MECHANICAL INSTRUMENTS. Must have strong technical understanding and hands-on skills in precision instruments. contact: 9840682273 (Vetrisree) Required Candidate profile Diploma/BE Mechanical Engineer with knowledge of air gauges & mechanical instruments. Skilled in troubleshooting, servicing & client handling. Freshers or 1–2 yrs experience preferred.

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

Job Overview: We are seeking a seasoned and dynamic professional helping organization to establish better Quality systems and compete with quality performance AGM/DGM - Quality to lead our Quality Team in the Aerospace Manufacturing industry. The ideal candidate will have deep knowledge of AS9100 Standards, QA, Calibration, Metrology, Metallurgy, Supplier Quality and Well versed with Quality Tools, Techniques, Standards & OEM requirements Responsibilities Rich experience in AS9100, AS9102 standards and NADCAP requirements, implementation, as a Auditor/Quality professional and Certified for self release system per SAE 13001 Certified DQR. Well versed with Quality Tools/Techniques, Standards & OEM requirements. Expertise to Lead and build the team, Innovative and positive towards challenges. Effective usage and implementation QMS and core tools like, PPAP, SPC, MSA, 8D Methodologies, QC tools, GD&T and QUALITY CLINIC system etc. Expert in FAI-related activities, monitoring all quality activities of respective assigned projects Interaction with Customers, Training on customer-specific requirements to the QA Project Leads Analysis of Customer Complaints and internal rejections Monitoring of corrective action implementation and validating the results Knowledge in GD&T, CMM programming Expert in Quality planning for gauge instruments and inspection methods Good knowledge of the Raw Material Approval process Educational Qualifications Diploma / B.E in Mechanical / Aeronautical Experience Required: 20 to 30 Years Experience working with senior leadership and managing Quality Tools/Techniques, Standards & OEM requirements. Industry Type: Aerospace / Aviation Industry

Supervise and schedule all Final Inspection and Lab and testing activities inorder to achieve maximum effectiveness and efficiency. Design and prepare procedures to support Quality operations. Maintain effective operations selection, development, training andmotivation of personnel. Coordinate and conduct customer and accreditation audits of the Qualityoperations. Ensure that Gage/Tools/Dies calibration system is effective and complieswith company operating procedures. Ensure that testing operations are performed within guidelines of customerand accreditation requirements. Maintain a record and documentation system for testing and calibration thatcomplies with both internal and customer accreditation requirements. Maintenance of all necessary requirements of the ISO9000/API approvedsystem Acts as a key contact with customers, suppliers, auditors, manufacturing, andsupport resources to ensure the execution of corrective actions and that theQuality Assurance systems are meeting objectives and continuouslyimproving. Management of external quality and special process audits assuring a highlevel of performance as exhibited by audit results. This includes preparationof necessary documentation to support an international customer base Enhance and implement effective measurement on quality performance withspecific focus on customer complaints and product consistency Job Type: Full-time Pay: ₹700,000.00 - ₹800,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Job Title : Machine Operator Location : Ernakulam, Kerala Experience : 1–2 Years Industry : Manufacturing / Engineering / Industrial Employment Type : Full-time Job Summary : We are seeking a skilled and motivated Machine Operator with 1–2 years of hands-on experience in operating, maintaining, and troubleshooting production machinery. The ideal candidate will be responsible for ensuring machine functionality, quality output, and safety in our Ernakulam-based manufacturing facility. Key Responsibilities : Operate and monitor machines (e.g., CNC, lathe, milling, printing, or packaging) efficiently Perform basic setup, calibration, and routine maintenance of machines Inspect finished products for quality assurance and report deviations Adhere to standard operating procedures (SOPs) and safety guidelines Maintain cleanliness and safety of the work area Record production logs and report daily outputs Required Qualifications : ITI / Diploma in Mechanical, Production, Tool & Die, or related field 1–2 years of machine operation experience in a factory or plant environment Ability to read technical drawings and basic measurements Basic knowledge of machine safety protocols Preferred Skills : Familiarity with CNC or lathe machine operation Problem-solving ability and attention to detail Willingness to work in shifts (rotational, if required) Job Types: Full-time, Permanent Pay: ₹8,086.00 - ₹18,000.00 per month Benefits: Food provided Schedule: Day shift Supplemental Pay: Performance bonus Experience: Machine operator: 1 year (Required) Work Location: In person Application Deadline: 28/06/2025

Dialysis Procedure Management : Set up and operate hemodialysis machines and related equipment. Prepare dialysis solutions and ensure proper functioning of the machine before each session. Initiate, monitor, and terminate dialysis sessions for patients according to prescribed protocols. Patient Care & Monitoring : Monitor patients’ vital signs before, during, and after treatment. Recognize and report any adverse reactions or complications during dialysis. Assist in managing vascular access (AV fistula, graft, catheter). Infection Control and Hygiene : Maintain a sterile environment to prevent infections. Disinfect machines and clean dialysis stations thoroughly after each session. Record Keeping : Maintain accurate patient records including treatment parameters, duration, and any issues noted during dialysis. Document machine calibration and maintenance logs. Equipment Maintenance : Conduct regular checks and basic maintenance of dialysis machines. Report any technical issues or need for repairs to the biomedical/maintenance team. Patient Communication & Support : Provide emotional support and guidance to patients undergoing long-term treatment. Educate patients on pre- and post-dialysis care, fluid restrictions, and dietary guidelines (in coordination with dietitian/nurse). Emergency Handling : Respond promptly to any complications or emergencies during dialysis. Assist in basic life support procedures if needed.

Key Responsibilities: Develop and implement quality assurance standards, processes, and procedures for HVAC products and installations. Conduct inspections and audits on raw materials, in-process components, and finished HVAC units to ensure conformity to specifications. Collaborate with engineering and production teams to resolve quality issues. Analyze test data and root causes of defects or failures, and recommend corrective and preventive actions (CAPA). Maintain calibration records for all testing equipment and ensure timely recalibration. Assist in the preparation and execution of ISO, ASHRAE, or customer-specific audits. Ensure compliance with industry standards and customer requirements. Develop quality documentation including inspection reports, SOPs, and quality manuals. Conduct training for shop floor staff on quality practices and product standards. Monitor supplier quality performance and initiate corrective actions for non-conformities. Support continuous improvement initiatives Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Company Description SAA Vishnu Bakers Pvt. Ltd. is a leading manufacturer and supplier of high-quality bakery products, committed to delivering taste, hygiene, and innovation. Established with a vision to create wholesome snacking experiences, we specialize in producing a wide range of biscuits, cookies, and baked treats that cater to diverse consumer preferences across India. Role Description This is a full-time on-site role for a Lab Chemist at Saa Vishnu Group located in Ranchi. The Lab Chemist will be responsible for conducting analytical tests, operating laboratory equipment, carrying out laboratory procedures, ensuring quality control measures, and performing calibrations. Qualifications • Analytical and Laboratory Skills • Experience with Laboratory Equipment • Knowledge of Quality Control and Calibration Processes • Attention to detail and precision • Strong problem-solving abilities • Ability to collaborate effectively in a team • Bachelor's degree in Chemistry or related field in Food Tech

As an Instrumentation Engineer is responsible for designing, installing, maintaining instruments that measure & control industrial processes. Design, Installation, Commissioning, Calibration, Maintenance Troubleshooting, Spares & Material Management Required Candidate profile Nature of exp: Chemical, Pharma, Argo industries, Instrumentation Engg. must have specific exp. & skills to ensure the effective operation, calibration & maintenance safety & regulatory compliance. Perks and benefits Canteen, Transportation/GTLI/GPA/GMC

Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management.

Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management.

Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management. 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. 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.

Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management. 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. 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 Title: Quality Analyst Location Hyderabad/Chennai Functional: Digital Sales Sub Department Digital Channel Reference / Version No: Last Updated Date: PURPOSE OF THE POSITION: Looking for a result-driven Quality Analyst to be responsible for monitoring and supervising a team of non - sales to achieve the organization’s objectives and increase sales through Digital Process DUTIES & RESPONSIBILITIES: Analyze /Audit Calls to identify the areas of Improvement which did not meet the predefined performance standards of Medvarsity. Provides Structured and timely feedback of the audits Verbal/Written to all the stakeholders within the organization and helps ISM's in improving their performance. Performs Mock -Calls with new hires post-training to determine readiness for moving into teams. Quality Analyst is responsible for facilitating calibration/group sessions regarding quality programs Need the ability to work in a constructive, unbiased, and collaborative manner by establishing positive work relationships & partnering with the Leadership team & Training Team. This Position requires the ability to gain the confidence and trust of others by demonstrating professionalism and expertise in an ever-changing environment. The Quality Analyst is responsible for the overall quality of the customer interactions, making improvement recommendations to the sales team leader and monitoring the result of the stated recommendation Desired Candidate Profile: 7 QC tool experience Excellent communication skills Outbound calls quality check Contact/whatsapp:7801027439 Job Type: Permanent Pay: ₹4.00 - ₹5.00 per year Benefits: Provident Fund Schedule: Day shift Application Question(s): Do you have experince as Quality Analyst Experience: BPO /Telecalling: 3 years (Required) Language: Do you speak Kannada or Marathi (Required) Work Location: In person Speak with the employer +91 7801027439

Job Description: Skills: High Analytical skills Investment operations exposure is mandate (Stock, Bond, Mutual Funds). Strong project management orientation. Ability to extract information with apt precision and shorter timelines and communicate to others. Ability to navigate, research, and utilize processing guidelines...And add value as needed. Strong problem-solving and decision-making skills through effective calibration of inputs. Strong Numerical ability…needs to be a role model for peers. Ability to innovate with new ideas for continuous process improvement. Ability to work in a team-oriented, collaborative environment…proactive help offering as needed. Strong customer service orientation, with close watch on set procedures. Quick learner with attention to detail. Comfortable with Night shifts. Knowledge: Advance knowledge in MS Excel / any other tools used in the process required Enhanced knowledge on SOPs & procedures for aligned process. Possess significant investment domain expertise to align with our processes. Ability to develop dashboard & measures to proactively manage multi- client level impacts and shares with the appropriate audience as per expected schedules Location: This position can be based in any of the following locations: Chennai, Gurgaon Current Guardian Colleagues: Please apply through the internal Jobs Hub in Workday