11381 Qc Jobs - Page 33

QC Head Position Overview : The QC Head at Peejay Max oversees the entire Quality Control department, ensuring that all materials and products meet the company’s high standards. This leadership role involves supervising the QC Engineer, QC Analyst (Physical Test), and Research Analyst (Chemical Test), while ensuring that testing processes, quality certifications, and compliance with industry standards are consistently maintained. The QC Head is also responsible for implementing continuous improvement initiatives and managing customer-related quality concerns. Reporting to : Managing Director Reported by : QC Engineer, QC Analyst, Research Analyst. Key Responsibilities: Oversee all activities in the QC department, including physical and chemical testing, quality certifications, and project coordination. Provide leadership and direction to the QC Engineer, QC Analyst (Physical Test), and Research Analyst (Chemical Test). Ensure all materials and products meet industry quality standards and regulatory requirements. Source and procure the necessary chemicals and testing equipment, ensuring timely availability and quality. Manage vendor relationships and ensure that all supplies meet the required specifications. Maintain compliance with ISO standards and ensure all audits are passed with no major non-conformities. Supervise the certification of test results for incoming raw materials, ensuring they meet the company’s quality standards. Approve final product certifications and ensure that all documentation is complete and accurate. Lead innovation and optimization initiatives in quality testing and material performance to enhance product quality. Implement best practices and introduce new methodologies to improve testing accuracy and efficiency. Implement and monitor safety procedures for handling hazardous chemicals, ensuring compliance with all safety regulations. Oversee the management and resolution of customer complaints related to material quality. Provide technical support to resolve issues and prevent future occurrences both through calls and direct visits as and when required. Ensure the team is continuously trained on the latest testing procedures and industry standards. Conduct technical training sessions for the sales and operations teams, keeping them updated on quality processes and product features. Collaborate with the operations department to ensure smooth integration of materials into production. Act as the primary point of contact for ISO audits and other regulatory inspections. Ensure all necessary documentation is maintained and all internal systems are audited regularly to meet compliance standards. Skills & Competence Requirements: Educational Qualification : Master’s Degree / Bachelor’s degree in Civil Engineering (mandatory). Candidates from Kerala preferred , Malayalam Mandatory. Other state people are also preferred but should be fluent in malayalam. Hindi is an added advantage. Salary & Benefits Upto 8,00,000 Per annum ; CTC Rs. 65000 ; Take home Rs.50,000 pm Other Benefits: Food & Accommodation will be provided Gratuity Bonus Health Insurance Cab facility during travels Interested Candidates can send your updated resume to hr@peejaymax.com Contact No-9072052225 Job Type: Full-time Pay: ₹50,000.00 - ₹65,000.00 per month Benefits: Food provided Health insurance Internet reimbursement Ability to commute/relocate: Palakkad, Kerala: Reliably commute or planning to relocate before starting work (Preferred) Education: Bachelor's (Preferred) Work Location: In person

Job Title: Production Manager – Pharmaceutical Manufacturing Department: Production Location: Pirana, Ahmedabad Qualification: B. Sc, M. Sc, B Pharm & Mpharm Experience: 3-8 yrs Salary: upto 50 K p.m. Joining: Immediately Interview: offline Employment Type: Full-Time Job Summary: We are looking for a results-driven Production Manager with experience in pharmaceutical manufacturing to oversee and manage daily production activities. The role involves ensuring that production processes meet Good Manufacturing Practices (GMP), quality standards, and regulatory compliance while optimizing efficiency and safety. Key Responsibilities: Plan and execute production schedules as per monthly targets while maintaining compliance with cGMP and regulatory standards (e.g., USFDA, MHRA, WHO). Supervise production activities across various dosage forms (e.g., tablets, capsules, injectables, ointments – as applicable). Ensure strict adherence to batch manufacturing records (BMR) and standard operating procedures (SOPs). Coordinate with Quality Assurance (QA), Quality Control (QC), Engineering, and Warehouse departments to ensure uninterrupted operations. Ensure proper documentation, review of logs, and batch records in compliance with regulatory norms. Monitor yields, wastage, equipment efficiency, and line productivity, initiating corrective actions where necessary. Manage manpower deployment, shift planning, and workforce development. Train and mentor production staff on GMP, safety protocols, and hygiene practices.

Key Responsibilities: Conduct analysis using instruments Perform routine and non-routine chemical and physical analysis of materials and products. Review and approve test results; ensure timely reporting and documentation. Investigate OOS (Out of Specification) results and ensure CAPA implementation. Maintain GLP (Good Lab Practices) and ensure all instruments are calibrated and maintained. Prepare and review Standard Operating Procedures (SOPs), COAs, and protocols. Train and mentor junior chemists and interns. Coordinate with production for sampling and process validation requirements. Support internal and external audits, documentation, and regulatory inspections. ⸻ Qualifications: M.Sc. in Chemistry (Organic preferred) 3-5 years of experience in a chemical manufacturing QC lab Proficient in handling analytical instruments and documentation Knowledge of ISO, EHS ⸻ Preferred Skills: Strong analytical and troubleshooting skills Attention to detail and commitment to quality Good documentation and communication skills Ability to lead small teams and manage priorities under tight timelines Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Commuter assistance Ability to commute/relocate: Turbhe Khurd, Navi Mumbai, Maharashtra: Reliably commute or willing to relocate with an employer-provided relocation package (Required) Experience: chemical manufacturing QC lab: 3 years (Required) Work Location: In person

Preferred Total Experience: 5- 8 Years Qualifications: Mandatory Bachelors in Electrical or Mechanical Engineering Responsibilities Ensures QC & T standards for all services. (HVAC, Electrical, Plumbing, Fire suppression, Gas bank, Security systems, Filtration systems & IT systems). Creates detailed design for all services. Obtains sign off on the drawings. Manage and control energy consumption through efficient design. Prepares & recommends the standard budget for services based on current McDonald’s standards and specification. Presents rate contract and presents it to Design & Purchase Lead on an annual basis for services. Identifies and builds a network of consultant for MEP for the region. Designs and presents a training programme for execution team on MEP. Ensures EVA of Store Energy consumption to be +/-5 %.

eview findings from various quality audits oversee investigations and guide measures to minimize cases of deviation Prepare Schedule and conduct of quality reviews for in-production, in-process and during new product development stages to ensure compliance with prescribed quality procedures and processes Review all instances of non-conformation and ensure communication with the Sourcing & Vendor Development, Inventory Management, Stores and Logistics, Production and Projects team and support them in taking corrective measures Periodically review the adherence to quality standards by external vendors devise plans for addressing any discrepancies Review quality reports on performance of external vendors on quality standards, including raw material inspection, service quality, etc. Drive coordination with Customer Care and Coordinating & Monitoring team Resolve customer complaints related to product quality. Oversee investigation and interactions with production, design and development teams to address the root causes of such quality complaints Monitor investigation of warranty / replacement issues (as and when required) and warranty costs Implement Operational Excellence activities like Kaizen, poka-yoke, TQM, QC tools and coordinate with the production team for uniform implementation Job Types: Full-time, Fresher Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Food provided Health insurance Leave encashment Ability to commute/relocate: Sachin, Surat, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Preferred) Experience: Quality control in textile industries: 2 years (Preferred) Work Location: In person

Job Title: Team Member – Quality Control Experience: 3–5 years Industry: Pharmaceutical / Biotechnology Location: Hyderabad Employment Type: Full-Time Overview Our client – one of the largest and most respected pharmaceutical companies – is seeking to hire a Team Member – Quality Control (QC) with 3–5 years of experience in pharmaceutical or biotech laboratory environments. The ideal candidate will possess proven hands-on expertise in analytical testing, instrumentation, and quality documentation to ensure product compliance and integrity. Key Responsibilities Execute analytical testing of raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV, IR , and dissolution Operate and maintain laboratory instruments, ensuring calibration and preventive maintenance are aligned with SOPs and cGMP protocols Record and analyze results using LIMS , SAP , or equivalent systems; prepare and review Records of Analysis (ROA) Investigate and report deviations—such as OOS or OOT —and support corrective action processes with documentation Support stability studies, including sampling, trend analysis, and documentation of stability batches Collaborate closely with cross-functional teams (e.g., QA, Production, Validation) to resolve quality-related issues Qualifications & Experience Bachelor's or Master’s degree in Chemistry , Analytical Chemistry , B.Pharm , or a related scientific discipline 3–5 years of experience in pharmaceutical or biotech QC laboratories, with practical exposure to routine testing and instrumentation

(Only for 6+ Years of experience) Company Description Gohra Technologies helps businesses transform their operations with the full power of Microsoft Dynamics 365 ERP. Based on the latest Microsoft cloud technology, we provide end-to-end solutions, including implementation, customization, system integration, and data migration. We serve businesses across various industries such as manufacturing, F&B, logistics, IT, and retail, and are known for our client-first approach and ability to quickly scale teams. Our solutions reduce manual work, improve decision-making, and enable real-time visibility. Total Experience - 6+ Yrs (Do Not Apply If You Dont Have 6+ Years of Experience) If you still wants to share your profile, please share it through hr@thegohra.com No. of Implementation Projects - At least 5- 6 End-to-End ERP Implementations in MS Dynamics Finance & Operation or AX No. of Support Projects - At least 6 ERP Support Projects Job Description - Role and Responsibilities The Technical Consultant should: Understand technical requirements. Create and review technical documents for the requirements. Provide estimations for proposed solutions and deliver customizations by respecting the committed/estimated efforts. Perform technical development, customization, reports, workflows, data entities etc. Build and release management, deploy models, and deployable packages. Develop interfaces from/to D365FO to other systems or applications using DMF, Logic App, APIetc. Follow the standards and best practices on all interfaces and modifications. Assists in Troubleshooting and resolving issues. Unit testing and QC to ensure quality. D365FO Security Management. Data Migration. Provide accurate estimation and timelines of tasks. Prioritize work and spend time on the most important, business identified concerns. Work independently and/or with team members to resolve escalated support tickets. Provide technical support to customers. Collaborate on the creation of application requirements and fit/gap analysis. Write technical specifications and collaborate with the functional team to ensure functional and technical requirements are understood and well defined. Collaborate with client technical resources around the definition and implementation of system integrations. Develop ‘proof of concept’ solutions where required. Code release management, ensuring successful build and deployment to relevant environments with appropriate release notes. Solve technical issues encountered, raising to Microsoft support as required. Good integration skills. Experience of Microsoft Common Data Service and the Microsoft Power Platform would be an advantage. Essential Skills/Abilities Possess at least 6 years of significant practical and technical experience in a D365 FO technical development/implementation installation, configuration, source code deployment and all subsidiary software needed for a successful Implementation. Knowledge of .NET (C#, XML, Web Services, etc.), Morph X, X++ Strong experience with SQL server, SSIS, SSRS. Experience using Azure DevOps. Strong Experience in Customizations (Pages, Tables, Views, Entities, Workflows, Class…) Experience with Dynamics AX2012 and D365FO. Experience Power BI Excellent documentation skills especially Technical Documents. Possess good oral and written communication skills, in English. Desirable Skills/Abilities D365 FO certifications a plus D365 Commerce, CRT, MPOS and CPOS Development experience is a plus. Power Apps/Power Automate/Logic Apps, Azure functions is a plus. Be able to adapt and summarize. Strive to continually increase knowledge. Have team spirit.

At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. Job Description - Staff Mobile Tester As ‘Test Analyst’ you will be responsible for Testing of Applications developed for Mobile devices against Requirements, meeting the Quality and Project Testing needs. You will work closely with Test Manager/ Lead for the projects under test. The candidate should be flexible to work on desktop, web applications across domains. Responsibilities Testing of Mobile Applications developed for various Mobile devices on different platforms for Functional, Usability, Performance and Security aspects Understand the Requirements (Business & Technical) for the Application developed for a specific Mobile device and its Operating platform Work closely with Mobile Solution Engineering team to understand the specifics of the Application, Mobile device & operating platform on which the Application would run and due considerations Review Design and provide feedback considering Testability of the Application/ Solution Provide inputs to Test Lead/ Manager on Test Strategy and Test Planning Perform Test Case design, identify any opportunity for Test Automation and Perform automation. Develop Test Cases both Manual and Automation Scripts as applicable Perform Test Environment readiness check Execute Testing, log defects and report the progress to Test Lead/ Manager. Liaise with Mobile Solution Engineering Team & other relevant team for Defect resolution Provide Test Results and other inputs for creating Test Report and Test Sign off documentation Participate and provide updates on Testing in Project/ Release meetings Assist Test Lead/ Manager in capturing and reporting Test Metrics. Provide required support in Analysis of metrics and implementation of improvement actions, as necessary People responsibilities Should come up with innovative and smart ways of doing work, without compromising on quality Understand and follow workplace policies and procedures. Requirements Other details BE/BTech/MCA Overall 3-6 years of hands on experience in Testing Mobile Applications on handheld devices is a must. Hands on experience in different type of mobile applications (Native, Hybrid, Mobile web) Should have excellent communication skills & should be able to articulate concisely & clearly Should play the role of an individual contributor Should have experience in Functional Testing of Mobile Applications for Android Platform, iPhone/ iPad (iOS), Windows phone. Good understanding of SDLC, Agile testing methodologies Nice To Have Skills Exposure to Mobile application test automation is desirable Experience/ exposure to Application testing on Windows Mobile platforms is desirable Good understanding of Mobile Technologies like 4G, 3G, GPRS, Wi-Fi etc Knowledge of MAM (Mobile Application Management), MDM (Mobile Device Management) & Security aspects is preferred Exposure to Web service testing,API testing,SOA testing Hands on experience with Test Management and Defect Management tools including HP QC. JIRA, Azure DevOps Responsive & adaptable to customer and project needs. Exposure to Global Projects and working with Clients at onsite is desirable Experience in Usability (User experience) & Accessibility Testing which covers industry standards like WCAG2.0/ 2.1 for mobile applications is a plus. EY | Building a better working world EY exists to build a better working world, helping to create long-term value for clients, people and society and build trust in the capital markets. Enabled by data and technology, diverse EY teams in over 150 countries provide trust through assurance and help clients grow, transform and operate. Working across assurance, consulting, law, strategy, tax and transactions, EY teams ask better questions to find new answers for the complex issues facing our world today.

At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. Job Description - Staff Mobile Tester As ‘Test Analyst’ you will be responsible for Testing of Applications developed for Mobile devices against Requirements, meeting the Quality and Project Testing needs. You will work closely with Test Manager/ Lead for the projects under test. The candidate should be flexible to work on desktop, web applications across domains. Responsibilities Testing of Mobile Applications developed for various Mobile devices on different platforms for Functional, Usability, Performance and Security aspects Understand the Requirements (Business & Technical) for the Application developed for a specific Mobile device and its Operating platform Work closely with Mobile Solution Engineering team to understand the specifics of the Application, Mobile device & operating platform on which the Application would run and due considerations Review Design and provide feedback considering Testability of the Application/ Solution Provide inputs to Test Lead/ Manager on Test Strategy and Test Planning Perform Test Case design, identify any opportunity for Test Automation and Perform automation. Develop Test Cases both Manual and Automation Scripts as applicable Perform Test Environment readiness check Execute Testing, log defects and report the progress to Test Lead/ Manager. Liaise with Mobile Solution Engineering Team & other relevant team for Defect resolution Provide Test Results and other inputs for creating Test Report and Test Sign off documentation Participate and provide updates on Testing in Project/ Release meetings Assist Test Lead/ Manager in capturing and reporting Test Metrics. Provide required support in Analysis of metrics and implementation of improvement actions, as necessary People responsibilities Should come up with innovative and smart ways of doing work, without compromising on quality Understand and follow workplace policies and procedures. Requirements Other details BE/BTech/MCA Overall 3-6 years of hands on experience in Testing Mobile Applications on handheld devices is a must. Hands on experience in different type of mobile applications (Native, Hybrid, Mobile web) Should have excellent communication skills & should be able to articulate concisely & clearly Should play the role of an individual contributor Should have experience in Functional Testing of Mobile Applications for Android Platform, iPhone/ iPad (iOS), Windows phone. Good understanding of SDLC, Agile testing methodologies Nice To Have Skills Exposure to Mobile application test automation is desirable Experience/ exposure to Application testing on Windows Mobile platforms is desirable Good understanding of Mobile Technologies like 4G, 3G, GPRS, Wi-Fi etc Knowledge of MAM (Mobile Application Management), MDM (Mobile Device Management) & Security aspects is preferred Exposure to Web service testing,API testing,SOA testing Hands on experience with Test Management and Defect Management tools including HP QC. JIRA, Azure DevOps Responsive & adaptable to customer and project needs. Exposure to Global Projects and working with Clients at onsite is desirable Experience in Usability (User experience) & Accessibility Testing which covers industry standards like WCAG2.0/ 2.1 for mobile applications is a plus. EY | Building a better working world EY exists to build a better working world, helping to create long-term value for clients, people and society and build trust in the capital markets. Enabled by data and technology, diverse EY teams in over 150 countries provide trust through assurance and help clients grow, transform and operate. Working across assurance, consulting, law, strategy, tax and transactions, EY teams ask better questions to find new answers for the complex issues facing our world today.

Use Your Power for Purpose As an Associate in Labeling Operations at Pfizer, you will play a crucial role directly contributing to the improvement of patients' lives. Your work will ensure that our products are accurately labeled, meeting regulatory requirements and providing essential information to healthcare professionals and patients. This role offers a unique opportunity to make a tangible impact on global health while working with a team of dedicated professionals. What You Will Achieve In this role, you will provide operational support for Global Labeling which includes; Generate necessary renditions in GDMS (e.g., clean and marked PDF, clean and marked MS Word) and bookmark renditions as appropriate. Facilitate workflow through corporate document repository, e.g., GDMS. Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.). Manage the document status in GDMS and notify internal stakeholders of the availability of labeling documents. Order SPL for USPIs, check and upload to GDMS upon receipt, notify internal stakeholders of its availability (e.g., Regulatory, Drug Listing). Responsible for ensuring compliance to Company’s submission standards, policies and procedures. Ensure all actions taken within role follow applicable SOPs and associated documents so that high quality delivery of outputs and compliance is maintained. Consolidate labeling versions. Consolidate comments from Labeling reviewers and Regulatory Authorities. Prepare comparison tables for labeling team discussions. Edit and format labeling documents- Ensure the document complies with the appropriate template (e.g., QRD, PLR). Update and maintain the CDS log. Set clear targets for review and approval timelines for labeling documents using effective project management. Follow up with Labeling Team members to ensure timely review and approval deadlines are met. Ensure appropriate tracking of labeling projects via defined procedures and optimal use of systems. Here Is What You Need (Minimum Requirements) Bachelor’s degree required preferably in a science / life sciences related degree. 0-2 years practical experience Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) Basic understanding of regulatory requirements for labeling Strong organizational skills Excellent written and verbal communication skills Ability to work independently and as part of a team Attention to detail and accuracy Ability to manage multiple tasks simultaneously Basic project management skills Bonus Points If You Have (Preferred Requirements): Experience in the pharmaceutical or biotechnology industry Familiarity with labeling software and databases Knowledge of global labeling regulations Experience with electronic document management systems Strong interpersonal skills Strong analytical skills Ability to interpret and apply regulatory guidelines Effective problem-solving skills Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Regulatory Affairs

Use Your Power for Purpose As an Associate in Labeling Operations at Pfizer, you will play a crucial role directly contributing to the improvement of patients' lives. Your work will ensure that our products are accurately labeled, meeting regulatory requirements and providing essential information to healthcare professionals and patients. This role offers a unique opportunity to make a tangible impact on global health while working with a team of dedicated professionals. What You Will Achieve In this role, you will provide operational support for Global Labeling which includes; Generate necessary renditions in GDMS (e.g., clean and marked PDF, clean and marked MS Word) and bookmark renditions as appropriate. Facilitate workflow through corporate document repository, e.g., GDMS. Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.). Manage the document status in GDMS and notify internal stakeholders of the availability of labeling documents. Create/Update SPL for USPIs, check and upload to GDMS upon receipt, notify internal stakeholders of its availability (e.g., Regulatory, Drug Listing). Responsible for ensuring compliance to Company’s submission standards, policies and procedures. Ensure all actions taken within role follow applicable SOPs and associated documents so that high quality delivery of outputs and compliance is maintained. Here Is What You Need (Minimum Requirements) Bachelor’s degree required preferably in a science / life sciences related degree. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) Basic understanding of regulatory requirements for labeling Excellent written and verbal communication skills Ability to work independently and as part of a team Ability to manage multiple tasks simultaneously Basic project management skills Bonus Points If You Have (Preferred Requirements): Knowledge of global labeling regulations Strong interpersonal skills Strong analytical skills Ability to interpret and apply regulatory guidelines Effective problem-solving skills Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Regulatory Affairs

Shadow design discussions the Senior Designer does with clients; prepare Minutes of Meetings and keep track of project milestones to ensure a timely and high-quality delivery Assist the Senior Designer in 3D designs using SpaceCraft (HomeLane Software) and Sketchup; recommend enhancements and be a sounding board for the Senior Designer Be available for Site Visits, Masking along with the Senior Designer; take on the responsibility of file management across HomeLane tech systems Assist the Senior Designer in creating commercial proposals using SpaceCraft and other quoting tools; validate quotes to ensure customers get a transparent and fair estimate. Coordinate with various stakeholders to ensure a great design outcome; build relationships with teams like sales, drawing QC, project management teams and planners. Mandatory Qualifications: Design education background - B.Arch, B.Des, M.Des, Diploma in Design 0-1yr of experience in Interior Design / Architecture Good communication & presentation skills Basic knowledge of Modular furniture Practical knowledge of SketchUp A great attitude.

We’re Hiring! Join Our Growing Team! 🌟 💥 Urgent Vacancy at Surat - Head Office. 💥Position :- QA/QC Engineer💥 As part of our expansion journey, Saurashtra Enviro Projects Private Limited is inviting skilled and experienced professionals to be a part of our project execution team across multiple locations! 🎓Key Responsibilities 1. Material & Equipment Inspection Inspect raw materials and critical equipment at vendor sites and stores for compliance with project specs, QAPs, and datasheets. Conduct final inspections before dispatch of rotary and static equipment. 2. Vendor Surveillance & StageWise Inspection Monitor vendor fabrication, assembly, and testingusing approved ITPs. Verify WPS/PQR, welder qualifications, NDT results, and test certificates. Issue clearance or NCRs based on findings. 3. ThirdParty & Client Coordination Liaise with clients, consultants, and TPIs for joint inspections and approvals. Schedule inspections, track punchpoint closures, and expedite timely signoffs. 4. Site Quality Control Activities Supervise installation and erection of mechanical machinery onsite. Conduct alignment, fit-up, welding, and quality checks at installation stage. Proactively implement corrective/preventive actions to avoid delays. 5. Documentation & Reporting Prepare inspection reports, NCRs, MTCs, quality dossiers, and test records. Maintain log of inspection status, approvals, and non-conformances. Ensure full documentation is available for dispatch releases and final project handovers. 6. Compliance to Codes & Standards Uphold engineering codes such as ASME, IS, API, IBR across pressures vessels, heat exchangers, piping, and rotating machinery. Validate thickness checks, hydro-tests, radiography, dyepenetrant, and other NDT methods. 7. QA/QC Plan Development Support creation of project-specific QAPs, ITPs, and SOPs. Drive continuous improvement in quality processes based on lessons learned. 8. Safety & Risk Management Drive safe inspection practices; report unsafe conditions during handling or lifting heavy equipment. 9. Cross-functional Coordination Collaborate with procurement, engineering, logistics, and project teams for smooth inspection flow and issue resolution. Experience 5+ years in mechanical QA/QC roles; experience with MSW, ZLD, or industrial projects Education UG: B.Tech/B.E . in Mechanical Skills Welding inspection, NDT review, root cause analysis, inspection tools, documentation, teamwork, communication Role: Quality Assurance and Testing - Other Industry Type: Water Treatment / Waste Management Department: Engineering - Software & QA Employment Type: Full Time, Permanent Role Category: Quality Assurance and Testing

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description Main Responsibilities: 24 x 7 audit readiness. Participation in internal, external, regulatory audits. Ensure 100% participation in training's against CAPA's. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Supporting to share required documents from QC to RA/ other requirement. Detern1ining team priorities in accordance with the plant's needs, while coordinating with the team leader /Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms. Perform analytical test according to the monograph and SOP. Responsible for calibration and verification of instruments. Responsible to work in shift as per requirement. Maintaining of reserved samples room and chambers / autoclaves / incubators. Help in preparation of documents related to department (like STP's, SOP's and etc.) Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis. Must be ensured sampled, approved and rejected labels timely as required. Responsible to maintain the stock record of chemicals and reconciliation of standards. Responsible to maintain safety CAPA. Responsible to maintain 5-S in QC. Online documentation (based on requirement) must be ensured as per data integrity norms and awareness to team against data integrity. Responsible to support analysis reduction/QC efficiency enhancement programs. Any other job assigned by the Manger - QC Manger or group leader - QC Preferred Skills Preferred experience with Wet lab instruments/techniques including but not limited to Karl Fischer Titrator, Auto-titrator, analytical balance, FTIR, Polarimeter, UV, X-ray Diffraction, etc. Qualifications The ideal candidate will have: Education: B.Sc. / M.Sc. in Chemistry. Experience: Minimum 8 years of industrial experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description Key Responsibilities: 24 × 7 audit readiness. Participation in internal, external, regulatory audits. Ensure 100% participation in training’s against CAPA’s. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Supporting to share required documents from QC to RA/ other requirement. Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader /Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms. Perform analytical test according to the monograph and SOP. Responsible for calibration and verification of instruments. Maintaining of reserved samples room and chambers / autoclaves / incubators. Responsible to work in shift as per requirement. Help to in charge in preparation of documents related to department (like STP’s, SOP’s and etc.) Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis. Must be ensured sampled, approved and rejected labels timely as required. Responsible to maintain the stock record of chemicals and reconciliation of standards. Any other job assigned by the Manger -QC Manger or group leader-QC Preferred Skills Preferred experience with Wet lab instruments/techniques including but not limited to Karl Fischer Titrator, Auto-titrator, analytical balance, FTIR, Polarimeter, UV, X-ray Diffraction, etc. Qualifications The ideal candidate will have: Education: B.Sc. / M.Sc. in Chemistry. Experience: Minimum 5 years of industrial experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Job Description The position is required to lead all manufacturing activities at Joka to ensure defect free, quality products being delivered to the customers. Position is required to anticipate Technological and Engineering variations in the Indian Metering market, review opportunities to optimize productivity and business growth in India.The incumbent will coordinate with cross-functional teams and drive operational excellence, compliance, and continuous improvement. Ensure a harmonious productive environment. AREAS OF RESPONSIBILITIES Plan, organize, and oversee daily operations to ensure smooth production of energy meters. Ensure production targets are met in terms of quantity, quality, and timeline. Implement lean manufacturing and Six Sigma practices to reduce waste and increase efficiency. Liaise with R&D, Quality, SCM, and Sales and other concerned Departments for order execution and product improvements. Ensure strict adherence to quality standards (ISO, BIS, etc.). Coordinate with QA/QC teams for regular inspections, testing, and audits. Strategize to minimize quality defects and field failures Drive product improvement processes Manage NQC/NCC Strengthen operational model for EMS (vendors) Oversee preventive and breakdown maintenance of machinery and equipment. Enforce EHS protocols as per ISO 14001 & ISO 45001 standards. Coordinate with the stores, procurement, and planning departments to ensure availability of raw materials. Prepare and control factory operating budget. Provide thought-leadership and build internal competencies Requirements Educational Qualification: B. Tech/B.E. in Communication from reputed institute Work Experience: "Around 20 years, out of which around 5 years must be in similar capacity / responsibility. Having adequate exposure in automation & software in the following industries -" Metering, Electronic Component, Energy Or Telecommunication

Shadow design discussions the Senior Designer does with clients; prepare Minutes of Meetings and keep track of project milestones to ensure a timely and high-quality delivery Assist the Senior Designer in 3D designs using SpaceCraft (HomeLane Software) and Sketchup; recommend enhancements and be a sounding board for the Senior Designer Be available for Site Visits, Masking along with the Senior Designer; take on the responsibility of file management across HomeLane tech systems Assist the Senior Designer in creating commercial proposals using SpaceCraft and other quoting tools; validate quotes to ensure customers get a transparent and fair estimate. Coordinate with various stakeholders to ensure a great design outcome; build relationships with teams like sales, drawing QC, project management teams and planners. Mandatory Qualifications: Design education background - B.Arch, B.Des, M.Des, Diploma in Design 0-1yr of experience in Interior Design / Architecture Good communication & presentation skills Basic knowledge of Modular furniture Practical knowledge of SketchUp A great attitude.

Job Responsibilities : Carrying out inspection as per inspection and test plan. Carrying out Inspection as per responsibility and Inspection & Test Plans, Procedures, specifications and Issue/certify reports within specified time. Carrying out testing within specified time and report the results. (Where applicable). Correctness of Inspection process. Correctness of inspection process w.r.t. Codes/Standard / Specification/Procedures. Carrying out technical surveillance/audit and timely prepare report. Ensure availability of latest revision of documents. Ensure latest revisions of ITP, procedures, formats, checklist, etc. are being implemented. Skill Encasement Attendance to Seminars / Training organized Identified training modules successfully completed as planned. Education Requirement : Graduate/Diploma Engineer in relevant discipline Experience Requirement : Necessary: Graduate Engineer: Min 1-7 years Diploma Engineer: Min 7-14 Years in QA/QC functions of Refinery, Petrochemical, Infrastructure projects. Desirable: NDT, Level - II in RT, UT, PT, MT & VT. (Mech.) Skills & Competencies : Preparation of inspection reports Knowl edge of job procedure, ITP, specifications and formats For Construction Quality Engineer - Mechanical: Knowledge of codes and standards for welding Materials and Metallurgy including heat treatment Welding symbols, processes, defects, consumable classifications, applicable codes Knowledge about measurement instruments needed for various type of inspection. Knowledge on warehouse inspection system and Method of welding inspection & Testing for the job Knowledge of inspection and testing for wrapping & coating and painting processes Pressure testing and Post weld Heat treatment Requirements For Construction Quality Engineer - Civil: Knowledge of civil construction practices, fire proofing, insulation, refractory Batching plant operation activities Knowledge of the Civil material, their properties and testing equipment Testing methods as per applicable testing codes, result monitoring, report preparation Knowledge of the specification and code requirement for various jobs. Various applicable type of testing in civil jobs covering, cube, water, cement sand and aggregates Knowledge of earthworks & bituminous work

Job Responsibilities : Carrying out inspection as per inspection and test plan. Carrying out Inspection as per responsibility and Inspection & Test Plans, Procedures, specifications and Issue/certify reports within specified time Carrying out testing within specified time and report the results. (Where applicable) Study of Drawing & Specification applicable to job Clear Knowledge of drawings and specification of the job being inspected Carrying out technical surveillance/audit and timely prepare report Review of ITPs, Procedures, formats submitted by Contractors/Vendors Complete review of ITPs, procedures, formats submitted by Contractors/Vendors within specified time. Skill Encasement Attendance to Seminars / Training organized Identified training modules successfully completed as planned. Education Requirement : Graduate/Diploma Engineer in relevant discipline Experience Requirement : Necessary: Minimum 7-12 years for graduate and 14-19 years for Diploma in discipline specific QA/QC functions in EPC activities of Refinery, Petrochemical, Infrastructure projects etc. Desirable: NDT, Level #II in RT, UT, PT, MT & VT. (Mech.) Skills & Competencies : Application of statistical techniques Code & Standard interpretation System of related job to be audited e.g. ITP, Quality Plan, Work Procedures, and Specifications etc. Knowledge of quality planning and implementation of process controls by Quality Control Procedures (QCPs) Preparation of Presentation & Training Booklets / Document & Report writing Field quality control, inspection and testing Organizing and conducting technical audits. Knowledge of SAP Modules For Construction Quality Engineer - Mechanical: Knowledge of codes and standards for welding Materials and Metallurgy including heat treatment Knowledge of fabrication codes and standards covering Inspection, Welding technology, PWHT, etc. Welding process qualification, different types of welding, problems and their effective solutions Knowledge of advantages and limitations of various welding and NDT processes Reviewing fabrication drawings to minimize welding NDT and PWHT problems Knowledge of ITP and dossier booklets and record compilation For Construction Quality Engineer - Civil: Knowledge of all Civil construction, fire proofing, insulation, refractory Batching plant operation activities Civil materials, their properties and testing Concrete Mix Design Knowledge of the specification and code requirement for various jobs. Knowledge on all types of civil material testing Earthworks & Bituminous work

Job Title: Quality Control (QC) Executive – Onsite & Offsite Location: Onsite: In-house QC Lab / HO / Warehouse Offsite: Third-party Manufacturing / RM Suppliers Employment Type: Full-Time Website: www.dermatouch.com About Dermatouch Dermatouch creates safe, effective, and clinically backed skincare products trusted by dermatologists and loved by customers across India. We ensure top-tier quality in every batch we release. Key Responsibilities: Conduct physical, chemical, and microbiological testing of raw materials, packaging materials, bulk, and finished skincare products. Prepare and maintain COAs , test reports, and sample records. Ensure quality standards across product appearance, pH, viscosity, stability, and fragrance . Handle third-party lab coordination for additional compliance testing (like dermatological tests, preservative efficacy, etc.). Perform stability studies and assist in shelf-life determination. Visit offsite vendors to inspect RM/PM and finished product QC processes. Candidate Profile: Education: B.Sc / M.Sc in Chemistry, Cosmetic Science, Microbiology, or B.Pharm. Experience: 2–5 years in QC for skincare / personal care / cosmetics . Familiar with instrumentation testing (e.g., pH meter, viscometer, UV, HPLC) and cosmetic testing parameters. Understanding of cosmetic BIS/ISO standards . Strong documentation, coordination, and observation skills. Open to travel for offsite checks.

Attention Jobseekers ! We are hiring for a Quality Control Role in our food manufacturing unit. Job Title: Quality Control Executive – Food Technology Company: Tanvi Foods India Ltd. Location: Seetharampuram , Nuzvidu District Qualifications: B.Sc / M.Sc / B.Tech in Food Technology or related discipline. Experience: 0–2 years (Freshers can apply). Salary: As per market standards. Job Responsibilities: Conduct routine quality checks on raw materials, in-process products, and finished goods to ensure compliance with company and regulatory standards. Maintain accurate and detailed QC documentation and reports. Support implementation of quality control procedures and standard operating protocols. Monitor hygiene, sanitation, and safety standards across production areas. Assist in calibration and maintenance of laboratory equipment. Coordinate with production and R&D teams to resolve quality issues promptly. Skills Required: Strong knowledge of food safety regulations, quality systems, and testing procedures. Basic understanding of HACCP, GMP, and ISO standards. Good communication skills and ability to work in a team environment. Attention to detail and problem-solving skills. How to Apply: Interested candidates can send their resume to hrvza@cornclub.info Phn no : 9133576333 with the subject line: Application for QC Executive – Food Technology. Job Types: Full-time, Fresher Pay: ₹15,000.00 - ₹44,136.20 per month Benefits: Health insurance Provident Fund Ability to commute/relocate: Sitaramapuram, Andhra Pradesh: Reliably commute or planning to relocate before starting work (Preferred) Experience: QC: 1 year (Preferred) Work Location: In person

Job Title Project Engineer Job Description Summary We are looking to hire for Project Engineer - Civil & Finishes, experienced with project execution. Job Description About the Role: Supervise daily activities at site mainly concentrating on civil works. Assist Project Manager in execution of civil activities. Execute work at site as per the drawings and specification. Prepare MIS report (Daily report) Coordinate with contractor ensuring quality of execution with safety and timely completion of job as per schedule. Monitor contractor’s work. Assist QA/QC – in charge ensuring quality parameters are met. Other Skills Should have good communication skills. Should be able to speak, read and write in English and local language. Should have strong knowledge of MS office. Why join Cushman & Wakefield? As one of the leading global real estate services firms transforming the way people work, shop and live working at Cushman & Wakefield means you will benefit from. Being part of a growing global company. Career development and a promote from within culture. An organization committed to Diversity and Inclusion We're committed to providing work-life balance for our people in an inclusive, rewarding environment. We achieve this by providing a flexible and agile work environment by focusing on technology and autonomy to help our people achieve their career ambitions. We focus on career progression and foster a promotion from within culture, leveraging global opportunities to ensure we retain our top talent. We encourage continuous learning and development opportunities to develop personal, professional, and technical capabilities, and we reward with a comprehensive employee benefits program. We have a vision of the future, where people simply belong. That's why we support and celebrate inclusive causes, not just on days of recognition throughout the year, but every day. We embrace diversity across race, colour, religion, sex, national origin, sexual orientation, gender identity or persons with disabilities or protected veteran status. We ensure DEI is part of our DNA as a global community - it means we go way beyond than just talking about it - we live it. If you want to live it too, join us. INCO: “Cushman & Wakefield”

Shadow design discussions the Senior Designer does with clients; prepare Minutes of Meetings and keep track of project milestones to ensure a timely and high-quality delivery Assist the Senior Designer in 3D designs using SpaceCraft (HomeLane Software) and Sketchup; recommend enhancements and be a sounding board for the Senior Designer Be available for Site Visits, Masking along with the Senior Designer; take on the responsibility of file management across HomeLane tech systems Assist the Senior Designer in creating commercial proposals using SpaceCraft and other quoting tools; validate quotes to ensure customers get a transparent and fair estimate. Coordinate with various stakeholders to ensure a great design outcome; build relationships with teams like sales, drawing QC, project management teams and planners Mandatory Qualifications: Design education background - B.Arch, B.Des, M.Des, Diploma in Design 0-1yr of experience in Interior Design / Architecture Good communication & presentation skills Basic knowledge of Modular furniture Practical knowledge of SketchUp A great attitude.

Job Title: Manager - QC Location: M/s.Analogics Tech India Ltd.,Plot No.9/10, Road No.6,IDA Nacharam, Hyderabad - 500 076. Department: QC Qualification &Skills: Diploma / B.E./B.Tech. / M.E./M.Tech.in Electrical or Electronics Engineering) OR Certificate-NSQF (Level-5 in Quality Engineer) with 5+ Years of experience in the relevant field & mainly in defense related projects is an added advantage. Candidate must have the Knowledge of Inward and outward QC of materials received according to the specifications, initial quality and manufacturing planning, Handling the inspection process, Develop and manage electronic record database, Technical writing skills that include quality procedures and test plans, perform product ,process, and system audits and verify effectiveness or corrective actions, Exposure on ISO and EMS & other related certification processes, implementation, control procedures, Candidate must be specialized in trainings related to ISO-9001(QMS) &14001(EMS). Gross Salary: Rs.25,000/- To Rs.35,000/- Brief Job Description: A Quality Manager is responsible for managing quality in all organizational operations. It starts from ensuring the quality of components received from the supplier to the quality of finished goods, including the quality of the production process. The individual also trains and manages a team of quality inspectors and supervisors, apart from driving quality initiatives in the organization to ensure it remains competitive in the market. Must be well acquainted with ISO QMS, EMS, ISMS, CMMI , internal training & Audits procedures. Personal Attributes: The individual in this job role must possess strong leadership & management skills apart from analytical and problemsolving abilities. The person must be adept at using various computer applications for efficient data and record management. The individual must have good communication skills, attention to detail and a strong sense of quality in all the activities. Working knowledge & thorough understanding of Advanced Product Quality Planning (APQP): Prepare a plan and define the program as per the customer needs and expectations from the existing or proposed product(s) · determine the material specifications and equipment requirements · design and develop the production process with a focus on product specifications, quality and production costs · determine the capability and reliability of the manufacturing process and product quality acceptance criteria. · develop the verification and validation plans, and effective quality control processes · carry out benchmarking with the top competitors’ products to ensure the relevance and quality of the product · arrange for carrying out production trial runs · collect and assess the data related to quality planning effectiveness · evaluate and test the product output to confirm the effectiveness of the deployed manufacturing approach · carry out necessary adjustments to the product and process, if required. Contact Person: P.Sreenivas S. / K.Amala , 8019610574,9000731133/ 8019058015 Company Address / Head Office: M/s.Analogics Tech India Ltd.,Plot No: 9/10, Road No.6, Nacharam,Industrial Estate, Hyderabad – 500 076, Telangana. Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Ability to commute/relocate: NACHARAM , Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (Required) Experience: total work: 4 years (Preferred) Work Location: In person

🚨 Hiring Alert – Sales Executives & Sales Managers (Lab Instruments & Software) 📍 Location: Hyderabad & Vizag 🏢 Company: Arizona Automation & Technologies 📨 Apply at: Hiring@arizonaautomationtech.com Arizona Automation & Technologies is expanding! We’re looking for dynamic and experienced Sales Executives and Sales Managers to drive our growth in the Hyderabad and Vizag markets. 🔍 Who Should Apply? ✅ Professionals with 2–8 years of sales experience in: • Lab instruments / Analytical instruments • Lab software such as LIMS, ELN, EQMS, CDS integration • Scientific equipment sales or digital lab solutions • Pharma, chemical, life sciences, or food industries preferred ⸻ 🧪 Key Responsibilities: • Promote and sell lab software solutions like LIMS, ELN, EQMS, EDMS, CDS integration, and compliance tools • Generate and manage leads for analytical instruments and lab automation tools • Identify client needs and recommend suitable software/hardware solutions • Conduct detailed demos and presentations to QC, QA, R&D, and IT teams • Build and maintain strong relationships with pharma, biotech, and food industry clients • Collaborate with technical/implementation teams for client onboarding and support • Stay updated on regulatory requirements (e.g., 21 CFR Part 11, GAMP 5, Annex 11) • Meet monthly and quarterly sales targets and provide regular reporting ⸻ 🎓 Qualifications: • Bachelor’s or Master’s in Science, Engineering, Pharmacy, or related field • Strong communication, presentation, and negotiation skills • Experience in lab instrument or software sales preferred • Willingness to travel across the assigned region ⸻ 📌 Why Join Us? • Work with a leading digital transformation partner for the pharma industry • Be part of cutting-edge lab automation and compliance software projects • Competitive salary + performance incentives + travel allowance • Career growth in a fast-scaling company with top pharma clients ⸻ 📧 Interested? Send your CV to: Hiring@arizonaautomationtech.com 📌 Subject: Application – Sales Executive/Sales Manager – [Preferred Location] ⸻ #HiringNow #SalesJobs #LabInstruments #AnalyticalInstruments #LIMS #ELN #EQMS #LabSoftwareSales #PharmaSales #ScientificSales #FieldSales #LifeSciences #PharmaceuticalJobs #SalesManager #SalesExecutive #KarnatakaJobs #TamilNaduJobs #SouthIndiaJobs #ArizonaAutomation #PharmaAutomation #DigitalPharma #JoinOurTeam