4809 Quality Control Jobs - Page 37

1. Act as customer relationship manager for product quality at corporate. 2. Monitor & improve ORM-social media complaints by analysis of product complaints/feedback/comments on social media. 3. Coordinate with plants for Timely reporting and resolution of Safety Issue, Zero Hour Issue and Critical Customer Complaints. Monitor and Improve TAT of Complaint Resolution. 4. Warranty/Customer complaints analysis and ensure improvement projects initiation & implementation against top contributors. 5. Monitor and improve of e commerce rating of product on various on-line sales portal e.g. Amazon, Flip cart and other portals etc. 6. Monitor and improvement Net Promotor Score (NPS) through product actions. 7. Conduct Customer Delight Survey across product categories and publish product category wise score.

Quality control & Assurance Engineer with 2-3 years experience and should be worked in aerospace/automobile/mechanical industry.

Position - QC Chemist Location - Alwar(Toll Manufacturing unit) Role & responsibilities Testing of all powder-finished products, Testing of raw materials packing materials and trading goods. Responsible for MSDS and TDS of all raw materials. Make Test Certificates for powder FGs Maintaining powder product and RP/PM testing records Random FG testing at shop floor of powder product and RM/PM SECONDARY Total HSE, Safety and Hazardous involvement in the laboratory Maintaining counter sample room Calibration of Lab Equipments and adherence of the calibration frequency Assigning of responsibilities for shift operators Preferred candidate profile BSc/MSc in Chemistry with 3-5 years of experience Perks and benefits If interested, please share your updated cv to renuka.thimmanaik@fosroc.com

About Company Founded in 2011, ReNew, is one of the largest renewable energy companies globally, with a leadership position in India. Listed on Nasdaq under the ticker RNW, ReNew develops, builds, owns, and operates utility-scale wind energy projects, utility-scale solar energy projects, utility-scale firm power projects, and distributed solar energy projects. In addition to being a major independent power producer in India, ReNew is evolving to become an end-to-end decarbonization partner providing solutions in a just and inclusive manner in the areas of clean energy, green hydrogen, value-added energy offerings through digitalisation, storage, and carbon markets that increasingly are integral to addressing climate change. With a total capacity of more than 13.4 GW (including projects in pipeline), ReNew’s solar and wind energy projects are spread across 150+ sites, with a presence spanning 18 states in India, contributing to 1.9 % of India’s power capacity. Consequently, this has helped to avoid 0.5% of India’s total carbon emissions and 1.1% India’s total power sector emissions. In the over 10 years of its operation, ReNew has generated almost 1.3 lakh jobs, directly and indirectly. ReNew has achieved market leadership in the Indian renewable energy industry against the backdrop of the Government of India’s policies to promote growth of this sector. ReNew’s current group of stockholders contains several marquee investors including CPP Investments, Abu Dhabi Investment Authority, Goldman Sachs, GEF SACEF and JERA. Its mission is to play a pivotal role in meeting India’s growing energy needs in an efficient, sustainable, and socially responsible manner. ReNew stands committed to providing clean, safe, affordable, and sustainable energy for all and has been at the forefront of leading climate action in India. Job Description Key Responsibilities of the Role : Preparation of Audit schedule for Preventive maintenance audits. Executing process & post maintenance Preventive maintenance audits. NC analysis and Coordinating with site team effective closure of the issues. 1st level root cause analysis of major component failure. Large component replacement inspection. Driving special project like -5S Audit and Kaizen Monitoring Horizontal deployment of Kaizen Analyzing repeated failure of components & repeated breakdowns. NCR management for the deviations observed in internal/ external audits Coordination with the internal/ external stakeholders for audit management NC analysis and Coordinating with site team effective closure of the issues Peroxidic meeting with cross functional team for effective resolution of the issues. Providing theoretical and on job training to site team Essential: GWO work at height certified

Analysis of different in process samples for Drying study Reaction monitoring by HPLC and other samples on GC Impurity profile and hold time study of process validation samples calibration activities reputed API industry having regulatory approvals

Inspection of Raw material, fabricated material, Finish goods & Development samples, TC verification, report preparation & documentation. NC Identification, SAP entries, QCP preparation. Third party testing of raw material. MIS, Third Party Inspection. Co-ordinate & perform Spark test, Light test, Visual test, Hydro test, NDT Test activities.

Conduct chemical testing of raw materials & final products using pH meter, viscometer & titrator Handle detergent formulation, batch validation, QC checks, documentation, lab safety, and coordinate with production & R&D teams Perform QC of detergents Travel allowance Job/soft skill training Assistive technologies Performance bonus

Role & responsibilities Conducting every day syncs across the team to ensure streamlined operations Training junior chefs Do the prep work themselves as well Regular updates to reporting managers to be provided on tasks All briefings conducted to be reported back to reporting managers in a timely and structured manner (MOM) Responsible for overseeing a specific section or station, managing the kitchen team, and ensuring the smooth operation of that area. Cross check checklists filled out by jr. staff and get it authorised by Head chef Supervise and lead the Commie 1, Commie 2, and other junior kitchen staff within your section. Ensure the quality, taste of all the ingredients before get it in the operations Organise and prioritise the preparation and cooking of dishes according to the restaurant's requirements and standards. Assist in developing and refining recipes and menus. Maintain inventory levels, conduct stock checks, and coordinate with the senior chefs for timely ordering. Train and mentor junior kitchen staff, providing guidance and feedback. Maintain cleanliness, hygiene, and safety standards in your section. Collaborate with other kitchen sections and front-of-house staff to ensure smooth operations. Submit Daily stock inventory and stock requisitions to head chef Make sure kitchen is running its operations as per stated SOPS

Examine and treat animals on a first-come, first-serve basis as well as by appointment Cultivate positive relationships with customers and their animals through regular communication and excellent record-keeping Prioritize traumatic injuries and serious illnesses to ensure that all animals receive time sensitive care Educate clients on the importance of vaccinations, heart worm treatments, flea and tick treatments and other aspects of preventive care Perform or assist with surgeries Train new veterinary assistants and other members of the support staff Job Type: Part-time Pay: ₹20,000.00 - ₹30,000.00 per month Schedule: Day shift Work Location: In person Application Deadline: 22/06/2025

Role & responsibilities FSMS Documentation : Prepare, update, and control SOPs, manuals, forms, and HACCP plans as per BRCGS, ISO 9001:2015, and FSSC 22000 standards. Internal Audits : Plan and execute audits; identify non-conformities; implement CAPA; maintain audit schedules and readiness. Compliance & Certification : Ensure adherence to statutory, regulatory, and customer-specific requirements; support certification processes and third-party audit activities. Licensing & Annual Returns : Oversee timely renewal of licenses (e.g., FSSAI) and submission of required annual returns. Raw Material Analysis : Monitor and record daily analysis of raw materials to ensure compliance with quality and safety standards. Artwork Compliance : Provide inputs for artwork and labelling requirements for both export and domestic markets, ensuring compliance with relevant regulations such as USFDA, CFIA, EU, FSSAI, and other country-specific standards. Preferred candidate profile Experience in food processing industry handling FSMS documentation and audits. Hands-on experience with BRCGS Issue 9 and FSSC 22000 v6 implementation and maintenance. Familiarity with ISO 9001:2015, and GFSI benchmarked schemes. Female candidate preferred

Role & responsibilities Responsible for Overall production quality, QC's and take care of cutting & fabrication production and sub process adherence as per standard and SOP. Need to identifies and sets appropriate quality standards and parameters for products. Need to analysis data of customer complaints and finding the areas to improve our quality to fulfil customer needs. Develops, implements, and manages processes to ensure that products meet required specifications for quality, function, and reliability prior to delivery. Prepare Quality documents, QC's and establish Production. Setting requirements for raw materials and products from suppliers and monitoring their compliance. Oversee all product development procedures to identify deviations from quality standards. Need to approve the right products in production and to reject defectives. Need to find opportunities for improvement and develop new efficient procedures Responsible for plant production productivity both individual, and teams goals. Prepare ISO formats for all stages of production, operation, stock, wastages management. Ensure Cutting and fabrication production with job card for daily weekly output target achievement. Prepare production plan and need to ensure the flow of production with QC's To ensure all process from fabrication, powder coating, as per the project schedule and timely completion. To introduce strict measure through checklist for quality check in all stages of production. Job reports of all production need to analysis with document and update to Managing Director in weekly production review meeting. Need to do gap analysis in process and close the gaps for better process flow. Plan products line with invention and develop new products in domain specific service Like Panels, HVAC, AHU and other specific requirements of market needs. Discuss with sales and marketing team for developing newer products in line with customer expectation. Co-ordinate with sales and marketing team, Engineering, design for smooth production to supply to achieve customer delight

Role & responsibilities Responsible for the encoding of Digital Cinema Packages (DCP). Ensures proper handling of DCP creation processes, meeting industry standards. Manages content and source files with a high degree of care and attention to detail. Adheres to strict protocols to prevent any damage or loss of critical files. Conducts Quality Control (QC) checks for both JPEG and MPEG versions of content. Ensures the integrity and quality of digital cinema content before finalization. Possesses in-depth knowledge of encryption methods for securing DCP content . Proficient in using Key Delivery Messages (KDM) for authorized decryption of DCPs . Follows stringent security measures to safeguard digital cinema assets . Complies with industry regulations and standards to maintain the confidentiality and integrity of content

• Monitored quality issues and provided feedback to production teams. • Executed tasks assigned by senior manager. • Conducted vendor factory audits for new developments. • Prepared final project inspection reports.

Walk-In Interview Drive Bhilad Vapi We are hiring for multiple positions at our Bhilad Vapi facility. If you are looking for a new opportunity, walk in for an interview and join a dynamic team! Positions Available: MIS Executive Strong analytical and reporting skills Proficient in MS Excel, ERP knowledge is a plus Shift Incharge Experience in managing shop floor operations Ability to lead and coordinate shift teams Inventory Control Knowledge of inventory management processes Attention to detail and good organizational skills Warehouse Manager Experience in warehouse operations and team managemen Ability to optimize warehouse processes Assistant Manager Quality Experience in quality assurance and quality control Knowledge of relevant quality standards and audits Candidates located outside Vapi who are interested in relocating can participate in the interview via virtual call. Please share your details at: DHURVE.HARSHAL@mahindralogistics.com DESAI.DHROOVIN@mahindralogistics.com

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Officer Onco Solid Oral Job Requisitions No : 13898 Job Description Purpose of Job Skill Required Roles and Responsibilites Qualification Required Relevant Skills / Industry Experience Relevant professional / Educational background Any Other Requirements (If Any) Compensation / Reward Location: SEZ, Ahmedabad, GJ, IN, 382213 Travel: 0% 25% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 26 May 2025

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Manager Corporate Q A Job Requisitions No : 13776 Job Description Purpose of Job Skill Required Roles and Responsibilites Qualification Required Relevant Skills / Industry Experience Relevant professional / Educational background Any Other Requirements (If Any) Compensation / Reward Location: SEZ, Ahmedabad, GJ, IN, 382213 Travel: 50% 75% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 26 May 2025

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Officer Quality Control Job Requisitions No : 13777 Job Description Purpose of Job For HPLC Analysis Skill Required For Analysis of HPLC , UV, IR, Karlfisher Roles and Responsibilites For RM analysis Qualification Required SC/M Relevant Skills / Industry Experience Relevant professional / Educational background Pharmaceuticals Back ground required Any Other Requirements (If Any) Compensation / Reward Location: SEZ, Ahmedabad, GJ, IN, 382213 Travel: 0% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 26 May 2025

Teslas Supplier Industrialization team is responsible for critical raw materials, component production and qualification activities at suppliers This role will be responsible for selecting, qualifying, scaling battery cell materials (such as NMC, LFP, precursor, graphite, LiOH, cathode electrode, PVDF, LiPF6, etc ) manufacturing processes and quality system at Tesla supplier locations In this role, you will work closely with many organizations both internal and external to Tesla, taking new battery designs from initial concept through into full production, The battery cell is a critical component in Tesla vehicles and storage systems This role will have the opportunity to make meaningful contributions to our products The work environment is demanding, fast-paced and incredibly exciting The ideal candidate should be ready to push their limits, as they join in highly motivated and capable team to make unbelievable things into reality, Responsibilities Review/setup, qualify& scale process flow for battery cell material manufacturing, Monitor production output at existing facilities and support expansion programs with existing suppliers Setup In-process, OQC and corresponding IQC material quality controls; qualified required metrology for the same, Work together with suppliers on production process optimization and quality yield improvement e-g Metalic Impurity control, Support material related FA @ Supplier location Project manage activities at supplier locations and ensure all required milestones are meeting Tesla product qualification on time Act as a technical contact point for battery cell material manufacturing processes and co-ordinate activities within internal and external teams, Requirements BS/MS in Chemical, Material Science & engineering, or related areas 3+ years of industrial experience in battery material manufacturing process & quality control, Experience in characterizing materials using techniques like PSD, BET, GCMS, Titration, XRD, FTIR, SEM, EDS, Stress-strain diagram, DSC, DTA, hardness test, etc Experience in developing OQC/IQC quality controls, metrology qualification for cell materials Must be well versed in statistical data analysis & process capability analysis Working knowledge of battery cell manufacturing requirements, cell performance requirements and corresponding relationship to material characteristics Experience in high volume manufacturing is desired, Good communication and presentation skills, Ability to travel domestically and internationally 75%,

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Senior Officer QC Micro Job Requisitions No : 13757 Job Description Purpose of Job To perform Microbiological analysis, Skill Required Microbiological skill require to perform the microbiological analysis, Roles and Responsibilites Role of microbiologist and responsibilities to perform the microbial analysis, Qualification Required Sc Relevant Skills / Industry Experience Microbiological skills required and having experience related to pharma industries, Relevant professional / Educational background Master of Science in microbiology field and having two to three years of experience, Any Other Requirements (If Any) Compensation / Reward Location: SEZ, Ahmedabad, GJ, IN, 382213 Travel: 0% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 26 May 2025

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Sr Executive Quality Assurance Job Requisitions No : 13749 Job Description Purpose of Job Preparation and Review of PQR, Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software, Skill Required Having basic knowledge on Microsoft Word and Microsoft Excell Have knowledge of Minitab software for statstical evaluation of data, Roles and Responsibilites Preparation and review of PQR schedule, Planining of PQR compilation as per PQR schedule, Collection of data from all the CFT teams for compilation of PQR, Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software, Based of the PQR data recommendation to be recommended to concern department and ensure implemenation of the same, Qualification Required Pharm or M Relevant Skills / Industry Experience Should have relevant experience in Regulatory approved plant, Relevant professional / Educational background Any Other Requirements (If Any) Compensation / Reward Location: SEZ, Ahmedabad, GJ, IN, 382213 Travel: 0% 25% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 26 May 2025

The Person should be Job Conscious, Knowledge of BUSY SOFTWARE is MUST Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹25,000.00 per month Schedule: Day shift Supplemental Pay: Overtime pay Experience: Paper Manufacturing: 1 year (Preferred) Shift availability: Day Shift (Preferred) Work Location: In person

Hatsun Agro Product Limited Walaja Poly Film Division QA Officer Roles and Responsibility Overall Responsibility of QA from RM to FG. Ensure and monitor to meet RM, PM , SFG and FG as per specifications . ¢ Document and records management. ¢ Control over sanitation and Calibration. ¢ Process monitoring and control ¢ Product clearance and confirmation. ¢ Analysis of results of verification activities ¢ Customer complaint investigation and Reporting. ¢ Control of non conforming products Corrections, CA and PA. ¢ Validation and Verification of control measures. ¢ Daily and Monthly report consolidation and submission of report to right time.

Role Summary: We are seeking a detail-oriented Revit Draftsman & Site Supervisor to join our dynamic team. This hybrid role requires strong technical proficiency in Revit for preparing accurate and coordinated construction drawings, along with hands-on experience in managing site execution, contractor coordination, and quality control. Key Responsibilities:Revit Draftsman Duties: Develop and manage detailed architectural and interior drawings using Revit. Coordinate with design teams to ensure accuracy in working drawings, layouts, and technical documentation. Prepare 3D views, construction details, schedules, and BOQs. Maintain and update Revit models based on design changes or site feedback. Collaborate with consultants and vendors to integrate structural, MEP, and design elements. Site Supervisor Duties: Oversee day-to-day site execution in accordance with drawings, specifications, and timelines. Coordinate with contractors, vendors, and labor teams to ensure quality workmanship. Monitor site progress and provide regular updates to the design and management team. Ensure adherence to safety standards and compliance with local regulations. Resolve on-site challenges and discrepancies between drawings and execution. Required Skills & Qualifications: Proficient in Revit , AutoCAD, and MS Office Suite. Strong understanding of architectural detailing and construction methods. Ability to read and interpret architectural, structural, and MEP drawings. Good communication and team coordination skills. Willingness to travel to sites as required. Degree/Diploma in Architecture, Interior Design, or Civil Engineering. Preferred: Experience with luxury residential or hospitality projects. Familiarity with local bylaws and construction norms. Basic knowledge of material specifications and vendor coordination. Job Types: Full-time, Internship Contract length: 2 months Pay: ₹15,000.00 - ₹30,000.00 per month Benefits: Paid time off Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

As part of a global team, you will be the second level contact to support our commercial organizations/customer facing functions with quality & regulatory knowledge for our global Life Science product portfolio. You will assist and advise our customers on quality and regulatory topics such as but not limited to providing consultative services and documentation support. You will interact with various internal functions (e.g. Quality, Regulatory, Business) to come up with resolution to address our customers Quality (Q) & Regulatory (R) related inquiries. Being the interface between customers and our internal functions, you will give advice to our customers as well as our internal stakeholders, explain complex topics including to non-experts and support the development of market leading solutions. Create/Continue to improve our digital solutions and workflows with aim to achieve better customer satisfaction. As a Subject Matter Expert for a specific group of product portfolio and/or Quality/Regulatory topic, you will drive the continuous improvements and implementation of digital workflows to improve our service level support. Who You Are: Masters Degree in Life Sciences, Chemistry, Biology, or equivalent. Minimum 4 years professional working experience in a customer service-oriented environment in Life Science, Biotechnology, or related industry. Good understanding of quality & regulatory guidelines is a plus especially for pharmaceutical raw materials (e.g. Excipient & API). Digital savvy in using digital tools are necessary and important in daily work. Proficiency in using relevant software applications such as SFDC, SAP & Microsoft 365. Act as a voice of our customers by advocating the importance to support when necessary and work with relevant stakeholders to find feasible solutions to resolve challenges faced. Global mindset and willing to attend global calls outside office hours (e.g. night calls). APAC regional exposure experience will be an added advantage.

Provision of differentiated Quality Support for Strategic Partnership Account(s) Responsible for customer quality and regulatory resolution and follow-up of quality incidents Foster customer intimacy and provide customers with interim updates during extended site investigations Demonstrate expertise in project management, typically in the form of coordinating complex customer inquiries or investigations across global sites Deliver Quality Services, adopting a consultative approach to understand customer needs, explain our quality systems capabilities and communicate that commitment Implement standards to ensure customer satisfaction for quality and regulatory matters for the whole Life Science portfolio. Implement policies, procedures and methods to provide quality and regulatory product and service information and continuously improves the same. Ensure sustainable relationship with key customers. Collect data in partnership with CRM colleagues and Business partner for the Commercial and Business Areas to monitor, report and improve quality performance from a customers perspective. Direct / support in the resolution of highly complex or unusual business problems applying advanced analytical thought and judgment. Applies broad industry and commercial awareness to drive quality performance across LS. Contributes/ Leads internal facing relevant (quality services, operations, marketing, sales, etc.) training/ education courses. Who you are: Masters or Bachelors degree (chemist, pharmacist, biologist, engineer) or equivalent experience in a relevant Life-Science-based position. Professional experience, more than 10 years industry experience. Excellent verbal and written communication skills, fluent in English. Understanding of basic Quality Assurance concepts and knowledge of FDA and/or EMA, cGMP regulatory requirements.