11381 Qc Jobs - Page 34

Graphic Designer - Volume Adaptation Full Time Job, Shift: Night 7:30 PM to 4:30 AM IST (US overlap - will be in rotation), Remote Possible TRAILER PARK GROUP Trailer Park Group is a full-service agency specializing in content creation and entertainment marketing. By combining a storytelling expertise with large-scale production resources, Trailer Park is uniquely positioned to make, market, and distribute content for its diverse client portfolio of top entertainment studios and major brands. With content creation at the centre, we support our clients with strategy, creative and the latest in digital services. Trailer Park Group Mumbai is a creative agency with 140+ employees. We have an unparalleled team and believe that talent and passion have no limits. Our Mumbai office has an expansive portfolio spanning multiple digital first OTT campaigns across different Indian languages, and high-profile theatrical, gaming and ed-tech campaigns as well as content production. White Turtle Studios, a Trailer Park Group company, is looking for an experienced and highly passionate AV leader who is eager to take on diverse scaled video projects for our global clients. In this role you will collaborate, learn, and get to work on the creative campaigns of some of the biggest content brands. We're looking for a Graphic Designer with a can-do attitude. The right candidate is also very well-organized and meticulous in nature, paying attention to the smallest of details—which is a necessity to perform this role. Responsible for adapting and resizing creative assets (posters, banners, visuals) into multiple formats and platforms for clients. You'll be part of a fast-paced, deadline-driven team that handles large-scale, high-volume design adaptation work (resizing creative assets for multiple platforms). The Role: Key Responsibilities: Adapt and resize creative assets as per brand guidelines for web, mobile, OTT, social, and print. Ensure consistency, accuracy, and high-quality output across all deliverables. Collaborate with art directors, client servicing, and QC teams to manage feedback and ensure timely delivery. Manage multiple adaptation briefs and prioritize work to meet aggressive deadlines. Maintain organized files, version control, and adapt to rapid changes or last-minute requests. Qualifications: 2-5 years' experience in graphic design or volume adaptation, preferably for OTT, studios, or major brands. Proficient in Adobe Photoshop, Illustrator, and related tools. Strong attention to detail, with an eye for layout, alignment, and brand consistency. Experience handling high volumes of repetitive, template-based work. Ability to work night shift (7:30 PM - 4:30 AM IST) for US market alignment (Will be in rotation) Strong team player, open to feedback, quick learner. Please provide a portfolio of your work with your application. WORKING AT TRAILER PARK GROUP: We believe that great work is only possible with great people. We want to find people who believe in our mission, vision and values and feel inspired to grow while they are here. Our approach to flexibility is called “Work Your Way,” have flexibility to work remotely or in the office. Work where you can do your best work. OUR PEOPLE AND CULTURE We strive to create an inclusive culture that empowers our people to be who they are, contribute their unique perspectives, and make a difference individually and collectively. It enables us to leverage different ideas and bring more creativity and innovation to everything we do. We want Trailer Park Group to be one of the most rewarding places you will ever work. PROFESSIONAL DEVELOPMENT From entry-level employees to senior leaders, we believe there’s always room to learn. We offer a best-in-class training programs and opportunities to build new skills, develop as managers and leaders and connect and grow through mentorship. From on-the-job learning experiences to formal development programs, our staff have a variety of opportunities to continue to grow throughout their career. At Trailer Park Group (Trailer Park, Art Machine, Mirada Studios, Mutiny, MXW, White Turtle Studios, and Dark Burn Creative) we want to improve the state of our world. Each of us has a responsibility to drive equality and inclusion in our communities and workplace. We are committed to hiring and retaining a diverse workforce. We view everyone as an individual, and we understand that inclusion is more than just diversity – it is about belonging. We celebrate the fact that everyone is unique, and that is what makes us so good at what we do. We pride ourselves on being a company that embraces difference and truly represents the global clients we work with.

We are hiring QA/QC Engineer (Civil Projects) for a leading Construction Company Key Responsibilities Ensure quality control and assurance in civil construction projects. Conduct site inspections, monitor progress, and identify defects. Develop and implement quality control plans, procedures, and checklists. Collaborate with project teams, contractors, and clients to ensure quality standards. Conduct tests, inspections, and audits to ensure compliance with specifications. Identify and report non-conformities, recommend corrective actions. Requirements Degree in Civil Engineering Experience in QA/QC in construction projects Knowledge of construction standards, codes, and regulations Strong attention to detail, analytical skills Excellent communication, reporting, and documentation skills Objective Ensure high-quality construction projects, meeting client expectations, industry standards, and regulatory requirements. Site Location: Kallakurichi,Tamil Nadu. Immediate Joiners are preferred. For more details contact us at 9176033506/9791033506. Skills: communication,reporting skills,attention to detail,site inspections,quality control plans,skills,regulatory compliance,civil engineering,assurance in civil construction,procedures development,construction standards knowledge,construction,civil engineering standards,projects,testing and auditing,collaboration skills,testing and inspections,checklists,quality control,inspection,civil construction,construction standards,progress monitoring,codes and regulations,contractors,reporting,site inspection,analytical skills,auditing,codes,quality assurance,project collaboration,documentation,documentation skills,defect identification,communication skills,qa/qc

The Role This position is for VTBA Systems & Solutions Pune Plant for undertaking Production activities in the organization in line with the defined global VTBA Standards. Ensure all production activities are carried on in an appropriate, cost-effective way Improve production management systems, processes, and best practices Guide and monitor the Production Systems and Collection team to perform in line with expectations Follow up with the Production in charge of the Daily Plan. Detail study of fabrication, P&ID, PIPING ISO, SKID PACKAGE ASSEMBLY drawings. Set targets & create benchmarks accordingly, Monitoring & controlling sequential day-to-day shop floor activities & raw material brought-out components directly/indirectly to achieve desired scheduled dates while maintaining quality and safety norms. Daily & timely monitoring with production & inspection regarding completion of stage activities as per the ITP & dispatch of equipment as per dates described in the job completion schedule. Make a daily production plan, follow up on material from the project, sourcing, and store team, and update project status on every weekend. Proper & timely interdepartmental coordination for the timely arrival of required material & drawings, resolution of discrepancies observed in the drawings, execution of the job smoothly, completion & dispatch within the prescribed time frame as per scheduled delivery dates well before contractual delivery dates. Hand over materials/consumables/bought-out items to the contractor through the SAP system. Check the status of the material in SAP and update shortages to the project engineer. Inspect the stages of fabrication and offer to QC engineer for inspection and maintain 6S and documents such as ITP, QAP, and Traveler list to shop floor. Daily GEMBA walk on the shop floor. To Succeed, you will need University Degree/Diploma in Mechanical Engineering or related discipline. Minimum 3-5 years of experience in a similar role. Have the ability to communicate effectively, work, and perform in a team environment. Sound Knowledge of weld and Piping standards followed in the Industry Working Knowledge of NDT, Hydro test, etc. Working knowledge of ASME/API/TEMA/IEC/IS/DIN/ ATEX/CCOE and other international Codes. Should be self-driven and should have a creative approach to improve and maintain quality. Fluency in spoken and written English. Proficient in Microsoft Office suite, orientation in modern IT structures and processes. Proficient in SAP PP. Should be a team player and take organization's ambitions forward together as a team with other disciplines Expert in piping fabrication, needs to understand the piping inch Dia /inch meter. Expert in the handling of the shop floor team. Required Knowledge in Lean manufacturing, Kaizen,6S. In return we offer you At Atlas Copco we believe in challenging the status quo, always looking for a better way. Our leading-edge technology enables us to innovate for a sustainable future. We believe that people make it happen and with us you are empowered to act. Your ideas can make a real difference and contribute to the quality of life for people everywhere City : Pune About Edwards Edwards is a leading developer and manufacturer of sophisticated vacuum products, exhaust management systems and related value-added services. Edwards solutions are integral to manufacturing processes for semiconductors, flat panel displays, LEDs and solar cells. They are also used within an increasingly diverse range of industrial processes including power, glass and other coating applications; steel and other metallurgy; pharmaceutical and chemical; and for scientific instruments in a wide range of R&D applications. Edwards has over 4,000 employees worldwide engaged in the design, manufacture and support of high technology vacuum and exhaust management equipment. Edwards has state-of-the-art manufacturing facilities in Europe, Asia and North America.

The client is looking at hiring a Production Supervisor for their team at Al Khobar / Dammam, Saudi Arabia. Candidates who are open to relocate to Saudi Arabia should apply. The Production Supervisor is responsible for managing and coordinating the activities of the production team to ensure efficient and timely production of panels while maintaining high standards of quality and safety. Responsibilities : Team Supervision: - Supervise and coordinate the activities of production workers. - Monitor technicians’ performance and provide coaching and guidance as necessary. - Schedule work assignments and ensure proper staffing levels. Production Management: -Oversee the production process to ensure production targets are met. -Monitor production schedules and adjust workloads as needed to meet deadlines. -Ensure that production is carried out in accordance with company policies and procedures. -Prepare equipment and device tags. -Prepare wiring ferrules. -Responsible for production machines maintenance with relevant record. Quality Control: - Maintain high standards of product quality. - Coordinate with QC team for regular inspections, quality checks, and punch closing. - Address any quality issues and implement corrective actions as necessary in coordination with QC team. Safety and Compliance: -Ensure compliance with health and safety regulations. -Promote a safe working environment and enforce safety policies. -Conduct regular safety meetings and training sessions. Process Improvement: - Identify opportunities for process improvements and implement changes to increase efficiency. - Work with management to develop and implement production strategies. - Analyze production data and prepare reports on performance. Resource Management: -Manage inventory levels and coordinate with the procurement team to ensure the availability of necessary materials. -Maintain equipment and machinery in good working condition. -Coordinate maintenance and repair activities as needed. Functional Requirement: -More than five (5) years in a production environment. -Proven track record in supervising production teams. -Proven experience in managing production schedules and meeting production targets. -Experienced in coordinating maintenance and repair activities.

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description To perform the preventive and breakdown maintenance of analytical equipment’s or Instruments. To ensure that all the QC lab analytical equipment’s/instruments are updated in SAP. To update the preventive maintenance plan whenever addition of instruments or to match the calibration schedule. To prepare the task lists for all analytical equipment’s and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performing the PM. To generate the breakdown maintenance notification or order based on the breakdown request received. To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP. To close the breakdown notification or order of the instrument /equipment after the Completion of breakdown maintenance. Responsible for the maintaining of required spares for all instruments in warehouse. To get the quotations for the required spares and services for the maintenance of the instruments. To generate the purchase requisitions for the required spares and services. To perform the PM in the given frequency within the given period. To get the controlled copies for master PM list, task lists and SOP. To maintain all the PM and Break down Prints. To raise the change controls as when required. Any other responsibility assigned by Group leader. To raise the Gate passes as when required. To ensure the safety measures while operating in Lab. Qualifications Educational qualification: B.Tech (Electronics and communications) Minimum work experience : 6 to 8 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry Skills & attributes: Technical Skills To perform the preventive and breakdown maintenance of analytical equipment’s or Instruments. To ensure that all the QC lab analytical equipment’s/instruments are updated in SAP. To update the preventive maintenance plan whenever addition of instruments or to match the calibration schedule. To prepare the task lists for all analytical equipment’s and update them in SAP. To perform the preventive maintenance as per the PM schedule. maintenance and management of analytical equipment and instruments across the QC Laboratory, ASAT Laboratory, and AMC Laboratory. His key responsibilities include: Routine maintenance and calibration of analytical instruments Troubleshooting and repair of equipment issues Coordination with vendors for AMC and service support Ensuring compliance with regulatory standards Supporting laboratory teams during audits and inspections Exp: 3-8yrs with B Tech EIE, ECE and EEE is must Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Designation: QC In-charge Industry: Ready Mix Concrete (RMC) Experience: 3-5 Years in Quality Control (RMC preferred) Salary: As per industry standards Location: Vadodara Joining: Immediate joiners preferred Key Responsibilities: Quality Assurance: Ensure strict compliance with quality standards for raw materials, mix design, and final concrete production. Concrete Testing: Conduct slump tests, cube testing, and other quality checks as per IS standards. Batching Plant Supervision: Oversee concrete production and batching operations to maintain consistency. Site Coordination: Work closely with site engineers, production teams, and customers to ensure quality requirements are met. Material Inspection: Check incoming raw materials (cement, aggregates, admixtures) for compliance with specifications. Report & Documentation: Maintain test reports, quality records, and audit compliance. Troubleshooting & Improvement: Identify quality issues, suggest corrective actions, and improve production processes. Required Skills & Qualifications: 3-5 years of experience in Quality Control for RMC or construction materials. Strong knowledge of concrete mix design, testing procedures, and IS standards. Hands-on experience with batching plant operations and material inspections. Ability to analyze test reports and troubleshoot quality deviations. Strong coordination and communication skills. Preferred Qualifications: Diploma/Degree in Civil Engineering or related field. Certifications in concrete technology or quality control will be an advantage. Immediate joiners will be preferred. Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Ability to commute/relocate: Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Required) Location: Vadodara, Gujarat (Preferred) Work Location: In person

Job Title: Lead QA/QC Engineer – Nafta Cracker Project (Panipat) Location: Panipat, Haryana, India (On-site) Employment Type: Full-time / Contract (Project-Based) About the Job: We are looking for a Lead QA/QC Engineer with 5 to 7 years of experience for the Nafta Cracker Project – Panipat . Immediate joiners will be prioritized. Key Responsibilities: Implement and monitor quality assurance and control procedures. Ensure compliance with industry codes, standards, and project specifications. Prepare and maintain QA/QC documentation and reports. Requirements: 5–7 years of QA/QC engineering experience in Oil & Gas / Petrochemical projects. Strong knowledge of quality standards and inspection processes. Available to join immediately. Salary: Negotiable – based on interview performance. How to Apply: Send your CV via WhatsApp to +91 7318546574 with the subject "Lead QA/QC Engineer – Panipat" . Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Work Location: In person

Job Title: Jr.Engineer/Technician- QC Location: M/s.Analogics Tech India Ltd.,Plot No.9/10, Road No.6,IDA Nacharam, Hyderabad - 500 076. Job Rolls & Responsibilities : Inward QC : Inward Material Inspection: ICs, Adaptors, Resistors, Batteries , Diodes , Capacitors, Mosfets, etc. How to Check: Their part numbers and Values and Working Conditions. PCB Inspection : Types of PCBs : SMPS, Mother Boards, Key Pads & Defense PCBs etc.. How to Check: Dry solders, Wrong Orientation, Wrong Values, Missing Components, etc... Final QC : Types of Units: SBMs. CAMR,Rider, 2I Lotus, Blutooth 2T & 3T , Android Units etc. How to check : Unit Working Conditions: Like key pad , Display, GPRS /GSM & GPS, printing test, charging condition, Proper finishing of unit etc. Department: QC Qualification &Skills: Diploma / B.E./B.Tech. in Electrical or Electronics Engineering) OR Certificate-NSQF (Level-5 in Quality Engineer) with 1+ Year 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.13,000/- To Rs.17,000/- Brief Job Description: A Quality Engineer 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/ 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: ₹13,000.00 - ₹17,000.00 per month Ability to commute/relocate: NACHARAM , Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (Required) Experience: total work: 4 years (Required) Work Location: In person

Title: Senior Manager - Production (OSD) Date: Aug 11, 2025 Location: Sikkim I - Plant Company: Sun Pharma Laboratories Ltd Job Title: Senior Manager -I (Production) Business Unit: Sun Global Operations Job Grade G9A Location : Gangtok (Sikkim) At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key responsibilities: Responsible for timely delivery of products as per the Rolling Forecast (RFC). To ensure the delivery of quality products to market. Review and approval of QMS (Quality Management System) documents such as Change controls, Events, Market complaints, Annual Product Quality reviews. To ensure up-keep of building facilities, equipment's through regular preventive maintenance calibration and requalification. To ensure that the required initial and continuous training of personnel are carried out. Participation in manufacturing and packing operations of Scale up, Clinical trial batches with FDD. Co-ordinate with Warehouse, EHS, Engineering, QA and QC in implementation of policies and guidelines. Review of SOP's and Qualification documents To ensure the implementation of Environment, Health and Safety policy requirements in plant operations. To ensure the compliance of internal/ external audit and to ensure timely adequate response of audit finding from the department to the auditor to close the issue. Involvement in New Project with right to production. To develop team member to take up responsibility in absence. Travel Estimate Job Requirements Educational Qualification B.Pharm / M.Pharm Experience Tenure : 15/20 yrs (OSD manufacturing experience) Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Position Title: Operator ETP Position Type: Regular - Full-Time Position Location: Mehsana Grade: Grade 01 Requisition ID: 37753 Job Details: Function/Department : QA Global Job Grade Job Title* : Operator ETP Region** : APMEA Global Grading System Job Code: Global Job Grade : Evaluation Date : March 14, 2012 Global Pay Band : Global Benchmark Job : Yes This is a generic job title to be used for Job Administration. Job titles used by individuals may vary by country but the position should be aligned to the generic job title for Job Administration purposes. ** e.g. Global/APMEA/NA/CE/etc. Instructions for Position Summary : Brief description of the primary purpose of the position, with emphasis on the outcomes or results expected (rather than what is specifically done). This should briefly describe why the job exists. Consider how you would describe the job to someone you’ve just met. Position Summary : To ensure that residents have safe and clean water in accordance with federal, territorial and municipal legislation, policies and standards. To Monitor & maintain Effluent Treatment Plant as per Pollution Control Board. To perform a variety of skilled and semi-skilled technical and maintenance work in the operation, maintenance and repair of the wastewater treatment facilities and systems. Instructions for Responsibilities and Accountabilities : List the major responsibilities and accountabilities of the position in order of importance with most important being first etc. Each item should describe what the person in this position have to accomplish at McCain. (i.e. what the job produces) as well as the key activities that lead to the outcomes: Responsibilities and Accountabilities : MANAGE THE KPA’s (Key Performance Areas) OF SUBORDINATES Performance of subordinates is achieved against their agreed KPA’s. Maintain ETP operation cost like Electrical, consumable and chemicals. Full implementation of training / development plan for all subordinates Coordinate with shop floor staff to achieve desired end quality. Manage the ETP Plant and general requirements for GPCB specifications and standards for effluent water quality. Support the ETP Chemist to ensure that effluent water quality and all parameter comply with the relevant requirements of the GPCB and water reclamation plant. Responsible for planning, organizing and managing the overall activities of ETP and Filter press operation. Responsible for preparing the shift schedules for all ETP sub ordinates. Preparation of an updated ETP manual, consisting of all relevant SOPs, Work Instructions and Formats. Development of operators of ETP and FP area. Operators to be groom to McCain level. PLANT AND MECHANICAL OPERATIONS Monitors the performance of all equipment, gauges and charts in the treatment plant and pump stations. Records statistical data concerning plant operations. Maintains, operates, repairs and replaces equipment as necessary. Operates, maintains, and repairs malfunctions at the wastewater treatment plant. Repairs gauges, pumps, filters and other controls and equipment. Maintains, modifies or repairs instrumentation and control equipment including recorders, flow meter and other water quality monitoring equipment. Cleans wet wells and operates pumps and valves to control and adjust flow and treatment process. Charts lab test results for trend analysis and maintains accurate records of analyses and test results. Evaluates data and writes reports as required. And manage the plant. Evaluates procedures and results for accuracy and determines appropriate methods. Records daily flow of influent, waste and return sludge. Maintains and operates sludge thickening equipment. Obtains certified land for sludge disposal according to soil specifications. Maintain and monitors sludge drying beds. NEATNESS OF WORKPLACE Ensure that the walls, walkways and floors are clean at all times during production. Ensure that the equipment in ETP area is clean at all times. All waste is disposed of in the correct containers and is removed / emptied into the appropriate waste areas MAINTENANCE & GENERAL DUTIES Report any defects in equipment performance to the Supervisor. Carryout simple adjustments to keep equipment running at optimal efficiency. Replace consumable parts as required and any other duties deemed reasonable. To perform any other reasonable work related tasks as instructed by the QC Manager. Assures that plant operates within required standards. Train other juniors in acceptable lab methods and procedures to assure accuracy of test results. Monitors performance of electrical systems, circuits or equipment of the treatment plant. SAFETY Ensure all equipment / motor covers are fitted securely. No loose wires or electrical panels are open to the environment (Only engineers have access to electrical panels). All floors are kept dry to minimize slips. OTHER DUTIES Calibrate instruments in-house. Add new procedures, work instruction, formats in QA procedures. Attends training as necessary. Performs other duties as apparent or assigned. Instructions for Requirements : Record the ideal qualifications for someone to take on this job (note: current incumbents may have different backgrounds). If you were looking to hire someone for this job, what background and qualifications would be required and/or desired ? This should briefly describe what a person needs to be successful in this position. Requirements: Academic: Must have: Minimum ITI or Degree in science or relevant field Nice to have: Professional/Technical Accreditations: Must have: Nice to have: Related Work Experience (Internal to the organization or external): Minimum Minimum 4-5 years in ETP Plant Instructions for Working Relationships and Key Contacts : Record the typical contacts both internal and external that someone in this position would have during a normal working day/week. Please do not record names - identify contacts by broad category (e.g. “clients”) if external to the organization, or by title (“Manager, Finance”) for contacts within the organization. Describe the purpose of the communication in a few words (i.e. “provide information”, “confirm transaction”). Working Relationships and Key Contacts: Contact Purpose Internal: 1 Manger QA / ETP Executive For day to day reporting 2 Plant Manger For west water/ water Quality and ETP Operation 3 Maintenance Manager / Executive /Area Leader For Maintenance and repairing purpose External 1 Govt. Authority To Explain how the EPT / environment related Parameters are implemented and follow and verification / validation Process 2 External Auditor To Explain how the EPT / environment related Parameters are implemented and follow and verification / validation Process 3 Authorities: Budget: Managing People (# of direct reports): Other: Competencies: Critical TECHNICAL (Function-Specific) Competencies: He should have effective report writing skills. He should have excellent analytical abilities to grasp the key points from complicated details. He should have awareness regarding ISO and GMP practices, Must be adept in use of MS Office 2000 or later, particularly Excel and Word, and ideally Access or similar database to basic level, Internet and email. He should have good leadership capabilities to lead projects to successful completion. He should be able to run machines of Effluent Treatment Plant, Multi-Effect-Evaporator & Incinerator, to ensure the smooth running of the ETP plant. Must have knowledge of general boiler operation, plumbing and electrical, and various styles of pumps. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, blue prints, City maps, and procedure manuals. Ability to prepare routine reports and correspondence. Must have the ability to perform control calculations Critical CORE (General Behavioral and Business) Competencies: Must have Analytical and decision making skill Must have communication & Presentation Team Work Ability to work weekends and holidays, be on call and respond to calls during non-work hours. Must be able to produce quality, accurate work. Must be able to detect and correct errors. Must be able to utilize work time properly and productively. Instructions for Additional Information : Record the description of other information relevant to the position, such as travel requirements, details about the team. This should briefly describe what else we need to know about this position in order to recruit the right person. Additional Information: Organization Relationships: Immediate Manager/Supervisor (title) Manager - QA Peer Job (title) Job Title Peer Job (title) Area Leader Title(s) of those reporting directly to the job ETP - Chemist ETP Associate McCain Foods is an equal opportunity employer. As a global family-owned company, we strive to be the employer of choice in the diverse communities around the world in which we live and work. We recognize that inclusion drives our creativity, resilience, and success and makes our business stronger. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, age, veteran status, disability, or any other protected characteristic under applicable law. McCain is an accessible employer. If you require an accommodation throughout the recruitment process (including alternate formats of materials or accessible meeting rooms), please let us know and we will work with you to find appropriate solutions. Your privacy is important to us. By submitting personal data or information to us, you agree this will be handled in accordance with McCain’s Global Privacy Policy and Global Employee Privacy Policy , as applicable. You can understand how your personal information is being handled here . Job Family: Manufacturing Division: India Department: Environment Line 4 Location(s): IN - India : Gujarat : Mehsana Company: McCain Foods(India) P Ltd

Job Description You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise. Officer - Quality Control Company: Ahlcon Parenterals IN Ltd Job Posting Location: Bhiwadi, Rājasthān, India Functional Area: Quality Working Model: Onsite Requisition ID: 6849 Are you a Officer Quality Control professional passionate about HPLC techniques? Join our QC team at Ahlcon Parenterals, a B. Braun company, where your expertise in High-Performance Liquid Chromatography (HPLC), analytical instrumentation, and regulatory compliance will play a key role in ensuring the quality and safety of raw materials used in sterile manufacturing. Your key responsibilities: High-performance liquid chromatography (HPLC) Titration Polarimeter What you will bring to the team: Technical expertise in HPLC, along with a deep understanding of analytical chemistry and regulatory standards. Ability to work independently and as part of a cross-functional team. Ensuring accurate and reliable test results. M.Sc. and B.pharma qualification with 1 - 2 years of experience in instrument use in the pharmaceutical industry. What sets B. Braun apart? Ahlcon Parenterals (India) Limited is a B. Braun group company, located at Bhiwadi, Rajasthan. We are a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic and export markets. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision - to protect and improve the health of people around the world. What can we offer you? Convenient transport and subsidized canteen services. Mediclaim and Life Insurance. Learning programs and workshops to drive your development. Mental Wellness Support with counselling and mindfulness sessions. Paternity & Birthday Leave for life’s special moments. Fun activities and team building events. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on social media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube

Job Description You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise. Executive - Quality Control Company: Ahlcon Parenterals IN Ltd Job Posting Location: Bhiwadi, Rājasthān, India Functional Area: Quality Working Model: Onsite Requisition ID: 6889 Are you a Quality Control professional with expertise in raw material sampling, analysis, and instrument handling? Join our QC team at Ahlcon Parenterals, a B. Braun company, where your skills in analytical techniques, equipment operation, and regulatory compliance will play a key role in ensuring the quality and safety of raw materials used in sterile manufacturing. Your key responsibilities: Sampling of raw materials Instrument experience - Ultraviolet-Visible Spectroscopy (UV-Vis) , Infrared Spectroscopy (IR) , Potentiometric Automatic Titrator , total organic carbon (TOC) analysers What you will bring to the team: Ability to work independently as well as collaboratively in a cross-functional team environment. Commitment to delivering accurate, reliable, and timely test results. Ensuring accurate and reliable test results. M.Sc. or B.pharma qualification with 3 – 4 years of experience in QC within the pharmaceutical industry. What sets B. Braun apart? Ahlcon Parenterals (India) Limited is a B. Braun group company, located at Bhiwadi, Rajasthan. We are a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic and export markets. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision - to protect and improve the health of people around the world. What can we offer you? Convenient transport and subsidized canteen services. Mediclaim and Life Insurance. Learning programs and workshops to drive your development. Mental Wellness Support with counselling and mindfulness sessions. Paternity & Birthday Leave for life’s special moments. Fun activities and team building events. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on social media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description OBJECTIVES : The Senior Manager, External Quality Vaccines will lead and oversee quality assurance activities for late-phase clinical programs and commercial vaccine launches. This role ensures that manufacturing, testing, packaging, and shipment processes comply with Takeda's Quality Management System (QMS), current Good Manufacturing Practices (cGMP), and global regulatory requirements. The position requires a strategic focus on quality assurance systems, product technology transfer, and lifecycle management to maintain product quality and compliance across multiple Contract Manufacturing Organizations (CMOs) and global markets. ACCOUNTABILITIES: Provide strategic leadership and oversight for quality assurance activities, ensuring alignment with Takeda’s global quality standards. Responsible for day-to-day interactions with contract facilities (CMOs, CTLs, and/or CSPs): Conducts/supports investigations on Good Manufacturing Practice (GMP) related issues or observations associated with audits, batch records and complaints. Reviews and approves (where applicable) manufacturing and testing deviations and investigations into out-of-specification results. Supports timely execution and completeness of change management at interface with CMOs (incl. supplier notification of changes) and of internal Takeda change management Reviews and approves batch production records and test records. Reviews and approves validation documentations Reviews and approves shipment or material transfer request Performs batch disposition (Diluent, DS, DP, FDP) as per MAH requirements Ensures collaboration with and provides guidance to external manufacturing, project management, supply chain, Manufacturing Science and Technology and CMOs to ensure Q-Systems compliance and manages compliant and timely closure of deviations, CAPA, change controls and interim batch assessment as applicable. Executes regular Person in Plant QA oversight and leverages insights to ensure compliance and drive performance and continuous improvement. Manages document life cycle (incl. reviews, approval, make-effective and retirement) of GMP related documents, such as master batch records, risk assessments, etc. according to Takeda QMS requirement. In early stages of project, support, review and approve development, technology reports where applicable. Review of submission document ensuring data integrity to source data. Provides guidance for technology transfer and validation of manufacturing processes, ensures compliance to Q-systems and regulatory guidances; reviews and approves applicable documents. Supports regulatory or Takeda global audits (including product specific inspections at CMOs), VBU Self-Assessment activities and risk mitigation activities identified in Risk Register. Maintains culture of teamwork, cooperation and continuous improvement. Other duties as assigned. EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: Minimum of Bachelor’s Degree in Pharmacy, Chemistry, Microbiology, or Life Sciences, or equivalent scientific discipline. Minimum of 6 years of experience in quality or regulatory compliance within the pharmaceuticals, biologics, or other related industry(ies) with Pharmaceuticals/biologics with demonstrated analytical (QC) expertise and leadership experience Experience of cGMPs, ICH and other relevant regulations. A broad based knowledge of domestic, and general knowledge of international regulations associated with manufacturing, testing and packaging. Excellent communication skills both oral and written. Experience with supporting product inspections from global Regulatory Authorities. Effectively represent Quality Assurance, both internally and externally. Experience in routine office software packages and specialized software applications as appropriate. Exhibit and promote Takeda Core Competencies. LICENSES/CERTIFICATIONS: NA PHYSICAL DEMANDS: Manual dexterity required to operate office equipment (i.e. computers, phones, etc.). TRAVEL REQUIREMENTS: Some international travel may be required. Approximately 5 – 20% Locations Telangana, Virtual Worker Type Employee Worker Sub-Type Regular Time Type Full time #LI-Remote

Title Senior Technical Professional - Instrumentation/Controls Job Description ROLE - Instrumentation Engineer Perform Project technical tasks assigned by the Instrumentation Discipline Lead consisting in design, checking, layout definition, installation drawings and material definition, validation, testing and engineering of process measuring sensors, process actuators, installation elements and process safety elements Interface and coordinate with the other Project Team Specialists and Designers Coordinate technical activities performed either by insourcing either by outsourcing Experience required is between 8-12 years The Engineer executes the activities within his area of responsibility, ensuring the compliance with the QA/QC and HSE requirements Tasks Include A - Development Technology know how and Commercial support B - Feasibility C - Bidding phase/Commercial proposal development Prepare Instrumentation elements (tagged items and bulk material), quantities for cost and erection works estimates Support Discipline Lead to define man hours and cost estimates D - Project Execution Review Client technical documentation and requirements Coordinate subcontracted engineering activities and control subcontracted engineering documents Define engineering design basis and guidelines Prepare the technical documentation for Instrumentation elements material and services requisitions and prepare, according to internal procedures, the technical evaluations Provide technical support to Project Team Optimize Instrumentation design ensuring minimal cost and complexity in compliance with the contractual and safety requirements Prepare Instrumentation technical specifications Prepare Instrumentation data sheets Prepare Instrumentation installation specifications and drawings Prepare Instrumentation BOQs and MTOs Participate to P and ID mechanization Validate Vendor control valves and safety valves sizing calculations Validate Vendor measurements elements sizing calculations Coordinate engineering activities Ensure Instrumentation 3D modeling design activities Participate to F.A.T. activities ad Vendor workshop E - Construction and Start up Provide technical and engineering support to construction Team Perform site engineering activities during construction and commissioning phases. R2100702

At Takeda, Quality has always been a priority for us, throughout our long history. Today, what we do in Global Quality touches every part of our diverse organization. It’s reflected in our end-to-end Quality Management System that encompasses R&D, Manufacturing & Distribution, Commercial, Vaccines and our BioLife Plasma collection network. When you’re a part of our team, you’ll do meaningful work that makes an impact on the lives of patients. Learn more about us and explore the opportunities to build a remarkable career. Back to nav Job ID R0160216 Date posted 08/11/2025 Location Remote By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sPrivacy Noticeand Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description OBJECTIVES : The Senior Manager, External Quality Vaccines will lead and oversee quality assurance activities for late-phase clinical programs and commercial vaccine launches. This role ensures that manufacturing, testing, packaging, and shipment processes comply with Takeda's Quality Management System (QMS), current Good Manufacturing Practices (cGMP), and global regulatory requirements. The position requires a strategic focus on quality assurance systems, product technology transfer, and lifecycle management to maintain product quality and compliance across multiple Contract Manufacturing Organizations (CMOs) and global markets. Accountabilities Provide strategic leadership and oversight for quality assurance activities, ensuring alignment with Takeda’s global quality standards. Responsible for day-to-day interactions with contract facilities (CMOs, CTLs, and/or CSPs): Conducts/supports investigations on Good Manufacturing Practice (GMP) related issues or observations associated with audits, batch records and complaints. Reviews and approves (where applicable) manufacturing and testing deviations and investigations into out-of-specification results. Supports timely execution and completeness of change management at interface with CMOs (incl. supplier notification of changes) and of internal Takeda change management Reviews and approves batch production records and test records. Reviews and approves validation documentations Reviews and approves shipment or material transfer request Performs batch disposition (Diluent, DS, DP, FDP) as per MAH requirements Ensures collaboration with and provides guidance to external manufacturing, project management, supply chain, Manufacturing Science and Technology and CMOs to ensure Q-Systems compliance and manages compliant and timely closure of deviations, CAPA, change controls and interim batch assessment as applicable. Executes regular Person in Plant QA oversight and leverages insights to ensure compliance and drive performance and continuous improvement. Manages document life cycle (incl. reviews, approval, make-effective and retirement) of GMP related documents, such as master batch records, risk assessments, etc. according to Takeda QMS requirement. In early stages of project, support, review and approve development, technology reports where applicable. Review of submission document ensuring data integrity to source data. Provides guidance for technology transfer and validation of manufacturing processes, ensures compliance to Q-systems and regulatory guidances; reviews and approves applicable documents. Supports regulatory or Takeda global audits (including product specific inspections at CMOs), VBU Self-Assessment activities and risk mitigation activities identified in Risk Register. Maintains culture of teamwork, cooperation and continuous improvement. Other duties as assigned. Education, Behavioural Competencies And Skills Minimum of Bachelor’s Degree in Pharmacy, Chemistry, Microbiology, or Life Sciences, or equivalent scientific discipline. Minimum of 6 years of experience in quality or regulatory compliance within the pharmaceuticals, biologics, or other related industry(ies) with Pharmaceuticals/biologics with demonstrated analytical (QC) expertise and leadership experience Experience of cGMPs, ICH and other relevant regulations. A broad based knowledge of domestic, and general knowledge of international regulations associated with manufacturing, testing and packaging. Excellent communication skills both oral and written. Experience with supporting product inspections from global Regulatory Authorities. Effectively represent Quality Assurance, both internally and externally. Experience in routine office software packages and specialized software applications as appropriate. Exhibit and promote Takeda Core Competencies. Licenses/Certifications NA Physical Demands Manual dexterity required to operate office equipment (i.e. computers, phones, etc.). Travel Requirements Some international travel may be required. Approximately 5 – 20% Locations Telangana, Virtual Worker Type Employee Worker Sub-Type Regular Time Type Full time Apply Now Back to nav

In this role you will be responsible for project delivery, design management & project management, for positioning and winning projects involving a range of services. The role will be instrumental in collaborating with commercial, project management, engineering and design technical leaders to create opportunities for Jacobs to plan, develop, deliver and operate a range of projects. * Review and understand the scope of works along with BOQ (based on contract provided by client). * Candidate should have sound knowledge of basic engineering principles and be well versed with the Standard Codes. * Supervise to ensure that contractor is executing the construction activities as per the drawings, specifications, relevant codes/standards. * Technical knowledge to supervise execution of construction work for Mechanical Equipment erection, Piping including clean piping, structural fabrication/erection, package units etc. * Study of drawings and obtain clarification through RFI’s for any discrepancies - missing details / mismatches - from Projects and Engineering. * Review and approve the quality plan, Inspection & Test plan and work procedures submitted by contractors. Monitor the compliance of quality requirement as per approved quality plan and ITP during execution. * Issuing of quality noncompliance note to contractors in case of sub-standard works and follow up with contractors for get it corrected. Maintain a tracker for the same. * Performing of tests through contractor, witness and recording and maintaining documentation. * Monitor through contractors that QC check sheets are prepared and maintained for the works being executed * Co-ordinate with other discipline engineers for release of fronts to contractors. * Prepare and issue punch list on completion of each area. Follow up with contractors for attending and closing the punch lists. * Scrutiny and certification of contractor’s RA bills and final bills, whenever required. * Follow up with Projects / Engineering team to release the "Holds" if any in the drawings so that schedule is not affected. * Prepare and maintain joint measurement records for all the approved variations / changes. * Study the drawings issued for construction in detail well in advance and identify if there is any mismatch between drawings and specifications / BOQ description / construction already carried out as well as any missing details and get required details in time from the concerned. * Review and approve the quality plan, Inspection & Test plan, erection scheme, resource requirements and work procedures submitted by contractors and ensure contactor is executing the work and meeting the approved plans and procedures. * Identify the piping MTO requirement based on the piping GA and isometrics issued to site and take up with concerned for any discrepancies. * Inspection of materials received at site. Knowledge to identify the contractor resource requirement to execute the job. * Understanding and experience in implementation of HSE procedures. * Monitoring of work progress and Follow- up with contractors for ensuring the adequacy of required labour resources, machineries and materials to complete the works as per schedule. * Should have effective communication skill to convey discrepancies /problem faced / expected at site to the respective lead and client as required. * Should have specific experience of supervising Finishes of Paint/ Pharma/FMCG / Industrial projects. Graduate in Engineering in Mechanical with 8 to12 years in a leading position including working in PMC /EPCM role. Candidates from Consultancy background would be preferred . Alternatively experience with large EPC contractors. Must be very good in written and verbal communication with leadership skill.

The Quality Control (QC) Inspector ensures that products manufactured meet quality and safety standards as specified by the company and regulatory guidelines. This role involves conducting inspections, identifying defects, documenting findings, and ensuring corrective actions are implemented to maintain high product standards. Key ResponsibilitiesInspection and Testing: Inspect raw materials, in-process products, and finished goods to ensure compliance with specifications. Perform routine and non-routine testing using specialized equipment and techniques. Monitor production processes to ensure adherence to quality standards. Documentation and Reporting: Record inspection results, test data, and deviations from quality standards. Prepare detailed reports on quality issues and provide suggestions for improvement. Maintain accurate records of inspections and tests in compliance with company policies. Collaboration and Communication: Work closely with production teams to address quality concerns. Communicate findings to supervisors, engineers, and management. Assist in training production staff on quality standards and processes. Compliance and Standards: Ensure all products comply with relevant industry standards and regulations. Participate in internal and external audits as required. Stay updated on changes in manufacturing standards and best practices. Problem-Solving and Corrective Actions: Identify root causes of defects or production issues. Recommend and oversee corrective actions to prevent recurrence. Follow up to ensure corrective measures are effective. QualificationsEducation: High school diploma or equivalent; a degree or certification in quality assurance, engineering, or a related field is preferred. Experience: Proven experience as a Quality Control Inspector in a manufacturing environment. Skills: Attention to detail and strong observational skills. Knowledge of quality control standards, tools, and methodologies (e.g., ISO 9001, Six Sigma). Ability to read and interpret blueprints, specifications, and technical documents. Proficiency in using inspection equipment (e.g., calipers, micrometers, gauges). Basic computer skills for data entry and reporting. Physical Requirements: Ability to stand for extended periods and lift/move materials as needed. Key CompetenciesStrong analytical and problem-solving skills. Effective communication and teamwork abilities. Commitment to upholding safety and quality standards. Ability to work in a fast-paced and dynamic environment.

Job Title: Quality Head Department: Quality Control & Assurance Job Location: Faridabad, Haryana Number of Vacancies: 1 Job Type: Full-Time Shift Timings: 9:30 AM – 6:30 PM Working Days: Monday to Saturday Experience Required: Minimum 10 years in quality control in precision manufacturing/testing instruments Education Qualification: B.Tech/Diploma in Mechanical/Electrical/Electronics/Instrumentation Gender Preference: Male/Female Age Range: 32 – 50 years Industry Preference: Packaging machine manufacturing or testing instruments manufacturing Job Brief: We are looking for a Quality Head to oversee all quality control operations from incoming raw materials to final product inspection, ensuring compliance with ISO & other international standards. Preference will be given to candidates from packaging machine manufacturing units or testing instruments manufacturing units. Key Responsibilities: Develop and implement QC plans. Inspect incoming materials, in-process assemblies, and final products. Handle customer complaints & corrective actions. Lead supplier audits & quality improvements. Ensure calibration of measuring instruments. Prepare quality documentation, inspection reports, and MIS. Train teams on quality standards & inspection techniques. Liaise with certification bodies for ISO audits. Maintain FTR at all stages. Skills Required: Knowledge of ISO 9001 & quality standards. Proficiency in precision measuring tools. ZOHO Quality Module knowledge. MS Excel, Google Sheets & data analysis. CAPA, problem-solving, and 7 QC tools expertise. Benefits & Perks: PF, ESIC, Annual Bonus.

We are looking for a seasoned crane design professional to lead the design, costing, and execution of EOT Cranes, Hoists, and Jib Cranes. This role demands full technical ownership — from structural design to drive system integration — ensuring that every project meets performance, safety, and compliance requirements. Key Responsibilities Lead structural and mechanical design of crane girders, end carriages, trolleys, and runway systems in line with IS/FEM/CMAA standards. Engineer complete load paths — from hook to runway — including wheel load distribution, deflection control, and fatigue life. Specify and validate rope systems, drums, sheaves, gearboxes, motors, brakes, VFDs, and associated safety systems. Develop and approve motor torque–speed profiles, drive system sizing, duty cycle ratings, braking energy management, and power distribution architecture. Prepare comprehensive calculation dossiers (mechanical + electrical) for client approval and statutory compliance. Deliver BOMs, cost models, and execution schedules while coordinating with procurement, manufacturing, and QC teams. Oversee fabrication, assembly, commissioning, and load testing, ensuring strict adherence to design intent. Requirements B.E./B.Tech in Mechanical Engineering (M.E./M.Tech preferred). 5+ years in crane system design, with proven delivery of high-capacity EOT, gantry, winches or jib cranes. Expert in SolidWorks (3D modeling, assemblies, load simulation) and AutoCAD. Demonstrated ability to integrate structural, mechanical, and electrical design disciplines into a unified, standards-compliant crane solution. Strong track record in cost-optimised engineering without compromising safety or performance. Preferred FEA validation of structural members. Exposure to PLC-based crane automation. ERP/MRP workflow experience for engineering-to-production linkages. Can be a remote job with occasional travel to Kolkata factory if residing outside Kolkata.

We are seeking a skilled and detail-oriented Production Engineer to oversee and optimize the manufacturing processes of stainless steel heavy tanks. The ideal candidate will have hands-on experience in metal fabrication, welding, and large-scale industrial production, with a strong focus on quality, efficiency, and safety. 🎯 Key ResponsibilitiesProduction Planning & Execution Develop and implement production schedules to meet delivery timelines. Coordinate with design and procurement teams to ensure material availability. Process Optimization Analyze and improve manufacturing workflows to reduce waste and increase throughput. Implement lean manufacturing and Six Sigma principles where applicable. Technical Oversight Supervise fabrication, welding, and assembly of SS tanks. Ensure compliance with ASME, ISO, and other relevant standards. Quality Assurance Monitor product quality and conduct root cause analysis for defects. Collaborate with QA/QC teams to maintain high standards. Team Coordination Lead and train shop-floor technicians and welders. Ensure adherence to safety protocols and company policies. Documentation & Reporting Maintain production logs, process documentation, and performance reports. Support audits and inspections with accurate technical records. 🧠 Required Skills & QualificationsBachelor’s degree in Mechanical Engineering, Production Engineering, or related field. 3–5 years of experience in heavy fabrication or tank manufacturing (preferably SS). Proficiency in CAD software and production planning tools. Strong knowledge of welding techniques (TIG, MIG, etc.) and metallurgy. Familiarity with pressure vessel codes and standards (ASME Section VIII, etc.). Excellent problem-solving, communication, and leadership skills.

The Senior Production Merchandiser is responsible for executing and monitoring all merchandising activities post-order confirmation. The role ensures seamless coordination between buyers, suppliers, and internal teams to achieve on-time production, quality, and shipment. This position is pivotal in bridging the gap between merchandising and manufacturing to deliver consistent results under tight deadlines. ⸻ Key Responsibilities: 1.⁠ ⁠Order Execution & Coordination • Manage the production process from order handover to shipment. • Follow up on pre-production approvals (fabric, trims, PP sample, etc.). • Coordinate with the sampling, fabric sourcing, and production departments for smooth order flow. 2.⁠ ⁠Time & Action (TNA) Management • Create and maintain TNA calendars for each style/order. • Ensure all milestones (fabric in-house, trims, production start, finishing, inspection) are met. • Flag delays and bottlenecks to the concerned department head. 3.⁠ ⁠Production Tracking • Monitor daily production output across stitching, finishing, and packing units. • Coordinate with the planning and production teams to align production as per shipment schedules. • Update daily production status and highlight risk areas. 4.⁠ ⁠Material Follow-Up • Track fabric, trims, and accessories inward as per BOM. • Coordinate with the sourcing team to ensure timely availability of raw materials. • Resolve material issues (shortages, quality deviations) on priority. 5.⁠ ⁠Quality Coordination • Work closely with QA/QC teams to ensure inline and final quality checks are done. • Address buyer comments, PP approvals, and any fit or spec changes. • Support during audits or third-party inspections. 6.⁠ ⁠Buyer Communication (Production Stage) • Provide regular production updates to buyers or buying offices. • Arrange and attend production review meetings and address buyer concerns on timelines and quality. 7.⁠ ⁠Documentation & Reporting • Maintain production files, order trackers, material trackers, and approvals. • Prepare weekly production status reports for internal reviews and buyer sharing. ⸻ Skills & Qualifications: • Degree/Diploma in Apparel Merchandising, Textile Technology, or Fashion Management. • Strong understanding of garment production processes, TNA planning, and BOM management. • Good knowledge of fabric types, trims, construction techniques, and industrial engineering. • Excellent follow-up skills and coordination ability across departments. • Proficient in Excel, Google Sheets, ERP/PLM systems. ⸻ Preferred Traits: • Sharp attention to detail and commitment to deadlines. • Proactive problem solver with an ability to work under pressure. • Strong interpersonal and communication skills (Hindi + English).

As a Production Supervisor for injectable formulations, you will be responsible for supervising daily production activities. Your primary focus will be to ensure compliance with cGMP, safety, and quality standards. In this role, you will coordinate closely with QA, QC, Maintenance, and Warehouse teams to maintain operational efficiency. Additionally, you will lead and train production staff to meet production targets effectively. To be successful in this position, you should have 8 to 10 years of relevant experience in the pharmaceutical industry. The ideal candidate will hold a degree in B.Pharma, BSC, or a Masters degree. This is a full-time, permanent position that offers benefits such as paid sick time and Provident Fund. If you are a detail-oriented individual with strong leadership skills and a background in pharmaceutical production, we encourage you to apply for this exciting opportunity. Join our team and contribute to the production of high-quality injectable formulations in a compliant and efficient manner.,

The role of Assistant Manager, Contract Manufacturing Sourcing involves being responsible for identifying, evaluating, and onboarding new manufacturing partners for Nutraceutical and personal care products. You will manage new projects under New Product Development (NPD), possess good negotiation skills, handle contract management, implement cost-saving initiatives, and ensure timely coordination with cross-functional teams. A strong understanding of formulations, regulatory frameworks, costing methodologies, and supplier relationship management is essential. You will be proactive in presenting business cases and proposals to leaders with a positive approach. Your contributions will include: Costing & Commercial Negotiations of contract manufacturers: - Driving open book costing discussions to evaluate true cost structures. - Benchmarking costs and negotiating competitive pricing while maintaining quality standards. - Supporting cost-saving initiatives through alternate sourcing and scale efficiencies. New Product Development (NPD) Support: - Collaborating with R&D, Marketing, and QA to identify sourcing needs for new product concepts across various dosage forms. - Coordinating supplier scouting and capability evaluation for NPD requirements. - Ensuring timely availability of samples, cost inputs, and trial materials from suppliers. - Leading commercial evaluation and techno-commercial feasibility of shortlisted products. - Tracking NPD timelines and supporting cross-functional teams to ensure launch readiness. New Contract Manufacturer Development: - Identifying and developing new CMOs/third-party manufacturers aligned with business growth. - Conducting technical, quality, and commercial assessments and supporting audit readiness. - Maintaining a database of approved and potential vendors by category and capability. Agreement & Contract Management: - Negotiating commercial supply agreements, development agreements, and NDAs. - Liaising with Legal, QA, and Regulatory teams to ensure end-to-end compliance. Cross-Functional Coordination: - Working closely with internal teams throughout the NPD and sourcing lifecycle. - Facilitating vendor meetings and supporting resolution of technical and operational issues. Data Management & Reporting: - Maintaining sourcing trackers, NPD dashboards, and vendor cost matrices. - Presenting timely reports on sourcing status, vendor performance, and risk areas. The Global Product Sourcing team is newly rebranded and reorganized to leverage global category management and expertise. This team collaborates with over 50+ Direct Sourcing colleagues worldwide, focusing on identifying opportunities for sourcing in different regions, delivering value and innovation back to the brand and customer. Skills required for this role include advanced computer skills, strong knowledge of healthcare formulations and machinery, experience in contract manufacturing and project management, familiarity with QA, QC, Manufacturing, and Supply topics, strong analytical and problem-solving skills, familiarity with industry standards and regulations, effective written and verbal communication, organized thought process in communication, and strong analytical skills. The ideal candidate should have a minimum of 5-8 years of experience in a Cost Negotiation/Contract Manufacturing/supply chain/Project/CM sourcing role in a GMP/FSSAI environment. A Bachelor's degree or university degree in Pharmacy, Food tech, Economics, Finances, Engineering, or related fields is required, while a Master's degree is a plus.,

The Lab Technician plays a crucial technical role in supporting the supervisor in the Trial Modification of Mortar, Grouts, Tile adhesive, etc. Your primary responsibility involves conducting various tests and trials for research and development purposes, ensuring accurate and reliable results. Your duties and responsibilities include: - Assisting in trial mix activities such as weighing, flow/slump testing, cleaning of mixing tools, water permeability test, rheology, RCPT, wash out, etc. - Supporting the application technician in physical parameter testing of competitor samples, raw materials, etc. - Conducting field tests at sites as per the supervisor's instructions. - Testing of sands, cement, chemical materials, and finished goods through various methods like sieving, flow testing, strength testing, etc. - Compiling laboratory test results including sieve analysis, water absorption, moisture content, specific gravity, marsh cone tests, and others. - Maintaining samples, testing apparatus, and tools for corrosion testing as per ASTM G 109 standards. - Assisting the supervisor in data collection for shrinkage and tamper study of admixtures. - Preparing stability samples and supporting the supervisor in sample observation. - Demolding, cleaning, and testing cubes in CTM machines and updating strength records. - Monitoring raw material stock availability for lab trials and ensuring proper use. - Supporting in equipment calibration, unloading raw materials, maintaining PPEs and essential tools, and ensuring a clean and organized work environment. - Providing assistance to the development team in technical activities and carrying out other duties as assigned for the smooth functioning of the R&D premises. Qualifications/Experience: - Graduate with a minimum of 2 years of experience in product development in a Chemical Manufacturing Company. - Knowledge of construction chemicals, application, R&D, and QC is preferred. - Familiarity with cement, concrete admixture, and related raw material functions. - Experience in handling analytical equipment and basic computer knowledge. Competencies: - Passion for innovation. Behavioral: - Self-starter. - Strong work management skills. This role requires a proactive individual with a keen interest in innovation and a structured approach to work management. If you meet the qualifications and are excited about contributing to the development of cutting-edge products in the chemical industry, we encourage you to apply for this position.,