41 Jobs in Pardi

Required Production Operator for a Reputed Chemical Company at Gundlav, Valsad. ITI or Diploma Chemical with 2 to 3 Years experience of plant operator. Apply or drop resume at 9879604156.

Job Requirements Role/Job Title: Branch Relationship Manager-Rural Function/Department: Rural Banking Job Purpose The role entails deepening relationships with Rural Banking accounts and ensuring best in-class service to the customers. The role bearer is responsible for understanding the client needs and working with customers to help them make the right decisions with their accounts. The role bearer must maintain updated knowledge on all bank products and services to ensure high quality assistance in resolving customer queries as well as developing new relationships with prospective clients. This is a critical role which leverages business generation opportunities to help achieve larger organizational objectives. Roles & Responsibilities Contribute to penetration of liabilities business in Rural markets through lead generations, account penetration and relationship deepening as per needs of customer. Ensure maintenance of Average Monthly Balance of Relationship of customers mapped to the incumbent. Deepen the relationship with existing customers of the branch. Ensure completion of account opening formalities with strict adherence to KYC norms. (Field verification Mandatory) Engage customers with multiple products at the time of account Opening. (viz: Mobile banking / Net banking registration / Recurring Deposit-Fixed Deposit activation) Ensuring account usage & constantly maintaining health of account. Ensure superior customer service to capture larger wallet share of population. Execute resolution of customer queries and issues. Recommend process changes in order to improve service efficiency and quality across the branch network. Provide support for implementation of livelihood advancement and community development initiatives. Education Qualification Graduation: Any Graduate Experience: 2 years & above relevant branch banking experience.

Responsible for front desk management, handling incoming calls and visitors, maintaining office records, coordinating administrative tasks, and supporting day-to-day office operations and Strong communication

Job Requirements Job Requirements Role/Job Title: Associate Relationship Manager-Micro Enterprise Loan(MEL) Function/Department: Rural Banking Job Purpose The role entails deepening relationships with Rural Banking accounts and ensuring best in-class service to the customers. The role bearer has a responsibility to support Relationship Manager in identifying Business owners / entrepreneurs in the defined catchment and assessing their business loan needs. The role bearer is responsible for driving client acquisition, building household level customer relationships and capitalizing on lifetime value in each relationship to achieve larger organizational goals. Roles & Responsibilities Manage zoning activity to map household needs in villages and areas allocated. Conduct end-user checks as specified post disbursal of loans while achieving monthly and annual group loan booking targets. Assess and evaluate the client needs and generate new sources of revenue by leveraging cross sell opportunities as per their lifestyle, risk profiling and requirements. Contribute to penetration of liabilities business in Rural markets through lead generations and account opening as per needs of customer. Achieve individual and branch sales goals through new business sales, referrals and retention of account relationship. Nudge behavioral changes in customers to drive them towards online banking. Maintain high collections efficiency through discipline and drive. Monitor preparation of accurate documentation of loans and saving account. Coordinate with operations officer to ensure timely and accurate data entry. Ensure compliance as per the bank requirements. Conduct field audits and customer verifications to ensure high quality of accounts. Gather latest Market intelligence and track and benchmark against best practices in competitor banks. Recommend process changes in order to improve service efficiency and quality across the branch network. Provide support for implementation of livelihood advancement and community development initiatives. Education Qualification Graduation: BA / BCom / BSc / BBA / BCA / BE / BTech or any other graduate. Experience: 0 to 1 years of relevant branch banking experience.

Responsibilities: * Create detailed designs using AutoCAD, Solid Works & 3D modeling software. * Ensure compliance with mechanical design standards. * Collaborate on machine development projects from concept to production.

Diploma in Industrial safety , PPE, HIRA, RCAT Monitor /Implement safety standards across all departments. Conduct safety audits, risk assessments, Investigate accidents, and implement corrective actions. Oversee PPE usage, emergency preparedness.

We are looking for a highly skilled and experienced Legal Officer to join our team at Equitas Small Finance Bank. The ideal candidate will have 3-5 years of experience in the BFSI industry, preferably with SBL. Roles and Responsibility Manage and oversee legal matters related to mortgages and other financial products. Provide legal support and guidance to internal stakeholders on various banking operations. Conduct legal research and analysis to ensure compliance with regulatory requirements. Develop and implement effective legal strategies to mitigate risks and protect the bank's interests. Collaborate with cross-functional teams to resolve legal issues and improve overall business performance. Stay updated with changes in laws and regulations affecting the banking industry. Job Requirements Strong knowledge of legal principles and practices applicable to the BFSI sector. Excellent analytical and problem-solving skills with attention to detail. Ability to work effectively in a fast-paced environment and meet deadlines. Strong communication and interpersonal skills to build relationships with internal stakeholders. Experience working with mortgage products and services is an added advantage. Familiarity with inclusive banking practices and legal frameworks governing the banking industry. Location - Nashik,Nagpur,Pardi

Job Title: Sales Executive/Sr. Executive / Asst. Manager / Manager Department: Sales & Marketing Experience Required: 0 to 10 Years Location: Mumbai, Vapi, Reports To: Sales Manager / Marketing Head Job Purpose: To generate leads, maintain customer relationships, and achieve sales targets by promoting corrugated box products to existing and new clients in various industries such as FMCG, Pharmaceuticals, Electronics, etc. Key Responsibilities: 1. Lead Generation & Client Acquisition Identify and contact potential customers through cold calls, emails, market visits, and referrals. Maintain and update a database of prospective and existing clients. Conduct regular field visits to understand client requirements and offer suitable packaging solutions. 2. Sales & Business Development Explain product features, advantages, and pricing to customers. Prepare and send quotations, negotiate prices and close orders. Ensure timely follow-up with clients and convert inquiries into sales. 3. Customer Relationship Management Maintain strong and long-term relationships with clients. Resolve customer complaints and coordinate with production/logistics to ensure on-time deliveries. Collect feedback for quality improvement and client satisfaction. 4. Market Research & Competitor Analysis Monitor competitor activity, market trends, and pricing strategies. Suggest improvements in product range or service offerings based on market feedback. 5. Reporting & Documentation Maintain daily/weekly reports of visits, leads, and order status. Assist in preparing monthly sales forecasts and targets. Coordinate with accounts for payment follow-ups. Key Skills Required: Good communication & presentation skills (Hindi, English, Gujrati, local language). Convincing and negotiation skills. Basic understanding of corrugated box materials, sizes, and applications (can be trained). Willingness to travel and meet clients regularly. MS Office & email writing proficiency. Educational Qualification: Graduate in any discipline (preferably BBA/Commerce). MBA in Marketing (optional but preferred). Growth Path: Sales Executive Sr. Sales Executive Area Sales Manager Regional Sales Manager Kindly apply - hr@vidhishapaper.com

Responsible for front desk management, handling incoming calls and visitors, maintaining office records, coordinating administrative tasks, and supporting day-to-day office operations and Strong communication

Responsibilities: Maintain inventory levels Input data into system accurately Manage stock movement & storage Ensure accurate record keeping Receive deliveries & issue products

load_list_page(event)"> Job listing Job details Job Information Date Opened 01/09/2025 Job Type Full time Work Experience 1-3 years Industry Manufacturing City Pardi State/Province Gujarat Country India Zip/Postal Code 396191 About Us MERIL DELIVERING WORLD-CLASS HEALTHCARE SOLUTIONS Founded in 2006, Meril is an India-based, global medical device company that is dedicated to the innovation, design and development of novel, clinically relevant and state-of-the-art devices. Our fundamental aim is to champion the alleviation of human suffering and improve quality of life. To enable this, we are committed to R&D, innovation in manufacturing medical technology, scientific communication, and contemporary distribution avenues. Meril was born with the aim of improving the quality of human life through innovative and advanced healthcare solutions. As a medical device manufacturer, we exist to improve the inventiveness in healthcare so that people’s lives are enriched. We continually seek excellence in providing answers to some of medicine’s toughest questions. Meril manufactures medical solutions in the form of vascular intervention devices, orthopaedic supplements, in-vitro diagnostics, endo-surgery and ENT products. It is our core commitment to ensure the delivery of advance healthcare solutions. Our inclination towards research and development is reflected in our diverse offerings. We ensure that we adhere to the best quality of standards in manufacturing, scientific communication and distribution to deliver path-breaking healthcare products to the world. We collaborate with physicians and global innovators to identify unmet clinical needs and develop revolutionary therapies. We encourage research and academic collaborations and remain available to interact on exciting opportunities. Headquartered in India with a manpower of more than 4000, Meril currently conducts business in more than 100 countries. We have 100% subsidiaries in India, USA, Germany, Brazil, Russia, South Africa, Bangladesh and Turkey. We have set up operations in China and Japan too. Job Description To develop and write clinical evaluation reports (CER) for pre- and post-market devices, while ensuring consistency with regulations, quality standards, commitments and goals. Writing coherent, convincing CERs by organizing and evaluating large amounts of scientific/clinical/medical data. Managing CER writing by planning, identifying, appraising and analyzing clinical data then writing the CER including conclusions based on expert knowledge. Ensuring quality by following internal and external SOPs, Work Instructions and Forms/Templates for successful preparation of robust CERs and other documents Assisting with other clinical, regulatory, quality and engineering projects as assigned Responsible to acquire, interpret, analyze and draw conclusions from clinical data from clinical trials, literature and experiences for a wide variety of medical devices Responsible to communicate scientific content in a clear, concise manner Other duties as assigned Requirements Must be focused, efficient, detail oriented and able to work independently. Able to read, analyze and implement regulations, standards and guidance. Demonstrated ability to manage projects (take minutes, multi-task, prioritize and ensure reliability and quality while executing projects on time and on budget). Strong written and oral communication skills. Bachelor's or Master’s Degree or PhD (preferred) in a scientific discipline. At least 1-3 years CER writing experience with solid knowledge of Med Dev 2.7/1, rev 4. At least 1-3 years clinical, regulatory, quality and/or engineering work experience. Able to productively interact with teams including corporate executives, research sites and research subjects. Advanced computer skills with Word, Excel, PowerPoint, etc. Benefits Fresh Perspectives Enhanced Skills and Expertise Increased Productivity Improved Morale Broadened Network Diversity and Inclusion Knowledge Transfer check(event) ; career-website-detail-template-2 => apply(record.id,meta)" mousedown="lyte-button => check(event)" final-style="background-color:#749DDB;border-color:#749DDB;color:white;" final-class="lyte-button lyteBackgroundColorBtn lyteSuccess" lyte-rendered="">

•Lead troubleshooting, diagnostics, and repairs other associated components. •Oversee and assist in the installation and commissioning of valves. • RCAT of failures and operational issues. •Create & maintain service reports and documents

Operate ERP. Maintain BMR, BPR, logbooks online. Perform in-process checks as per SOP. Plan PM & packaging as per schedule. Ensure instrument calibration. Allocate packing line manpower. Handle line clearance & changeovers. Reconcile BPR post-packing. Create batch/product master in Track & Trace. Coordinate with QA, QC, WH, Engineering. Support other tasks as assigned.

machine overhauls, manage in-house fabrication, and supervise motor/gearbox refurbishing. on-site mechanical service, troubleshooting, and maintenance. detailed reports on work progress, findings, and recommendations. Locals Prefered Annual bonus

For Valve Industries Plans, preparation of order/tender documentation, engineering drawings, production specifications and schedules to ensure customer contract requirements are met. Monitors status of project & documentation

load_list_page(event)"> Job listing Job details Job Information Date Opened 01/09/2025 Job Type Full time Work Experience 4-5 years Industry Manufacturing City Pardi State/Province Gujarat Country India Zip/Postal Code 396191 About Us MERIL DELIVERING WORLD-CLASS HEALTHCARE SOLUTIONS Founded in 2006, Meril is an India-based, global medical device company that is dedicated to the innovation, design and development of novel, clinically relevant and state-of-the-art devices. Our fundamental aim is to champion the alleviation of human suffering and improve quality of life. To enable this, we are committed to R&D, innovation in manufacturing medical technology, scientific communication, and contemporary distribution avenues. Meril was born with the aim of improving the quality of human life through innovative and advanced healthcare solutions. As a medical device manufacturer, we exist to improve the inventiveness in healthcare so that people’s lives are enriched. We continually seek excellence in providing answers to some of medicine’s toughest questions. Meril manufactures medical solutions in the form of vascular intervention devices, orthopaedic supplements, in-vitro diagnostics, endo-surgery and ENT products. It is our core commitment to ensure the delivery of advance healthcare solutions. Our inclination towards research and development is reflected in our diverse offerings. We ensure that we adhere to the best quality of standards in manufacturing, scientific communication and distribution to deliver path-breaking healthcare products to the world. We collaborate with physicians and global innovators to identify unmet clinical needs and develop revolutionary therapies. We encourage research and academic collaborations and remain available to interact on exciting opportunities. Headquartered in India with a manpower of more than 4000, Meril currently conducts business in more than 100 countries. We have 100% subsidiaries in India, USA, Germany, Brazil, Russia, South Africa, Bangladesh and Turkey. We have set up operations in China and Japan too. Job Description To develop and write clinical evaluation reports (CER) for pre- and post-market devices, while ensuring consistency with regulations, quality standards, commitments and goals. Writing coherent, convincing CERs by organizing and evaluating large amounts of scientific/clinical/medical data. Managing CER writing by planning, identifying, appraising and analyzing clinical data then writing the CER including conclusions based on expert knowledge. Ensuring quality by following internal and external SOPs, Work Instructions and Forms/Templates for successful preparation of robust CERs and other documents Assisting with other clinical, regulatory, quality and engineering projects as assigned Responsible to acquire, interpret, analyze and draw conclusions from clinical data from clinical trials, literature and experiences for a wide variety of medical devices Responsible to communicate scientific content in a clear, concise manner Other duties as assigned Requirements Must be focused, efficient, detail oriented and able to work independently. Able to read, analyze and implement regulations, standards and guidance. Demonstrated ability to manage projects (take minutes, multi-task, prioritize and ensure reliability and quality while executing projects on time and on budget). Strong written and oral communication skills. Bachelor's or Master’s Degree or PhD (preferred) in a scientific discipline. At least 3+ years CER writing experience with solid knowledge of Med Dev 2.7/1, rev 4. At least 3+ years clinical, regulatory, quality and/or engineering work experience. Able to productively interact with teams including corporate executives, research sites and research subjects. Advanced computer skills with Word, Excel, PowerPoint, etc. Benefits Fresh Perspectives Enhanced Skills and Expertise Increased Productivity Improved Morale Broadened Network Diversity and Inclusion Knowledge Transfer Benefits Fresh Perspectives Enhanced Skills and Expertise Increased Productivity Improved Morale Broadened Network Diversity and Inclusion Knowledge Transfer check(event) ; career-website-detail-template-2 => apply(record.id,meta)" mousedown="lyte-button => check(event)" final-style="background-color:#749DDB;border-color:#749DDB;color:white;" final-class="lyte-button lyteBackgroundColorBtn lyteSuccess" lyte-rendered="">

To lead and manage the Quality & Compliance function by ensuring robust Quality Assurance systems, regulatory and customer compliance, product quality standards, continuous improvement, and support for New Product Development (NPD). This role ensures that quality processes are proactive, standardized, and aligned with business and customer expectations while driving a culture of excellence and accountability Responsibilities 1. Quality Management Systems (QMS) Ensure the implementation and continual improvement of ISO, IMS, and GMP systems across the organization. Lead internal and external audits (customer, regulatory, certification). Oversee documentation and compliance related to QMS and CAPA systems. 2. Quality Control (QC) Supervise the QC Manager and team to ensure systematic inspection at Incoming, In-process, and FG stages. Analyze quality trends and drive preventive and corrective actions. Develop and maintain quality inspection standards, sampling plans, and test protocols. 3. Compliance Ensure compliance with all applicable national and international regulations related to product safety, customer requirements, and industry certifications. Maintain and update regulatory documentation as per customer or legal requirements. 4. New Product Development (NPD) Represent the Quality function in Stage-Gate NPD processes. Define quality criteria, critical parameters, and inspection protocols for new products. Collaborate with R&D, Production, and Customer Service to ensure first-time-right launches. 5. Process Excellence & Continuous Improvement Provide guidance to the Manager – Process Excellence & LEAN to drive CI projects using Six Sigma, and root cause analysis tools. Promote cross-functional Kaizen participation to improve product quality and process efficiency. Align improvement initiatives with customer feedback and internal KPIs. 6. Leadership & Team Development Build capability and engagement in the Quality team through training, coaching, and development plans. Ensure alignment and collaboration with Production, Maintenance, and Planning teams for shared quality and process improvement goals. Qualifications Bachelor's/ Master's degree in Packaging/ Engineering More than 15 years experience in QA/QC leadership. Experience in managing regulatory compliance as per country/ customer needs and leading compliance audits. Experience in leading IMS/GMP audits, managing product certifications such as BIS, managing NABL accredited lab Leading NPD experience.

load_list_page(event)"> Job listing Job details Job Information Date Opened 01/01/2025 Job Type Full time Work Experience 5+ years Industry IT Services City Pardi State/Province Gujarat Country India Zip/Postal Code 396191 About Us MERIL DELIVERING WORLD-CLASS HEALTHCARE SOLUTIONS Founded in 2006, Meril is an India-based, global medical device company that is dedicated to the innovation, design and development of novel, clinically relevant and state-of-the-art devices. Our fundamental aim is to champion the alleviation of human suffering and improve quality of life. To enable this, we are committed to R&D, innovation in manufacturing medical technology, scientific communication, and contemporary distribution avenues. Meril was born with the aim of improving the quality of human life through innovative and advanced healthcare solutions. As a medical device manufacturer, we exist to improve the inventiveness in healthcare so that people’s lives are enriched. We continually seek excellence in providing answers to some of medicine’s toughest questions. Meril manufactures medical solutions in the form of vascular intervention devices, orthopaedic supplements, in-vitro diagnostics, endo-surgery and ENT products. It is our core commitment to ensure the delivery of advance healthcare solutions. Our inclination towards research and development is reflected in our diverse offerings. We ensure that we adhere to the best quality of standards in manufacturing, scientific communication and distribution to deliver path-breaking healthcare products to the world. We collaborate with physicians and global innovators to identify unmet clinical needs and develop revolutionary therapies. We encourage research and academic collaborations and remain available to interact on exciting opportunities. Headquartered in India with a manpower of more than 4000, Meril currently conducts business in more than 100 countries. We have 100% subsidiaries in India, USA, Germany, Brazil, Russia, South Africa, Bangladesh and Turkey. We have set up operations in China and Japan too. Job Description Job title : Procurement Specialist / Sr. Manager - Information Technology (IT) IT Categories: The person procuring Information Technology (IT) related goods and services is typically responsible for acquiring technology solutions to support an organization's IT infrastructure and operations. Key roles and responsibilities include: Hardware (e.g., servers, laptops, desktops) Software (e.g., licenses, subscriptions) Networking and telecommunications Cybersecurity solutions Cloud services (IaaS, PaaS, SaaS) IT consulting and professional services Desirable Skills: IT knowledge (e.g., hardware, software, networking) Procurement expertise Contract negotiation and management Analytical and problem-solving skills Communication and project management skills Roles & Responsibilities: Staying up-to-date with IT market trends and technologies Collaborating with IT stakeholders to understand requirements Evaluating technical specifications and vendor capabilities Sourcing and evaluating IT vendors and service providers Conducting Request for Proposal (RFP) processes for IT goods and services Negotiating contracts and pricing for IT purchases Ensuring contract compliance and adherence Managing contract renewals and terminations Coordinating with legal and finance teams for Maintaining accurate contract records Coordinating with IT vendors and service providers for timely delivery of IT goods and services Managing vendor performance and quality Resolving disputes or issues with vendors Conducting vendor audits and due diligence Risk Management: Identifying and mitigating IT procurement risks Conducting risk assessments and due diligence Developing and implementing risk mitigation strategies Monitoring and reporting on risk exposure Compliance: Getting IT budget & forecasting for effectively managing procurment expenses Ensuring compliance with organizational procurement policies and procedures Conducting total cost of ownership (TCO) analyses Requirements Education and Certifications: Bachelor's degree in computer science, IT ,business, or related field Certified Procurement Professional (CPP) Certified Information Technology Procurement Specialist (CITPS) Certified Technology Procurement Specialist (CTPS) Desirable Skills: IT knowledge (e.g., hardware, software, networking) Procurement expertise Contract negotiation and management Analytical and problem-solving skills Communication and project management skills Benefits Enhancing and decentralization of Service procurement in terms of quality, TAT & Cost. check(event) ; career-website-detail-template-2 => apply(record.id,meta)" mousedown="lyte-button => check(event)" final-style="background-color:#749DDB;border-color:#749DDB;color:white;" final-class="lyte-button lyteBackgroundColorBtn lyteSuccess" lyte-rendered="">

Job Requirements Role/Job Title: Associate Relationship Manager-Loan against property Function/Department: Rural Banking Job Purpose To deliver a high-quality client service and customer retention. Enhance product sales and new client acquisition. Roles & Responsibilities Identifying New Markets, must work towards attracting new customers and generating leads through local activities like organizing canopy activities/leaflet distribution/cold calling and etc. To service, the leads referred by sales front/cross/selling or other channels. To deliver a high-quality client service and customer retention approach to managing client relationships to enhance product sales and new client growth targets. Achieve agreed individual performance targets for income generation, product sales and new client growth targets. Login to disbursement completion, fulfilment, counselling, and handholding the customer through the entire process of sanction and disbursement. Ensuring that customer doesn’t become a non-starter e.g. helping collections to recover EMI’s in case of default. Building the relationship in the Market by meeting the Local Builders, Business communities and new channels. Education Qualification Graduation: BA / BCom / BBA / BSc / BTech / BE or any other graduate. Experience: 2 to 5 Years in NBFCs/Banking.

Must know about Dispatch activities, Material Management, Manpower Management, Dispatch Scheduling

load_list_page(event)"> Job listing Job details Job Information Date Opened 01/09/2025 Job Type Full time Work Experience 1-3 years Industry Manufacturing City Pardi State/Province Gujarat Country India Zip/Postal Code 396191 About Us MERIL DELIVERING WORLD-CLASS HEALTHCARE SOLUTIONS Founded in 2006, Meril is an India-based, global medical device company that is dedicated to the innovation, design and development of novel, clinically relevant and state-of-the-art devices. Our fundamental aim is to champion the alleviation of human suffering and improve quality of life. To enable this, we are committed to R&D, innovation in manufacturing medical technology, scientific communication, and contemporary distribution avenues. Meril was born with the aim of improving the quality of human life through innovative and advanced healthcare solutions. As a medical device manufacturer, we exist to improve the inventiveness in healthcare so that people’s lives are enriched. We continually seek excellence in providing answers to some of medicine’s toughest questions. Meril manufactures medical solutions in the form of vascular intervention devices, orthopaedic supplements, in-vitro diagnostics, endo-surgery and ENT products. It is our core commitment to ensure the delivery of advance healthcare solutions. Our inclination towards research and development is reflected in our diverse offerings. We ensure that we adhere to the best quality of standards in manufacturing, scientific communication and distribution to deliver path-breaking healthcare products to the world. We collaborate with physicians and global innovators to identify unmet clinical needs and develop revolutionary therapies. We encourage research and academic collaborations and remain available to interact on exciting opportunities. Headquartered in India with a manpower of more than 4000, Meril currently conducts business in more than 100 countries. We have 100% subsidiaries in India, USA, Germany, Brazil, Russia, South Africa, Bangladesh and Turkey. We have set up operations in China and Japan too. Job Description To develop and write clinical evaluation reports (CER) for pre- and post-market devices, while ensuring consistency with regulations, quality standards, commitments and goals. Writing coherent, convincing CERs by organizing and evaluating large amounts of scientific/clinical/medical data. Managing CER writing by planning, identifying, appraising and analyzing clinical data then writing the CER including conclusions based on expert knowledge. Ensuring quality by following internal and external SOPs, Work Instructions and Forms/Templates for successful preparation of robust CERs and other documents Assisting with other clinical, regulatory, quality and engineering projects as assigned Responsible to acquire, interpret, analyze and draw conclusions from clinical data from clinical trials, literature and experiences for a wide variety of medical devices Responsible to communicate scientific content in a clear, concise manner Other duties as assigned Requirements Must be focused, efficient, detail oriented and able to work independently. Able to read, analyze and implement regulations, standards and guidance. Demonstrated ability to manage projects (take minutes, multi-task, prioritize and ensure reliability and quality while executing projects on time and on budget). Strong written and oral communication skills. Bachelor's or Master’s Degree or PhD (preferred) in a scientific discipline. At least 1-3 years CER writing experience with solid knowledge of Med Dev 2.7/1, rev 4. At least 1-3 years clinical, regulatory, quality and/or engineering work experience. Able to productively interact with teams including corporate executives, research sites and research subjects. Advanced computer skills with Word, Excel, PowerPoint, etc. Benefits Fresh Perspectives Enhanced Skills and Expertise Increased Productivity Improved Morale Broadened Network Diversity and Inclusion Knowledge Transfer check(event) ; career-website-detail-template-2 => apply(record.id,meta)" mousedown="lyte-button => check(event)" final-style="background-color:#749DDB;border-color:#749DDB;color:white;" final-class="lyte-button lyteBackgroundColorBtn lyteSuccess" lyte-rendered=""> Show more Show less

Company Description NIMIT KRAFTPACK INDUSTRIES, an ISO 9001-2015 Certified company, is based in Killa Pardi, Balda Industrial park, GIDC. With a focus on producing high-quality corrugated fiberboard boxes and paperboards, NIMIT KRAFTPACK serves its clientele with a fully automated 5-ply plant and state-of-the-art technology. The company prioritizes customer satisfaction, timely deliveries, and environmental sustainability by using 100% recycled paper and being FSC certified. Role Description This is a full-time on-site role for a Converting Supervisor in corrugated fiberboard boxes at our Pardi location in Gujarat. The Converting Supervisor will be responsible for overseeing the day-to-day operations of converting raw materials into finished corrugated boxes. This includes managing production schedules, quality control, and ensuring adherence to safety regulations. Qualifications Experience in corrugated box manufacturing industry Knowledge of converting processes and machinery Strong leadership and supervisory skills Attention to detail and quality control Ability to work in a fast-paced environment Excellent communication and problem-solving skills Experience with JIT inventory system is a plus Technical degree or certification in manufacturing is preferred Show more Show less

Having hands on experience in BIS testing 694 or 1293. 1–3 years of experience in quality control, quality assurance, or laboratory testing in a manufacturing or industrial setting. Hands-on experience with laboratory equipment calibration, testing procedures, and inspection documentation. Proficient in reading and interpreting technical drawings and quality standards (BIS, ISO, ASTM, IEC). Knowledge of Production Part Approval Process (PPAP). Familiarity with CAPA (Corrective and Preventive Action) processes and root cause analysis tools (e.g., Fishbone, 5 Whys). Ability to prepare inspection reports and maintain detailed quality documentation. candidate from Cable Industry will get preference.

Key Responsibilities: Operating and monitoring processing equipment in a cleanroom facility. Ensuring compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Accurate completion and maintenance of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Troubleshooting and resolving minor operational issues. Collaborating with other departments to optimize production processes. Adhering to all safety protocols and company policies. Qualifications & Experience: Male candidates only. Educational Background: Bachelor of Engineering (B.E.) in Mechanical / Bachelor of Science (B.Sc.) / Bachelor of Pharmacy (B.Pharm). Work Experience: 2 to 5 years of experience in the pharmaceutical industry is mandatory. Essential Skills: Proven experience working in a cleanroom facility. Strong understanding and practical experience with GDP, GMP, BMR, and BPR documentation. Ability to work effectively in a team environment. Good communication and interpersonal skills.

Key Responsibilities: Operating and monitoring processing equipment in a cleanroom facility. Ensuring compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Accurate completion and maintenance of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Troubleshooting and resolving minor operational issues. Collaborating with other departments to optimize production processes. Adhering to all safety protocols and company policies. Qualifications & Experience: Male candidates only. Educational Background: Bachelor of Engineering (B.E.) in Mechanical / Bachelor of Science (B.Sc.) / Bachelor of Pharmacy (B.Pharm). Work Experience: 2 to 5 years of experience in the pharmaceutical industry is mandatory. Essential Skills: Proven experience working in a cleanroom facility. Strong understanding and practical experience with GDP, GMP, BMR, and BPR documentation. Ability to work effectively in a team environment. Good communication and interpersonal skills.