476 Jobs in Baddi - Page 4

Role & responsibilities You will be working as Head QC for USFDA approved Formulation Plant at Baddi and will be responsible for: 1. You will be responsible for Establish the project goals and priorities. 2. You will be responsible for team management and leadership. 3. You will be handle 50 Plus Products and handle business turnover. 4. You will be reporting to Head Quality at Plant level at Baddi. 5. You will be good in handling regulatory audits starts to end. 6. You will be good in team leader to guide and trained and developed team members. 7. You will be good in team management and monitoring team Desired Candidate Profile 1. Candidate should be B.Pharm/M.Sc. Organic Chemistry or Ph.D in Organic chemistry. 2. Candidate should be 20-25 years of experience in Pharma Formulation industry with USFDA Approved Company in Quality Control department . 3. Candidate should be handle a team size of persons in pharma companies. 4. Candidate should be good in Management and improving production and quality and quantity of company. Preferred candidate profile

Company Description K.P. Manish Global Ingredients Pvt. Ltd. is one of India’s largest importers of Food, Pharma, Nutra, and Personal Care Ingredients. Representing many global manufacturers including Wuxi Jinghai, Evonik, Mitsubishi, and Firmenich, we act as authorized and exclusive distributors in India. Our clientele includes leading MNCs and domestic leaders such as AMWAY, Dabur, and Patanjali. Based in Chennai, we have a PAN India presence with branches in Ahmedabad, Delhi, Mumbai, and other key locations. Our state-of-the-art 5500 sq ft application lab is equipped to support a wide range of formulations. Role Description This full-time on-site role, located in New Delhi, is for a Sales Manager - Active Pharmaceutical Ingredient. The Sales Manager will be responsible for identifying and targeting key clients, developing and maintaining relationships with industry leaders, and driving sales growth. Day-to-day tasks involve executing sales strategies, preparing sales reports, attending industry events, and collaborating with internal teams to ensure client satisfaction. Additionally, the Sales Manager will oversee the negotiation of contracts and manage client communications. Qualifications Proven experience in sales and business development Knowledge of the pharmaceutical industry and Active Pharmaceutical Ingredients Strong negotiation and contract management skills Excellent written and verbal communication skills Ability to work independently and collaboratively within a team Bachelor's degree in Business, Marketing, or a related field Proficiency in CRM software and Microsoft Office Suite Experience with market analysis and sales forecasting Show more Show less

DY Manager - Innovation & Design (R&D Textile only) Qualification - B.Tech/M.Tech in textile Experience - 7 to 10 Years in spinning production (cotton/yarn) Responsible for all the Research & Development activities, research on product design, product development and cost effective manufacturing in line with the current and future world trends, management of shade cards, ensuring quality of all the sample etc. Essential Duties & Responsibilities: Appropriately sketching ideas from concepts, and drawing blueprints to create development samples, and selecting suitable raw materials and combining basic manufacturing principles to create a design in line with Customers. Ensuring that all developments are in line with the current and future world trends, so as to meet the technical specifications which are within the price range of the target retailers. Ensuring the research on product design, product development and cost effective manufacturing is carried out within the team. Managing the functions of Product Development process (Innovation & Design) and carrying out research, originating new concepts. Addressing and solving all technical issues with regards to new product development on a day to day basis. Coordinating with Internal & External parties to ensure that fabric and other materials required for the production of samples are available on time. Guiding the team in addressing technical issues. Liaisoning with Dyeing and fabric departments to arrange for the dyeing and fabric of newly developed samples. Liaisoning with the quality assurance lab to arrange for quality testing of newly developed samples. Maintain stock of new developments and melange shade cards. Providing technical advice and solutions to all production and quality issues which occur during bulk production. Monitoring Industry trends & accordingly develop product ranges. Designing & development of new shade cards from time to time and checking of each shade card before sending to market, as per requirement Fancy development-- hangers and swatch card availability. Proper house keeping and maintaining of 5S-- in record keeping . Quality assurance of all samples. System implementation in sample line for consistent quality and shade. Timely delivery of shade cards to market. Visit customers for presentation of new products along with Marketing team. Liaisoning with relevant departments to verify the status of bulk production and following up any technical product failures through appropriate corrective action. Preparing costing for developments and finalizing development specifications, taking into account any revisions or refinements made during the sample making process. Maintain a Library of all new products developed and index the same in easy search records. Designing and implementing stringent systems, detailed design and quality plans. Manuals to ensure high quality standards during all the stages of project. Assigning the Performance Targets to the team members, periodic monitoring of targets and submit the mid- year and annual performance plans to the management. Strategic planning and implementation of plan for ramp up of capacity. Show more Show less

Company Description 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 Job summary We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches, adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines. Roles & Responsibilities Your responsibilities encompass testing assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis. Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy. You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines, actively participate in laboratory investigations and discrepancy closures, fulfilling defined roles in audits. Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification. You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques. Qualifications Educational qualification: An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology Minimum work experience : 2 years Skills & attributes: Technical Skills Basic understanding of the Biologics/Biosimilar industry, including processes, regulations, and trends. Hands-on experience in High-Performance Liquid Chromatography (HPLC) techniques, including Size Exclusion, Reverse Phase, Ion Exchange chromatography, and Peptide mapping analysis, especially within the context of Analytics. Hands-on experience in Biochemical analysis techniques, specifically Electrophoresis, Enzyme-Linked Immunosorbent Assay (ELISA), and Polymerase Chain Reaction (PCR), with a focus on Analytics. Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). Basic knowledge in protein chemistry, including an understanding of protein structure, function, and relevant analytical techniques. Basic knowledge and hands-on exposure to Microbiology techniques, particularly relevant for individuals working in Microbiology Labs. Basic knowledge and hands-on exposure to cell culture techniques, specifically for working in Bioanalytics (BA) Labs. Behavioural Skills Prioritizes effective communication and demonstrates a performance-oriented mind-set. Effective verbal and written communication skills. Performance-oriented approach, consistently striving for high standards. Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Biologics Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon. With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products. With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation. Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs. We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date. 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/#!/ Show more Show less

Job summary We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches, adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines. Roles & Responsibilities • Your responsibilities encompass testing assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis. • Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy. • You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines, actively participate in laboratory investigations and discrepancy closures, fulfilling defined roles in audits. • Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification. • You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques. Qualification Educational qualification: An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology Minimum work experience : 2 years Skills & attributes: Technical Skills • Basic understanding of the Biologics/Biosimilar industry, including processes, regulations, and trends. • Hands-on experience in High-Performance Liquid Chromatography (HPLC) techniques, including Size Exclusion, Reverse Phase, Ion Exchange chromatography, and Peptide mapping analysis, especially within the context of Analytics. • Hands-on experience in Biochemical analysis techniques, specifically Electrophoresis, Enzyme-Linked Immunosorbent Assay (ELISA), and Polymerase Chain Reaction (PCR), with a focus on Analytics. • Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). • Basic knowledge in protein chemistry, including an understanding of protein structure, function, and relevant analytical techniques. • Basic knowledge and hands-on exposure to Microbiology techniques, particularly relevant for individuals working in Microbiology Labs. • Basic knowledge and hands-on exposure to cell culture techniques, specifically for working in Bioanalytics (BA) Labs. Behavioural skills • Prioritizes effective communication and demonstrates a performance-oriented mind-set. • Effective verbal and written communication skills. • Performance-oriented approach, consistently striving for high standards. • Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Biologics Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon. With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products. With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation. Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs. We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date. 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/#!/

Role & responsibilities Oversee the design, installation, and maintenance of HVAC, water, gas, and electrical systems to ensure efficiency and reliability. Supervise the installation of HVAC equipment and systems, ensuring full compliance with design specifications, safety standards, and regulations. Operate and maintain: Air compressors and air blowers, Gas and oxygen supply systems Air Handling Units (AHU) and ventilation systems, Dust collectors and wastewater treatment systems, Sewage Treatment Plant (STP), Uninterruptible Power Supply (UPS) and Diesel Generators. Install and troubleshoot Variable Frequency Drives (VFD), Programmable Logic Controllers (PLC), and control systems. Handle shift operations and troubleshoot utility system issues and resolve them promptly to minimize downtime and prevent operational disruptions. Conduct regular inspections and preventive maintenance on all utility systems, ensuring optimal performance, operational efficiency, and compliance with safety standards. Maintain accurate and up-to-date documentation of all utility systems, inspections, maintenance activities, and any modifications made to the systems. Coordinate with external vendors, contractors, and service providers for specialized maintenance, installations, and repairs. Ensure compliance with industry regulations, safety standards, and best practices in utility management. Implement and manage Corrective and Preventive Actions (CAPA) to address non-conformances and improve utility system reliability and safety. Understand and implement Quality Management System (QMS) documentation and Standard Operating Procedures (SOPs). Generate and analyse daily utility consumption reports for performance monitoring Preferred candidate profile We are looking for a skilled Utility Systems Engineer to manage the design, implementation, maintenance, and optimization of HVAC, water, gas, and electrical systems. The ideal candidate will have hands-on experience in utility systems management, including troubleshooting, inspections, and ensuring compliance with safety standards.

Key Responsibilities: Ensure timely updating of accounting entries in ERP. Validate Bills of Materials (BOM) in ERP and track actual consumption against BOM. Control manpower data and conduct efficiency analysis. Prepare and circulate MIS reports. Draft and implement SOPs for material accounting at the plant. Ensure timely closure of month-end activities in the factory. Ensure rejection accounting is performed as per SOPs. Account for stock differences in ERP on a monthly basis.

Role & responsibilities Key Responsibilities: Lead the Microbiology Laboratory operations for injectable manufacturing in accordance with cGMP and global regulatory guidelines. Oversee and ensure compliance in microbiological testing such as: Sterility Testing Bacterial Endotoxin Testing (LAL) Environmental and Personnel Monitoring Bioburden and Microbial Limit Tests (MLT) Water and utility microbiological assessments (WFI, purified water, compressed air) Design, execute, and review microbiological method validation protocols including: Validation of Sterility Test methods BET (LAL) method suitability and validation Disinfectant efficacy studies Antimicrobial effectiveness testing Microbial recovery studies from various matrices and surfaces Lead cleanroom validations, aseptic process simulations (Media Fills), and HVAC system qualification from microbiological perspective. Serve as subject matter expert (SME) during inspections (EU, PICS, COFEPRIS, WHO-GMP, etc.) and customer audits. Drive root cause analysis (RCA), CAPA implementation, and continual improvement related to microbial excursions or contamination events. Maintain and periodically update SOPs, microbiological risk assessments, and QMS documents. Develop and mentor a team of qualified microbiologists. Coordinate with QA, Production, and Validation teams for cross-functional initiatives and technology transfers. Preferred candidate profile M.Sc. in Microbiology or related field. 1215 years of relevant experience in a sterile pharmaceutical environment with a strong background in injectables . Hands-on expertise in microbiological method validations and regulatory-compliant documentation practices. Proven track record of successful regulatory audits and inspections. Strong grasp of current regulatory guidelines: USP, EP, JP, ICH, WHO TRS , etc. Familiarity with laboratory instrumentation like isolators, automated endotoxin readers, particle counters, and bio-safety cabinets. Desired Competencies: Strong leadership and decision-making skills. Meticulous attention to detail and scientific integrity. Effective communication and team-building abilities. High level of regulatory awareness and industry best practices.

Any BFSI or insurance sales exp candidate can apply. Min 1 yr exp in insurance sales. urgent hiring for banca channel overall pan India location CTC + fixed travelling allowance interested candidate directly share their cv on: 7499211307

Following will be the responsibilities of the position holder : To develop, ensure, implement and maintain a GxP compliant Laboratory systems. To ensure training and effective implementation of current Good Laboratory Practices. To establish and ensure analysis, approval / rejection of starting materials, packaging materials, intermediate, bulk & finished products as per validated Pharmacopoeia / In — house method for Oral Dosages and LVP facility. To ensure that the appropriate validations, including analytical procedures, and calibrations of equipment are done. To Ensure the Maintenance of the Department, Premises and Equipment. To ensure all necessary testing and stability studies are carried out for Oral Dosages and LVP facility as per the approved specifications and applicable guidelines. To ensure that the specifications and the testing methods are in line with the latest guidelines and applicable pharmacopoeias To approve specifications, sampling instructions, test methods & other Quality control procedures for oral and liquid injectable facility. To approve and monitor all contract analysis. To Ensure the required initial and continuing training of Quality Control personnel is carried out and adapted as per requirement. To assist in the investigations related to the laboratory, product failure, incidents and Risk assessments. Review and disposition of the non-conforming materials in co-ordination with Quality Assurance. To ensure the compliance of the Quality Management System and CAPA effectiveness related to the Laboratory. To apply total quality management tools and approaches to analytical and reporting processes. Create and direct environmental monitoring programs in line with the regulatory requirements. To continuously review quality control processes, procedures and capabilities in order to sustain the most cost effective and efficient methods for meeting quality requirements and making recommendation for improvement as appropriate. To monitor and report quality control progress, notify any discrepancies or potential concerns to the site Quality Head. Support the development of quality goals and targets as part of the organization’s strategic plan. Maintain active role on internal continuous improvement initiatives. To Design, develop and implement quality control training programs. To ensure the self-training in the ISO train within the stipulated time frame. Business Administrator for Darius System, to ensure the review and approval of documents in Darius. To be responsible for Laboratory Quality management system and internal Audit as per NABL ISO/IEC 17025. In absence of the position holder, the Manager/ Group manager working in the respective section or shall be responsible for day to day working. Minimum Education M.Sc / B.Pharm / M.Pharm / Ph.D in pharmacy having relevant experience of around 15+ years in quality control functions in a formulation plant. Should have faced and managed regulatory audits such as USFDA / EU GMP independently Show more Show less

Following will be the responsibilities of the position holder : To develop, ensure, implement and maintain a GxP compliant Laboratory systems. To ensure training and effective implementation of current Good Laboratory Practices. To establish and ensure analysis, approval / rejection of starting materials, packaging materials, intermediate, bulk & finished products as per validated Pharmacopoeia / In — house method for Oral Dosages and LVP facility. To ensure that the appropriate validations, including analytical procedures, and calibrations of equipment are done. To Ensure the Maintenance of the Department, Premises and Equipment. To ensure all necessary testing and stability studies are carried out for Oral Dosages and LVP facility as per the approved specifications and applicable guidelines. To ensure that the specifications and the testing methods are in line with the latest guidelines and applicable pharmacopoeias To approve specifications, sampling instructions, test methods & other Quality control procedures for oral and liquid injectable facility. To approve and monitor all contract analysis. To Ensure the required initial and continuing training of Quality Control personnel is carried out and adapted as per requirement. To assist in the investigations related to the laboratory, product failure, incidents and Risk assessments. Review and disposition of the non-conforming materials in co-ordination with Quality Assurance. To ensure the compliance of the Quality Management System and CAPA effectiveness related to the Laboratory. To apply total quality management tools and approaches to analytical and reporting processes. Create and direct environmental monitoring programs in line with the regulatory requirements. To continuously review quality control processes, procedures and capabilities in order to sustain the most cost effective and efficient methods for meeting quality requirements and making recommendation for improvement as appropriate. To monitor and report quality control progress, notify any discrepancies or potential concerns to the site Quality Head. Support the development of quality goals and targets as part of the organization’s strategic plan. Maintain active role on internal continuous improvement initiatives. To Design, develop and implement quality control training programs. To ensure the self-training in the ISO train within the stipulated time frame. Business Administrator for Darius System, to ensure the review and approval of documents in Darius. To be responsible for Laboratory Quality management system and internal Audit as per NABL ISO/IEC 17025. In absence of the position holder, the Manager/ Group manager working in the respective section or shall be responsible for day to day working. Minimum Education M.Sc / B.Pharm / M.Pharm / Ph.D in pharmacy having relevant experience of around 15+ years in quality control functions in a formulation plant. Should have faced and managed regulatory audits such as USFDA / EU GMP independently

Government department Railway Undertaking job requirement as a cab Driver Job Types: Full-time, Permanent Pay: ₹11,500.00 - ₹14,000.00 per month Schedule: Day shift Work Location: In person Expected Start Date: 02/06/2025

Experience/Qualifications: 10+ years in construction safety in FMCG. Technical diploma/degree (Mechanical/Civil/Electrical). Diploma in Industrial Safety, Fire & Safety, Occupational Health & Safety. NEBOSH and First Aid certified. Strong computer/reporting skills (MS Office). Certified in scaffolding, WAH, rigging, and lifting. Responsibilities: Manage health & safety plans, audits, SOPs, JSAs, emergency response, and permit systems. Conduct training, incident investigations, walkthroughs, and vendor evaluations. Oversee safety reporting and inspections. Work across multiple disciplines (Civil, Mechanical, Electrical).

Company Description Kaiser Appliances is a well-renowned manufacturer specializing in a comprehensive range of gas stoves and induction cookers. As a sole proprietorship firm, we are dedicated to providing high-quality appliances known for their reliability and performance. Our long-standing reputation in the industry is built on innovative design and meticulous craftsmanship, making us a trusted name in home appliances. Role Description This is a full-time on-site role for a Data Analyst, located in Baddi. The Data Analyst will be responsible for collecting, processing, and performing statistical analyses on large datasets. The role includes developing data models, identifying trends, and using data analytics to support decision-making processes. The Data Analyst will also communicate findings and insights through clear and concise reports and presentations. Qualifications Strong Analytical Skills and expertise in Data Analytics Proficiency in Statistics and Data Modeling Excellent Communication skills for reporting insights and findings Bachelor's degree in Data Science, Statistics, Computer Science, or a related field Experience with data visualization tools and statistical software Ability to work independently and collaboratively in a team Experience in the manufacturing industry is a plus Show more Show less

Job description Position Type: Permanent Qualification: MBA Marketing (Preferred) / Any Graduate Work Location: As per the location aligned for the job role Experience: 4-8 years Preferred Candidates: From NBFC, Sales SME and Business Banking, Trade Finance Role: Individual Contributor Company: L&T SuFin is a B2B Ecommerce Platform which will leverage L&Ts deep knowledge and capabilities in Procurement (through its huge volume of annual procurement) and Logistics, Financing, and IT solutions.This platform is essentially a digital marketplace for SME buyers and sellers (mainly focused on construction and industrial products & services) to connect in an efficient manner, thereby enabling sellers to expand their sales reach, and for buyers to find required products and services at optimal cost and quality. Key Responsibilities: Bringing Buyers to the platform and inducing transactions on the platform. Attaining the numbers and revenue targets Identifying the opportunities and offering platform centric solutions Candidate must be from Finance Acumen and have handled SMEs and MSMEs. Recommending banks/ NBFCs depending on customer profile and coordinating for loans/ finance Deepening the relationship through cross sell and up sell Key Competencies: Should have demonstrated abilities to nurture relationships and generate revenue. Communicate persuasively in English & Hindi and Local language. Stable Career record

Technician Maintenance (Electrical)/Mechanical Breakdown Maintenance Breakdown Maintenance Preventive Maintenance PMS, PM Reports Utility

Were continuously seeking talented individuals who bring fresh perspectives, a problem-solving mindset, and sharp technical expertise We know you have choices, so our team of collaborative, innovative professionals are at the ready to support your professional development At Citrin Cooperman, we offer competitive compensation and benefits and most importantly, the flexibility to manage your personal and professional life to focus on what matters most to you!We are looking for a highly experienced and effective NetSuite Manager to join our NetSuite team This person will utilize best practices and methodologies to architect solutions, lead implementations and enforce project governance for our clients They will work extensively with internal leadership, consulting resources, clients, and vendors throughout the project, providing ongoing management, solution architecture, configuration, deployment and support assistance Furthermore, they will engage in business development activities such as project estimation, pre-sales tasks, and deal closure This is a hands-on role working with clients and leading project resources to complete projects successfully and with a high degree of satisfaction Responsibilties: Overall project lead and facilitator relative to solution design, delivery and execution Design and architect solutions based on requirements and business models Facilitates the gathering of client requirements and documenting functional specifications Applies standardized and consistent project delivery methods across all projects assigned Drives utilization of project team members by directing work and resource planning to meet project profitability goals Understands and configures various modules within NetSuite Draft and manage data migration plans/tasks moving master records, activity and balances from legacy to current NetSuite solution Complete project tasks as assigned, on time and within budget Perform assessment of existing NetSuite solutions, recognize opportunity for optimization and provide associated recommendations, roadmap and estimated effort Lead client status meetings in conjunction with project managers providing regular project updates Involved in business development and pre-sales activities such as soliciting high level solution requirements, business application demonstrations, proposal development, and drafting project plans with scope, associated assumptions and estimated effort Participates in candidate screening and interviewing process Qualifications7 plus years working with the NetSuite application5 plus years team management and project experience Experience with implementation/deployment of ERP systems, management and hands-on configuration capacities Strong understanding of primary business processes including SFM (Campaigns and Promotions), CRM (Leads, Opportunities, Quotes), Procure to Pay, Design to Build (Manufacturing), Order to Cash, Project Accounting, Return to Credit, Customer Support, Core Financial and CPM Experience with multi-subsidiary, multi-currency and intercompany based transaction flow and accounting Understands and leverages appropriate project management methodologies (ie, waterfall, agile, scrum) Exceptional understanding of strategy and operations related to technical consulting and delivery of projects Ability to independently manage individual time and tasks Ability to quickly adapt to new requirements and changing situations Ability to effectively generate new business Education: Bachelors degree in Accounting/Finance, Business Systems or related field NetSuite certification preferred

We're Hiring: Assistant Manager / Manager – Marketing (PU Synthetic Leather) 📍 Location: Baddi, District Solan, Himachal Pradesh 🏢 Company: Winner Nippon Leatherette Pvt. Ltd. Winner Nippon Leatherette Pvt. Ltd., a leading manufacturer of PU and PVC synthetic leather, is looking for an experienced and dynamic Assistant Manager / Manager – Marketing to join our growing team. 🔍 What We're Looking For: ✔️ Strong knowledge and understanding of PU synthetic leather products ✔️ Established market connections in the PU synthetic leather industry ✔️ Ability to identify new business opportunities and grow our customer base ✔️ Excellent communication and relationship-building skills ✔️ Proven track record in marketing or sales roles within the synthetic leather industry 📌 Responsibilities: Develop and implement marketing strategies for PU synthetic leather Build and maintain relationships with clients and distributors Conduct market research to identify trends and customer needs Drive sales growth and meet monthly/quarterly targets Collaborate with production and design teams to align customer requirements 🧠 Experience Required: Minimum 5+ years of experience in marketing/sales of PU synthetic leather or similar industry 📞 How to Apply: Interested candidates can reach out directly at: 📧 hr_admin@winnernippon.com 📱 +91 8544770893 Join a leading name in synthetic leather manufacturing and take your career to the next level! Show more Show less

Job title Manager QC Reports to : Plant Head CTC : Salary no bar for deserving candidates Job Description: We are seeking a dedicated and skilled QC Manager for our pharmaceutical manufacturing facility. The ideal candidate will have extensive experience in chemical and instrumental testing, along with in-depth knowledge of pharmaceutical quality control standards. The role will require leadership in overseeing the quality control processes for all types of pharmaceutical products, ensuring compliance with regulatory standards, and maintaining high-quality practices within the lab environment. The QC Manager will be responsible for the testing, calibration, documentation, and preparation of various QC materials, including analytical method validation (AMV), specifications, standard operating procedures (SOPs), and Standard Testing Protocols (STP). The role also requires proficiency in microbiological testing and leadership in managing a team of professionals. Duties and responsibilities: The role would encompass a variety of responsibilities, including and not necessarily limited to the following points: · Chemical and Instrumental Testing : Perform testing using various methods including but not limited to HPLC, FTIR, UV Spectrophotometry, Karl Fischer Titrator, Dissolution, and other chemical and instrumental techniques. · Calibration & Equipment Maintenance : Ensure calibration and proper maintenance of all testing equipment and instruments as per regulatory standards. · Pharmacopeia Adherence : Implement and interpret pharmacopoeia standards for testing and establishing procedures, ensuring compliance with USP, BP, IP, and other relevant pharmacopeia. · Quality Control Documentation : Prepare and review all QC documentation as per the Drugs and Cosmetics Act , New Schedule M , WHO guidelines , and other relevant standards. This includes the preparation of AMV, specifications, SOPs, and STPs. · Regulatory Compliance : Ensure compliance with national and international regulatory requirements such as FDCA , WHO , and MNC guidelines . · Team Management : Lead and train a team of QC analysts and technicians, providing guidance on best practices, troubleshooting, and complex testing. · Microbiological Testing : Oversee and manage microbiological testing, including environmental monitoring, sterility testing, endotoxin testing, and pyrogen testing. · Analytical Method Development : Develop new analytical methods for products not listed in current pharmacopeia. · Inspection and Audit Support : Assist in inspections by regulatory authorities (e.g., FDA , WHO , MNC , TP ) and ensure that the facility meets the required quality standards. · Reporting and Communication : Provide detailed reports on testing results, compliance audits, and other QC activities. Clearly communicate QC issues and resolutions to management and external auditors. Key Requirements: In order to perform your role well, the following qualities will be required: · Educational Qualification : B.Sc., M.Sc., B. Pharm, M. Pharm, or PhD in Pharmaceutical Sciences or Chemistry. · Certifications : FDCA approval for Chemical & Instruments. · Experience : Minimum 15 years of experience in a pharmaceutical quality control department, with at least 5 years in a managerial capacity. Hands-on experience with all types of pharmaceutical formulations, including Tablets, Capsules, Syrups, Ointments, and Liquids. · Testing Expertise : Proficiency in chemical (all types of titration) and instrumental methods (including but not limited to HPLC, UV, FTIR, Karl Fischer Titrator, Dissolution, GC, AAS, etc.). · Documentation Skills : Experience in preparing and reviewing AMV, specifications, STPs, SOPs, and other regulatory documentation. · Microbiological Testing : Basic knowledge of microbiological testing including environmental monitoring, sterility, pyrogen, and toxicity testing. · Regulatory Compliance : In-depth knowledge of Drugs and Cosmetics Act , New Schedule M , WHO guidelines , and other regulatory standards. · Leadership and Training : Ability to handle a team and train others in both technical and analytical skills. · Personal Attributes : Must have a disciplined, compliant, and positive attitude. Strong character, adaptable to changing requirements, and committed to the company’s growth. Good to have skills (not mandatory): · Strong experience in handling FDA , WHO , and MNC inspections. · Ability to work extended hours as required and a flexible attitude toward work demands. · Proficient in ERP systems and familiar with computer-based testing documentation. · Ability to communicate effectively in English (both written and spoken) for internal and external communications, including audits. · Ready to live on the factory campus and demonstrate flexibility as needed. Ideal Candidate Profile: Age: Between 40-50 years . · Demonstrated leadership ability in a QC team and a proactive, solution-oriented approach to problem-solving. · Ready to take on new challenges in a dynamic, fast-paced environment, prioritizing work and the company’s growth. Candidates who wish to apply for the above position may register for interview using the below link/QR code: https://bit.ly/QCManagerMedipol Show more Show less

Looking to hire Executives, AM, Managers Sales & Marketing of Epoxy Pultruded Products Managing Existing relationships Developing new clients, Channel Partners Good understanding of Products around Pultrusion, Resins, Polymers, etc Required Candidate profile 4+ years of sales & marketing experience Good experience of selling Epoxy Pultrusion products Good understanding of various applications of Epoxy Pultruded products Good communication & Attitude Perks and benefits Great opportunity to work with growing Orgn

Have sales experience for Water Treatment chemicals, Eg. Cooling water Treatment chemical , Boiler water Treatment Chemical and, water treatment Plant & Project sales and chemical sales Eg, RO, DM, UF and STP , ETP Required Candidate profile Able to Generate Leads and Enquiries for Water Treatment chemical and Plants & Projects. Market Research for business development and Marketing the products & Generate lead to achieve the target

Production Head Required for Finishing In Textile Ind in Baddi Location Diploma/ BE in Textile Chemistry/ Technology 15+ Year Exp Interested Candidates Mail Your CV on sdpbharuch@gmail.com Subject with HOD Baddi Free Recruitment Required Candidate profile Must have Textile Industries Exp Join Our Group: https://chat.whatsapp.com/EQ6mtr9AaR8693uaaoCNi3 Share Job with Your Friends Visit Our Bharuch Office Best Job Placement Consultancy in Gujarat

1. Preferable Male Lab Technician/Phlebotomist requirement at Doctor G Path Labs, Baddi. 2. Sample collection and sample transportation. 3. Baddi and Nalagarh Labs of Doctor G Path Labs Job Type: Full-time Benefits: Flexible schedule Schedule: Day shift Supplemental Pay: Overtime pay Performance bonus Work Location: In person Expected Start Date: 07/06/2025

Ø Responsible to ensure the cGMP compliance in the department. Ø Responsible for the execution of production plan. Ø Responsible to keep the documents online. Ø Responsible to keep the cleanliness in the department. Ø Responsible for the preventive maintenance of equipments. Ø Responsible to keep the gowning system in the department. Ø Responsible to coordinate with supporting departments for the smooth functioning of department. Ø Responsible to maintain the discipline in the department. Ø Responsible for the compliance of established procedures in the department. Ø To participate in process validation batches. Ø Review of documentation as per requirement. Ø Friability test apparatus Ø Disintegration test apparatus Ø Hardness tester Ø L.O.D. test apparatus Ø Bulk Density Apparatus Ø RMG(rapid mixture granulator) Ø FBD(fluid bed dryer) Ø OGB(octagonal blender) Ø Paste kettle HR-Contact Detail-9218548147 ( 09-05:30) Timing Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Food provided Leave encashment Life insurance Paid sick time Schedule: Day shift

v Preparation and review of Validation master plan v Handling of qualification and Validation related activities. v Qualification of new equipments at site and preparation of DQ, IQ, OQ and PQ. v Responsible for communicating with approved outside laboratories to perform all validations as per validation master plan. v Responsible for review of outside laboratories reports. v Responsible for review routine validation of all validations like HVAC Validation, cartridge filter validation, CIP/ SIP validation, autoclave validation etc. v Handling of final release of batch of finished product through ERP. v Implementation of Good documentation Practices v Preparation and Compilation of Protocol and Report. v Active participation in Internal Audits and Vendor Audit. v Preparation and Review of Sops. Of concerned Department. v Review of environmental monitoring records of all areas. v Handling of QMS activities. v Handling of artwork. v Preparation of new BOM in ERP. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Food provided Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Work Location: In person