476 Jobs in Baddi

Computer System Validation, QMS and IT

Position Overview: We are seeking a dynamic and detail-oriented PPIC Master Planner to join our team. The ideal candidate will be responsible for developing and managing the production and inventory plans to ensure optimal production flow, timely delivery, and cost efficiency. This role requires a strategic thinker with strong analytical skills and the ability to collaborate effectively across various departments. Key Responsibilities: Production Planning: Develop and maintain detailed production schedules based on demand forecasts, inventory levels, and production capacity. Inventory Management: Monitor and control inventory levels to meet production requirements while minimizing excess stock and associated costs. Cross-Functional Collaboration: Work closely with procurement, production, and logistics teams to ensure seamless execution of production plans. Data Analysis and Reporting: Utilize ERP systems and Excel to analyze production data, identify trends, and prepare regular reports for management. Continuous Improvement: Identify opportunities for process improvements to enhance efficiency, reduce lead times, and improve product quality.reddit.com Compliance and Documentation: Ensure all planning activities comply with company policies and industry standards. Maintain accurate records and documentation. Qualifications: Education: Bachelors degree in Engineering, Supply Chain Management, or a related field. Experience: Minimum of 3 years of experience in production planning, inventory control, or a related role, preferably in a manufacturing environment. Technical Skills: Proficiency in ERP systems (e.g., SAP, Oracle), advanced Excel skills, and familiarity with data analysis tools. Analytical Skills: Strong problem-solving abilities with a keen attention to detail. Communication Skills: Excellent verbal and written communication skills in English. Gender Preference: Female candidates are preferred to promote diversity and inclusion within our team

Role & responsibilities 1. Structure Fabrication drawings. 2. Anchor bolt and Templet drawings. 3. PEB Structure drawings. 4. Built up structure members drawings. 5. BOM for structure. 6. Connection drawings. 7. pre Estimation of structure. Preferred candidate profile 1. Must have hands on Experience on AUTOCAD. 2. Additional - Advance Steel.

Location: Baddi, Himachal Pradesh, India Job Type: Part-Time / Contract Industry: Logistics / Courier Services Salary: ₹10,000 – ₹15,000 per month (depending on experience and location) Job Summary: We are looking for a reliable and hardworking Delivery Boy to join our team in Baddi , Himachal Pradesh. The primary responsibility is to deliver/pickup packages or goods to customers on time and in good condition, ensuring excellent customer service and route efficiency. Key Responsibilities: Pick up and deliver goods to customers safely and on time Follow the assigned delivery routes and schedules Verify delivery details and get confirmation/signature from customers Maintain delivery logs and submit daily reports Ensure proper handling of packages during transit Follow traffic laws and safety regulations Communicate with dispatch team or supervisor in case of delays or issues Requirements: Minimum 10th Pass (preferred) Valid driving license (Two-wheeler/LMV as per job need) Own vehicle (optional but preferred, depending on employer) Familiarity with local roads and geography of Baddi and Nalagarh Basic smartphone knowledge (for delivery apps, maps, etc.) Good communication and customer service skills Physically fit and willing to work in different weather conditions *Contact Vikash Sharma - +91-9816154472* Job Type: Part-time Pay: ₹10,000.00 - ₹15,000.00 per month Expected hours: 40 per week Schedule: Evening shift Work Location: In person

Urgent Hiring for Electrical Engineer ( Delta/Plc) Location : Baddi Experience : 5to 7y Salary : 35k to 40k Gender Male Qualification : B.tech / Diploma Electrical Must : Delta, Plc Interested candidate can share cv on this number 9780685477 Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Division Department Sub Department 1 Job Purpose Perform sampling, execute and document the analysis of raw materials, packing materials, products assigned for testing and complete all the stability studies in order to ensure its compliance to the laid down quality parameters and predefined specifications / standards and meet SRB targets Key Accountabilities (1/6) Analyse the assigned samples and chromatographic tests for analysis by using the suitable valid procedure and calibrated instruments to ensure the compliance to the set specification / standards Perform analysis for release of RM, PM, FP & water analysis and process/cleaning validation as per commitment dates Perform analysis for stability samples without any errors as per schedule Check the results of the tests performed, evaluate them against the specifications Review the TDS printed through LIMS for its completion before release Key Accountabilities (2/6) Perform all activities as per current standard procedures by referring to all approved procedures/specifications to ensure compliance to GLP and safety norms Gather all the samples for analysis by checking the consignment for sampling Gather the essentials like standards, glassware, solvents to perform the analysis as per specification Operate the instruments and perform routine/stability as per SOP and safety norms Key Accountabilities (3/6) Document all activities performed as per valid procedure online by using standard/approved formats or templates to ensure that all entries done are correct, accurate and authentic Maintain system integrity by updating documentations and deviations on CipDox while performing operations Maintain all the online documentation and timely entries and supporting documents Prepare new documents and update existing documents as per GMP requirement Key Accountabilities (4/6) Maintain and upkeep the laboratory working area by disposing off all analysed solutions and samples after review as per valid disposal procedures to ensure compliance to GLP Maintain equipment, facility and block premises as per SOP Perform validation, qualification and calibration as per schedule and update output of all activities in the systems Key Accountabilities (5/6) Provide suggestions and ideas by exploring new possibilities to achieve cost saving and work simplification Conduct operational studies to find improvement areas and implement new development projects Strive for continuous automation of processes through implementation of new processes Key Accountabilities (6/6) Major Challenges Delay in performing analysis or re-planning due to frequent changes in production plans. Overcome by conducting performance dialogues and handshakes meetings identifying priorities Delay in performing laboratory activity due to instrument breakdown. Overcome by ensuring timely availability of parts and engineers Delay in releasing the batches due to non-availability of standards, glassware, chemicals. Overcome by coordinating with CFTs and escalations Key Interactions (1/2) Unit Planning for daily release of RM,PM and FP (Daily) Site QC (Non-Routine) for essentials of analysis (Daily) CDC for specification changes implementation (Need Basis) Unit QA for non-conformances (Need Basis) Stores for inventory (Daily) Key Interactions (2/2) Service Engineer to resolve instrument related issues, breakdown (Need Basis) Dimensions (1/2) Number of FP batches released: 3-4 Number of RM analysis conducted : 3-4 Number of studies conducted for Stability samples : 10 Non-conformance OOS/OOT to be closed within 7 working days Non-conformance rate should be below 1.5% Dimensions (2/2) Key Decisions (1/2) Suggestions for improvement of QC productivity to Team Leader (Routine/Stability) Procurement of required instruments and glassware standards to Team Leader (Routine/Stability) Key Decisions (2/2) Education Qualification B. Sc. (Chemistry) or B. Pharm. Relevant Work Experience 0-3 years of experience in quality control function of a pharmaceutical organisation 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 a Technology Transfer team member to support the development and implementation of robust manufacturing processes, including authoring validation protocols and reports, conducting risk assessments, and utilizing advanced tools for process monitoring and analysis. Your role will involve active participation in technology transfers, continuous improvement initiatives, and ensuring compliance across manufacturing operations. Roles & Responsibilities Responsible for Validation which shall include: Preparation/Review/Approve of MPR. Preparation/Review/Approve of process validation protocols. Preparation/Review/Approve & compilation of validation report. Responsible for Tech transfer which shall include: Coordination with Vendor/cross functional teams for Tech transfer activities. Execution of Tech transfer products at Receiving Units. Responsible for QIP which shall include: Identifying root cause for QIP. Execution of QIP. Conclusion/Recommendation of QIP. Responsible for OOS/OOT investigation which shall include: Identifying probable and most probable root cause for OOS/OOT. Ensure that validations is carried out as per the protocol & qualification protocols meets the cGMP & regulatory requirements. Follow up & coordinate with cross functional team for execution of validation. Give the input for the monthly reporting system, participate in the internal & external audits, present the documents to auditor’s/inspection team. Qualifications Educational qualification: Masters/Bachelors/Ph.D in pharma Minimum work experience: 6 -8 years of experience in Process development / MSAT / Tech transfer Skills & attributes: Technical Skills Experience in the scale up/ technology transfer of products in relevant dosage forms or technologies. (OSD) Experience in process Engineering, Quality by Design (QbD) principles and risk assessment approaches. Knowledge of International Council for Harmonization (ICH) guidelines related to Product development or Process Development. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Show more Show less

Company Description KP Manish Global Ingredients Pvt. Ltd. is one of India’s largest importers of food, pharmaceutical, nutraceutical, and personal care ingredients. Representing top global manufacturers as authorized or exclusive distributors in India, we serve leading MNCs and domestic companies like AMWAY, Dabur, and Patanjali. With our head office in Chennai and branch offices across major cities, we have a strong sales force and a state-of-the-art 5500 sq ft application lab. Our lab offers a wide range of ready-made formulations equivalent to world-leading brands. Role Description This is a full-time, on-site role located in Baddi for a Sales & Marketing Manager - Ingredients (API, Food, Nutra) role. The responsibilities include managing sales and marketing activities, designing and implementing marketing strategies, building and maintaining relationships with clients, and overseeing the sales team’s performance. The role also involves market research, identifying new business opportunities, and ensuring customer satisfaction through high-quality service. Qualifications Proven experience in Sales, Marketing, and Business Development Experience in the Food, Pharmaceutical, Nutraceutical, or Personal Care ingredients industry Excellent communication and interpersonal skills Strong analytical and problem-solving abilities Ability to lead and motivate a team Proficiency in market research and analysis Bachelor’s degree in Business, Marketing, or a related field; MBA preferred Show more Show less

He should have knowledge of Institutional Sales . He should be fluent in English.Knowledge of SAP is must.He should have experience of Key Account Management, Sales, Institutional Sales etc. Required Candidate profile He should be B Tech Mech with exp of 8 to 10 years in Sales. He should be fluent in English. He should be ready to relocate to Chandigarh.

VETERINARY DOCTOR EXPERIENCE IN PRE CLINICAL STUDIES ANIMAL HUSBANDRY ANIMAL TESTING EXPERIENCE ANIMAL LAB TESTING STUDIES AND ANIMAL HANDLING

Job Title: Manager / Sr. Manager Projects Sales B2B/B2G Sales _Jammu Br, Chandigarh & Himachal Br. **Job Description:** **Key Responsibilities:** 1. **Sales Expertise:** Leverage your 10 to 15 years of proven experience in B2B and B2G (Lighting Division only) sales to drive revenue growth and establish strong business relationships. 2. **Communication Skills:** Demonstrate excellent communication skills to effectively convey the value of Havells' electrical and electronics products to clients, architects, builders, and government organizations. 3. **Team Leadership:** Showcase your leadership abilities by managing and motivating a sales team to achieve and exceed targets. 4. **Industry Network:** Utilize your existing network to foster connections with architects, builders, and government officials in the Amritsar regions. 5. **Team Handling** Should have experience in team handling . 6. **Location:** The position is based in Jammu Br., providing a unique opportunity to contribute to the growth of Havells in these regions. **Qualifications:** - 10 to 15 years of experience in B2B/B2G (lighting division only) sales, - Having MBA or equivalent degree if its B.tech or B.Arch with MBA is preferred. - Strong communication and interpersonal skills. - Proven track record in team management. - Existing network and connections within the architectural, builder, and government sectors. - Results-driven with a passion for achieving and exceeding sales targets. **Benefits:** - Competitive salary and performance-based incentives. - Opportunity for career growth within a dynamic and diverse work environment. - Work with a market leader in the electrical and electronics industry. Join Havells and be part of a team that values diversity, innovation, and excellence in the world of electrical solutions. Apply now and power up your career with us!

. Implementing Quality management systems . Review & approval of Process validation, cleaning validation, Water Validation, HAVC Validation, Analytical Method Validation. . Annual product reviews and reviews of stability reports Required Candidate profile 20+ years of experience in Pharmaceuticals Industry with Quality Management Systems, Quality Assurance, Validation, Greenfield Projects in dosage form -. Solid orals ,liquid injectable,

Respond to Customer Inquiries: Resolve Customer Issues Provide Product Information. Troubleshoot Issues Document Customer Interactions: Meet Customer Satisfaction Targets Collaborate with Internal Teams Stay Up-to-Date with Product Knowledge

to manage & monitor costings, budgeting & financial control at plant & branch. The ideal one will have a key role in cost optimisation, variance analysis to have efficient operation and profitability. manage production & consumption data.

We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them for the company Identify industry trends, shifts, and disruptions and put them into perspective with the company's strengths and capabilities."

Urgent requirement for Injection Officer contact person Mr. Mani Sharma (8219395110) Job Type: Full-time Benefits: Food provided Health insurance Leave encashment Paid sick time Provident Fund Schedule: Monday to Friday Rotational shift Weekend availability Supplemental Pay: Yearly bonus Work Location: In person

1. Production Planning Develop and maintain monthly, weekly, and daily production plans based on: Sales forecasts Customer orders Inventory levels Capacity constraints (equipment, labor, shift availability) Coordinate with manufacturing, QA/QC, and maintenance to ensure realistic and achievable schedules. Optimize plant capacity utilization and minimize downtime. 2. Material Requirements Planning (MRP) Calculate and plan for raw materials, packaging materials, and consumables based on the production plan. Monitor stock levels and lead times to avoid shortages or overstocking. Generate material requisitions/purchase requests in coordination with the procurement team. 3. Inventory Control Track inventory of raw materials, intermediates, packaging, and finished goods. Implement FIFO/FEFO principles and ensure GMP-compliant warehousing . Prevent material expiry, obsolescence, or deviations by managing inventory accuracy. Conduct cycle counts and physical inventory reconciliations . 4. Coordination Across Departments Act as a liaison between: Production Quality Assurance (QA) & Quality Control (QC) Procurement Sales & Marketing Warehouse & Logistics Ensure alignment between supply and demand to meet customer and market needs. 5. Monitoring & Reporting Track production vs. plan and provide daily/weekly/monthly reports on: Line efficiency Inventory status Schedule adherence Material variances Identify bottlenecks and propose corrective actions. 6. Demand Forecasting & Sales Coordination Collaborate with sales and business development teams to: Forecast product demand accurately Adjust plans for urgent market needs or product launches Manage Make-to-Stock (MTS) or Make-to-Order (MTO) strategies based on product category. 7. GMP & Documentation Compliance Ensure all planning and inventory documents are: Properly recorded Aligned with GMP guidelines Ready for internal/external audits Maintain batch-wise traceability of materials used and products manufactured. 8. Change Management & New Product Planning Plan for scale-up, validation, or launch of new products. Adjust production and material planning to accommodate formula or process changes. 9. Supply Chain Risk Management Identify and mitigate risks in supply and production (e.g., supplier delays, equipment breakdowns). Develop contingency plans for critical materials and SKUs. 10. Continuous Improvement Use Lean, Six Sigma, or other tools to: Improve planning accuracy Reduce waste Enhance production flow Implement ERP/MRP software solutions effectively (e.g., SAP, Oracle, or Pharma-specific tools). Immidiate Joiner Preffered Salary Upto 40k Job Type: Full-time Pay: ₹35,000.00 - ₹40,000.00 per month Benefits: Cell phone reimbursement Health insurance Schedule: Day shift Work Location: In person

Wings Biotech LLP is steadfast in creating drugs in the Prescriptions and Branded Formulations segments with solutions to counter the problems. We are on a constant hunt for talented professionals. If you are an experienced healthcare professional who is skilled, qualified, and innovative. If you are one of those who redeem challenges to meet success with cutting-edge creative ideas and growth in life, Wings is the place for you. Walk in to explore a world of change that assures bright career and growth prospects. Profile Requirements: Company Name: Wings Biotech LLP Profile : QC chemist Vacancy : 1 Position Location : Baddi CTC : Best in market, Negotiable as per current package Exp : 1 to 2 years in Chemical Analysis RM Qualification: B Pharma, B.sc or M.Sc Email ID : amhr.plant@wingsbiotech.com (*If interested share updated CVs on the provided email address )* Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹220,000.00 per year Benefits: Leave encashment Paid sick time Paid time off Provident Fund Schedule: Day shift Night shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Yearly bonus Education: Bachelor's (Preferred) Location: Baddi, Himachal Pradesh (Preferred)

Urgent requirement for IPQA Officer contact person Mr.Vishal Kumar(8219501366) Job Type: Full-time Benefits: Food provided Health insurance Leave encashment Paid sick time Provident Fund Schedule: Monday to Friday Rotational shift Weekend availability Supplemental Pay: Yearly bonus Work Location: In person

Role Summary: We are seeking a highly competent and detail-oriented Manufacturing QA Personnel with substantial experience in Sterile Injectable manufacturing , specifically focusing on Small Volume Parenterals (SVP) including Dry Powder, Liquid, and Lyophilized Injections . The selected candidate will ensure shop floor compliance and enforce GMP practices to maintain a state of readiness for inspections and regulatory compliance. Role & responsibilities : Ensure cGMP compliance on the shop floor during all stages of sterile manufacturing (formulation, filtration, filling, lyophilization, sealing, and visual inspection). Conduct and supervise line clearance, in-process checks, and aseptic practices adherence. Monitor and record activities for Dry Powder, Liquid, and Lyophilized Injectable production lines. Perform real-time batch record review and initiate necessary corrections. Ensure cleanroom behavior compliance , including gowning validation, personnel movement monitoring, and hygiene compliance. Coordinate with Production, QC, and Engineering for investigation of deviations, change controls, and CAPAs related to the manufacturing process. Participate in the qualification/validation activities including media fills, equipment qualification, and cleaning validation . Review SOPs, protocols, and BMRs for compliance with regulatory standards and internal policies. Provide training and on-floor guidance to production teams regarding QA best practices and compliance expectations. Ensure readiness for audits and inspections by maintaining appropriate documentation and control practices. Collaborate with cross-functional teams for continuous improvement and risk mitigation in manufacturing QA processes. Required Skills and Competencies: Strong understanding of sterile injectable manufacturing processes and controls, especially for SVP, Dry Powder, and Lyophilized dosage forms. Hands-on knowledge of cleanroom classifications, aseptic techniques, environmental monitoring , and equipment sterilization/cleaning . In-depth knowledge of cGMP, WHO, EU GMP, and PICS regulations . Experience handling deviations, OOS, CAPA, change controls, and batch record reviews . Ability to work in cross-functional teams and provide real-time QA support to operations. Proficiency in documentation practices and QA audits/inspections . Good communication, observation, and leadership skills.

Onboarding buyer on platform by through cold calls, reference meeting, direct meeting Training and guiding buyers to raise buying requirement (RFQ) Coordinating with supply team for quotes and ensure maximum conversion of RFQ Cross selling platform Required Candidate profile Male Candidates only Good Communication skills with B2B sales experience Qualification: Graduation/ Post Graduation/Diploma Experience: Minimum 4 + years in B2B Sales (Industrial Sales/Banking/NBFC) Perks and benefits TADA and Unlimited Incentives

Location: Baddi, HP, IN Work Arrangement: Hybrid Markem-Imaje is a trusted world manufacturer of product identification and traceability solutions, offering a full line of reliable and innovative inkjet, thermal transfer, laser, print and apply label systems. Markem-Imaje delivers fully integrated solutions that enable product quality and safety, regulatory and retailer compliance, better product recalls and improved manufacturing processes. Markem-Imaje is a trusted global manufacturer of product identification and traceability solutions. Our connected solutions help manufacturers to reduce waste, increase efficiency, achieve compliance and protect their brand. We offer the most complete range of market-leading marking and coding systems along with software, services and consumable solutions so you can streamline all your printing needs from one supplier. The Role The Technical Service Engineer is responsible for performing on-site installation, maintenance, service repair and support for Markem-Imaje products and services. What You Will Do The engineer has to provide on site service and customer support study different type of packaging machines and site readiness for printer installation. Conduct onsite (online) printer trial Perform on-site product installation on customer premises. He shall be responsible for on- site services such as Installation & Maintenance of Markem products to ensure maximum up-time and customer satisfaction. He needs to meet service & spares budget for assigned geographical territory. Job requires travelling to manufacturing facilities of Markem customers What You Need To Have The engineer must have 3 - 5 years of hands on experience in on site service and customer support of capital goods relating to industrial automation. He must be Graduate with Degree in Electrical/Electronics/ BSc (maths/Physics) with at least 60% marks from reputed college. Good organizational skills and ability to set priorities and manage time effectively. Good level of customer relationship management skills. Candidates applying for this position must have own vehicle that can be used for business travel purpose. You’ll only be the right candidate if you are aligned to our values and culture: Collaborative entrepreneurial spirit Winning through customers High ethical standards, openness and trust Expectations for results Respect and value people Work Arrangement : Hybrid Salary Range : - We consider several job-related, non-discriminatory factors when determining the pay rate for a position, including, but not limited to, the position’s responsibilities, a candidate’s work experience, a candidate’s education/training, the position’s location, and the key skills needed for the position. Pay is one of the Total Rewards that we provide to compensate and recognize employees for their work. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other factors prohibited by law. Attention Applicants: If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, please let us know. Likewise, if you are limited in the ability to access or use this online application process and need an alternative method for applying, we will determine an alternate way for you to apply. Please contact Drajesh@dovercorp.com for assistance with an accommodation. Kindly specify Job Requisition Number / Job Title and Location in response. Job Function : Customer Service Job Segment: Thermal Engineering, Manufacturing Engineer, Electronics Engineer, CRM, Relationship Manager, Engineering, Technology, Customer Service Show more Show less

Role & responsibilities :- Prepare and maintain daily, weekly, and monthly production reports. Collect and analyze production data (e.g., output, downtime, rejects, efficiency). Support production planning and scheduling by providing real-time data. Ensure timely and accurate entry of production data into ERP/MIS systems. Generate dashboards, charts, and data visualizations for management review. Coordinate with cross-functional teams (QA, Maintenance, Stores) to ensure data flow. Assist in inventory control, raw material consumption tracking, and variance analysis. Identify and recommend improvements in data management and reporting processes. Ensure compliance with internal standards and audit requirements for reporting. Proficiency in MS Excel (Pivot tables, VLOOKUP, charts), PowerPoint, and MIS tools. Working knowledge of ERP systems (SAP, Oracle, Tally, etc.). Analytical mindset with attention to detail. Strong communication and coordination skills.

Job Title: Process Technologist Location: Baddi, Himachal Pradesh (We can look for candidates from Anywhere in India) CTC Range: Open Qualification: Bachelor’s/Master’s/PhD degree in Materials Science, Physics, Chemical Engineering, or related field. Years of Experience: 6+ years of experience of Research & Development in the area of semiconductor, solar cell/module, optical fibre and allied field. Job Summary: The Solar Cell and Module Process Technologist is responsible evaluate & develop science-based process optimization method and technique in the manufacturing processes used in the production of solar cells and modules. The ideal candidate combines strong technical knowledge of materials science, semiconductor processing, or photovoltaic technology with hands-on experience in a cleanroom or manufacturing environment. Key Responsibilities:  Evaluate & Develop science-based process optimization method and technique for solar cell and module manufacturing processes, including wafering, texturing, doping, metallization, vacuum deposition, lamination, and encapsulation.  Acquire new knowledge through research, collaboration with external R&D institution & experimental trials and implement.  Analyze process data and metrics to identify trends, pattern and build library of knowledge for performance improvement.  Support root cause analysis and corrective actions for yield losses and defects.  Participate in continuous improvement projects and Lean/Six Sigma initiatives. Experience & Qualifications:  Understanding of crystalline silicon and/or thin-film solar cell technologies and knowledge of device simulation/modelling preferred.  Proficient in data analysis tools and statistical process control (SPC).  Experience with process automation tools, cleanroom protocols and vacuum deposition, etching, and laser processes are desirable.  Strong analytical thinking and problem-solving abilities. If your Cv is matching with the Requirement then kindly share your updated Cv: nirajita@hireduo.com Reachable @ 6290477087 Thanks and Regards Nirajita Roy Chowdhury Show more Show less

Role & responsibilities qc Purchase R&D Production Engerineering Preferred candidate profile Experience in any of the above in Manufacturing Set up - Preferably in Consumer Durables - Small Medium Home appliances ,kitchen appliances Location is Baddi Details will be discussed Please share your resume on - florance.dias@schsearch.com Ping me - 877 977 8980