476 Jobs in Baddi - Page 19

Responsibilities: Conduct heat load calculations, Ensure compliance with industry standards & codes Collaborate with project team on design & BOM creation Prepare detailed HVAC designs, approvals, coordination with vendor & site Annual bonus Provident fund

We are hiring for a Plant HR role with key focus areas in Employee Relations, Statutory Compliance, Time Office, Employee Engagement, PMS, and HR Analytics. Required Candidate profile Experience: 6–10 years in core HR, preferably in a manufacturing/plant setup (MBA/PG in HR preferred) Employee Relations & Grievance Handling Statutory Compliance (Factories Act, PF, ESI, etc.)

We are looking for QA Manager / QA Executive to join our dynamic team and embark on a rewarding career journey You will also be responsible for identifying and resolving quality-related issues and ensuring that the company's products and services meet the requirements of customers Conduct regular quality audits to identify and resolve quality-related issues Develop and maintain quality metrics to track performance and identify areas for improvement Manage the documentation process for quality assurance procedures, including the creation and maintenance of standard operating procedures (SOPs).

Responsible for performing the analytical activities as per Analytical competency matrix (Format No.BDI-QCSG004F23) and On job training and Practical Demonstration for Chemical and Instrumentation (Format No.BDI-QCSG004F19). Analysis of In process, SFG, Finished Goods, Raw material & stability sample, Analytical method validation/Verification, of OSD and LVP as per defined Protocol or procedure and related documentation as per GLP and GMP in time. Responsible for receiving sample and their documentation. Responsible Data entry in SAP. Responsible for sending the sample to outside laboratory and ensure their analysis as per requirement from Outside Commercial Lab as and when required. Calibration of instruments, as and when required. Preparation of volumetric solution, reagent, and test solution, as and when required. Ensuring the timely updation in the documents as per the Pharmacopeial amendments. Responsible for maintaining the resource in the quality control department. To ensure the compliance of the requirement of cGDP/cGDP and Data integrity while performing all activities in the laboratory. Ensuring the Compliance to EPD Global Guidelines. Facing internal and external audits and ensuring compliance. Implementation of GLP / GMP requirements. Coordinating and aligning the practices and procedures in line with the COBC requirements. SOP training in Isotrain of self-train within stipulated time.

Education / Qualification D. Pharma/B.Sc. Experience 1-2 years Followings will be the Core Job Responsibilities of the position holder: Compliance cGMP norms in warehouse as well as dispensing area. Compliance warehouse respective area SOP in daily routine work. Compliance EHS norms in warehouse as well as dispensing area. Compliance Good Documentation Practice in warehouse as well as dispensing area. Timely completion of raw material dispensing plan as per plan with error less raw dispensing. Update WMS system on daily basis as when movement of materials. Timely perform physical stock verification as per specified SOP. Timely provide training to NMS as per scheduled training matrix. Timely completion of warehouse related project. JOB FAMILY: Supply Chain t

Role & responsibilities -ELECTRICAL MATERIAL HANDLING EQUIPMENTS SERVICING, Preferred candidate profile Perks and benefits

Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift Accountabilities I. Operate the equipment efficiently without error and deviation as per SOP to meet shift targets II. Provide suggestions for optimization of processes to manufacture quality product III. Execute and update online documentation to meet cGMP requirements IV. Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations Education Qualification Diploma in Pharmacy / Mechanical Engineering Relevant Work Experience 2 years of experience in a manufacturing organisation preferably in pharmaceutical industry Competencies/Skills Collaborate to Succeed Innovate to Excel Perform with Accountability Lead with Empathy Act with Agility Strong Domain Knowledge People Management

The incumbent is a team member of Engineering Maintenance & Reliability Team and carries overall responsibility to: 1. Execute the maintenance activities in the plant & ensure the minimum breakdown with maximum efficiency by following safety & GMP Standards 2. Support Senior Engineer in carrying out Functional EM&R Planning, Detailed Scheduling and Execution of CMP to- ensure continuity of availability of plant & equipment at optimal cost; achieve standard capacity; ensure overall plant & equipment integrity & reliability - in compliance with Cipla Policies, Standards & Procedures; Reporting of EM&R MIS, Incidents & Deviations at SOP; Functional Engineer is responsible for executing maintenance tasks as assigned by Senior Engineer for his function in the Manufacturing, Packing and utility areas. Where outsourced, 3rd Party Functional Engineer is accountable for the Service Floor / Technical Floor maintenance execution Key Accountabilities I. Shift Maintenance Activity: Execute maintenance activities in a shift by managing available resources to achieve shift maintenance plan. Execute assigned tasks as per planned maintenance activity to meet maintenance targets for a shift Cater to machine and facility maintenance requirements of Unit as a responsible member of the team with overall ownership of Unit Operations. Increase the efficiency of area by ensuring better utilization of equipment and by reducing downtime in manufacturing area Prepare and submit Shift Engineer report to ensure smooth shift handover Analyse breakdowns, diagnose faults and supervise time critical equipment repairs. Offer technical expertise to maintenance people like supervisor, foreman, fitters and technicians. Function as project development member to maintain new equipment. Work with reliability engineers to extend equipment life cycle. II. Comprehensive Maintenance Plan Execution: Give inputs for preparing & adhere to unique planner for planned preventive maintenance & instrument calibrations for effective maintenance and adherence to standards. Schedule shift activities in line with the CMP including PM, Calibration, and condition monitoring activities. Execute planned maintenance and update related documentation o Preventive Maintenance o Calibration o Condition Monitoring o Planned Corrective Actions Follow good Engineering practices during planned preventive activity. Perform validation, qualification and calibration as per schedule and update output of all activities in the systems Prepare new documents and update existing documents as per GMP requirement Update Metrics on Schedule compliance III. Breakdown Maintenance: Handle breakdown maintenance to avoid recurrence and maintain continuous process operations Execute breakdown work expeditiously but safely and in compliance with cGMP. Receipt and tracking the job card for the break down activity Maintain critical spares inventory of all machines to reduce resolution time IV. Efficient Equipment Operation: Operate the equipment efficiently without error and deviation as per SOP to meet shift targets Operate an equipment only when trained and authorized to do it. Perform unit operations as per SOP & unit processes as per work instructions Maintain equipment, facility and block premises as per SOP for audit readiness. Ensure equipment, facility and block premises are maintained as per regulatory compliance Ensure all operations are performed as per GMP & Safety norms by reviewing all processes and documents for compliance Maintain system integrity by updating documentations and deviations on CipDox while performing operations V. New Technology / Capex: Use new technologies initiated by Management while adhering to CAPEX and OPEX targets to improve Machine/system performance Implement new technologies in the plant initiated by management Attend planned trainings and incorporate the learnings on the floor for improving machine performance Implement and close ideas generated through internal audits / Idea generation sessions Monitor present energy use of the plants to identify and report areas for energy conservation Implement Energy Conservation activities to improve the equipment efficiency, reduce error and reduce production cost Identify areas of improvement for waste & work simplification Manage activities to operate within budget and to reduce operating expenses Verification of the contract invoices and making of the job orders as per estimates. VI. Spares Management: Perform Material and Spare management and issue Consumables, spares, materials, log books etc to avoid delays due to unavailability of materials Issue required materials (spares and consumables) to the contractors from stores and make SAP entries for the receipts and issuance Maintain the inventory of critical spares and consumables by tracking consumption and monitoring of stocks Assess log book requirements, raise the request to QA and issue them within required timelines Classify the unused / spare / usable scrap materials or components and reuse the same where ever possible VII. EHS Compliance: maintain high level of Safety during maintenance to avoid major breakdown and report accidents/ incidences Complete preplacement Safety Training before starting the work in any area. Monitor safe operations of the machine as per SOP and timely report any safety deviations Maintain proper procedures for safety permits in plant Ensure safety systems and procedures followe'd by the operators in the shift Issue work permits to contractual staff after verifying the safety aspects, monitoring and communicating safety hazards and safety near miss to the concern. Ensure availability and usage of PPEs in the shift by coordinating with EHS department for requirements and shift schedule; Ensure usage and maintenance of PPEs by self & other workmen during shifts Report any safety incident to the Shift In charge as we'll as the Senior Engineer for the following o Near Miss o Safety Incident o Work Place Inspection o Unsafe Act o Unsafe Condition Attend safety meetings and ensure implementation of actions planned during departmental safety meeting at shop floor Ensure compliances to safety training targets by monthly reconciling VIII. cGMP Compliance: Execute and update online documentation to meet cGMP requirements Complete preplacement cGMP Training before starting the work in any area. Monitor cGMP compliance in the impact domain and report any incident / cGMP deviation to the Shift In charge as we'll as the Senior Engineer. Maintain online documentation and timely entries in all document in cGMP environment and their supporting documents Check documentation before submission to ensure data integrity. In case of any deficiency or errors in documents and rectify them as per SOP Conduct training related to cGMP, equipment operation, safety and housekeeping for workmen Optimize the use of resources in housekeeping; Ensure good housekeeping and sanitisation as per the guidelines Operate software such as SAP, CipDox and QMS as required and basis training & certification. Execute CAPA as guided by the Senior Engineer. Prepare and maintain engineering documents wrt cGMP and Good Engineering Practices IX. Continuous Improvements: Provide suggestions for optimization of processes to manufacture quality product Propose and implement new idea to enhance production, optimise the use of consumable goods and maximum utilization of resources Provide new ideas and simplify processes to reduce process cycle time and achieve new targets Participate in internal audits / Idea generation sessions to improve on deficiencies to verify GEP and GMP. Implement action plans for improving on deficiencies observed through internal / external audits X. [E] Self Development on Electrical engineering & leadership aspects Keep self-updated on regulatory guidelines and product regulatory requirements of all markets to which product manufactured by the Site is exported. Undergo training on Electrical engineering & Leadership capability building as per guidance from HR function and the Global Operations Team. Major Challenges CapEx and OpEx Adherence to the budget Cost vs performance trade off in equipment Ageing Asset leading to escalating OpEx Cost Challenges around capability & competence of personnel and service providers Key Interactions Internal Central Engineering for technical standards and guidance EHS for safe operations and near-misses Site head & Unit heads for Proposals, breakdowns and developments Indirect purchase for Spares, scope, insurance and new vendors Central purchase for provide Technical inputs and clarifications for CAPEX Global Leadership Team Guidance & Updates in TLT, Focus Calls & Reviews Corporate Affairs & Legal Team Guidance & Updates on Compliance matters External OEMs for projects , automations, alternate vendor development , quality issues and maintenance Facility maintenance contractors for Improve maintenance and quality standards Industry Bodies Connect on external benchmarking & information on technology evolution Statutory Bodies Connect for Regulatory compliance Dimensions Direct Reports: 0, Team Size 9-12 Unit Maintenance + Utility Budget: 15-20 CR [ Functional ~ 33% of this] Capex Budget: Sustenance 10 CR [ Functional ~ 33% of this] Revenue of Goa I: 300-400 CR Current Replacement value of Assets Maintained: Net Block > 50 CR; CRV > 200 CR Decisions Spends within Approved Budget Capex & Opx Maintenance & Reliability Strategies Engineering & Project Vendors & service Providers as per EA Technology for Manufacturing Resource Conservation initiatives Capability Programs Recommendations Opex & Project costs Proposal New vendor addition Facility audits Hiring consultants New equipment & Technology Key Decisions ( 2/2) Education Qualification BE / B Tech (Electrical) Relevant Work Experience 2-5 years of experience in manufacturing (Maintenance and Projects). Ability to implement new techniques, deep understanding of manufacturing process, planning and organizational skills, prioritization multi-tasking, understanding of financial concepts Good technical knowledge of Pharma / API machinery and utility requirements Good knowledge and experience in execution of green field / brown field projects Knowledge of GMP and various regulatory requirements Good leadership skills and experience in Electrical engineering activities.

Roles and Responsibilities Manage procurement activities for Raw Materials, Packing Materials, and other consumables across India. Develop and maintain relationships with vendors to ensure timely delivery of high-quality products at competitive prices. Plan and execute procurement strategies to meet business requirements while minimizing costs. Collaborate with cross-functional teams to identify opportunities for cost savings and process improvements. Ensure compliance with company policies, regulatory requirements, and industry standards.

QC Testing,HPLC,RP, Stability,GLP

Sales Business opportunities Strong relationships Sales targets Marketing Develop and implement marketing strategies research and analyze Content and promotional materials Collaboration Work closely with cross-functional teams Develop and execute

We are looking for a hard-working warehouse associate to help us in our warehouse. The warehouse associate is responsible for receiving, labeling, and storing incoming shipments, assessing stock for damages, keeping a concise record of inventory, and accurately filling customer orders. A successful warehouse associate is hard-working, organized and detail-oriented. You should be able to keep good records and keep track of incoming and outgoing stock to ensure inventory levels remain steady. Warehouse Associate Responsibilities Receiving, processing, labeling, and storing incoming stock. Maintaining clear records on all inventory and stock. Inspecting all stock for damages and keeping records of damages. Organizing the warehouse space. Preparing orders for shipment. Recording exact arrival and departure times for shipments. Operating stock management tools; for example, a forklift. Counting stock and keeping inventory records. Warehouse Associate Requirements A high school diploma. Experience with inventory software. Excellent time management and organizational skills. A forklift driver's certification. Physical stamina. The ability to be a team player. This job is provided by Shine.com

🔹 We're Hiring | AGM / DGM – Operations (Chemical Industry) 📍 Location: Baddi, Himachal Pradesh 💼 Department: Operations 📊 Reporting To: Vice President / Director 💰 CTC Range: ₹12 – ₹15 LPA 🎓 Qualification: B.Tech / B.Sc in Chemical Engineering / Chemistry 🧪 Experience: 12–15 years in Chemical Manufacturing (preferably Specialty / Performance Chemicals) 🔍 Job Overview We are looking for an experienced AGM / DGM – Operations to lead plant operations in the specialty chemicals domain. The ideal candidate will ensure smooth production, enforce safety and regulatory compliance, drive process optimization, and lead cross-functional coordination to support business goals. ⚙️ Key Responsibilities • Lead day-to-day plant operations: production, planning, quality, and process efficiency • Ensure compliance with HAZOP, MSDS, PPE, and other safety standards • Coordinate with R&D and QA/QC for trials and new product development • Drive continuous process improvement, reduce waste, and control costs • Ensure full compliance with statutory/regulatory norms • Develop and mentor a strong team of engineers and operators • Maintain audit-ready operational documentation and SOPs • Monitor raw material and inventory to avoid production disruptions 🧪 Technical Expertise Required • Strong understanding of Batch Processing, Chemical Reactions, and Process Safety • Experience with Acrylic Polyols, PU Specialty Coatings, PVC Chemicals, Auxiliaries • Background in Paint, Textile Coatings, and Specialty Chemicals for Technical Textiles • Hands-on with safety protocols: HAZOP, MSDS, PPE • Proven track record in audit readiness and documentation management 🧠 Soft Skills & Leadership • Strategic Leadership & Team Management • Analytical Thinking & Problem Solving • Excellent Communication across departments • Strong Time & Pressure Management • Commitment to Continuous Improvement 🏭 Preferred Industry Background • Specialty Chemicals • Performance Chemicals • Paints & Coatings • Textile Chemicals / Technical Textiles 📩 Interested or know someone suitable? Let’s drop your resume at vinod.hrd@cel.co.in. #ChemicalIndustryJobs #OperationsLeadership #AGM #DGM #HiringNow #SpecialtyChemicals #ProcessEngineering #PlantHead #TextileChemicals #PUCoatings #BaddiJobs #LinkedInJobs

Division Manufacturing Department Manufacturing Employment Type Permanent Job Purpose Operate & maintain packing machines to achieve quality product & shift wise targeted output with maximum utilisation Accountabilities I. Prepare the machine for packing operation as per production plan by using proper resources to ensure smooth operations II. Operate the packing machines by using minimum resources to get quality product III. Execute and update online documentation to meet cGMP requirements and maintain data integrity Fill Machine logs. Document entries/SOP and process simplification to meet cGMP. IV. Perform packing machine operations safely to avoid safety incidences by appropriately handling the machines and thereby maintaining high standard of safety V. Deliver training to workmen and adhere cGMP and safety guidelines in production process to ensure smooth operations Education Qualification Diploma in Pharmacy / Engineering Relevant Work Experience 5 years of experience in packing with knowledge of handling of QMS activity, qualification and other related documents Competencies/Skills Collaborate to Succeed Innovate to Excel Perform with Accountability Lead with Empathy Act with Agility Strong Domain Knowledge People Management Job Location Baddi Shift Hours

Company Description SAMSON LABORATORIES PRIVATE LIMITED is a pharmaceutical company based in Baddi, located at Baddi Himachal Pradesh, India. The company focuses on delivering high-quality pharmaceutical products and services. Role Description This is a full-time on-site role for a Head of Quality Assurance at SAMSON LABORATORIES PRIVATE LIMITED. The role involves overseeing quality control, quality auditing, analytical skills, quality management, and quality assurance processes to ensure compliance with industry standards and regulations. Qualifications Experience in Quality Control, Quality Auditing, and Quality AssuranceStrong analytical skills and attention to detailKnowledge of Quality Management principles and practicesExcellent communication and leadership skillsExperience in the pharmaceutical industry is a plusBachelor's or Master's degree in a relevant field (e.g. Pharmaceutical Sciences, Chemistry, Quality Assurance)

Civil Engineer, Site Supervisor, Auto Cad Designer, Pharma Project Management, Construction Supervisor, Site Management, Building Construction

Lead and manage the QC operations for injectable products, ensuring that all products meet the highest industry standards for quality, safety, and regulatory compliance. Work closely with senior management to set strategic goals for quality improvement and oversee the performance of quality control teams across the organization. Key Responsibilities: Leadership & Strategy: Develop and implement the quality control strategy for injectable products, ensuring alignment with overall corporate goals and regulatory requirements. Lead and mentor the QC team, fostering a culture of excellence and continuous improvement. Collaborate with cross-functional teams, including R&D, production, regulatory affairs, and supply chain, to ensure seamless operations and product quality. Provide strategic oversight on the quality control program for injectable products from raw materials through to finished goods. Compliance & Regulatory Management: Ensure compliance with relevant regulatory bodies , industry standards , and internal policies. Oversee the preparation and submission of quality control documentation for regulatory inspections and audits. Stay current on changes in pharmaceutical regulations, guidelines, and best practices related to injectable drugs. Ensure timely resolution of any compliance issues or regulatory findings related to quality. Quality Control Operations: Oversee the management of QC laboratories and testing for injectable drug products, ensuring the effectiveness and accuracy of all quality tests. Review and approve QC specifications, protocols, and methods for injectable products. Direct stability testing programs and ensure appropriate data handling and reporting. Develop and maintain appropriate procedures and systems for tracking quality-related incidents, complaints, and corrective actions. Continuous Improvement & Risk Management: Lead the continuous improvement initiatives within QC processes to enhance efficiency, reduce defects, and improve overall product quality. Conduct root cause analysis for quality failures and implement corrective and preventive actions (CAPA) to mitigate risks. Establish and monitor key performance indicators (KPIs) for the QC department to measure effectiveness and ensure objectives are met. Collaboration & Communication: Communicate with executive leadership to report on quality control performance and initiatives, providing insights for decision-making. Ensure effective communication and coordination between QC and other departments to streamline workflows and resolve issues in a timely manner. Represent the company during external audits and inspections, ensuring that QC practices are appropriately showcased. Training & Development: Develop training programs for QC personnel to ensure they are equipped with the necessary knowledge and skills to perform their duties effectively. Stay abreast of new developments in the pharmaceutical industry and injectables, and integrate relevant advancements into the QC strategy.

Ointment & External Preparation Block Manufacturing Leading A dynamic professional with 11 -15 years of experience in Production Planning and Control. Management, Process Enhancements and Resource Management with expertise of Equipment /instrument handling in manufacturing, filling and packing of External Preparation. Identifying production targets and achieving the same within time, quality and cost parameters. Functional expertise in managing production operations with key focus on top line profitability by Ensuring optimal utilization of resources. Activitly participate in various Regulatotry audits like USFDA,MHRA,MCC,WHO,QP,&Internal audit etc, Role & responsibilities

Serve as the primary point of contact for our key customers Regularly conduct client meetings to review performance, introduce new products & Business opportunities. Assist building RFQs /Costing/Price Adjustments /Development PO’s & invoicing.

Req. Executive Purchase for machine tools manufacturer near Chandigarh. B Tech Mech with exp of 5 to 7 years can apply.He should have knowledge of Prod Plans, Prod Scheduling, Raw Material Planning, etc. Required Candidate profile He should be B Tech Mech. Regular only with exp of 5 to 7 years in Prod Planning, Monthly Prod Scheduling, Raw Material Planning .He should be fluent in English with leadership Qualities

This position is accountable for below activities on routine basis. Personnel Hygiene Plant Housekeeping as per GMP requirment Linen Management Pest Control Management To face various audits internal/external related to falities & ensure compliances Vendor Bill checking and processing Contract Labour Management. Induction of new employees. Preparation and implementation of SOP s & Change control Timely closure of QMS Documents To arrange Skill development programme for workmen To arrange the works committee meetings Dealing with site manufacturing and other departments for day to day activities Any other work assigned by HOD

Knowledge of injection molding machines of Engineering Industries, Knowledge of computer controlled injection molding machines.Knowledge of ISO Documentation. Team Handling, Leadership Qualities etc Required Candidate profile He should be B Tech Plastic Tech or CIPET from Govt Institutes only. He should have have experience of 4 to 5 years in Injection Molding. He should be ready to shift to Baddi.

HDB Financial Services Ltd. Hiring for Sales Manager - Retail Commercial Vehicle Product - Sales Manager - Commercial Vehicle Exp - min 3 Yrs. experienced in Retail Commercial Vehicle CV shared with - Aditya.rajawat@hdbfs.com. Contact No - 7440798286

Role & responsibilities To carry out investigations related to OOS, OOT, Incident and Extraneous Peaks to ensure their closure and implementation of CAPA. Responsible for execution of Regulatory Notification as per SOP. To ensure implementation of all proposed actions identified as a CAPA of investigations related to OOS, OOT, and incident. Review of investigation reports, hypothesis protocol and hypothesis reports related to OOS/OOT and Incidents. Co-ordination with R&D, Production, Central Cell, CQA and other responsible for investigations. To prepare and review Quality documents such as (but not limited to) protocols, reports, SOPs STPs Specification, Investigation. Preferred candidate profile Perks and benefits

Role & responsibilities Investigation of market complaints, OOS/OOT result related to product. To ensure that the manufacturing and packing operation are carried out as per the instruction given in the batch production Record. To Handle (Initiation /Evaluation/Closure) Change control, Deviation/Incident management System. To verification and Check the dispensed raw material and packing material before batch processing and during dispensing. Preferred candidate profile Perks and benefits