975 Jobs in Baddi - Page 27

Key Responsibilities : Perform quality inspections throughout the manufacturing process Identify and resolve quality-related issues in coordination with production teams Maintain accurate quality records and documentation as per ISO/QMS standards Assist in root cause analysis and implementation of corrective and preventive actions Ensure compliance with internal quality standards and customer specifications Candidate Profile : Diploma in CEPIT / Polymer Engineering / Plastic Technology Relevant experience in quality assurance/control in the polymer industry Knowledge of ISO 9001 / quality tools (like 5 Why, Fishbone, Pareto) Strong communication and analytical skills Team player with a proactive attitude How To Apply? Copy and Paste the below link in your browser to apply online on The Search House: https://recruitcrm.io/apply/17496273446310029714rVP

Job Summary: We are looking for a dynamic and skilled R&D Manager to oversee the development of innovative and high-quality cosmetic and personal care products. The ideal candidate should have hands-on experience in formulation development, strong knowledge of cosmetic regulations, and the ability to lead projects from concept through commercialization. Key Responsibilities: Product Development: Lead the formulation and development of skincare, haircare, and personal care products, ensuring alignment with brand goals and consumer expectations. Project Management: Manage multiple R&D projects, timelines, and deliverables across various product categories. Formulation & Testing: Supervise lab trials, stability studies, performance testing, and scale-up processes. Documentation & Compliance: Prepare and maintain formulation records, product dossiers, and ensure regulatory compliance (BIS, FDA, EU, etc.). Raw Material Evaluation: Source and evaluate new raw materials in collaboration with procurement and suppliers. Team Supervision: Manage and mentor junior chemists, technicians, and interns within the R&D lab. Cross-functional Coordination: Collaborate with marketing, QA/QC, production, and packaging teams to ensure product feasibility and quality. Innovation & Trends: Stay updated with market trends, consumer insights, and technological advancements to fuel innovation. Qualifications & Experience: Bachelors or Master’s degree in Cosmetic Technology, Chemistry, Pharmaceutical Sciences, or related field. 5–8 years of hands-on experience in the cosmetic or personal care industry. Solid understanding of formulation chemistry, manufacturing processes, and cosmetic regulations. Proficiency in managing lab operations, stability testing, and product documentation. Preferred Skills: Experience in natural/organic/clean beauty product development. Familiarity with global cosmetic ingredient standards and labeling regulations. Strong organizational, analytical, and communication skills.

1. Quality Assurance • Conduct quality checks at multiple stages of production and final inspection. • Maintain quality standards as per company and regulatory guidelines. • Coordinate with vendors and internal teams to resolve quality issues. • Maintain and update QA documentation including checklists, defect logs, and audit reports. • Support audits and regulatory inspections with accurate data and records. 2. Production Supervision • Monitor daily production activities and ensure adherence to production schedules. • Track key metrics such as output, downtime, and efficiency. • Collaborate with production teams to implement process improvements. • Identify bottlenecks and troubleshoot operational issues in real-time. • Maintain updated production documentation and reports. • QC check of PPS before dispatch to HO for approval • Physical inspection of stability samples and regular audits of RM/PM/ STABILITY SAMPLES/ BATCHES/ stability reports 3. Procurement Coordination • Assist the procurement team in raising purchase orders and following up with suppliers. • Coordinate with vendors for update of manufacturing status and schedules • Help track inventory levels of critical raw materials and packaging. • Flag any potential delays in procurement that could impact production. • Maintain supplier master data and purchase records. Required: • Bachelor’s degree in Engineering, Supply Chain, or a related field. • 2–4 years of experience in quality control, production planning roles. • Strong analytical and problem-solving skills. • Proficiency in MS Excel, ERP systems, and documentation. • Excellent communication and coordination skills. Preferred: • Experience in Colour Cosmetics and Personal Care. • Knowledge of ISO, GMP, or other quality frameworks. • Hands-on exposure to lean manufacturing or Six Sigma principles. • Experience preferably in color cosmetics/personal care Show more Show less

Urgent requirement for Vial Washing operator Qualification : ITI Experience : 02 to 04 years Contact : 8091773947 Job Type: Full-time Pay: ₹14,500.00 - ₹25,000.00 per month Benefits: Food provided Health insurance Paid sick time Paid time off Provident Fund Schedule: Day shift Monday to Friday Work Location: In person

CONTACT PERSON = PANKAJ BHATIA - 9599417801 (jobs@viownmettube.com) ITI ELECTRICIAN CANDIDATE SHOULD HAVE GOOD KNOWLEDGE OF ELECTRICAL DRAWINGS, UTILITIES LIKE PUMPS, DG DETS, AIR COMPRESSORS, EOT CRANES, ELECTRICAL PANELS, VFD, PLC SYSTEMS, LT PANELS, ACB, VCB, TRANSFORMERS, AC/DC DRIVES, ELECTRICAL CONTROL AND POWER CIRCUIT, THERMOCOUPLES, SENSORS, RTD etc.. SHOULD MAINTAIN PROPER RECORDS OF DAY TO DAY MAINTENANCE PROBLEMS AND REPORT TO THE MAINTENANCE HEAD. WORKING EXPERIENCE = 3 - 5 YRS Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Leave encashment Provident Fund Schedule: Day shift Evening shift Morning shift Supplemental Pay: Overtime pay Yearly bonus Work Location: In person

Job Title: Sr. Officer / Executive – QC DRA Department: Quality Control / Drug Regulatory Affairs (DRA) Reporting To: DRA Manager / QC Head Employment Type: Full-time Experience Required: Minimum 2 Years Qualification: M.Sc. / B.Sc. (Science/Pharmacy stream preferred) Job Summary: We are seeking a motivated and detail-oriented Sr. Officer / Executive for QC DRA to support the preparation, compilation, and review of regulatory documents required for product registrations and regulatory submissions. The ideal candidate should have experience working in QC or DRA functions within a pharmaceutical manufacturing setup and should be well-versed with regulatory compliance requirements (domestic and international). Key Responsibilities:1. Dossier Compilation & Review: Assist in preparation and review of CTD / ACTD / eCTD dossiers for domestic and international regulatory submissions. Compile and verify quality-related documents including specifications, STPs, validation protocols, and COAs for submission. Coordinate with internal teams (QA/QC/Production/R&D) to collect and organize required data for regulatory filings. 2. Regulatory Documentation: Prepare and maintain Product Master Files (PMFs) and Site Master Files (SMFs) . Support submission of Annual Product Reviews (APRs) , and DMFs (Drug Master Files) as per regulatory timelines. 3. Compliance and Coordination: Ensure all documentation aligns with current regulatory guidelines (e.g., WHO, USFDA, MHRA, EU, TGA). Coordinate with external consultants or agents for country-specific dossier submissions. 4. QC Interface: Liaise with the QC team to obtain data such as method validation, stability studies, and analytical results required for regulatory submissions. Review analytical data and reports to ensure correctness and readiness for regulatory review. 5. Audits & Queries: Assist in addressing regulatory queries and deficiencies. Support audit preparations and participate in internal and external audits as required. Candidate Requirements: Education: M.Sc. or B.Sc. (Chemistry, Microbiology, Biochemistry, or related disciplines) Experience: Minimum 2 years of experience in Quality Control or DRA in a pharmaceutical company. Skills: Good understanding of ICH guidelines, regulatory documentation structure , and technical writing. Hands-on experience in document review , dossier compilation , and data coordination . Proficiency in MS Office and regulatory software tools (if any). Soft Skills: Strong attention to detail and data accuracy. Good communication and coordination skills. Ability to meet deadlines and manage multiple priorities. Work Schedule: 6-day working week (as per company policy) Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹28,000.00 per month Benefits: Flexible schedule Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Morning shift Weekend only Supplemental Pay: Overtime pay Performance bonus Yearly bonus Work Location: In person

Greeting customers and directing them to available mechanics. Consulting with mechanics regarding necessary repairs and possible alternatives to expensive repairs. Using your knowledge of our products and services to sell or provide in-depth information about available parts and service options to customers. Answering questions about service outcomes and scheduling and booking appointments, vehicle drop-off, and vehicle pick-up. Providing customers with information and advice on warranty protections, potential cost savings, and the advantages of trading in versus fixing their vehicle. Managing and overseeing the dealership's workflow and schedule. Calling customers to advise them about service changes or car pick-up times. Maintaining positive customer relationships to ensure repeat business. Ensuring all details on services rendered and costs are related to customers and processing their payments. Liaising with service technicians about parts ordering and ensuring parts are available when needed. Job Types: Full-time, Permanent Pay: ₹10,000.00 - ₹15,000.00 per month Benefits: Cell phone reimbursement Provident Fund Schedule: Day shift Weekend availability Supplemental Pay: Performance bonus Yearly bonus Experience: total work: 1 year (Preferred) Work Location: In person Application Deadline: 07/02/2025

Department: Production Reporting To: Production Supervisor / Production Manager Employment Type: Full-time Salary: ₹15,000 – ₹18,000 per month Experience Required: Minimum 5 Years in tablet compression (bilayer preferred) Qualification: Minimum 12th Pass (Higher Secondary) Job Summary: We are hiring an experienced Operator – Bilayer Compression for our tablet production department. The ideal candidate should have strong hands-on experience in handling bilayer tablet compression machines , ensuring consistent product quality and adherence to cGMP norms. Key Responsibilities:1. Machine Operation: Independently operate bilayer compression machines (e.g., Cadmach, Korsch, Fette, etc.). Set up, start, monitor, and shut down machines as per production requirements and SOPs. Monitor weight variation, hardness, thickness, and appearance of tablets during production. 2. Production Execution: Follow the Batch Manufacturing Record (BMR) and production plan to meet daily output targets. Conduct in-process checks and maintain consistency in product quality. 3. Equipment Handling & Maintenance: Perform routine cleaning and minor maintenance of compression equipment. Ensure proper lubrication and part replacement when necessary. 4. Documentation & Compliance: Accurately record production data, machine logbooks, and cleaning records. Follow GMP and safety protocols strictly on the shop floor. 5. Coordination: Work closely with QA, maintenance, and warehouse teams for smooth production flow. Report any machine or process deviations immediately to the production supervisor. Candidate Requirements: Education: Minimum 12th Pass (Science/technical stream preferred) Experience: At least 5 years of experience in tablet compression, especially bilayer compression Technical Skills: Proficient in machine settings, tooling changes, and troubleshooting. Understanding of compression machine parameters and production SOPs. Soft Skills: Disciplined and safety-conscious Team player with good communication skills Work Schedule: 6 days working Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Flexible schedule Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Morning shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Yearly bonus Experience: Bilayer Compression: 4 years (Required) Location: Baddi, Himachal Pradesh (Required) Work Location: In person

 WORKING KNOWLEDGE OF EXCEL AND GMAIL  KNOWLEDGE OF MARG SOFTWARE  FORECASTING INVENTORY REQUIREMENTS  PROCUREMENT  INVENTORY CONTROL  MONITORING INVENTORY LEVELS  PLANNING PRODUCTION SCHEDULES  MONITOR PRODUCT BATCHES MANUFACTURING  FOLLOW UP WITH VENDOR TO TIMELY DELIVERY OF PENDING ORDER AS PER PRODUCTION PLAN Job Types: Full-time, Permanent Schedule: Day shift Work Location: In person Application Deadline: 23/06/2025 Expected Start Date: 16/06/2025

Job Summary: We are seeking a skilled and detail-oriented Officer for our Tablet Manufacturing Department to support and supervise daily production operations in accordance with GMP standards. The ideal candidate should have at least 2 years of hands-on experience in tablet manufacturing in a pharmaceutical environment, with a strong understanding of production processes, documentation, and quality compliance. Key Responsibilities: Manufacturing Operations: Execute and monitor daily manufacturing operations for tablet production including granulation, compression, coating, and packing. Ensure batch manufacturing activities are conducted as per the Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs). Operate and calibrate equipment such as RMG, FBD, tablet presses, and coating machines. Maintain strict compliance with cGMP and safety guidelines. Documentation: Ensure timely and accurate documentation of BMR, logbooks, cleaning records, and other production records. Assist in deviation, change control, and CAPA documentation when required. Quality & Compliance: Ensure adherence to quality standards and report any deviations to QA/QC. Coordinate with QA for in-process checks, line clearance, and sampling. Inventory & Equipment Management: Monitor availability of raw materials, granules, and consumables for uninterrupted production. Ensure cleanliness and proper maintenance of machines and production area. Team Support: Coordinate with team members, technicians, and support staff to ensure smooth workflow. Train junior operators on machine handling and SOP adherence. Desired Candidate Profile: Education: B.Pharm is mandatory Experience: Minimum 2 years of experience in tablet manufacturing in a regulated pharma company (USFDA/WHO-GMP approved preferred) Good understanding of manufacturing processes and production planning. Sound knowledge of GMP, safety standards, and pharmaceutical regulations. Strong documentation and communication skills. Ability to work in shifts and under pressure situations. Work Schedule: 6 days working (as per company policy) Job Types: Full-time, Permanent Pay: ₹12,000.00 - ₹16,500.00 per month Benefits: Flexible schedule Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Morning shift Night shift Rotational shift Weekend only Supplemental Pay: Overtime pay Performance bonus Yearly bonus Education: Bachelor's (Preferred) Experience: Tablet Manufacturing: 2 years (Required) Location: Baddi, Himachal Pradesh (Required) Work Location: In person

Job Title: Officer / Sr. Officer – Quality Control (FG & RM) – HPLC Department: Quality Control Reporting To: QC Manager / Head – Quality Control Employment Type: Full-time Experience Required: 3 to 6 Years Minimum Qualification: B.Pharm (Bachelor of Pharmacy) Job Summary: We are looking for a highly skilled and experienced Officer/Sr. Officer – QC (Finished Goods & Raw Materials) with hands-on expertise in HPLC analysis . The candidate will be responsible for testing and analysis of raw materials (RM), finished goods (FG), and packaging materials, ensuring compliance with quality standards and regulatory requirements. Key Responsibilities: 1. Sample Analysis: Perform chemical and instrumental analysis of Raw Materials (RM), Finished Products (FG), and Packaging Materials using HPLC, UV, IR, GC etc. Ensure timely release of RM and FG based on QC test results. 2. Instrument Handling & Maintenance: Operate, calibrate, and maintain HPLC and other QC instruments. Troubleshoot minor instrument issues and ensure periodic calibration and preventive maintenance. 3. Documentation & Compliance: Prepare and review analytical documents including STPs, SOPs, COAs, and logbooks. Maintain proper records and ensure data integrity and compliance as per cGMP , GLP , and regulatory guidelines . Involve in deviation handling, out-of-specification (OOS) results, and corrective/preventive actions (CAPA). 4. Quality Assurance Support: Support QA in internal and external audits. Participate in investigations and support regulatory inspections (USFDA, WHO-GMP, MHRA, etc.). 5. Inventory & Sample Management: Maintain inventory of laboratory chemicals, standards, and consumables. Ensure proper sample management – storage, labeling, disposal as per SOP. Candidate Requirements: Education: B.Pharm (mandatory); candidates with M.Pharm or additional certifications in Quality Control or Analytical Techniques may apply. Experience: Minimum 3 to 6 years of relevant experience in pharmaceutical QC (RM & FG) with strong hands-on HPLC exposure. Technical Skills: Proficiency in HPLC operation and method validation. Soft Skills: Good communication and analytical thinking. Attention to detail and strong documentation practices. Ability to work independently and in a team. Work Schedule: 6-day working week (as per company policy) Job Types: Full-time, Permanent Pay: ₹18,000.00 - ₹29,000.00 per month Benefits: Flexible schedule Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Morning shift Weekend only Supplemental Pay: Overtime pay Performance bonus Yearly bonus Education: Bachelor's (Preferred) Location: Baddi, Himachal Pradesh (Required) Work Location: In person

Job Title: Officer – Quality Control (Microbiology) Department: Quality Control – Microbiology Reporting To: QC Microbiology Manager / Quality Head Employment Type: Full-time Salary: ₹20,000 per month Experience Required: Minimum 2 YearsQualification: M.Sc. / B.Sc. (Microbiology or related life sciences field) Job Summary: We are looking for a dedicated and detail-oriented Officer – QC Microbiology to join our Quality Control team. The selected candidate will be responsible for performing microbiological testing of raw materials, finished products, water, and environmental monitoring to ensure compliance with quality and regulatory standards. Key Responsibilities: 1. Microbiological Testing: Conduct routine microbiological analysis of raw materials, finished products , and in-process samples . Perform water testing (WFI, Purified Water, RO Water) for microbial limits. Execute sterility testing, BET (Bacterial Endotoxin Test) , and Microbial Limit Testing . 2. Environmental Monitoring: Carry out environmental monitoring of production and sterile areas , including air, surface, and personnel monitoring. Maintain and review EM records, trends, and reports. 3. Media Preparation & Validation: Prepare, sterilize, and validate media for microbiological testing. Perform growth promotion tests and media control checks. 4. Documentation & Compliance: Ensure timely and accurate documentation of all microbiological activities as per cGMP and GLP . Maintain logbooks, worksheets, test reports, and analytical records as per SOPs. 5. Instrument Handling: Operate and maintain laboratory equipment such as Incubators, LAF, Autoclave, pH meter, Conductivity meter, and Particle counter . Ensure instruments are calibrated and maintained as per schedule. Candidate Requirements: Education: M.Sc. / B.Sc. in Microbiology or Life Sciences Experience: Minimum 2 years in pharmaceutical QC microbiology Knowledge Required: Strong understanding of microbiological techniques and regulatory standards. Familiarity with GMP , GLP , and ISO guidelines. Skills: Good observation and documentation skills. Ability to follow SOPs and work in a sterile environment. Basic computer proficiency for record-keeping and reporting. Work Schedule: 6 days working Job Types: Full-time, Permanent Pay: ₹216,000.00 - ₹240,000.00 per year Benefits: Flexible schedule Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Morning shift Weekend only Supplemental Pay: Overtime pay Performance bonus Yearly bonus Location: Baddi, Himachal Pradesh (Required) Work Location: In person

Desired Candidate Profile: Candidate should have an experience of 1-3 years in a packaging development role. Experience of Packaging development of Personal Care Products is desirable. Candidate should possess excellent communication and analytical skills apart from domain knowledge. He / She should be well versed with packaging development activities in a user industry. Should have knowledge of various printing processes and decoration techniques. Must have strong technical understanding of major Packaging materials i.e. Plastics, Paperboard, Glass, Metal etc. Should have basic technical understanding of various package dispensing systems like pumps, valves, tubes etc. Candidate should have good knowledge of various package testing methods. Must be familiar with operations of common packaging machines like Bottle Filling, Form-fill-seal, Flow wrapping, Labelling etc. Candidate should be able to define packaging component specifications. Job Description: To handle entire packaging development as per brief. To identify new material, technology, suppliers for packaging material and processes. Packaging material testing, transit trials, machine trials etc. To support product development and brand team in various new product development initiatives. Finalizing PM Specifications, BOMs and other documents after completion of successful tests & trials. Developing New/Alternate vendors for procurement of existing & new packaging material in coordination with procurement team Artwork approvals/proofing of packaging designs. Handle quality & process improvement Projects to facilitate higher productivity and/or user convenience. To Identify and implement PM related cost optimization initiatives for the business. Preference - Experience in fmcg domain such as personal care, foods

Role & responsibilities Achieve Individual Targets Document Collection from Landlords and follow-ups Rental negotiations with Landlords in-line with Rental Band and rent policy. Explore alternate options in case of Site Terminations and resolution of Old sites by doing Full and Final Co-ordinate with Landlords for Lease Registration Achieving Target for rental cost Reduction Meet LL and clear estate issue as per ask of customer like Fiber ,Tenancy addition ,5G any kind of upgradation Preferred candidate profile Field Sales Executive Bike is a must have Distance education wont be accepted Perks and benefits TA + DA upto 7500 per Month

Title: Unit Sales Manager Job Responsibilities - Hiring new health agents or advisors on a regular basis is the first job role. licensing and routinely monitoring the same's activation. Managing the health retail item Developing connections with health agents. Frequent field visits to sell health coverage to agents or individuals. Working in tandem with other divisions like operations, claims, and underwriting To maintain records in an organized way and to regularly interact with agents, lead providers, and intermediates. Educating and inspiring the health agents to enter competitions and generate additional revenue. If interested, kindly share your update resume at [HIDDEN TEXT]

Urgent opening for Key Sales Executive profile RSPL Ltd Shimla/Rohru/Baddi locations Please share your resume Salary Range - 13500 to 17000 gross (Based on experience and Qualification= Minimum High School Minimum 2 years of Experience in FMCG is must Profile of the Key Sales Executive as follows (JD) Candidate Profile from the SAMT (Stand Alone Modern Trade) Handling Large Self Service Stores or SAMT (Stand Alone Modern Trade) Good Communication Skills Having a exposure of at least 1 to 3 years in same category of outlets. Will be handling in shop promoters at SSS (Super Saver Store). Merchandising at stores BTL activities for the consumers at these category of SELF SERVICE Plus outlets. Ability to travel 25 to 30 km per day Please share your updated resume dalip.sharma@adecco.com WhatsApp 7973360541 Regards Dalip Sharma

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

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.

He should have knowledge of Sales & Business Devolpment . He should be fluent in English.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.