960 Jobs in Baddi - Page 10

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Officer - Production Date: Jul 11, 2025 Location: Baddi - Operations - Cosmetic Company: Sun Pharmaceutical Industries Ltd Responsible for Quality and quantity (% yield) of products packed and delivered. Responsible for cGMP compliance of the areas, preparation & updating of SOP. Responsible for Liquid orals packing, Steroid products packing, non-steroid products packing. Responsible for manufacturing of liquid, non-steroid and steroid products To ensure cGMP compliance in the manufacturing, primary & secondary packing area. Deliver the products as per the monthly plans given by HOD. To allocate the job to the workmen to achieve the best productivity. To ensure the up-keep of facilities and equipment’s by making the notification to the concern departments for the preventive maintenance, calibration and requalification. To keep the packing area always ready for inspection through good documentation/ cGMP compliance of the plant and personnel hygiene. To motivate the workmen by proper training in activity and safety matter, timely guidance in shop floor monitoring so that they can achieve results successfully first time and for every time. To provide training to all employees. Set Production goals & objective for the production team with maximum output of best quality. Collaborate with QA/QC, warehouse and other departments for day to day activities Participate in Self inspection programs. Updating Production manager regarding Day to Day production activities. Investigate and answer market complaints, deviations and CAPA. Work distribution. Prepare & Review SOPs. Coordinate with Eng. Department for installation of new machines. Coordinate with R&D for new product manufacturing on site Apply Now » Apply Now Start applying with LinkedIn Please wait...

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Officer - Validation Date: Jul 11, 2025 Location: Baddi - Plant Company: Sun Pharmaceutical Industries Ltd Equipment qualification (IQ,OQ,PQ) Utility Qualification ( HVAC Validation,Compressed air validation) Apply Now » Apply Now Start applying with LinkedIn Please wait...

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Officer Date: Jul 11, 2025 Location: Baddi - Warehouse Company: Sun Pharmaceutical Industries Ltd Dispensing of Raw material to production Storage and Labeling of Raw and Packaging material. Handling stock of raw material Ensure Quality & quantity of all materials to be issued. Proper storage & labeling, Identification of materials. Compliance of Current Good Manufacturing Practices. Maintain document in accordance with cGMP & statutory requirements. Develop & Improve of Warehouse systems. Monitoring the compliance of issuance of materials as per SOPs. Apply Now » Apply Now Start applying with LinkedIn Please wait...

Efficiently monitor all operations which affect the quality. Devise procedures for inspecting and reporting all the persisting quality issues. Assure the consistency and reliability of production with thorough checking procedures and final output. Supervise and guide inspectors, technicians, and all other staff. Report all malfunctions to production executives only to ensure immediate action. Appraise all the requirements of customers and ensuring they are quite satisfied. Facilitate proactive solutions by collecting and analyzing quality data. Keep permanent records of quality reports, statistical reviews, and relevant documentation. Review the current standards and policies. Communicate with external quality assurance officers during on-site inspections. Efficiently ensure that all the legal standards are met with great care. Provide assistance during the recruiting process. Efficiently create reports for tracking progress.Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications. Perks and benefits: Mention available facilities and benefits the company is offering with this job.

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities Comprehensive Oversight: Manage day-to-day activities in Quality Control . Instrument Expertise: Demonstrate hands-on experience with a variety of QC instruments, including HPLC, Dissolution, and other chemical and analytical tools. Lab Development: Utilize your expertise to develop the lab, ensuring compliance with the latest Revised Schedule M requirements. Team Training: Share your knowledge and experience to train and mentor the team, fostering continuous improvement in quality. Software Proficiency: Utilize your proficiency in relevant software tools to streamline processes and enhance efficiency. Preferred candidate profile Experience: A minimum of 7 years in a Quality Control role within the pharmaceutical industry. Qualification: Hold an Approval in Quality Control. Education: Bachelor's degree in Pharmacy or above. Dedication: Exhibit a strong work ethic and dedication to maintaining the highest quality standards. Leadership Skills: Possess strong leadership and training skills. Perks and benefits

Roles and Responsibilities Operate granulation equipment such as roller compactor, fluid bed dryer, etc. to produce high-quality granules. Monitor and control process parameters to ensure product quality and consistency. Perform routine maintenance tasks on equipment to prevent breakdowns and optimize performance. Collaborate with other departments (e.g., formulation, packaging) to ensure smooth production operations. Ensure compliance with cGMP regulations and company policies. Desired Candidate Profile 2-7 years of experience in OSD (Oral Solid Dose) manufacturing or related field. B.Pharma degree from a recognized institution. Strong understanding of FBD (Formulation & Bulk Drugs), USFDA guidelines, RMG (Revised Manufacturing Guidelines). Proficiency in operating various types of granulation equipment.

Equipment qualification (IQ,OQ,PQ) Utility Qualification ( HVAC Validation,Compressed air validation)

Dispensing of Raw material to production Storage and Labeling of Raw and Packaging material. Handling stock of raw material Ensure Quality & quantity of all materials to be issued. Proper storage & labeling, Identification of materials. Compliance of Current Good Manufacturing Practices. Maintain document in accordance with cGMP & statutory requirements. Develop & Improve of Warehouse systems. Monitoring the compliance of issuance of materials as per SOPs.

Job Description Role : - Associate Director – Finance Baddi Qualification: CA Experience: 20+ years of experience. Team Size: 7-9 Location: Baddi (Himachal Pradesh) Followings Will Be Core Responsibilities Of The Position Holder Direct and manage manufacturing related finance and accounting functions (ie., cost, capital , payroll and inventory) for manufacturing plant. Active involvement in the development and establishment of the plant strategic functional goals and initiatives. Ensures complete and accurate financial reporting over cost performance, inventory control, general accounting processes, payroll and all other financial activities. Oversee and direct all general ledger accounting activities including maintenance of the accounts and monthly reconciliations. Ensure items are correctly classified and all reporting is prepared in accordance with GAAP. Ensure SOX compliance and updates documentation as required. Handle Indirect Taxes like Central Excise, Sales Tax, VAT etc. and its compliance. Controlling the Plant Functional cost & Highlight Operations Head at Plant areas of cost saving opportunities. Establishing cost management systems/techniques for monitoring various overheads and achieving maximum cost control in operations. Calculating and releasing the Standard Cost of products once a year. Control on Capex / RCE raised at the Plant and its capitalization. Control and release of MIS on an accurate and timely basis.

Responsible for Quality and quantity (% yield) of products packed and delivered. Responsible for cGMP compliance of the areas, preparation & updating of SOP. Responsible for Liquid orals packing, Steroid products packing, non-steroid products packing. Responsible for manufacturing of liquid, non-steroid and steroid products To ensure cGMP compliance in the manufacturing, primary & secondary packing area. Deliver the products as per the monthly plans given by HOD. To allocate the job to the workmen to achieve the best productivity. To ensure the up-keep of facilities and equipment’s by making the notification to the concern departments for the preventive maintenance, calibration and requalification. To keep the packing area always ready for inspection through good documentation/ cGMP compliance of the plant and personnel hygiene. To motivate the workmen by proper training in activity and safety matter, timely guidance in shop floor monitoring so that they can achieve results successfully first time and for every time. To provide training to all employees. Set Production goals & objective for the production team with maximum output of best quality. Collaborate with QA/QC, warehouse and other departments for day to day activities Participate in Self inspection programs. Updating Production manager regarding Day to Day production activities. Investigate and answer market complaints, deviations and CAPA. Work distribution. Prepare & Review SOPs. Coordinate with Eng. Department for installation of new machines. Coordinate with R&D for new product manufacturing on site

Responsible for Quality and quantity (% yield) of products packed and delivered . Responsible for cGMP compliance of the areas, preparation & updating of SOP . Responsible for Liquid orals packing, Steroid products packing, non-steroid products packing. Responsible for manufacturing of liquid, non-steroid and steroid products To ensure cGMP compliance in the manufacturing, primary & secondary packing area. Deliver the products as per the monthly plans given by HOD. To allocate the job to the workmen to achieve the best productivity. To ensure the up-keep of facilities and equipment’s by making the notification to the concern departments for the preventive maintenance, calibration and requalification. To keep the packing area always ready for inspection through good documentation/ cGMP compliance of the plant and personnel hygiene. To motivate the workmen by proper training in activity and safety matter, timely guidance in shop floor monitoring so that they can achieve results successfully first time and for every time. To provide training to all employees. Set Production goals & objective for the production team with maximum output of best quality. Collaborate with QA/QC, warehouse and other departments for day to day activities Participate in Self inspection programs. Updating Production manager regarding Day to Day production activities. Investigate and answer market complaints, deviations and CAPA. Work distribution. Prepare & Review SOPs. Coordinate with Eng. Department for installation of new machines. Coordinate with R&D for new product manufacturing on site

The ideal candidate will be involved with preparing financial reports and statements, bank reconciliations, and conducting cyclical audits. Moreover, the candidate must have strong interpersonal skills and possess a strong business acumen. Responsibilities Create ad-hoc reports for various business needs Prepare tax documents Compile and analyze financial statements Manage budgeting and forecasting Qualifications Bachelor's degree in Accounting or related field Ability to interpret and analyze financial statements and periodicals Fluency in Microsoft Office suite (Outlook, Excel, Word, PowerPoint, etc.)

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. If you are looking for an opportunity for a job Wings Biotech LLP provides a platform for candidates to prove themselves. Profile Requirements: 1) Qualification- B.Pharma 2) Profile- Chemist 3) Department- Production 4) Experience-1 to 2 years in Liquid Syrup Section 5) Salary- Hike on current package as per your interview performance

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 3 years in GLP 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 - ₹250,000.00 per year Benefits: Leave encashment Paid sick time Paid time off Provident Fund Education: Bachelor's (Preferred) Location: Baddi, Himachal Pradesh (Preferred) Work Location: In person

Key Responsibilities: Environmental Monitoring: Conduct routine environmental monitoring of Quality Control, Production, and Warehouse areas, including but not limited to, viable and non-viable particle counting, surface sampling, and air sampling, all in strict adherence to approved procedures. Sampling: Perform accurate and timely sampling of Active Raw Materials (ARMs) and Inactive Raw Materials (IRMs), as well as final lot samples of finished products, according to established protocols. Microbiological Analysis: Execute microbiological analysis of various samples, including environmental swab samples and compressed air samples, utilizing validated methods. Trend Analysis & Reporting: Prepare and submit comprehensive monthly and annual microbiological trend summary reports for environmental monitoring procedures, identifying any deviations or critical trends. Documentation & Compliance: Maintain meticulous logbooks within the Quality Control department, review generated reports for accuracy and completeness, and actively participate in the preparation and revision of Standard Operating Procedures (SOPs). Media Fill Support: Participation in media fill, sample incubation and perform diligent vial observation to assess aseptic processing performance. Team Collaboration: Collaborate effectively with cross-functional teams and proactively take on any additional responsibilities assigned by the Head of Department to support overall QC operations. Qualifications: Bachelor's or Master's degree in Microbiology, Biotechnology, or a related scientific discipline. 1-5 years of experience in Quality Control Microbiology, preferably within a pharmaceutical, vaccine, or sterile manufacturing environment. Proficient in environmental monitoring techniques, microbiological testing, and aseptic practices. Strong understanding of cGMP guidelines and regulatory requirements for pharmaceutical manufacturing. Excellent data analysis, report writing, and documentation skills. Ability to work independently and as part of a team in a fast-paced environment. Detail-oriented with a strong commitment to quality and compliance.

Role & responsibilities Creates and implements company quality standards at Loan License sites. Accomplishes quality assurance objectives by monitoring, reviewing, and enforcing policies and procedures at all sites. Trains and motivates employees to ensure that quality standards are met. Achieves quality assurance operational objectives by contributing to information analysis. Meets financial objectives by estimating requirements, preparing annual budgets, and scheduling expenditures. Develops quality assurance plans by conducting hazard analyses and monitoring procedures. Validates quality processes by establishing product specifications and quality attributes. Assists in the recruiting process. Maintains and improves product quality by completing product, company, system, and compliance audits. Prepares quality documentation and reports by collecting, analyzing, and summarizing information and trends.

Company Description Shiva Testing & Research Laboratory Private Limited is a NABL and ISO 9001:2015 approved testing laboratory located in Baddi, Distt Solan (H.P.). We provide comprehensive testing facilities for Geo Tech investigation work, building materials including coarse and fine aggregates, admixtures, building bricks, paver blocks, soil and earth fill material. Our services also cover highway materials such as bitumen, emulsion, job mix formula, and mix design within the laboratory. Role Description This is a full-time role for a Civil Surveying Draftman. In this on-site position located in Baddi, the Civil Surveying Draftman will be responsible for creating technical drawings and engineering designs, preparing civil engineering drafting, and producing accurate engineering drawings using Computer-Aided Design (CAD) software. Daily tasks will require close collaboration with engineers and other team members to ensure all designs meet project specifications. Qualifications Civil Engineering Design and Technical Drawing skills Proficiency in Engineering Drawings and Civil Engineering Drafting Experienced in using Computer-Aided Design (CAD) tools Excellent attention to detail and accuracy Ability to work collaboratively within a team Strong organizational and time-management skills Bachelor's degree or Diploma or equivalent in Civil Engineering field.

Oversee clinical operations, staff duties, patient care, training, quality control, emergency protocols, and compliance. Ensure Ashtavaidya tradition, adopt new methods, manage audits, optimize resources, and uphold treatment excellence.

Programming, configuring, testing, and commissioning PLC and HMI systems for industrial automation projects.

A leading client of Empower Resources requires SCM- Head for a manufacturing company Key Responsibilities:1. Procurement Strategy & Execution Develop and implement procurement policies, procedures, and strategies. Lead sourcing initiatives to ensure cost-effective and timely purchasing. Negotiate major contracts and manage supplier relationships. Monitor procurement KPIs (cost savings, vendor performance, etc.). 2. Supply Chain Planning Design and oversee end-to-end supply chain operations including demand forecasting, supply planning, and inventory control. Optimize supply chain networks to reduce lead times and costs. Coordinate with production, sales, and finance to ensure alignment with business goals. 3. Vendor Management Identify, evaluate, and onboard key suppliers and service providers. Conduct regular supplier audits and performance reviews. Develop strategic partnerships and mitigate supplier risks. 4. Logistics and Distribution Oversee inbound and outbound logistics. Ensure cost-effective and timely delivery of goods. Manage warehousing, transportation contracts, and 3PL relationships. 5. Compliance & Risk Management Ensure adherence to local and international procurement regulations. Mitigate risks in sourcing and logistics through strategic planning. Drive sustainability and ESG compliance in supply chain operations. 6. Team Leadership Lead, mentor, and develop the SCM and procurement team. Build a high-performance culture with strong accountability and collaboration. Foster cross-functional coordination with other departments. Required Qualifications: Education: Bachelors degree in Engineering, Commerce, or Supply Chain Management. MBA or PGDM (preferably in Operations or Supply Chain) is highly desirable. Certifications: Additional certifications like CSCP (Certified Supply Chain Professional), CPSM (Certified Professional in Supply Management), or Six Sigma are advantageous. Experience: Years of Experience: 20+ years, with at least 5+ years in a leadership role in Procurement and SCM. Industry Exposure: Manufacturing, FMCG, Automotive, Pharma, Retail, Proven track record in strategic sourcing, cost reduction, and vendor management. Experience with ERP systems (e.g., SAP, Oracle) and data-driven decision-making. Key Skills: Strategic sourcing and negotiation Supply chain analytics and planning Logistics and inventory optimization Strong leadership and people management Stakeholder and vendor relationship management Risk and compliance management Excellent communication and analytical skills Interested candidate can mail their resume at jayvardhan@empowerresources.in A leading client of Empower Resoruces requries

Provide day-to-day support to the Purchase Head in scheduling meetings, preparing reports, and coordinating with internal and external stakeholders Proficiency in MS Office (Excel, Word, PowerPoint); SAP knowledge is a must Required Candidate profile Graduate in any discipline; preference for candidates with a background in supply chain or commerce experience in a similar role preferably in a procurement or supply chain environment

Profile: Tig Welder || Mig Welder Location: Baddi Himachal Pradesh Experience: 1-2 years Salary: 13500 per month+ Pf/Esi+ Accomodation Responsibilities: Material preparation: This includes cutting, grinding, and shaping metal pieces to fit properly and removing impurities. Setting up equipment: Welder will assist in preparing welding equipment, including setting up machines, selecting the correct electrodes or filler metals, and ensuring proper ventilation. Welding tasks: They will perform all welding tasks under the supervision of experienced welders and Fitters. Quality control: Welders will have to inspect welds for flaws and ensure they meet quality standards. Following safety guidelines: They must always follow safety procedures, wear appropriate personal protective equipment (PPE), and maintain a safe work environment. Maintaining equipment: They will clean and maintain welding equipment and tools. Keeping the workspace clean: They will contribute towards maintaining a clean and organized workspace. Moving Material & Equipment: They may be tasked with moving materials and equipment to other sections. Collaborating with team members: They will work collaboratively with other team members to complete projects on time and to the required standards. Communication: They will communicate with supervisors and other team members to ensure projects are completed efficiently. Interested candidates can call on 7011867274 or share your resume Job Types: Full-time, Permanent Pay: ₹13,500.00 per month Benefits: Health insurance Provident Fund Schedule: Weekend availability Supplemental Pay: Overtime pay Experience: TIG welding: 1 year (Required) MIG welding: 1 year (Preferred) 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 Officer Vacancy : 1 Position Location : Baddi CTC : Best in market, Negotiable as per current package Exp : 3 to 5 years in HPLC 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 - ₹300,000.00 per year Benefits: Leave encashment Paid sick time Paid time off Provident Fund Education: Bachelor's (Preferred) Location: Baddi, Himachal Pradesh (Preferred) Work Location: In person

Job Profile- Purchase Executive Job Location- Baddi (Field job) Location- Company based in Ludhiana Experience required- Min. 1 year in field job Salary- 20-22k (Negotiable) + Petrol Expenses Gender- Male Age- 22 to 50 Qualification- School Pass Timings- 9AM to 6PM Note:- Local Baddi candidates will be preferred Candidate must have his own vehicle Candidates with Sales or Marketing Experience can also apply Interviews will be conducted virtually Job Description- Visit factories and scrap dealers in Baddi and nearby areas * Find places where LDPE / LLDPE plastic film scrap is available * Talk to vendors and fill their details in a simple mobile form (Google Form) * Fix meetings for the company owner with good vendors * Go with the owner once a week to meet vendors * Re-visit the vendor if: * Scrap needs checking before sending * Vehicle loading support is needed "What You Don’t Need to Do * No rate negotiation – boss will do this himself * No work related to payment or unloading – office staff will do that * No computer or office work – only field visits and lead filling" Job Type: Full-time Pay: ₹20,000.00 - ₹22,000.00 per month Schedule: Day shift Work Location: In person Application Deadline: 12/07/2025