40 Jobs in Nālāgarh

Coordinating communication between MD and team. Keeping daily monitoring on the mails received, their response time, and pending assigned tasks. Communication and following up with team of managers and report back to MD daily. Coordination of travel planning for the MD. Competencies Required Excellent written and verbal communication skills Confidence in Public Speaking Good Interpersonal Skills Problem Solving Skills Cross Cultural Sensitivity Learning attitude Strategic thinking Efficiency in Microsoft Word, Excel & PowerPoint Job Type: Full-time Pay: ₹250,000.00 - ₹264,000.00 per year Ability to commute/relocate: Nalagarh, Himachal Pradesh: Reliably commute or planning to relocate before starting work (Required) Language: English (Required) Work Location: In person

Company type : Waste water treatment company Education : MSC(Chemistry) Experience : 0-5 Years Location : Nalagarh CTC :5 LPA Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Work Location: In person

Key Activities Safety, Quality & Compliance  Enforce EHS protocols and conduct regular safety audits and training.  Ensure adherence to SOPs, ISO standards, and internal quality benchmarks.  Lead incident investigations and implement corrective actions. Production & Process Excellence  Execute daily production plans and ensure timely booking in ERP (e.g., SAP).  Monitor batch processing, line performance, and troubleshoot deviations.  Drive Lean Manufacturing practices and implement Root Cause Analysis (RCA) for process optimization.  Ensure established Operational process are implemented  Ensure procedures and practices for smooth plant operation in co-ordination with stakeholders like maintenance, Quality, Dispatch & Stores in relevant shifts. Utility & Infrastructure Oversight  Knowledge about compressors, DM plants, DG sets and effluent treatment systems would be an added advantage  Monitor energy and water usage, and support sustainability targets.  Ensure CIP usages, WIP management to reduce waste generation & effect on environment  Ensure smooth Effluent Treatment Plant Operation and Control effluent discharges from process, identify & implement techniques to improve various processes. Documentation & Reporting  Maintain accurate records for ISO, GMP, and statutory audits.  Circulate daily MIS reports and track KPIs including OEE, yield and downtime.  Support digital transformation initiatives for real-time data visibility. Team Leadership & Collaboration  Plan and manage manpower allocation, shift rosters, and leave schedules.  Mentor operators and contract staff; conduct performance reviews and skill assessments.  Collaborate with cross-functional teams (Quality, Maintenance, Stores, HR) to resolve operational challenges. Continuous Improvement & Innovation  Lead Kaizen projects and drive cost reduction through process improvements.  Support trials for new formulations, packaging, and equipment upgrades.  Promote a culture of innovation and accountability across shifts.  Lead actively Continuous Improvement activities in the plant through sub-team involving DMC & Contract workers and train them time to time as required  Ensure set KPI’s are met by self & team (operators)  Encourage adoption of digital tools for production monitoring, predictive maintenance, and real-time analytics to improve decision-making and reduce downtime.

We are hiring for QA- Officer for Nalagarh(Himachal Pradesh) Location Minimun Exp Required 2 Years Candidate must have exp in QMS Qualification-Bsc/Msc/B.pharm/M.phar Preferred API Background Job Type: Full-time Pay: ₹15,000.00 - ₹32,000.00 per month Application Question(s): Is your Qualification is Bsc/Msc/B.pharm/M.phar? Experience: Pharmaceutical: 2 years (Preferred) Work Location: In person

Job Opening: MBBS Doctor (Part-time/Full-time) – Jalandhar We are looking for an MBBS registered doctor with a minimum of 2 years of clinical experience for our healthcare operations in Jalandhar . Requirements: MBBS degree with valid registration (MCI/State Medical Council) Minimum 2 years of experience Good patient-handling and clinical skills Location: Jalandhar Type: [Specify – Full-time / Part-time / Visiting] Remuneration: As per industry standards Documents Required: Resume MBBS Degree & Registration Certificate Experience Certificates ID & Address Proof 9560138792 Job Type: Part-time Pay: ₹10,000.00 - ₹12,000.00 per month Benefits: Paid sick time Paid time off Work Location: In person

Knowledge of Electrical panels, Injection Molding Machine maintenance, 5s, Safety, Basic knowledge of IATF audits and ISO Audits, Monthly PM and report, Training. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹32,000.00 per month Benefits: Leave encashment Provident Fund Work Location: In person

Job Description Head of Quality Assurance (Pharma)Position: Head – Quality Assurance (QA) Department: Quality Assurance Reports To: Managing Director / Plant Head / VP – Quality Location: Nalagrah HP Role Summary The Head of Quality Assurance is responsible for leading the QA function to ensure that all pharmaceutical products are manufactured in compliance with cGMP, regulatory guidelines (USFDA, EMA, MHRA, WHO, CDSCO, etc.) , and company quality standards. This role oversees quality systems, documentation, audits, training, compliance, and continuous improvement initiatives to maintain a state of inspection readiness at all times. Key Responsibilities Quality Systems & Compliance Establish, implement, and monitor Quality Management Systems (QMS) in line with global regulatory requirements. Ensure compliance with ICH, WHO, USFDA, EMA, MHRA, CDSCO, and other regulatory guidelines . Oversee change control, deviations, CAPA, OOS/OOT, risk management, and product quality reviews . Documentation & Records Approve SOPs, Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs) , and quality policies. Maintain data integrity and electronic documentation compliance. Audits & Inspections Prepare the site for regulatory and customer audits/inspections . Lead internal audits and vendor audits; ensure timely closure of audit findings. Team Leadership & Training Lead and mentor the QA team, ensuring continuous training on GMP and quality standards. Foster a culture of compliance, integrity, and continuous improvement. Product Quality & Release Ensure timely review and approval of batch manufacturing and analytical documents. Authorize batch disposition/release in compliance with regulatory requirements. Cross-functional Collaboration Work closely with Production, QC, R&D, Supply Chain, and Regulatory Affairs teams. Provide QA support for technology transfer, validation, and new product launches . Continuous Improvement & Risk Management Drive initiatives for operational excellence and quality improvements. Implement Quality by Design (QbD) and risk-based approaches in manufacturing. Qualifications & Experience Education: M. Pharm / B. Pharm / M.Sc. (Chemistry / Biotechnology / Microbiology). Experience: Minimum 15+ years in Quality Assurance/Quality Control in the pharmaceutical industry, with at least 5 years in a leadership role . Strong knowledge of global regulatory requirements (USFDA, EU, MHRA, WHO, TGA, CDSCO, etc.) . Proven experience in handling regulatory inspections and audits . Excellent leadership, communication, and decision-making skills. Key Competencies Strong understanding of cGMP, GLP, GDP . Leadership and people management. Analytical thinking and problem-solving. Strategic planning and execution. Inspection readiness and compliance mindset. Job Type: Full-time Pay: ₹80,000.00 - ₹90,000.00 per year Benefits: Food provided Health insurance Provident Fund Work Location: In person Speak with the employer +91 7657867748

Shiva International is a growing organization committed to delivering high-quality products and services to our clients worldwide. We believe in innovation, integrity, and excellence in everything we do. To strengthen our quality standards, we are looking for a dedicated and detail-oriented Quality Analyst to join our team. Job Type: Full-time Pay: ₹11,830.39 - ₹15,000.00 per month Work Location: In person Speak with the employer +91 7018951077

Knowledge about SAP, GRN, Gate Entry, cash handling Job Types: Full-time, Permanent Pay: ₹14,000.00 - ₹18,000.00 per month Benefits: Leave encashment Provident Fund Language: English (Preferred) Work Location: In person

Key Responsibilities: Coordination and Scheduling: Organizing and scheduling deliveries, pickups, and service appointments, often using transportation management software. Communication: Maintaining clear communication with drivers, customers, and other relevant parties regarding delivery details, schedules, and any potential issues. Route Optimization: Planning and optimizing delivery routes to ensure efficiency and minimize delays. Issue Resolution: Addressing and resolving any problems that arise during the dispatch process, such as traffic delays, vehicle issues, or customer inquiries. Record Keeping: Maintaining accurate records of all dispatched orders, driver information, vehicle maintenance, and other relevant data. contact-9812001068 Job Type: Full-time Pay: ₹25,000.00 - ₹30,000.00 per month Work Location: In person

Job Title: Manufacturing Excellence (ManEx) Officer Location: Nalagarh ICD Reports To: Factory Manager Job Purpose: To lead the governance and performance of Manufacturing Excellence systems including the Unilever Management System (UMS), SU League KPIs, TPM deployment, and Digital Transformation Index (DTI), ensuring the factory operates with high efficiency, digitization, and compliance. Key Responsibilities: UMS (Unilever Management System) Governance Coordinate all 10 UMS pillars (AM, PM, FI, EEM, Safety, Quality, PD, CSL etc. Facilitate monthly reviews with pillar leads and maintain audit readiness Track pillar maturity, visual management, and document compliance SU Factory League Performance Own and report KPIs like OEE, CPT, QI, OR, Energy, Waste, Inventory, SRS Drive monthly governance reviews to track score improvements Ensure accuracy and on-time data submission for Power BI dashboards DTI (Digital Transformation Index) Execution Manage DTI roadmap including Adoption (DFOS, EMS, SPC, etc.), VC creation, Deployment OTIF, and Capability Track scoring, implementation, and compliance with business group expectations Collaborate with digital enabler leads to close gaps TPM & OEE Management Support deployment of TPM tools across pillars (AM, PM, FI, EEM) Examine line losses, drive kaizens, and lead OEE improvement programs Track daily/weekly OEE performance, loss tree and RCA actions Capability Building Maintain and track training plans for factory teams Conduct workshops, drive kaizen engagement, and promote shopfloor ownership Foster digital and lean culture through structured rollout of tools Key Metrics: SU League Score > 90 DTI Score in Green Zone (across 4 pillars) OEE > 81% Audit and Pillar Maturity Scores Required Qualifications: B.E./B.Tech. in Mechanical, Electrical, or Industrial Engineering 2–5 years’ experience in manufacturing excellence, TPM, or digital systems Proficiency in Power BI, Excel, and manufacturing systems TPM/UMS exposure and cross-functional coordination ca

Key Responsibilities Executive Support: Own the Director’s calendar, e-mail, calls and daily briefing notes; anticipate needs and prioritise requests. Communication Hub: Draft letters, presentations, MIS reports and investor/ customer correspondence in clear, professional English. Meeting & Travel Management: Schedule internal / external meetings, prepare agendas, record minutes, and arrange domestic & international travel logistics. Project Tracking: Monitor action items for ongoing projects (plant upgrades, ISO initiatives, wellness-retreat spin-offs, etc.) and chase deadlines across departments. Stakeholder Liaison: Act as the first point of contact for senior clients, vendors, auditors and government bodies; maintain absolute discretion with sensitive information. Office Coordination: Oversee small administrative tasks—stationery, visitor arrangements, expense claims—ensuring the Director’s office runs like clockwork. Job Type: Full-time Pay: ₹30,000.00 - ₹45,000.00 per month Benefits: Cell phone reimbursement Commuter assistance Health insurance Internet reimbursement Life insurance Paid sick time Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Nalagarh, Himachal Pradesh: Reliably commute or planning to relocate before starting work (Preferred) Experience: PA: 5 years (Required) Location: Nalagarh, Himachal Pradesh (Required) Work Location: In person

We are hiring for Chiller operator having exp of 2 Years Location: Nalagarh Experience: Minimum 200 TR chiller system Job Type: Full-time Pay: ₹8,493.67 - ₹29,475.15 per month Application Question(s): What is your salary? Do you have exp. in Minimum 200 TR chiller system? Experience: Ciller Operation: 1 year (Preferred) Work Location: In person

Quality Control (QC) Roles and Responsibilities 1. Inspection and Testing Inspect raw materials, in-process components, and final products. Perform routine tests to ensure products meet specifications. Use instruments like calipers, micrometers, spectrometers, etc., as needed. 2. Documentation and Reporting Maintain detailed records of inspections, test results, and deviations. Document and report non-conformities or quality issues. Generate inspection reports, certificates of analysis (COA), and quality logs. 3. Compliance and Standards Ensure products comply with company standards, regulatory requirements (e.g., ISO, GMP, FDA), and customer specifications. Participate in audits and quality reviews. 4. Root Cause Analysis Investigate the root cause of defects or process deviations. Assist in implementing corrective and preventive actions (CAPA). 5. Process Monitoring Monitor production processes to ensure consistency and repeatability. Work closely with production teams to minimize defects and rework. 6. Calibration and Equipment Maintenance Ensure measuring and testing equipment is calibrated and maintained. Keep records of equipment calibration schedules and certificates. 7. Training and Guidance Train production staff on quality standards and inspection procedures. Promote awareness of quality requirements across departments. 8. Continuous Improvement Suggest process improvements to enhance product quality. Participate in Six Sigma, Lean, or Kaizen initiatives where applicable. 9. Safety and Hygiene Ensure QC operations are carried out safely and hygienically (especially in pharma/food industries). Report unsafe practices or equipment malfunctions. 10. Sample Collection and Handling Collect and label samples for lab testing. Ensure proper storage, handling, and transport of test specimens. Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹70,000.00 per month Benefits: Food provided Paid sick time Paid time off Provident Fund Schedule: Day shift Work Location: In person

Role: Production Chemist (Liquid/Injection) – ApprovedKey Responsibilities: Batch Manufacturing: Execute batch manufacturing and filling operations for liquid and injectable formulations as per GMP guidelines. Ensure adherence to approved Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs). Documentation & Compliance: Maintain accurate and timely documentation of production activities. Ensure compliance with regulatory norms (e.g., WHO, GMP, FDA) and in-house quality standards. Line Clearance & Area Monitoring: Coordinate with QA/QC for line clearance and maintain hygiene and environmental conditions in manufacturing areas. Ensure proper cleaning and sanitization of production areas and equipment. Equipment Handling: Operate, calibrate, and monitor equipment used in the production of liquids and injections (e.g., mixing vessels, filtration systems, filling machines, autoclaves). Report any deviation or malfunction to the production head or engineering team. Material Management: Ensure availability of raw materials, excipients, and packaging materials before batch initiation. Coordinate with stores and planning departments for material requisition and reconciliation. In-process Checks: Perform in-process checks during production (pH, volume, visual inspection, etc.). Take necessary corrective actions in case of deviations. Training & Safety: Follow safety protocols and ensure team compliance with PPE usage and hazard guidelines. Participate in training programs related to GMP, equipment handling, and SOP updates. Regulatory Readiness: Prepare documentation and support audits (internal, regulatory, and client). Ensure traceability and compliance in all production-related activities. Job Types: Full-time, Permanent Pay: ₹15,628.89 - ₹30,837.90 per month Benefits: Food provided Paid sick time Paid time off Provident Fund Schedule: Day shift Work Location: In person

Roles and Responsibilities: 1. Manufacturing Operations: Supervise and execute day-to-day manufacturing activities for liquid or injectable dosage forms as per production plan. Operate, monitor, and troubleshoot machines like Liquid Filling, Sealing, Autoclave, Sterilizers, Vial Washing Machines, Ampoule/Vial Filling Lines, etc. Ensure batch processing is done as per Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs) . Monitor cleanroom conditions and ensure aseptic practices are followed during injectable production. 2. Documentation & Compliance: Prepare and maintain accurate production-related documentation like BMR, logbooks, equipment usage logs, cleaning records , etc. Ensure Good Manufacturing Practices (GMP) , Good Documentation Practices (GDP) , and regulatory norms (e.g., WHO-GMP, USFDA, EU-GMP) are followed. Participate in self-inspections, audits , and implementation of CAPA (Corrective and Preventive Actions). 3. Quality & Safety: Coordinate with QA/QC for in-process quality checks , sampling, and line clearance. Ensure proper cleaning, sterilization, and validation of equipment and area before and after batch production. Identify and report deviations, OOS (Out of Specification), and OOT (Out of Trend) to the QA department. Follow all EHS (Environment, Health & Safety) protocols strictly, including the use of PPE. 4. Inventory & Material Handling: Monitor and request raw materials, packaging materials, and consumables as per production requirements. Ensure correct dispensing, usage, and reconciliation of materials. Maintain inventory of critical spares, tools, and equipment. 5. Team Coordination & Training: Coordinate with engineering, QA/QC, warehouse, and other departments for smooth production flow. Guide and supervise operators and workers under the shift. Participate in training sessions related to GMP, machine operation, safety , and SOPs . Job Types: Full-time, Permanent Pay: ₹15,586.79 - ₹25,778.31 per month Benefits: Food provided Paid sick time Paid time off Provident Fund Schedule: Day shift Work Location: In person

Job Responsibilities;- Control manufacturing activities in the respective section to ensure activities carried out are as per requirement of cGMP & safety to meet the quality and manufacturing targets in time. I. Monitor and control planned production by daily activity review as per production plan to meet production targets and quality standards II. Ensure maintenance is carried out as per standards to realise optimum utilisation of manufacturing consumables III. Prepare, review and update GMP documents to meet regulatory compliance and quality of product IV. Ensure adequate and trained manpower availability across shifts to ensure production continuity V. Monitor employee and workplace safety to maintain safe environment VI. Implement management initiatives and manufacturing excellence practices for continuous improvement Educational Qualification M.Sc /B.Pharm / M.Pharm intrested candidates can send your cv hrsupport@prgpharma.com Job Type: Full-time Pay: ₹70,000.00 - ₹90,000.00 per year Schedule: Day shift Work Location: In person

We are Hiring for ETP Executive having Min 2 Years of Experience in API Pharma Job Type: Full-time Pay: ₹251,298.03 - ₹522,635.64 per year Benefits: Health insurance Provident Fund Schedule: Day shift Application Question(s): What is your Salary? Do you have exp of API Pharma? Work Location: In person

Key Responsibilities Conduct microbiological analysis of wastewater and treated effluents, including tests for coliforms, E. coli, Legionella, and other pathogens. Perform routine microbial testing such as bacterial counts and coliform testing to ensure compliance with quality standards. Develop and maintain microbiological monitoring programs for water maintenance and treatment operations. Identify microbial trends in treated water systems and recommend corrective measures to optimize water filtration efficiency. Support the design and implementation of disinfection protocols in industrial water treatment systems. Prepare detailed microbiological reports for internal stakeholders and external clients in the water purification sector. Ensure laboratory equipment is properly maintained, calibrated, and operated in line with regulatory standards. Experience - 2 to 5 years Education : M.Sc. - Microbiology Salary - 2 to 3.5 LPA Location : Nalagarh Conduct research on advanced microbiological methods and technologies for improving commercial water purification systems. Adhere to health, safety, and environmental guidelines in all laboratory and field activities. Provide training to junior staff on microbiological testing methods and best practices Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Work Location: In person

We are hiring a Machine Operator experienced in operating IBM(Injection Blow Moulding ) and EBM (Extrusion Blow Molding) machines. The ideal candidate will be responsible for running, monitoring, and maintaining, and maintaining blow holding machines to ensure efficient and high-quality production. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹40,000.00 per month Benefits: Cell phone reimbursement Paid time off Provident Fund Schedule: Day shift Morning shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Yearly bonus Work Location: In person

Company Name: Elfin drugs Pvt Ltd Location: Nalagarh Himachal Salary: 8000-12000 Experience: Fresher Qualification: ITI / 12th Pass (Preferred: Mechanical, Fitter, Electrician, etc.) Shift: Rotational / Day-Night Industry: Pharmaceutical / Manufacturing Roles and Responsibilities: Operate and monitor machinery as per standard operating procedures (SOPs). Ensure machines are running efficiently with minimal downtime. Assist in machine setup, loading/unloading materials, and basic maintenance tasks. Maintain cleanliness and hygiene of the working area and equipment. Report any malfunction or deviation to the supervisor immediately. Follow safety protocols and wear proper PPE while on duty. Maintain daily production records and logs. Work as part of a team to meet production targets. Follow instructions from seniors and quality control teams. Willing to learn and grow under guidance. Key Skills Required: Basic understanding of machinery operation Ability to read and follow instructions Discipline and punctuality Teamwork and adaptability Willingness to learn and work in shifts Job Types: Full-time, Permanent Pay: ₹8,123.49 - ₹13,976.39 per month Benefits: Food provided Paid sick time Paid time off Provident Fund Schedule: Day shift Work Location: In person

Himachal Pradesh, Nalagarh Plant, Himachal Pradesh, India Department Employee Resource Management (HP) Job posted on Apr 21, 2025 Employment type Blue Collar Job Summary: TVS Motor Company is looking for dynamic and hardworking trainees to join our production team. The trainees will be responsible for assembling two-wheeler and three-wheeler vehicles, inspecting products, and ensuring quality standards are met as per company guidelines. Key Responsibilities: Assembly Work: Perform assembling of two-wheeler and three-wheeler products as per the standard operating procedures. Inspection: Conduct pre- and post-assembly checks to ensure vehicles meet production specifications. Quality Assurance: Identify defects and report any deviations from quality standards. Process Compliance: Adhere to safety and operational guidelines in the production line. Team Coordination: Work collaboratively with supervisors and team members to achieve production targets.

1. Material Planning & Procurement Support Forecasting the requirement of packing materials based on production plans. Ensuring timely availability of approved packing materials. Coordinating with the purchase department for ordering materials from approved vendors. 2. Incoming Material Inspection & Quality Check Conducting visual and physical inspection of all incoming packing materials (e.g., blister packs, cartons, labels, inserts, outer boxes, seals, etc.). Sampling and sending materials for quality testing. Handling rejected, damaged, or non-conforming materials as per SOPs. 3. Material Storage & Handling Proper storage of packing materials following GMP guidelines. Segregating and labeling different batches for easy identification. Maintaining inventory using FIFO (First In First Out) or FEFO (First Expiry First Out) system. 4. Documentation & Record Keeping Maintaining accurate records like Goods Receipt Note (GRN), Inspection Reports, Release Notes, etc. Tracking materials according to the Bill of Material (BOM). Issuing material slips and maintaining consumption records. Ensuring traceability and batch-wise material reconciliation. 5. Line Clearance & Material Issuance Issuing the correct packing materials to the production floor as per batch requirements. Conducting line clearance along with QA before the start of any packing process. Performing reconciliation of issued, consumed, and returned materials after batch completion. 6. Compliance & Audit Readiness Following Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). Ensuring readiness for regulatory audits such as USFDA, MHRA, WHO, EU GMP, and customer audits. Participating in handling deviations, change controls, CAPA, and other quality events related to packing materials. 7. Vendor Management & Development Supporting the qualification and periodic evaluation of packing material vendors. Assisting in new vendor development and approval processes in coordination with QA and purchase teams. 8. Cost Control & Waste Management Optimizing the use of packing materials to minimize waste. Managing the disposal of damaged, obsolete, or expired packing materials in compliance with SOPs. Contributing to cost-saving initiatives without compromising quality. Key Packing Materials in the Pharmaceutical Industry: Primary Packaging: Blisters, Alu-Alu, Bottles, Tubes, Vials, Ampoules Secondary Packaging: Cartons, Leaflets, Labels Tertiary Packaging: Outer Boxes, Stretch Films, Pallets Qualifications & Skills Required: Graduate/Diploma in Pharmacy, Science, or Packaging Technology. Good knowledge of GMP, GDP, and pharmaceutical regulatory standards. Strong documentation skills and attention to detail. Familiarity with ERP systems like SAP (preferred). Job Types: Full-time, Permanent Pay: ₹8,770.92 - ₹20,492.84 per month Benefits: Paid sick time Paid time off Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Key Roles and Responsibilities: 1. HPLC Operation & Analysis Routine operation of HPLC for raw materials, in-process, finished products, and stability samples. Method development and validation as per pharmacopeia or client requirements (if applicable). Troubleshooting HPLC instruments and resolving minor errors. Calibration and qualification of HPLC instruments as per schedule. 2. Sample Management Receiving, labeling, and maintaining records of incoming samples. Performing chemical and instrumental analysis of raw materials, intermediates, and finished goods. Maintaining proper documentation of sample testing, observations, and results. 3. Documentation & Compliance Preparation and review of Standard Operating Procedures (SOPs), test procedures, and calibration protocols. Ensuring all testing is done as per GMP, GLP, and regulatory compliance. Proper entry of data in analytical records, logbooks, and electronic systems (if any). 4. Quality Assurance Support Investigate out-of-specification (OOS) and out-of-trend (OOT) results related to HPLC testing. Supporting deviation handling, change control, and CAPA related to QC activities. 5. Equipment Maintenance Performing routine preventive maintenance of HPLC and other QC instruments. Coordinating with service engineers for major repairs and breakdowns. 6. Training & Development Training new joiners or junior analysts on HPLC operation and lab safety practices. Continuously updating self on regulatory guidelines, pharmacopeial updates, and new technologies. 7. Regulatory & Audit Compliance Ensure readiness for regulatory audits like USFDA, MHRA, WHO, or client audits. Participate in internal audits and implement corrective actions. 8. Safety & Housekeeping Following all lab safety protocols. Maintaining cleanliness and orderliness of the QC lab area. Preferred Skills and Qualifications: B.Sc / M.Sc in Chemistry, Pharmaceutical Sciences, or equivalent. 2-5 years experience in QC department with hands-on experience in HPLC operation. Familiarity with software like Empower, LabSolutions, or Chromeleon (if applicable). Knowledge of regulatory requirements (GMP, GLP). Job Types: Full-time, Permanent Pay: ₹16,745.43 - ₹30,694.27 per month Benefits: Paid sick time Paid time off Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Handle both sales executives and marketing executives work towards the same goal of increasing a company’s revenue, there are some key differences in their roles and responsibilities. A sales executive’s main objective is to deal with consumers and clients to sell products and services, generating revenue and achieving or exceeding sales targets. On the other hand, a marketing executive develops and implements marketing strategies, advertising the business’s goods and services and raising brand recognition. Job Types: Full-time, Permanent Pay: ₹11,000.00 - ₹15,000.00 per month Benefits: Cell phone reimbursement Provident Fund Compensation Package: Performance bonus Schedule: Day shift Weekend availability Experience: total work: 1 year (Preferred) Work Location: In person