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2.0 - 7.0 years

3 - 7 Lacs

Baddi

Work from Office

QC Testing,HPLC,RP, Stability,GLP

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7.0 - 12.0 years

35 - 50 Lacs

Baddi

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Job Summary We are looking for an individual for the SIT Team to oversee the investigation of major and critical deviations, working closely with Cross-Functional Team (CFT) members to identify root causes and implement corrective and preventive actions. The role involves active participation in investigating Out of Specification (OOS) cases, ensuring accurate classification in the DCMS deviations log, and providing support during regulatory inspections. Roles & Responsibilities • You will be responsible for overseeing the investigation of major and critical deviations from the outset, collaborating closely with Cross-Functional Team (CFT) members to identify root causes, corrective actions (CA), preventive actions (PA), and preparing comprehensive reports. Your will also be working on the trending of the deviations and identification of adequate action items for reduction of the same. • Your role involves active participation in investigating OOS (Out of Specification) and other relevant cases, working closely with CFT members to determine root causes, CA, PA, and report writing. • You will review minor and critical , providing constructive feedback for improvement. • Your responsibilities include periodically assessing the trending of minor deviations, highlighting or escalating key observations, regularly reviewing the deviations log to ensure accurate classification, and utilizing the Rubrics template for crafting investigation reports. • You will offer necessary support to the site in readiness for or during regulatory inspections related to investigations. Qualification Educational qualification: A Bachelor's or Master's degree in a relevant scientific field, such as Chemistry, Biochemistry, Pharmacy, or related discipline Minimum work experience : 7 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance Skills & attributes: Technical Skills • In-depth knowledge and experience in overseeing investigations, and familiarity with root cause analysis, corrective actions (CA), and preventive actions (PA). • Expertise in investigating valid OOS and other relevant cases. • Familiarity with reviewing deviations / OOS log and ability to perform classification of data. • Ability to craft comprehensive investigation reports. • Experience in providing necessary support for regulatory inspections related to investigations. • Knowledge of regulatory requirements pertaining to deviations investigations. Behavioural Skills • Ability to collaborate closely with CFT members. • Analytical mind set for identifying root causes and developing effective solutions. • Strong problem-solving skills and attention to detail in reviewing deviations, reports, and trending data and implementing corrective actions. • Effective communication skills for report writing and escalation of key observations. • Commitment to ensuring compliance with regulatory requirements in investigations. • Ability to offer necessary support to the site in readiness for or during regulatory inspections. Additional Information looking someone with strong QC Microbiological investigation background. Should have exp in Microbiological compliance. Education :M.Sc. Microbiology Exp : 8-10 Years Industry : Injectable preferred/ OSD will be second preference Person will be responsible to manage 3 sites Microbiological compliance at Baddi

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1.0 - 7.0 years

3 - 9 Lacs

Panipat, Noida, Baddi

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Safety Officer Candidate would be responsible for all safety related activities at site for Fired Heater / Piping related projects in Refineries or similar locations. Job Includes : Handling all the safety issues at site. Coordination with client, consultant and company head office. Safety Reporting Tool Box Talks Any other activity required to ensure safe work at site as per client requirements. Desired Candidate Profile : Recognized degree or diploma in any branch of Engineering or Graduation Degree in Science and Advance Diploma in Industrial Safety. (from any Indian institutes recognized by AICTE or state Council of Tech. Education of any Indian State) with practical experience of working in a building, plant or other construction works (as Safety Officer) for a period of not less than ten years.

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0 years

0 Lacs

Baddi, Himachal Pradesh, India

On-site

Company Description Chitkara University Himachal Pradesh is located in Baddi, India. Join us in our mission to foster research and innovation in the field of education. Role Description PhD Research Scholar at Chitkara University Himachal Pradesh. The role involves conducting research, writing papers, collaborating with faculty members, attending seminars, and contributing to the academic community. Qualifications Research and analytical skills Strong writing and presentation abilities Ability to work collaboratively with a team Experience in academic research Strong background in the relevant field of study Effective time management and organizational skills Excellent academic record M. Pharm. (Preferably with GPAT qualified)

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12.0 - 18.0 years

10 - 20 Lacs

Rudrapur, Baddi, Delhi / NCR

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Overseeing the quality assurance function at our manufacturing sites located in Baddi & Rudrapur. Ensure that all products manufactured at the sites adhere to the required quality standards, regulatory requirements, and internal procedures. Required Candidate profile M.Sc/B.Pharm/M.Pharm 12+ year QA experience in a regulated pharma/CDMO environment Strong knowledge of cGMP, ICH & regulatory guidelines Hands-on experience in audits, documentation, quality systems

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0.0 - 2.0 years

0 - 2 Lacs

Baddi, Chennai, krinagiri

Work from Office

ONLY DIPLOMA CANDIDATES SHOULD APPLY. NO B TECH's JOB Location- Mumbai/Pune/Krishnagiri/Bengaluru/Chennai/Tamil Nadu/Baddi NOTE : Candidates who are flexible with working in different shifts and are open to relocation should apply. SALARY- 2,66,000/- Detailed Job Description: Role & responsibilities 1. Routine Plant Operations & Records 2. Issue Identification & Escalation Adherence to industrial safety practices during operations & maintenance procedures. Ensuring optimal operations of all equipment (Pre-treatment generation, storage & distribution) following prescribed SOPs. Preparation and maintenance of comprehensive reports & records including log-sheets, Chemical consumption Records, and PM Record. Monitoring utility and feed water parameters to ensure they comply with specified limits. Verification of sensor calibration using test kits. Coordination with the QC team for sampling and analysis. Conducting non-critical maintenance tasks (e.g., fixing leakages) utilizing available tools. Maintaining meticulous records of operational issues as per QA documentation procedures. Participation in both classroom and hands-on trainings provided by CN & Customer to attain and sustain certifications in Plant Operations. Conducting hands-on training sessions for operators periodically and certifying their competence upon successful completion. Developing and ensuring adherence to shift schedules, including contingency management at the site. Performing essential administrative duties as scheduled (HR compliance, invoicing, payment follow-up, etc.). Preferred candidate profile Proven experience in industrial operations and maintenance within the specified field. Comprehensive knowledge of industrial safety protocols and procedures. Proficiency in interpreting and implementing standard operating procedures (SOPs). Strong analytical skills to monitor and manage utility and feed water parameters. Familiarity with calibration techniques and sensor functionality. Excellent organizational and record-keeping abilities. Capability to deliver hands-on training and assess operator competencies. Effective time-management skills with the ability to handle contingencies. Proficient in essential administrative tasks related to operations and maintenance

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1.0 - 6.0 years

4 - 6 Lacs

Ludhiana, Baddi

Work from Office

COMPANY PROFILE Brief - Delhivery is Indias leading fulfillment platform for digital commerce. With its nationwide network extending beyond 18,000 pin codes and 2,500 cities, the company provides a full suite of logistics services suchas express parcel transportation, LTL and FTL freight, reverse logistics, cross-border, B2B & B2C warehousingand technology services. Delhivery has successfully fulfilled over 550 million transactions since inception andtoday works with over 10,000 direct customers, which includes large & small e-commerce participants, SMEs, and over 350 leading enterprises & brands. Vision - Since its inception in 2011, Delhivery has become India’s leading supply chain services company. Our vision is to become the operating system for commerce in India, through a combination of world-class infrastructure, high-quality logistics operations, cutting-edge engineering, and technology capabilities. Team - Delhivery was founded in 2011 by Sahil Barua, Mohit Tandon, Bhavesh Manglani, Suraj Saharan, and Kapil Bharati and is now 40,000+ people strong. Roles and Responsibilities Ability to identify customer’s LTL/PTL requirements and clearly communicate the product offerings to match their needs. Service a geographical area/client segment to generate leads & sign new customers. Responsible for negotiation & pricing closure. Manage a portfolio of customers and potential customers via personal sales visits, using face to face contact to provide a personal service. Build a strong client relationship to ensure that the account performs and grows to its maximum potential, reducing attrition rate and minimizing opportunities for competitors to gain business. Conversion of qualified leads into customers (First Time Buyers) across Major, Small and MediumBusiness Accounts and develop and penetrate existing accounts (Retention and Development). Act as the customer’s main point of contact, by liaising closely with the relevant departments within Delhivery to ensure that their queries, problems or issues are dealt with appropriately. Monitor the health of accounts, service levels and enhace SOW growth. Prepare and present weekly/monthly reports detailing sales achieved and those predicted against targets. To continually develop knowledge of Delivery’s products/services and general commercial awareness to provide the best possible solutions to the customers. Desired Skills and Experience Candidate should have 4-7 yrs. experience in Logistics / SCM BD Role Candidate should have excellent communication skills, good negotiation & co-ordination, market intelligence, generate business inquiries, expanding sales & ensure the profitability of the company New acquisition skills required Analytical bent of mind and good data analysis skills Willing to travel and are ready to visit as per the company ask A positive attitude and a desire to promptly resolve potential customer issues or complaints to support business growth.. Go getter and responsibility taker who will ensure that we hit monthly targets with given margins

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10.0 - 15.0 years

0 - 3 Lacs

Baddi

Work from Office

Job Title: AutoCAD Draftsman (Site-Based) Location: Baddi, Himachal Pradesh Industry: FMCG (Fast-Moving Consumer Goods) Experience: 10+ Years Qualification: B.Tech / M.Tech (Mechanical / Civil / Architectural preferred) Employment Type: Full-Time, Site-Based Job Overview: We are seeking an experienced AutoCAD Draftsman with a strong background in FMCG projects. The ideal candidate will have extensive hands-on expertise in 2D & 3D AutoCAD drafting, structural & architectural drawings, fabrication design, and machine part detailing. The role requires frequent interaction with the ongoing site project team, ensuring drawing accuracy, quality checks, and design updates in real-time. Key Responsibilities: Prepare and update 2D/3D AutoCAD drawings including layout, sectional, and architectural plans. Develop detailed as-built, fabrication, and structural drawings . Create and maintain P&ID and isometric drawings for piping and instrumentation. Assist in process-related R&D and conceptual designs. Perform floor visits for measurements, quality checks, and dimension verifications. Support the execution team during project implementation on-site. Handle machine part designs , including machining process understanding. Generate 3D interior models and prepare BOM/BOQ . Implement drawing revision control and maintain proper documentation. Use measurement tools effectively to support design and execution. Required Skills & Qualifications: B.Tech/M.Tech with minimum 10 years experience in FMCG or similar industries . Expert proficiency in AutoCAD 2D & 3D . Strong understanding of fabrication engineering , structural modifications , and machinery design . Proficient in design documentation and drawing management systems . Familiar with building codes , standards , and engineering best practices . Hands-on experience with site supervision and drawing updates . Preferred Traits: Strong attention to detail and visualization skills. Ability to work independently and collaboratively on-site. Excellent communication and coordination skills with multidisciplinary teams.

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0 years

0 Lacs

Baddi, Himachal Pradesh, India

On-site

The Job Responsibilities Of The Position Holder Include Ensure timely and compliant management of all QC documentation—including Change Controls, SOPs, Raw Data Sheets, GTPs, STPs, and Specifications—in alignment with Abbott AQD/EQD and applicable regulatory guidelines. Lead the preparation, review, and approval of SAP specifications to ensure accurate material and test parameter alignment with regulatory and internal standards. Drive timely evaluation, feasibility analysis, and risk assessment of pharmacopeial updates, ensuring seamless integration into QC systems and documentation. Conduct impact assessments of new and revised regulatory guidelines, ensuring proactive updates to QC practices and documentation. Evaluate and implement QRI actions within defined timelines, ensuring risk analysis and implementation of actions identified. Oversee analytical method validation and verification activities in compliance with ICH, USP, and internal standards, ensuring robustness and regulatory readiness. Manage QC-related activities for new product introductions and technology transfers, ensuring analytical readiness, method transfer, and documentation compliance. Lead preparation and timely closure of audit responses for internal and external audits, ensuring adherence to commitments and continuous audit readiness. Champion continuous improvement initiatives such as Lean Lab, Opti-Q, and method optimization to enhance efficiency, reduce waste, and improve data integrity. Review and approve analytical reports to ensure accuracy, completeness, and compliance with regulatory and internal quality standards. Ensure training compliance by coordinating laboratory training activities through ISOTrain, maintaining up-to-date training matrices and records.

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0 years

0 Lacs

Baddi, Himachal Pradesh, India

On-site

Followings Will Be The Responsibilities Of The Position Holder 1. Handling shift maintenance activity for Oral dosage manufacturing area. 2. To ensure compliance of GMP/GEP/GDP. 3. To ensure safety compliance as per Abbott Safety Guide lines 4. Work all shifts flexibly when job demands. 5. Diagnose malfunctioning systems, apparatus, and components, using test equipment and hand tools, to locate the cause of a breakdown and correct the problem. 6. Knowledge of PLC, SCADA, Servo Motors & Drives, control valves & switches, VFDs, Relays, and different electronic circuits, motors, star delta starters, relay, Panel & switch gear, Contractor 7. Basic Knowledge of Electrical system. 8. Knowledge of handling equipment’s with safety like applying LOTO during maintenance activity. 9. Working in collaboration with the production team to formulate the best cost-effective manufacturing process 10. Supervise electrical works when new installations are undertaken. 11. Learn new skills and attend training programs in other to increase knowledge of trends and best practices in the industry 12. Provide safe working environment for members of staff, and ensure electricity induced accidents and mishaps are prevented

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0 years

0 Lacs

Baddi, Himachal Pradesh, India

On-site

Followings will be the Core Job Responsibilities of the position holder: 1. Preparation, Issuance, Retrieval & archival of Mastet documents SOP (Forms & Records), Spec & STP (RM, SFG & FG) and other Master documents (List, SMF, VMP, Quality Manual), Master Lists. 2. DARIUS - Software Handling and Compliance 3. Master List – SOP, Spec & STPs etc. 4. Issuance of requested Uncontrolled Master documents for closure of CCP/ Exception & requested by cross function department outside the Plant for Reference Purpose. 5. Controlling of General Document Number. 6. To ensure documentation of out of specification, Exception, and Change Control. 7. To ensure the effective implementation of QMS through SolTRAQs application system. 8. To ensure the effective artwork through harmony. 9. Preparation of Maximum Retail Price List. 10. Annual Product Quality Review –Preparation of Annual Product Quality Review as per SOP timelines and to identify the improvement areas or recommendations. 11. To perform CAPA effectiveness check activity related to Audit Compliance CAPAs. 12. Preparation for the Training Materials, Coordination with the cross functions for the execution of the trainings as per plan. 13. Updation of the Employee, courses, modules, and other amendments in ISOtrain system. 14. Past due trainings follow – up and reconciliation. 15. Maintaining the records of GMP/Technical training and QA department training. 16. To follow all the practices related to Safety and COBC. 17. All miscellaneous activities as assigned by seniors. In absence of the position holder, the sub-ordinate Executive / Manager working in the section, or the authorized designee (as applicable) shall be responsible for day to day working.

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1.0 - 6.0 years

2 - 3 Lacs

Baddi, Jaipur, Delhi / NCR

Work from Office

Promote & Sell Commercial Lab testing services to industries & Business identify new clients / generate new leads and convert prospects onto customers . visit client in the field regularly maintain client relationship for repeat business & raffles Required Candidate profile Graduate MALE 1-6yrs exp. in sales in Lab /Analytical LAB expert with computers Fresher can also apply Must have own conveyance

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3.0 - 6.0 years

3 - 4 Lacs

Baddi

Work from Office

Key Responsibilities : 1. Store Operations Receive, inspect, and verify materials (engineering spares, tools, lubricants, PPEs, etc.). Ensure timely and accurate issuance of materials as per approved requisitions. Maintain proper identification, storage, and traceability of all items. Ensure FIFO/FEFO compliance wherever applicable. 2. Inventory Management Maintain minimum and maximum stock levels for critical spares. Regularly update stock records in ERP or manual registers. Conduct periodic stock audits (monthly/quarterly/yearly) and reconcile discrepancies. Coordinate with purchase/procurement for timely replenishment of materials. 3. Documentation & Compliance Maintain all records as per GMP and audit requirements (GRNs, Issue Slips, Return Notes, etc.). Ensure proper labeling of materials and shelf-life tracking for time-sensitive consumables. Comply with safety, EHS, and 5S practices in the store area. Support regulatory inspections and internal audits. 4. Coordination Liaise with engineering, production, QA, and purchase departments for material planning. Coordinate with vendors and procurement for delivery follow-ups or quality issues. Assist in vendor development by identifying alternate sources for critical items. 5. System and Tools Operate and manage store transactions in ERP (e.g., SAP, Oracle, Tally, etc.). Use barcoding/RFID systems (if implemented) for inventory control. Prepare and submit periodic MIS reports on inventory status, consumption, and reordering.

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10.0 - 13.0 years

9 - 11 Lacs

Baddi

Work from Office

Key Responsibilities : 1. Operational Management Plan and execute daily packing activities for injectable formulations (ampoules, vials, prefilled syringes). Ensure adherence to approved Batch Packing Records (BPR) and SOPs. Coordinate with production, QA, QC, and warehouse teams for smooth operations. Monitor packing line efficiency and downtime; initiate corrective actions as needed. 2. Compliance and Documentation Ensure packing operations comply with cGMP, WHO ,EU-GMP,and other regulatory requirements. Review and approve packing-related documents (SOPs, BPRs, logbooks). Handle regulatory and customer audits related to the packing department. Ensure traceability and documentation of each stage of packing. 3. Team Management Supervise, train, and develop packing line operators and staff. Prepare shift schedules and manpower planning. Conduct periodic performance evaluations and ensure training on SOPs and cGMP. 4. Equipment and Maintenance Ensure proper functioning, calibration, and maintenance of packing equipment (labeling machines, blister packing, serialization, etc.). Coordinate with the engineering/maintenance department for preventive and breakdown maintenance. 5. Quality and Continuous Improvement Monitor in-process quality checks and take immediate corrective actions for deviations. Lead initiatives for yield improvement, cost reduction, and packaging material optimization. Participate in investigations of deviations, OOS/OOT, and implement CAPAs.

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0 years

3 - 12 Lacs

Baddi

On-site

QC Manager – Key Responsibilities Oversee testing of raw materials, packing materials, finished products, and stability samples as per pharmacopeial standards. Ensure compliance with cGMP, GLP, Schedule M, and WHO guidelines. Manage QC documentation, review COAs, STPs, SOPs, and ensure timely release of batches. Handle OOS, OOT, deviations, and implement CAPA effectively. Supervise calibration, maintenance, and qualification of lab instruments. Coordinate with the microbiology team for environmental monitoring and water testing. Lead stability studies and ensure regulatory compliance as per ICH. Train and supervise QC staff; ensure audit readiness at all times. Ensure data integrity and proper record-keeping (ALCOA+ compliance). Job Types: Full-time, Permanent Pay: ₹28,085.45 - ₹100,000.00 per month Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

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0 years

1 - 2 Lacs

Baddi

On-site

Job description SKILLS REQUIRED : Supervise packaging department operations to ensure efficient and accurate packaging of cosmetic products Oversee packaging staff, including training, scheduling, and performance management Monitor production schedules to meet deadlines and targets Ensure compliance with packaging specifications and quality standards Coordinate with other departments such as production and quality control to maintain smooth workflow Identify and implement process improvements to enhance productivity and efficiency Conduct regular inspections of packaging equipment and maintain inventory levels of packaging materials on job floor Enforce safety regulations and company policies within the packaging department Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift Morning shift Shift availability: Day Shift (Required) Night Shift (Required)

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4.0 - 6.0 years

4 - 5 Lacs

Baddi

Work from Office

Act as NABL Tech

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10.0 - 15.0 years

10 - 13 Lacs

Baddi

Work from Office

The Manager/Sr Manager - SCM is responsible for overseeing and optimizing the entire supply chain process from procurement to delivery. This role involves strategic planning, inventory management, supplier management, logistics coordination, and ensuring the timely dispatch of goods. The Manager/Sr Manager will work closely with various departments to ensure that the supply chain operates efficiently, cost-effectively, and meets customer demands. Role & responsibilities Supply Chain Management (SCM): Develop and implement supply chain strategies that align with business objectives. Optimize end-to-end supply chain processes to ensure efficient production and delivery. Manage supplier relationships, negotiate contracts, and ensure timely procurement of materials. Warehouse Management: Oversee the daily operations of the warehouse, ensuring inventory accuracy and efficient space utilization. Implement inventory control systems and conduct regular audits to maintain stock levels. Ensure the warehouse is compliant with safety regulations and standards. Store Management: Manage store operations, including stock management, order processing, and delivery scheduling. Develop and maintain relationships with key suppliers and vendors. Ensure timely availability of materials for production and maintain optimal stock levels. Production Planning and Control (PPC): Develop production plans and schedules to meet customer demands and minimize downtime. Monitor production progress and adjust schedules as needed to ensure on-time delivery. Coordinate with production, engineering, and quality teams to ensure seamless operations. Logistics Management: Oversee the logistics operations, including transportation, distribution, and freight management. Optimize logistics processes to reduce costs and improve delivery times. Ensure compliance with legal and regulatory requirements for transportation and logistics. Skills: Strong leadership skills with the ability to manage and motivate a diverse team. Experience in training, developing, and evaluating team performance. Excellent verbal and written communication skills. Ability to effectively communicate with internal teams, suppliers, and customers. Demonstrated leadership capabilities with a strategic mindset. Ability to drive change and implement process improvements.

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2.0 - 7.0 years

2 - 4 Lacs

Baddi, Jaipur

Work from Office

Promote & Sell Commercial Lab testing services to industries & Business identify new clients / generate new leads and convert prospects onto customers . visit client in the field regularly maintain client relationship for repeat business & raffles Required Candidate profile Graduate MALE 3-6yrs exp. in sales in Lab /Analytical LAB expert with computers Must have own conveyance

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0 years

1 - 1 Lacs

Baddi

On-site

Analyzes, troubleshoots and resolves Tier 1 level software & hardware issues for internal end users (i.e. Windows 7 OS & MS Office 2010 support issues, and hardware & peripherals). Processes IT equipment/hardware and software delivery and installation requests. Engages, delegates and coordinates Tier 2 & Tier 3 level issues to IT Team Members (i.e. Systems Administrators) for issue resolution and support as needed. Maintains communication with internal customers, keeping them informed of the status of their request - follows-up with internal customers to ensure that requests were completed to the user’s satisfaction. Reviews and follows-up with IT team members on a daily basis concerning open requests. Job Type: Full-time Pay: ₹12,000.00 - ₹15,000.00 per month Shift: Day shift Work Days: Monday to Friday Weekend availability Work Location: In person

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1.0 years

1 - 1 Lacs

Baddi

On-site

We are seeking a details oriented Billing/accounts persons to join our Ayurveda/Naturopath hospital (vrindavan Ayurveda Chikitsalayam) Baddi. Responsibilities OPD registration Manage outpatient billing process with accuracy and efficiency Coordinate with patients , doctors and departments keep recor of patients HAndle cash, card and digital payments Requirements Fresher with good knowledge of computer can apply prior experience in hopsital/OPD registration and billing preferred send your Resume to admin@vrindvanachikitsalayam.com or whatsapp 7901777680 Qualificateions Proven experience as a billing specialist,billing clerk or in a similar role Excellent attention to detail and ability to work with numers Good knolwedge of Tally Experience in billing Job Types: Full-time, Permanent, Fresher Pay: ₹12,000.00 - ₹15,000.00 per month Benefits: Food provided Schedule: Morning shift Night shift Experience: total work: 1 year (Preferred) Work Location: In person Application Deadline: 27/01/2025 Expected Start Date: 01/07/2025

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0 years

2 - 4 Lacs

Baddi

On-site

CONTACT PERSON = PANKAJ BHATIA (OPERATIONS MANAGER) - 9599417801 Email = jobs.viown@gmail.com CANDIDATE should be responsible for finding, attracting, and hiring talent for our organization. Their duties include writing job descriptions, sourcing candidates through various channels, screening resumes, conducting interviews, and coordinating the hiring process. CANDIDATE should keep accurate and up-to-date records of candidate interactions and progress within. Effective communication is crucial for interacting with candidates, hiring talent. Also they need to manage multiple tasks, prioritize effectively, and keep track of the hiring process. Building rapport with candidates and establishing strong relationships with hiring managers is essential. Working Experience = 2-4 yrs Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹35,000.00 per month Benefits: Cell phone reimbursement Leave encashment Provident Fund Schedule: Day shift Evening shift Morning shift Supplemental Pay: Yearly bonus Work Location: In person

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0 years

7 - 12 Lacs

Baddi

On-site

Position -QA Head LOCATION -BADDI OSD EXPERIENCE MUST GOOD STAYBILTY INTERESTED ONE SEND ME RESUME-7719715392 admin@addiibiotech.com Job Type: Full-time Pay: ₹60,000.00 - ₹100,000.00 per month Schedule: Day shift Work Location: In person Speak with the employer +91 7719715392

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4.0 - 7.0 years

4 - 6 Lacs

Baddi

Work from Office

Key Responsibilities: 1. QMS Implementation & Oversight: Maintain and continually improve QMS elements such as deviation handling, change control, CAPA, OOS/OOT, risk assessments, and quality reviews . Ensure compliance with GMP, GAMP, ISO, ICH (Q9, Q10), and regulatory agency requirements (e.g., USFDA, MHRA, WHO, EU GMP) . 2. Deviation & CAPA Management: Investigate deviations in manufacturing, QC, and support areas. Perform root cause analysis (RCA) and drive timely and effective CAPA implementation. Monitor the closure timelines and effectiveness verification of CAPAs. 3. Change Control & Document Control: Evaluate and manage changes in equipment, facility, process, and documents. Review and manage controlled documents including SOPs, protocols, risk assessments , etc. Ensure document lifecycle management in compliance with GDP . 4. Audit Readiness & Regulatory Compliance: Support internal audits, regulatory inspections, and third-party audits. Prepare and maintain audit documentation, observation responses, and compliance tracking . Coordinate self-inspections and site quality risk assessments . 5. Training & Quality Culture: Conduct GMP training programs related to QMS and quality culture. Monitor training compliance across functions and maintain training matrices. 6. APQR/PQR & Quality Metrics: Participate in the preparation of Annual Product Quality Reviews (APQRs) . Compile, monitor, and report Quality KPIs and metrics to management. 7. Sterile Manufacturing Support: Ensure QMS processes support sterility assurance practices. Review and ensure compliance for media fill protocols, aseptic area controls, and environmental monitoring deviations.

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7.0 years

0 Lacs

Baddi, Himachal Pradesh, India

On-site

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 looking for an individual for the SIT Team to oversee the investigation of major and critical deviations, working closely with Cross-Functional Team (CFT) members to identify root causes and implement corrective and preventive actions. The role involves active participation in investigating Out of Specification (OOS) cases, ensuring accurate classification in the DCMS deviations log, and providing support during regulatory inspections. Roles & Responsibilities You will be responsible for overseeing the investigation of major and critical deviations from the outset, collaborating closely with Cross-Functional Team (CFT) members to identify root causes, corrective actions (CA), preventive actions (PA), and preparing comprehensive reports. Your will also be working on the trending of the deviations and identification of adequate action items for reduction of the same. Your role involves active participation in investigating OOS (Out of Specification) and other relevant cases, working closely with CFT members to determine root causes, CA, PA, and report writing. You will review minor and critical , providing constructive feedback for improvement. Your responsibilities include periodically assessing the trending of minor deviations, highlighting or escalating key observations, regularly reviewing the deviations log to ensure accurate classification, and utilizing the Rubrics template for crafting investigation reports. You will offer necessary support to the site in readiness for or during regulatory inspections related to investigations. Qualifications Educational qualification: A Bachelor's or Master's degree in a relevant scientific field, such as Chemistry, Biochemistry, Pharmacy, or related discipline Minimum work experience : 7 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance Skills & attributes: Technical Skills In-depth knowledge and experience in overseeing investigations, and familiarity with root cause analysis, corrective actions (CA), and preventive actions (PA). Expertise in investigating valid OOS and other relevant cases. Familiarity with reviewing deviations / OOS log and ability to perform classification of data. Ability to craft comprehensive investigation reports. Experience in providing necessary support for regulatory inspections related to investigations. Knowledge of regulatory requirements pertaining to deviations investigations. Behavioural Skills Ability to collaborate closely with CFT members. Analytical mind set for identifying root causes and developing effective solutions. Strong problem-solving skills and attention to detail in reviewing deviations, reports, and trending data and implementing corrective actions. Effective communication skills for report writing and escalation of key observations. Commitment to ensuring compliance with regulatory requirements in investigations. Ability to offer necessary support to the site in readiness for or during regulatory inspections. Additional Information looking someone with strong QC Microbiological investigation background. Should have exp in Microbiological compliance. Education :M.Sc. Microbiology Exp : 8-10 Years Industry : Injectable preferred/ OSD will be second preference Person will be responsible to manage 3 sites Microbiological compliance at Baddi

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