476 Jobs in Baddi - Page 12

The Business Development Manager - Emerging Corporates role at IndusInd Bank involves overseeing key operations, ensuring compliance, and driving business growth. Responsibilities include managing customer interactions, improving service efficiency, and coordinating with various teams to achieve operational excellence. The ideal candidate should possess strong analytical skills, excellent communication, and a proactive approach to problem-solving. Prior experience in a similar role is preferred. Candidates must demonstrate leadership qualities and adaptability to dynamic banking environments. This position offers a great opportunity to grow within the banking sector.

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

Oversee the construction process to ensure adherence to design specifications and safety standards. Manage and coordinate construction activities, including scheduling, resource allocation, and material procurement. Cv -9812001068

Investigation ofmarket complaints, OOS/OOT result related to product. To check and ensurethe cleaning activity in Production area as per SOP. To ensure that themanufacturing and packing operation are carried out as per the instruction givenin the batch production Record. To Handle (Initiation/Evaluation/Closure) Change control, Deviation/Incident management System. To supervise theworking activity of the officers and junior officers. To verification andCheck the dispensed raw material and packing material before batch processingand during dispensing. To coordinate with QAdept. for preparation of protocol for Qualification and requalification of theequipment s

Experience Required: Diploma in engineering/ D.Pharma with 1-2 years of experience in core compression area Exposure to Korsch XT 600 compression machine candidate shall be preferred. Should have expertise in compression department also Should have exposure in machine installation qualification activity. Should have exposure to regulatory audits such as MHRA, USFDA etc. Person working in a containment facility are preferred. Followings will be the responsibilities of the position holder: 1. Responsible for Operation, cleaning and primary maintenance of AWC based compression machine. 2. Competent for (entry) recording of activity in logbooks, Batch manufacturing record Responsible for completing documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP s and good documentation practices. 3. To perform all in-process checks and monitoring of all intermediate processes in compression, to prepare new recipes set process parameters in PLC/SCADA as per BMR ensure its correctness before Compression machine run. 4. Issuance, utilization, cleaning, polishing, buffing and retrieval of tablet tooling (Die punches) Proper handling of machine change parts with its inventory. 5. Responsible for set up, changeover, and operation of various manufacturing equipment s but not limited to compression department. 6. Ability to read, write and communicate in English, Strong work ethic, professional approach, and ownership of lines production performance. 7. Ability to read understand SOP s, Batch Records, training documents Basic computer knowledge. 8. Ensures accurate and timely completion of all equipment logs and documentation. Understands and adheres to all cGMP and FDA regulations. 9. Responsible for reporting and/or escalating any conditions or problems that may affect the quality or integrity of product to supervisor and HOD production. 10. Responsible for maintaining a neat, clean and safe working environment at all times and notifies supervisor immediately of any safety concerns, accidents or injuries are observed. 11. Understands and adheres to all Company policies, procedures, SOPs and Safety regulations. 12. Willingness to do overtime as needed responsible for performing additional task, related duties as assigned. 13. Responsible for completing all training requirements and maintaining 100% compliance with all assignments.

Minimum 1 Years Experience in solid dosage form- Tablets. Person shall be well versed with manufacturing and packaging operations, Compression Machines, Isolators, Blenders, Bulk packing lines, Investigation , QRM Process Validation. Person with Experience in Hormone Facility shall be preferred. Followings will be the responsibilities of the position holder: Ensure compliance to cGMP Regulations, established SOPs, FO/MI and PO/PI and for all operational activities, area and equipment. Perform QA review of executed batch production records and ensure the submission of Batch production record in the document cell. Calibration maintaining documentation of In-process Quality Assurance (IPQA) instruments. Data back-up activities of IPQA instruments as per defined SOP frequency. Monitor the environmental conditions mentioned in the batch production record and SOP. Certification of batch production records for compliance and stage-wise compliance. Reporting any GMP related discrepancies, non-conformances and deviations to superiors immediately. Collection and entry of data for APR preparation. Line Clearance: Ensure physically that the area and equipment to be used for manufacturing and packaging of next product/batch are free from any material/remnants of previous product. Ensure to prevent mix up and cross contamination. Check for proper environmental conditions with respect to temperature, Relative humidity, differential pressure etc. Ensure that the Batch Production record is completed up to the previous stage. Verify the material with respect to the container labels and quantity from the batch production record. In-Process Checks: Ensure the calibration of instruments for in-process checks. In-process checks as per the approved manufacturing and packaging instructions. Enclose all the printouts generated during in-process checks along with the batch production record. All printouts shall be duly signed after checking. Inform the production manager, supervisor and quality assurance manager about the in-process failure observed during in-process checks. To record all the observations in the Batch Production Record Inspection: Inspection of the Tablets/Capsules as per SOP. Inspection of the Finished Goods as per SOP and clearance of Transfer Ticket by ensuring the quantity and batch details. Sampling: Ensure for usage of appropriate sampling tool for sampling. Ensure sampling device cleaning prior to the sampling. Sampling procedure to be followed as per SOP No. SOP019995 (Sampling of intermediates, finished product and stability samples) SOP020059 (Collection and shipment of Analytical samples of EU market). Ensure sampling of in-process finished product, process validation, cleaning validation, control samples, EU Lab testing samples stability samples, Reference Retention sample as per SOP.

Compliance of current Good Manufacturing Practices in the Hormone Facility to follow GDP with data-integrity compliance. Responsible for achieving monthly and yearly target of production department. Alarm Identification and management as per SOP. To ensure all in-process checks and monitoring of all intermediate processes, to check set process parameters in PLC/SCADA as per BPR. Responsible to operate the Packaging machine as per respective equipment operation SOP. To identify the problems with the machine and undertake trouble shooting activity where required, to ensure work is carried on in the Packing section according to the SOPs, to coordinate with departmental colleagues HOD QA in cases of discrepancies in Packing Section. Responsible to minimize breakdown and support engineering Department. Responsible to maintain primary packing machine (Unscrambler machine, Bulk packing machine, induction sealing) spare parts. Responsible for operation and cleaning at packing stage. Packing process compliance in accordance with approved BPR and SOP. Follow the safety compliance as per Abbott policy. Responsible to inform Safety incident, accident, near miss and BBS. Complete the training and training record as per stipulated time. To carry out In-process checks at the different stages as per batch packing record. Responsible to update all logbooks of packing area. To follow the safety compliance and SOP. To support the team on additional responsibilities assigned time to time.

Design manufacturing models, engineering drawings and customer drawings for all product manufactured by the company.

Responsibilities: * Process accounts payable, GST returns, TDS deductions * Maintain general ledger, journal entries & voucher entry * Ensure accurate financial reporting through tally erp software

Role & responsibilities skilled in creating prototypes and optimizing fromulations through iterative trials. experience in scaling up processes from lab-scale to pilot and commercial production. Preferred candidate profile expertise in selecting excipients for stability, bioavailability and desired release profiles. Perks and benefits

Job Description: Cell Culture Specialist Monoclonal Antibodies Production Position: Cell Culture -Scientist Department: Medipath- Cell culture -RND Location: [Baddi, Himachal Pradesh] Reporting To: [ Cell Culture Senior Scientist] Job Summary We are seeking a highly skilled and experienced Cell Culture Specialist to join our monoclonal antibodies team. The ideal candidate will have 3-4 years of hands-on experience in cell culture techniques, with a strong background in biotechnology. This role involves maintaining and optimizing cell lines, scaling up production processes, and ensuring high- quality monoclonal antibody yields. Key Responsibilities 1. Cell Culture Management: Maintain and expand mammalian cell lines used in monoclonal antibody production. Monitor cell health, viability, and productivity through routine checks and assays. 2. Process Optimization: Optimize media composition, feeding strategies, and environmental conditions to maximize antibody yields. Implement scalable production processes for large-scale monoclonal antibody manufacturing. 3. Quality Control: Conduct regular contamination testing and ensure cell line integrity. Perform routine analytical assays, including protein quantification and activity testing. 4. Documentation and Compliance: Maintain accurate and detailed records of all cell culture processes and experiments. Adhere to GMP/GLP standards and ensure compliance with regulatory requirements. 5. Equipment Handling and Maintenance: Operate and maintain bioreactors, incubators, and other cell culture equipment. Perform calibration and troubleshooting of equipment as needed. 6. Cross-Functional Collaboration: Work closely with upstream and downstream teams to streamline production workflows. Provide technical support and training to junior team members. Required Qualifications • Bachelor’s degree in Biotechnology or a related field. • 3-4 years of proven experience in mammalian cell culture for monoclonal antibody production. • Strong knowledge of aseptic techniques and cell culture process optimization. • Familiarity with bioreactor operations and scale-up processes. • Experience with analytical techniques such as ELISA, SDS-PAGE, and Western Blot is a plus. Preferred Skills • Excellent problem-solving and troubleshooting abilities. • Strong organizational and documentation skills. • Ability to work in a fast-paced, team-oriented environment. • Familiarity with regulatory and quality guidelines, including GMP/GLP. What We Offer • Competitive salary and benefits package. • Opportunities for professional growth and development. • A collaborative and innovative work environment.

Manages a large cluster, collaborates with the objective to support and contribute to bank strategy, achieve operations excellence, ensure systems are deployed and help build the channel WITHIN the company guidelines and the achieve business targets Required Candidate profile Segment Heads and Branch Heads With the advent of cluster formation relationship management with the Branch Heads in order to achieve business targets and builds a progressive partnership with

Urgent Hiring Position- Executive Assistant Location-Himachal Pradesh Experience- 3+ Years Qualification- Bachelors degree Job Description 1. To manage and coordinate the daily schedule, meetings, Conferences and appointments. 2. To prepare agendas, reports, and briefing materials for meetings. 3. To take minutes during meetings and ensure follow-up on key action points. 4. To handle travel arrangements, itineraries, and accommodations. 5. To prepare reports, presentations, and correspondence on behalf of the CEO. 6. To maintain confidential documents, records, and databases. 7. Responsible for Screening emails, calls, and requests, responding where appropriate. 8. Responsible for Drafting and proofreading emails, letters, and presentations. 9. To facilitate communication between different departments and executives. 10. To handle office-related administrative duties as required

Role & responsibilities :- Lead the development, implementation, and continuous improvement of our Quality Management System (QMS). Ensure adherence to industry standards and regulatory requirements (e.g., EMA, WHO). Collaborate with cross-functional teams to drive quality initiatives and foster a culture of quality. Oversee audits and inspections, ensuring timely resolution of findings and implementation of corrective actions. Analyze quality metrics to identify trends and recommend improvements to enhance product quality and safety. Develop and implement quality management system policies and procedures. Identify, analyze, document and report on system deficiencies. Monitor and evaluate the effectiveness of the quality management system. Ensure compliance with applicable standards and regulations Train employees on quality management system procedures and processes Perform internal audits and lead external audit activities Develop and maintain quality management system documentation. Manage and investigate customer complaints Analyze data and produce reports to present to management. Monitor performance and implement corrective action plans.

Role & responsibilities To manage and coordinate the daily schedule, meetings, Conferences and appointments. 2. To prepare agendas, reports, and briefing materials for meetings. 3. To take minutes during meetings and ensure follow-up on key action points. 4. To handle travel arrangements, itineraries, and accommodations. 5. To prepare reports, presentations, and correspondence on behalf of the CEO. 6. To maintain confidential documents, records, and databases. 7. Responsible for Screening emails, calls, and requests, responding where appropriate. 8. Responsible for Drafting and proofreading emails, letters, and presentations. 9. To facilitate communication between different departments and executives. 10. To handle office-related administrative duties as required Experience required: 3 to 5 years of experience in a factory/corporate in Secretarial/Executive Assistant role. Preferred candidate profile Any Graduate with good communication Perks and benefits

Roles and Responsibilities Manage distributor sales, ensuring timely delivery of products to customers. Develop and maintain strong relationships with retailers, identifying new business opportunities. Collaborate with internal teams to resolve customer issues and improve overall satisfaction.

Facility : 1. Manage ETP (Effluent Treatment Plant), DI Plant, ZLD (Zero liquid Discharge), Operation of NH3 Stripper operations to ensure compliance with regulatory requirements and plant standards. 2. Collaborate with cross-functional teams to resolve issues related to waste water treatment, sewage treatment, and water quality management. 3. Candidate having experience in preparation of design, costing in ETP, STP, RO and ZLD. 4. Develop the down the line team, Strong interpersonal skills and team building capability 5. Developments of indigenous vendor to reduce the cost of spares to reduce the operation and maintenance cost. 6. Identify significant environmental aspects and impacts of operational activities and recommend possible mitigating measures. 7. Submit Self-Monitoring Reports (SMRs) and Compliance Monitoring Reports (CMRs) periodically. 8. Report any environmental incidents or exceedances in effluent and/or emission standards within a stipulated time frame. 9. Act as the liaison officer to the Pollution Control Board (PCB) and coordinate regulatory programs with local government units 10. Well ware about all permitting and registration requirements prior to the construction or operation of pollution sources and control facilities

Key Responsibilities: Execute preventive and predictive maintenance strategies to minimize equipment downtime. Perform fault diagnosis and rectification of mechanical and electrical systems. Maintain and troubleshoot PLC, HMI, Servo, Robotics, Conveyor Systems, Pneumatics, Valves, Actuators, Vacuum Pumps, and Exhaust Systems . Ensure compliance with safety protocols and industry regulations. Maintain departmental logs and daily shift reports . Collaborate with cross-functional teams to optimize plant operations. Preventive & Predictive Maintenance Electrical & Mechanical System Maintenance Fault Diagnosis & Troubleshooting Safety & Compliance PLC, HMI, Servo, Robotics Pneumatics, Valves, Actuators, Vacuum & Exhaust Systems Understanding of electrical drawing and P&ID Report & Log Maintenance Interested candidate can mail their resume at jayvardhan@empowerresources.in

Candidate should have Exp. to Sell "Water Treatment chemicals" Products "/ Industrial sales, Exp. & Knowledge of Cooling tower & Boiler " Chemicals And" Plants eg, STP, ETP & DM, RO, filtration Plants Capable of generating relevant enquiries. Required Candidate profile Calculating Target Pricing & Converting into Orders Capable of meeting out the Monthly & Annul Sales Targets in a defined territory. Capable of Developing Dealer Network in prescribed Area

Campus Owner / Program Manager @ Kalvium ***Work Timings: Monday to Saturday, 8:45AM-6:15PM About Kalvium: Kalvium is an exceptional startup with a mission to make the world's education more relevant and engaging. Our flagship offering is India's BEST Undergrad program in Computer Science Engineering which is offered across 20+ Universities in India. We are backed by 30+ industry stalwarts like top executives from Google, Microsoft, Flipkart, and PhonePe, as well as luminaries of India's unicorn ecosystem like Anupam Mittal, Kunal Shah, Rahul Chari, and Ankit Bhati. We are on the lookout for passionate minds to champion our vision and join us on a journey to redefine the global tech education landscape. Responsibilities: 1. Program Management Ensure smooth execution of the Kalvium program on the assigned campus. Monitor and improve student learning progress, outcomes, and experience through data analysis and dashboards. Collaborate with internal and external stakeholders to ensure effective program operations. Manage student / parent / university stakeholder interactions. Manage on-ground operations for assessments, events, and other program-related activities. Take up and drive execution of various initiatives from time to time. 2. Mentorship Facilitate professional development and career outcomes of a cohort of Kalvium students, ensuring successful placements and optimal performance reviews from recruiting tech companies. Provide counselling, guidance and support to students to help them overcome challenges during their learning journey and at work. 3. Team Management Manage a team of academic mentors on campus to deliver and drive the necessary outcomes. Qualification: B.E/B.Tech and Masters Degree in any related field with a minimum of 5+ years of relevant experience. A Kalvium Campus owner serves as the glue that ties the program together and acts as a role model for our future Software Engineers. Before applying, consider the following questions: Are you interested in helping students succeed in their careers? Do you enjoy mentoring students? Do you possess good communication and presentation skills? Are you a good listener? Are you proficient in working with data? Are you obsessed with productivity? Location and Work Mode: (1) Rajpura (Punjab) (2) Jalandhar(Punjab) (3) Bangalore (Karnataka) (4) Chennai (Tamil Nadu) Work Timings: Monday to Saturday, 8:45AM-6:15PM CTC:- 8LPA to 15LPA (Fixed + Variable) Actual CTC Will Be Decided Based On: (A) Your Current/Last Drawn CTC (B) Your Interview Performance Kalvium Benefits: Opportunity to be part of an impactful movement to transform higher education for the better, with a competitive salary. Challenging role designed to significantly enhance your professional profile and skills. Work closely with the founders and the founding team. Enjoy an awesome work culture that helps you thrive with the team. Kalvium's Core Values: We obsess about student experience and outcomes above all. We embrace extreme ownership, focusing on outcomes over tasks. We respect and trust each other. We disagree with candor and courtesy We improve things regularly, rather than chase perfection We learn continuous and seek discovery If you resonated with the description and answered 'Oh, that's so me' while reading along, this role is an ideal fit for you.

Responsibility for Chemical/ Instrumental testing of Raw materials sample. Responsible for assure the quality of Sun s products manufactured at Sun Pharmaceutical Industries Ltd for the domestic market as well as export to emerging markets. Responsible for system up-gradation as per CQ and regulatory guidelines To analyze and report the stability sample FG sample if needed. Monitoring of gowning and sanitation practices in area of operation. Monitoring of compliance of standard operation procedure for operation of analytical instrument. To operate the analytical equipment in quality control as per the allotment works in shift. To follow the procedure of good documentation and recording of result as per SOP on GDP and good execution of laboratories practices. To support the internal audit/Regulatory/FDA audit with best of practices Following all regulations of cGMPs as per schedule M. To maintain the safety procedure in handling analytical equipment and hazards. Completing the training assigned as per the training need identified by participating in trainings organized or self-reading. To calibrate the analytical equipment s as per the calibration procedure for assigned responsibility of calibration. To maintain the analytical equipment s and laboratories in good state of operation .To maintain the stock of working standard, column, reagent, chemicals, glass ware etc. To follow procedure for non-conforming result as it is applicable in SOP of OOT, Lab Incident OOS. To follow the administrative procedure of compliance with respect to term and condition for attendance, leave and other benefits .

Ensure Compliance with laid procedures and standards of the current Good Manufacturing Practices. Carrying setup, operation, cleaning, troubleshooting, and maintenance of Production equipment (Granulation, Compression, Coating and Packing). Handling of manufacturing and packing equipments. To fill and maintain the BPR/ BMR/ DPR and related documents online. Carrying operation of SCADA system. Ensure proper handling of instruments like Moisture analyzer, DT apparatus, Friability apparatus, Hardness Tester, Leak test apparatus. To exercise effective control over the environmental conditions in Manufacturing and other related activities, which may adversely affect the product quality. Continuous monitoring and improving the production output on daily basis. To exercise effective control over the process variable affecting the quality of the product.

The Technical Service Engineer is responsible for performing on-site installation, maintenance, service repair and support for Markem-Imaje products and services. What you will do: The engineer has to provide on site service and customer support study different type of packaging machines and site readiness for printer installation. Conduct onsite (online) printer trial Perform on-site product installation on customer premises. He shall be responsible for on- site services such as Installation Maintenance of Markem products to ensure maximum up-time and customer satisfaction. He needs to meet service spares budget for assigned geographical territory. Job requires travelling to manufacturing facilities of Markem customers What you need to have: The engineer must have 3 - 5 years of hands on experience in on site service and customer support of capital goods relating to industrial automation. He must be Graduate with Degree in Electrical/Electronics/ BSc (maths/Physics) with at least 60% marks from reputed college. Good organizational skills and ability to set priorities and manage time effectively. Good level of customer relationship management skills. Candidates applying for this position must have own vehicle that can be used for business travel purpose. You ll only be the right candidate if you are aligned to our values and culture: Collaborative entrepreneurial spirit Winning through customers High ethical standards, openness and trust Expectations for results Respect and value people Work Arrangement : Hybrid

Followings will be the Core Job Responsibilities of the position holder: Analysis and review of Inprocess, SFG, Finished Goods, Raw material stability sample and related documentation as per GLP and GMP in time. Ensure analysis and Review of RM, Stability and FG samples for Fenopenta, and other Export project sample. Ensuring the timely updation in the documents as per the Pharmacopoeial amendments. Timely charging and withdrawal of samples from stability chambers and their documentation within the time frame Sample reconciliation and destruction record of stability sample. Data entry in Starlims. Monitoring of stability chamber data. Reporting of stability/Finished product sample as per report received from outside laboratory and check the compliance against respective specification. Calibration of instruments, as and when required. Preparation of volumetric solution, reagent and test solution, as and when required. Implementation of GLP / GMP requirements. Coordinating and aligning the practices and procedures in line with the COBC requirements To play a training coordinator role in Isotrain system for training and compliance as per electronic system within timeline 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.

Followings will be the responsibilities of the position holder: 1.0 Microbial Culture Media Preparation and qualification of Microbial Culture Media. 2.0 Surface and Personnel Monitoring of Production and Microbiology laboratory. 4.0 Transportation of all required items from Microbiology laboratory to sampling site and vice versa. 6.0 Sampling and analysis of In-process samples from production area. 7.0 Sampling and analysis of WFI, PSC and Purified water from production area. 9.0 To perform sampling and bioburden testing.