476 Jobs in Baddi - Page 18

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job Summary We are seeking a Technology Transfer team member to support the development and implementation of robust manufacturing processes, including authoring validation protocols and reports, conducting risk assessments, and utilizing advanced tools for process monitoring and analysis. Your role will involve active participation in technology transfers, continuous improvement initiatives, and ensuring compliance across manufacturing operations. Roles & Responsibilities Responsible for Validation which shall include: Preparation/Review/Approve of MPR. Preparation/Review/Approve of process validation protocols. Preparation/Review/Approve & compilation of validation report. Responsible for Tech transfer which shall include: Coordination with Vendor/cross functional teams for Tech transfer activities. Execution of Tech transfer products at Receiving Units. Responsible for QIP which shall include: Identifying root cause for QIP. Execution of QIP. Conclusion/Recommendation of QIP. Responsible for OOS/OOT investigation which shall include: Identifying probable and most probable root cause for OOS/OOT. Ensure that validations is carried out as per the protocol & qualification protocols meets the cGMP & regulatory requirements. Follow up & coordinate with cross functional team for execution of validation. Give the input for the monthly reporting system, participate in the internal & external audits, present the documents to auditor’s/inspection team. Qualifications Educational qualification: Masters/Bachelors/Ph.D in pharma Minimum work experience: 6 -8 years of experience in Process development / MSAT / Tech transfer Skills & attributes: Technical Skills Experience in the scale up/ technology transfer of products in relevant dosage forms or technologies. (OSD) Experience in process Engineering, Quality by Design (QbD) principles and risk assessment approaches. Knowledge of International Council for Harmonization (ICH) guidelines related to Product development or Process Development. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Show more Show less

Company Description Hotel Gianz, Baddi is a modern hotel located on the Chandigarh - Baddi - Manali Highway. The hotel offers 35 stylish bedrooms and suites with contemporary amenities, 24-hour room service, a Multi-Cuisine Restaurant, and Conference Banqueting Space for corporate and social events. It is an ideal stopover hotel for travelers exploring Himachal's touristic destinations. Role Description This is a full-time on-site Executive Chef role located in Baddi. The Executive Chef will be responsible for overseeing the kitchen operations, menu planning, food preparation, and ensuring high-quality standards of food production. The role also involves managing the kitchen staff, controlling food costs, and maintaining inventory levels. Qualifications Culinary Arts, Food Production, and Menu Planning skills Leadership and Team Management skills Food safety and sanitation knowledge Creativity and Innovation in culinary creations Excellent communication and interpersonal skills Time management and organizational skills Experience in a similar role in the hospitality industry Certification in Food Handling and Safety Show more Show less

Job Description Grow Distribution and Market share in the assigned area of operations. Visibility Accountability through Extensive QR & Sound box deployment and sale of the product. Identify and Recruit the sales team to align and drive business in the market. Skilled in coaching and mentoring, a quick learner who grasps and puts into application new learned ideas and concepts. Plan the market size, span and geographies for FSE. Should be able to devise the best methods for communication of plans/targets to the team so as to minimize the expectations vs delivery gap. Monitor the Quality parameters as suggested by the management. Validate and conduct the audits on the acquisitions and sales done by the team. Ensure the team members are in the market where sales & usage are done regularly Should have good networking capabilities and be willing to travel extensively throughout their specified area. Show more Show less

Experience : 0-2 Years Education : MSC(Microbiology) Salary : 3.5-4 LPA Location : Baddi/ Nalagarh

We are seeking a highly skilled and motivated Process Engineer to join our team at Morepen Laboratories Ltd, a leading organization dealing in manufacturing of home diagnostics medical devices. The Process Engineer will play a crucial role in optimizing manufacturing processes, ensuring product quality, and driving continuous improvement initiatives. This role requires a strong understanding of manufacturing principles, medical device regulations, and process improvement methodologies. Role & responsibilities Process Optimization: * Analyze and optimize manufacturing processes to improve efficiency, reduce costs, and enhance product quality. * Develop, implement, and validate process improvements, including new equipment, procedures, and technologies Technical Support: * Provide technical support to production teams to resolve process issues, equipment malfunctions, and quality concerns. * Collaborate with cross-functional teams, including R&D, quality assurance, and production, to ensure smooth integration of new products and processes. Compliance and Documentation: * Ensure all processes comply with regulatory requirements, including FDA, ISO 13485, and other relevant standards. * Develop and maintain process documentation, including Standard Operating Procedures (SOPs), Work Instructions, and Process Flow Diagrams. Process Development: * Design and execute process validation studies, including installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). * Identify and implement best practices for process design, control, and monitoring Preferred candidate profile Qualifications: Education: Bachelors degree in Engineering (Electrical, ECE). Advanced degree or certifications (e.g., Six Sigma, Lean) preferred. Experience: Minimum of [3-5] years of experience in process engineering within a medical device or regulated manufacturing environment. Perks and benefits

Environment health and safety, safety compliance

Job Summary We are looking for a detail-oriented engineering team member to coordinate preventive maintenance schedules, manage breakdown records, and ensure adherence to SOPs, critical for maintaining operational efficiency and equipment reliability. This role plays a pivotal part in inventory control, and CAPA closure, contributing to seamless production operations, compliance with regulatory standards, and effective resource utilization. Roles & Responsibilities • To maintain the facility as per cGMP, and GMP requirements of country where product is being exported and strict adherence of Good Engineering practices during task execution. Can handle Water system operation and maintenance. Can handle HVAC system operation and maintenance. Must have knowledge of RO membranes & EDI replacement and its troubleshooting. Must Have knowledge of SCADA system and cGMP documentation. Spare management, Vendor management, MIS reports etc. Do the planned work on time. e.g. PM, PR, PO's etc. To carry out upkeep round as per schedule and updating of the records. To follow the instructions relating to engineering operations and to ensure their strict implementation. Ensuring continuous improvements and engineering excellence. To follow good documentation practices. To ensure EHS procedures and practices are followed at site to achieve zero lost time accident and compliance. Responsible for documentation related to upkeep of water system and HVAC. Must have knowledge of RCA, FMEA, Change Control, deviation and other GxP documentation. You will be accountable for ensuring implementation of Good Engineering Practices (GEP) at Site. Qualification Educational qualification : A Diploma or a B.Tech in Mechanical or Electrical Engineering Minimum work experience : 5 to 8 years Skills & attributes: Technical Skills Responsible for documentation related to upkeep of water system and HVAC. Responsible of Operation oif water system and HVAC Managing contractors at site. Their Work permits etc. Water system Maintenance and upkeep of HVAC in proper manner. Spare management for water system and HVAC Spares Experience in managing RO Mem. and EDI maintenance plans. Ability to manage maintenance budget of an area/unit. Knowledge of GMP and GEP. Behavioural skills • Communication and collaboration skills to coordinate with cross functional teams, external contractors and agencies. • Attention to detail to ensure preventive maintenance, documentation, and inventory control. • Commitment to quality and compliance. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Finalization of accounts & financial reporting Product costing, variance & inventory analysis GST, TDS, and statutory compliance Budgeting, MIS, and audit coordination Strong in cost accounting, ERP (SAP/Tally) & Excel Required Candidate profile Qualified CA or ICWA (mandatory) 3–5 yrs of relevant experience in a manufacturing company Strong knowledge of cost accounting, GST & financial reporting ERP systems (SAP / Oracle / Tally preferred)

Basic Section No. Of Openings 1 External Title Branch Relationship Officer - Used Car Employment Type Permanent Employment Category Field Closing Date 30 May 2025 Organisational Entity Equitas Small Finance Bank Business Unit Assets Division/Function (SBU) Emerging Enterprise Banking Department Used Car Sub-Department Sales Generic Role Sales Officer External Title (Job Role) Branch Relationship Officer - Used Car Division Emerging Enterprise Banking Zone North State Himachal Pradesh Region Punjab Area Punjab Cluster Punjab PT Location Himachal Pradesh Branch Code 15021 Branch Name Baddi Skills Skill Highest Education Bachelor of Arts Working Language English About The Role SNO.OBJECTIVE1Deliver UC disbursemet as per productivity norms by managing SO productivity2Maintain branch profitability WIRR to be 17% and PF to be 1.1%3PDD Collection Plan4Manage and monitor the portfolio quality and follow up with ED cases for timely resolution5Training Mandays6Process Orientation7Team Management

Basic Section No. Of Openings 1 External Title Receivable Officer Employment Type Permanent Employment Category Field Closing Date 13 Jun 2025 Organisational Skills Skill Highest Education Bachelor of Arts Working Language English About The Role SNO.OBJECTIVE1Resolution in Fresh NPA2Arresting Flow forward from Current month NPA3Contact recording updation4To ensure collection of over due charges 5Timely collection and deposition of payment

QC(Foil/PVC), min 4-5 years experience in packaging line. Ensure product packaging quality, inspect packaging materials, check labels & compliance with industry regulations. Ensure consistent quality throughout production process Required Candidate profile Male Candidates BSc/MSc/BPharma having: - Knowledge of packaging materials (FOIL/PVC). - Understanding of industry regulations. - Excellent reporting skills & proficiency in quality control tools.

good knowledge of in process quality

Need to take care of the joining formalities and other basic works Interested candidates should call Sanghamitra @ 90519-83261 Female candidates only. Candidates should be good in English Communication and having MBA HR will be great Required Candidate profile Candidate should have good communication skills Female Only

Job description Candidate will be based at corporate office of reputed Pharma company as a Manager- IT and he will be responsible for handling following:- Job Responsibilities: 1 Candidate would be responsible for the Servers and Computers, Printer and accessories are working properly any given time. 2) The Master Creation in the SAP Batch master is to be done properly. Backup of Servers and Computers are done from time to time. And functions of all camera system installed at plant to ensure proper support to the users.to prepare Presentation, SOPs and participate etc. for the IT compliance training. 3) He have good knowledge of administer LAN, WAN, EPABX & Video Conferencing. 4) Candidate would be responsible Daily Monitoring of all IT compliance with respect to Quality Assurance activities. IT compliance and data integrity Training to IT Team Members. Creation and Review of Qualification/ Validation related documents. Review of IT Training Matrix and Internal Trainer list. 5) Candidate would be responsible impart GSP, GLP, Behavioural, Motivational and other kind of trainings (Classroom & QC), ensuring compliance of the specified procedures / guidance and review of qualification documents such as URS, DQ, IQ, OQ, PQ and validation protocols and validation study report. 6) Candidate would be responsible for various Regulatory and Customer audits and assist management in providing compliance to audit observations and to review performance of juniors and recommend for higher punishment in case of their indulgence in any kind of misconduct including any data integrity. 7) Candidate would be responsible implementation and operation of Document Management (DMS), Quality Management System (QMS), Training/Learning management system (LMS), Lab Info. Management (LIMS) Software. 8) Candidate would be responsible troubleshooting any issues in SAP and subsequent validation and documentation of any modifications, enhancement or upgrades in any and all softwares implemented in the facility. 7) Candidate will be responsible for monitoring the performance of factory network, conduct regular internal audits and implement necessary modifications or adjustments to optimize resources.and CSV Activities with GAMP5 Approach with a yearly planner. And define and manage IT Disaster recovery strategy and Compliance and security for all IT related systems and infrastructure. Required candidate profile Qualification- Bachelors degree in Computer Science, Computer Application. . Candidate should have 8 to 12 yrs. in relevant experience in Hardware & Software. Candidate should have good experience in SAP, of Document Management (DMS), Quality Management System (QMS), Training/Learning management system (LMS). Candidate should have good Knowledge of LAN, WAN, EPABXETS. Should have good Knowledge of Daily Monitoring of All IT Compliance

Lead product development teams to design and launch new home appliances Develop product strategies and roadmaps Conduct market research and analysis Collaborate with cross-functional teams (engineering, mfg, supply chain)

Job Description Position : Senior Executive Quality Assurance Section : Quality Assurance Grade/Band : 1C Qualification : M.Sc. /B. Pharm. Desirable Experience: 06 - 10 years Followings will be the responsibilities of the position holder: To ensure effective implementation of system and procedure as per cGMP, cGLP and other Regulatory requirements, and monitor its compliance in laboratory. To participate in investigation of laboratory error report, incidents, out of trend and out of specification results and review the investigation report. To handle & coordinate QMS through SolTRAQs. To ensure the effective implementation of QMS through SolTRAQs application system. To participate in investigation exceptions, market complaints and out of specification results and review the investigation report. To act as a laboratory compliance administrator for creation of new users and projects and to review the audit trials. Compliance of QMS related SOPs and records. Ensuring the Compliance to EPD Global Guidelines. Facing internal and external audits and ensuring compliance. Implementation of GLP / GMP requirements. Coordinating and aligning the practices and procedures in line with the COBC requirements. Any other task assigned by reporting manager. JOB FAMILY: Operations Quality t

• Heat Load Calculations for cleanroom projects • Layout development & BOQ preparation • Equipment Selection & Approvals • Documentation (DQ, IQ, OQ, PQ) • Coordination/reporting with Internal design/project team, Vendors, Consultant & Client

HIRING FOR SENIOR LEADERSHIP POSITIONS PHARMA MANUFACTURING Credo Signature Solutions is inviting applications for Two Prestigious Senior Leadership Roles with one of our esteemed pharmaceutical clients engaged in the manufacturing of tablets and liquid formulations. The manufacturing facilities are located across the Northern Himachal region and Punjab . 1. PLANT HEAD 2. QUALITY HEAD Key Requirements (Common to Both Positions): Minimum 20+ years of experience in the pharmaceutical industry Proven track record in a similar leadership capacity (Plant/Quality Head) Prior experience working with top 10 Indian pharmaceutical companies Strong leadership qualities with the ability to drive performance and foster cross-functional collaboration Thorough knowledge and hands-on experience in handling regulatory audits such as USFDA, EU-GMP, WHO, and other RoW markets Excellent interpersonal and communication skills Qualification: B.Pharm/M.Pharm/M.Sc or equivalent Additional Role Expectations: For Plant Head: Comprehensive understanding of end-to-end plant operations including Production, Quality, Engineering, Supply Chain, and EHS Ability to create synergy among departments and align them with business goals Strategic mindset with a focus on compliance, operational excellence, and people development. For Quality Head: Deep expertise in Quality Assurance, Quality Control, and Compliance Strong exposure to QMS, CAPA, data integrity, and regulatory documentation Capability to lead a large quality team and maintain a culture of quality and compliance across the site. Compensation: CTC in the range of INR 40 Lacs to 50 Lacs PA (negotiable for exceptional candidates) Location: Manufacturing sites in Northern Himachal Pradesh and Punjab. How to Apply: Interested candidates may share their updated resume at: info@credosignaturesolutions.com Only shortlisted candidates will be contacted for further discussions.

Job description Candidate will be based at corporate office of reputed Pharma company as a Manager- IT and he will be responsible for handling following:- Job Responsibilities: 1 Candidate would be responsible for the Servers and Computers, Printer and accessories are working properly any given time. 2) The Master Creation in the SAP Batch master is to be done properly. Backup of Servers and Computers are done from time to time. And functions of all camera system installed at plant to ensure proper support to the users.to prepare Presentation, SOPs and participate etc. for the IT compliance training. 3) He have good knowledge of administer LAN, WAN, EPABX & Video Conferencing. 4) Candidate would be responsible Daily Monitoring of all IT compliance with respect to Quality Assurance activities. IT compliance and data integrity Training to IT Team Members. Creation and Review of Qualification/ Validation related documents. Review of IT Training Matrix and Internal Trainer list. 5) Candidate would be responsible impart GSP, GLP, Behavioural, Motivational and other kind of trainings (Classroom & QC), ensuring compliance of the specified procedures / guidance and review of qualification documents such as URS, DQ, IQ, OQ, PQ and validation protocols and validation study report. 6) Candidate would be responsible for various Regulatory and Customer audits and assist management in providing compliance to audit observations and to review performance of juniors and recommend for higher punishment in case of their indulgence in any kind of misconduct including any data integrity. 7) Candidate would be responsible implementation and operation of Document Management (DMS), Quality Management System (QMS), Training/Learning management system (LMS), Lab Info. Management (LIMS) Software. 8) Candidate would be responsible troubleshooting any issues in SAP and subsequent validation and documentation of any modifications, enhancement or upgrades in any and all softwares implemented in the facility. 7) Candidate will be responsible for monitoring the performance of factory network, conduct regular internal audits and implement necessary modifications or adjustments to optimize resources.and CSV Activities with GAMP5 Approach with a yearly planner. And define and manage IT Disaster recovery strategy and Compliance and security for all IT related systems and infrastructure. Required candidate profile Qualification- Bachelors degree in Computer Science, Computer Application. . Candidate should have 8 to 12 yrs. in relevant experience in Hardware & Software. Candidate should have good experience in SAP, of Document Management (DMS), Quality Management System (QMS), Training/Learning management system (LMS). Candidate should have good Knowledge of LAN, WAN, EPABXETS. Should have good Knowledge of Daily Monitoring of All IT Compliance

Create dyeing recipes for new shades based on customer needs, considering the required color. Handling and supervising shift in spinning production. We have 2 vacancies, 1 in Lab dyeing as TDT and another is in spinning production as TDT.

Role & responsibilities : The candidate should also possess practical experience in the following techniques: Bacterial characterization Maintenance of bacterial cultures Phenotypic and genotypic characterization Antimicrobial susceptibility testing using disc diffusion and broth dilution methods Time-kill curve studies Fractional Inhibitory Concentration (FIC) studies Bioburden analysis in biological samples

Dear candidate we are hiring for fresher ITI OR DIPLOMA FOR apprenticeship qualification - ITI( ANY TRADE) EXPECTED ELECTRICIAL OR ELECTRONICS SALARY- 13,500/- Department - Assembly interested candidate contact- 904166549

Customer service- Machine maintenance, ITI electrician required, Ac technician required , Field Work

Wanted Home Tutors who can handle CBSE, ICSE, State Board & college students. If you are good in any subject(s) and can teach any classes from KG to 12th then you are welcome to apply. You can teach students of any class near your home or online Perks and benefits You get 100% of the fee paid by students/parents

Min 2 yr must have experience in production soap/detergent industry and willing to relocate to Dhule Maharashtra for cv whatsapp 9216321822