56 Jobs in Anklesvar

Urgent Hiring || QA Head || Ankleshwar -Gujarat Designation : QA - Head Experience : Minimum 15 to 19 years’ experience in pharma from QA Department. Salary : upto 15 lpa (Depend on the interview) Location: Ankleshwar -Gujarat Essential Duties and Responsibilities : Knowledge of all regulated Guideline & Pharmacopoeia. Preparation & implementation of SOPs related to the concerned department & Justification of Specification. Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing. collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications. The conducts regular internal audits of the manufacturing facility to ensure that the facility meets the required quality standards. handles the Regulatory and Customer audit and its compliance. Responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements Responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented. Responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA). Responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations. Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing. Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC. Implementation & verification, in-process checks, online entries in BPR Review of Manufacturing Processes. Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site. Monitoring and ensuring the good laboratory practice (GLP) by laboratory personal during the routine analysis and instrument operation ensure adherence to procedure Preparation & review of Quality Risk Assessment. Preparation & review of process validation, cleaning validation, equipment qualification To prepare/review the Validation Master Plan, Site Master File, Drug Master File, Annual Product Quality Review, Plant Layout and other documents related to QA Show more Show less

Company Description Glindia Chemicals has over 30 years of expertise in supplying niche, difficult-to-source chemical materials. We provide real solutions by matching customer needs with our extensive network of qualified suppliers to ensure the best fit for quality and performance. Role Description This is a full-time onsite role for a Pharma Intermediates Sales and Marketing Specialist. The specialist will be responsible for developing and maintaining client relationships, identifying and pursuing sales opportunities, conducting market research, creating and implementing marketing strategies, and achieving sales targets. The role also includes preparing and delivering sales presentations, negotiating contracts, and collaborating with internal teams to ensure customer satisfaction. Qualifications Sales and Marketing skills, including developing and implementing strategies, pursuing opportunities, and achieving sales targets Market Research and Analysis skills, including understanding market trends and identifying potential clients Client Relationship Management skills, including maintaining strong client relationships and ensuring customer satisfaction Excellent Communication and Negotiation skills Ability to work independently and remotely Bachelor’s degree in Marketing, Business, Chemistry, or a related field Experience in the pharmaceutical industry is a plus Minimum Experiance of 2 years Show more Show less

Company Description We suggest you enter details here. Role Description This is a full-time on-site role for a Plant Supervisor at Navjivan Chemicals in Anklesvar. The Plant Supervisor will be responsible for overseeing plant operations, maintenance, training staff, and implementing preventive maintenance measures. Qualifications Supervisory Skills and Training experience Plant Operations and Plant Maintenance skills Experience in Preventive Maintenance Good communication and leadership skills Ability to work in a fast-paced environment Knowledge of chemical plant operations is a plus Bachelor's degree in Engineering or related field Show more Show less

Urgent Hiring || Production Head || Ankleshwar, Gujarat Designation : Production Head Experience : Min 15 years in pharma API pharma Salary : Upto 15 lpa (Depend on the interview) Location : Ankleshwar, Gujarat RESPONSIBILITIES: Responsible for reviewing, approving and distributing work instruction for manufacturing activities. Carry out production activities as per production plan. Responsible to decide new batch production. Responsible for monitoring batch process. Review online documentation related to production activities like BMR, BPRs, logbooks and daily records. Qualification of production equipments and participation in validation activities. To check quality system in production department. To prepare equipment master list and equipment qualification plan. Review of MFRs, BMRs, BPRs, SOPs and formats. Review URS, DQ, IQ, OQ, PQ protocol with reports and validation protocol with reports. To ensure that all production deviations are reported, evaluated and that critical deviations are investigated, and the conclusions are recorded. Evaluation and investigation of all market complaints and necessary corrective and preventive actions jointly with QA. Initiating any change by originating change control request and to evaluate proposed changes in product, process or equipment. Review proper segregation of material, labeling and identification, area cleaning and disinfection. Review Preventive maintenance and calibration done according to schedule of equipments/ utilities and recorded. Check on production yields and reconciliation at various stages of manufacturing. Responsible for giving training to the personnel working in the production area. Responsible for handling of manpower and proper allocation of manpower. Responsible for Internal audit preparation. Participate in external audit preparation and handling activities during audit. To comply the requirements of technical audit. cGMP documentation and their revision as and when required. Identifying need and procurement of new machines and equipments. Resource identification (up gradation of existing equipments and manpower). Shift scheduling and sanctioning of production personnel. To comply the requirements of safety audit. Interaction with warehouse / quality control for material availability / release of raw material and packaging material, semi-finished and finished good. Co-ordination with engineering for maintenance / machine breakdown/ Modification. Control on scrap going out of department. To assure batch uniformity and integrity of drug products through written procedure followed by in process controls and tests of each batch. To monitor outputs and to validate the performance of manufacturing process. Periodical review of SOP related to production functions and inform QA to incorporate revisions for betterment of work/developments. Responsible to raise the deviation and change related issues to intimation the QA department. Responsible to participate in investigation and preparation of CAPA. To verify the function and performance of equipments/ utilities. To check and verify labeling and packing activity. Effectively Participate in re-processing and reworking activity. To check and verify the gowning, usage of PPE’s in processing and controlled area. Compliance with cGMP norms. To ensure that all decisions, rules and policies related to environmental management system is followed. Investigation and CAPA implementation for environment related incident/deviation. Show more Show less

Urgent Hiring || QA Head || Ankleshwar -Gujarat Designation : QA - Head Experience : Minimum 15 to 19 years’ experience in pharma from QA Department. Salary : upto 15 lpa (Depend on the interview) Location: Ankleshwar -Gujarat Essential Duties and Responsibilities : Knowledge of all regulated Guideline & Pharmacopoeia. Preparation & implementation of SOPs related to the concerned department & Justification of Specification. Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing. collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications. The conducts regular internal audits of the manufacturing facility to ensure that the facility meets the required quality standards. handles the Regulatory and Customer audit and its compliance. Responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements Responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented. Responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA). Responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations. Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing. Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC. Implementation & verification, in-process checks, online entries in BPR Review of Manufacturing Processes. Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site. Monitoring and ensuring the good laboratory practice (GLP) by laboratory personal during the routine analysis and instrument operation ensure adherence to procedure Preparation & review of Quality Risk Assessment. Preparation & review of process validation, cleaning validation, equipment qualification To prepare/review the Validation Master Plan, Site Master File, Drug Master File, Annual Product Quality Review, Plant Layout and other documents related to QA Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Data Coordinator Date: Jun 6, 2025 Location: Panoli - Prodcution Block 1 Company: Sun Pharmaceutical Industries Ltd YOUR TASKS AND RESPONSIBILITIES: Preparation & Review of start-up Documents: eCRF completion Guidelines, DMP, SAE reconciliation plan, Clinical Coding Plan Preparation of Edit specification document (ESD), Test Plan and Data Entry Guideline Screen design UAT Edit checks UAT in CDMS as per ESD Discrepancy Management Support Data Manager in URS review for IWRS Ensure timely completion of SAE reconciliation activities Ensure timely completion of closeout activities including database lock Preparation and update of Master Data Management File to ensure its completeness Preparation & Review of Data Management Report WHO YOU ARE: Pharmacy / Science Post-Graduate At least 5 years of experience in the clinical data management domain in Pharma/CRO industry. Experience in, development of data management documents, development of validation plan, screen UAT, edit check UAT, clinical data query management etc. Job Location: Remote working job opportunity Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Tips: Provide a summary of the role, what success in the position looks like, and how this role fits into the organization overall. Key Responsibilities: Understand manpower requirements from department heads. Source candidates through job portals, social media, campus hiring, employee referrals, etc. Screen resumes and conduct telephonic interviews. Schedule and coordinate interviews with hiring managers. Maintain candidate database and provide timely feedback. Coordinate and manage onboarding process for new hires. Support in developing and maintaining the recruitment process and metrics. Maintain MIS reports and recruitment trackers. Assist in employer branding and HR activities like job fairs or campus drives. Key Skills: Good understanding of recruitment tools and techniques Excellent communication and interpersonal skills Ability to manage multiple positions simultaneously Attention to detail and strong follow-up skills Proficiency in MS Office (especially Excel and Word) Preferred Experience: Experience in bulk/mass hiring (preferred) Prior recruitment experience in Pharma, Chemical, or Manufacturing is an added advantage Show more Show less

Urgent Hiring || Production Head || Ankleshwar, Gujarat Designation : Production Head Experience : Min 15 years in pharma API pharma Salary : Upto 15 lpa (Depend on the interview) Location : Ankleshwar, Gujarat RESPONSIBILITIES: Responsible for reviewing, approving and distributing work instruction for manufacturing activities. Carry out production activities as per production plan. Responsible to decide new batch production. Responsible for monitoring batch process. Review online documentation related to production activities like BMR, BPRs, logbooks and daily records. Qualification of production equipments and participation in validation activities. To check quality system in production department. To prepare equipment master list and equipment qualification plan. Review of MFRs, BMRs, BPRs, SOPs and formats. Review URS, DQ, IQ, OQ, PQ protocol with reports and validation protocol with reports. To ensure that all production deviations are reported, evaluated and that critical deviations are investigated, and the conclusions are recorded. Evaluation and investigation of all market complaints and necessary corrective and preventive actions jointly with QA. Initiating any change by originating change control request and to evaluate proposed changes in product, process or equipment. Review proper segregation of material, labeling and identification, area cleaning and disinfection. Review Preventive maintenance and calibration done according to schedule of equipments/ utilities and recorded. Check on production yields and reconciliation at various stages of manufacturing. Responsible for giving training to the personnel working in the production area. Responsible for handling of manpower and proper allocation of manpower. Responsible for Internal audit preparation. Participate in external audit preparation and handling activities during audit. To comply the requirements of technical audit. cGMP documentation and their revision as and when required. Identifying need and procurement of new machines and equipments. Resource identification (up gradation of existing equipments and manpower). Shift scheduling and sanctioning of production personnel. To comply the requirements of safety audit. Interaction with warehouse / quality control for material availability / release of raw material and packaging material, semi-finished and finished good. Co-ordination with engineering for maintenance / machine breakdown/ Modification. Control on scrap going out of department. To assure batch uniformity and integrity of drug products through written procedure followed by in process controls and tests of each batch. To monitor outputs and to validate the performance of manufacturing process. Periodical review of SOP related to production functions and inform QA to incorporate revisions for betterment of work/developments. Responsible to raise the deviation and change related issues to intimation the QA department. Responsible to participate in investigation and preparation of CAPA. To verify the function and performance of equipments/ utilities. To check and verify labeling and packing activity. Effectively Participate in re-processing and reworking activity. To check and verify the gowning, usage of PPE’s in processing and controlled area. Compliance with cGMP norms. To ensure that all decisions, rules and policies related to environmental management system is followed. Investigation and CAPA implementation for environment related incident/deviation. Show more Show less

Urgent Hiring || QA Head || Ankleshwar -Gujarat Designation : QA - Head Experience : Minimum 15 to 19 years’ experience in pharma from QA Department. Salary : upto 15 lpa (Depend on the interview) Location: Ankleshwar -Gujarat Essential Duties and Responsibilities : Knowledge of all regulated Guideline & Pharmacopoeia. Preparation & implementation of SOPs related to the concerned department & Justification of Specification. Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing. collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications. The conducts regular internal audits of the manufacturing facility to ensure that the facility meets the required quality standards. handles the Regulatory and Customer audit and its compliance. Responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements Responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented. Responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA). Responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations. Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing. Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC. Implementation & verification, in-process checks, online entries in BPR Review of Manufacturing Processes. Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site. Monitoring and ensuring the good laboratory practice (GLP) by laboratory personal during the routine analysis and instrument operation ensure adherence to procedure Preparation & review of Quality Risk Assessment. Preparation & review of process validation, cleaning validation, equipment qualification To prepare/review the Validation Master Plan, Site Master File, Drug Master File, Annual Product Quality Review, Plant Layout and other documents related to QA Show more Show less

Objectives of the Position To handle QA/QC activities in shifts, provide decision on running production and update to HOD (QA/QC) if required. Main Areas Of Responsibilities And Key Activities Responsibilities & Key Activities: All day-to-day shift activities. Approval of WIP, RM , FG as per specification. Colour inspection and adjustment. Injection moulding and testing of the lab samples. Enter QC data in the SAP . Implementation of 5S in lab area. Responsible for any production issue i.e. customer complaints, rejection, losses etc. Reporting of daily reports. All other activities related to QA/QC. Implementation of QMS system. Recording, investigating all the accidents departmentally and identifying, potential hazards, unsafe conditions/ near misses and reporting to the QA/QC Head / HSE department. Implementation of suggestions and recommendations. Giving feedback to QA/QC Head in the safety matters and suggest improvements in the working conditions, methods, procedures etc. EHS Responsibility Follow safety rules and use of PPE in QA/QC lab & ensure safe environment in lab area. To find out near miss, unsafe condition in whole plant & report it on yellow card for mitigation of major accident & close it in proper way action plan. Follow regulatory compliance and company policies etc. Participation in Mock Drills. Ensuring safe and clean environment in lab area Follow that all Sustainability Requirements, procedure, regulations, and safe working practices. Job Basic Skills Basic operation of computer. On the job skill like operation or testing of different lab equipment’s. Communication Presentation Job Technical Skills Hands on experience of Tensile Test, Flexural Test, Specific gravity, Impact, HDT, DSC, UL 94 FR rating , Viscosity, MFI, Ash content, Shrinkage, Moisture content etc. Job Requirements Education : B. Sc.in Mathematics, Chemistry, Physics and Diploma in plastic testing Working Experience: 3 – 6 years in plastic testing Technical & Professional Knowledge: Knowledge of plastic testing etc. and operation of injection molding machine. Knowledge of core QC tools, QMS/EMS , IATF16949 Show more Show less

O bjectives of the Position To operate process plants for manufacturing of finish product by monitoring and control of process parameter Operates, regulates, and monitors batch productions to produce Engineering Plastics products during shift. Works in field under supervision of the shift leader M ain Areas of Responsibilities and Key Activities Performs routine tasks and assignments through practical application of industry standards involving production operations, Mixing & feeding of RM & packing of FG. Applies considerable knowledge in the operation, maintenance, methods, procedures and techniques of applicable plant equipment and safety requirements specific to the area of assignment. Basic House Keeping of machine and workplace Performs routine troubleshooting. As per site layout responsible for Production area. RCMS Responsibilities Familiarize themselves with MSDS of hazardous substances within workplace. Perform the role as defined in On-site Emergency Plan to mitigate the emergencies. Follows requirement / procedure related to EMS/ RCMS. To take EHS requirements into consideration prior to any activity or work to make sure that the launching work is safe to prevent/minimize the safety risk, environment pollution and other potential hazards. Attend all EHS training as required. Have the responsibility for promptly reporting to direct supervisor in case of any incidents and near miss or exposure to hazardous substances. Always practice good housekeeping and keep workplace clean. Risk analysis. Develop safe working skills and habits. Familiarize themselves with MSDS of hazardous substances within workplace. Key Activities Maintain the Production, Quality & Safety Smooth Plant operation House Keeping Job Skills Equipment Knowledge of production / packaging equipment, and knowledge of instrumentation / control system, and automation, including technical standards Process Unit Operations Safety Communication Job Requirements Diploma in plastic processing / ITI with 3year experience in polymer plant 3 -15 Years Working Experience Technical & Professional Knowledge in Extrusion equipment & compounding process Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: QA Head API Date: May 15, 2025 Location: Panoli - Quality Assurance Company: Sun Pharmaceutical Industries Ltd JOB DESCRIPTION Position : QA Head Effective Date: Reports to : Quality Head Job Code: Department: Quality Grade: Functional Area: QA Location: Panoli POSITION SUMMARY Manage overall quality assurance oversight and site activities wrt to quality systems: documentation review and SOP update, in-process quality assurance, sampling and batch release, preventive maintenance/calibration/qualification/validation, internal audit, compliance, quality oversight of electronic systems, budget, and continuous improvement of quality systems, RA support, monitoring of pest control, retention sample management as per Good Manufacturing Practices requirements. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures. Key Responsibilities: Responsible for defining operational strategy and road map for quality assurance management at site. Define site quality assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at site. Provide strong leadership and expertise to ensure achievement of all Quality Assurance accountabilities at site. Identify and implement solution for improving existing site quality assurance systems and processes. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. Ensure that performance issues are managed in a consistent and timely manner. Develop site quality assurance revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams. Responsible for executing Quality Management Reviews at site, monitor individual Performance and set improvement areas. Responsible for ensuring market complaints, failures, deviations are investigated and corrective and preventive actions are implemented as per set timeline. Responsible for ensuring compliance to regulatory requirements on product, process and release procedures. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. Responsible for ensuring smooth collaboration with all Sun Pharma sites and leveraging synergies. Review & tracking of quality assurance metrics e.g. deviation, change control, OOS/OOT, CAPA effectiveness, market complaints with site manufacturing / QC Management and driving them down. Ensure processes for supply chain management / Global Material Sourcing for vendor selection is followed for vendor selection, qualification and monitor vendor quality performance Provide inputs to manufacturing, R&D and PDL work processes to ensure Quality by Design. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and QA systems at the site. Facilitate internal and regulatory agency audits, ensuring that findings from site audits are understood, assessed and addressed site wide in a comprehensive manner. Monitor industry trends/issues faced internally and identify scope for improving Site quality assurance management and processes. Responsible for fulfilling all training requirements of quality assurance employees. Ensure the quality policies, standards and procedures for computerized systems are implemented and adhered at site. Ensure all GxP computerized systems are validated in compliance with the quality policies, standards and procedures and are maintained in validated state throughout the lifecycle with adequate security and controls to ensure data security. Review and approve the documents as per quality procedures. Work in partnership with the site cross functions and corporate functions for implementation of new initiatives. MINIMUM EDUCATION/EXPERIENCE REQUIREMENTS Science or Pharmacy Graduate Equivalent 15 years REQUIRED SUCCESS ATTRIBUTE Knowledge of GxP’s, cGMP and other regulatory requirements. Planning and Prioritization Collaboration Accountability Compliance Customer Service orientation Secondary Success Attributes People Connect Attention to detail Emotional control Effective Communication & Problem solving Roles WORKING ENVIRONMENT/PHYSICAL REQUIREMENTS Additional responsibilities can be assigned as required. Incumbent performs work assignments in both normal office and non-aseptic manufacturing/packaging environments. Moderate to loud noise level is common in production rooms. The incumbent must be able to comply with the gowning requirements for entry into controlled non-aseptic manufacturing areas, and wear personal protective equipment as required. DELEGATION OF RESPONSIBILITY In the absence of job holder, delegation of responsibility will be as follows: Upward Delegation – Strategic site responsibilities to higher level Downward Delegation – Operational responsibilities to direct reports or similar job role ___________________ __________ Department Head Date ____________________ __________ Human Resources Date This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Manager - Production (API) Date: May 24, 2025 Location: Panoli - Prodcution Block 6 Company: Sun Pharmaceutical Industries Ltd Role : Sr.Manager Production (API) Role: Sr. Manager - API Production Location: Panoli (Baroda) Grade: Sr. Manager Educational Qualification B.Pharma/M.Pharma Work Experience 17 to 19 years of work experience. Handle team size of 150 to 200. Handle Production capacity of minmum 50 Cr. In Current role, he should be heading block. Apart from this experience of handling QMS, Capacity Enhancement, Solvent recovery. API regulatory plant experience. Roles & Responsibilities : Production Planning and scheduling (day to day basis) Ensuring resources available (BMR, Raw Material Manpower etc.) Liaison with QC/QA/STORE/Eng. Dept. for solving of trouble shooting problem. Implementation and monitoring of GMP Standard. Introduction and scale up of technology transfer. (New Prod 1ct) Constantly monitoring and improvement of product process, efficiency, services etc. Documentation work, Monthly Report, data preparation (Process trend analysis) and root cause analysis. Ensure the availability of consumable items & Planning of RM require as per campaign basis. Ensure the documents related to process I cleaning / House Keeping. Control on fresh as well as recovered solvents/ spent solvent. Ensure the solid and process waste transfer to respective area and record maintaining. Other activities entrusted from time to time. Review the prepared/ Revision of BMR and SOP. Operation of electronic system i.e.ONE HR portal, Metis Track wise, Minitab, Out Look etc. Ensure Preventive Maintenance of Plant Equipment's in time frame. Ensure the training to subordinates. Extended Facility of reactor Area of production Planning and scheduling (day to day basis) Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Manager - Production Date: May 19, 2025 Location: Panoli - Prodcution Block 6 Company: Sun Pharmaceutical Industries Ltd Job Description Position: Sr. Manager - Production Job Title: Job Grade: G9A Function: Global API Business Sub-function: Manager’s Job Title: Skip Level Manager’s Title: Function Head Title: Location: Panoli No. of Direct Reports (if any) Areas of Responsibility Production planning and scheduling (day to day basis.) Ensuring resources available (BMR, Raw Material Manpower etc.) Maintain GMP norms and trained the subordinates accordingly. Review the BMR, incident and change control etc. and accordingly co-ordinate with R&D. Co-ordination with Engg. Dept. for preventive maintenance and calibration Ensure to maintain the online documentation and accordingly train the subordinate. Close co-ordination with service dept. like QA, QC, Store, Egg, Safety etc. for Routing work of plant. Ensure create and confirm the process order and ensure to complete the daily entry in SAP HANA. Liaison with QC/QA/Store/Engg. Dept. for solving of trouble shooting problem. Constantly monitoring and improvement of product process, efficiency, services etc. Reporting to higher authority. Ensure Training to subordinate. Ensure Documentation work, monthly reports, data preparation, root cause analysis, incident and change control etc. (process trend analysis). Ensure Preparation/ Revision of BMR & related accessories and SOP. Procurement of consumable items. Actively involves the Process and cleaning validation. (where applicable) Ensuring the Maintaining of documents related to Process/ Cleaning/ HouseKeeping. Control on fresh as well as recovered solvents/ spent solvents Responsible for administrative work related to plant Co-ordination with other department for solid waste, process waste and spent solvent transfer to respective area and record maintaining. To maintain discipline as per company's rules and regulation. Other Activities entrusted from time to time Preparation, review and revision of SOP. Working as a Department Training coordinator in LMS Operation of electronic system like SAP HANA, Leave Portal etc. Travel Estimate Job Scope Internal Interactions (within the organization) External Interactions (outside the organization) Geographical Scope Financial Accountability (cost/revenue with exclusive authority) Job Requirements Educational Qualification MSC / BE/ B.Tech – Chemical Specific Certification Skills API Production Experience 17 to 19 years of work experience. Handle team size of 150 to 200. Handle Production capacity of minimum 50 Cr. In Current role, he should be heading block. Apart from this experience of handling QMS, Capacity Enhancement, Solvent recovery. API regulatory plant experience. 2 | P a g e Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Engineering Head Date: Jun 2, 2025 Location: Panoli - Engineering Company: Sun Pharmaceutical Industries Ltd To maintain facility and equipment. To procure engineering consumables, proprietary spares and to maintain inventory of the same. To perform and to approve Qualification studies for equipment (Plant and Utility) and Facility. To schedule and to execute preventive maintenance program for plant equipment and utility equipment. To review and to participate in process validation program. To maintain and to update drawing like plant layout, equipment layout, P & ID for equipment (Plant and Utility), HVAC system etc. To schedule and to execute Annual Maintenance Program for Utility and material handling equipment. To arrange instruments for plant equipment and accessories. To review, authorize and to comply all Quality documents. To ensure statutory compliance of boiler/electrical inspector & standard weights. To execute modifications in plant as per approved capex and requirement by plant. To ensure cGMP & EHS compliance. To arrange the training of department employees for SOP, new system, Qualification etc. To review maintenance report and energy consumption to ensure corrective action for control of same. To review annual engineering budget. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Engineering Head - API Date: May 22, 2025 Location: Panoli - Engineering Company: Sun Pharmaceutical Industries Ltd Engineering Head – API Grade : DGM / GM Location : Panoli (Vadodara) Job Purpose Lead, plan and directs all aspects of engineering activities within the API plant Organization. Conduct effective reviews of the team and portfolio, provide direction and guidance to the team, and develop team competence with the object of ensuring all engineering projects, initiatives, and processes are in conformance with organization's established policies and goals Duties And Responsibilities Conduct effective reviews of the team and portfolio, provide direction and guidance to the team, and develop team competence Monitor operation and maintenance of Utility and services including water, air ,steam, nitrogen refrigeration , HVAC system in the plant to achieve the desired targets Monitor the maintenance of equipment Modify the equipment as per process requirement / mandates /new projects Monitor the Civil and building management activities Ensure 100% availability of electrical system including DG power and transformers Ensure sterile plant process equipment maintenance Adhere to compliances related to boiler ,factory ,electrical and any other compliance related to Engg Adhere to CGMP compliance for audits participation etc. Ensure plants Energy conservation and cost reductions as per required mandates Ensure adherence to safety compliances are followed in the Engg team Prepare annual budgets ( CAPEX /OPEX) Overall Engineering including Mechanical Maint. of plant, Utility operation, Electrical, Instrumentation, Quality Engineering and execution of capex and Plant modification. Total No. of reactors is 400 with a combined capacity of 1000 KL spread over 14 Production modules. Experience- 20 years. Qualifications Include: Requires a bachelor's degree in engineering preferably Mechanical Knowledge of SAP/ERP systems will be an added advantage. Minimum experience of 20 years with 10 years’ experience in the API industry Having exposure to Energy conservation Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Role & responsibilities Checking VTOP/ PLC/FDS/DQ compilation. Follow up for drawing approval. Informing marketing/Commercial department in case of commercial implication in all approved drawing. Visit to clients site for clearing tech issues and closure of pending info from client. Check drawing logs. Check for conformity of design for cable conducting PLC/FDS/ID & Drawing. Updating Drawing Approval Report. Maintaining of correspondences between factory and between clients in the Job file. Corresponding with factory and client for closure of technical issues. Clearing of technical bottlenecks in any Projects Master monitor for change controls. Communication within organisation and with client for Techno commercial clarity for drawing execution. To get GA drawing approval from client in consultation with VTOP / Marketing. Data live jobs updating Timely closure of open issues. Ensure technical inputs are properly filtered and archived. Ensure preparation and updating of documents like VTOP/PLC/FDS/DQ. Co-ordinate with factory & other departments for completion of processes for on time delivery to time. Weekly compliance report communication to client.

Sales Development

Objectives of the Position Maintenance of plant equipment including twin screw extruders, pelletizers, loss in weight feeders, pneumatic conveying systems, classifiers, packaging and sealing machines, etc. Utility In charge: Responsible for smooth operation of Utility equipment at site, Preventive maintenance planning and Execution for all utility equipment including chilled water system, air compressor system, fume scrubber system and dust collector system. Spare part management for Smooth operation of Plant. Regular Monitoring of Plant equipment to reduce the breakdown. Supervision of Mechanical and Civil Projects. Ability to handle Mechanical breakdown in the Plant. Main Areas Of Responsibilities And Key Activities Responsibilities & Key Activities Manage all maintenance activity related to mechanical dept according to plant requirement with utmost Safety measures. Day to day planning and execution in co-ordination with production team for maintenance work (Preventive maintenance, other maintenance activity) as per priority defined in SAP. To carry out Preventive Maintenance as per the PM planner prepared. To attend all Breakdown/ other maintenance activity with optimum usage of available resource and minimum repair time. To come up with improvement ideas and suggestions. To participate in 5Why/ RCA for major breakdown Maintain housekeeping and ensure plant in good condition. Maintain records, Logbooks of day-to-day activity. Ensure maintenance work with desired quality, safety and reliability Manpower handling and planning. Ensure Implementation of PPE & Work Permit requirements. Checking and maintaining of Spare parts & inform supervisor for Procurement, Sending Material outside for repairing Follow up with Vendor for Repairing. Action against each Yellow card/Near Miss/MOC reports. Job Skills Ability to handle all maintenance activities, planning & its implementation, Internal projects planning & Execution. Equipment Knowledge of Extrusion & Compounding Process, packaging equipment, loss in weight feeders, spiral conveyors, classifiers and pelletizers. Computer Operation Ability to handle Problem Individually Follow all EHS guidelines Communication ISO/TS/EMS basic understanding Job Requirements Education: Diploma in Mechanical Engineering, ITI (fitter) or equivalent Working Experience: 5 Years’ experience in Mechanical Maintenance Technical & Professional Knowledge: Ability to handle all Mechanical maintenance activities, planning & its implementation. Manpower Handling. Show more Show less

At FMC , our employees are guided by our purpose: Innovation for Agriculture, Solutions for the Planet. We provide farmers innovative solutions that increase the productivity and resilience of their land. From our industry-leading pipeline to novel biologicals and precision technologies, we are passionate about the power of science to solve agriculture’s biggest challenges. For more than a century, FMC has successfully delivered some of the of the industry's most advanced, innovative solutions that protect farmers’ crops from destructive pests and disease, while also protecting the environment. We are committed to fulfilling our mission of discovering new herbicide, insecticide and fungicide active ingredients, product formulations and pioneering technologies that are consistently better for the planet. Job Responsibility:- Having experience of Operation and maintenance of equipment like Fire tube Boiler, Water tube boiler, cooling tower, Chiller, Air compressor, Nitrogen generating system, steam network and steam traps. Reducing wastage and losses of Energy, improving efficiency through technological upgrades and improved operation and maintenance (Energy Conservation). Using Computing skills to prepare machine performance report preparation and its presentation. Calculation of cost of Utility service and optimizing it as minimum as possible. Equipment BOM preparation and inventory control like filter stock, Oil stock, spares. Reduce down time of machine using operational trend chart, solving problem and improving reliability. Maintain safety standard & Safety rules in dept. Maintaining, updating the Departmental documents and the records Maintain Environment related documents & adhere to policy for related activities. Looking after Day To day Routine maintenance jobs Trouble shooting jobs Required material Intend Compile data and write reports regarding existing and potential engineering studies and projects as well as day to day activities Installing, servicing, calibrating, Preventive Maintenance and updating Mechanical systems. Having Knowledge of SAP Requirements:- Experience- 5 to 8 Years of experience. Education - ITI OR Diploma in Mechanical / ITI or Diploma in Refrigeration and Air conditioning. Location - Panoli, Gujarat Show more Show less

Job Title: Sales Officer (On Roll) Salary: Rs. 12,500 to 14,500 + (Incentives) Week off: All Sunday Job Time: 9:30 am to 7:00 pm Key Responsibility: Generate leads and acquire new customers for two-wheeler loans through field visits, referrals, and dealership tie-ups. Establish and maintain relationships with two-wheeler dealerships to drive loan business. Explain loan products, eligibility criteria, interest rates, and documentation requirements to potential customers. Collect and verify customer documents as per KYC norms and internal guidelines. Coordinate with credit and operations teams for loan processing and disbursal. Achieve monthly sales targets and maintain high customer satisfaction.

Sales Development

Company Description We suggest you enter details here. Role Description This is a full-time on-site role for a Junior Accountant located in Anklesvar. The Junior Accountant will be responsible for day-to-day accounting tasks, financial record-keeping, assisting with audits, preparing financial reports, and reconciling accounts. Qualifications Accounting, Finance, and Bookkeeping skills Knowledge of financial regulations and compliance Strong analytical and mathematical skills Proficiency in MS Excel and accounting software Attention to detail and accuracy Excellent organizational and time management skills Ability to work collaboratively in a team Bachelor's degree in Accounting, Finance, or related field Show more Show less

responsibility is to identify, attract, and engage potential candidates, particularly for field roles, by directly connecting with them in their work environments or at field events. This involves building relationships, participating in job fairs and networking, and managing the recruitment process from sourcing to onboarding. Job Location :- Ankaleshwar, Gujrat Experince :- min 1-2 Years In recruitment. Only Male Candidate Required 2 Wheeler Mandatory Salary 15000 To 20000 NTH