1494 Jobs in Ankleshwar - Page 44

We are looking for a motivated Field Sales Executive to promote our hardware shop in the Panoli and Ankleshwar industrial area . The candidate will be responsible for visiting nearby companies, meeting with purchase managers, distributing business cards, introducing our products , and generating regular orders . Responsibilities: Visit companies in Panoli and Ankleshwar region Meet purchase or store managers to explain our product offerings Share business cards and promote our hardware store Build strong relationships and follow up regularly Collect orders and coordinate with our store for delivery Requirements: Good communication and presentation skills Should be comfortable with fieldwork (daily visits to companies) Basic knowledge of hardware/building materials is a plus Own vehicle preferred Location: Panoli / Ankleshwar Job Type: Part Time Salary: Based on experience + incentives Job Types: Full-time, Part-time, Contractual / Temporary, Freelance Pay: From ₹10,000.00 per month Compensation Package: Commission pay Performance bonus Location: Ankleshwar, Gujarat (Required) Work Location: In person

Job Title: Sr. Executive – Production, Pharma Educational Qualification and Experience: M. Pharm / B. Pharm from a reputed university, having 7 to 10 years in the pharmaceutical Primary and secondary packing section, and also exposure in manufacturing in Granulation, compression, and Coating. Production Implementing a monthly production schedule with consistent quality, adhering to Regulatory, GQS, and HSE guidelines, with proper utilization of resources and optimum cycle time. Performing the production activities in assigned areas to achieve 100 % customer service. Performing the SAP-related activities Able to handle a team consisting of Contractual persons, FTC & Operators in the allocated shift Able to do troubleshooting in the allocated area ISO 14001 and SAP Adhering to ISO 14001 activities and objectives in Pharma Mfg. Performing all the SAP-related activities as and when needed. Compliance Implementing and ensuring compliance with GQS, HSE, and ISO guidelines/standards and maintaining documentation for the same, including process validation and qualification. Coordination Coordinating with Engineering department for preventive and breakdown maintenance, modifications etc. The purchase department for procuring and controlling auxiliaries. Quality department for all quality-related matters. Packaging department for bulk availability. Yield monitoring Implementing and making efforts for the continuous improvement of the yield of assigned products Training Impart training to the operative staff (like contractual persons, FTC & operators ) on GMP, Data Integrity ,HSE, ISO requirement & process improvement and maintaining good industrial relation in the plant by effective grievance process. Others Carrying out any other assignments or projects like qualifications and validations as per the instruction of the Dept. Head to meet the organizational priorities. Identifying and correcting unsafe conditions or behavior and promptly reporting other potentially hazardous situations. Maintaining plant assets in good condition and making optimum use of all resources. Ready to work in each shift & in any allocated areas

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Supervision and Leadership, Production Planning and Scheduling, Safety and Compliance, Communication and Collaboration, Monitoring and Reporting

Roles and Responsibilities Develop formulations for solid oral dosage forms (tablets) and liquid orals. Conduct formulation research development, stability studies, and analysis to ensure product quality. Prepare trial batches of formulations and document them accurately. Collaborate with cross-functional teams to resolve formulation-related issues. Ensure compliance with regulatory requirements during all stages of formulation development.

Role & responsibilities Able to do Cycle count independently. Able to perform Inventory count independently. SAP knowledge is must at transactional T-Code level. Able to do reconciliation independently. Reporting of results of Cycle count and Stock Count. Fluent E-Mail communication. Able to handle team of 5-6 members. Required good co-ordination skills. Able to work in stretched hours as well as on Sunday as per business requirement.

Role & responsibilities : End-to-end warehouse operations / floor operations Organize and maintain inventory storage area Ensure accuracy in transactions Vendor / contractor management Labor management Maintaining and assessing safety, hygiene and welfare of employees at warehouse Transportation management

Process Maintenance Management Ensure the proper operation and maintenance of equipment used in the production of vaccines and injectable, including sterile systems, filling lines, and aseptic processing equipment. Develop and implement preventive maintenance programs that adhere to GMP standards to minimize downtime and ensure continuous production. Manage maintenance activities for critical production and utility systems, including HVAC, autoclaves, sterilization systems, and other aseptic equipment. Lead troubleshooting efforts for any process or equipment failures, ensuring prompt corrective actions are taken while complying with safety and regulatory standards. Instrumentation and Control Systems Supervise the installation, calibration, and ongoing maintenance of all instrumentation and control systems in the plant, including those that monitor and control critical manufacturing parameters. Ensure compliance with GMP, FDA, and other regulatory standards for instrumentation used in the production of vaccines and injectables. Collaborate with quality assurance (QA) and validation teams to validate control systems and instrumentation for accuracy, reliability, and compliance with regulatory requirements. Lead troubleshooting and maintenance activities for any failures in instrumentation, ensuring immediate corrective action and minimal impact on production. Water Systems Management Oversee the operation, maintenance, and monitoring of water systems, including water for injection (WFI) systems, ensuring that they meet the required pharmaceutical-grade quality and regulatory standards. Ensure compliance with regulatory requirements for water quality, including microbial control and endotoxin levels. Manage water treatment and distribution systems, coordinating routine cleaning, sanitization, and validation of these systems. Ensure water systems are maintained to prevent contamination and safeguard product quality. Utility Systems Management Manage and maintain critical utility systems, including steam, compressed air, HVAC, and cooling systems, ensuring they meet stringent pharmaceutical manufacturing standards. Implement and maintain energy efficiency and sustainability practices, in line with regulatory standards and corporate sustainability goals. Oversee the maintenance and calibration of systems used in temperature and humidity control, which are critical for sterile production environments. Regulatory Compliance & WHO Audits Lead preparation for WHO audits, FDA inspections, and other regulatory audits, ensuring all maintenance practices, systems, and equipment are fully compliant with GMP and regulatory requirements. Ensure the engineering and maintenance documentation, including calibration logs, preventive maintenance records, and validation documents, are accurately maintained and ready for audit. Collaborate with the QA team to support the resolution of audit findings and the implementation of corrective actions. Stay up to date on the latest regulatory changes and industry standards, ensuring the plant operates in full compliance at all times. Validation and Qualification Oversee the qualification and validation of critical equipment, systems, and processes to ensure they meet all required regulatory and operational standards. Work closely with the validation team to develop, execute, and maintain qualification protocols for equipment, systems, and utilities. Ensure that all maintenance activities are aligned with the requirements of the validation master plan (VMP) and that any changes are appropriately documented and validated.

We are hiring Q.A Officer for our pharma intermediate organization. Requirements:- Qualification :- Pharm/M. Pharm/M.Sc. Location :- Panoli (Gujarat) Experience :- 0 TO 3 year Benefits:- PF/Bonus Salary :- 15000-20000

Job Requirements Role/Job Title: Relationship Manager-Kisan Credit Card Function/Department: Rural Banking Job Purpose The role entails providing financial solutions to meet the requirements of the KCC customers and ensure value added customer service. The role will closely collaborate with the product and operations teams to drive effective customer acquisition, servicing and deepening. The role bearer would be responsible for providing customers with the best in-class experience to become their banking partner of choice. The role bearer is responsible for NTB clients and manage the relationship for a designated branch contributing to the larger branch banking channel objectives. Responsibilities Roles & Responsibilities: Responsible for increasing liabilities size of relationship via balances in accounts of existing KCC customers and enhancing customer profitability by capturing larger share of wallet. Review the inflows and outflows in the mapped accounts and also proactively identify potential business opportunities. Establish closely connect with the existing customers through mailers and phone calls and share insights on the fluctuations in interest rates, exchange rates and various product offerings. Generate new sales leads for KCC customers through referrals from existing clients, brokers, etc. Responsible for acquiring new customers for KCC with a detail understanding of Credit assessment. Leverage knowledge on Liability, Fx, Trade and Client Relationship, Delinquency management, Relationship management and Analytical mind-set to increase volume of business. Managing portfolio effectively through continuous monitoring of accounts and renewals enhancement, retention and ensure Portfolio Hygiene with minimal open deferral and covenants. Develop a superior working relationship with Branch banking for cross leveraging and synergy optimization and work within the Overall Bank Eco System with other Stakeholders. Evaluate the growth strategy based on competitor analysis and feedback from different channels/customers. Recommend process changes in order to improve service efficiency and quality across the branch network. Demonstrated Ability in sales planning and conceptualize promotions and marketing initiatives. Understanding of Financial statements, Credit Assessment and title- security documents. Managerial & Leadership Responsibilities Attract and retain best-in-class talent for key roles in their reporting structure. Monitor key parameters on employee productivity, hiring quality and attrition rates and make necessary improvements. Enable teams to drive growth targets by providing necessary support. Education Qualification Graduation: Bachelor’s in Engineering / Technology / Math’s / Commerce / Arts / Science / Biology / Business / Computers / Management. Experience: 3+ years of relevant experience. Show more Show less

Qualification: ITI AOCP/Bsc /Diploma Chemical Experience : 5 to 10 Years CTC: Up to 7.0 LPA Work Location : Dahej Experience In Agrochemical Company is Prefer send cv on sdpbharuch@gmail.com with Sub : Plant Operator Dahej Required Candidate profile Interview Venue: SDP HR SOLUTION 610, GOLDEN SQUARE BESIDE DMART ABC CIRCLE BHARUCH Share CV on sdpbharuch@gmail.com with Subject: Plant Operator Dahej No Charges Share with Friends & Colleagues

Urgent Opening For Bharuch Gujarat Location for QualityController should be B.S.C graduate working experience of 5yrs from food industry share resume on fatima.prospectus@gmail.com or Whatsapp on 8928384830/9082705936

Knowelgde of Tally Prime ERP 9 , E invocie , Eway bill , GST

Roles and Responsibilities Ensure timely completion of civil construction projects on site. Conduct regular site monitoring to identify potential issues and implement corrective actions. Manage labor resources effectively to meet project deadlines. Coordinate with other departments for smooth site operations.

JD: 1) To be prepared document related to audit as per audit agenda. 2) Filled vendor questionnaires & prepared related documents. 3) Keeping record of key Customer. 4) To be prepared process validation protocol and report as per seniors guidance. 5) To be prepare cleaning validation protocol and report as per seniors guidance. 7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement. 8) To help the senior for preparation of CAPA according to audit report. 9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook. 10) To be prepared BPCR as per procedure. 11) To be issue BPCR to all blocks as per prerequisite. 14) To be handle change control, market complaint, deviations, CAPA. 15) To be issue documents, protocols, log book and format to all department as per prerequisite. 16) Retrieval of documents. 17) To be controlled all master documents. 18) To be prepared schedule & conduct Internal audit. 19) To be prepared APQR of all products. 20) Preparation of documents for Certification & product registrations work i.e. FDA, Halal, Kosher, Reach. etc. Review specification, test procedure and SOP's for their deficiencies according to audit points 1) To be prepared document related to audit as per audit agenda. 2) Filled vendor questionnaires & prepared related documents. 3) Keeping record of key Customer. 4) To be prepared process validation protocol and report as per senior’s guidance. 5) To be prepare cleaning validation protocol and report as per senior’s guidance. 6) To be conduct training and evaluation done as per Schedule. 7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement. 8) To help the senior for preparation of CAPA according to audit report. 9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook. 10) To be prepared BPCR as per procedure. 11) To be issue BPCR to all blocks as per prerequisite. 13) To be prepared data for monthly report as per QMS and submit to senior. 14) To be handle change control, market complaint, deviations, CAPA. 15) To be issue documents, protocols, log book and format to all department as per prerequisite. 16) Retrieval of documents. 18) To be prepared schedule & conduct Internal audit. 19) To be prepared APQR of all products.

Designation : QA - Head Experience : Minimum 15 to 19 years’ experience in pharma from QA Department. Salary : 15 lpa Location: Ankleshwar -Gujrat 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 Job Types: Full-time, Permanent Pay: ₹1,500,000.00 per year Schedule: Day shift Morning shift Application Question(s): are you most comfortable with location Ankleshwar? what is your expected annual salary / ctc? what is your current annual salary / ctc? what is your notice period? (in days) How many years of Proven experience in QA HEAD? How many years of Proven experience in API ? Work Location: In person Speak with the employer +91 9289321002

Hi Everyone Exciting Opportunity Qualifications : Graduate in science-related field, such as chemistry or pharmacy Experience : 20 years Experience Location: Ankleshwar -Gujrat JD: 1. 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 Please share me Your Resume if Your Interested: 86570 17224 Job Type: Full-time Pay: ₹1,400,000.00 - ₹1,600,000.00 per year Benefits: Flexible schedule Internet reimbursement Leave encashment Life insurance Provident Fund Schedule: Day shift Work Location: In person Speak with the employer +91 86570 17224

Lead and manage raw material planning, purchasing, inventory control, forecasting. Manage vendor relationships. Oversee organization wide management of the strategic sourcing, procurement, contracting, and evaluation of services Manage / coordinate the sales and operations planning process including supply / demand forecasting, inventory management, and on time delivery. Identify and manage risk within the supply chain. forecasting levels of demand for services and products to meet the business needs and keeping a constant check on stock levels. conducting research to ascertain the best products and suppliers in terms of best value, delivery schedules and quality. liaising between suppliers, manufacturers, relevant internal departments and customers. identifying potential suppliers, visiting existing suppliers, and building and maintaining good relationships with them. negotiating and agreeing contracts and monitoring their progress, checking the quality of service provided. Responsible for All IMPORTS of Raw Material and EXPORTS of Finish products. Obtaining of Advance License / DFRC / RoDTeP Licenses against exports anticipated / made and clearance of consignment custom duty free. Responsible for cost effectiveness in import & export transactions. Negotiations with Shipping companies, CHAs, Transporters for charges for their services. Responsible for All documentation with CHAs, DGFT, Customs, Port Authorities, Surveyors, Transporters, Export Inspection Agency, Chambers of Commerce, Consultants.

Lead and manage raw material planning, purchasing, inventory control, forecasting. Manage vendor relationships. Oversee organization wide management of the strategic sourcing, procurement, contracting, and evaluation of services Manage / coordinate the sales and operations planning process including supply / demand forecasting, inventory management, and on time delivery. Identify and manage risk within the supply chain. forecasting levels of demand for services and products to meet the business needs and keeping a constant check on stock levels. conducting research to ascertain the best products and suppliers in terms of best value, delivery schedules and quality. liaising between suppliers, manufacturers, relevant internal departments and customers. identifying potential suppliers, visiting existing suppliers, and building and maintaining good relationships with them. negotiating and agreeing contracts and monitoring their progress, checking the quality of service provided. Responsible for All IMPORTS of Raw Material and EXPORTS of Finish products. Obtaining of Advance License / DFRC / RoDTeP Licenses against exports anticipated / made and clearance of consignment custom duty free. Responsible for cost effectiveness in import & export transactions. Negotiations with Shipping companies, CHAs, Transporters for charges for their services. Responsible for All documentation with CHAs, DGFT, Customs, Port Authorities, Surveyors, Transporters, Export Inspection Agency, Chambers of Commerce, Consultants.

Job Title: Officer/Senior Officer Location: Ankleshwar Experience: 2-5 Year Department: Production Role and Responsibilities: Production Operations Check labels and verify identity of raw materials, packing materials, and solvents before use. Maintain appropriate storage conditions for raw materials and intermediates in the plant. Execute batch processes as per approved Batch Production Records (BPRs). Follow instructions from Shift In-charge or Production Manager for batch charging and monitoring. Monitor and maintain process parameters during manufacturing. Complete allocated tasks within the stipulated timeline with accuracy. Ensure contamination-free production and proper packing/repacking of materials. Adhere to proper gowning, hygiene, and entry protocols for classified production areas. Operate plant equipment and utilities safely and efficiently. Maintain cleanliness and proper segregation in the production area as per SOP. Documentation & SAP & GDP Perform online documentation of BPRs, cleaning logs, and equipment usage records during the shift. Maintain differential pressure, centrifuge bag records, and other PP/Intermediate area logs. Update SAP transactions for material consumption, yield recording, and inventory movements. Ensure timely entries in equipment logbooks and SAP-based process entries . Label all process equipment, HDPE/fiber drums, and accessories correctly per batch and SOP requirements. Ensure Good Documentation Practices (GDP) by making real-time, legible, complete, and traceable entries in all logs and records. GMP & Compliance Guide and train workmen on cGMP practices and technical SOPs. Ensure finished product yield and quality meet predefined specifications. Participate in internal audits, regulatory inspections, and SOP reviews. Perform calibration of instruments such as weighing balances and pH meters. Keep equipment status boards updated and follow QMS standards. Safety & Environmental Compliance Understand MSDS of all materials handled and ensure safe handling practices. Supervise plant operators to ensure chemical and equipment handling safety. Use scrubbers and proper exhaust systems to control emissions and avoid air pollution. Coordinate with the EHS department for required safety permits and compliance. Wastage Reduction Prevent solvent/material spillage and reduce wastage through proper process control. Ensure utilities (valves, pumps) are turned off when not in use to conserve resources. Cross-Functional Coordination Coordinate with QC for sample analysis and batch release. Liaise with engineering for breakdown and preventive maintenance activities during shift. Work closely with Warehouse, QA, and EHS departments for smooth operations. Interested candidate can share there cv at meet.chauhan@cadilapharma.com .

Requirements: 1-3 years of experience in Injectable Plant production. Expertise in sterile manufacturing. Strong understanding of regulatory compliance & quality standards Educational qualification in Pharmacy, Biotechnology, or related fields.

Candidate must have perfection in English communication. Knowledge of all regulated Guideline & Pharmacopoeia. Must have Knowledge all documentation of QA 18 to 20 Years in API Pharma Industry Experience

Role & responsibilities - Ensure that all processes have documented SOPs (Standard operating procedures) - Ensure that P&IDs (Piping and instrumentation diagrams) and PFDs (Process flow diagrams) of all the process are maintained and updated as per the defined timelines - Plan and approve safety studies like HAZOP (Hazard operability ) HAZAN (Hazard analysis) etc. of existing and new processes and ensure take corrective actions to rectify the findings - Design various documents like DDS, PFD, P&ID, autoCAD drawings, equipment drawings etc, compile basic engineering and transfer it to project team for execution - Develop material and energy balance calculations and maintain records of the same - Prepare a set of SOPs and operations manual as per the built plant / project and other related project details and hand it over to the operating staff - Strategize to ensure that plants run at design capacity and ascertain Aarti Standards of HSE are adhered - Ensure continuous research to improve processes to meet technical challenges like corrosion, exposure, leakages; remain continuously updated with latest and emerging technological advances and trends - Identify any deviations in the processes and conduct root cause analysis to identify the cause and suggest corrective actions to ensure that deviations are under control - Ensure all the applicable legal requirements are fulfilled before commissioning of the project [safety audits, HAZOP, What If, PSSR (Pre-startup safety review) , licenses, plan approvals, building stability etc.] - Initiate technical improvements w.r.t Catalyst, Process Efficiency, to reduce breakdowns and improve uptime of plant - Assign process engineering resources for specific Jobs as and when required based on the priority of the organization - Ensure standardization of process / technology based on critical outcomes from the RCAs and communicating it company wide - Monitor various processes for critical parameters which impact quality, capacity, efficiency, safety, maintenance etc. and conduct review meetings with the technical teams to identify process improvements areas - Follow Management of Change procedure for proposed modification with the respective Plants teams - Plan and design PSSR activities prior to handover to the operations team - Define parameters of general plant conditions for ensuring high quality and healthy work environment for optimum operations activities - Review ERCP documents & it's approval. Training of operating staff for ERCP related to new technologies - Prioritize the pilot plant trials and ensure availability of proper infrastructure of the pilot plant operations - Explore new avenues to initiate new projects in the existing facilities, initiate cost saving / improvement projects and plan implementation - Follow up with the suppliers for the timely delivery of the equipment / other project related items to ensure its timely commissioning for uninterrupted functioning - Ensure active involvement in introducing new technologies within the organisation, its technical evaluation and implementation"" - Explore new avenues to initiate new projects in the existing facilities, initiate cost saving / improvement projects and plan implementation - Review and complete different phases of project on time with respect to cost, quality and time matrix - Conduct periodic review of all the projects under implementation and maintain the executive summary of its progress by updating MS Project software - Monitor the project cost budgeting and reviews any escalation from time to time - Submit a closing report for the projects to the management indicating achieved outcome (Planned vs Actual parameters) - Lead planning and/or implementation of new projects, conduct a cost benefit analysis, develop complete plan for the projects pertaining to cost, resources and timelines - Review and approve the budget estimations & new proposals on technical parameters - Approve and update detail engineering design of equipments for process during projects - Prepare equipment selection and installation guidelines as per industry best practices for optimum operations - Approve detail engineering design of process aspects of projects - Select the right vendor(s) and validate the selection based on vendors performance and capability - Contribute towards industry benchmarking of guidelines for vendor selection and qualification - Prepare incident reports for various equipments - Support procurement team in selection of the right vendor and ensure timely delivery to ensure availability of equipments Preferred candidate profile Notice period :- 1 Month Education :- BE / B.Tech Chemical Experiance :- 2 to 7 Years

HR Operations, Recruitment, Managing Factory Contract Labours, Statutory, Bills checking & on-time Labour payments, Oversee Attd, late coming OT & payroll. Enforcing discipline. Managing employee transport, Canteen, Housekeeping etc. + Govt. Liaison Required Candidate profile Min 10 years of experience in managing HR & Admin in a Factory. Must be good in IR and Admin aspects including Contract Labour Mgt. Should be excellent in Excel & payroll processing to check workings.

Key Accountabilities Analysis and approval Supporting in-process control sample testing by online analysis to support production activities Sampling, analysis and ascertaining quality of intermediates, In-process samples and API for Chemistry Ankleshwar. Testing of the method validation samples and process validation samples and cleaning validation. Perform analysis and documentation of API finished product stability study as per stability study protocol. Coordinating with Production, CWH and QA for Approval / Rejection of raw materials/finished product. Validation and verification of analytical procedures as per requirement. Reporting OOS / OOT results and deviations. Maintaining retained samples as per standard procedure. Assisting in investigation of customer complaint. Testing of new samples (Vendor approval) Give required suggestion for corrective actions and to plan effective preventive actions for the up gradation of the quality system. To ensure proper maintenance of the stability samples and their management. Disposal of waste according to the approved procedures. Continual reduction in the waste generation and effluent management. Co-ordination with microbiology lab (Pharmaceuticals) for microbial analysis of products and utilities. Documentation Generation, managing and archiving Documents including raw data, reports, COA etc as per requirements. Preparation and implementation of the SOPs in the laboratories system. Specification preparation and implementing for API raw material and API finished product according to requirement Maintaining LIMS data entries Providing technical support in compiling Annual Product Review. Analytical method development when required. 2.6.Executing on line documentation Laboratory Management Qualification and Validation of instruments/equipment Appropriate training and guidance to the subordinates. Safety in the laboratory. Regular housekeeping and upkeep of the work area. Maintaining adequate inventory of chemicals and reference standards. Adapting relevant technologies and systems in Quality control. Laboratory equipment calibration and their maintenance. Developing training modules for improvement / training for HSE and Quality systems Generate up gradation plans as need basis. Any other activity assigned by the In charge, Quality control Quality, HSE and Compliance Adhere to current GMP guidelines Following ALCOA+++ practices during documentation and related activities Compliance to local and international HSE norms Regulatory compliance ISO 14000 related activities Regular Pharmacopoeia and regulatory requirement review for compliance To participate in any regulatory/Customer inspection takes place at the site Training of self and subordinates on quality and HSE systems Team member Member of validation team. Member of Analytical transfer team. Participating in discussions and giving feedback to Manager, Quality control regarding on-going activities. Other Projects Trouble shooting activities. Participation in Industrial Excellence projects. Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations Plant round in absence of QA and during IInd and IIIrd shift. Online checking of critical process parameters during round. Requirements Education / Experience M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry Min. 2 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment Technical Skills & Competencies / Language Technical competence Leadership skills Analytical ability Planning ability Communication skills Problem solving Team Building Show more Show less