274 Jobs in Dholka - Page 6

1. Strategic Sourcing & Procurement Develop and implement procurement strategies aligned with business objectives. Manage sourcing of raw materials, packaging materials, and indirect purchases for multiple locations. Ensure timely procurement while optimizing cost, quality, and delivery timelines. 2. Vendor Development & Management Identify, evaluate, and develop reliable suppliers (domestic & international). Negotiate contracts, pricing, and terms with vendors to secure favorable terms. Conduct periodic vendor audits in coordination with QA/QC to ensure compliance. 3. Budgeting & Cost Control Prepare annual purchase budgets and monitor adherence. Analyze market trends and pricing to control...

Sales & Operations Planning: Conducting Sales & Operations Planning meetings (Pre-S & OP and S & OP), to providing visibility and communication on sales, demand, distribution, and supply trends in support of business growth. Close coordination with Logistics Team for timely, appropriate documentation & dispatch. Inventory Management: Maintenance of RM & PM (Long lead-time RM.S & PM.S and APIS) as per the defined lead times to avoid stock outs/under stock of products for all business units across the all plants. Tracking of Non-Moving & Slow moving, retest/ to be expired materials to reduce Obsolescence and Design of Safety stocks & Re-order levels to meet the Customer needs or Business needs...

Overall supply and demand planning lead for US Tracking- PR-PO-GRN and RM availability 25th of previous month and PM availability by 5th of the month for planning. MIS / Tracking plan vs actuals for USBU

- Carry out repair and maintenance of all machines in the parenteral manufacturing and aseptic areas. - Operate all equipment in the parenteral manufacturing area, including PFS filling, vial and ampoule filling, Autoclave, DHS, TS, and all compounding vessels. - Monitor and record in-process parameters such as temperature, RH, and DP at defined intervals as per MMDI and SOPs. - Ensure aseptic operations across all production lines. - Operate and oversee processes in the aseptic area, including compounding activities. - Handle vial and ampoule washing, stoppering, sealing, and labeling operations. - Operate lyophilizers and ensure smooth functioning of all compounding vessels in the manufact...

Responsible for operating vial/bottle and ampoule washing, filling and capping machine and PFS filling Machine at Dholka premises. Should have knowledge of Operating and maintenance of vial/bottle filling, Washing and capping m/c, Depyrogenation tunnel, Labeling Machine. To do aseptic and processing area entry exit procedure properly with proper gowning. Should have knowledge of working in aseptic and processing area. Repair and maintenance of all machines of parenteral manufacturing area. To check and ensure that differential pressure and Temperature of the aseptic area and processing area are within limit and record it properly. To check and ensure that pressure differential of all Laminar...

Major Purpose of the Job: 1) Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Specification and Standard test procedure. 2) Calibration of HPLC system and auto titrator. 3) To maintain GLP in working environment. 4) Preparation of analytical data and submit for review. 5) Method development of Classical wet analysis. Principal Tasks and Responsibilities: 1) Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Specification and Standard test procedure. 2) Method development of Classical wet analysis as well assay and content method by auto titrator. 3) Calibration of HPLC's as per SOP and maintenance of HPLC Systems...

Principal Tasks and Responsibilities: - Literature search and compliance to ensure designing of product development strategies for formulation development and helping scientists to perform trial based on the same. - Compliance to regulatory requirements of domestic and regulatory market. - To maintain lab inventory and perform equipment calibration and maintain calibration and usage log of the same. - Periodic compilation of stability data and discussing with concerned scientist for evaluation and planning further development of different projects. - Participate in training as per training need identification and seminars for technical knowledge up-gradation of people in group based on scien...

Major Purpose of the Job: Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Specification and Standard test procedure. Calibration of HPLC system and auto titrator. To maintain GLP in working environment. Preparation of analytical data and submit for review. Method development of Classical wet analysis. Principal Tasks and Responsibilities: Routine HPLC Analysis for Raw Material, Intermediate, in process and Final API as per the Specification and Standard test procedure. Method development of Classical wet analysis as well assay and content method by auto titrator. Calibration of HPLC's as per SOP and maintenance of HPLC Systems. Trouble shooting durin...

Have working knowledge of lyophilized product development and transfer to plant. Have good knowledge on documentation practices with respect to preparation and review. Timely development and delivery of allotted formulations and any other assigned project as per agreed timelines and budget. Completion of document preparation and formulation activities to support pre-clinical, clinical supplies and technology transfer, exhibit batch manufacturing of developed product. Development of non-infringing strategies for novel formulations in compliance to regulatory requirements for US, EU, and ROW market. To write Lab note books, stability data compilation and tracking of project progress. To prepar...

To prepare and maintain SOP and documents related to Plant preventive maintenance. To conduct routine breakdown maintenance of Main Pharma Block equipment's. To follow and implement PPM schedule for effective implementation in shortest duration of time for all equipment's in close co-ordination with production dept. To allocate maintenance job to all the technicians with routine breakdown requisition. To co-ordinate with inter department staff for any breakdown or any abnormality in equipment's. To provide support to Execution of CAPEX project of process equipment side. Ensure timely indenting of spares required for preventive maintenance / breakdown maintenance with close follow up with sen...

To prepare BOM for new UID activities with respect to costing of NPDs. Timely development and delivery of allotted formulations and any other assigned project as per agreed timelines and budget. Completion of document preparation and formulation activities to support pre-clinical, clinical supplies and technology transfer, exhibit batch manufacturing of developed product. Development of non-infringing strategies for novel formulations in compliance to regulatory requirements for US, EU, and ROW market. To write Lab note books, stability data compilation and tracking of project progress. Preparation and request of spec for raw material, packaging material, in-process controls and finished pro...

This role is responsible for industrial relations, trade union management, contract labor management, labor-related statutory compliances, manufacturing productivity as well as employee safety and welfare across all manufacturing sites of the Company with the objective of ensuring harmonious, productive and engaged manufacturing workforce at all sites. Industrial Relations Maintaining harmonious & cohesive industrial relations across all sites Negotiating productivity linked wage settlements in a win-win manner Building a productivity mindset in the industrial relations environment Trade Union Management Developing a win-win relationships with trade unions wherever applicable Ensuring that t...

- Carry out repair and maintenance of all machines in the parenteral manufacturing and aseptic areas. - Operate all equipment in the parenteral manufacturing area, including PFS filling, vial and ampoule filling, Autoclave, DHS, TS, and all compounding vessels. - Monitor and record in-process parameters such as temperature, RH, and DP at defined intervals as per MMDI and SOPs. - Ensure aseptic operations across all production lines. - Operate and oversee processes in the aseptic area, including compounding activities. - Handle vial and ampoule washing, stoppering, sealing, and labeling operations. - Operate lyophilizers and ensure smooth functioning of all compounding vessels in the manufact...

Key Responsibilities: Contract Management: Drafting and Negotiation: Reviewing, drafting, and negotiating contract terms with vendors and agencies, ensuring compliance with company policies and legal requirements. Onboarding and Offboarding: Managing the process of onboarding new contract workers, ensuring they have the necessary resources and information, and managing their offboarding when their contract ends. Compliance and Legal: Ensuring all contracts adhere to legal and regulatory requirements, as well as company policies. Contract Monitoring: Tracking contract start and end dates, renewals, and performance metrics. Contract Repository: Maintaining an organized system for storing and a...

1. Strategic Procurement Management Develop and execute procurement strategies aligned with production and compliance needs. Plan sourcing of APIs, excipients, packaging materials, lab chemicals, and consumables. Ensure procurement planning supports uninterrupted manufacturing and new product launches. 2. Vendor Development and Management Identify and qualify new vendors, ensuring they meet regulatory and GMP standards. Conduct vendor audits (in coordination with QA/Regulatory teams). Establish long-term supply agreements with key suppliers to ensure continuity and quality. Monitor supplier performance (delivery timelines, quality, cost competitiveness). 3. Regulatory and Quality Compliance ...

1) Maintain GLP in the laboratory as per regulatory requirement. 2) Issuance and Maintain the records of reference standards, working standards and impurities standards 3) Issuance and Maintain the records of HPLC columns 4) Calibration of all laboratory instrument/Equipment likewise HPLC/Dissolution/UV/FTIR/GC/LCMS MS/Autotitrator/Analytical Balance 5) To perform daily calibration of Instruments/Equipment likewise Analytical Balance, pH meter, Temperature record for Refrigerator and thermometer etc. 6) Preparation and revision of Analytical laboratory's SOP. 7) Issuance and Maintain the records of LNB for validation group, development groups. 8) Issuance and Maintain the records of MRS for ...

Supervise daily operations in the assigned manufacturing area (e.g., granulation, compression, coating, packaging). Ensure production activities are carried out as per Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs). Monitor area-wise manpower allocation, machine utilization, and shift-wise productivity. Coordinate with QA/QC, maintenance, and warehouse departments for line clearance, sampling, and material movement. Ensure adherence to current Good Manufacturing Practices (cGMP), safety, and hygiene standards at all times. Review and ensure timely completion of BMRs, logbooks, and other GMP documents. Provide on-the-job training and guidance to operators and junio...

Follow cGMP and GLP practices in Quality Control Lab. To follow safety procedure in qc department. To analyze the Sample of in process validation and finish product on instrument such HPLC, GC, UV, FTIR etc. by following test procedure. To attend the training as per schedule. To follow safety procedure in QC department. To receive the samples for analysis and making entry in Inward register. To maintain the Instruments log books related to sample analysis. To analyze the sample and compilation of documents. Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS. Responsible for online documentation. To do any other Work assign by HOD.

Strategic Procurement: Develop and implement procurement strategies aligned with organizational goals. Lead cost reduction initiatives and supplier consolidation efforts. Identify new sourcing opportunities to improve cost, quality, and lead time. Team Leadership & Development: Manage and mentor the procurement team across multiple categories. Define KPIs for the team and ensure continuous performance improvement. Foster a culture of accountability, continuous learning, and ethical procurement. Vendor Management: Establish and maintain strategic relationships with key suppliers. Lead supplier selection, onboarding, evaluation, and audits. Negotiate contracts, prices, and terms to maximize va...

1. Understanding the process in details with concerned scientist with experiments in the lab. 2. Study the operational parameters of different operations like crystallization, distillation, drying and extraction and optimize those parameters based on energy, cost , safety accordingly. 3. Preparing list of facility requirements like equipment, utilities at production. 4. To find out the root cause of the failed batches at plant and take up an experiment based on proposed solution. 5.Solvent recovery and system capacity enhancement. Scale up of products from R&D to plant scale by doing engineering calculations and observing the kinetics involved in the reaction. 6. To maintain quality and safe...

1. To develop Stable & Bioequivalent for solid oral products for Europe, ROW & Domestic Markets. 2. Technology transfer of developed products to plant level, this includes all TTD-related works. 3. To collect and compile all data and submit to respective regulatory agencies. 4. To address DCGI/ regulatory agency queries as per requirement. 5. To extend support to plant for any commercial trouble shooting.

To operate the CVC Bulk packing machine as per the norms of cGMP To supervise the machine activity as per the standard output with GMP requirements To carryout in process checks during packing machine activities To arrange packing materials as per shift plan & planning for next shift packing materials To minimize the rejections during packing operation To maintain online and offline packing activity along with time management To ensure timely transfer of finished goods to the BSR

1. Method verification of new HPLC method for all stages of new molecule as well as modified old molecule method as per regulatory guidelines. 2. Calibration and maintenance of HPLC systems as per SOP. 3. Maintaining records for all analytical reports by entering all the data in raw note book and timely release of analytical report. 4. To maintain analytical data and report.

Induct employees through appropriate induction mechanism as per organization and strive for constantly improving the quality of induction Responsible for implementation of all HR programs & initiatives in the location department/division. Play a key role in talent identification, development and retention. Undertake employee engagement in identifying interventions that motivate employees, make Cadila a great Place to Work. Address employee grievances on time. Building and maintaining a culture of continuous improvement to make Cadila, a better palce to work. To ensure the joining formalities of all new joiners. Participate in various meetings of Dholka Manufacturing and ensure the HR issues ...

Receipt of Raw Material for main Pharma stores. SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. To check the environmental parameters like Temperature, RH, pressure difference etc. Daily verification of weighing balance and daily documentation. Reconciliation of materials. Stock verification with internal and external auditors. Maintain of Rack location in SAP as per physical. Preparation of packing list and keep ready the material for Ethiopia. Dispatch of material to Loan license and Ethiopia plant. Handling of retest, rejected, expired materials. Co-ordinate with quality control / production / maintenance /QA / SCM/ Purchase / Contract Mfg e...