274 Jobs in Dholka - Page 5

Monitor and track project activities from inception to closing. Proactively interact with managers within the organization during the course of the project. Working towards increasing the project management competency and capability within the organization as a whole and involved in both tacit and explicit knowledge transfer and integration initiatives. Works closely in collaboration with other roles, such as organizational managers, subject matter expert and those involved in business analysis. Focus on critical project management elements not limited to schedule, cost, resources and risks for each project. Make time to plan thoroughly and prioritize diligently. Principal Tasks and Responsi...

To ensure compliance of procedure and practices in line with GMP guidelines and regulatory expectations for concerned manufacturing facilities and products of Biotech division, Cadila Pharmaceuticals Ltd. . Review and release of Batches of API (Drug substance of STR, VLP, BOT, GCSF, EPO and IMM) including intermediate stages of production, In-process quality assurance checks, Area clearance for scheduled manufacturing activities and day to day compliance for manufacturing facilities during batch manufacturing activity. Review BMR related ROA for Release of Drug Substance (Bulks) manufactured in Biotech Division (STR, VLP, BOT, GCSF, EPO and IMM) Cell Bank management, such as issuance, trendi...

1 Ensure Freedom to operate of CPL's product (Formulation) 2 Design a strategy to secure CPL's invention effectively 3 Handling of Patent Prosecution 4 Effective Management of CPL Patent Portfolio 5 Support to New Product Selection Activity

Principal task: 1) Analytical Method Development by HPLC for all Project. 2) Review the analytical method development data, validation study data and method transfer protocol and reports. 3) Calibration of HPLC system. 4) To maintain GLP/GDP in working environment. 5) Preparation of analytical data and submit for review. 6) Analytical Method Development and Validation. Responsibilities: 1) Calibration of HPLC's as per SOP and maintenance of HPLC Systems. 2) Maintaining record for all analytical reports by entering all the data in raw data note book and timely release of analytical reports. 3) Preparation & Review of analytical method validation protocol and report as per the current regulato...

1. To develop Stable and Bioequivalent solid oral products for US and EU markets. 2. Technology transfer of developed products to plant level this includes all TTD related works 3. To collect, compile of all data of plant batches and submit to regulatory department as per market specific requirement 4. To address agency's queries as per requirement 5. To extend support to plant for any trouble shooting

To assure Quality and cGMP compliance of the products being manufactured and Packed for Liquid Manufacturing Block. To give Area /Equipment clearance i.e. checking and approval of all manufacturing & filling. To verify environmental condition i.e. Temperature, Relative Humidity & Pressure Differential condition in all for said areas are within acceptable range at all the time during operation throughout the shift. To ensure daily verification of weighing balance with standard weights. To perform filled volume & weight method and leak test as per MMD-I & SOP. To perform sampling of bulk and finished product for each batch at the end of the batch as per SOP entry into sampling log and submit t...

1. Procurement & Sourcing Assist in sourcing of raw materials, excipients, and packaging materials as per production requirements. Raise and process purchase orders (POs) in ERP systems (e.g., SAP). Coordinate with approved vendors to ensure timely delivery and best commercial terms. Maintain procurement records and supplier documentation in compliance with audit norms. 2. Inventory & Material Management Monitor stock levels to ensure optimum inventory without overstocking or stock-outs. Coordinate with production and warehouse teams for material availability and replenishment planning. Conduct regular inventory audits and resolve discrepancies. 3. Logistics & Distribution Ensure timely disp...

1. Procurement Operations Ensure timely purchase of raw and packaging materials as per production requirements. Issue purchase orders, track deliveries, and ensure timely inward of materials. Coordinate with production planning and inventory control (PPIC) to avoid shortages. 2. Vendor Management Identify, qualify, and develop vendors for key materials. Maintain vendor relationships and monitor performance (delivery, quality, cost). Handle negotiations to achieve cost savings and favorable terms. 3. Inventory Coordination Monitor inventory levels and initiate timely replenishment. Ensure minimum stock levels are maintained for uninterrupted production. Coordinate with stores and warehouse fo...

1. Procurement & Sourcing Assist in sourcing of raw materials, excipients, and packaging materials as per production requirements. Raise and process purchase orders (POs) in ERP systems (e.g., SAP). Coordinate with approved vendors to ensure timely delivery and best commercial terms. Maintain procurement records and supplier documentation in compliance with audit norms. 2. Inventory & Material Management Monitor stock levels to ensure optimum inventory without overstocking or stock-outs. Coordinate with production and warehouse teams for material availability and replenishment planning. Conduct regular inventory audits and resolve discrepancies. 3. Logistics & Distribution Ensure timely disp...

Principal task: Analytical Method Development by HPLC for all Project. Review the analytical method development data, validation study data and method transfer protocol and reports. Calibration of HPLC system. To maintain GLP/GDP in working environment. Preparation of analytical data and submit for review. Analytical Method Development and Validation. Responsibilities: Calibration of HPLC's as per SOP and maintenance of HPLC Systems. Maintaining record for all analytical reports by entering all the data in raw data note book and timely release of analytical reports. Preparation & Review of analytical method validation protocol and report as per the current regulatory requirement. As per Prot...

To prepare BOM for new UID activities with respect to costing of NPDs Timely development and delivery of allotted sterile 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 of developed product Development of non-infringing strategies for novel formulations in compliance to regulatory requirements for US, EU, and ROW market To maintain 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 product specification. Pre...

Principal task: Analytical Method Development by HPLC for all Project. Review the analytical method development data, validation study data and method transfer protocol and reports. Calibration of HPLC system. To maintain GLP/GDP in working environment. Preparation of analytical data and submit for review. Analytical Method Development and Validation. Responsibilities: Calibration of HPLC's as per SOP and maintenance of HPLC Systems. Maintaining record for all analytical reports by entering all the data in raw data note book and timely release of analytical reports. Preparation & Review of analytical method validation protocol and report as per the current regulatory requirement. As per Prot...

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.

1) Based on production requirement generate the production plan for next 3 month. 2) Run MRP for next 3 month in System (SAP) 3) Share the shortages to RM / PM based on requirement to Purchase team. 4) Discuss and coordinate with purchase team for timely supply RM / PM 5) Discuss with Production team for scheduling of products. 6) Delivery has to completed for M0 for ISBU / USBU on 22nd and for BSBU on 25th 7) Prepare the plan Vs Actual on daily basis. 8) Generate the LL requirement separately after discussion with LL team. 9) Closely coordinate with cross function department for Ach goal. 10) Daily discuss with Production / QC and purchase team for ach daily schedule. 11) To provide technic...

1) Based on production requirement generate the production plan for next 3 month. 2) Run MRP for next 3 month in System (SAP) 3) Share the shortages to RM / PM based on requirement to Purchase team. 4) Discuss and coordinate with purchase team for timely supply RM / PM 5) Discuss with Production team for scheduling of products. 6) Delivery has to completed for M0 for ISBU / USBU on 22nd and for BSBU on 25th 7) Prepare the plan Vs Actual on daily basis. 8) Generate the LL requirement separately after discussion with LL team. 9) Closely coordinate with cross function department for Ach goal. 10) Daily discuss with Production / QC and purchase team for ach daily schedule. 11) To provide technic...

To supervise the Manufacturing & Packing Line Activities with compliance of cGMP and Regulatory requirements to ensure timely completion of the work. Setting daily/weekly/monthly objectives and communicating them to employees Organizing workflow by assigning responsibilities and preparing schedules To supervise Packing and Manufacturing Activities as per requirement. To carry out in process checks during Packing and Manufacturing Activities. To ensure that all products are produced to the specified specifications. Target and deadlines are met to achieve the orders. To arrange ensure dispensing of Raw and Packing material as per shift plan & planning for next shift.

To ensure timely development and delivery of allotted Injectable & NDDS project, sterile formulation and any other assigned project as per agreed timelines and budget. To ensure completion of document preparation and formulation activities to support pre clinical, clinical supplies and technology transfer of developed product. Ensuring development of non-infringing strategies for novel formulation in compliance to regulatory requirement of domestic and regulatory market. To mentor, support & Guide team to select new excipients to improve process/stability/cost effectiveness of the product under development

Maintain GLP in the laboratory as per regulatory requirement. Analytical method development as per ICH Guidelines. To perform In-process, routine and stability sample analysis. Perform the analytical method verification / validation as per protocol. Analytical method transfer to QC Laboratory. Documentation as per the GLP requirement. Trouble shooting during day to day analysis with proper instrument care. Perform dissolution development, multimedia dissolution and CDP activity. Working standard preparation as per SOP.

Review of Literature summary report, patent summary report and development protocols. New product development, Planning and Resource allocation for Domestic and ROW Market. Alternate source development for API and Excipients, GC improvement of existing products. Timely execution of scale up/ exhibit/process validation of allotted projects. Process improvement and troubleshooting of existing commercial products. Overall review of Formulation Development data during stage gate clearance. Execution of allotted projects in stipulated timeline & within budget. To check feasibility of manufacturing and costing of all new projects for UID. Timely review of LNB and project files for allotted project...

Major Purpose Of The Job: 1. Negotiation with vendor for lowest price. 2. New vendor development for alternate source. 3. SAP operation. 4. Market information. 5. Resolving day to day issues with internal and external customers. 6. Team work. 7. Cross functional meeting with internal customers for update and issue resolution. 8. Follow up with vendors for delivery / quotation and if any requirement for our internal customers 9. Ensure timely delivery of primary & secondary packaging materials for each location 10. Ensure timely vendor payments Principal Tasks and Responsibilities: 1. Negotiation Ensure Quotations from different vendors are arranged as per SOP Verification of Comparative Anal...

1. LCMSMS Operation Maintenance and Calibration 2. Method Development, Method Validation and Project Study sample analysis as per ICH M10 Guidelines and in house SOPs 3. Documentation as per GDP, GLP and in house SOPs 4. Daily Performance activity of Bio analytical Equipments

Major Purpose of the Job: - To develop cost effective and robust process of API. - To manage lab activity as per current GLP guideline. Principal Tasks and Responsibilities: 1. To develop chemical process which is having least hazardous chemicals and cost effective process of API in lab and the technology to be transferred at plant scale. 2. To check the proof of concept of selected synthetic route. 3. To plan the experiments, execution of experiments and record in Lab Note Book. 4. Prepare standard samples for KSM, Intermediates, Impurities and Finish products. 5. To do characterization and identification of finished product, impurities and intermediates. 6. To transfer the technology from ...

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.

The Senior Manager Raw Material is responsible for end-to-end management of sourcing, procurement, quality compliance, and inventory planning of raw materials including Active Pharmaceutical Ingredients (APIs), excipients, and solvents. The role involves building strong vendor relationships, driving cost optimization, ensuring timely material availability, and maintaining strict compliance with regulatory requirements. Key Responsibilities: 1. Raw Material Procurement & Sourcing: Develop and execute sourcing strategies for APIs, excipients, solvents, and intermediates. Ensure timely procurement of quality raw materials as per production planning. Identify and onboard qualified suppliers (dom...

Ensure the cGMP Compliance and schedule M compliance in production. Ensure the proper utilization of men and machine of Granulation area. Ensure the training of production staff and worker. Ensure the development progress periodically of personals and take necessary corrective action. To lead the Granulation department with respect to developing the second line. To ensure the delivery of products as per the production target. To ensure and monitoring yield, Wastage, WIP & operation expenses of Granulation area. To co-ordinate with tablet sub- department, Quality Assurance, Quality Control and engineering department to achieve production delivery as per production schedule. To ensure daily pr...