274 Jobs in Dholka - Page 7

Verify Receipt of Raw Material & Packaging Material for stores. Verify SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. Verify the environmental parameters like Temperature, RH, pressure difference etc. Verify Daily verification of weighing balance and daily documentation. Verify Reconciliation of materials. Stock verification with internal and external auditors. Verify to Maintain of Rack location in SAP as per physical. Verify Preparation of packing list and keep ready the material for Ethiopia. Verify timely dispatch of material to Loan license and Ethiopia plant. Verify handling of retest, rejected, expired materials. Co-ordinate with qualit...

Follow cGMP and GMP PRACTICES. Responsible for charging the stability sample of Finished Product as per SOP. To follow and maintain stability study schedule. Pulling out samples from chambers as per the schedule Maintain all stability chambers daily temperature and humidity monitoring. To follow safety Procedure in QC department. Responsible for withdraw the stability sample for analysis as per schedule. To maintain stability study log book of stability sample. Responsible for preparation of stability study protocol and maintain all relevant records. Ensure working of all the stability chambers as per the condition and in case of any problems take the correction action. Ensure cleanliness of...

To plan daily compression activity per norms of cGMP. To supervise cleaning and compression activity as per requirement in Cephalosporin block. To carry out in process checks during manufacturing activities. To arrange batches as per shift plan and planning for next shift material to make easy to perform manufacturing operation. To maintain document (BMR) as per cGMP and also filled and maintain the daily, weekly, monthly record as per cGMP requirement and confirm in SAP. To coordinate with RM stores Raw materials procurement in time. To carry out proper line clearance procedure and follow SOPs To ensure discipline from workers and get systematic work to improve quality. To Comply cGMP and o...

1. To develop Stable and Bioequivalent solid oral products for EU, ROW (Rest Of World) and Domestic 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 perform vendor management activity to assure that vendors are complying with Cadila procedure on vendor management and GMP requirements in order to source quality materials and products. To perform self-inspection activity to assure that the facility remains in the state of cGMP compliance, to evaluate and identify gaps for future needs and to regularly review the effectiveness and applicability of the quality assurance system. Responsible to assist for handing of day to day activities related to Vendor Approval. To assist for evaluation of vendor documents and maintain current status. To assist for preparing vendor grading of RM/PM based on rejection of supply from vendors on yearly basi...

New Product Development of Domestic, ROW and EU markets Revision of Products of Domestic, ROW and EU markets as per Requirements of various stake holders PM selection, Machinability as per existing Automization of the pack Cost competitive pack development Monitoring of Stability and Exhibit batch packaging of the development batches Co-ordination with plant for the Registration sample packaging Digital print proof, Shade card approval

The Senior Manager Purchase to Pay (P2P) is responsible for managing the end-to-end P2P process, including purchase requisition, procurement, vendor onboarding, invoice processing, GRN, payments, compliance, and reporting. This role ensures accurate, timely, and compliant processing of procurement transactions in alignment with business objectives, internal controls, and regulatory standards relevant to the pharmaceutical industry. Key Responsibilities: 1. P2P Process Management: Manage the entire Purchase to Pay lifecycle: requisition, PO generation, goods receipt, invoice verification, and payments. Oversee SAP/ERP system transactions to ensure accurate and real-time processing. Monitor an...

1. To develop stable solid oral products for Domestic Markets and ROW 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.

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.

1. Planning, conducting, supervising and reporting of BA/BE studies in accordance with Protocol, ICH-GCP guideline and regulatory requirements. 2. Coordination with external service providers and cross-functional teams 3. Data submission of clinical studies as per requirement to Pharmacovigilance and RA department. 4. Regulatory inspection compliance 5. SOP preparation, review, revalidation, and training to all team members. 6. Plan Calender training. External training such as ACLS BLS, GCP. Mock drills , internal trainings and seminars.

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...

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 and Responsibilities: - Perform laboratory experiments to optimize critical process parameters to make process robust. - Process feasibility study, cycle time estimation, capacity mapping, material compatibility test etc. for implementation in plants. - Process safety analysis, scale-up studies and technology transfer. - Plant support for process troubleshooting, debottlenecking, effluent reduction, utility reduction (energy conservation) etc. - Business/marketing support by meeting various API PSD demands of customers. - Basic engineering for new projects preparation of PFD, budgeting of the project, evaluation of mass & energy balances, utility & effluent load evaluations, e...

To co-ordinate with supply chain , dispensing and Q.C. CFT meetings. To release of raw material as well as packing material. To co-ordinate with vendor and maintenance if any technical m/c breakdown. IQ , PO and PQ for new machine installation. Reconcile batches at each stage of Manufacture and Packing. Investigate and report any deviations. Monitor Yields of all products. Initiate corrective actions where ever necessary. Ensure that all documents / records required for Regulatory Compliance are maintained properly. Review SOP's for regulatory compliance and actual practice.

- Liaison with Food & Drugs Control Administration, Gandhinagar/circle offices/CDSCO for various applications including but not limited to Product Permissions for manufacturing COPPs Various certificates for tender (FSC, Performance certificate, Non-conviction certificate) Inspections for WHO GMP/Schedule M GMP certification Technical persons approval Technical person application verification. - Liaison with CDSCO, West Zone, Form 29 Export licenses Loan license Manufacturing licence renewal for all plants Wholesale licences - Submission of commercial batches to CDL Kasauli for testing - Submission of quarterly returns to NCB/CBN - Handling NSQs Experience in submissions through Sugam, NSWS ...

Sample Preparation, Daily Calibration, and maintain log of equipment. Method Development and method validation and study sample analysis as per ICH M10 guidelines. Operation, maintenance and Calibration of LCMS Documentation as per Bio analytical SOPs and ICH M10 guidelines. Data & Report review

1. Act as TICO officer for receiving, handling and issuing of vehicle / reference/ test for pre clinical studies. 2. Maintaining document of test item control. 3. Communicate with the sponsor for TIDS, COA, and discrepancies about test material receipt, label and other issues. 4. Communicate with SD, archivist, and TFM for test material-related works. 5. Maintaining TICO facility & preparation for regulatory and sponsor's audit.

To prepare and review the PQRs. To compile the quality attributes & In-Process parameter in PQR as per current version of SOP. To verify & review of Ingredient manufacture name (Vendor Name) & TSE-BSE certificate for PQR Compilation. Review for Qualification & validation data for compilation of PQR. To perform continuous process verification of the product. To initiate & review Change Control in LIMS, Deviation & CAPA in EPIQ. Any other job assigned time to time by HOD as per requirement.

Job Purpose This position is open with Bajaj finance limited Duties and Responsibilities Responsibilities: Responsible for overall branch operations,performance & profitability of the branch. Drive & participate in field-marketing activities of various financial products along with the team to improve brand visibility Plan,conduct & monitor the branch & field level marketing activities to ensure health pipeline of leads resulting into business conversion & branch growth Focus on customer engagement for new customer acquisitions & retainment of old customers Conducting error free valuation & appraisal of gold ornaments being pledged in branch with correct weight & purity assessment as per com...

Role: Pre-Clinical Pathology Lab Executive Job Location: Dholka (Near Ahmedabad), Gujarat Experience: 3-5 Years Job description: Core responsibility related to GLP:  Planning and execution of blood collection from various laboratory animals  Monitoring anesthesia / euthanasia of laboratory animals  Planning for necropsy examination.  Preparing and conduct of necropsy examination of laboratory animals.  Responsible for conducting and monitoring of tissue trimming, processing, block making, sectioning, slide staining of various studies.  Histopathological slide reading for toxicity and efficacy studies.  Responsible for monitoring Histopathological slide preparation  Slide reading and ...

INDEL MONEY PVT. LTD is looking for Internal Auditor to join our dynamic team and embark on a rewarding career journey. Develop and execute audit programs to test the effectiveness of internal controls and compliance with policies and proceduresAssist in the preparation of audit reports for presentation to senior management and the Audit CommitteeStrong knowledge of internal auditing standards, accounting principles, and financial reportingExcellent analytical and problem-solving skillsStrong written and verbal communication skillsExperience with data analytics and visualization tools a plus Disclaimer: This job description has been sourced from a public domain and may have been modified by ...

Role : Senior Manager Regulatory Affairs Job Description: Handling submissions in Sugam & NSWS Portal Preparation & Submission of o New Drug applications, Subsequent New Drug Applications Clinical trial application - Phase I, II, III, IV (Form CT-04) BA/BE Export application (Form CT-05) Test License application (Form CT-10, Form CT-13, Form CT-14, Form CT-16, Form-11) Manufacturing new drug & Marketing (MA) application (Form CT-21) Import new drug & Marketing application (Form CT-18) Form-40 & Form-10 application Post approval changes RCGM Submission o for R&D activities o Pre-clinical toxicity study of vaccines (Form C-1, Form C-3b) Dual use NOC application Import and export application of...

Machine Operation & Maintenance:- Operate assigned machines independently as per SOPs. Perform basic troubleshooting and routine maintenance of machinery. Ensure machines run efficiently to meet production timelines and reduce downtime. Monitor machine parameters and take corrective actions proactively. Quality Control:- Ensure pouches are sealed and printed (text/barcode) as per defined quality standards. Conduct visual and functional checks on output to maintain consistency. Report any defects, quality deviations, or equipment issues immediately. Team Handling :- Manage a small team of 56 labourers. Allocate tasks based on team members’ skills and capabilities. Supervise and support labour...

Shift Supervisor – Brick Production Department Location: Plot No. 282/9, Nr. Jai Parmeshwar Petrol Pump, Dholka Road, Badarkha, Ahmedabad-382260 (GUJ) Shift Timing: Night Shift (9:30 PM – 9:30 AM, 11–12 hours) Job Summary: We are looking for an energetic and responsible Shift Supervisor (Fresher to 2 years of experience) to oversee night shift operations in our Brick Production Department. The role involves supervising production activities, dispatch operations, and loading/unloading work while ensuring safety and quality standards. Key Responsibilities: Monitor and supervise daily shift activities in brick production. Oversee dispatch, loading, and unloading of raw materials and finished go...

Role 1. Segment the market and identify potential direct clients, approach them and generate business through customized loan structure offerings that meet client requirements and also generate good margins for business 2. Deliver on sales targets for Business by building strong relationships in the DSA/ DST / Connector network 3. Carry out meetings and sales calls with prospective clients on a regular basis to source business 4. Drive faster TATs through effective loan sanctioning by building strong relationships with internal stakeholders in order to expand channel presence and customer base 5. Track and report on sales operations and productivity metrics, and work towards building a high...