275 Jobs in Dholka - Page 9

Bachelor's Degree in Mechanical / Chemical Engineering with 3 + Years of experience in FMCG & hygiene manufacturing preferred. Proficient in manufacturing processes, safety standards & quality protocols. Strong leadership & team management skills. Required Candidate profile Oversee daily production operations to ensure efficiency & product quality. Enforcing safety & hygiene regulations. Managing production data & inventory level. Upholding quality standards & procedure. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Graduate / Post Graduate with 1 to 5 years of experience in Sales field. Experience in B2B sales, preferably in South India market. Strong understanding of sales techniques, negotiation & closing strategies. Strong communication & negotiation skills. Required Candidate profile Knowledge of the local languages spoken in South India ( Telugu ) is a plus. Be prepared to travel within the South India region and attend industry events to network & build relationships. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Industrial experience in - VALVE AND PUMP INDUSTRY - Quality department Supplier Inspection, In-process Casting Inspection, Inward Inspection. Knowledge on Engineering Drawings, CMM - gantry type Zeiss, Faro - CAM2measure , Documentations Annual bonus Provident fund Office cab/shuttle Over time allowance Travel allowance Mobile bill reimbursements Gratuity Capability building program Job/soft skill training

Job Description: Cadila Pharmaceuticals is seeking a proactive and detail-oriented Assistant Manager to support the procurement of intermediate raw materials , including solvent chemicals and APIs . The role requires hands-on experience in pharma-related purchasing and coordination with suppliers and internal stakeholders. Key Responsibilities: Assist in sourcing and procurement of intermediate materials, solvent chemicals, and APIs Raise purchase orders and ensure timely material deliveries Liaise with vendors for quotations, negotiation, and order confirmation Maintain accurate records of procurement data and purchase reports Support inventory tracking and reordering processes Qualificatio...

Location: Dholka / Corporate Office, Ahmedabad Experience Required: 1520 Years Department: Purchase Job Description: Cadila Pharmaceuticals is seeking a strategic and experienced General Manager to head the procurement of intermediate raw materials , especially solvent chemicals and APIs . The role requires a high level of expertise in pharma supply chains, cost control, and vendor management. Key Responsibilities: Lead the complete procurement lifecycle for solvent chemicals and APIs Develop global sourcing strategies and establish long-term supply contracts Coordinate with senior stakeholders in QA, Regulatory, Finance, and Manufacturing Drive supplier audits and ensure compliance with ind...

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

" Ensure the c-GMP Compliance and schedule M compliance in production. Ensure the completion of production targets with zero quality issue. Ensure the compliance of inspection /Audit in coating area and follow of procedures/SOPs. To work at designated place in Coating & Capsule machine where they are trained to work for as allocated by supervisor. To make and attach the status labeling on the equipment, utensils and miscellaneous items during operation/cleaning and after operation/cleaning. To follow the SOPs, BMR procedures while performing the activity in accurate form what is mentioned. To document the process with real time (i.e. start time, end time, process parameters recording, proces...

Location: Dholka / Corporate Office, Ahmedabad Experience Required: 15–20 Years Department: Purchase Job Description: Cadila Pharmaceuticals is seeking a strategic and experienced General Manager to head the procurement of intermediate raw materials , especially solvent chemicals and APIs . The role requires a high level of expertise in pharma supply chains, cost control, and vendor management. Key Responsibilities: Lead the complete procurement lifecycle for solvent chemicals and APIs Develop global sourcing strategies and establish long-term supply contracts Coordinate with senior stakeholders in QA, Regulatory, Finance, and Manufacturing Drive supplier audits and ensure compliance with in...

Location: Dholka / Ahmedabad Experience Required: 7–10 Years Department: Purchase Job Description: We are hiring a Manager to independently manage the procurement of intermediates, solvent chemicals, and APIs . The candidate should have strong vendor management skills, a deep understanding of pharma raw materials, and the ability to coordinate across departments. Key Responsibilities: Source and negotiate with vendors for solvent chemicals and APIs Develop procurement plans in line with production forecasts Track supplier performance and ensure adherence to quality and timelines Handle cost optimization while maintaining material quality standards Coordinate with QA/QC, R&D, and production d...

Job Description: Cadila Pharmaceuticals is seeking a proactive and detail-oriented Assistant Manager to support the procurement of intermediate raw materials , including solvent chemicals and APIs . The role requires hands-on experience in pharma-related purchasing and coordination with suppliers and internal stakeholders. Key Responsibilities: Assist in sourcing and procurement of intermediate materials, solvent chemicals, and APIs Raise purchase orders and ensure timely material deliveries Liaise with vendors for quotations, negotiation, and order confirmation Maintain accurate records of procurement data and purchase reports Support inventory tracking and reordering processes Qualificatio...

Location: Dholka / Ahmedabad Experience Required: 11–14 Years Department: Purchase Job Description: We are looking for a Senior Manager to lead procurement activities for solvent chemicals, intermediates, and APIs across multiple manufacturing units. The role involves high-level coordination, cost control, and vendor development. Key Responsibilities: Strategically manage the procurement of key solvent chemicals and APIs Identify reliable vendors and build long-term partnerships Ensure on-time material delivery aligned with production needs Implement cost-saving initiatives and monitor price trends Ensure regulatory and documentation compliance Qualifications: Graduate in any discipline 11–1...

Role & responsibilities: 1. Act as Study Director for various Pre-Clinical studies as per guidelines 2. Conduct, schedule & report toxicological studies for various products in pre-clinical studies 3. Conduct Pharmacological evaluation of various pharmaceutical products 4. Preparation of SOP & documentation as per guidelines 5. Ensuring facility readiness as per regulatory guidelines & audits Preferred candidate profile: Local candidates

L2 engineer in Ahmedabad Job Description - Candidate needs to have enterprise level Infrastructure operations and deployment experience. Must have hands-on the core networking technologies including security too. A good communication skill is a must. Need to have end to end support and problem-solving attitude. Professional level certification - CCNP or similar would be an added advantage. Hands on experience on CISCO Nexus, ASR, Catalyst switches and routers, Firewalls, SD-WAN and wireless.

Formulation R&D Finance Function 1 Concurrence of all expenses & Indents with respect to Budget and justification 2 Vendor Invoice checking with budget for approval & Concurrance 3 Travelling / Petty Cash Vouchers - All R & D Employees documents are verified and entered in SAP. 4 Monthly MIS Activities 5 Customer invoicing for External Projects 6 Vendor Creation on Vendor Portal for Creation in SAP. 7 Material Code approval for R & D Projects through MDM. 8 UID (Unique Identification Number) working, payback verification, approval and UID creation in SAP for Formulation projects 9 Payment follow up for vendors with corporate treasury team. 10 Yearly Revenue Budget to be prepared 11 Yearly CA...

Role : Senior Executive Qualification: M. Pharma/B. Pharma Experience : 4 to 8 Years Location : Dholka, Gujarat Responsibilities 1. Preparation and submission of registration and re-registration dossiers as per country requirements of ROW (Preferable Russia, CIS countries and WHO) 2. Arrangement for indent of Samples, Packing Material specimen, Impurities, Reference Standards as per submission requirement. 3. Query evaluation and submission with respective countries requirement within the required time frame. 4. Establish coordination with other departments like QA/QC, R&D, Marketing and Purchase for ensuring the filings and query response within time frame. 5. Post approval activities: Subm...

Job Responsibilities: · Preparation of CTD/eCTD format drug master file and its submission to various regulatory authorities including USA, Europe, Canada, Australia, China, Japan, Korea, Brazil and ROW market · Preparation of query response of drug substance for various and less regulated markets and customers. · Preparation of applicant part and closed part for various authorities for different customers. · Preparation of annual updates and amendment of drug master files US via ESG, ASMF via CESP, KDMF via MFDS Korea, · Preparation and submission of CEP applications and responses to EDQM via CESP. · Preparation of CEP LOA’s & LOA’s and declarations of various customers and authority. · To ...

Major Purpose Of The Job To developed Analytical Method Development, Routine analysis and Validation by GC & GC-MS To maintain and observe cGLP and cGDP in working environment in GC & GC-MS. Timely respond development of the Regulatory Queries of products. Preparation of COA’s. Follow and update periodic Preventive Maintenance & Calibration schedule of GC & GC-MS DSC; TGA instrument. Responsibilities Preparation of NewAnalytical method validation and Method Transfer Protocol and Report as per the current Regulatory requirement. Prepare Protocol of analytical method validation and method transfer report and routine analysis data. Preparation of standard operating procedure. Maintaining GC & G...

Preparation of CTD/eCTD format drug master file and its submission to various regulatory authorities including USA, Europe, Canada, Australia, China, Japan, Korea, Brazil and ROW market Preparation of query response of drug substance for various and less regulated markets and customers. Preparation of applicant part and closed part for various authorities for different customers. Preparation of annual updates and amendment of drug master files US via ESG, ASMF via CESP, KDMF via MFDS Korea, Preparation and submission of CEP applications and responses to EDQM via CESP. Preparation of CEP LOA’s & LOA’s and declarations of various customers and authority. To collect and evaluate scientific data...

Job Requirements Job Requirements Role/Job Title: Associate Relationship Manager-Micro Enterprise Loan(MEL) Function/Department: Rural Banking Job Purpose The role entails deepening relationships with Rural Banking accounts and ensuring best in-class service to the customers. The role bearer has a responsibility to support Relationship Manager in identifying Business owners / entrepreneurs in the defined catchment and assessing their business loan needs. The role bearer is responsible for driving client acquisition, building household level customer relationships and capitalizing on lifetime value in each relationship to achieve larger organizational goals. Roles & Responsibilities Manage zo...

Job Requirements Role/Job Title : Associate Relationship Manager-Personal Loan Function/Department: Rural Banking Job Purpose To Start Personal Loan in Rural Market and service and source the product. Roles & Responsibilities Identifying Business owners / entrepreneurs in the defined catchment and identifying / assessing their business loan needs. Map out prospects in the town to scope business potential. Disburse Personal loans based on needs assessment. Conduct end-use checks as specified post disbursal of loans. Achieve monthly and annual loan booking targets. Cross-sell products and services to both new and as well as existing customers as per their lifestyle, risk profiling and requirem...

Major purpose of the Job: Overall monitoring & handling of all BA/BE studies Principal / Clinical Investigator for all BA/BE studies Responsibilities / Job Description: Work as Clinical / Principal Investigator for the BA/BE and PK studies Responsible for planning, conduct, monitor and reporting of BA/BE and PK studies in accordance to specifications laid down in protocol / applicable SOPs and regulatory requirements Responsible for monitoring and ensuring safety of the volunteers participating in BA/BE and PK Studies Responsible for adherence to ICH-GCP and conduct of the studies as per ICMR guidelines for Ethical Conduct of Biomedical Research Involving Human Subjects Responsible for prepa...

Role & responsibilities 1. Act as Study Director for various Pre-Clinical studies as per guidelines 2. Conduct, schedule & report toxicological studies for various products in pre-clinical studies 3. Conduct a Pharmacological evaluation of various pharmaceutical products 4. Preparation of SOP & documentation as per guidelines 5. Ensuring facility readiness as per regulatory guidelines & audits

Role & responsibilities 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 throug...

Principal task and Responsibilities: • IT Strategy: Develop and implement IT Infra and OT strategies leveraging new age tools and technology and ensure it should be aligned with the business goals and regulatory requirements. • IT Infrastructure Management: Overseeing the management of IT and OT infrastructure, including hardware, software, networks, and data centers. Ensuring the availability, reliability, and security of IT systems. Ensuring minimal downtime and optimal performance. • System Performance: Ensure the reliability and availability of IT and OT systems and applications critical to manufacturing processes as per business requirements. • Security and Compliance: Ensure IT and OT ...

Role & responsibilities • Raw materials and Consumables transfer from Warehouse to Drug substance manufacturing area • Transfer of Raw material from Day store to Drug substance manufacturing area • Transfer of Formulated bulk from Drug substance manufacturing area to Injection manufacturing • Cleaning of Glass ware, Vessel and Utensils • Operation of Dry Heat Sterilizer, Steam sterilizer, Decontamination Autoclave and Particle Counter • Perform Manufacturing activities in strict accordance with standard Operating procedures and cGMP guideline • Arrangement of Equipment/ Instruments and Cleaning of Equipment/ Instrument • Online Documentation for the operations • Assist vendors during annual ...