225 Jobs in Daman & Diu - Page 7

The Production Supervisor will be responsible for overseeing day-to-day production activities, ensuring smooth operations, maintaining quality standards, and meeting production targets.

Role & responsibilities Experience in creating purchase order SAP HANA MS Excel

We need Electrical and Mechanical Maintenance Head for a Reputed Plastic Injection Molding Company at Daman. BE Mechanical or Electrical with 12 to 15 years experience. Candidate from South Gujarat who can join immediately will be preferred.

We are hiring Maintenance Engineer Mechanical Engineer

We are hiring quality control Engineer Mechanical Engineer

Sourcing & creating job description for various roles Recruitment, Onboarding and Induction training for HR to new joiners Preparation of various letters like joining, relieving, experience certificate, Appreciation etc. Maintain Employees' database Required Candidate profile Applicant must be MBA HR with 5= years of experience into end to end recruitment in pharma manufacturing plant. Good exp of recruitment as well as contract management is desirable

Responsible for operations and maintenance of HVAC systems, Dust Collector Systems, Air Compressors, Chillers. Maintaining Documents as per GMP & Safety norms. Installation & commissioning of HVAC equipment’s Review of Logbooks of HVAC equipment’s. Required Candidate profile Applicant must be Mechanical Engineer with experience of HVAC Maintenance and Operations. Understanding of concepts and principles of industry and technical skills in HVAC

Role & responsibilities To operate fermenters (50L to 4KL), Nutrient dosing vessels, Media preparation vessels and CIP tanks. • To perform raw material dispensing monitoring, media preparation, media transfer and CIP solution preparation. • Preparatory work required for actual production batches which includes (but not limited to) issuance of material, preparation of stock solutions, sterilization of glassware, sterilization of filters etc. • Execution of production batches as per production schedule. • To perform fermenter and process vessel sterilization and cleaning activities. • To perform downstream activities such as centrifugation, slurry preparation, spray drying, Blending and sifting. • Adherence to SOPs, BMRs and product specifications. • Seed and production fermenter operation, batch monitoring, harvesting and CIP. In process sampling and analysis as per STP. • Participate in Equipment and system qualification and documentation. • To Maintain log records, batch records, deviation report and shift handover reports. • Adherence to good manufacturing practices, good documentation practices and safety compliance. • Follow up of calibration and validation of equipment as applicable as per schedule. • To work in shifts and monitoring of all production activities in Shift. • To participate in SOP ,BMR and production formats preparation • To ensure the production documentation completion by team. • To coordinate with maintenance team for planning preventive maintenance activities • To issue MRN to stores, Batch booking to QA, issue the finished product analytical testing report to QC. • Training, supervising, monitoring plant assistants / helpers. • To supervise housekeeping activities.

To receive, analyze & assign ITSM calls to respective engineer, software developer to ensure that the end user get the IT support. To support end user technology, fixed telephony & associated operating systems, software & administration platforms. Required Candidate profile 5-7 years of relevant experience of IT support, MIS, Troubleshoot, Diagnose and fix the issue in reputed pharma company

Objective: Execute and monitor overall administration and efficient daily operations of a full service branch office; including operations, lending, product sales, customer service, security and safety in accordance with the Bank's objectives. Principal Accountabilities Sales & Business Development: 1. Achievement of incremental number and value targets for Liabilities (CA, SA, FD); Assets (Home, Auto & other assets) and Fee Products (MF, LI, GI, Gold & other fee products) 2. Prepare and monitor Sales plan for the branch 3. Build a healthy asset and liability book. 4. Increase market share in the catchment area (3 to 5 kms radius) Major Activities Sales & Business Development: 1. Sales Planning : Prepare and track product wise - liabilities, assets & fee AOP for the full financial year. Commerce and catchment mapping Prepare and review monthly activity calendar of outbound activities of BSM / JO Roll out MOP for outbound and inbound sales on 1st of every month followed by weekly and monthly reviews. Review all employees in branch quarterly. Review productivity of BSMs / BOMs/ JOs on a weekly basis. 2. Review and handhold BOMs & BSMs on a daily basis and Sales Officers (JOs) on a weekly basis. 3. Conduct Daily Morning Huddles to discuss daily plan and agenda for employees. 4. Ensure proper on-boarding of all new customers acquired. 5. Sale of 3 products per customer within 90 days of account opening. 6. Track inflow outflow reports, account closures, FD renewals, FD closures, overdue FD, locker occupancy, Sales and thus daily business generation 7. Maintain quality of customer acquisition through sourcing mix and on-boarding process. 8. Monitoring DSRs on a regular basis. 9. Lead management proper assignment and closure of leads. 10. Tapping markets or customer segments within the catchment of the branch, which are hitherto untapped, to increase the GL Base of the branch. Principal Accountabilities Customer Service : 1. Manage Key Branch Relationships 2. Ensure Wait Time within permissible limits as per segmental service approach 3. Achievement of branch Customer Service Scores target 4. Nil Critical Requests at branch 5. Nil Escalations at branch and complaint handling If interested share your cv on Sagar.namaha@rblbank.com or refer it someone.

. To prepare GRN of all categories i.e Capital/ Raw material on daily basis. . Tracking of Indents of Raw material. . Proper storage of materials .Dispensing of Raw Material as per Batch Manufacturing Record . Physical Verification of Material Required Candidate profile Applicant must be Pharmacy graduate / post graduate with experience of warehouse operations, ,Inventory Control, Purchase Order ,Store Keeping, Store Management, Basic SAP

. Prepare and review the Product Quality Review. . Investigation related to Deviation, Queries received from the customers and regulatory department related to Product Quality Review. . Adherence and compliance to cGMP requirements. Required Candidate profile Applicant must be Pharmacy graduate / post graduate with experience of IPQA Activity in Oral Liquid / Tablets/ Capsule/Dry Syrup.

Analysis of Finished Products, Raw Material, In-Process, Solid oral doses form Test, Process Validation, Stability Samples , To Maintain Good Laboratory Practices. Handling Lab Samples &Reports. Required Candidate profile Applicant must be Pharmacy graduate / post graduate with experience of QC functions in Solid Oral dosage form. He must be well versed with instruments like GC, HPLC, UV, Karl Fischer, Dissolution etc

Assist with day-to-day accounting tasks, including data entry and bookkeeping. Prepare & maintain financial records, ledgers, and journals. Process invoices, payments, and receipts. Reconcile bank statements

Prepare and send client drawing & GTP for Link Box and Cable cleats Co-ordinate with client on request received for revised drawing & GTP Discuss queries with client Prepare new drawing & GTP of Link box and Cable cleats as per new requirement. Required Candidate profile Prepare and send QAP of Link Box Enter 60-90 Nylon cleat FG stock at the time of dispatch Submit vendor approval form and other technical documents to client in case of emergency.

1.To handle activities related to Injection moulding shop floor, IML robot process & Hot runner moulds process. 2. Side entry & Top Entry IML robot experience. 3. IMS, ISO documentation part should be handled 4. Experience of rigid packaging.

Post: Export-Import Manager Education :B.Com Experience: - Min 8 to 15Yrs Salary: - Min 8 to 9 Lacs PA Location:- Sanjan, Umargam Notes: Candidates must have good knowledge in Export & Import. Interested candidate Call on +91 9157895300 Required Candidate profile Thanks Mr priyanka +91 9157895300 (Call & Whatsapp) hr@creativehr.in Creative HR Services Visit Us on: SA-05, Solitaire Business Centre, GIDC Char Rasta, Vapi.

Position: Civil Engineer Company: Cable and wire Manufacturing Location: Daman Employment Type: Contractual (Third-party payroll CIEL HR Services) Contract Duration: 12 months (renewable based on performance and project needs) Education: B.E./B.Tech in Civil Engineering (Diploma holders can also apply) Experience: 3 to 4 years Salary: Based on current CTC and interview performance Required Skills: Experience in construction, foundations, and maintenance work Project execution and quality checks Bill checking, rate analysis, BOQ preparation Bar chart preparation and team coordination Key Responsibilities: Oversee industrial construction projects Execute and inspect work per project requirements Assist in bill verification and BOQ-related tasks Support ongoing maintenance and project work Prepare progress reports and coordinate with teams Apply Fast

- Education: Diploma / B.E. / B.Tech. in Mechanical or Tool Engineering. - Experience: 10-15 years in mould design, 5+ years in managerial role. - Industry: Electricals, plastics, automotive, appliances. Skills & Competencies - CAD tools: UG NX, SolidWorks, CATIA, AutoCAD. - Simulation: Moldex3D or Autodesk Moldflow. - Leadership, problem-solving, manufacturing knowledge. - Familiarity with ISO, RoHS, safety standards. 1. Mould Design & Development: - Lead end-to-end design of moulds for injection, compression, and die-casting. - Conduct feasibility studies and mould flow analysis. - Validate designs for manufacturability and durability. 2. Team & Project Management: - Manage team of designers and engineers. - Oversee project timelines and deliverables. 3. Vendor Coordination & Tooling Procurement: - Coordinate with internal/external toolmakers. - Approve vendor drawings and supervise mould trials. 4. Process Optimization & Innovation: - Improve cycle time and mould efficiency. - Apply DFM and DFA principles. 5. Documentation & Standards: - Maintain design records and BOMs. - Establish internal standards and best practices.

Degree or Diploma in Plastic, or CIPET with Minimum 15Years Experience in Injection Molding Manufacturing Plant followed by minimum 5 Years in Managerial role Require a candidate with rich 15+ years of relevant work experience in Injection Molding Manufacturing Plant. Primarily Laying down policies and procedures for the department - to ensure the department functions to meet focal points of the organization, customers and stake holders. Responsible for compliance. Responsible for maintaining Overall P/L of the department Responsible and Contributing in departmental Budget activities Define, Recruit and train of technical staff related to production. Setting departmental goals KPIs & KRAs ensure compliance to QMS /EHS, driving continual improvement plans and CA Implement Quality policy in his function, establish systems in place, participate in IQA and ensure observation closure Goal deployment & performance appraisals for the team membersDefine & Implement MIS template for the Department • Ensure the Records and Documents are maintained properly • Drive the Department team to get maximum throughput of the equipment and machineries with On time delivery and Quality • Work Closely with the Internal stakeholders to define policies and systems • Expertize in Various polymer processing technics, Polymers and Its troubleshooting • Should Contribute in development of New products, tool, process, machineries and/or designing of any systems, process flow.

. Implementing Quality management systems . Review & approval of Process validation, cleaning validation, Water Validation, HAVC Validation, Analytical Method Validation. . Annual product reviews and reviews of stability reports Required Candidate profile 20+ years of experience in Pharmaceuticals Industry with Quality Management Systems, Quality Assurance, Validation, Greenfield Projects in dosage form -. Solid orals ,liquid injectable,

To ensure the machines availability as required for production at optimum cost by maintaining safety through work permits and compliance to safety requirement on machine To support erection and commissioning of equipment as per plan. Required Candidate profile BE (Electronics & Instrumentation) with 8 yrs plus exp in EngigPreferably from Process Industry of the respective sections Viz. Plastic, Tire building, handling PLC based equipment trouble shooting

Role & responsibilities 01 Quality Control Functions: 1.1 To ensure that the laboratory carrying out its testing, calibration, validation and all other technical activities in such a way to meet GLP requirements. 1.2 To carry out all technical activities and implementation of documented quality system. 1.3 To plan, schedule and monitor analysis of Raw Materials, Premix, Packing Materials, In-process materials, Finished products, Microbiological analysis, Water analysis and ensure that they meet defined relevant quality standards. 1.4 Periodically review logbooks, reports and test protocols related to Raw Materials, Premix, Packing Materials, Microbiological analysis, In-process and Finished products for proper entries, accuracy and completeness and ensure that they meet defined relevant quality standards. 1.5 To handle Quality management events according to SOP and complete its documentation with corrective and preventive actions. 1.6 To ensure that updated Specifications, Standard Testing Procedure, Test protocol and documents are available for use. 1.7 To review the resources of Manpower, Instruments, Equipment, Material and advise Management on the provision with justification. 1.8 To train the personnel in the department regarding Chemical Testing, Instrument qualification & current regulatory guidelines. 1.9 To establish effective communication systems with other departments including Commercial departments to achieve effective and efficient service from Quality Control Department. 1.10 To ensure implementation of cGMP in laboratory. 1.11 To ensure Qualification, Annual Maintenance and Calibration of QC instruments. 1.12 To ensure Management of Standards, Chemicals, Reagents and Glasswares. 1.13 To Review and approval of new or revised SOPs. 1.14 To handle instrument troubleshooting and interact with service Engineer in case of instrument breakdown. 1.15 To ensure compliance of Laboratory safety practices and firefighting devices. 2.0 General function 2.1 To provide compliance of Audit observations. 2.2 To take adequate measures to ensure updating of information and knowledge of the key people in the Quality control. 2.3 To provide support to planning, production, finish product for timely release of the goods for dispatch. 2.4 To monitor the microbiological analysis and ensure that all testing is carried out. 2.5 To create SOP awareness by continuous training. 2.6 To ensure good housekeeping of laboratory and up-keep of laboratory. 2.7 Self-updation of current regulatory guidelines. 2.8 Self inspection of other departments, as and when scheduled. . 2.9 Take necessary measures to prevent accident/incident and help in accident/incident Investigation. 3.0 Adherence and compliance to cGMP requirements. 3.1 Undertaking any other work, either for this department or any other department which the organization, which may be requested by the Plant Manager, for which training and/or an explanation has been provided and understood.

1.Recruitment & Manpower Planning, Time Office & Attendance Management 2.Statutory Compliance & Labour Laws, Employee Relations & Welfare 3.MIS & Reporting, Training & Development.

Role & responsibilities : ISO 9001/ISO 13485. Manage the Quality Management System. To provide QA support in all quality related matters and to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements. Risk Management & CAPA. Establishing procedures and records as per requirement of standards and regulatory authorities. Responsible for establishing, managing, and implementing Records Management policy, Records. Retention and retrieval procedures are in place. To manage and execute internal and external audit schedules and follow up on action plan, Quality Auditing of External suppliers - maintain an annual auditing program. Regular Internal Quality Audit and maintain the company anytime audit ready. Participate in and/or lead audits, manage action plans and follow up on agreed upon CAPAs & NCs. To monitor & handle market complaints. Conduct Management review at site. Conduct Calibration of instrument & Maintain Calibration Matrix . Ensure that a respective Change Control procedure is in place and adhered to . Process validation protocol preparation & implementation. Provide leadership and expertise on all aspects of product regulatory compliance to ensure that products are successfully introduced and maintained domestically and globally pursuant to regulatory compliance. Must be capable to handle all types of Audit. To Lead and face the regulatory audits and close all queries and NC in stipulated time. To maintain all documents related to compliances. Create Maintain & update Device Master/ Product Technical File. Preferred candidate profile: Graduate in Science or Engineering . Post Graduation preferred. Thorough Experience in quality and regulatory areas. Thorough experience in ISO 13485, GMP, US FDA, EU MDR, CDSCO, ISO 9001. Regulatory functions throughout the organization including monitoring , improvement , audits, and team building. Thoroughly conversant with technical documentation requirement and preparation. Excellent MS office skills. Should have faced multiple audits from multiple agencies Should have thorough knowledge of the applicable standards Perks and benefits: Medical Insurance for Spouse , 2 Kids Below 18 years upto Rs. 3lac.