35 Injection Jobs - Page 2

GCS Medical College Hospital & Research Centre is looking for Dialysis Technician to join our dynamic team and embark on a rewarding career journey. Conducting electrocardiogram (EKG), phonocardiogram, echocardiogram, and stress tests by using electronic equipment. Ensuring cardiology patients are comfortable by answering any questions they have about the tests. Recording the results of cardiological tests and consulting with the physician on duty to schedule any follow-up tests. Assisting physicians during non-evasive cardiological procedures by monitoring the patients' heart rates and alerting the physicians to any readings outside normal ranges. Maintaining cardiological equipment and supplies with daily cleanings and adjustments. Recording supply inventory levels and restocking the supply storeroom accordingly. Troubleshooting problems with cardiological equipment and reporting any malfunctions to superiors. Staying up-to-date with cardiological developments by attending conferences and participating in research projects

Skills: . Machine operation, Tool maintenance, Precision measurement, Problem solving, Safety procedures, AutoCAD,. As a Tool Maker Trainee, you will be responsible for designing and manufacturing precision tools and mold parts used in plastic injection molding. This is a full-time position with a Junior level of experience required only Freshers.*. Responsibilities. Design, fabricate, and repair precision tools and mold parts according to specifications. Operate various machine tools such as lathes, milling machines, grinders, and EDM. Read and interpret blueprints, drawings, and specifications. Inspect finished tools and mold parts for accuracy and quality. Collaborate with engineers and technicians to optimize tool and mold designs. Troubleshoot and resolve tooling and mold-related issues. Perform preventative maintenance on tools and equipment. Maintain accurate records of tooling activities and inventory. Adhere to safety and quality standards. Qualifications And Skills. Freshers with valid degree in tool making. Proficient in using various machine tools and equipment. Strong knowledge of tool and mold design principles. Ability to read and interpret blueprints, drawings, and specifications. Detail-oriented with excellent problem-solving skills. Strong attention to detail and quality. Good communication and teamwork skills. Ability to work independently and meet deadlines. Experience in plastic injection molding is an advantage. Job TypeFresher. Pay180,000.00 240,000.00 per month. BenefitsProvident Fund. Work LocationIn person. Show more Show less

About The Role Experience in Injection Moulding Process Analyze production for the previous day (and/or shift). Compare against target to identify deviations and help plan for next steps to enable recovery of losses in the day / shift Participate in daily review meetings with the Section Incharge to understand the daily production targets, inhouse rejection (IHR) targets, maintenance schedules and discuss variances (if any) in prodution Create a work plan for production activities (during the day/shift) basis the daily section production requirement Oversee end to end production process including all cell operation routines aimed at achieving the production target Maximize plant production efficiency by monitoring and controlling production bottleneck areas Resolve various issues impacting production capacity of plant; Escalate to Section Incharge for critical issues Collaborate with maintenance teams as and when required to assess various maintenance requests basis risks involved to production. Aim at limiting machine breakdown to 3-4% and minimizing downtime Monitor actual production vs scheduled production; Understand the causes for the deviation and implement corrective actions to prevent future occurrences Provide daily updates regarding production activities, actual production, IHR, consumables utilization etc Monitor consumables per unit of product hence estimate the cost of manufacturing. Ensure consumption in-line with the consumables plan by optimizing utilization of the consumables Study and analyze previous day rejections to identify processes getting rejected and its subsequent causes and effects. Submit the IHR report to the Section Incharge for further analysis and planning Implement process modifications suggested by supervisor to control IHR thereby avoiding wastage of both quantity and cost Contribute to the implementation of Kaizen and initiatives suggested by ME ensuring plant is operated in compliance with best engineering practices Contribute to the review of plant operating procedures by provide inputs to modify the same to improve quality and performance of system Ensure all documents such as QMS requirements, log books, log sheets and safety documents are properly stored and maintained for future reference Ensure timely reporting and investigation for any HSSE related incident; Ensure effective and timely implementation of formulated action plan to prevent its reoccurrence Conduct timely trainings and talks for all production personnel and contract workforce on all HSSE, legal, environmental and fire compliances and management Facilitate internal / external audits and ensure compliance of all production processes to applicable environmental, health and safety policies, laws and regulations.

Dear Aspirant , Greetings From Eugia Pharma Specialties , Unit ..! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit. Department - Production (Injectable) Qualification - M. Pharmacy / B. Pharmacy / M. Sc /B Sc / Diploma / ITI Designation - Sr. Executive / Executive/ Operators Experience - 2Yrs to 8 yr. Skills - Vial Filling/ Sealing / Autoclave / Lyo and etc Work Location : Eugia Unit -3, Pashamylaram Walk In Details: Date : 23.03.2025 Time : 10 AM - 02 PM Venue : Eugia SEZ (Aurobindo Pharma Limited-Unit 16), Balanagar, Ambatapur, Telangana 509202 Google Maps: https://maps.app.goo.gl/KxN3JSa7wL8MoYpm6 Contact : Mr Prabhakar / Ms Rama

Dear Aspirant , Greetings From Eugia Pharma Specialties , Unit ..! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit. Department - Production (Injectable) Qualification - M. Pharmacy / B. Pharmacy / M. Sc /B Sc / Diploma / ITI Designation - Sr. Executive / Executive/ Operators Experience - 2Yrs to 8 yr. Skills - Vial Filling/ Sealing / Autoclave / Lyo and etc Walk In Details: Date : 23.03.2025 Time : 10 AM - 02 PM Venue : Eugia SEZ (Aurobindo Pharma Limited-Unit 16), Balanagar, Ambatapur, Telangana 509202 Google link : https://maps.app.goo.gl/TpvUmrAjTBXakHv77 Contact : Mr Prabhakar / Ms Rama

Can handle the production and packing line independently. To exercise effective control over the environmental conditions in process areas activities, which may affect the product quality. Compliance to Quality Management System as per cGMP and regulatoryrequirements at all levels of Manufacturing. CAPA implementation for observed non-conformance/exceptions. Training and evaluation of the Production Technicians, Production Associates and Trainee Production Associates for their qualification to specific task or to operate specific equipment. Preparation of Standard Operating Procedures for production equipments. Co-ordination for installation and Qualification of Production equipment with Engg.,QA and other departments. To co-ordinate for calibration / preventive maintenance for all production equipments and instruments with Engineering / QA / QC & outside agencies. To carry out routine documentation as per Regulatory Requirements and to complete BMR/BPR, Formats& related documents online and timely with all respects. Coordination with production Planning department for Process Order and Batch Records document with QA. Organizing the job responsibilities to the Technicians/ITIs as per daily plan and execute the defined targets as per standard outputs. Checking of dispensed input materials against process orders and co-ordination with WarehouseDeptt. Continuous monitoring of In-process controls in the production areas. Continuous monitoring and improving the production output on daily basis and control on absenteeism of Technicians/ITIs. To work within the specified working hours and mainly responsible for Process areas. To ensure proper maintenance of Production Area and equipments in the state of cleanliness as per the SOPs at all points of time and its upkeep. To ensure all time readiness for audits. Have basic knowledge of SAP&Track wise. Have skills pertaining to QMS handling in packing and production line. Flexible to work in shifts and extended hours in case of production requirement. Knowledge of Manual Visual Inspection, Automatic visual inspection machine (Antares Vision), Automatic case packer machine (Fuji), Automatic setup caser machine (Fuji), Automatic palletizer machine (Fuji) & Printers (Domino). Good knowledge of Track and Trace system (Optel). Well familiar with Knapp Test and challenge test of the automatic inspection machine. Shall effectively co-ordinate with External contract giver i.e. Piramal Pharma and shall ensure timely packing and deliverance of export batches as per plan. Shall be responsible for the process improvisation w.r.t packing operations.

To handle the niche category core customers To provide Clinical Facilitation for the upcoming aesthetic Drs To revive the previous prescribers as well as create new customers To conduct Grow Hands-on workshops in clinic & institutions for Basic & Advance indications along with Complication management To achieve primary and secondary sales targets and growth objectives assigned for his / her territory. Prepare monthly, quarterly sales forecasts and chase it with meticulous planning and Account Management. Establish productive and professional relationships with all the stake holders of his / her territory such as HCPs, Stockists, Pharmacies, Purchase department of different accounts and support staff of the account to name a few. Implement effective sales strategies for his territory under the guidance of the National Head and with the help of Brand promotion, Strategies Implementation and Execution effectively to achieve his territorys budget. Identify the key accounts for negotiation and closing the business agreements. Provide timely feedback and suggestions to the National Head on his / her territorys clients needs. Ensure implementation of CRM and KOL engagement plans in his / her territory in conjunction with marketing and medical affairs team. Identify new potential customers and new market opportunities from his territory. Accountable for his / her territorys Collections / Management of accounts receivables. Prepare & participate in periodic sales review of his territory by the National Head and suggest way-forward to surpass his / her territory revenue targets. Critical Competencies, Skills, Knowledge & attributes: Should be a peoples person with Strong team work attitude. Should possess Professional manners and etiquettes. Self-motivated with a results-driven approach excellent with negotiation skills. Enthusiastic with strong interpersonal skills. High achievement orientation Effective communication skills Should be learning Agile and passionate about sales. Good at using MS Office / EXCEL. Education and Work Experience Requirements: Science Graduate , minimum 4 Years of experience in Derma cosmetics and preferably in Pharma Aesthetic Injectable Sales / Speciality divisions Desirable: MBA / Diploma in Sales & Marketing.

Role & responsibilities Responsible for Drup Product Manufacturing Ensure compliance to Current Good Manufacturing Practices (cGMP)& documentation thereof for various production activities. Filling line in built CIP, SIP operations Knowledge of Isolator VHP, Blending vessels- CIP, SIP Good at QMS Regulatory inspection exposure WHO-PQ, USFDA, EU GMP, TGA,ROW Experience in O RABS, Isolator filling lines Lyophilizers - ALUS, Manual operations Blending of viral, bacterial vaccines Media fill activities , TRS 1044 updates Responsible for preparing production plan in consultation with PPIC department and execution thereof with effective planning and utilization of Men, Materials and Machineries for quality linked productivity. To approve the instructions relating to production operations and to ensure their strict implementation. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. To ensure that the production records are evaluated and signed by an authorized person. Review investigation of Quality Management System (QMS) including market complaint, Out of Specification (OOS), change controls of manufacturing, risk assessment, Corrective Action and Preventive Action (CAPA) etc. To ensure the qualification and maintenance of department, premises and equipment. Ensure compliance to master formula and process provided in the Batch Manufacturing Record (BMR). To ensure that the appropriate validations are done. Reviewing document like of Standard Operating Procedures (SOPs), Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR)etc. and compliance reports thereof with training of personnel on the same. Ensure appropriate inventory of Consumable in the Department for smooth functioning. Responsible for Co-ordination with Technical Services, Quality Assurance / Quality Control, Finance, Purchase, Warehouse and Administration Departments for effective management of Production targets. Ensure wastage control and optimization of yield at various stages of manufacturing and packaging operations. Ensure compliance to various In-process control guidelines provided in the batch documents. Ensure periodic preventive maintenance of plant and machineries as per schedule worked out by Engineering for optimum performance. Ensure that personnel follow basic safety guidelines during operations. Responsible for the preparation of training calendar for employees and to ensure that the required initial and continuing training of department personnel is carried out and adapted according to need on cGMP and various operational activities. Responsible for preparation of accurate and timely reports of various production activities showing performance and shortcomings against agreed/planned parameters (monthly presentation, work in progress (WIP) statement yield report, monthly planning, expense budget stationary, housekeeping material, production item &capital budget etc). Preferred candidate profile M.Pharm/ B.Pharm / MSc ; Experience- 18 to 25 years Candidate Must have exposure of regulatory Audits should be willing to relocate with family to ahmedabad

Manufacturing of lyophilized product, liquid injection, Liposome, microsphere product and filling activities of Lyophilized vial, Liquid vial, PFS, Cartridges, Glass ampoule Preparation and review of documents like product BMR, media fill BMR, PVP,

Role & responsibilities Key Responsibilities: Participate in new product development and supplier selection processes. (Support in Supplier Feasibility study.) Initiate the PPAP process and conduct SOD kick off. Perform manufacturing feasibility study along with design and Industrial team. Define the measurement method and criteria for the new parts. Ensure suppliers are capable of delivering the required quality standards by RPN reduction, Poka-yoke implementation and training. Conduct PPAP audit and ensure PPAP approval. Evaluate and audit supplier quality systems and processes. Closure and Monitoring of issues observed during PPAP and initial lots. Ensure Project timeline adherence. Collaborate with suppliers on quality improvement and RPN reduction initiatives. Conduct root cause analysis and implement corrective actions for quality issues. Provide training and support to suppliers on PPAP process and other SE quality standards as well as best practices. Coordinate with cross-functional teams to ensure Component validation (PVP/CVP) and Production Trial Run is completed successfully. Handover the new component to respective plants after PTR. Qualifications: Bachelors degree in mechanical engineering with 5 to 7 yrs. of exp. Experience in Part development & Qualification, supplier quality process. Good Knowledge on manufacturing process (Injection Moulding, Stamping and casting ). Good experience on Metrology and Knowledge of GD&T. Strong analytical and problem-solving skills. Knowledge of quality management systems (e.g., VDA 6.3 / IATF). Excellent communication and interpersonal skills.