We are hiring *Microbiologist* For Pharmaceuticals Company, Experience : 0 to 3 years (Must experience in pharma base company.) Location : Chhatral, Kalol (Gujarat) Time : 09:00AM to 17:30PM Salary : up to 25k For more details please feel free to call or WhatsApp us on 9925232909 / mail me your CV on hr@memphisvisioncare.com Show more Show less
Company Description Memphis Vision Care Pvt. Ltd. (MVCPL) is an innovation-led transnational pharmaceutical company dedicated to improving the health and wellbeing of mankind through the development, production, and marketing of high-quality medical products. MVCPL manufactures a wide range of parenteral formulations packed in sterile PFS under hygienically controlled environments. The company's state-of-the-art manufacturing facility has received international recognition and approval from various regulatory authorities for its adherence to cGMP standards, surpassing WHO quality standards. Experience : 0 to 1 year Location : Chhatral, Gujarat Qualification : BSc - Msc & B.Pharm - M.Pharm Time : 09:00AM to 17:30PM For more details please feel free to call or WhatsApp us on 9925232909 / mail me your CV on hr@memphisvisioncare.com Show more Show less
Company Description Memphis Vision Care Pvt. Ltd., (MVCPL) is an innovation-led transnational pharmaceutical company that manufactures a wide range of parenteral formulations in a hygienically controlled environment. The company is committed to enhancing the quality of life through the development, production, and marketing of excellent medical products. MVCPL's state-of-the-art manufacturing facility has gained international recognition for its adherence to cGMP standards and exceeding WHO quality standards. Designation : QA Executive Department : QUALITY ASSURAMCE Qualification : B.Pharmacy / M. Pharm / M.Sc. Experience: 03 to 05 Years Sections : Validation / Qualification / Calibrations & Stability Section Equipments / Instruments / Process Validation / Cleaning Method Validation / HVAC / Media Fill / Packing Validation RESPONCIBILITY : 1) Responsible for all the validations / Qualifications & calibrations related activities & its documentation 2)Preparation, execution & maintenance of validation / qualification & calibration protocols, executions its reports & related documents for all Validations / Qualification & Calibrations. 3)Qualification of Newly received equipment 4)Preparation of PQ protocols for the newly received equipment's, execution of PQ & Report preparation. 5)Responsible for stability planning and execution. 6)Responsible for handling of stability chambers including alarms acknowledgement & breakdowns (if any). 7)Charging & withdrawal of stability samples as per the schedule & its documentations. 8)Follow up with QC & tracking for the analysis data. 9)To ensure analysis is completed as per the timeline. 10)Compilation of stability data & preparation of stability summary reports 11)To maintain all the log books / Records related to the stability chambers & stability studies. 12)Record the temperature and humidity of stability chamber and control sample room Show more Show less
Company Description Memphis Vision Care Pvt. Ltd. (MVCPL) is an innovative transnational pharmaceutical company dedicated to enhancing the well-being of humanity through the development, production, and marketing of high-quality medical products. Specializing in a wide range of parenteral formulations packed in sterile PFS, MVCPL operates under strict hygienic and cGMP standards to exceed WHO quality norms. Located in Chhatral, our state-of-the-art manufacturing facility has garnered international recognition from regulatory authorities for its excellence. JOB RESPONCIBILITY 1.Packing Execution and supervision as per plan 2.Online Entry in SAP and Pharma cloud system 3.Online Documentation 4.Stream line the activity with parties for Dispatch 5.material Procurement as per packing planning EXPERIANCE : 3 TO 5 YEARS LOCATION : Chhatral(Gujarat) For more details please feel free to call or WhatsApp us on 9925232909 / mail me your CV on hr@memphisvisioncare.com Show more Show less
Job description Company Description Memphis Vision Care Pvt. Ltd. (MVCPL) is an innovation-led transnational pharmaceutical company dedicated to improving the health and wellbeing of mankind through the development, production, and marketing of high-quality medical products. MVCPL manufactures a wide range of parenteral formulations packed in sterile PFS under hygienically controlled environments. The company's state-of-the-art manufacturing facility has received international recognition and approval from various regulatory authorities for its adherence to cGMP standards, surpassing WHO quality standards. Location : Chhatral, Gujarat Time : 09:00AM to 17:30PM For more details please feel free to call or WhatsApp us on 9925232909 / mail me your CV on hr@memphisvisioncare.com
Responsibility: 1. Analysis of samples for batch release, stability testing, validation and other testing activities along with proper documentation as per approved STPs and approved protocols with complete documentation. 2. Preparation of reagents and solutions as per test requirements. 3. Troubleshooting in HPLCas when required. 4. Support in investigation of Deviation, OOS or OOT 5. Preparation and review of documents as & when required 6. Participate in training/ qualification/ validation of methods during technology transfer 7. Perform verification/calibration/ qualification/monitoring activities of instruments/ equipment as per schedule 8. To support in internal as well as external audit compliance
Qualifications : Graduate Experience : 3 to 5 Years in SAP Role Description To prepare, review and revise the entire SOP as and when required related to ware house department. To ensure training of the personnel involved in handling and dispensing of RM, PPM and SPM and strict adherence of safety precautions . To ensure per proper receiving, storage as define storage condition for RM, PPM and SPM and make necessary entries in software and documents. To submit request to QC department for sampling of received Raw Material, Primary Packing Material and Secondary Packing Material, and ensure proper labeling of all received material as per different stages like Quarantine, Under test, sampled, released etc. To maintain the respective records of received materials and their consumption for all RM, PPM and SPM. To ensure dispensing of the required batch materials as per request by manufacturing department mentioned in BMR’s and BPR’s. To ensure that all the material dispensed shall belong to approved stock containing proper approved labels on container or box. To Execute qualification/Re-qualification as per qualification planner of all equipments belong to ware house department. To ensure proper labeling and transfer of dispensed material to respective department as per material request form. To intimate QC dept. About the sampling Employee shall intimate QC about the material due for retesting. To ensure proper handling, storage and the dispatch of the finished goods and related documentation of excise. Employee shall be responsible for calibration of the balances used in Warehouse facility. To maintain all online entries in software (SAP & Pharmacloud) related to warehouse. To initiate any QMS document as when required related to warehouse dept. To implement training of all relevant CFT member as per training matrix. Any other responsibility assigned by superiors.
This is a full-time on-site role for a Production Manager - Injectable Manufacturing based in Chhatral, Gandhinagar. The Production Manager will oversee the daily operations of the manufacturing facility, ensuring adherence to production schedules and quality standards. Key responsibilities include supervising production staff, developing production plans, optimizing manufacturing processes, and coordinating with other departments. The role also involves maintaining compliance with regulatory requirements and implementing continuous improvement initiatives to enhance productivity and efficiency. Qualifications : M.sc/ B.Pharm/ M.Pharm Experience : 5+ Years of experience in injectable plant. Role Description : Responsible to update on self-hygiene. Responsible for preparation, review, revision, control, and implementation of standard operating procedures of sterile manufacturing department. Responsible for preparation and review of Protocols and reports based on the requirements. Responsible for Document management like BMRs, BPRs, Master SOPs etc. Responsible for the handling of Change Control, Deviations, CAPA, Investigation etc. To generate general purchase indent for departmental general items. Responsible for preparation of production planning on monthly and daily as per the requirement and availability of materials. Responsible to prepare daily production report as per the production achieved. Responsible to ensure that all equipment’s and lines are in validated and calibrated status. Responsible to follow cGMP, GDP, and discipline in the department and to ensure that all employees follow the same. Responsible to give training to all the subordinates, technicians, and operators of the department. Activities other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance. Responsible to attend the training as per training schedule and to ensure training as per TNI(Training Needs Identification). Responsible for preparation & review of the all-master documents of production . Responsible to ensure cleaning & sanitization and operation of machines as per Standard operating procedures. Responsible for Control and Aseptic Area operation like sterilization, manufacturing, washing & dehydrogenation, filling and sealing etc. Responsible for line clearance activity before commencing the operations like manufacturing, filling & sealing. Skills : Complying with Good Manufacturing Practices (GMP) and Regulatory Standards. Completing Batch Manufacturing Records(BMRs), Batch Packing Records(BPRs), Logbooks, and Deviation Reports. Maintaining traceability and following SOPs strictly
As a Production Manager - Injectable Manufacturing based in Chhatral, Gandhinagar, your role will involve overseeing the daily operations of the manufacturing facility. You will be responsible for ensuring adherence to production schedules and quality standards. Your key responsibilities will include: - Supervising production staff to ensure smooth operations - Developing production plans to optimize efficiency - Coordinating with other departments for seamless workflow - Maintaining compliance with regulatory requirements - Implementing continuous improvement initiatives for enhanced productivity Qualifications required for this role include: - M.sc/ B.Pharm/ M.Pharm - 5+ years of experience in an injectable plant In your role, you will be responsible for various tasks such as: - Updating on self-hygiene - Preparation, review, revision, and control of standard operating procedures - Document management including BMRs, BPRs, Master SOPs - Handling Change Control, Deviations, CAPA, Investigation - Generating purchase indents for departmental items - Preparation of production planning on a monthly and daily basis - Ensuring equipment and lines are validated and calibrated - Providing training to subordinates, technicians, and operators - Following cGMP, GDP, and maintaining discipline in the department - Attending training sessions and ensuring training as per TNI - Preparation and review of all master documents of production - Ensuring cleaning, sanitization, and operation of machines as per SOPs - Control and operation of Aseptic Area activities Skills required for this role: - Complying with Good Manufacturing Practices (GMP) and Regulatory Standards - Completing Batch Manufacturing Records(BMRs), Batch Packing Records(BPRs), Logbooks, and Deviation Reports - Maintaining traceability and strictly following SOPs,
Company Description Memphis Vision Care Pvt. Ltd. (MVCPL) is a transnational pharmaceutical company committed to enhancing human health through innovative development, production, and marketing of high-quality products. We produce a wide range of parenteral formulations (packed in sterile PFS) in a hygienically controlled environment. Our state-of-the-art manufacturing facility has received international approval from various regulatory authorities. Strict adherence to cGMP standards allows MVCPL to exceed WHO quality standards, ensuring customer satisfaction through continuous improvement. Role Description This is a full-time on-site role for a Human Resources Executive, located in Kalol. The Human Resources Executive will oversee day-to-day HR operations, manage employee relations, develop and implement HR policies, and handle various HR management tasks. Responsibilities will include recruitment, performance management, employee engagement, and ensuring compliance with labor laws and company policies. Qualifications HR Management and Human Resources (HR) skills Experience in HR Operations and developing HR Policies Strong Employee Relations skills Excellent communication and interpersonal skills Ability to work independently and collaboratively Bachelor's degree in Human Resources, Business Administration, or related field Prior experience in the pharmaceutical industry is a plus