148 Sterile Jobs

Position - CSSD Technician (Female Candidates Only) - Mumbai Experience: 0 – 1 Year (Freshers are welcome; training will be provided) B.Sc in Chemistry or Biology Interested? Share your CV shubha@hireindians.com OR Call/WhatsApp at +918178223314 Required Candidate profile If you're a recent graduate looking to start your career in the healthcare sector, this is a great chance to gain hands-on experience in a reputed hospital setting.

Roles and Responsibilities Manage daily operations of the CSSD department, ensuring compliance with hospital policies and procedures. Oversee sterilization processes using autoclaves and other equipment to maintain high standards of sterility. Supervise a team of technicians and support staff, providing guidance on best practices and quality control measures. Develop and implement effective training programs for new employees, promoting knowledge sharing among team members. Collaborate with other departments to resolve issues related to inventory management, supply chain logistics, and patient care. Contact Number Mail ID: hodhr@kmchihsr.edu.in Land Line Number: 0422-680-6170/6171 Mobile Number: 7339475252

Immediate requirement of CSSD Senior Technician Position - CSSD Technician Experience - Min. 10 Years of experience Qualification - Diploma Interested candidate can share their resume on :- Gaurav Bisla- 7838858533 (Whatsapp/Call)

Immediate requirement of CSSD Technician Position - CSSD Technician Experience - 1-4 Years Qualification - Diploma Interested candidate can share their resume on :- Gaurav Bisla- 7838858533 (Whatsapp/Call)

Responsible for leading production operations, coordinating production staff and equipment, ensuring product quality and profitability, and overseeing and managing the production operations involved in injectable products.

Job Title: Senior Nurse - Operations Theatre Company Name: Manipal Hospitals Job Description: The Senior Nurse in the Operations Theatre at Manipal Hospitals is responsible for providing high-quality nursing care to patients undergoing surgical procedures. This role involves coordinating and managing nursing activities in the operating room, ensuring a safe and efficient environment for both patients and the surgical team. The Senior Nurse will assist in the preparation and maintenance of the operating theatre, manage surgical instruments and supplies, and support the surgical team before, during, and after procedures. Key Responsibilities: - Monitor and assess patients' condition before, during, and after surgery. - Prepare patients for surgical procedures, including explaining the procedure and obtaining informed consent. - Ensure that the operating room is properly set up and stocked with necessary supplies and instruments. - Assist the surgical team during procedures by passing instruments, suctioning, and maintaining sterility. - Maintain accurate and detailed patient records related to surgeries and post-operative care. - Collaborate with other medical staff to develop and implement patient care plans. - Provide guidance and mentorship to junior nursing staff and students. - Stay updated with current trends and best practices in surgical nursing care. - Participate in quality improvement initiatives to enhance patient safety and care. Skills and Tools Required: - Advanced clinical nursing skills, particularly in perioperative care. - Strong knowledge of surgical procedures, aseptic techniques, and infection control protocols. - Excellent communication and interpersonal skills to interact with patients, families, and the healthcare team. - Critical thinking and problem-solving abilities to manage unexpected situations. - Ability to work effectively in a fast-paced and high-pressure environment. - Familiarity with electronic health records (EHR) and relevant healthcare software. - Leadership and organizational skills for managing nursing staff and operational tasks. - Current nursing registration and relevant certifications in perioperative nursing or surgical specialties. This position offers an opportunity to make a significant impact on patient care within a dynamic healthcare environment. Candidates should possess a high level of professionalism and a commitment to delivering excellence in nursing care. Roles and Responsibilities About the Role As a Senior Nurse in the Operations Theatre at Manipal Hospitals, you will play a vital role in delivering high-quality perioperative care. You will be responsible for assisting in surgical procedures, ensuring patient safety, and maintaining sterile environments. Your expertise will contribute to the overall efficiency of the operating room and the well-being of patients. About the Team You will work as part of a dedicated team of healthcare professionals, including surgeons, anesthetists, and nursing staff. The team emphasizes collaboration and communication to provide optimal patient care. You will have the opportunity to work alongside experienced colleagues and participate in continuous professional development to enhance your skills. You are Responsible for - Assisting surgeons and anesthetists during surgical procedures by preparing instruments and equipment. - Monitoring patient vital signs and ensuring their comfort throughout the surgical process. - Maintaining a sterile environment and adhering to infection control protocols. - Educating patients and their families about pre-operative and post-operative care. To succeed in this role – you should have the following - A Bachelor’s degree in Nursing and a valid nursing license. - Significant experience in the perioperative setting, preferably as a surgical nurse. - Strong knowledge of surgical procedures and aseptic techniques. - Excellent communication and teamwork skills, with the ability to remain calm under pressure.

Experience in Sterile injectable, specifically in vial washing and tunnel areas Sound knowledge of cGMP, aseptic operations, and production documentation. communication and team coordination. Maintain production documentation and logbooks accurately.

Job Title: Production Manager Department: Production Production Manager Injectables with full manufacturing knowledge including formulation, filling, sterilization, and packaging. Strong technical knowledge of sterile/injectable manufacturing. Supervise and manage day-to-day production activities for injectable formulations. Prepare and review production plans, BMRs, SOPs, and validation protocols. Key Responsibilities: Formulation / Compounding Filling & Sealing Sterilization Visual Inspection Packaging Team Management & Training

Multiple Positions open for Officer/Manager Role & responsibilities : Managing the production line with end to end responsibility for Quality and Quantity. Also required to complete requisite documentation and MIS as desired by management. Preferred candidate profile: S cience Graduate with 3-11 years of experience in managing Filling Lines/Batch Manufacturing/Packing operations in the pharmaceutical industry. Preference will be given to candidates with Injectable operations experience. Should be able to handle 6-10 supervisors Perks and benefits : Best in Industry salaries, growth opportunities within the organization and a fair minded organization which respects individuals as contributors.

Title: Block Head (Parenteral Production) Job Grade: G8 Deputy General Manager Educational Qualification: B.Pharm / M.Pharm Location: Baska, Gujarat Experience: Knowledge of parenteral manufacturing operations Understanding regulatory guidelines Leadership & Team Management Skills Problem Solving & Decision-Making Proficiency in handling production documentation & compliance Min. 15 years of experience working in sterile manufacturing plant or Block In-charge experience Position Summary Responsible for plant operations from material procurement to product dispatch along with operational activities, manufacturing actions, lean management, training, regulatory compliance, cross functional coordination, new product projects, new CAPEX projects, safety and administrations. Monitoring and control of the manufacturing environment, plant hygiene, compliance to requirement of current Good Manufacturing Practice, EHS, local and international regulatory norms. To coordinate for external/regulatory GMP audits at plant and to ensure timely compliance of audit observations. Optimum utilization of man, material and machinery of pharmaceutical products and assuring adequate resource arability with focus of safety and quality first. Ensuring lean management, operation excellence, GEMBA, yield improvement and waste reduction etc. with action plan and its implementation. Responsible to review and approve the qualification related documents as URS, DE, FAT, SAT, IQ, OQ, PQ etc. To coordinate with FDD/PDD (R&D)/ MSTG for execution of trial/ exhibit/ process validation batches and trouble shooting. Implementation of effective control on budgetary provisions and cost reduction measures. Supervision of proper production planning, plan execution as per schedule and ensure that products are produced and stored according to appropriate safety, cGMP requirement. Ensuring protection of the product from contamination and maintain quality as required. Participate in management reviews of process performance, product quality and of the quality management system and advocating continual improvement.

KEY FUNCTIONS / RESPONSIBILITIES Project initiation activities:- To understand project timelines and required activities for the timely execution. To perform literature search required for idea generation form (IGF) upon receiving IGF. To review DMF received from suppliers. To prepare product feasibility based on IGF received. To create the item codes for material and procure material and Reference Listed Drug (RLD). To assist AD lab for Q1 Q2 estimation of RLD. To draft tentative specification for API, RM and finished good. To plan laboratory trials and stability batches. To finalize proposed manufacturing process. To initiate filter validation process with the filter supplier. To handle Bead mill and high pressure homogenise . Documentation:- To prepare tech transfer documents including MFR, BOM, Process flowchart, Critical process parameters and critical quality activities. To review product specifications, manufacturing documents. To prepare documents for trial batches. To prepare product development report. To prepare and review SOPs and prepare response for internal audits. To review documents related to filter validation. Product Specification/ Tech Transfer/ Commercialization To organize and execute trial pre exhibit and exhibit batches at plant. To execute first three commercial batches at plant. To provide technical support for existing commercial batch. To perform investigation of failures during exhibit batches/ stability (Out of Specification). Innovation To come up with innovative and patentable formulations proposals. To come up with novel ideas which can reduce workload or expenses. Train, mentor and supervise the team To mentor RAs in planning the project activities in minute and actionable details. Help RAs in carrying out literature search. Help RAs in carrying out procurement of RLD, API and excipients. Plan and execute Knowledge sharing session for compatibility studies, reverse engineering, laboratory batches planning, filter compatibility, process optimization and recent updates in the field to emphasize importance of timeline adherence to team member

1. Preparation, review and revision of SOPs, GTPs and Work sheets. 2. Execution of analytical method validation protocols for product samples. 3. Testing and review of product / Miscellaneous samples for AET. 4. Operation and maintenance of laboratory Instruments. 5. Monitoring of temperature, DP and RH of the Microbiology laboratory. 6. Involve in the execution of Media fill validations. 7. Cleaning, verification of laboratory cleaning and glassware cleaning in the Microbiology laboratory. 8. Receipt, storage, preparation, sterilization and maintenance of sterile media and reagents. 9. Performing the isolation, identification and confirmation tests for test organisms and Isolates. 10. Responsible for Growth promotion, inhibition test of Microbiological culture media. 11. Responsible for Biological indicator qualification, usage and testing. 12. Culture maintenance in Microbiology department. 13. Preparation and usage of disinfectants. 14. Review of outside COAs. 15. Review, checking and verification of all types Microbiology laboratory documents. 16. Responsible for implementation activities related to resource manager and sample manager of Laboratory information management System #40;LIMS#41;. 17. Verification of cleaning in the Microbiology laboratory. 18. Responsible for compliance to cGLP.

1. Operation and maintenance of Instruments. 2. Receipt, storage and usage of microbiological dehydrated media and other microbiology laboratory consumables. 3. Reconciliation and maintenance of sterile media. 4. Preparation of dilute disinfectants, cleaning, reagents solutions / indicator solutions. 5. Responsible for handling of Bio-waste in Microbiology department. 6. Monitoring of temperature, DP and RH of the Microbiology laboratory. 7. Preparation, sterilization and maintenance of sterile media and reagents. 8. Review, checking and verification of all types Microbiology laboratory documents. 9. Verification of cleaning in the Microbiology laboratory. 10. Responsible for compliance to cGLP. 11. Performing the isolation, identification and confirmation tests for test organisms and Isolates. 12. Responsible for Growth promotion, inhibition test of Microbiological culture media. 13. Responsible for Biological indicator qualification, usage and testing. 14. Culture maintenance in Microbiology department. 15. Preparation and usage of disinfectants. 16. Any job allotted by Department head.

1. Following GMP, safety practices in production facilities and work place. 2. Responsible for buffer preparation activities Area drains cleaning and documents updation. Verification and receiving of material required for buffer preparation activities. Execution of Buffer preparation activities. Preparation of area, equipments before batch activities. Updation of batch parameters. Samples handling (Sampling and labelling). Intimation of incidents to Shift in-charge. Updation of room / equipment status labels. Arrangement of sterile material. 3. Handling of documents Updation of log books. Updation of BMRs and protocols/reports 4. Responsible for operation of following production equipments Mixing systems Conductivity meter Weighing balance Peristaltic pumps Walk in Cold room Freezer room Magnetic Stirrer pH meter Heat exchanger 5. Attending training on SOP's / GMP as per schedule

Business Development GIFT City Branch Department BMU Location Gandhinagar Number of Positions 01 Reporting Relationships VP GIFT City Position Grade M5 (AVP) Kotak Mahindra Bank Gift City Branch is the International Financial Services Center Banking Unit [IBU] set up in Gujarat International Finance Tec - (GIFT) City. It deals with non-individual entities across the globe for their funding (Non INR) requirements; extending ECBs to Indian corporates, Trade and other transaction banking products. Business development Liaising with various business groups in KMBL for lead generation Liaising with various banks globally for borrowing / lending Liaising with various product teams / subsidiaries of KMBL to explore permissible business opportunities Documentation, negotiation and Conclusion of transactions Product structuring Understanding client requirements Liaising with compliance, risk and product teams Setting up process flow for the product Keep the business teams updated with the regulations and products availability. Salary Budget- 19 LPA to 23 LPA Experience Required- 10 to 12 Years Reporting- SVP/ EVP

Microbiological evaluation of raw materials, components, drug product intermediate, finished drug product and stability samples. They will also be responsible for the managing the environmental monitoring and aseptic process simulation programs.

Crystalline Manager Production for the distribution of the instructions and producing API’s/intermediate as per production plan.This includes responsibility for safety,cleanliness of system during product change over or after non/production activity

Reviewing submission related documents including Inactive Ingredient Evaluation, Q1/Q2, Product Development Report, Quality Plan, Product Manual, Trade dress, Specifications, Master Packaging Card and Validation Protocols/Reports etc. DMF Review for ANDA submissions. Outlining requirements for labelling, storage and packaging for FDA submission. Compilation of ANDA sections of US market for sterile dosage form. Review of manufacturing related documents such as BMR, BPR and Stability study Protocols /Reports etc. To draft response and timely submission for regulatory deficiencies. To coordinate with cross-functional teams for regulatory requirements. Keeping up to date with regulatory guidelines

Sterilization and Decontamination: Cleaning, decontaminating, and sterilizing medical instruments, equipment, and supplies using various methods like autoclaving. Equipment Operation and Maintenance: Operating and maintaining autoclaves, low-temperature sterilizers, and other sterilization equipment, ensuring proper functioning and adherence to safety protocols. Instrument Inspection: Inspecting instruments and supplies for cleanliness, proper function, and any defects before they are sterilized. Assembly and Packaging: Assembling and packaging sterile instruments and supplies in appropriate containers or trays for storage and distribution. Inventory Management: Maintaining accurate inventory records of sterile supplies and instruments, ensuring adequate stock levels. Distribution: Providing sterile supplies and instruments to various departments within the hospital or healthcare facility as needed. Documentation: Maintaining detailed records of sterilization processes and quality control measures, ensuring compliance with regulations. Collaboration: Collaborating with other healthcare staff, such as surgeons and nurses, to ensure timely availability of sterile supplies and address any needs.

Walk In Drive For Production Injectables In Formulation Division @ RK Puram Department:- Production Injectables Qualification :- B Tech | B Sc | B Pharmacy | M Sc | M Pharmacy Experience :- 2-4 Years Skills :- Documentation :- BMR & Process validation protocol document preparation & Review | SOP Preparation & Review | QMS Elements | Production & Audit Compliance Qualification :- ITI | Diploma Experience :- 2-4 Years Skills :-Filling Operator Qualification :- ITI | Diploma | B Sc |B Tech Experience :- 10-12 Years Skills :- Senior Filling Operators :- ALUS | Vial filling | Stoppering | Sealing Machine | PFS Division :- Formulation Interview Date:19-07-2025 (Saturday) Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-V, RK Puram Venue Location :- MSNF Unit-V, Rk Puram 25GX+XHX, Solipur, Telangana 509216 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Role & responsibilities 1. Follow the instruction & procedure given in Entry- Exit SOP (Standard Operating Procedure) of Grade C, decartoning area and Grade B’ area. 2. Responsible a procedure for proper functioning or behaviour in aseptic area. 3. Follow the personnel hygiene practices in factory premises. 4. Follow the GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices) as per given in SOP. 5. Responsible for monitoring of temperature, relative humidity and differential pressure. 6. Responsible for monitoring of differential pressure of laminar air flow units and pass boxes. 7. Responsible for handling of material movement in production area. 8. Responsible for maintain the document as per GDP and area as per cGMP. 9. Responsible for to maintain day to day records. 10. Responsible for training to new joining chemist, workers and operators for their respective job. 11. Carrying out the line clearance before starting the operation. 12. Responsible for planning of manufacturing as per availability of RM and PM. 13. Responsible for supervision of preparation and filtration of cleaning/ disinfectant solutions and fogging solutions. 14. Responsible for supervision of equipments/ machines and utility readyness before batch manufacturing. 15.Responsible for supervision of operation and cleaning of steam sterilizer, compounding vessel and holding vessel, vial washing machine, sterilization and depyrogenation tunnel, washing and drying and wrapping of garments and pass box and laminar air flow. 16. Responsible for supervision of handling of filters, filter integrity testing apparatus, silicon tubing, decartoning area and hose pipes and cleaning and wrapping of glassware, auxiliary items and machine parts. 17. Responsible for supervision of operation of pH meter and stirrer. 18. Responsible for supervision of aseptic process stimulation, post media fill cleaning and sanitization of machine and area as per procedure. 19. Responsible for destruction of media filled vials. 20. Responsible for supervision for general area cleaning and sanitization of grade ‘C’ and ‘D’ area and fogging activity of respective area. 21. Responsible for verification of load cell. 22. Responsible for verifying the handling of waste generated in production area. 23. Responsible for non viable particle count (online and offline) monitoring. 24. Recording the operation and cleaning details in batch manufacturing record and equipment uses log book. 25. Responsible for handling of equipment like homogenizer, rota evaporator, magnetic stirrer, ultrsonicator, pH meter and fogger. 26. Follow the procedure for dispensing room and responsible for RM and PPM dispensing and additional materials issuance. 27. Responsible for all data entry for batch manufacturing process in pharmacloud system. 28. Responsible for audit preparation and execution. 29.To undergo periodic medical checkup arranged by the company. 30.Performing the task assigned by the supervisor. 31. Reporting regarding unsafe act/ unsafe condition/ accident/ incident to supervisors. Preferred candidate profile Candidate Should have Exposure of Pharma Injectable Plant. Candidate Should well familiar with Pharma Guidelines. Candidate should have good Verbal and Written Communication Willing to Relocate in Navsari, Gujarat, Willing to Work in a Shift.

Overview We are seeking a highly organized, proactive, and detail-oriented Executive Assistant to support our Senior Vice President (SVP). This role requires a high level of professionalism, discretion, and the ability to anticipate needs while managing a wide range of administrative and executive support tasks in a fast-paced environment. Responsibilities Manage and optimize the SVPs calendar, scheduling meetings, appointments, and travel arrangements. Prepare, review, and organize correspondence and other confidential documents. Coordinate internal and external meetings, including logistics, agendas, and follow-ups. Serve as a liaison between the SVP and internal/external stakeholders. Handle expense reports, invoices, and budget tracking as needed. Maintain strict confidentiality and discretion in all interactions. Taking care of all activities related to SVPs office. Visa processing. Maintaining & Updating tracking tracker. Qualifications Bachelors degree preferred; equivalent experience considered. Minimum of 5 years of experience in an executive support role, preferably supporting C-level or SVP executives. Exceptional organizational, time management, and multitasking abilities. Strong verbal and written communication skills. Proficient in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint); familiarity with collaboration tools like Teams and Concur is a plus.

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile and Allergy Therapy Products, and Generics Solid Dosage Formulations. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma which is subsidiary to Jubilant Pharmova Limited. Jubilant Generics have 2 manufacturing sited at Roorkee, Uttarakhand and Salisbury, Maryland, USA engaged in manufacturing of Tablets and Capsules. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business team focusses on B2B model for EU, Canada and emerging markets. Kindly refer www.jubilantpharmova.com for more information about organization. JOB RESPONSIBILITIES : ;;;;;;;;;;;;; Accountabilities;;;;;;;;;;;;;;;;;;;;;;;;;;; Scope of work US Drug Dossier Authoring, Reviewing and Submission of ANDA (US) Product life cycle management (LCM) activities Assessment of post approval changes eCTD publishing Thorough knowledge of CMC and Module 1 requirements Labelling submission, SPL preparation Preparation and Submission Authoring and review, compilation and submission of ANDA, DMF review and assessment, Query evaluation and response for under review ANDA within timeline. Assessments of post approval changes and submissions (Annual report, CBE-30, PAS), life-cycle maintenance and ensure timely post approval regulatory activities. Artworks (PIL, labels) and labeling files preparation along with SPL preparation. Coordinate with cross-functional teams for desired regulatory data and accordingly plan and complete regulatory filing activities Review and finalization of artwork/label as per current guideline. Regulatory Intelligence and develops up-to-date knowledge with regard to technical guidelines and regulatory requirements, as well as technical trends eCTD publishing Coordination Interface with R and D and other business functions on a regular basis to ensure project-specific regulatory strategy is met as agreed in timely manner Co-ordination with API vendors to resolve technical quires w.r.t. regulatory requirements To review technical documents like process validation, AMV, Stability and composition etc. received from Site QA or R and D/ADL against DMF/Dossier requirements Reporting and Maintenance Maintain regulatory files/database

Walk In Drive for Engineering Services Department In Formulation Division @ RK Puram Department:- Engineering Services OSD Skills- Instrumentation | Utility | Process Maintenance | HVAC | Electrical | Water System Qualification :- Diploma | B Tech Mechanical & Electrical Experience :- 2-8 Years Division :- Formulation Work location :-MSNF-V, RK Puram Interview Date-16-07-2025 Interview Time:- 9.00AM To 2.00PM Venue Location:- MSN Formulation Unit-V RK Puram, 25GX+XHX, Solipur, RK Puram,Telangana 509216 Contact No:- 040-304338701 | 8787 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Must to have Exp into sterile (injectables) production Prepare & review SOPs Responsible for daily smooth operation of Production Lead & Collaborate to implement process improvements, automation initiatives, and technology upgrades effectively Required Candidate profile Good in Communication Good in Leadership Quality