147 Sterilization Jobs - Page 6

Role & responsibilities To maintain a clean and sterile OT. To clean and pack the instruments and autoclave and provide enough sets and linen. To maintain the autoclave-machine and eto machine. To pack and autoclave sufficient dressing sets, other set’s like bone-marrow, ICD etc. For use in the floors. To help in cleaning and fumigation of the OT. To dispatch the specimen as and when required. To see that all hospital policies are followed. Preferred candidate profile Immediate Joiners will be preferred.

Qualification : Bsc in OT Tech. / Diploma in OT Tech. Must have exposure as Operation Theatre Technician with comprehensive exposure to various surgical specialties including Urology, Neurosurgery, Orthopedics, Gynecology, General Surgery, and Laparoscopy etc. Maintains and keeps the operating room and ensures everything is running smoothly before the conduct of surgery. Cleanse and disinfect surgical instruments and or equipment after surgeries. Prepare surgical instrument and equipment for autoclaving/sterilization per protocol Maintains and keeps all surgical tools sterile and orderly. Maintains and keeps all equipment clean and functional. Order and maintain adequate necessary supplies in the operating room. Prepares the patient before and after surgery by washing and disinfecting the area for surgery. Prepare necessary equipment and instrument prior to procedure/surgery. Assists in bringing the patient to the operating room. Attends to the needs of the patient while inside the operating room. Assist surgeon during the procedure. Assist nursing staff in keeping patient safe during the procedure by assisting RN with the application of restraints and following the recommended protocol. Provides assistance to the surgical team and coordinates very closely with the doctors, nurses and laboratory staff. Clean and disinfect operating room area after each procedure/surgery. Reports any defective equipment and instrument for repair or replacement. Assist other staff in discharging patient as needed.

Roles and Responsibilities Required Sales Manager with experience in Sales of Hospital Disinfectants and Sterilization solutions. Candidate is required to visit Hospitals, Meet Microbiologist, Infection control and nursing departments ; conduct cme programs and presentations, demonstration up to order finalization. Desired Candidate Profile Experience in Sales of Hospital Disinfectants and Sterilization solutions. Perks and Benefits Salary + Commission

Responsible for cleaning, sterilizing, inspecting, & packing surgical instruments; maintaining records; ensuring infection control; coordinating with OT/ICU. Requires knowledge of sterilization,attention to detail, & physical stamina.NABH guildeline.

1. Role & Responsibilities: Perform facial massages and apply our Korean skincare products to clients. Showcase and promote the features and benefits of our Korean skincare product line during treatments. Provide excellent customer service and build rapport with clients. Educate clients on proper skincare routines and recommend suitable products. Maintain a clean and organized work environment. Provide feedback on product performance and customer preferences. Collaborate with the team to achieve overall business goals. 2. Preferred Candidate Profile: Female candidate. Educational background in skincare or cosmetology is preferred. Some prior experience in skincare application or facial massage is necessary. Strong interest in skincare, particularly Korean beauty and cosmetic products. Excellent communication and interpersonal skills. Demonstrates proactive and enthusiastic personality. Possesses sales-oriented skills with the ability to effectively promote products. Eagerness to learn and grow within the beauty industry. Positive attitude and a team-oriented mindset. Willingness to represent the brand positively.

Working Experience in Production/Packing : 2 to 10 years in Parenteral Manufacturing unit *For Production (Parenteral/Injectable exposure only) : > Process Incharge/Sr. Process Incharge : - To ensure the cleanliness, environmental norms and other process of various area like Dispensing, Mixing, Filling and Terminal Sterilizer. -To complete CIP, SIP and batch manufacturing process timely. -To ensure the batch manufacturing process is done as per Batch Manufacturing record. -To co-ordinate with other departments like QA, QC, Stores, Engineering, etc. as and when required. *For Packing (Parenteral/Injectable exposure only) : >Process Incharge/Sr. Process Incharge: - To make sure that issued material is as per requirement and the material quality is as per specification. -To check the availability of packing material with proper labels and status. -To ensure that the packing activity does not start without line clearance. -To check, verify and destroy the rejection generated during packing and ensure recording of all such material. -To update the Batch Packing Record online. -To check the packing online at frequent intervals as defined in the Standard Operating Procedure. -To train personnel for the critical operations like visual inspection and labeling. Candidate Profile: Ready to work in rotational shifts. Excellent understanding about working area. Initiator and Learner. Decision making ability. Team player and if required, can provide training to other team members. Good communication. -The above positions are for shift (rotational) operations for the plant location (Vasana-Chacharwadi) and only for experienced candidates. -Fresher candidates can share their profile on hrm.opmf-amd@otsukapharma.in Note: Otsuka Pharmaceutical India Pvt Ltd does not hire any such consultants/agents who promise interviews/jobs for monetary consideration/registration fees. Beware of such fraudulent calls.

Media Preparation, (GPT). Instrument like Autoclave, Hot air Oven, pH Meter, Balance, (LAF), Sampler, BOD Incubator, Deep Freezer, analysis of Water, documentation, Limit testing of Finished Product as Per Specification. Required Candidate profile Preference for Male Candidate ONLY

Decontamination, sterilization, and preparation of surgical instruments, equipment, and supplies in accordance with established protocols and standards. Ensure all sterile processing activities in a safe & efficient manner.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere For 70 years, our team has driven meaningful innovations in kidney care As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients? that is what Vantive aspires to deliver, We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us At Vantive, you will become part of a community of people who are focused, courageous and dont settle for the mediocre Each of us is driven to help improve patientslives worldwide Join us in advancing our mission to extend lives and expand possibilities, Vantive: A New Company Built on Our Legacy Since last year, we have been on a journey to separate our Kidney Care segment into a standalone company Vantive will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us, At Vantive, you will become part of a community of people who are focused, courageous and dont settle for the mediocre Each of us are driven to help improve patientslives worldwide Join us as we revolutionize kidney care and other vital organ support, Job Summary Job Title Engineer IILab, Sterility Assurance & Microbial Sciences Location Whitefield, Bangalore Shift General This position will report to Sterility Assurance & Microbial Sciences Lab Manager and is primarily responsible for laboratory contract support This role will be responsible for the overall operation, maintenance and execution of various sterilization cycles in steam sterilizer The candidate should learn the technical aspects of sterilizer and should be able to troubleshoot routine challenges related to sterilizer by coordinating with vendors The candidate should have a strong understanding of the scientific aspects related to Microbiology and Sterility Assurance, Job Responsibilities Candidate working with a Device / Drug Company (Device preferred but would consider Pharma/ Biopharma)Microbiology & Quality Assurance/Control Should have a good knowledge of Regulations and GMP working environment Exposure to multiple products life cycle desirable, Contribute to technical feasibility analysis of complex research and design concepts including a lot of microbiology inputs for Sterility Assurance and related controls for the products, Good understanding of the Science & microbiology principles, guidance, regulations around sterilization validation & related to Sterility Assurance, Design, development & Technical Understanding of Microbial Method Validation & Sterilization Engineering principles for devices/ Solutions, Support Lab Manager by assuring contract laboratories documentation and internal lab documentation are audit ready and team can effectively respond to auditor inquiries, Work with Quality team to ensure adequate documentation, input into computer systems, and being the point person for addressing quality issues, Operation of steam sterilizer as per set procedure for various Sterility Assurance studies (Class-C & B studies), Prioritization of sterilizer cycles as per project need and urgency ensuring timely completion of project deliverables, To document all the sterilization study records manually or by using ELN templates, To learn and develop expertise in execution of different CCI methods (Air Under Water & Gurley), Responsible for calibration and maintenance of all laboratory equipment, Responsible for maintaining optimum inventory of lab consumables, Responsible for maintaining anytime audit readiness of Sterilization lab, Design and draft various study protocols as per project need, Equipment procurement and assure necessary validations and documentation, Support Lab Manager to maintain lab operations, Provide regular/timely updates to Sterility Assurance Management, Assure all work complies with Vantives QMS and cGDP/cGMP/cGLP practices, Perform standard Sterility Assurance assignments for application, validity and conformance to specifications, Utilize analytical process tools to solve complex process problems (e-g , FMEA, Risk Analysis, Process Modeling, Design of Experiments) Lead small project teams as needed to accomplish project objectives, Study and recommend techniques to improve existing products/processes and process controls, Provide sterilization support for Renal R&D projects and technical trouble shooting & to evaluate results relative to product requirements, definitions and/or program goals Analysis and evaluation of sterilization studies data and assist in the preparation of documentation using Good Documentation Practices (GDP), Employ appropriate techniques and methods to successfully conduct specific assignments within negotiated deadlines after receiving general instruction, Demonstrate working knowledge of basic technical theories and principles within area of expertise for routine tasks, Devise new approaches to complex problems through adaptations and modifications by use of standard technical principles, Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities, Display a solid understanding of theories/practices utilized by other disciplines outside primary area of expertise, Ability to convince management on courses of action with minimal assistance using both written and verbal methods, Knowledge around microbiological aspects of biological indicators, Adventitious Agents and related microbiological concepts, Qualifications Masters degree in a scientific discipline (Microbiology/Technology/ Science/ Pharmacy) with minimum 6 years or BS with minimum 8 yearsexperience in sterilization validation or equivalent, Prefer experience with Sterilization, Global sterilization regulations & TQM methods (e-g "six sigma") Display a solid technical understanding of Microbiological principles and qualification practices & application of these principles on individual/small projects, Technical writing skills, remote support for projects, strong interpersonal skills and a quick adaptive mindset for the new technologies, Strong Microbiology background and experience, Demonstrated ability to utilize resources available to ensure compliant and required documentation for contract testing laboratories and the internal R&D microbiology department, Experience managing multiple simultaneous projects and work activities, In-depth knowledge of cGDP/cGMP/cGLP practices and compliant documentation, Effectively operates in, and capable of facilitating, cross-functional teams, Knowledge of Terminal sterilization and/or pharmaceutical industry, Skills Excellent English verbal and written communication skills, skilled to coordinate with global stake holders and support across the different time zones, Proficient with Sterilization principles and related testing for Biological indicators etc Hands on experience cycle design and development and performing the sterilization studies for devices with use of PCD /biological indicators, Highly adept at grasping and solving complex problems using root-cause analysis techniques, Ability to objectively identify technical solutions and make sound decisions Project management experience for Quality & value improvement projects Self-driven, resourceful, and able to work on multiple projects and priorities, Strong organization, attention to detail, and documentation skills, Strong acquaintance with technology, QMS tools and collaboration tools over the web: e-g Trackwise, Document tools, WebEx, Teams, Microsoft Office products, etc Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information To learn how you can protect yourself, review our Recruitment Fraud Notice, Show more Show less

Greetings from Continental Hospital Hiring CSSD Technician Experience : 1 to 6 In hospitals, the Central Sterile Supply Department (CSSD) is responsible for ensuring the cleanliness, sterilization, and distribution of medical equipment and supplies . It plays a crucial role in preventing hospital-acquired infections and maintaining patient safety. Here's a breakdown of CSSD functions: 1. Cleaning and Decontamination: CSSD personnel receive soiled items from various departments and disassemble them. They utilize automatic washers and ultrasonic cleaners to ensure thorough cleaning and disinfection, following established protocols. Inspections are conducted to confirm that items are free of debris and contaminants. 2. Packing and Sterilization: Cleaned items are inspected, assembled, and packaged using appropriate materials and methods. Sterilization is performed using various methods, such as autoclaves or ethylene oxide, to eliminate all microorganisms. Sterilization is monitored using chemical and biological indicators to ensure its effectiveness. 3. Storage and Distribution: Sterilized items are stored in designated areas, maintaining their sterility until needed. CSSD provides a readily available supply of sterile equipment and supplies to various departments, including operating rooms, clinics, and emergency rooms. 4. Other Functions: CSSD may also handle the recycling of certain medical equipment and supplies. They play a vital role in controlling nosocomial infections by ensuring strict hygiene practices. CSSD staff work closely with other hospital departments to meet the demands of patient care.

Job Role : Analyst - Microbiology Job Description : 1. To Follow Good Laboratory Practices as Laid Down In quality Control Standard operating procedures. 2. carry out calibration of the instruments in Microbiological department. 3. Daily Monitoring of Pressure Differentials, Temperature- Humidity of Microbiological Laboratory Rooms and Equipment's. 4. Microbiological Analysis of purified water, potable water and finished product. 5. Environmental monitoring of MF2, MF3, MF4, store and Microbiological Department. 6. Sterilization and destruction of media. 7. analysis of purified water for TOC content. 8. Daily data downloading of incubators.

Roles and Responsibilities Assist in production activities such as BMR, sterilization, dispensing, mixing, formulation, and parenteral operations. Monitor and control process parameters to ensure compliance with quality standards. Maintain accurate records of production data and batch logs. Collaborate with team members to resolve issues and improve productivity. Ensure adherence to cGMP guidelines and company policies. Desired Candidate Profile Strong understanding of BMR, sterilization techniques, dispensing procedures, mixing processes, formulation development, and parenteral manufacturing principles. Ability to work effectively in a fast-paced environment with attention to detail and ability to multitask.

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.

Responsibilities: * Provide exceptional patient care during treatments. * Assist dentists with procedures such as RCT, capping, scaling, filling, registration & fillers. Annual bonus Referral bonus Leave encashment Job/soft skill training

Walk In Drive For Production Injectables In Formulation Division @ Corporate Office Department:- Production Injectables Qualification :- Diploma | ITI | B Tech | B Pharmacy | BSc | MSc | M Pharmacy Experience :- 2 to 8 Years Division :- Formulation Interview Date:-10-05-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-II, Kothur & MSNF-V, RK Puram Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 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.

Multiple positions open for various operators who are responsible to operator vial filling/ sealing machine, autoclave, ampoule filling machine, manufacturing of injectable.

May support in the development, review and approval of sterilization process and equipment validation/qualifications (IQ, OQ & PQ). Be the point of contact for suppliers/development engineers for new process development, quality issues and process improvements for assigned projects. Participate in the development and improvement of the manufacturing processes for existing and new products. Support product transfers to other plants/facilities. Review/approve nonconforming material and system documentation. Review/approve product and process change control documentation and specifications. Actively participate on teams to support new product development activities. Support design verification and validation test requirements that ensure appropriate objective evidence is available to support acceptance criteria. Specific Job Skills: Must understand the fundamentals of at least one of the following sterilization techniques: gamma irradiation, ethylene oxide (preferred), hydrogen peroxide gas plasma, moist heat, or dry heat and be an expert in one of the techniques. Demonstrated knowledge about a variety of microbiological concepts, practices, and procedures. Ability to use ISO, AAMI, USP, ANSI, EPA, EU and related guidelines toward the design, manufacturing, development, and launch of initiatives. Experience with ISO 17025, Lab Quality Management System. Desired Profile Education: M.Sc. in Microbiology Experience: Min 5 years of experience in applied device or pharmaceutical microbiological or biological testing, research and development, or sterility assurance experience.

- Sterile Injectable Manufacturing (Core) - Liquid ampoules, vials, lyophilized products - BMR/BPR Documentation - cGMP - Production Line Operation - Pharmaceutical Equipment Handling - Cleaning/Sterilization - Internal Audit/Validation - Maintenance

Key Responsibilities: Sales: * Promote and sell our range of medical devices to hospitals, clinics, and other healthcare facilities. * Identify potential customers and generate new business opportunities. * Build and maintain strong relationships with clients to understand their needs and provide appropriate solutions. * Meet and exceed sales targets and objectives. * Conduct Application Demonstration and primary level of service, if required in coordination with servicing department Qualifications: * A degree or diploma in Biomedical Engineering, Electronics, or any healthcare-related field. * Basic knowledge of critical medical instruments and equipment. * Strong technical aptitude and a willingness to learn about new technologies. * Excellent communication and interpersonal skills. * Ability to work independently and as part of a team. * Customer-focused with a strong service orientation. * Willingness to travel frequently. Preferred Skills: * Previous experience in a similar role or internship in the medical device industry is a plus. * Knowledge of sterilization equipment and operating theatre (OT) instruments. * Sales experience in a healthcare or medical device setting. Benefits: * Competitive salary and performance-based incentives. * Comprehensive training and development programs. * Opportunities for career growth and advancement. * Health insurance and other employee benefits. * A supportive and collaborative work environment

RETORT- TECHNICAL Position: Retort Technical Officer Department: Retort Operations Location: Sonipat, Haryana. Salary Range- 50-55K CTC Only Male Candidate is preferred Job Summary: As a Retort Technical & Competent in Retort Operations at Snackstime Pvt. Ltd. (A Subsidiary of Chandigarh Sweets Limited), you will oversee the day-to-day operations of the retort process, ensuring food safety, quality, and efficiency. This role involves managing personnel, maintaining equipment, adhering to safety protocols, and contributing to process improvement initiatives. Job Responsibilities: Supervising Retort Operations: Overseeing the entire retort process, including loading, processing, and unloading of products, ensuring adherence to established procedures and schedules. Staff Management: Training, supervising, and scheduling retort operators and other related personnel, ensuring proper execution of tasks and maintaining a safe working environment. Quality Control: Monitoring product quality throughout the retort process, conducting regular checks, and identifying and resolving any deviations from established standards. Equipment Maintenance: Ensuring all retort equipment is properly maintained, calibrated, and functioning correctly, coordinating maintenance and repairs as needed. Safety Compliance: Enforcing strict adherence to safety regulations and procedures related to retort operations, including proper handling of chemicals and equipment. Process Improvement: Identifying areas for improvement in the retort process, recommending and implementing changes to enhance efficiency, safety, and product quality. Record Keeping: Maintaining accurate records of retort operations, including processing parameters, quality control data, and equipment maintenance. Inventory Management: Managing the inventory of retort supplies, ensuring adequate stock levels to support continuous operations. Collaboration: Working closely with other departments, such as production, quality control, and maintenance, to ensure smooth and efficient operations. Reporting: Preparing and submitting regular reports on retort operations, including production data, quality metrics, and any issues encountered. Required Qualifications: Education: A Bachelor's/Masters degree in food science, Food Technology, Biotechnology, or a related field like Chemistry, Microbiology, or even Biology is required. Experience: Minimum 5-6 years of experience in food processing specifically with retort operations, preferably within the food industry (sweets, confectionery, or similar). Skills: Technical Skills: Deep understanding of retort processes, sterilization temperatures, and shelf-life studies, thorough knowledge of product wise cycle timing, heat penetration in gravy products, rice items, vegetables, etc. Strong knowledge of food safety standards like HACCP and GMP , as well as regulatory requirements. Ability to analyze data, identify issues, and implement effective solutions. Controlling retort chamber (steam pressure cooker) to cook canned/Pouched foods according to specifications Pushing trucks or lowers baskets of canned foods into chamber of retort, using hoist Observing dials and thermometers Time & Temperature Knowledge about temperature penetration validation Controlling valves to admit steam to retort Opening retort and moving basket of canned food for cooling trough, using hoist Managing valves to control temperature, pressure and cooking time Closing retort door or lid to seal chamber Turning valves to release steam Admitting cooling water into chamber to prevent overcooking at end of cooking cycle Knowledge about retort packaging material Microbiology Operational Skills: Project Management: Managing projects related to retort operations, including planning, execution, and reporting. Cost Management: Understanding and managing costs associated with retort operations, including energy consumption, material usage, and labor. Scheduling: Creating and managing production schedules for retort operations, ensuring optimal utilization of resources. Supervisory Skills: Overseeing and guiding the retort team, ensuring adherence to procedures and maintaining a safe work environment. Key Competencies: - Knowledge of relevant tools and equipment Knowledge of safety and hygiene regulations Knowledge of controlling/handling valves Ability to handle and control temperature regularly Skilled in controlling pressure inside a chamber Skilled in monitoring gauges, dials or other indicators to make sure machine is working properly Ability to handle equipment like hoists, etc.

Role & responsibilities Working as a Production Chemist. Experience into BMR, BPR. Experience in Sterile, sterilization. Batch Planning, Batch Manufacturing

Cleaning, disinfecting, sterilizing, and distributing surgical instruments and medical equipment. Ensures proper functioning of sterilization processes, maintains hygiene standards, and follows infection control protocols.