85 Sterilization Jobs - Page 2

Company Description Role Description This is a full-time, on-site role for a CSSD Technician located in Jorhat. The CSSD Technician will be responsible for tasks related to decontamination, sterilization, and infection control. The technician will ensure all medical instruments and equipment are properly sterilized and maintained for safe use in the operating room. The role involves understanding and utilizing medical terminology pertinent to sterilization and operating room procedures. Qualifications Skills in Decontamination and Sterilization Experience with Infection Control Proficient in Operating Room procedures Knowledge of Medical Terminology Attention to detail and ability to follow strict protocols Excellent organizational and communication skills Previous experience in a healthcare setting is a plus Relevant certification or training in sterilization techniques preferred,

Witnessing of manufacturing processes for sterile drug products including cleaning, sanitization, environmental monitoring and personnel monitoring to ensure compliance with CGMP regulations and regulatory standards Oversight of cleanroom behavior, contamination control and aseptic techniques To report any observations to site operations and quality and ensure compliance to the observations Review of media fill protocol and reports and witnessing aseptic process simulations Review of batch documentation to ensure product quality, regulatory compliance and meeting ALCOA++ requirements Review of environmental monitoring reports Review of unplanned deviations and CAPA

Roles and Responsibilities Operate autoclave equipment to sterilize medical instruments and equipment according to established protocols. Perform cleaning, washing, and drying procedures on surfaces and objects using various cleaning solutions. Ensure proper functioning of all CSSD (Central Sterile Supply Department) equipment by performing routine maintenance tasks. Maintain accurate records of inventory management, including tracking stock levels, ordering supplies, and receiving deliveries. Collaborate with other team members to ensure efficient workflow and maintain high-quality standards. Desired Candidate Profile 3-8 years of experience in a hospital setting with exposure to CSSD operations. Diploma or equivalent qualification in relevant field (e.g., NABH). Strong understanding of sterile techniques, sterilization methods (autoclave), quality control measures. Ability to work effectively under pressure while maintaining attention to detail.

Greetings from Adecco , A Leading Manpower Consulting Company!!! We have been retained by Leading Pharmaceuticals Company in Ahmedabad for their Manpower Requirements. We have an following Openings as of now. 1) Vial Washing Operator 2) Filling Machine Operator 3) Aseptic Operator 4) Autoclave Education: ITI/Diploma Experience: 3 to 10 Years. Interested candidates please connect on below contact details.

As a Product Assessor, you will play a crucial role in our organization by overseeing Sterilization product assessments and conducting technical file reviews in strict adherence to regulatory requirements, including the European Medical Device Directive and Medical Device Regulation for Class IIa/IIb and/or Class III. Your primary focus will be to ensure the technical soundness of reviews and compliance with all relevant standards. Responsibilities: Conduct comprehensive Sterilization product assessments in line with regulatory requirements for medical devices. Support CE marking activities conducted by SGS, contributing to the overall certification process. Effectively communicate with colleagues and clients regarding product assessments and related activities. Work proactively to minimize risks associated with medical device certifications. A degree or equivalent qualification with Microbiology modules or relevant studies (e.g., medicine, pharmacy, engineering, or other related sciences). Four years industrial experience with medical device manufacturing that includes a

Manager - Processing (Production) Role: We are seeking a dynamic and seasoned individual responsible for overseeing day-to-day processing operations in sterile manufacturing, ensuring alignment with production schedules and regulatory standards. The role focuses on identifying process inefficiencies, leading improvement and automation projects, and collaborating with cross-functional teams to drive productivity, reduce waste, and enhance product quality. This position demands strong technical knowledge of sterile processing equipment and a proactive approach to maintaining seamless production workflows and continuous operational improvements. Location: Umarsadi (Vapi, Gujarat) Main Tasks: Manage and oversee work orders for our product lines, ensuring efficient execution of production plans to maximize machine performance. Plan and implement batch production on a product-specific basis, optimizing throughput and minimizing downtime. Collaborate with cross-functional departments to ensure uninterrupted operations and timely execution of preventive maintenance schedules. Lead initiatives to reduce market complaints, aiming to maintain a production ratio of over 20 million units per justified complaint. Review BMR for new products to be processed on syringe lines. Review and approve BMRs for new products prior to processing and verify completed BMRs for submission to Quality Assurance. Develop, review, and implement SOPs for syringe processing operations, ensuring thorough training and compliance among line operators. Monitor and enhance line yield while working to minimize rejection rates through process improvements and quality control measures. Ensure timely preparation of customer samples as per specifications, with accurate documentation in BMRs and logbooks. Oversee SAP activities related to batch processing, including data entry, reconciliation, and return of unused materials to inventory.. Ensure optimal shift-wise performance of SPRC machines, maintaining complete and accurate documentation in SAP, BMRs, and logbooks. Prioritize and coordinate the ETO process of completed batches, ensuring all related entries are updated in both BMRs and SAP. Maintain audit readiness by ensuring no critical observations in the production area through strict compliance and monitoring. Ensure NVPC records are correctly attached to the respective BMRs and submitted to QA within the designated timeline. Lead training programs for staff and operators on cleanroom protocols and enforce adherence to cGMP standards. Ensure full compliance with the most recent EHS guidelines across all production activities. Drive continuous improvement of the EHS management system through effective implementation, monitoring, and periodic review. Requirement: M.Pharm /B.Pharm /B.Sc /M.sc / BE (Chemical, Electrical, Instrumentation, Mechanical) from an accredited institution. Experience: Proven record of 12+ years in Junior Management in any Pharmaceutical industry with relevant experience in the area of Process Engineering. Competencies: Strong organizational skills and attention to detail. In-depth knowledge of sterile processing equipment: Washing Systems, Depyrogenation Tunnels, Sterilizers, Siliconization Systems. Sound understanding of cGMP, GEP, FDA/ regulatory requirements, and cleanroom operations. Strong command over lean manufacturing, root cause analysis, CAPA, and risk assessment tools. Strong leadership with proven ability to motivate and guide cross-functional teams. Skills: Proficiency in local languages and English, both written and spoken, to facilitate effective communication with employees and stakeholders. Knowledge of SAP, MS Excel, PowerPoint, etc. Strong learning agility and continuous improvement mindset. Contact: careers.hr@schott-poonawalla.com

The CSSD Technician is responsible for the effective sterilization and disinfection of surgical instruments and medical equipment. This role involves preparing, sterilizing, and ensuring the safe handling of instruments to maintain the highest standards of hygiene and safety within the hospital environment. The technician will also be responsible for the quality control of sterilization processes and will work closely with various departments to support surgical procedures. Roles and Responsibilities - Clean, decontaminate, and sterilize instruments and medical equipment using appropriate methods and technologies. - Ensure the proper functioning of sterilization equipment and report any malfunctions. - Monitor and maintain sterilization logs and quality assurance records. - Prepare and package instruments for surgery, following established protocols. - Collaborate with surgical teams to meet instrument and equipment needs during procedures. - Follow infection control standards and safety protocols to prevent contamination. - Conduct routine checks and maintenance of CSSD supplies and inventory management. - Participate in ongoing training and professional development related to sterilization techniques and infection control practices. Skills Required: - Knowledge of sterilization techniques, principles of infection control, and safety standards. - Familiarity with surgical instruments and medical equipment. - Attention to detail and strong organizational skills. - Ability to work under pressure and manage time effectively. - Excellent communication and teamwork skills. - Analytical skills to monitor sterilization processes and troubleshoot issues. Tools and Equipment: - Autoclaves and sterilization equipment. - Decontamination tools and instruments. - Personal protective equipment (PPE). - Inventory management software. - Quality control systems and logging tools.

Role & responsibilities Prepare and maintain operation theatre Maintain equipment support in an acute care environment Identify and move to maintain a sterile field Follow infection control policies and procedures Manage and maintain theatre equipment Prepare patient for operative procedures Provide intra-operative equipment and technical support Assist anesthetist in handling emergencies outside of OT Room Preferred candidate profile Qualification - Diploma / B. Sc. (Operation Theater) Experience - 0-2 yrs Perks and benefits As per market standards

Preparing the operating room for surgery, including setting up equipment and ensuring a sterile environment. Sterilizing surgical instruments & equipment. Ensuring the availability of necessary medical and diagnostic supplies.

GITAM School of Technology is looking for Lab Technician to support the smooth functioning of our Chemical Engineering and Bioinformatics laboratories. Role & responsibilities Ensure all equipment and instruments in the Chemical Engineering laboratories - including PDC (Process Dynamics & Control), HT & MT (Heat and Mass Transfer), BCRE (Biochemical Reaction Engineering), and MO (Mechanical Operations) - are functional and regularly calibrated. Assist in the setup, operation, and maintenance of Bioinformatics software tools and systems. Maintain laboratory-related software and ensure smooth functioning of lab computer systems. Provide technical support to faculty and students during lab sessions and project work. Manage inventory, consumables, and enforce lab safety protocols. Skills required Proficiency in computer operations, including MS Office and scientific / lab software. Ability to troubleshoot IT/software-related issues in lab environments. Strong communication and team coordination skills. Education & Experience M.Sc. in Life Sciences, Biotechnology, Biochemistry, Microbiology, or any related discipline. or Diploma in Chemical Engineering

Role & responsibilities Prepare and maintain operation theatre Maintain equipment support in an acute care environment Identify and move to maintain a sterile field Follow infection control policies and procedures Manage and maintain theatre equipment Prepare patient for operative procedures Provide intra-operative equipment and technical support Assist anaesthetist in handling emergencies outside of OT Room Manage hazardous waste Ensure availability of medical and diagnostic supplies Work effectively with others Manage work to meet requirements Maintain a safe, healthy, and secure working Environment Follow radiation safety guidelines Follow biomedical waste disposal protocols Monitor and assure quality.

The Senior Nurse - OT at Manipal Hospitals will be responsible for providing high-quality patient care in the operating theatre. This role involves assisting surgeons during procedures, ensuring a sterile environment, and monitoring patients' vital signs preoperatively and postoperatively. The Senior Nurse will also oversee and mentor junior nursing staff, collaborate with healthcare professionals to implement patient care plans, and maintain accurate patient records. The ideal candidate should be proactive in educating patients and their families about surgical procedures and aftercare. Roles and Responsibilities About the Role: As a Senior Nurse-OT at Manipal Hospitals, you will play a crucial role in ensuring the smooth operation of the operating theatre. Your expertise will be vital in delivering high-quality care to patients undergoing surgical procedures. You will work closely with surgeons and other healthcare professionals to maintain a safe and efficient environment. About the team: You will be part of a dedicated team of healthcare professionals committed to providing exceptional perioperative care. The team consists of skilled surgeons, anesthetists, and fellow nursing staff who collaborate to deliver the best patient outcomes. A supportive culture encourages continuous learning and professional development. You are Responsible for: - Preparing the operating room and ensuring all necessary equipment and instruments are sterile and ready for use. - Assisting the surgical team during procedures, providing necessary support and anticipating needs. - Monitoring patients' vital signs and providing post-operative care to ensure their comfort and safety. - Maintaining accurate and detailed records of patient information and surgical procedures. To succeed in this role – you should have the following: - A valid nursing degree with specialization in operating theatre nursing. - Strong communication and interpersonal skills to effectively interact with patients and healthcare colleagues. - A thorough understanding of surgical instruments and sterilization processes. - The ability to work efficiently in a fast-paced environment and manage multiple tasks simultaneously.

*For Production (Parenteral/Injectable exposure only) : > Process Incharge/Sr. Process Incharge (Officer/Sr. Officer/Executive) : - 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 (Officer/Sr. Officer/Executive): - 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. *For Stores (Pharmaceutical exposure only) : >Process Incharge (Officer/Sr. Officer): -Manage inventory levels by receiving, storing, and issuing materials according to GRN (Goods Received Note) and challans. -Ensure accurate recording of stock movements using FIFO (First-In-First-Out) method. -Maintain store cleanliness and organization to prevent damage or loss of goods. -Monitor inventory turnover ratios to optimize storage capacity utilization. -Perform regular physical counts to verify accuracy of recorded stock levels. 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.

Executive/AM/DM for Production-DPT(Bacterial Vaccines) Experience: 4 to 14 Years Qualification: M.Sc.(Biotechnology/Biochemistry/Microbiology) Job Responsibilities: 1.Executives: Should possess experience in Bacterial Vaccines, with a preference for DPT Vaccines with a total industrial experience of 04-07 years. Should have practical experience in handling, Sterilization of the reactors, Vessels, Media Preparation, Seed cultures, Fermentation and Downstream Activities, including Centrifugation, TFF and filtration techniques. 2.AM/DM: Should possess experience in Bacterial Vaccines, with a preference for DPT Vaccines with a total industrial experience of 10-14 years. Should have practical experience in handling Seed cultures, preparing cell banks, conducting Fermentation and Downstream Activities, including Centrifugation, TFF, Chromatography, and filtration techniques. Must have experience in a team leadership role, managing a team of at least 10-15 members. Should also be well-versed in Quality Management Systems, including Risk Assessment, Deviations, Change Controls, and CAPA. Should have experience with regulatory audits, ideally with 3-5 years in this area.

Roles and Responsibilities Maintain Proper Inventory of surgical instruments & also update the usage of records, breakage records (if any) from the time to time. Ensure the check on instruments proper usage to avoid any damages. Ensure all technicians follow the SOP's strictly in the department. Check records of steam sterilizer, Plasma & ETO gas sterilizer from time to time. Verify Physical & chemical & Biological monitoring are done properly. Indent to be processed for requirements of any instruments from time to time. Arrange duty roster for the staff and updating the of stocks on a day-today consumption. Ensure that the sterile items reach the end user in proper condition. Keep proper records for the Machines-calibration certificates To ensure the quality of water used for the machines are as per required norms. Make sure that all staff are familiar with SOP's & follow the same. Re allocate duties to staff as per department requirement. Supervise the documentrary procedures and completion of documentation in time. Quality monitoring & record keeping maintenance. Replenish such instruments sent for repairs to see it that the work does not suffer at the user end. To comply with quality & standards. Knowledge of JCI/NABH regulations & Standards. Computer Skills. Infection control practices & Procedures.

Dear Aspirant , Greetings From Eugia Pharma Specialties Limited (Aurobindo Group)!!!! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit. Department : Quality Assurance (IPQA) No. of Vacancies : 30 Education Qualification : B. Pharmacy / M Pharmacy Experience : 2-5 Years Designation : Executive Required Skills : Aseptic Area Monitoring / Environmental Monitoring / Aseptic behavior / Media Fill / Gowning Practices / Sterility Assurance/ In Process checks in Injectable Work Location : Eugia Unit -3, Pashamylaram Walk In Details: Date : 29.06.2025 Time : 09 AM - 02 PM Venue : Aurobindo Pharma Limited - Unit - 3 Sy. No. 313, Bachupally, Hyderabad, Telangana 500090 Google Map : https://maps.app.goo.gl/qoL8vZ6EwDm5GcWb8 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 Work Location : Eugia Unit -3, Pashamylaram Walk In Details: Date : 29.06.2025 Time : 09 AM - 02 PM Venue : Aurobindo Pharma Limited - Unit - 3 Sy. No. 313, Bachupally, Hyderabad, Telangana 500090 Google Map : https://maps.app.goo.gl/qoL8vZ6EwDm5GcWb8 Contact : Mr Prabhakar / Ms Rama

POSITION: FILLING OPERATOR (entry level) runs machines that fill sterile medicines Production of sterile injectable products like vials, ampoules, cartridges, and pre-filled syringes (PFS). COMPANY: OneSource CDMO Known for sterile injectables, prefilled syringes, autoinjectors, and soft gel capsules. Department: production, manufacturing, formulation Aseptic Filling Operations: Operate machines inside cleanrooms or isolators to fill sterile drug products without contamination. Machine Setup & Maintenance: Set up, calibrate, clean, and dismantle equipment like vial filling machines, lyophilizers, and sterilizers, cartridge filling/washing, Ampoule filling Visual Inspection & Leak Testing: Check for particulate matter, proper sealing, and container integrity.

Roles and Responsibilities Responsible for Water sampling and analysis. Responsible for Media Preparation and consumption, sterilization. Responsible for Environmental Monitoring. Responsible for Growth Promotion test. Responsible for FG/RM/Swab/Stability/ Hold time analysis. Desired Candidate Profile Must have Experience in OSD plant (tablet & capsule)

Role & responsibilities Job summary We are looking for an individual to perform filling/washing and sterilization operations within GMP (Good Manufacturing Practices), regulatory, and organizational guidelines. The objective is to produce products within defined volumes and timelines, ensuring compliance with quality standards, GMP, and regulatory requirements as per schedule. " Roles & Responsibilities Perform filling, washing, sterilization operations as per the day plan, executing batch production records. Participate in filling area line clearance activities and perform machine cleaning operations. Handle material dispensing and issuance from the warehouse. Issue discrepancies, work with cross-functional departments to close discrepancies, and implement appropriate corrective actions. Compliance with GMP, safety standards, and SOPs (Standard Operating Procedure) for designated manufacturing equipment. Maintain records in machine operation log books. Maintain manufacturing equipment to ensure correct functionality and calibration compliance. Actively engage in validation and qualification activities for all manufacturing area machines. Promote safety awareness and improvements, engage in continuous improvement activities, and adhere to the company's safety rules. Report all unsafe matters, near misses, and accidents. Preferred candidate profile Educational qualification and work experience Educational qualification: A Diploma or B.Pharm. Minimum work experience: 4 to 6 years of experience in batch formulation operations Skills & attributes Technical Skills Proficiency in comprehending and overseeing sterile and fill finish operations in pharmaceutical manufacturing, demonstrating familiarity with the processes involved. Practical experience and hands-on knowledge in executing sterile and fill finish operations, showcasing the ability to actively participate in and manage these critical manufacturing processes. Practical expertise in equipment validation, process validation, and cleaning validation, demonstrating the ability to validate and ensure the reliability of manufacturing equipment and processes. Behavioral skills Effective listening skills, ensuring a comprehensive understanding of information. A keen eye for detail, ensuring accuracy and precision in tasks. Awareness and sensitivity to deadlines, ensuring timely completion of tasks. Analytical skills and the ability to troubleshoot, enabling effective problem-solving. Strong interpersonal skills and the ability to work well in a team, fostering collaboration and positive team dynamics. Location: Pydibhimavaram Dr Reddy's Formulations Limited(DFL-02) Injectable Facility, Aseptic Manufacturing Hiring For : Filling,Compounding,Autoclave,Lyo Operators, PM(Preventive Maintenance),Documentation, MS Office

JOB DESCRIPTION OF C.S.S.D. TRAINEE/TECHNICIAN AT WOCKHARDT HOSPITALS MIRAROAD Only Male required Qualification: Science graduate in microbiology, botany, zoology or chemistry. Basic course in computers is desirable. Reporting to: Head of the Department. Job Summary: Responsible for decontamination, assembly, sterilization, storage and distribution of medical and surgical supplies and equipment used in the care and treatment of patients following infection control practices. Job duties: To collect, receive, sort, test, sterilize and pack contaminated instruments, containers, treatment trays and other supplies and equipment that have been used in the operation theatre, ICU, wards, emergency (casualty) room and CATH lab and prioritize sterilization depending on emergency requisitions. To operate automatic and semi-automatic sterilizing equipments like steam sterilizers, Ethylene oxide sterilizers, Ultrasonic cleaners. Report problems and information of operational nature to the department head or supervisor. To inspect or replace missing or damaged equipment, make minor repairs on them, maintain inventory of supplies and materials to include documenting usage, issuing, receiving and reordering as assigned. To maintain an accurate record regarding the effectiveness of the various processes of cleaning, disinfections and sterilization. To accurately compute the sterilization process for all items using the method determined by the manufacturer and Infection control. To carry out biological checks to ensure proper functioning of sterilizers. To carry out manual cleaning and cleaning by machines. To maintain high standard of environmental cleanliness. To ensure care and maintenance of autoclaves. To carry out preliminary check of supplies, i.e. check reusable items that need to be sterilized. To maintain Quality Control parameters for all methods of sterilization and to document the effectiveness of each method. To perform other related duties incidental to work described as assigned. Skill Set: Verbal ability Ability to comprehend verbal instructions given by the supervisor or head of the department. To understand and apply knowledge of medical terminology. Problem solving/ Decision-making To think independently and exercise ones own judgment in determining actions during emergencies. Other skills Have an affinity for teamwork. Technical skills required for using and maintaining the various sterilization equipments and the computer . Ability to comprehend written instructions given by the supervisors and the other related departmental personnel. Ability to plan & organize ones work schedule effectively. Being a service provider listening speaking and are essential requirements to understand and carry out the instructions given by users

Company Overview LINQ Corporate Solutions Private Limited is a market research and strategic advisory firm based in Vadodara, working with clients in 41 countries across 8 dynamic industriesincluding Oil & Gas, Biotech, Pharmaceuticals, Healthcare, and more. We operate in two shifts, with over 150 professionals at our Vadodara HQ and 200 international team members. While our night shift team works directly with our international clients (primarily in the US), the day team focuses on in-depth research, data mining, analytics, and execution. Our support extends into web development, graphics, SEO, and digital operations as wellgiving us full-stack capabilities for global research delivery. Role Overview We are seeking a dynamic and driven Senior Associate Medical Science & Technology to join our growing team. The ideal candidate will support global projects through in-depth research, data analysis, and technical insights in the fields of healthcare and related technological advancements. You will work closely with company leadership and international clients, contributing to innovative solutions shaping the future of healthcare and medical science. Key Responsibilities Conduct comprehensive primary and secondary research in medical science and healthcare technology. Develop insightful reports, databases, and white papers to support client acquisition and strategic initiatives. Analyse academic publications and provide concise feedback to internal stakeholders. Support the development and refinement of technical documents and proposals. Participate in brainstorming sessions and collaborative solution development. Organize tasks and manage project timelines efficiently. Communicate findings and insights clearly across internal and external teams. Utilize tools such as Google, MS Office (Word, Excel, PowerPoint), LinkedIn, and online research platforms. Receive ongoing training and mentorship aligned with our organizational processes. Required Qualifications Bachelor of Medicine and Bachelor of Surgery (MBBS), Biomedical Engineering, or a related degree in Medical Science & Technology. Strong foundational knowledge in: Anatomy, Physiology, Cardiology, Orthopaedics, Radiology, Neurology, Speech & Hearing Biomedical Instrumentation and Medical Imaging Drug Delivery Systems, Artificial Organs, Rehabilitation, and Tissue Engineering Additional understanding in: Medical Robotics, Automation, Lasers & Optics Telehealth, Health AI, Point-of-Care Testing Prosthetics & Robotics, Sterilization, Emergency Medicine, and Operating Room Management Desired Skills & Attributes Excellent internet-based research skills, knowledge and experience in use of ChatGPT and strong academic reading comprehension. Outstanding verbal and written communication skills. Ability to manage multiple priorities and adapt to shifting deadlines. Proactive and self-motivated with a strong learning mindset. Collaborative team player capable of independent initiative. Compensation & Benefits Remuneration: Negotiable, based on experience and qualifications. Incentives: Competitive performance-linked structure. LINQ Corporate is an Equal Opportunity Employer. Shaping tomorrow together

Freshers can also welcomed for interview. QC Executive To monitor all process steps (physical, chemical & microbiological testing) and control points as per defined parameters and standards. To monitor effectiveness of overall cleaning and sanitation of the plant including all warehouses. To monitor GLP practices in lab, resources needed as per laboratory requirement. To monitor the product quality through compliance of specification for raw material, packaging material & finished products. To monitor testing plan, calendar & standard for inside & outside testing & to ensure outside testing as per schedule. To check and verify the daily deviation report, taking appropriate actions against the same. Determining and agreeing on in-house quality procedures, standards and specifications. Specifying quality requirements of raw materials with suppliers. To ensure that all the products confirm the quality specification. To identify, plan, documents and manage the practices, activities and resourced needed to meet quality goals and objectives. Responsibility for review and analyze quality index and carry out root cause analysis for failure and corrective action plan. Oversee the pre dispatch inspection related activities and ensure that the products dispatched meet the required standards. Analyze and resolve all matters related to quality issues and closure of customer complaints. Responsible for reviewing all customer complaint and provide RCA & CAPA. Continuous endeavor for zero customer complaint. Provide support to other departments in managing quality within their processes. Preparation labels for domestic and Export as per requirement. And Make data records as per buyer requirement in case of export /domestic example COA, Serial Number of Items to be dispatched etc. Provide trainings to workforce related with quality & food safety. Microbiologist Preparation of media and sterilization of media &glasswares. Microbiological analysis of raw material & finished products. Microbiological analysis of complaint samples. (whenever required) Perform hygiene tests like environment monitoring, hand swab, surface hygiene & swabs of packing material Microbiological analysis of RO & CIP water & testing Responsible for daily quality documentation & record keeping. Micro analysis of R&D & market samples with record keeping. Micro analysis of trial batches upto required time with record keeping. Assisting in calibration of laboratory equipment with documentation. To monitor & maintain incubation samples with record keeping. Validation of CIP, hygiene & environmental hygiene Preparation, Handling and destruction of media Good lab practices and arrangement of micro items. Provide trainings to workforce related with quality, microbiology & food safety. Product shelf life checking and its records. Lab Chemist / Process Controller Implementation of quality system schedule, preparation and recording Online quality control reports. In case of any deviation from standard and safety of product inform immediately to Lab In charge. Monitoring of CCPs & OPRPs and its Records and Control. Incoming Raw material ad Finished Product Testing and Records. Instrument Calibration of lab and Weighing scales. Recopies Verification and Online Parameters Check and Control if any deviation observed. Online Training to Plant Workers on Food safety/GMP/Personal Hygiene/product Parameters and Packing Parameters. Finished Product Coding Printing Verification and its records. Verification Plant GMP/ GHP . Incoming and Outgoing Vehicle checks and its records. Maintaining Keeping samples and its records. Monitoring all line labeling and Packaging of Finished product. Supervision of Plant cleaning through Housekeeping team. Ensure the PPEs monitoring wearing by Food handlers during Food Product packing. Freshers can also welcomed for interview.

HIRING FOR FORMULATION UNIT - INJECTABLE JOB DESCRIPTION AND EXPERIENCE: WORK LOCATION: Hetero Labs Limited, UNIT VI, Polleypally, Jadcherla, Mahabubnagar PRODUCTION Experience: (02-06Years) Autoclave, Compounding, filling, QMS, Vial Washing, Lyophilizer, Visual Inspection PACKING Experience: (01-05Years) Blister Primary Packing, Bottle Primary Packing. QUALIFICATION : I.T.I, Diploma, B.Com, B.Sc, B.Tech, B. Pharm, M.Sc with relevant experience DESIGNATIONS: Operator, Sr.Operator, Jr.Officer, Officer & Jr.Executive INTERVIEW VENUE: PHARMA JOBS: Talent Acquisition center, Bhagyaradhi Degree College, 1st Floor, IDPL X Road, Jeedimetla Road, Hyderabad DATE &TIME: 22nd June'2025 (Sunday); From 09.00 A.M. to 03.00 P.M NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID Proofs CONTACT INFO: E-mail: Harishwar.m@hetero.com & Cont: 8121005416, 8121036004 for further info

Job Description: Cleaning the all equipment in CSSD. Collecting the unsterile instruments from various department in the hospital. Arrange the instruments for washing process. Prepare the dressing materials. Distributing the sterile things to the end user. Collect the raw materials from stores (consumables) Requirement of any instruments or consumables from time to time & keep documentation. Make sure the proper packing technique as per SOPfor for packing. Follow the instructions and do the proper loading & Unloading. Sterilization process has to be done as per the SOP's. Documentation should be done for alll receipts & issues on the same time. Follow the FIFO (first in first out)