35 Injection Jobs

About Us tms unites technology, marketing, and sourcing to drive transformational change for the worlds leading brands With 1,200+ employees across 26 countries, we offer an impressive range of solutions from inspiration and innovation to category management and delivery Operating as a creative agency, a strategic consultancy, a sourcing business, and a technology provider, we engage with over 110 million customers every single day for our clients, including McDonalds, T-Mobile, O2, Starbucks, and adidas Most importantly, we're a place where you can achieve great things, and be recognized as the best What Matters The Most Breakthrough, business-driving ideas come from extraordinary people with the freedom to be their most authentic selves at work Authenticity and diversity are critical elements of our business They can only be realized when we create access and equity for all We foster a culture of inclusion and belonging and aspire to be ever-evolving tms is a place where brilliant people are better together If you want your ideas to be heard and to contribute to a culture of inclusion and authenticity, bring us your voice! Visit us at tmsw com Job Summary This position is responsible to provide full support and oversight the tooling development and manufacturing locally on-site in the area During development stage, works with Tool Makers / Manufacturing Vendors to ensure the product meets all the safety and quality requirement, injection molds are properly fabricated, the optimized manufacturing processes are adequate for mass production and the tooling development milestones are met During mass production stage, works with factories to ensure production processes are under controlled and meets all TMS/client product safety and quality requirements To follow up on quality issues found To assist and support the Quality and Safety team to handle/manage quality and safety issues (e g- Intervention test failure, customer complaint, etc-) at factory level Job Relationships Internal Global Quality & Safety Team, Product Development Engineers (based in Hong Kong and China), Supply Chain Operations, TMS Agency External Manufacturing Vendors, Tool Makers, Factories, Subcontractors, Raw Material Suppliers Job Responsibilities Actively participate in the new product turn over activities organized by Development Engineer (based in Hong Kong and China) such as Design Review and VTO meeting to provide technical opinions on the product design Manages the new product development schedule to ensure the product could be released for production on time Organizes and leads the EP meetings during tooling development stage to resolve the issues found at EP stage Working closely with tool makers and factories to ensure the molds are properly built and delivered on time Ensure the factories prepare the approval and testing samples at development stage are properly made and meet TMS/client requirements Oversight the tool manufacturing process and schedule Monitor factories that optimized manufacturing processes are being setup and proper process control are implemented for mass production Oversight the Production Pilot in factories to ensure all the issues are resolved before mass production Follow up on quality and safety issues found during inspection and Feasibility/Intervention testing at factory level Conduct, facilitate, advise on corrective action and preventive action preparation in product failure and defect analysis and monitor their effectiveness in implementation Provide support and follow up on TMS quality and safety initiatives Qualifications/Experience Solid experience and technical expertise in plastic toys, premium & childrens products Proven experience working with factories in high volume production Good knowledge in a variety of other product areas Education At least 5 years working experience in toys or hard plastic industry Degree in Mechanical or Manufacturing Engineering or relevant scientific/technical discipline Job Knowledge/Skills Strong analytic thinking with good problem-solving ability Good knowledge on plastic product design and mold making processes Solid experience on injection molding workshop procedures and best practice Good communication and influence skills Good spoken and written English Other Requirements Reliable and strong character High integrity and business ethics Team Player Proactive, self-motivated and able to work independently Able and willing to travel outside India Career Ladder Senior Production Engineer / Assistant Production Engineering Manager / Production Engineering Manager Show more Show less

Job Title: VMC Operator (Die Making) Location: Ambernath Job Requirement: Skilled VMC Operator with 3-5 years of experience in die making. Responsibilities: - Machine Operation: Set up and operate VMCs for die making. - Inspection / QC : Inspect parts using measuring instruments for accuracy. - Die Maintenance : Conduct routine maintenance and repairs. Candidate Profile: - 3-5 years experience with VMC Operations for die making. - Good in reading blueprints and using measurement tools - 12th Pass or Training in VMC Operation preferred - Immediate Joiner preferred

Proficient in Liquid, HTML, CSS, JavaScript, and Shopify APIs with expertise in theme and app Customization Design and develop high-performance Shopify stores tailored to client needs. Strong leadership skills with the ability to manage teams, take ownership, and deliver projects on time. Optimize speed, responsiveness, and overall user experience. Perform QA testing, fix bugs, and integrate third-party tools and secure payment gateways. Collaborate with teams to ensure store security, performance, and seamless functionality.

Amneal is coming in your city Hyderabad this 07th & 08th Jun 2025 for Walk In Drive Hiring for Projects & Engineering and Peptide expereince : Walk-In Interview Drive #Hyderabad We are coming to your city for a walk-in interview drive! If you're looking to build a rewarding career with a growing Global Pharmaceutical Company, dont miss this opportunity. Day 1: Saturday, 07th June 2025 Time: 9:00 AM to 5:00 PM Venue: Lemon Tree Premier Plot No. 2, Survey No. 64, HITEC City, Madhapur, Hyderabad 500081, Telangana Day 2: Sunday, 08th June 2025 Time: 9:00 AM to 5:00 PM Venue: Vivanta Hyderabad, Begumpet 1-10-147 & 148, Mayuri Marg, Begumpet, Hyderabad 500016, Telangana Opening in Engineering Department for the following opening : Designation : Sr Executive / Manager Yrs of Exp : 5-12 Yrs Qualification : M.Tech / B.E Expereince into Electrical : Experienced in electrical project execution, compliance, and commissioning, with strong knowledge of HT and LT electrical systems and a solid understanding of pharmaceutical equipment requirements. Expereince into Instrumentation Skilled in automation and instrumentation of equipment and utility systems, with hands-on experience in regulatory compliance, calibration, temperature mapping, and thermal validation. Expereince into Civil Civil engineer overseeing site execution, quality assurance, regulatory compliance, cross-functional coordination, and project documentation in pharmaceutical projects. Expereince into Mechanical Mechanical project scope includes HVAC systems, utility services, regulatory compliance, project timelines, and cross-functional coordination. In-depth knowledge of process equipment used in injectable pharmaceutical plants experience in the installation, commissioning, and qualification of water systems. Expereince into Process Strong expertise in equipment used for injectable manufacturing, with preferable knowledge of isolator systems. Experienced in the installation, commissioning, qualification, and documentation of process equipment Interested candidates who are unable to attend interview, can share their CV on below mentioned Email Id with subject line Application for Falcon indiacareers@amneal.com

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview TE Connectivity's Manufacturing and Process Development Engineering Teams significantly impact LEANPD driven new product development projects, driving for excellence in existing manufacturing technologies and methods and striving to implement new manufacturing technologies to provide improved process and tolerance control. They act as the binding element between product development and manufacturing engineering, ensuring the effectiveness and efficiency of this critical interface. They support Product Development in the optimization of designs and piece parts for manufacturability by realizing sample tooling/products/prototypes. They also design, develop, and qualify tooling and processes to meet TE quality and production standards, document all processes and tooling in applicable TE systems, support supply chain to verify supplier compliance and capability, initiate and implement programs to continuously improve quality, cost and cycle time and adhere to all appropriate specifications, regulatory requirements and customer requirements. Responsibilities Prepare RFQ for mold costing. Prepare mold component drawing and assembly drawings. Create concepts with at least moderate knowledge of manufacturing and assembly. Determining the type of material needed to create the mold and calculating its size and shape Should be able to prepare 2d detailed drawings inline to manufacturing tolerances and BOM for procurement of elements. Manage design related issues throughout the build process Work with Product Engineering to fully understand molded part design requirements and integrate these requirements in to mold design. Leverage Simulation studies, run by other experts, to improve and optimize mold designs for productivity and longevity Should understand the GD&T tolerances. Attention to detail, self-driven, result oriented. Good experience in 3D cad software s. Education and Knowledge BE / B-tech in Mechanical Engineering (with tooling background) Post Diploma in Tool design (NTTF /GTTC/CIPET). Knowledge on o Tool material, material specifications, heat treatment and its processes. o Tool building, Tool assembly, measurement, testing and tool room processes. o ISO/TS requirement. Critical Experience 2-3 years of relevant design experience in precise injection molds for automotive plastics parts. Connector mold design experience would be an advantage (1-2 years). Moldex3d/Moldflow will be added advantage. Assembly/Stamping design will be an added advantage. Working knowledge on MS Office tool. (MS Excel, Word & Power point). Hands on experience in SAP usage will be added advantage. Competencies Compensation Competitive base salary commensurate with experience$xxx - xxx (subject to change dependent on physical location) Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity. What TE Connectivity Internship Program offers TE has a robust internship program that provides our interns with an abundance of resources to feel included as part of our Team. Every summer we coordinate various educational and networking events for our interns. The TE University Relations team will be hosting virtual meetups, information sessions, tours, skill building presentations, and topping it off with National Intern Day celebration activities. A unique employee resource group we have is the Young Professionals (ERG). This group is committed to creating a highly engaged and empowered cross-functional network of young professionals by placing high value in Professional Development, Networking Opportunities and Community Involvement to drive the success of our interns. In addition to the ERG, we also provide our interns with complete access to our internal library of self-lead courses. These courses include academies like leadership to help the interns develop their development in becoming future leaders at our organization. To help with their professional growth, we provide access to Mentors via our NAVIGATE platform. Mentors serve as a guide to navigate the organization and provide additional support in their career endeavors at the company. Our program provides a holistic experience for interns that targets professional development and personal growth. Our internship program typically runs May thru August and gives students the opportunity to work on projects that contribute to the success of their team and build on their classroom experience. Throughout the 10-12-week program, interns will be provided with Onboarding & Orientation Professional Development Workshops Networking Opportunities Operations Experience Executive Exposure Timeline TE Connectivity recruits on campus between September and March for New Grad (FT), Rotational, Internship and Co-op positions beginning in May. Once you have applied to a position, your resume and application will be reviewed. If you are selected to move to the next step in the application process, you will be contacted by a recruiter. Once you accept an offer, the onboarding process will begin in January for interns who have committed to offers in the fall semester and upon acceptance for interns who have committed to offers in the spring semester. EOE, Including Disability/Vets Location

Sterile Operations Trainer Grade: G8 Designation: Deputy General Manager Location: Halol 1 Job Description: Education: B. Pharm / M. Pharm Overall responsibility of Aseptic Training Academy (ATA), Baska To plan, develop, and execute training at Aseptic Training Academy (ATA) - Sterile Operations for Sun Global Operations (SGO) Training. Creation of simplified training modules for technicians, scheduling and execution of training Creation of training evaluation and/or feedback systems Course creation according to levels (Level 1 - Technicians, Level 2 - Supervisors and above, Level 3 - Managers and above) pertaining to sterile operations Planning, scheduling & execution of technical training program relevant to sterile operations for new recruits/for existing employee by self/internal or external facility Identification of Certified trainer at various locations (sterile operations) based on additional training need of respective location Coordination with location head and Subject Matter Expert (SME) for conducting the additional training program according to training calendar on monthly basis pertaining to sterile operations To prepare and submit SGO training score card for sterile operations on monthly basis after plant review to Corporate Quality Policy and Training department (CQPT) To maintain the training records of training Periodical review of technical courses along with business units for site specific course and the head of course for suitable course content / design and pedagogy up gradation To coordinate in technical course scheduling and publishing of calendars and facilitate visiting faculty/guest faculty in course delivery Any other work assigned by superiors from time to time

Job Description We are looking for an experienced and dynamic Team Leader to head our Analytical Research team within the Pharmaceutical R&D division, focused on complex injectable products and 505(b)(2) submissions . This role is ideal for a candidate with a strong background in pharmaceutical R&D , robust team management skills , and deep understanding of injectable formulation analytics . Key Responsibilities Lead and manage the analytical research team supporting complex injectable development. Supervise daily lab operations, resource allocation, and project timelines. Drive method development, validation, and troubleshooting for injectable formulations. Provide scientific leadership and ensure data quality and regulatory compliance. Maintain high team morale and cultivate a positive, collaborative work environment. Guide preparation of analytical documents for regulatory filings (505(b)(2), ANDA, etc.). Impart training, develop team capabilities, and mentor junior scientists. Collaborate closely with formulation, quality, and regulatory teams. Ensure compliance with cGMP, GLP, and internal SOPs. Desired Candidate Profile Qualification: M.Pharm / Ph.D. in Pharmaceutical Sciences, Analytical Chemistry, or related field. Experience: 8+ years in Pharmaceutical R&D , minimum 3 years in a leadership/supervisory role . Hands-on experience in analytical method development for complex injectables (liposomes, suspensions, emulsions, etc.). Sound knowledge of 505(b)(2) regulatory pathway . Strong command of analytical techniques: HPLC, GC, spectroscopy, particle size analysis, etc. Proven track record in team leadership, project coordination , and technical problem-solving . Excellent communication and interpersonal skills. Key Skills Analytical R&D, Complex Injectables, Injectable Formulations, Team Management, 505(b)(2), Method Development, HPLC, GC, Troubleshooting, Pharmaceutical R&D, Training & Mentoring

Process Mechanical, Process Electrical, HVAC, Water System with WFI Knowledge, Utility Electrical (Chiller, DG, Air compressor, Heat pump, Boiler)

Focus on PART FEASIBILITY, PRODUCT DESIGN, TOOL FEASIBILITY, TOOL DESIGN CONCEPT, TOOL SPECIFICATION, MOLD FLOW STUDY, GATE DESIGN, ATTEND TOOL TRIALS, TOOL COMMISSIONING, MOLDING PROCESS PROVE OUT, FIXTURE DESIGN CHECKING, VQF CYCLE TIME etc Required Candidate profile DIP/BE/CIPET/NTTF 3-6yrs exp with AUTO / ENGG / PLASTIC Unit into INJECTION MOLDING TOOL ROOM function Strong skills in TOOL DESIGN, TOOL MAINT, TOOL TRIALS, MOLDING PROCESS etc Relocate to HOSUR Perks and benefits Excellent Perks. Send CV recruiter@adonisstaff.in

Walk-In Drive Hyderabad | June 1, 2025 Join our growing team at OneSource The new way to CDMO We're hiring for multiple roles across our R&D and Manufacturing facilities in Bengaluru. Walk-In Interview Details: Date: Sunday, June 1, 2025 Time: 9:00 AM 4:00 PM Venue: Oakwood Residence, 115/1, Road No. 2, Financial District, Gachibowli, Hyderabad, Telangana 500032 Open Positions: Process Development Lab (Unit 1, Bommasandra) Research Associate | Sr. Research Associate | Scientist Qualification: B.Tech / M.Tech (Biotechnology) Experience: 2 – 12 years Drug Substance Manufacturing (Unit 2, Doddaballapura) Executive | Sr. Executive Qualification: MSc / B.Tech / M.Tech (Biotech, Microbiology) Experience: 2 – 8 years Drug Product Manufacturing (Unit 2, Doddaballapura) Executive | Sr. Executive | Team Leader Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Experience: 2 – 12 years in sterile injectables

To provide effective disinfection and sterilization services. Assist in performing sterilization activities, such as reprocessing, segregation, decontamination and packing under supervision of medical and surgical equipment/instruments. Assist in performing sterilization activities, ensures all surgical items and instruments are sterilized as per the rules and with the required procedure. Essential duties and responsibilities Responsible for receipt of different un-sterile instrument packs with a checklist and record in appropriate register. Disassembling, decontaminating, inspecting and reassembling surgical/medical instruments in accordance with established procedures. Responsible for cleaning setting up the sets as per the protocol. Autoclave according to laid down protocol and dispatch to respective departments/sections. Ensure that each autoclave cycle is recorded. Packing and wrapping, sealing and labelling instruments and sets. Contributes to effective communication, facilitating teamwork and co-operation within the Department and with other Departments. Responsible for the care and handling of all surgical instruments, sterile stock, linen, supplies and equipment in line with competencies. Performs all duties in accordance with position description & CSSD Technician Competencies Initiates and maintains effective communication lines and teamwork/collaboration within the Operating Theatre & CSSD Maintains a safe clean environment using only authorized cleaning products and adheres to the principles of infection control Promotes & adheres to Occupational Health & Safety Policies & Procedures Any other tasks assigned by supervisor that you are capable to perform. Participates as a team member promoting and contributing to a supportive team environment Attends all compulsory core education and teamwork within the facility Set up instrument wash room with distinct areas for clean and dirty. Set up of all Sterilizers Apply the principles of microbiology & infection control to all activities in restricted and semi-restricted areas. To maintain Quality Control parameters for all methods of sterilization and to document the effectiveness of each method. Working conditions Will work in Shifts (Morning, Evening & Night) of 8.5 hours a day. Will remain on call for emergencies. Stretched working hours Skills & Abilities Should have very good assisting skill. Should have basic knowledge of computers. Should be polite & good in communication while handling patient. Role & responsibilities Preferred candidate profile Perks and benefits

Job Description Roles & Responsibilities You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval. You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections. You will be responsible to support in scale-up to pilot/plant scales for Injectable Products. You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will be responsible for technology transfer and execution of the batches. You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization, processes designing and scale up). You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documents for drug product at every stage of development. You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materials and ensure development studies are performed related to regulatory and internal system requirements. You will be responsible for designing and implementing stability studies for injectable formulations to ensure product quality and shelf life. You will be accountable for troubleshooting formulation and process-related issues during development and manufacturing stages. You will collaborate with cross-functional teams to ensure alignment of formulation development with regulatory requirements and commercial objectives. You will be responsible for staying current with emerging technologies and regulatory guidelines in injectable drug development and incorporating them into your work. You will mentor junior scientists and contribute to the continuous improvement of the formulation development process. Qualifications Educational qualification: Masters in Pharmaceutical/M.Tech in Chemical Engineering Minimum work experience: 5 to 8 years of experience in pharmaceutical company in Injectable products. Skills & attributes: Technical Skills Have work experience on Formulation Development and expertise in inhalation/injectable dosage form. Experience in areas of product development for Generic Injectable Experience in Quality by Design (QbD). Experience in Process Optimization and scale up. Experience in Operational Excellence. Knowledge on Good Manufacturing Practice and Good Laboratory Practice. Experience in Technology Transfer. Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams.

SUMMARY Job Summary: We are in search of a committed and empathetic Registered Nurse to become a part of our healthcare team. The perfect candidate will deliver exceptional patient care, assist physicians, and work collaboratively with the medical team to ensure optimal patient outcomes. Key Responsibilities: Deliver direct patient care following established protocols and nursing standards. Monitor, document, and communicate symptoms and changes in patient conditions. Administer prescribed medications, injections, and treatments. Aid in patient assessments and create personalized care plans. Maintain precise and comprehensive patient records. Educate patients and their families on healthcare plans, post-treatment care, and medication usage. Assist in emergency care situations when necessary. Qualifications: GNM or BSC in Nursing Valid nursing license/registration At least 1 year of bedside nursing experience Age: Up to 40 years Language Proficiency: A2/B1/B2 language proficiency Requirements Requirements: Strong communication and interpersonal skills Ability to work in a fast-paced environment Compassionate and empathetic demeanor Ability to work collaboratively in a team Attention to detail and accuracy in record-keeping

Deva Institute of Healthcare and Research Pvt Ltd is looking for Patient Attendant to join our dynamic team and embark on a rewarding career journey. Assist patients with daily living activities such as bathing, dressing, feeding, and mobility Monitor patient health by taking vital signs, reporting changes to nursing staff, and ensuring medication reminders are followed Maintain a clean and safe environment, support emotional well-being, and help patients move safely between rooms or for tests Collaborate with healthcare staff to ensure proper care and respond promptly to patient needs and requests Maintain patient dignity, confidentiality, and comfort at all times .

Key Responsibilities: Assess motor function, balance, tone, gait, and physical limitations of clients. Design personalized neurorehab plans to improve strength, coordination, and mobility. Deliver therapy using evidence-based neuro techniques (e.g., Bobath, PNF, task-specific training). Assist with transfers, posture correction, and use of mobility aids. Monitor progress and update treatment goals regularly. Educate caregivers and families on home-based exercises and safe handling. Requirements Skills Needed: Good knowledge of neurophysiology and neuroplasticity principles. Hands-on skills in neuromuscular facilitation, gait training, and posture management. Patience, empathy, and motivational approach toward clients. Ability to work with adults and children with long-term disabilities. Communication skills for patient education and team coordination. ","

Sodexo Food Solutions India Pvt. Ltd. is looking for Patient Care Assistant to join our dynamic team and embark on a rewarding career journey A Patient Care Assistant provides essential support to patients under the supervision of healthcare professionals Primary duties include assisting with daily activities such as bathing, dressing, and feeding patients, monitoring vital signs, and ensuring patient comfort and safety The role demands excellent interpersonal skills, compassion, and the ability to handle physically demanding tasks Prior experience in a healthcare setting is advantageous, and certification as a nursing assistant is often required Additionally, the ability to follow detailed instructions, maintain patient confidentiality, and contribute to a positive healthcare environment is crucial for this position

Job Summary : The Cloud Network Security Administrator shall have strong technical knowledge of perimeter, networking and security practices of key public cloud offerings such as Microsoft Azure and Amazon Web Services to build and administer cloud infrastructure platform. The Cloud Network Security Admin is expected to individually solve problems of higher complexity. The Cloud Network Security Admin shall also participate in the development and enhancement of the information security solutions and to ensure it maintains relevancy with prevalent threats and industry changes. Work Location: Mumbai. Roles and Responsibilities : Must understand various types of attacks like Cross site scripting, SQL Injection, Cookie Poisoning, DDoS attacks, Web scraping, brute force, etc. Must define, administer and manage policies accordingly. Creates WAF rules/signatures to mitigate threats and implements best practices Creation and implementation of custom alerting dashboards in SIEM for investigations Works extensively with different stakeholders for tuning WAF policies or creating custom signatures Design and Develop Cloud-specific security policies, standards and procedures e.g. Identity and Access Management (SSO, SAML), and Privilege Access Management (PAM), Firewall management, SSL/IPSec, Encryption Key Management (BYOK), Security incident and event management (SIEM), Data protection (DLP, encryption), Vulnerability Management in partnership with Infrastructure Services, and Application Development. Orchestrate & Automate security control (guardrails) in Azure and AWS compute &/or Container services. Follows automate-first automate-everything philosophy with use of technologies like Terraform. Focus on Platform Governance & Security and automating operational tasks wherever possible. Requirements : Bachelor's Degree in Computer Science, Software Development or related field. Working knowledge of AWS WAF administration and management, associated policy management, Ingress Egress rules, VPC setup and administration. Must understand and have working knowledge of AWS Landing Zone and Control Tower. Experience with Container technologies (Docker, Kubernetes) Experience with Vulnerability Management and Privilege Account management Strong understanding of TCP/IP, web protocols and networking concepts Excellent understanding of OWASP Risks, Vulnerabilities and Mitigation Mechanisms Experience with Web Application Firewall management and rules Well versed in system exploits (e.g. Buffer Overflows, PTH attacks, windows authentication framework etc.) Excellent understanding of DDoS techniques and mitigation mechanisms Ability to manage and prioritize tasks efficiently Solid resource planning and problem-solving skills Readiness to demonstrate a proactive attitude Excellent verbal and written communication skills Technologies : AWS WAF, VPC, related.

Alembic Pharmaceuticals is looking for Jr. Executive(Operator) - Manufacturing (Injectable) for our Formulation Unit-3, Karakhadi. Job Criteria: 1-7 years ITI/Diploma qualification Job Responsibility: Perform assembling as per defined procedure. Operate filling machine/ Ophthalmic/ PFS machine. Operate homogenizer. Perform batch filtration activity. Perform aseptic manufacturing activity. To unload steam sterilizer and bio-decontamination chamber in co-ordination with equipment preparation and sterilization area. To take part in area qualification activity. To take part in periodic area requalification activity. Aseptic area equipment qualification, filling machine qualification, media fill process. Interested candidates may share their resumes to " injectable@alembic.co.in "

Sets up and operates haemodialysis machine to provide dialysis treatment for patients with kidney failure Attach dialyzer and tubing to machine and prime the extracorporeal circuits with 0.9% normal saline to prepare machine for use. Label dialyser & blood lines with patient name & ID prior to the first use (excluded single use). Preparing dialysis solutions and mixing bicarbonate according to formula Explains dialysis procedure and operation of haemodialysis machine to patient before treatment to allay anxieties. Connects haemodialysis machine to patient s access site to initiate dialysis. Monitor haemodialysis machine for malfunction. Maintain all the log books, forms & registers.

Job Description: As a Certified Nursing Assistant (CNA) at Dahl Memorial Healthcare, you will play a key role in assisting patients with their daily activities and ensuring their comfort, safety, and well-being. You will work closely with a team of healthcare professionals to provide quality care and contribute to improving the lives of our patients. Responsibilities: Assist patients with daily living activities, such as bathing, dressing, grooming, and eating. Provide assistance with mobility and transfers, including repositioning patients as needed. Monitor and record vital signs (temperature, blood pressure, pulse, and respiration). Assist with patient hygiene and ensure a clean and safe environment. Report any changes in patients physical or mental condition to the nursing staff. Help with feeding, hydration, and medication reminders as directed. Maintain patient confidentiality and adhere to all healthcare regulations. Ensure patient comfort and emotional support, fostering a positive environment. Perform other duties as assigned by the nursing staff. Qualifications: High school diploma or equivalent. Current CNA certification (or eligible for certification will pay for certification). Previous experience as a CNA in a healthcare setting preferred. Strong communication skills and the ability to work as part of a team. Compassionate, patient, and detail-oriented with a focus on quality care. Ability to lift and transfer patients safely. Benefits (if applicable): Competitive pay and benefits package Health, dental, and vision insurance Paid time off (PTO) 401(k) retirement plan with employer matching Continuing education and career development opportunities

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

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

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

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

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