Gm Jobs

We need Consultant Anesthesia for Multispecialty Hospitals in Bhiwani & Narnaul, Haryana. The candidate should be MD or DNB or DA in Anesthesia Any experience. Salary 2.0 to 3.0 Lacs pm If interested, please send us your cv at the earliest on recruiterdoctors at the rate gmail dot com

... Address: Regd. Office 1st Floor Old Terminal Building Dr. Babasaheb Ambedkar International Airport Nagpur Maharashtra Facility: GMR NAGPUR INT. AIRPORT Qualification: 12th Experience: 1 - 2 years Source: Sodexo India | Job Code: IJP567531

... Address: Regd. Office 1st Floor Old Terminal Building Dr. Babasaheb Ambedkar International Airport Nagpur Maharashtra Facility: GMR NAGPUR INT. AIRPORT Qualification: 10th Experience: 1 - 2 years Source: Sodexo India | Job Code: IJP567527

... Address: Regd. Office 1st Floor Old Terminal Building Dr. Babasaheb Ambedkar International Airport Nagpur Maharashtra Facility: GMR NAGPUR INT. AIRPORT Qualification: 10th Experience: 1 - 2 years Source: Sodexo India | Job Code: IJP567528

... Address: Regd. Office 1st Floor Old Terminal Building Dr. Babasaheb Ambedkar International Airport Nagpur Maharashtra Facility: GMR NAGPUR INT. AIRPORT Qualification: 10th Experience: 1 - 2 years Source: Sodexo India | Job Code: IJP567526

... Address: Regd. Office 1st Floor Old Terminal Building Dr. Babasaheb Ambedkar International Airport Nagpur Maharashtra Facility: GMR NAGPUR INT. AIRPORT Qualification: 10th Experience: 1 - 2 years Source: Sodexo India | Job Code: IJP567525

... Address: Regd. Office 1st Floor Old Terminal Building Dr. Babasaheb Ambedkar International Airport Nagpur Maharashtra Facility: GMR NAGPUR INT. AIRPORT Qualification: 12th Experience: 1 - 2 years Source: Sodexo India | Job Code: IJP567532

The Manager, Business Intelligence leads a team of product owners and reporting engineers who build and maintain the reporting our corporate business areas and venues run on. You set the standard for how data is modeled, defined, and delivered in Amazon Quick Suite (Quick Sight) on top of Redshift and Snowflake, and you connect two halves of the team: the product owners who own the relationship with the business and the backlog, and the engineers who build against it. Success is measured less by dashboards shipped and more by decisions improved — how fast a venue GM or a corporate leader gets a reliable answer, and how much they trust it. Team leadership Lead, coach, and develop a team of BI product owners and reporting engineers; own hiring, onboarding, performance, and career growth across two distinct skill tracks. Develop product owners in requirements gathering, backlog management, stakeholder communication, acceptance criteria, and saying no well. Develop reporting engineers in SQL, data modeling, Quick Suite development, and engineering craft. Hold the line between the two: ensure requirements arrive well-defined and that engineers aren't absorbing unscoped work mid-sprint. Run the team's delivery cadence — intake, prioritization, sprint or release planning, and demo/review — balancing executive asks against roadmap commitments and technical debt. Establish and enforce team standards for SQL, data modeling, version control, code review, testing, documentation, and dashboard design consistency. Product management of the reporting portfolio Own the BI product roadmap across corporate functions and venue operations; make the trade-off calls when demand exceeds capacity. Ensure each business area — Finance, Operations, Marketing, F&B, Guest Experience — has a clear product owner relationship and a visible backlog.<

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: The Opportunity The Maintenance Technician IV is responsible for operating, maintaining, troubleshooting, and repairing facility related mechanical, electrical, instrumentation, refrigeration, control systems, and equipment located within office, R&D, and GMP manufacturing locations. Additionally, this position supports automated fill, cap, and labeling, conveying, and product finishing equipment from set-up, to change-over and supports associated maintenance and troubleshooting as requested. Shift: 8:00 p.m. – 8:30 a.m., Saturday through Monday (three 12-hour overnight shifts per week). What You’ll Work On Include but are not limited to the following: Communicate facility and safety related issues that arise from daily operations to the Facilities Management to coordinate with internal customers, property owner and/or outside vendors. Own the process in managing spare parts for facility utilities and supplies as needed to minimize equipment downtime. Oversee the facility and utility systems including but not limited to electrical distribution, plumbing, HVAC, compressed air systems, fire and life safety systems and emergency power. Enter, prioritize and complete work orders in the CMMS system. Provide first level review of completed work orders for assigned site. Execute building/facility projects (i.e. installation of new systems, commissioning of building systems). Execute preventive maintenance and demand maintenance tasks

Job Title Quality Control Technician Job Description In this role you Are responsible for supporting diverse complex quality control tasks, assisting in resolving malfunctions, analyzing quality control improvements. Your role: •Helps to execute diverse complex tasks based on individual understanding and technical knowledge to address abnormalities within operational manufacturing processes. •Assists in remedying complex malfunctions, helps to execute product quality inspection activities within the project scope. •Aids to implement quality control procedures and protocols, ensuring adherence to good laboratory practices (GLP) and good manufacturing practices (GMP). •Helps in the documentation of regulatory requirements for good manufacturing controls for medical devices as outlined in quality control plans, assisting in implementing the laboratory chemical hygiene program. •Provides support towards the execution of validation protocols and testing methods for new products and processes to ensure they meet quality standards. You're the right fit if: You have a High School Diploma or Vocational Education 2&#43; years of Quality Control experience. Prefer experience with Inspection, QMS, Technical documentation, Manufacturing in medical device. You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this <a target="_blank" href="https://eur01.safelinks.protection.outlook.com/?url&#61;https%3A%2F%2Fwww.careers.philips.com%2Fna%2Fen%2Foffice%2Fremote-sedentary-work-physical%2C-cognitive-and-environmental-pce-job-requirements&data&#61;05%7C02%7Cvenkata.damaraju%40philips

Job Title Quality Control Technician Job Description In this role you Are responsible for supporting diverse complex quality control tasks, assisting in resolving malfunctions, analyzing quality control improvements. Your role: •Helps to execute diverse complex tasks based on individual understanding and technical knowledge to address abnormalities within operational manufacturing processes. •Assists in remedying complex malfunctions, helps to execute product quality inspection activities within the project scope. •Aids to implement quality control procedures and protocols, ensuring adherence to good laboratory practices (GLP) and good manufacturing practices (GMP). •Helps in the documentation of regulatory requirements for good manufacturing controls for medical devices as outlined in quality control plans, assisting in implementing the laboratory chemical hygiene program. •Provides support towards the execution of validation protocols and testing methods for new products and processes to ensure they meet quality standards. You're the right fit if: You have a High School Diploma or Vocational Education Prefer 2&#43; years of experience with Quality Control, Inspection, QMS, Technical documentation, Manufacturing in medical device. You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this <a target="_blank" href="https://eur01.safelinks.protection.outlook.com/?url&#61;https%3A%2F%2Fwww.careers.philips.com%2Fna%2Fen%2Foffice%2Fremote-sedentary-work-physical%2C-cognitive-and-environmental-pce-job-requirements&data&#61;05%7C02%7Cvenkata.damaraju%40philips.com%7Cc673b7f662d14a95a61708dc704f3d4b%7C1a407a2d76

Job Title: Section 12 approved doctor - SPR shifts Grade: Specialty Doctor Location: London Working Hours: Adhoc Rate: Competitive, to be discussed upon application Locum SPR Psychiatrist - Ad Hoc Shifts | London We are currently seeking a Section 12 Approved Locum SPR Psychiatrist to cover a variety of ad hoc shifts across London. The role consists predominantly of non-residential on-call and night shifts, providing assessment and support within established mental health services. Flexible availability is welcomed, with regular shifts available for the right candidate. Applicants must hold full GMC registration, Section 12 approval, and have previous NHS psychiatry experience at SPR level. Qualifications and Experience: • GMC registration (essential) • Section 12 approval • 3+ Years experience working in a psychiatry position • Excellent communication and teamwork skills

Job Title: Aseptic Pharmacy Technician Banding: Band 5/6 Location: North Wales Start Date: ASAP Duration: 3 Months Initially Hourly Rate: Band 5 - £17 - £19 Band - 6 £22 - £24 Working Hours: Monday to Friday, Full-Time Job Overview Pulse is currently seeking an experienced and motivated Aseptic Pharmacy Technician to join the pharmacy team in Wrexham. This is an excellent opportunity for a skilled pharmacy technician to work within a specialist aseptic services environment, supporting the safe preparation, quality assurance, and supply of aseptically prepared medicines. The successful candidate will play a key role in ensuring high standards of pharmaceutical quality and patient safety, working closely with pharmacists and aseptic services staff to support the delivery of an efficient and effective service. Key Responsibilities Support the preparation and supply of aseptically prepared medicines in accordance with departmental procedures. Work within Good Manufacturing Practice (GMP) and quality assurance requirements. Assist with the maintenance of aseptic services documentation and records. Support environmental monitoring, validation, and quality control activities. Ensure compliance with relevant medicines legislation and governance requirements. Work collaboratively with pharmacists, technicians, and other healthcare professionals. Contribute to service development and continuous quality improvement initiatives. Maintain high standards of accuracy, safety, and professionalism at all times. Qualifications and Experience Be registered with the General Pharmaceutical Council (GPhC). Have previous NHS hospital pharmacy experience. Demonstrate experience working within an aseptic services environment. Possess a sound understanding of Good Manufacturing Practice (GMP) principles. Have knowledge of quality assurance processes and aseptic preparation standards. Be able to work accurately and effectively within a regulated environment. Demonstrate excellent commu

Work Flexibility: Field-based Due to the nature of this role and travel requirements associated with this role, we will accept candidates from the 48 continental United States. Job Summary: As a National Leaves Clinical specialist, you will work directly with a JR/MPS team to support robotic and manual joint replacement procedures. You will be required to work within RepSuite for scan and schedule management in multiple territories across the country for employee leave of absence and when otherwise needed by the business. The NLCS will directly report to the Senior Manager, LEAP but indirectly work alongside local Mako Manager, JR Sales Manager, and GM. When not deployed the NLCS will assist and train with local JR team and execute all necessary clinical functions with that team. Field assignments can be a short as two week and as long as 3 months or more. Essential Duties & Responsibilities: Clinical Expertise in robotic applications Develop and maintain expert-level knowledge of Mako robotic systems, their functionalities, and clinical applications. Develop and maintain expert-level knowledge of manual joint replacement instrumentation and implants. Serve as a clinical resource to healthcare professionals, offering insights, training, and support. Deliver comprehensive customer experience tailored to surgeons, nurses, and other clinical staff during the deployment. Ensure that healthcare teams are proficient in MAKO technology, understand clinical benefits and have access to program resources. Be a point of contact for clinical inquiries, troubleshooting, and technical support related to Mako and manual instrumentation and implants. Relationship Building: Build and maintain strong relationships with healthcare providers and hospital staff, internal team members and potential new c

We anticipate the application window for this opening will close on - 1 Oct 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72&#43; million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life This role supports laboratory operations through the maintenance, calibration, qualification, and troubleshooting of analytical instrumentation used in regulated testing environments. The team is responsible for ensuring laboratory equipment performs accurately and reliably while supporting compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and internal quality requirements. Responsibilities include preventive maintenance, calibration management, instrumentation documentation, vendor coordination, and continuous improvement of equipment processes and procedures. This position is located at the Rice Creek Campus in Fridley, Minnesota and is an onsite role requiring regular presence within the laboratory environment. No travel is required. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 5 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. Responsibilities may include the following and other duties may be assigned: Perform r