Job Description SummaryAt GE HealthCare, were transforming the way the world sees disease, through pioneering pharmaceutical diagnostics and precision imaging. As our Global Medical Governance Excellence Lead, youll be the architect behind the frameworks and processes that
Job Description SummaryBecome part of a winning team and help to deliver the Green Energy transition. GE Vernova is seeking a Lead Hardware Engineer to design and support embedded hardware platforms used in energy and power systems.
Join us in making sure no one is left without a voice At Smartbox, our assistive technology empowers people with disabilities who experience speech difficulties to express themselves, connect with others, and live more independent lives.
Serves as the engineering Subject Matter Expert (SME) for all data center delivery process related to maintenance and repair of critical infrastructure from liquid to chip. Leads and executes the needed efforts related to change management, administration
Job title: Shift Lead - nights (Temporary, fixed term for 6 months) Reporting to: Manufacturing Manager Location: Bury St. Edmunds, Suffolk Hours: 38 hours per week (Monday to Thursday, 20.45 – 06.15) The Opportunity Responsible for the
Location Ampthill - on site About the role Applies quality principles in the areas of: design, incoming material, production control, product evaluation, program performance, reliability, inventory control, and/or research and development as they apply to product
NOxBOX Ltd. Quality Regulatory Assurance Lead Sittingbourne, United Kingdom | req33235 What you will enjoy doing You will manage day to day responsibilities and support a small QA team performing Registration, Document control, training, Product release,Non-conformance and
Whether its the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isnt
What youll do. As Area Lead, you’ll take operational ownership of a defined manufacturing zone, ensuring production lines run safely, efficiently and in line with performance targets. You’ll oversee shift-level delivery across safety, quality, delivery and cost,
Work ScheduleThird Shift (Nights) Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed,
EHS Lead - EMEA Colorcon® is a world leader in the development, supply and technical support of formulated film coating systems, modified release technologies, specialty excipients and functional packaging for the pharmaceutical, nutritional, and animal health industries.
GLP Vendor Oversight and QA Lead The integrity of nonclinical data depends on more than what happens inside a companys walls. Much of the critical work in GLP-regulated research — safety studies, toxicology, analytical testing — is
We are seeking an IT Quality Engineer with a strong background in manufacturing environments to bridge the gap between our production operations and digital infrastructure. In this role, you will ensure the reliability, compliance, and performance
Work Flexibility: Onsite Operations Associate What you will do: Provides manufacturing, product and process co-ordination support to the manufacturing line. In addition, coordinates and evaluates production training and trains trainers. Responsible for ensuring the performance of
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Mylan Pharma UK Limited Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes
Quality in clinical development is a matter of operational resilience as much as regulatory mandate. This role serves as a GCP Auditor within our Research & Development Quality audit program, responsible for executing the global audit
Overview Reporting to the Lead Account Manager, you are responsible for the vendor performance management and governance of Stockless Fulfilment vendors, ensuring KPIs, service levels, and customer outcomes are met through accurate monitoring, reporting, and timely issue
Quality in a globalized drug safety network is a matter of operational resilience as much as regulatory mandate. This role serves as a GVP Auditor within our Research & Development Quality audit program, responsible for executing