7 lead cook jobs found

  Manufacturing Supervisor - Cell Therapy Location: Houston, Texas – Onsite Shift: 7 am -7 pm – 12-hour rotating schedule. As a Manufacturing Supervisor in Cell Therapy, you will lead frontline production teams and play a critical role in delivering high-quality, life‑saving therapies under cGMP conditions. This role offers the opportunity to combine people leadership, technical expertise, and cross‑functional collaboration in a fast‑paced, highly regulated manufacturing environment. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus Medical, dental and vision insurance 401(k) matching plan Life insurance, as well as short-term...

  Senior Process Engineer – Viral Vector Houston, TX The actual location of this job is in Houston, TX, USA. Relocation assistance is available for eligible candidates and their families, if needed. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. A variety of benefits dependent on role and location. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits . The Senior Process Engineer is responsible for leading the support to site operations by ensuring that equipment and related processes are designed and operating to meet the requirements of a regulated manufacturing site.  This role is also...

  Quality Assurance Specialist III - Viral Vector Location: Houston, Texas – Onsite Shift: Tuesday through Saturday, 11:00 PM – 8:00 AM As a Quality Assurance Specialist III - Viral Vector , you will serve as a senior representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector, cell therapy, and advanced therapy manufacturing operations. This role partners closely with Manufacturing, Quality Control, Engineering, Facilities, and other support functions to provide quality oversight of production activities, support complex quality investigations, maintain cGMP compliance, and help deliver life-changing therapies to patients. You will also provide informal leadership and guidance within the QA team while taking ownership of complex quality issues and continuous improvement initiatives. What you will get: A competitive compensation package. In addition, below you will find a comprehensive...

  Quality Assurance Specialist III - Viral Vector (Second Shift) Location: Houston, Texas – Onsite Shift: Monday through Friday, 3:00 PM – 11:30 PM As a Quality Assurance Specialist III - Viral Vector , you will serve as a senior representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector, cell therapy, and advanced therapy manufacturing operations. This role partners closely with Manufacturing, Quality Control, Engineering, Facilities, and other support functions to provide quality oversight of production activities, support complex quality investigations, maintain cGMP compliance, and help deliver life-changing therapies to patients. You will also provide informal leadership and guidance within the QA team while taking ownership of complex quality issues and continuous improvement initiatives. What you will get: A competitive compensation package. In addition, below you will find a...

  Quality Assurance Specialist III - Viral Vector Location: Houston, Texas – Onsite Shift: Sunday through Thursday, 11:00 PM – 8:00 AM As a Quality Assurance Specialist III - Viral Vector , you will serve as a senior representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector, cell therapy, and advanced therapy manufacturing operations. This role partners closely with Manufacturing, Quality Control, Engineering, Facilities, and other support functions to provide quality oversight of production activities, support complex quality investigations, maintain cGMP compliance, and help deliver life-changing therapies to patients. You will also provide informal leadership and guidance within the QA team while taking ownership of complex quality issues and continuous improvement initiatives. What you will get: A competitive compensation package. In addition, below you will find a comprehensive...

Job Description The job of the Motorhand is to safely and efficiently ensure that the regular preventative maintenance and repair activities for the generators, main engines, air compressors, portable water system, drill water manifold and pumps, and cold start air compressors occur in a timely manner to prevent downtime and ensure the efficient and continual functioning of the mechanical equipment used in the operation of the drilling rig. The Motorhand works under the direction of the Rig Manager. Qualifications Ability to perform essential functions of this position with or without reasonable accommodations Minimum of 3 months experience as a Floorhand for Nabors Drilling USA or 6 months experience as a Motorhand for another drilling company Ability to successfully complete Motorhand training at the NDUSA training center Ability to wear respiratory protective devices Ability to complete the essential functions of Floorhand duties when needed Must have reliable...

  Deviation Investigation Writer - Viral Vector Location: This is an on-site position located in Houston, TX. Available shift: Monday through Friday, standard office hours (approximately 8:00 a.m. to 5:00 p.m.) The Deviation Investigator III – Viral Vector is responsible for leading and executing deviation investigations within a cGMP-regulated viral vector manufacturing environment. This role independently manages minor and low-to-medium severity major process deviations while supporting higher-risk investigations to identify root causes, assess product quality impact, and implement effective corrective and preventive actions (CAPAs). The position serves as a key quality partner to Manufacturing, Quality Assurance, and MSAT teams, ensuring quality records are completed accurately, compliantly, and within established timelines while supporting operational excellence and continuous improvement initiatives. What you will get: This is a competitive salary...