Job Description The GMP Operational Quality Specialist works with a high degree of independence to provide QA Analytical support for release and stability program for commercial products. The GMP Operational Quality Specialist executes routine tasks and
The Microbiologist Technician is responsible for conducting routine microbiology tests, recording results, performing maintenance tasks, and assisting the Lead Microbiologist in maintaining the microbiology lab and conducting microbiological analyses under professional supervision. Key Responsibilities Conduct routine
Job Description The GMP Operational Quality Specialist works with a high degree of independence to provide QA Analytical support for release and stability program for commercial products. The GMP Operational Quality Specialist executes routine tasks and
We Put the World on VacationTravel + Leisure Co. is the world’s leading vacation ownership and travel membership company, with a dynamic and growing portfolio of resort, travel club, and lifestyle travel brands. Our dedicated associates
Job Description The Information School IT department has an outstanding opportunity for a Web Application Developer to join their team. About this Opportunity Reporting to the Web Development Technical Manager, the Web Application Developer is responsible
Job Description The Quality Shop Floor Specialist is responsible for the floor quality oversight of the production of autologous cell and gene therapy product in a controlled cGMP cleanroom environment. This position is responsible for quality
Job Description The GMP Operational Sr. Quality Specialist recognized as a subject matter expert in the principles and application of quality assurance and compliance. The Sr. Quality Specialist coordinates GMP activities in support of commercial disposition.
Job Description The Quality Shop Floor Specialist is responsible for the floor quality oversight of the production of autologous cell and gene therapy product in a controlled cGMP cleanroom environment. This position is responsible for quality
Job Description The operational Area Senior Quality Specialist will provide QA support of manufacturing operations, analytical laboratory operations and materials management for the external manufacturing programs at VCGT. This role will review batch data, including batch
Job Description The Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects with emphasis on
We Put the World on VacationTravel + Leisure Co. is the world’s leading vacation ownership and travel membership company, with a dynamic and growing portfolio of resort, travel club, and lifestyle travel brands. Our dedicated associates
MUST HAVE SECRET CLEARANCE DO NOT APPLY IF YOU DO NOT CURRENTLY POSSESS A CLEARANCE Description We are looking for you to join our team as a Embedded Software Engineer with the Software Engineering organization based
Maintenance Planner - Mechanical This is for a Mechanical Maintenance Planner role is located at Peach Bottom Clean Energy Center (CEC) in Delta, PA. Primary Purpose of Position Plan and prepare work packages for work to
QC Laboratory Chemist I | cGMP | FDA Charlotte Metro Area Salary range $70k - $80k plus discretionary bonus potential up to 12% Hours: Monday – Thursday 3:30pm – 11:30pm & Friday 1:30pm – 9:30pm US
QA Support Contractor The contractor will provide temporary QA support to maintain quality and compliance oversight of sterile pharmaceutical products manufactured by third-party partners. The focus will be on batch release, issue resolution, and regulatory compliance for
QC Laboratory Chemist | cGMP | FDA (Must have at least 2 years of INDUSTRY experience in a cGMP Laboratory and a BS in CHEMISTRY only). Charlotte Metro Area Salary range $70k - $80k plus discretionary
Documentation Control Specialist We are looking to hire a Documentation Control Specialist immediately. The candidate will be responsible for running the Quality Document Management System (QCBD). This includes processing Engineering Change Orders for Manufacturing Specifications and
Manager, QA Operations Jupiter, FL Who We Are Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing
In-Process Quality Assurance (IPQA) Specialist The In-Process Quality Assurance (IPQA) Specialist provides real-time quality oversight for sterile injectable manufacturing operations, ensuring that all activities comply with current Good Manufacturing Practices (cGMP), approved procedures, regulatory requirements, and
Who We Are As the largest private‑sector power producer in the world and the nations largest producer of clean and reliable energy, Constellation is focused on our purpose: lighting the way to a brilliant tomorrow for