GMP Officer California-Silicon Valley/Peninsula
9/20/2016 7:42 PM

The GMP Officer will provide support to the day-to-day site compliance needs on the shop floor to identify and resolve compliance issues within the Process Unit (PU) unilaterally and cross-functionally. Work closely with the PU and Quality Organization to ensure compliance with current FDA regulations through operational oversight, internal audits, deviation management, and proactive process impro  ...View Job
Quality Compliance Team Lead (Associate Director level) California-Silicon Valley/Peninsula
9/20/2016 7:23 PM

The Quality Compliance Team Lead will manage and lead the QA Compliance Department and is responsible for helping to interpret cGMP regulations and current industry practices for Pharma Operations. This person will ensure adherence to Novartis Quality System and Regulatory standards, internal audits, supplier quality, third party cGMP evaluations and approval, hosting health authority inspections   ...View Job
Process Unit Coordinator (Supervisor/Manager) California
9/20/2016 7:01 PM

The Process Unit Coordinator will manage and lead a team of direct reports to produce and deliver high quality products to customers in a compliant, timely, efficient, and cost effective manner. Ensure full compliance with Health, Safety and Environment (HSE), Good Manufacturing Practices (GMP), statutory, regulatory, and Novartis requirements. Responsibilities: • Translate Process Unit (PU)  ...View Job
Sr. Project Engineer - Equipment, Facility, Safety California
9/20/2016 6:21 PM

Novartis is looking for a top-notch Senior Project Engineer with skills in pharmaceutical engineering and construction safety management and oversight. This role will lead and support highly technical projects involving automated equipment implementations, enhancements, and facility systems engineering improvements. This person will manage engineering projects ensuring all applicable Novartis poli  ...View Job
Validation Lead California-Silicon Valley/Peninsula
9/16/2016 5:30 PM

Executing and managing process validation activities, primary packaging validation activities, cleaning validation activities and complex revalidation activities strategies to meet cGMP requirements on time and quality to ensure that programs are compliant with inspection agencies’ requirements and related SOPs. Validation Master Plan • Lead writing and maintaining Validation Master Plan for  ...View Job