Description: Senior Specialist QA Remote any time zone OK Does the thought of building an entirely new digital quality management system, excite you. Do you love to design and streamline processes within a hard-working team. If you hav...
Job Title: Sr. Analytical Engineer Location: Thousand Oaks, CA Zip Code: 91320 Start Date: Right away Job Type: Contract Keywords: #AnalyticalEngineer #EngineeringJobs #CAjobs JOB RESPONSIBILITIES: Will lead the troubleshooting, ve...
Job Title: Engineer Senior, CQV & Troubleshoot Biopharma Analytical Equipment (JP13477) Location: Thousand Oaks, Ca. 100% onsite. Business Unit: Facilities and Equipment Drug Substance Supply Employment Type: Contract Duration: 1+ years...
Description: Note: FULLY ONSITE AT USTO Must be flexible as it is possible worker will start on any shift. Rotate every 6 months. DAY 7 AM - 8 PM SWING 1 PM to Midnight NIGHT SHIFT 7 PM - 8 AM Will change on the business they are su...
Description: Note: Role and Responsibilities: Provide strong vendor management to deliver premium employee experience. This includes ensuring overall compliance in filing immigration petitions while partnering on strategic initiatives. ...
Description: Note: Will need to be onsite as needed (hybrid schedule) Responsibilities of this position will include: Support commercial training events for multiple business units (including logistical support during an event) Manage...
The Project Coordinator will be responsible for supporting the planning, execution, and completion of various product development projects. This role requires excellent communication skills, the ability to manage multiple tasks simultaneous...
Description: Note: Hybrid - 1 day a week in office + additional onsite support as needed. (flexible) Ideal Candidate: 3+ YOE. Familiarity with any project management software. Team currently uses Smartsheet. Strong communication and ini...
Note: Ideal candidate will have solid oral dosage formulation experience. Someone motivated to come in and learn something new and want to be an active part of the team. The Pivotal Synthetic Drug Product group of the Drug Product Technol...
Top 3 Must Have Skill Sets: 5+ years of clinical trials experience. Hands on SAS experience is required. Regulatory interaction payer experience. Day to Day Responsibilities: Position Summary: The primary role of this position is to...