31 to 45 of 50
Job Title QA Associate Job ID 24 02273 Location Bothell, WA, 98021 Duration 12 Months contract on W2 This is an Onsite role Work Schedule Wednesday Saturday, 6AM 4 30PM PST Maintains shop floor quality presence; disposition in process materials and finished product; investigates and resolves GDP errors; Performs batch record reviews. Assures the quality of manufactured pr
Posted 2 days ago
Job Title Rheumatology Review Group Eligibility Liaison Job ID 24 02297 Location Madison, NJ, 07940 Duration 12 Months contract on W2 Job Description Job Title Rheumatology Review Group (RRG) Eligibility Liaison Division R&D / Global Drug Development Functional Area Description The RRG Eligibility Liaison (REL) employs scientific and technical expertise to track, coordina
Posted 2 days ago
The successful candidate will manage department SharePoint sites, including permissions hierarchy, external partner access, and continuous improvement efforts. They will manage SharePoint user request queues, fulfilling requests and responding to inquiries. The role involves maintaining the department Project Staffing list and ensuring its accuracy. The individual will ma
Posted 3 days ago
Job Title Infrastructure Program Manager Job ID 24 02203 Location Libertyville, IL, 60048 Duration 12 Months contract on W2 Project/Domain Overview Libertyville is Client vector manufacturing facility part of the Cell therapy network. Client will be implementing next generation IT infrastructure capabilities at the site in accordance with global standards. Additionally, C
Posted 3 days ago
This individual contributor role has task level responsibility for in house and outsourced studies while ensuring adherence to the client's outsourcing strategies within a specific therapeutic area(s) and is accountable to support clinical trial vendor partnerships across select or multiple service categories of clinical trial activities in R&D. Must Have List 2 5 yea
Posted 3 days ago
Job Title Facility, Utility, and Equipment Reliability Specialist Job ID 24 02189 Location Warren, NJ Duration 12 Months contract on W2 Onsite Role Work Schedule Mon Fri, Business Hours Flexibility is required though as needs of the business warrant Position Overview The main purpose of the Facility, Utility, and Equipment Reliability Specialist is to evaluate facility an
Posted 3 days ago
This position will manage procure to pay transactions utilizing SAP Planning (MRP) and Procurement modules to support manufacturing operations, ARIBA to resolve accounts payable invoice issues, and other business systems (Microsoft Suite, etc.) while abiding by SOP’s and regulatory requirements. This role will collaborate closely with other professionals in Procurem
Posted 3 days ago
100% Onsite position
Posted 3 days ago
12 Months of W2 Contract
Posted 3 days ago
Sunrise Systems
- Fuquay-Varina, NC
? As an?Electrical Engineer Engine Management Systems?for?Client’s Turf Care?located in?Fuquay Varina, NC, you will develop Engine Management Systems in the Turf & Compact Utility division on low to medium complexity engine and transmission electronic control systems for products across our division.? In addition, you will You will be a key contact to provide expert
Posted 3 days ago
We are seeking a self motivated, detail orientated, and collaborative team member to partner effectively with research staff and support day to day laboratory operations at our new flagship building in Cambridge, MA. The successful candidate will be part of the Lab Operations (Lab Ops) team within Strategy & Research Operations and will play a critical role in maintaining
Posted 3 days ago
Job Title Controls Engineer Job ID 24 01872 Location Moline, IL Duration 12 Months contract on W2 Visa sponsorship is not available, now or in the near future, for this position. Onsite, first shift position. Hours are 6am 2 30pm and include overtime as the production line is scheduled. Metatarsals required from day one. This position will support manufacturing, quality a
Posted 3 days ago
will include, but are not limited to, the following 1. Participate in the development of the CMC regulatory strategy for post approval small molecule product submissions, including global supplements/variations and responses to health authority queries. 2. Prepare and review CMC submission documents, registration dossiers, and responses to health authorities through collab
Posted 3 days ago
5 day work week(4 days in office)
Posted 3 days ago
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