Location (mandatory): Portsmouth NH USA 03801 Small Description: The QC Specialist II will join the Quality Control department and assist with technical transfer activities, contributing to the testing and analysis of in-process samples, final product testing, and stability studies. This role requires familiarity with GMP (Good Manufacturing Practices) systems, quality records, and testing methodologies. The individual will work collaboratively to complete complex tasks while ensuring adherence to industry regulations, contributing to method transfers, instrument qualifications, and validation activities.

Location (mandatory): Pleasanton, CA 94588 The Product Manager / Product Evaluator II supports food product development by managing product samples, documentation, testing, and evaluations across multiple categories. This role plays a key part in new product demonstrations, sensory evaluations, and finished product specifications while ensuring food safety, quality, and accurate reporting—enabling product development teams to focus on strategic initiatives.

Location:- Cambridge, MA 02141 (Onsite) Work Schedule: Generally, Monday to Friday 08 Am to 05 Pm EST (slight flexibility in hours) potential weekends (max 40 hrs)

Location (mandatory): Vacaville California With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals.

Location : Cambridge, MA 02141. The CMC Synthetics Platform within the Client R&D organization is responsible for the process development of small molecule drug substances undergoing clinical studies. We are seeking a hands-on laboratory manager with excellent organizational skills to support our activities. The person will provide services to Client at the Cambridge Crossing (CX), Cambridge, MA site. • Provide on-site service to the Client for both laboratory functions and laboratory equipment and instrumentation maintenance and upkeep • Perform experimental protocols to support the Client’s technology platforms • Ensure compliance with health and safety teams and training as required for Client lab operations • Support inventory management, purchasing, and shipping of chemical compounds and laboratory supplies

Location - 11202 El Camino Real San Diego CA USA 92131 The Structural Biology and Protein Sciences group is seeking a highly motivated contractor to support recombinant protein production efforts, primarily utilizing insect cell expression systems. The successful candidate will be responsible for maintaining eukaryotic cell cultures, generating and managing high-titer baculovirus stocks, and performing multi-liter scale protein expression and harvest workflows. Additional responsibilities include executing plate-based expression and purification profiling to enable rapid screening of construct and condition variants. This role requires strong organizational skills, attention to detail, and the ability to operate efficiently in a fast-paced research environment.

Location : Princeton, NJ 08540. Experienced Regulatory Affairs professional responsible for supporting global regulatory operations, ensuring compliance, maintaining regulatory data accuracy in RIMS, and enabling timely market access across multiple jurisdictions. The role requires 5 days a week onsite presence in Princeton, NJ during normal business hours.

Location (mandatory): Chicago, IL The Video team is responsible for designing, implementing, and supporting video solutions across the City. The team partners with multiple city agencies to define requirements and deliver solutions that increase situational awareness for mission critical first responders.

Location (mandatory): 3340 Enterprise Way, Miramar, FL 33025 The Laboratory Technician is responsible for ensuring timely, accurate, and comprehensive processing during screening, admission, study conduct, and discharge procedures. The role supports clinical and laboratory operations while ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory standards.