Location: Westborough, MA, 01581 The Compliance Specialist will perform critical QA tasks in support of GMP and non-GMP manufacturing programs and Regulatory Submissions at AIRM. This role ensures data integrity, quality, and compliance across a broad range of Quality Assurance areas, working closely with team members to maintain high-quality standards and value delivery for patients.

Location (mandatory): Remote, Pacific Time, USA DESCRIPTION: Software Engineer III Seeking a Software Engineer to build and maintain internal tools, automate workflows, and set technical best practices for our legal department. This role is ideal for someone who has a strong attention to detail and enjoys collaborating with a variety of technical and non-technical cross-functional partners. This role will be responsible for supporting the Legal team. This includes full stack. Disqualifiers: Very short tenures: would prefer someone who has had one or more engagements lasting 2+ years. Someone who doesn’t have 5-7 years of explicit Full-Stack Software Engineering experience. Interview: Rounds: 2 Rounds (one screen, one follow-up for those who pass the screen). Details: Technical and Behavioral. Should be able to provide explicit examples of full-stack experience, building applications and/or tools from the ground up. Should have strong communication and XFN experience, and be able to provide examples articulating technical concepts in easy-to-understand language Duration: First sync: 30 min. Second sync: 1 hour

Location (mandatory): Fremont, CA Supply Chain Analyst III Ideal Candidate: Basic analysis skills, Warehouse/manufacturing experience, Committed, focused on reverse logistics Red Flags: Frequent job changes, Few desktop roles, Over 10 years of experience Summary: Our IT Logistics team is seeking a highly motivated, goal-oriented, and hands-on supply chain analyst to facilitate the implementation of industrial engineering and Lean principles within our warehouse operations and global supply chain processes. The successful candidate will possess a comprehensive understanding of warehouse operations, end-to-end supply chain functions, data analysis methodologies, and supply chain management software. This role requires collaboration with internal teams and external vendors to implement process improvements and manage projects from inception to completion, ultimately taking ownership of operational process enhancements. Day-to-Day Responsibilities: Identify and resolve process constraints and escalations Develop and implement new processes with Process Engineers Update SOPs and conduct time/resource studies Liaise with vendors and manage meetings/training Build metrics dashboards with data teams

Location (mandatory): Fremont, CA The IT Logistics Team is looking for a highly motivated, goal-oriented, and hands-on Supply Chain Analyst to help implement industrial engineering and Lean principles in the processes at our warehouse in Newark, CA. Through a detailed understanding of the warehouse’s objectives and in collaboration with internal and external teams, the Supply Chain Analyst will help improve processes to increase overall efficiency, capacity, quality, and safety. This Candidate will focus on improving efficiency and costs, working with different vendors and focus on customer satisfaction. Typical Day would look like: Factor 1: Supporting processes, set ups and overall management In the warehouse- deploying phones, laptops to users, focusing on the “Telco process” to improve warehouse efforts Reverse actions of these processes as well - data backups , data wipes Factor 2: Revamping / reengineering supply chain processes and increasing efficiencies Factor 3: Tasks outside of the warehouse – looking into how transportations work - ensuring the end-to-end process is a good experience for users, finding issues and gaps between these How will performance be measured: SOPs: Tasks closed on time Feedback from warehouse and partners Responsiveness and support Communication

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 (mandatory): Springfield OH USA 45505 This role will be responsible for reviewing insurance document images and entering missing information into a database quickly and accurately. This is a repetitive, computer-based data entry position.

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 (mandatory): Bridgeport, NJ 08085 Provide administrative and operational support for logistics, trade compliance, and site operations by maintaining organized physical and digital filing systems and ensuring accurate, timely document flow. Review import/export documentation for compliance, support audits and inspections, and assist with shipping, receiving, and inventory records. Coordinate with warehouse staff, carriers, and freight forwarders to align shipment documentation and track status updates across teams. Utilize Microsoft Office and ERP systems.

Location (mandatory): Colorado Springs, CO 80915 provides day-to-day support for the Document Control and Production Planning teams within manufacturing operations. Approximately 90% of the role focuses on Document Control tasks, including scanning, organizing, and preparing documentation used by Manufacturing and Test. The remaining 10% of the role supports routine Production Planning activities such as updating standard reports or assisting with basic order scheduling and release processes.

Location (mandatory): Zelienople, PA 16063 The Warehouse Associate will be responsible for receiving and stocking inventory, pulling orders for both pump and parts orders, parts identification, assembling parts orders, prepping and painting orders and final packaging for shipment.

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 : Taylor Texas 76574 Provides support, oversight, administration and facilitation of changes that affect facilities, infrastructure, hardware, operating systems, database platforms, firmware, network, and software environments for 24/7 IT Operations. Ensure audit tracking, reliability, availability, correct functionality, system integrity, and risk mitigation in IT Service Delivery model by coordinating, communicating and recording changes to non-development environments. [Coordinates & facilitates all Software, Hardware, and Infrastructure code and configuration changes.]