DOT NET Enterprise Architect

Join our dynamic team at Sonsoft Inc. as a DOT NET Enterprise Architect. In this role, you will leverage your expertise in .NET technologies to design and implement robust enterprise-level solutions. You will collaborate with cross-functional teams to ensure system integrity, scalability, and performance, while guiding best practices in software architecture…

Join our dynamic team at Sonsoft Inc. as an SOA Testing Specialist! We are seeking skilled professionals proficient in Soap UI and CA DevTest. This is a fantastic opportunity for individuals who enjoy tackling complex testing challenges and are eager to contribute to innovative projects.

Join our dynamic team as a Recruiting Coordinator (Level III) where you will play a pivotal role in enhancing our recruitment processes. In this position, you will collaborate with various stakeholders to streamline candidate sourcing, scheduling, and onboarding activities. Your organizational skills will ensure a seamless experience for candidates and hiring managers alike.

Join our team at Integrated Resources, Inc. as a Business Systems Analyst III, where you will play a critical role in bridging the gap between business objectives and technology solutions. We are looking for a proactive individual who is skilled in analyzing and improving business processes, collaborating with cross-functional teams, and implementing effective solutions.

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) stands as a global leader in biotechnology. Established in 2002, GenScript boasts a robust international presence in North America, Europe, Greater China, and Asia Pacific. Our operations are diverse, encompassing key areas fueled by our pioneering gene synthesis technology, including Life Science CRO services, enzyme and synthetic biology products, biologics development and manufacturing, and advancements in cell therapy.At GenScript, we are dedicated to realizing our vision of becoming the most dependable biotech company globally, enhancing human and environmental health through biotechnology.Job Scope:The Logistics Specialist will report directly to the Warehouse Supervisor, playing a vital role in supporting warehouse operations related to raw materials and finished products. The ideal candidate will be detail-oriented, possess strong problem-solving skills, and have the physical capability to manage shipment unloading effectively.Key Responsibilities:Coordinate both domestic and international shipments for raw materials, intermediates, drug substances, and drug products.Manage relationships with freight forwarders and carriers, monitor shipment statuses, and proactively resolve any issues that arise.Prepare, review, and maintain all necessary shipping and customs documentation.Support the logistics of temperature-controlled, time-sensitive, and high-value shipments.Ensure compliance of logistics activities with GMP/GDP standards and internal SOPs.Collaborate with Manufacturing, Quality Assurance, Quality Control, Procurement, and Project teams to align shipment schedules effectively.Track logistics costs while supporting cost control and optimization initiatives.

About GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a leading global player in biotechnology, established in 2002. With a strong international footprint across North America, Europe, Greater China, and Asia Pacific, GenScript excels in diverse areas such as Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cutting-edge cell therapy solutions.At GenScript, we are on a mission to enhance the health of humanity and the environment through innovative biotechnology solutions.Job Scope:The Facility Project Manager will take charge of coordinating and overseeing external facility services and capital engineering/construction projects for GXP and non-GMP facilities based in New Jersey. This role requires collaboration with external engineering firms, construction contractors, landlords, government entities, and various internal departments.Key Responsibilities:Oversee multiple facility services and construction projects, managing budgets from $0.05MM to $30MM concurrently.Direct daily project team activities to ensure effective project execution.Maintain a log of action items throughout each project’s lifecycle.Conduct bidding, awarding, and selection of engineering firms, construction companies, equipment vendors, CQV consultants, and service contractors.Guarantee that user requirement specifications are met with high-quality project deliverables.Develop and uphold project schedules to ensure accountability and identify staffing needs.

Join our dynamic team as a Project Coordinator at Artech Information Systems LLC, where you will play a pivotal role in managing and coordinating various projects. You will work closely with project managers and stakeholders to ensure timely delivery and execution of project plans. Your organizational skills and attention to detail will be essential in tracking progress and facilitating communication across teams.

Join our team as a Trust Administration Professional (Level I) where you will play a crucial role in supporting trust services and operations. This entry-level position is an excellent opportunity for individuals looking to kickstart their careers in the legal and administrative realm. Your responsibilities will include assisting with the management of trust accounts, maintaining accurate records, and ensuring compliance with regulations.

About the Role Monarch Communities in Pennington is looking for a Dining Server to help create a welcoming and comfortable dining experience for residents. This position plays a key part in daily meal service and resident satisfaction. What You Will Do Take meal orders from residents with attention to their preferences Serve food and beverages promptly and courteously Keep the dining area clean and organized Contribute to a friendly and inviting atmosphere during meal times

Role overview The (Senior) Environmental, Health, and Safety (EHS) Manager at GenScript USA Inc. leads initiatives to protect employee health and maintain compliance with environmental regulations. This position is based in Pennington, New Jersey and plays a key role in shaping safety strategies and programs across the company. Key responsibilities Design and implement workplace safety and health programs Identify workplace hazards and act to reduce risks Collaborate with teams from different departments to strengthen the organization’s safety culture Ensure all operations comply with environmental laws and regulatory standards Collaboration This role involves working closely with colleagues across multiple departments to foster safety awareness and support compliance throughout GenScript USA Inc.

We are seeking a dedicated and knowledgeable Drug Safety Specialist to join our dynamic team. This pivotal role involves monitoring and evaluating the safety of pharmaceutical products, ensuring compliance with regulatory standards, and contributing to the improvement of patient safety. If you are passionate about drug safety and thrive in a fast-paced environment, we would love to hear from you!

Join our dynamic team at Collabera as a Data Entry Specialist! In this role, you will play a crucial part in ensuring the accuracy and efficiency of our data processing operations. If you have a keen eye for detail and a passion for data management, we want to hear from you!

About GenScript Biotech Corporation GenScript Biotech Corporation (Stock Code: 1548.HK), founded in 2002, is a global biotechnology company with operations in North America, Europe, Greater China, and Asia Pacific. The company’s core business includes gene synthesis technology, a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript’s mission centers on building trust in biotechnology and improving health for people and the environment through new biotechnological solutions. About ProBio ProBio Inc., based in New Jersey, operates as an integrated contract development and manufacturing organization (CDMO). The team partners with biotech and pharmaceutical companies to accelerate the discovery, development, and production of new medicines. ProBio draws on multidisciplinary expertise and proprietary platform technologies to support advances in cell and gene therapies. Facilities in the US, including a 128,000-square-foot site in Hopewell, provide quality control and assurance from early development through clinical and commercial manufacturing. ProBio supports clients with tech transfer and manufacturing services for plasmid DNA and viral vectors. The team is committed to helping bring innovative therapies to patients and improving lives through scientific progress.