Network Automation Application Developer - Contract Position

Join our dynamic team at Software Technology Inc. as an IT Technician. In this vital role, you will support our IT infrastructure and ensure that our systems operate efficiently. You will be responsible for troubleshooting, maintaining hardware, and providing technical support to our staff.

We are seeking a skilled Python Developer with a focus on automation to join our dynamic team at Sonsoft Inc.. In this role, you will be responsible for developing and implementing automated solutions that enhance our software systems and improve operational efficiency.The ideal candidate will have a strong background in Python programming, experience with automation frameworks, and a passion for driving innovation through technology.

Speechify seeks a Senior Software Engineer to focus on Windows and desktop application development. This full-time position is located in Princeton, NJ. Key Responsibilities Design and build desktop applications for Windows platforms Maintain and enhance existing software to ensure reliability and quality Apply software development expertise to deliver robust products Improve user experience through careful engineering and attention to detail Location This role is based in Princeton, New Jersey.

Join our dedicated team at Software Technology Inc. as a C# Developer, where you will have the opportunity to work on exciting projects that drive innovation in software solutions. We are looking for a passionate developer who is eager to contribute to our collaborative environment and enhance our product offerings.

Join SciTec, a proud subsidiary of Firefly Aerospace, as we lead innovations in advanced technologies that bolster U.S. National Security and Defense. With over 45 years of dedicated service to Department of Defense clients, we excel in crafting cutting-edge remote sensing algorithms and tools that provide exceptional data exploitation capabilities for missile defense, intelligence, surveillance, reconnaissance, space domain awareness, and aircraft survivability missions.Important Notice: To maintain compliance with U.S. government contracts, all employees must be U.S. citizens. Applications from non-citizens will not be considered.We are urgently seeking a skilled Application Security Engineer to enhance the security of our Next-Generation Missile Warning software. This role is an exciting opportunity to contribute to vital national defense initiatives through the end-to-end processing of Overhead Persistent InfraRed (OPIR) sensor data, focusing on Missile Warning, Missile Defense, Battlespace Awareness, and Technical Intelligence.The ideal candidate will possess robust technical security expertise and demonstrate proficiency in collaborating with software engineers within a DevSecOps environment, ensuring security is seamlessly integrated into the development lifecycle.

Join our innovative team at Sonsoft Inc. as a Python Developer! We are looking for a skilled developer who is passionate about coding and eager to contribute to exciting projects. If you thrive in a dynamic environment and are excited to tackle challenging problems, this is the perfect opportunity for you.

WithumSmithBrown values individuality and talent. The firm supports growth and encourages team members to bring their full selves to work. Collaboration and an entrepreneurial mindset shape the way teams approach client service and professional development. The System and Process Assurance team is growing to meet increased demand for assurance services. Withum is hiring a Senior Consultant for Contract Compliance. This position focuses on contract compliance audits, including royalty, franchise, revenue participation, lease agreement, and vendor audits, as well as other contractual projects. The role can be based in New York, NY; Whippany, NJ; East Brunswick, NJ; Red Bank, NJ; Princeton, NJ; or Philadelphia, PA. Withum’s culture centers on teamwork, resilience, and a commitment to helping clients and communities thrive. The firm invests in both personal and professional growth for all team members. Learn more about the Withum Way. What You Will Do Assist audit teams with planning and evaluating franchisees’ and licensees’ compliance with financial and brand management requirements during contract compliance audits. Review financial records of franchisees and licensees to determine reportable income and fulfillment of other contractual obligations. Conduct independent research on franchisees, owners, and related parties to understand contractual relationships. Manage project workflow to meet deadlines and maintain effective communication with clients for cooperation throughout the process. Prepare work papers that summarize findings, conclusions, and outcomes for clients. Document franchisees’ and licensees’ responses to evaluations and verify compliance with contract terms.

Kardigan aims to change the future of heart health by focusing on prevention and cures for cardiovascular disease. The company works on multiple targeted treatments at once, with the goal of removing heart disease from the list of leading causes of death worldwide. The leadership team brings deep experience from guiding MyoKardia through the discovery and development of mavacamten, the first cardiac myosin inhibitor, which resulted in a successful acquisition by Bristol Myers Squibb in 2020. Kardigan's approach combines a modern discovery platform, a strong pipeline of late-stage candidates, and a dedicated group of professionals committed to improving outcomes for patients with heart disease. Values Patient-centric: Every decision prioritizes the needs of patients and their families. Authenticity: The team values acceptance and truth in daily work. Curiosity: A drive to learn and adapt fuels discovery and progress. Teamwork: Collaboration and support help move projects forward and maintain high standards. Enable the impossible: Risk-taking and bold thinking are encouraged to push scientific boundaries. These principles shape Kardigan’s culture and inspire the team to create lasting change for people living with cardiovascular conditions.

About Kardigan Kardigan focuses on heart health, working to shift cardiovascular disease from a global threat to a manageable condition. The company develops multiple targeted therapies at once, aiming to provide effective treatments for people living with cardiovascular diseases. Kardigan was founded by Tassos Gianakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D. The team previously led MyoKardia, where they developed mavacamten, the first cardiac myosin inhibitor. Their work led to MyoKardia's acquisition by Bristol Myers Squibb in 2020. The company uses advanced discovery and translational research platforms and has a pipeline of late-stage candidates. The team is committed to improving patient outcomes. Our Values Prioritize the well-being of patients and their families Embrace authenticity and foster inclusion Encourage learning, curiosity, and adaptability Support each other in striving for excellence Work together to achieve ambitious goals for patients These values shape daily work at Kardigan and support a lasting impact in the field of cardiovascular health.

We are seeking a skilled Python Developer with a strong background in Django to join our dynamic team at Career Guidant. The ideal candidate will possess proficiency in Python and Django, as these are critical to the role. Additionally, experience with JavaScript, JQuery, and various JS frameworks is highly desirable. If you are passionate about technology and eager to work in a collaborative environment, we would love to hear from you!

Join Sonsoft Inc. as a Lead Python Developer, where you will lead a team of talented developers in creating innovative software solutions. Your expertise in Python programming and leadership skills will contribute to our mission of delivering high-quality technology services. You will be responsible for overseeing project development, mentoring junior developers, and ensuring best practices are followed.

Join our dynamic team at Sonsoft Inc. as a Python Developer, where you will have the opportunity to work on innovative projects and develop cutting-edge solutions. We are looking for an individual who is passionate about technology and eager to contribute to the success of our clients. Your role will involve designing, developing, and maintaining robust applications using Python, collaborating with cross-functional teams to deliver high-quality software solutions.

Integrated Resources, Inc. is seeking a dynamic and experienced Director of Business Development to spearhead our growth initiatives. In this pivotal role, you will be responsible for identifying new business opportunities, forging strategic partnerships, and driving revenue growth in line with our corporate objectives. Your leadership will be essential in expanding our market presence and ensuring the successful execution of our business strategies.

Speechify creates tools to improve how people read and listen. The team is dedicated to making information easier to access and understand for all users. Role overview The Software Engineer - Platform Development position is based in Princeton, NJ. This role centers on building and maintaining the systems that support Speechify’s main products, which reach millions of users. The focus is on designing and implementing solutions that can scale as the company grows. What you will do Design and implement scalable features for core applications Work on backend systems that ensure reliability for Speechify’s products Support the growth and stability of platforms used by a large user base

About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific innovation into impactful solutions for underserved communities affected by neurological and rare diseases across the globe. Our commercial portfolio features the pioneering and sole FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are advancing the next generation of therapeutic breakthroughs with a robust pipeline that spans mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, alongside early-stage initiatives targeting other critical patient needs. At Acadia, we are committed to making a difference.This position is available in either San Diego, CA, or Princeton, NJ. Acadia operates on a hybrid model, requiring this role to be in the office an average of three days per week.

About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific advancements into impactful innovations for the global community facing neurological disorders and rare diseases. Our approved treatments for Parkinson's disease psychosis and Rett syndrome set us apart as pioneers in the field. With a dynamic pipeline that addresses critical needs in Alzheimer's disease psychosis and Lewy body dementia psychosis, as well as ongoing early-stage programs, we strive to be the difference for those we serve.Talent sought in: Princeton, NJ; San Diego, CAPosition OverviewThe Associate Director within the Early Stage Drug Product Development team at Acadia will lead the formulation development of pharmaceutical products intended for early-phase clinical trials and preclinical studies. This role will closely collaborate with drug discovery teams to identify optimal drug candidates through comprehensive physicochemical analysis and property assessment. Focused on early development strategies, the successful candidate will ensure that formulations are primed for initial safety and efficacy evaluations. Collaboration with both internal scientists and external partners is vital to overcoming technical challenges and advancing promising compounds to clinical readiness.Additionally, the role involves managing activities at Contract Service Providers (CSPs) and contributing to the resolution of complex technological issues, ensuring the selection of viable drug candidates, mitigating risks, and accelerating the introduction of new chemical entities into Acadia's pipeline.Key Responsibilities Design and develop pharmaceutical formulations to facilitate early-stage clinical trials, incorporating rapid development options such as on-site compounding.Assess and validate new drug product CSPs (Contract Service Providers) to support...

About Us Kardigan is a pioneering company dedicated to revolutionizing heart health by making cardiovascular diseases preventable and curable. Our mission is to develop a portfolio of targeted therapies that will provide effective treatments for individuals suffering from cardiovascular conditions. Founded by industry leaders Tassos Giannakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D., Kardigan emerged from their success with MyoKardia, where they played key roles in the discovery and development of mavacamten, the first cardiac myosin inhibitor, leading to a significant acquisition by Bristol Myers Squibb in 2020. We boast a state-of-the-art discovery and translational research platform, a robust pipeline of late-stage candidates, and an exceptional team committed to enhancing patient outcomes. At Kardigan, our core values shape every aspect of our work and interactions. We are driven by patients and their families, prioritizing their needs above all. We uphold a principle of authenticity, fostering an environment where everyone feels valued and accepted. Our curiosity fuels our eagerness to learn and adapt, while we emphasize team success through collaboration, urgency, and excellence. We dare to enable the impossible, taking calculated risks to drive innovation and scientific breakthroughs for the benefit of patients. These values empower us to make meaningful contributions every day. Position Title: Associate Director, Drug Substance Development Department: Technical Operations - Drug SubstanceReports To: Vice President, Head of Drug SubstanceLocation: Princeton, NJ...

We are seeking a highly experienced and strategic Senior Director of Drug Substance Development to lead our innovative team at Kardigan in Princeton, New Jersey. In this pivotal role, you will spearhead the development of drug substances from early-stage formulation through to commercialization, ensuring that our products meet the highest standards of quality and efficacy. The ideal candidate will possess a deep understanding of drug development processes, project management, regulatory requirements, and cross-functional collaboration. You will drive initiatives that enhance productivity and foster a culture of scientific excellence, providing mentorship and guidance to team members.

About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific potential into innovative solutions that significantly benefit underserved communities dealing with neurological and rare diseases globally. Our current commercial portfolio features the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are actively developing a diverse pipeline of therapeutic advancements, which includes mid- to late-stage programs targeting Alzheimer's disease psychosis and Lewy body dementia psychosis, alongside earlier-stage initiatives aimed at addressing various unmet patient needs. At Acadia, our mission is to make a difference in the lives of these patients.Seeking talent near: Princeton, NJPosition SummaryThe Associate Director of Drug Product Development will lead the formulation, primary packaging, and manufacturing process development for Acadia’s expanding portfolio of drug candidates across all development phases. This role involves providing technical oversight, expertise, and guidance for outsourced drug product development activities. The responsibilities encompass the development of formulations, packaging, and processes for various administration routes, including oral solid, liquid, and injectable dosage forms, managing candidates from clinical development through to process validation and lifecycle management. The successful candidate will oversee activities related to these tasks at Contract Service Providers (CSPs) and play a pivotal role in addressing complex technological challenges while implementing new manufacturing technologies for products intended for clinical and commercial distribution. This position is vital for optimizing development, mitigating risks, and expediting the launch of new assets into the market.Primary ResponsibilitiesDesign and develop pharmaceutical formulations and manufacturing processes to support clinical trials, regulatory submissions, and product launches.Evaluate and validate new drug product Contract Service Providers (CSPs) to facilitate development, scaling, and commercialization of new drug candidates within Acadia’s pipeline. Initiate and manage supplier contract agreements as necessary.