Python Developer (Automation) at Sonsoft Inc. | Princeton

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.

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.

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 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.

Join our dynamic team at Sonsoft Inc. as a Python Developer! We are looking for talented individuals who are passionate about coding and eager to contribute to innovative projects. If you are a U.S. citizen or a Green Card holder with a solid foundation in Python, we invite you to apply and be part of our tech-driven environment.

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.

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.

About UsKardigan is an innovative heart health company dedicated to transforming the landscape of cardiovascular disease, making it preventable and curable, and ultimately eliminating it as the leading cause of death worldwide.Our mission is to develop a range of targeted treatments simultaneously to ensure that individuals suffering from cardiovascular diseases receive the cures they truly deserve.Founded by experts Tassos Giannakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D., who previously led MyoKardia in the groundbreaking development of mavacamten—the first cardiac myosin inhibitor acquired by Bristol Myers Squibb in 2020—we have established a state-of-the-art discovery and translational research platform paired with a robust pipeline of late-stage candidates. Our team is passionately committed to enhancing patient outcomes.At Kardigan, our core values guide our operations and interactions. We are driven by patients and their families, authentically engaging with each other to foster a supportive work environment. Our eagerness to learn fosters curiosity and adaptability. We believe in winning as a team, demonstrating urgency and excellence, and supporting one another regardless of our roles. We also strive to enable the impossible, taking calculated risks to unlock innovation and promote scientific advancements.

Kardigan seeks a Vice President of Clinical Development for Tonlamarsen (TLA), based either in South San Francisco, CA or Princeton, NJ. This position reports directly to the Chief Medical Officer and is part of the Development department. The role is on-site four days a week, Monday through Thursday. Role overview This leadership position focuses on guiding the clinical development of Tonlamarsen (TLA), a key candidate in Kardigan’s late-stage pipeline. The Vice President will play a central role in advancing targeted therapies for cardiovascular disease, supporting Kardigan’s mission to transform heart health and improve patient outcomes. Work environment The role is embedded in a team known for its track record in cardiovascular drug development, including leadership with experience from MyoKardia and the successful development of mavacamten. Collaboration, urgency, and a patient-centered approach shape daily work. The company values authenticity, curiosity, and team success, aiming to achieve significant impact for patients with cardiovascular conditions. Location and schedule South San Francisco, California or Princeton, New Jersey On-site presence required Monday through Thursday

We are seeking a skilled Network Automation Application Developer to join our team on a contract basis. In this role, you will be responsible for developing and implementing automation solutions for network management and operations. This is an exciting opportunity to work with cutting-edge technologies and contribute to the efficiency of our network systems.

Join Prosidian Consulting as a Senior Executive Coach and lead transformative coaching initiatives that empower executives and enhance leadership capabilities. In this pivotal role, you will collaborate with senior leaders to foster growth, drive strategic objectives, and cultivate high-performance cultures.As a senior coach, you will utilize your extensive experience to provide tailored coaching solutions, deliver impactful workshops, and support leaders in navigating complex challenges. Your ability to inspire trust and foster meaningful relationships will be essential in driving positive change within organizations.

About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific potential into innovative solutions that significantly benefit underrepresented communities facing neurological and rare diseases globally. Our commercial offerings include the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are at the forefront of developing a new wave of therapeutic innovations with a robust pipeline that encompasses mid- to late-stage programs targeting Alzheimer’s disease psychosis and Lewy body dementia psychosis, as well as earlier-stage programs addressing various unmet patient needs. At Acadia, our mission is to make a tangible difference in patients' lives.We are seeking talent near: Princeton, NJ; San Diego, CAPosition SummaryThe Senior Manager of R&D Learning & Development plays a pivotal role in designing, implementing, and continuously refining onboarding and training strategies, systems training, and learning processes aimed at enhancing scientific, operational, and future-ready capabilities within the Research and Development organization and its pipeline.Primary ResponsibilitiesContribute to the design, implementation, and ongoing enhancement of a comprehensive onboarding and capability-building curriculum that aligns with the dynamic needs of the R&D pipeline, covering discovery, early development, and late-stage programs.Employ experiential learning methodologies to effectively engage adult learners and facilitate successful knowledge transfer.Assist in managing GxP, congress, and data training in collaboration with internal stakeholders.Work collaboratively with R&D subject matter experts to develop focused training on disease areas, modalities, platforms, and pipeline initiatives, including education on investigational assets and emerging scientific advancements.Lead and support training initiatives in partnership with internal stakeholders.Facilitate the management and development of learning modules in collaboration with external vendors.Oversee the creation of advanced, recurrent, and future-focused training materials.

Kyowa Kirin is an innovative and rapidly expanding global specialty pharmaceutical company that leverages cutting-edge biotechnologies to discover and deliver groundbreaking medicines across four key therapeutic areas: bone and mineral, intractable hematologic conditions, hematology oncology, and rare diseases. Headquartered in Princeton, New Jersey, we pride ourselves on our mission to transform scientific advancements into impactful therapies, particularly in areas where treatment options are limited. Our North American operations extend across various locations, including California, North Carolina, and Mississauga, Ontario.Position Overview:The Senior Director of GRA Development & Product Strategy Team Lead will spearhead the formulation and execution of regulatory strategies while leading a talented team and overseeing global projects. This pivotal role includes managing a team of Global Regulatory Leads (GRLs) and may involve acting as a Regional Regulatory Lead (RRL) as dictated by business needs.Key Responsibilities:Develop and implement comprehensive global regulatory strategies for all products within the designated disease area, ensuring alignment with corporate objectives and maximizing the value of products.Lead and cultivate a high-performing team of Global Regulatory Leads (GRLs), providing direction and building capabilities to foster an accountable culture.Integrate regulatory strategies into global product development and lifecycle plans in close collaboration with cross-functional partners.Ensure the successful execution of regulatory strategies, encompassing global submissions, approvals, and post-approval activities for assigned products and projects.Represent the organization in engagements with health authorities, leading negotiations and overseeing agency meeting strategies.Oversee and approve global regulatory submission plans, including marketing applications and key lifecycle deliverables.Coordinate regulatory activities, timelines, and deliverables across internal teams and external partners to ensure timely execution.Maintain compliance with global regulatory requirements and internal policies, supporting inspections and audits.Monitor and communicate regulatory risks, emerging trends, and competitive intelligence, recommending mitigation strategies as necessary.Drive operational excellence by leading process improvements and standardization efforts.