Lead Python Developer

Sonsoft Inc.Princeton

On-site Full-time

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Experience Level

Mid to Senior

Qualifications

Proven experience in Python developmentStrong leadership and team management skillsExperience with software development methodologiesExcellent problem-solving and analytical abilitiesFamiliarity with Agile frameworks

About the job

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.

About Sonsoft Inc.

Sonsoft Inc. is a leading technology solutions provider based in Princeton, New Jersey. We specialize in delivering innovative software solutions that empower businesses to achieve their goals. Our team is dedicated to providing exceptional service and driving technological advancements.

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Enterprise Solutions Quality Tester

Integrated Resources Inc.

Full-time|On-site|Princeton

Join our dynamic team as an Enterprise Solutions Quality Tester in Princeton, NJ. As a key player, you will be responsible for ensuring the quality and reliability of our enterprise software solutions. Your contributions will directly impact our ability to deliver exceptional products to our clients.

Mar 16, 2015

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Physical Therapist Assistant (PTA) at Gotham Enterprises | Princeton, NJ

Gotham Enterprises

Full-time|$70K/yr - $85K/yr|On-site|Princeton, New Jersey, United States

Join Our Team as a Physical Therapist Assistant (PTA)Location: Princeton, NJSchedule: Monday–Friday | 9:00 AM–5:00 PMCompensation: $70,000–$85,000/year + full benefitsPosition OverviewWe are seeking a dedicated Physical Therapist Assistant (PTA) to become part of our outpatient orthopedic clinic where patient-centric care is our top priority. In this role, you will facilitate patient recovery by providing tailored treatments under the guidance of a licensed Physical Therapist. Our team emphasizes achieving excellent clinical outcomes, maintaining ethical caseloads, and fostering a supportive, collaborative environment that prioritizes both exceptional care and professional development.New graduates are encouraged to apply!Key ResponsibilitiesImplement skilled interventions under the supervision of a licensed Physical Therapist according to the established care plan.Administer PTA-specific treatments including therapeutic exercises, functional training, neuromuscular re-education, balance and gait training, and other scope-appropriate interventions.Accurately document patient information in the EMR in compliance with clinic policies and payer requirements.Communicate patient progress, clinical observations, and any changes to the supervising Physical Therapist.Educate patients on home exercises, movement strategies, and the proper use of equipment to promote safe independence.Adhere to New Jersey practice regulations, APTA ethical standards, and documentation requirements set by Medicare and private insurance.Contribute to maintaining a clean, organized, and professional clinical environment.Engage in team meetings and clinic initiatives as appropriate.QualificationsGraduation from a CAPTE-accredited PTA program.A valid New Jersey PTA license (or eligibility pending).Current CPR certification.Exceptional communication skills, professionalism, and a patient-focused approach.A reliable, team-oriented mindset committed to maintaining high standards of care.BenefitsSign-on Bonus: Up to $7,500 for full-time PTA roles, based on experience and commitment, distributed through structured retention milestones.401(k) plan with company matching.Comprehensive health, dental, and vision insurance.Generous paid time off and six paid national holidays.Continuing education support.If you're searching for a clinic that values outstanding patient care and a supportive team culture, we invite you to apply. Submit your CV today for consideration!

Mar 6, 2026

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Associate Director of Clinical Quality Management

Kyowa Kirin, Inc.

Full-time|$190K/yr - $190K/yr|On-site|Princeton, New Jersey

Join Kyowa Kirin, a rapidly expanding global specialty pharmaceutical company, committed to innovating life-changing medicines through cutting-edge biotechnologies. We focus on four key disease areas: bone and mineral disorders, intractable hematologic conditions, hematology oncology, and rare diseases. Our mission is to convert scientific advancements into therapeutic solutions, ensuring that patients receive the care they need when existing treatments fall short. Our North America headquarters is based in Princeton, NJ, with additional offices in California, North Carolina, and Mississauga, Ontario.Position Overview:The Associate Director of Clinical Quality Management acts as the primary Risk-Based Quality Management (RBQM) Lead within Clinical Operations. This pivotal role oversees proactive risk management strategies across clinical trials, implementing a comprehensive RBQM framework that encompasses risk identification, assessment, mitigation, centralized monitoring, lessons learned, and the upkeep of a clinical risk library. This ensures uniform risk management practices across studies, programs, vendors, and regions. Collaborating with various departments, this role integrates risk-based decision-making into all aspects of study design, execution, oversight, and continuous enhancement, in accordance with ICH E6 (R3), GCP, and global regulatory standards.

Feb 3, 2026

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Senior Solutions Architect

Ensono

Full-time|$151K/yr - $204K/yr|On-site|Princeton, NJ

Join Ensono as a Senior Solutions Architect!At Ensono, we are dedicated to being an unyielding ally, challenging conventional norms, and empowering our clients to achieve extraordinary results! Our mission is to help clients realize transformative business outcomes that redefine global operations. As a leading technology advisor and managed service provider with comprehensive cross-platform certifications, we equip our clients to navigate continuous change and embrace innovation.We thrive because of our exceptional team members. Our core values—Honesty, Reliability, Curiosity, Collaboration, and Passion—form the foundation of how we conduct business and achieve our mission.About the Role:We are in search of a seasoned Solutions Architect with extensive knowledge of AWS, Nutanix on AWS (NC2), and enterprise security and observability solutions. Your role will involve designing, constructing, and modernizing robust, secure cloud and hybrid solutions.This pivotal position is essential for migrating workloads from on-premises data centers to AWS, facilitating standardized cloud solutions, and integrating automation, security, and monitoring capabilities. You will collaborate with various teams—Infrastructure, Application, Security, and Operations—to deliver resilient, compliant, and cost-effective solutions on an enterprise scale.

Apr 10, 2026

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Managing Consultant, Air Quality

Ramboll

Full-time|On-site|Princeton

Join our dynamic team at Ramboll as a Managing Consultant in Air Quality, where you will leverage your expertise to drive impactful environmental solutions. In this pivotal role, you will lead projects that enhance air quality standards, working closely with a diverse range of clients including governmental agencies and private sector organizations.Your responsibilities will include developing innovative strategies, collaborating with multidisciplinary teams, and ensuring compliance with regulatory frameworks. This position offers a unique opportunity to make a significant difference in environmental management and public health.

Feb 3, 2026

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Physical Therapist Assistant (PTA)

Gotham Enterprises

Full-time|$70K/yr - $85K/yr|On-site|Princeton, New Jersey, United States

Join Our Team as a Physical Therapist Assistant (PTA)!Position Type: Full-TimeLocation: Princeton, NJSchedule: Monday–Friday | 9:00 AM–5:00 PMCompensation: $70,000–$85,000/year + Comprehensive BenefitsAbout the RoleWe are looking for a dedicated Physical Therapist Assistant (PTA) to enhance patient care at our outpatient orthopedic clinic. In this role, you will play a crucial part in our patients' rehabilitation journey by providing skilled treatments under the guidance of a licensed Physical Therapist. Our clinic prides itself on delivering excellent clinical outcomes, maintaining manageable caseloads, and fostering a collaborative team environment that emphasizes quality care and professionalism.New graduates are warmly welcomed to apply!Key ResponsibilitiesDeliver physical therapy interventions as directed by a licensed Physical Therapist, adhering to the established care planAdminister treatments within the PTA's scope of practice, including therapeutic exercises, functional training, neuromuscular re-education, and orthopedic-focused interventionsTrack patient progress and relay clinical observations to the supervising Physical TherapistGuide patients on home exercise routines, safe movement techniques, and equipment usageAccurately document patient treatments, responses, and progress in the EMR, following clinic policies and payer guidelinesComply with New Jersey practice regulations, APTA ethical standards, and Medicare/private insurance documentation rulesContribute to a clean, organized, and professional clinical workspaceEngage in team meetings and clinic initiatives as neededQualificationsGraduate from a CAPTE-accredited Physical Therapist Assistant programPossession of an active New Jersey PTA license (or pending eligibility)Current CPR certificationExceptional communication skills and a professional approach to patient careDependable, team-oriented attitude with a commitment to maintaining high standardsBenefits We OfferSign-on Bonus: Up to $7,500 for full-time PTA positions, based on experience and commitment, paid through structured retention milestones401(k) with company matchingHealth, dental, and vision insuranceGenerous paid time off and six paid national holidaysSupport for continuing educationInterested candidates are encouraged to submit their CV today!

Mar 9, 2026

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Principal Air Quality Specialist

Ramboll

Full-time|On-site|Princeton

Join our dynamic team at Ramboll as a Principal Air Quality Specialist. In this pivotal role, you will leverage your extensive expertise in air quality management to lead innovative projects that enhance environmental performance and compliance. Collaborate with a diverse team of professionals to develop sustainable solutions that address complex air quality challenges.Your contributions will be vital in shaping our approach to air quality assessments, regulatory compliance, and stakeholder engagement. As a leader in the field, you will have the opportunity to mentor junior staff and contribute to the development of best practices within the industry.

Mar 18, 2026

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Senior Consultant - Air Quality Expertise

Ramboll Group

Full-time|On-site|Princeton, New Jersey

Join Ramboll as a Senior Consultant specializing in Air Quality, where your expertise will directly contribute to environmental sustainability. In this pivotal role, you will leverage your analytical skills to assess air quality data and formulate strategies aimed at improving air quality standards. Collaborate with a dynamic team of professionals dedicated to advancing environmental solutions.

Apr 10, 2026

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Senior Managing Consultant - Air Quality

Ramboll

Full-time|On-site|Princeton

Join Ramboll as a Senior Managing Consultant for Air Quality, where you will play a pivotal role in driving sustainable solutions in air quality management. You will collaborate with a diverse team of experts and contribute to innovative projects that address critical environmental challenges. Your expertise will help shape strategies to improve air quality and promote sustainable practices.

Mar 18, 2026

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Manager, R&D Quality Assurance - GCP

Kyowa Kirin, Inc.

Full-time|$155K/yr - $170K/yr|On-site|Princeton, New Jersey

Join Kyowa Kirin, a rapidly expanding global specialty pharmaceutical company dedicated to harnessing cutting-edge biotechnologies to innovate and provide groundbreaking therapies across four critical disease areas: bone and mineral disorders; intractable hematologic conditions; hematology oncology; and rare diseases. With our headquarters located in Princeton, New Jersey, and additional offices in California, North Carolina, and Mississauga, Ontario, we are committed to translating scientific advancements into meaningful treatments, addressing unmet medical needs from drug discovery through to product development and commercialization.Position Summary:The Manager of R&D Quality Assurance will oversee Quality Assurance systems and processes, conducting comprehensive internal and external audits, and ensuring adherence to global standards of quality. This role is crucial in supporting the QA program to ensure the accuracy and integrity of scientific data submitted to regulatory authorities for new drug applications and biological licensing agreements. You will collaborate closely with the R&D teams to provide essential quality insights.Key Responsibilities:Act as the primary liaison for GCP/GLP quality concerns, offering continuous feedback to management on potential quality risks. Engage in clinical trials through independent review and approval of deviations and CAPAs, GCP guidance, and the preparation of quality agreements.Conduct and document assigned GCP/GLP audits of clinical investigator sites, vendors/CROs, internal systems, and clinical data/documents.Prepare timely, high-quality audit reports; assess audit responses; and supervise CAPA development, implementation, and tracking in accordance with corporate standards.Maintain in-depth knowledge of global GCP/GLP regulations and industry standards. Serve as a subject matter expert for internal teams, interpreting regulatory requirements, and actively contributing to the Regulatory Intelligence program.Design and deliver GCP training sessions to enhance compliance awareness and foster a culture of quality across the organization.Support continuous improvement initiatives by developing, revising, and managing SOPs and controlled documents, ensuring effective maintenance within quality document management systems.Participate in Health Authority inspections for domestic and international projects as required.

Feb 18, 2026

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Microsoft Dynamics CRM Solution Architect

Sonsoft Inc.

Contract|On-site|Princeton

We are seeking a talented and experienced Microsoft Dynamics CRM Solution Architect to join our dynamic team at Sonsoft Inc. In this role, you will leverage your expertise in Microsoft Dynamics CRM to design, implement, and optimize solutions that meet our clients’ needs. You will work collaboratively with cross-functional teams to deliver high-quality solutions that enhance customer relationship management processes.

Jul 21, 2017

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Business Information Solutions Consultant

Coface

Full-time|On-site|Princeton

Join Coface as a Business Information Solutions Consultant, where you will leverage your analytical skills and industry knowledge to provide innovative solutions that empower our clients. You will work closely with cross-functional teams to deliver exceptional service and insights, ensuring our clients achieve their business objectives efficiently.

Apr 8, 2026

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Associate Director of GLP/GCP Quality Audits and Compliance

Acadia Pharmaceuticals

Full-time|$145.2K/yr - $181.5K/yr|Hybrid|Princeton, New Jersey, United States; San Diego, California, United States; San Francisco, California

About Acadia Pharmaceuticals At Acadia Pharmaceuticals, we are dedicated to transforming scientific breakthroughs into impactful solutions for underserved populations affected by neurological and rare diseases globally. Our portfolio features the first and only FDA-approved therapies for Parkinson’s disease psychosis and Rett syndrome. We are advancing innovative treatments through a diverse pipeline, including programs targeting Alzheimer’s disease psychosis and Lewy body dementia psychosis. At Acadia, we strive to be the difference for those in need.Please be aware that this role can be located in San Diego, CA; Princeton, NJ; or San Francisco, CA. Acadia operates under a hybrid work model, requiring in-office attendance three days per week on average. Position OverviewThe Associate Director of GLP/GCP Quality Audits and Compliance is pivotal in safeguarding data integrity and ensuring regulatory compliance across the company's nonclinical and clinical operations. This role encompasses the planning, execution, and reporting of both internal and external GLP/GCP audits, ensuring adherence to U.S. and international regulations while promoting ongoing enhancements in quality systems.As a valued quality partner, this role will provide expert advice on GLP/GCP compliance, assist in regulatory inspections, and collaborate closely with internal teams and Contract Service Providers (CSPs) to sustain inspection-ready operations. The ideal candidate will possess strong audit leadership skills, sound regulatory judgment, and the ability to positively influence quality practices throughout the organization.Key ResponsibilitiesPlan, schedule, coordinate, and conduct internal and external GLP/GCP audits of company functions and Contract Service Providers (CSPs) according to company standards and global regulatory requirements.Manage the complete audit lifecycle, including preparation, execution, documentation, reporting, follow-up, and validation of corrective and preventive actions.Prepare, review, and approve clear, compliant audit reports, ensuring that observations, risks, and responsibilities are effectively communicated to relevant stakeholders.

Feb 11, 2026

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Managing Consultant in Air Quality Compliance & Permitting - Chemical/Pharmaceutical Sector

Ramboll

Full-time|On-site|Princeton

Join Ramboll as a Managing Consultant focusing on Air Quality Compliance and Permitting within the Chemical and Pharmaceutical sectors. In this role, you will leverage your expertise to guide clients in navigating complex environmental regulations, ensuring compliance, and implementing effective air quality management strategies. Your analytical skills and industry knowledge will contribute to impactful projects that promote sustainable practices and environmental stewardship.

Mar 10, 2026

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Senior Manager, IT Business Analyst - Development & Quality

Kardigan

Full-time|$171K/yr - $223K/yr|On-site|Princeton, New Jersey, United States

Kardigan is dedicated to improving heart health by pursuing both prevention and cures for cardiovascular disease. The company aims to develop several targeted treatments at once, ensuring people with cardiovascular conditions have more options for care. Founded by Tassos Gianakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D., Kardigan's leadership previously led MyoKardia to discover and develop mavacamten, the first cardiac myosin inhibitor, which was acquired by Bristol Myers Squibb in 2020. Today, the team continues to advance cardiovascular medicine through a strong research platform and a late-stage pipeline focused on patient outcomes. Our Values Patient-centric: Every decision starts with the needs of patients and their families. Authenticity: Honesty and acceptance shape the work environment. Curiosity: Learning and adapting are part of daily work. Collaborative success: Team members support each other, no matter their role. Unlocking innovation: The team embraces risk to advance care, knowing patients depend on progress. These values guide daily work and reflect the impact the team aims to achieve.

Apr 20, 2026

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QUMAS Consultant

Sonsoft Inc.

Contract|On-site|Princeton

Join our dynamic team at Sonsoft Inc. as a QUMAS Consultant, where you will play a crucial role in enhancing our clients' regulatory compliance and quality management systems. As an integral part of our consulting team, you will leverage your expertise to implement effective QUMAS solutions, ensuring that our clients meet industry standards and regulations. This position offers an exciting opportunity to work with cutting-edge technology and contribute to the success of various projects.

Jan 18, 2017

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Associate Director, ERP Functional & Solutions Architect - D365

Kyowa Kirin, Inc.

Full-time|$165K/yr - $190K/yr|On-site|Princeton, New Jersey

Kyowa Kirin is a rapidly expanding global specialty pharmaceutical company leveraging advanced biotechnologies to discover and deliver groundbreaking medicines across four key disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare diseases. Headquartered in Princeton, NJ, with additional offices in California, North Carolina, and Mississauga, Ontario, our mission is to transform scientific innovation into therapeutic solutions where effective treatments are currently lacking.Position Overview:The Associate Director, ERP Functional & Solutions Architect, ICT will play a pivotal role in managing the Microsoft Dynamics 365 (D365) Enterprise Resource Planning (ERP) system within our organization. This position is essential for implementing business process enhancements and ensuring the ERP system operates at peak functionality. The role involves planning, designing, configuring, and customizing MS D365/ERP modules and functionalities, ensuring they integrate seamlessly with existing systems while adhering to industry standards, security protocols, and regulatory requirements. As a business process analyst, the Associate Director will collaborate closely with various corporate functions including Supply Chain Management, Manufacturing, Quality, Finance, Human Resources, Legal, Compliance, and Procurement to ensure the successful development and delivery of technical solutions.Key Responsibilities:The D365 ERP F&O Functional Architect will oversee the comprehensive functional design, configuration, and optimization of Microsoft Dynamics 365 Finance & Operations, supporting business functions across Finance, Procurement, Supply Chain, Manufacturing, and Quality. This role will involve partnering with business stakeholders, technical teams, and implementation partners to align solutions with corporate strategies, ensure compliance with applicable GxP/GAMP 5 standards, and facilitate scalable solutions for future growth.Solution Architecture & Design:Lead the functional design and architecture of the D365 F&O solution across critical modules including Finance, Supply Chain, Manufacturing, Procurement, Inventory, and Quality. Translate complex business requirements into clear, scalable, and compliant functional solutions, emphasizing proactive leadership in solution architecture aligning with business objectives.

Mar 2, 2026

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Network Automation Application Developer - Contract Position

USTech Solutions

Contract|On-site|Princeton

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.

Jun 8, 2016

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Lead Python Developer

Sonsoft Inc.

Full-time|On-site|Princeton

Apr 26, 2017

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Product Event Demonstrators in Princeton, NJ

Crossmark

On-site|On-site|Princeton

Join our dynamic team as a Product Event Demonstrator in Princeton, NJ! In this engaging role, you will have the opportunity to showcase and promote various products at events, assisting customers in understanding their benefits and features. Your enthusiasm and communication skills will play a crucial role in enhancing the customer experience and driving product sales.

Nov 23, 2016

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