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Generis Tek Inc

Generis Tek Inc

www.generistek.com

7 Jobs

41 Employees

About the Company


Generis Tek is an elite IT staffing firm headquartered in Chicago, IL offering long-term, short-term, temporary-to-permanent and direct placement staffing. Our team has 15 years of experience providing talented professionals to several Fortune 1000 clients.

We at Generis Tek very highly value our relationship with our consultants. Our dedicated professionals help consultants reach their career objectives. We provide a competitive, fast-paced environment that promotes open communication to form a long term relationship built on mutual understanding, respect and trust. What sets us apart is the high level of service we provide to our clients after each employee is placed.

Our client relationships are backed by unparalleled understanding of workforce strategies, industry insight and expertise. As a trusted partner that has a strong recruiting focus, clients look at Generis Tek to meet their Talent acquisition needs. Our fundamental success lies in understanding our clients' specific needs and working very closely with our consultants to create a right fit for both sides.

Our business heavily relies on technology that gives a seamless solution to our clients and consultants. We offer our client intelligence about the talent market which helps them in their decision making and formulating workforce strategies at an optimum cost. We aspire to be our clients most trusted business partner.

Listed Jobs

Company background Company brand
Company Name
Generis Tek Inc
Job Title
Filenet developer/administrator-Hybrid
Job Description
Job Title: Filenet Developer/Administrator Role Summary: Design, develop, and maintain Java applications that interact with IBM FileNet P8 and KnowledgeLake ECM environments, build and customize workflow components, and support data migration and high‑availability operations. Expectations: 3+ month contract, hybrid work model, hourly rate $70‑72, W2 employment. Key Responsibilities: • Develop Java programs using FileNet P8 and KnowledgeLake APIs for CRUD operations on documents. • Design and implement workflow maps, queues, and subscriptions in FileNet P8 (Content Platform Engine / Process Engine). • Configure and integrate scanning/indexing solutions (IBM DataCap, Kofax AutoStore, KnowledgeLake Capture Professional). • Migrate and ingest data from multiple sources into FileNet P8 and KnowledgeLake platforms. • Troubleshoot and resolve issues in highly available, clustered FileNet environments, including SSL certificate management. • Conduct demos and provide technical guidance to ECM staff. • Perform system administration tasks and support cloud technologies. • Participate in business analysis and project design activities. Required Skills: • Java development with FileNet P8 and KnowledgeLake APIs. • Experience with FileNet P8 Content Platform Engine, Process Engine, Content Navigator. • Knowledge of KnowledgeLake API and ability to learn. • Familiarity with IBM WebSphere Application Server and application deployment. • Experience with SQL Server, DB2, Oracle relational databases. • Proficiency in scanning and indexing solutions (IBM DataCap, Kofax AutoStore, KnowledgeLake Capture). • Strong problem‑solving, analytical, and troubleshooting skills; log and trace analysis. • Basic .NET development knowledge is a plus. • Experience with Windows Server 2019+, Microsoft SQL Server 2019+, IBM WebSphere 8.55+, FileNet P8 5.x+. Required Education & Certifications: • Bachelor’s degree (or equivalent) in Computer Science, Information Technology, Mathematics, or related field.
Nashville, United states
Hybrid
02-03-2026
Company background Company brand
Company Name
Generis Tek Inc
Job Title
IoT-UI Developer
Job Description
Job Title: IoT-UI Developer Role Summary: Contract (11+ months, W2) position developing end‑to‑end IoT web applications, combining front‑end UI components with AWS cloud services and backend APIs. Expectations: Deliver scalable, secure, high‑performance web interfaces and microservices; collaborate cross‑functionally; maintain documentation and best practices. Key Responsibilities: - Design and develop full‑stack web applications using modern frameworks (React, Angular, Vue). - Build scalable REST and server‑less APIs with AWS Lambda, API Gateway, and related services. - Create responsive UI components with React or Angular, and implement client‑side logic in JavaScript/TypeScript. - Integrate Python UI frameworks (Tkinter, PyQt/PySide, Dash, Streamlit) for desktop or hybrid interfaces. - Optimize application performance, ensuring high availability, fault tolerance, and security. - Collaborate with UX designers, product managers, and QA to deliver quality releases. - Maintain technical documentation and contribute to knowledge sharing. Required Skills: - 3+ years of UI/Front‑end engineering experience. - Proficiency in React (preferred) or AngularJS, including component architecture and state management. - Strong JavaScript/TypeScript, HTML5, CSS3, responsive design. - Experience building backend/UI layers with Flask. - Knowledge of REST, asynchronous programming, and debugging across front/back ends. - Familiarity with Git, Webpack/Vite, npm/yarn, and Docker containerization. - Experience with AWS services (Lambda, API Gateway, S3, DynamoDB) and server‑less architecture. - Exposure to GraphQL, WebSockets, real‑time data handling, and monitoring tools (Datadog, New Relic, Prometheus). Required Education & Certifications: - Bachelor’s degree in Computer Science, Engineering, or related field. - AWS Certified Developer or Solutions Architect (preferred).
Lexington, United states
On site
Junior
04-03-2026
Company background Company brand
Company Name
Generis Tek Inc
Job Title
Cybersecurity Coordinator
Job Description
Job title: Cybersecurity Coordinator Role Summary: Provide end‑to‑end protection of digital assets across manufacturing, IT, engineering, and compliance functions; design secure architectures; conduct risk and threat assessments; implement and enforce cybersecurity controls; ensure compliance with industry and regulatory standards. Expectations: Deliver cybersecurity solutions on a 12+ month contract, maintaining robust posture for food and medical device manufacturing environments. Key Responsibilities: • Perform risk assessments, threat modeling (STRIDE), vulnerability assessments, and penetration tests. • Enforce compliance with ISO 27001, NIST SP 800‑82, FDA, HIPAA, GDPR, PCI DSS, SOX, and other applicable regulations. • Support internal/external audits, coordinate remediation, and integrate regulatory updates into policies. • Design secure system architectures with engineering teams; uphold secure coding and encryption practices across SDLC. • Monitor cyber‑threat landscape, develop mitigation strategies, and investigate incidents (root cause analysis, recovery). • Manage security technologies: firewalls, IDS/IPS, endpoint protection, DLP, SIEM, log aggregation. • Deploy and operate Governance, Risk, and Compliance (GRC) platforms. • Collaborate with cross‑functional teams and vendors to document and enforce controls, ensuring timely, budget‑aligned delivery. Required Skills: • 5+ years cybersecurity experience in regulated industries (food, beverage, healthcare, medical devices). • Expertise in threat modeling, risk management, vulnerability management, incident response, and secure SDLC. • Strong knowledge of cloud security (SSL/TLS, VPN, IPsec, secure cloud applications), network protocols, and secure hardware. • Proficiency with security frameworks (ISO 27001, NIST, SOC 2, HITRUST). • Ability to interpret and apply evolving cybersecurity regulations. Required Education & Certifications: • Bachelor’s degree in Computer Science, Engineering, Information Security, or related field. • CISSP, CISM, or equivalent certification preferred.
Columbus, United states
On site
Mid level
06-03-2026
Company background Company brand
Company Name
Generis Tek Inc
Job Title
Senior Clinical Data Coordinator
Job Description
**Job Title** Senior Clinical Data Coordinator **Role Summary** Coordinate and oversee Investigator Sponsored Study (ISS) data management activities. Capture, verify, and maintain clinical documentation, resolve data quality issues, and support regulatory compliance within a medical device/pharmaceutical environment. Works independently while collaborating with cross-functional teams to improve processes and ensure data integrity. **Expectations** * Manage ISS documentation within a 6‑month contract environment. * Demonstrate high proficiency in Microsoft Excel (pivot tables, formulas). * Exhibit strong written communication with minimal errors. * Learn and adapt quickly to study-specific systems and processes. * Maintain confidentiality and adhere to FDA and internal quality procedures. **Key Responsibilities** - Enter and verify incoming forms and data into the database accurately and on time. - Review, audit, and correct entered data; resolve discrepancies proactively. - Organize clinical documentation (forms, correspondence, supporting materials). - Identify data quality issues, perform root‑cause analysis, and recommend corrective actions. - Provide administrative support (mail merges, faxing, filing, data postings). - Communicate with customers to clarify missing or incomplete data. - Participate in process improvement initiatives and quality management programs (QMS, EMS). - Collaborate with field clinical engineers and study coordinators to resolve complex issues. **Required Skills** - Proficient with MS Office suite: Excel (advanced), Word, PowerPoint. - Strong accuracy, organizational and time‑management skills. - Ability to work under limited supervision and manage multiple concurrent projects. - Excellent written and verbal communication; strong grammar and proofreading. - Quick learner; comfortable with new software (I‑Envision, Concur, Contract Hub/Salesforce, Onit, OCR, Ariba). - Ability to handle confidential information with discretion. - Understand FDA regulatory requirements and relevant company processes. **Required Education & Certifications** - Some college coursework acceptable; bachelor’s degree preferred. - Experience in a clinical research or data management setting; ISS experience advantageous. - No specific certifications required, but familiarity with FDA, Good Manufacturing Practices (GMP) and related quality systems is a plus.
Pleasanton, United states
On site
Senior
09-03-2026