JOB OVERVIEW

We are seeking a highly skilled and experienced Senior Network Specialist and Solution Architect and System administrator for an enterprise healthcare client to carry on specific project for them. The ideal candidate will be responsible for designing, implementing, and maintaining their network infrastructure while ensuring optimal performance and security. This role requires a deep understanding of network protocols and technologies, as well as the ability to troubleshoot complex network issues.

CORE SKILLS (ESSENTIAL REQUIREMENTS)

These are the foundational skills required to perform the role effectively.

ASSETS / NICE-TO-HAVE SKILLS

These skills are beneficial and add significant value but are not strictly essential core requirements for the architecture/design focus of the role.
· Specific Domain Expertise:
o Hands-on experience operating, maintaining, or troubleshooting specific manufacturing/lab equipment, such as packaging lines (e.g., Uhlmann, IMA), scientific instrumentation (e.g., spectrophotometers, scanners, analyzers), or process equipment (e.g., dryers, washers).
· Specific System/Software Experience:
o Experience with various manufacturing/lab systems and platforms, potentially including:
§ PLC/HMI/SCADA Systems: In-depth programming and advanced troubleshooting (e.g., iFix, Raft).
§ Lab Software: Configuration and management (e.g., LabX Server, Chromeleon, Raman Scanner software, AA software).
§ Integration Platforms: Experience with tools like Kepware for protocol conversion and data aggregation.
§ Thin Client Management: Familiarity with systems like ThinManager.
§ Data Transfer/Storage: Experience with platforms like FTPS for EBR/eLogs.
§ Serialization Systems: Implementation or management (e.g., Optel Line Master).
§ Document Management Systems: (e.g., Sotax Qdoc).
§ Other Systems: BMS, RFID, ERP/MES integrations.
§ Security Tools: Familiarity with standard endpoint security stacks (Threat Detection / Anti-Virus) and specific OT threat detection tools like Claroty.
· Compliance & Process Familiarity:
o GxP & Regulations: Strong understanding of GxP regulations, particularly FDA 21 CFR Part 11 and ALCOA+ principles for electronic records, signatures, and audit trails in manufacturing/lab environments.
o Data Integrity: Deep knowledge of data integrity principles, policies, and risk assessment procedures applicable to OT systems.
o Validation Lifecycle Support: Understanding the validation lifecycle (VMP, IQ, OQ, PQ) and providing necessary design documentation (URS, DS) and technical expertise to support the Infrastructure Qualification (IQ) phase for OT systems.
o Change Management: Strict adherence to formal change control processes for regulated environments.
o Regulatory Standards: Familiarity with relevant standards (e.g., FDA, EU GMP, ISO) for regulated environments.
o Project Management: Experience in managing or coordinating OT-related projects or workstreams.
o Advanced Documentation Skills: Demonstrated excellence in creating clear, concise, and comprehensive technical documentation beyond core requirements.
Job Type: Full-time
Pay: $71,549.85-$127,687.19 per year

Application question(s):

• Do you have past experience working in Manufacturing in Healthcare industry?

Work Location: In perso

Please refer the Job description for details