Cybersecurity
Security staffing, assessments, audits, and recovery planning.
South 6 staffs cybersecurity roles and runs the assessment work that tells you which roles you need. Our consultants hold active certifications across Microsoft, Oracle, Dell/RSA, VMware, Cisco, and IBM. Most placements are contract or contract-to-hire, which means people start in days rather than at the end of a normal recruiting cycle.
Security Staffing
We place security architects, forensic analysts, network engineers, and cloud security engineers on contract, contract-to-hire, and direct-hire terms. The bench skews senior, including CISSP-credentialed practitioners who run threat emulation and incident response in the field. Roles span Microsoft 365 and Azure, Oracle, Dell/RSA, VMware, and Cisco environments, from a single specialist covering a gap to a full team standing up a monitoring practice.
Security and
Threat Assessments
An assessment finds the vulnerabilities in your environment, ranks them by what they would actually cost you, and tells you what to fix first. Ours go past automated malware and virus scanning to look at configuration, access control, and the gaps between systems. You get a prioritized list of recommendations you can act on, not a raw scanner dump.
System Audits
An IT system audit examines the management controls inside your infrastructure and gathers the evidence to prove they work. We check whether your safeguards protect the assets they are supposed to protect, and whether your data holds its integrity end to end.
Disaster Recovery
Disaster recovery is the plan, the tools, and the procedures that get you running again after an outage, a natural disaster, or a cyberattack. We help write the plan and staff the people who execute it. The starting question is how long your business can run without its systems, because that number determines everything else in the plan.
REGULATORY AND COMPLIANCE: LIFE SCIENCES
South 6 places quality assurance managers, regulatory affairs associates, and validation engineers with pharmaceutical, biotechnology, and medical device companies. Consultants work independently under your direction or fill gaps on an existing team. The work maps to FDA, CE Marking, and ICH requirements.
REGULATORY AFFAIRS
510(k) submissions, PMAs, IDEs, adverse event reports, remediation and resolution management, technical papers, complaint handling.
QUALITY ENGINE
Complete quality systems: CAPA, change control, deviation and complaint management, document control, training. Gap and risk assessment. Recalls and MDRs. Auditing against Part 11, quality systems, vendors, and IT compliance.
VALIDATION
SOPs, validation master plans, and IQ/OQ/PQ protocols. Execution and reporting across computer systems, software, process, cleaning, methods, facilities and utilities, equipment, IT infrastructure, and 21 CFR Part 11.
STATISTICAL ANALYSIS
Design and analysis across all phases of clinical trials, from planning through study completion and reporting.
Tell us the role or the project, and we will come back with people who have done it before.