MEDVACON LIFE SCIENCES, LLC Tech Stack

FDA compliance consulting and validation services for pharma manufacturers

Pharmaceutical Manufacturing Sparta, NJ 51–200 employees Founded 2012 Privately Held

MEDVACON provides FDA quality compliance and technical consulting to life sciences manufacturers. The tech stack reveals a regulatory-operations-first organization: SolidWorks and JMP for engineering/statistical work, SAP and LIMS for manufacturing systems, and heavy reliance on spreadsheets and document management (Excel, Word, SharePoint, Nitro). Active hiring is concentrated in engineering (8 roles) and skews senior (12 of 19), suggesting customer-facing validation engagements and internal scaling of complex compliance projects rather than entry-level hiring.

Tech Stack 18 technologies

Core StackSolidWorks Zoom SAP Smartsheet JMP Excel LIMS Teams ImageJ GraphPad Prism Microsoft Office JazzHR SharePoint Nitro Ariba Word PowerPoint

What MEDVACON LIFE SCIENCES, LLC Is Building

◆Challenges

Patient safety risk
Risk to product quality
Optimizing tmf and rim processes
Identifying gaps in regulatory workflows
Automation of clinical regulatory processes
Ensuring compliance of statistical analysis processes
Securing excel spreadsheets
Conducting onsite ioq protocols
Bimo inspection modernization
Bimo compliance consolidation

▲Active Projects

Validation protocol development
Full scope gmp audit
Clinical packaging audit
Ioq protocol execution
Jsl unit testing framework implementation
Bimo inspection modernization
Risk-based prioritization validation
Stability study design and execution
Stability protocol review
Digital tools implementation

Hiring Activity

Accelerating20 roles · 9 in 30d

Department

Engineering

Healthcare

Manufacturing

Quality

Compliance

Legal

Ops

Product

Seniority

Senior

Mid

Junior

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About MEDVACON LIFE SCIENCES, LLC

MEDVACON is a consulting firm based in Sparta, NJ that serves life sciences and pharmaceutical manufacturers seeking FDA compliance and operational quality improvements. Their service portfolio spans validation protocol development, quality systems design, IT/software validation, audit preparation and response, tech transfers, and training. The company operates at the intersection of manufacturing operations and regulatory affairs, working with mid-market and enterprise pharma customers to manage both compliance risk and costs. With 51–200 employees and accelerating hiring, MEDVACON is scaling field validation and audit support capabilities.

HeadquartersSparta, NJ

Company Size51–200 employees

Founded2012

Hiring MarketsUnited States

Frequently Asked Questions

What software does MEDVACON use for validation work?

MEDVACON uses SolidWorks for engineering documentation, JMP and GraphPad Prism for statistical analysis, LIMS for lab data management, SAP for manufacturing systems, and Smartsheet for project tracking. Excel and SharePoint are also core tools for protocols and compliance documentation.

What are MEDVACON's main service offerings?

MEDVACON provides FDA Quality Compliance and Technical Consulting Services including validation protocol development, GMP audits, computer system validation, FDA audit preparation and remediation, quality systems design, tech transfers, and training. They work with life sciences companies across manufacturing, clinical packaging, and regulatory workflows.