Our Facility

A scalable manufacturing environment built for clean, consistent production

ZivaQ's East Brunswick facility is designed around efficient material flow, ISO-oriented cleanroom standards, high-volume production capacity, and the documentation discipline dietary supplement brands expect from a dependable contract manufacturer.

45,000 sq ftEast Brunswick, NJMulti-format productionISO Class 8 planned
Production Capacity

Built for high-volume output

Planned capacity across the five core supplement formats, with warehouse infrastructure to support large-scale ingredient procurement and finished goods distribution.

45,000sq ft

Manufacturing footprint

1,600pallets

Storage capacity

15,000kg / shift

Powder processing

10Mper shift

Tablet output

11Mper shift

Capsule output

Facility Overview

One integrated facility — every format, every stage

Located in East Brunswick, New Jersey, our 45,000 sq ft facility consolidates raw material warehousing, multi-format production, in-process quality controls, packaging, and finished goods storage under one roof. The layout is designed for clean handoffs between each stage of manufacturing, with minimal material backtracking and full documentation at every step.

The floor plan follows a linear flow from receiving through to shipping, with segregated cleanroom zones for production and dedicated spaces for quality review — suited for both new product launches and high-volume repeat programs.

Facility Highlights

  • East Brunswick, New Jersey — centrally located for East Coast distribution
  • Designed for multi-format supplement production under one roof
  • High-bay warehouse with organized pallet racking and FIFO material flow
  • Dedicated receiving, quarantine, and release zones for incoming materials
  • Positive-pressure production areas with controlled air handling
  • Scalable floor plan supporting phased capacity expansion
Production Zones

Dedicated zones for every stage of production

Each production area is physically separated, purpose-designed, and documented. From raw material receipt through finished goods release, every zone operates on controlled workflows with clear handoff points.

Receiving & Incoming Materials

Organized dock-to-floor receiving workflow with dedicated quarantine holding areas. Incoming materials are logged, labeled, and staged for quality review before release into production.

Material loggingQuarantine holdQuality release

Raw Material Warehousing

Climate-monitored warehouse with 1,600-pallet capacity. Rack organization supports FIFO inventory management and clear separation of active, quarantine, and rejected materials.

1,600 palletsFIFO inventoryClimate monitoring

Blending & Powder Processing

High-capacity powder blending area designed for sports nutrition, functional supplement, and custom formula programs. Supports 15,000 kg of blended output per shift.

15,000 kg / shiftCustom blendsBatch documentation

Tablet Production

High-speed tableting lines capable of producing up to 10 million tablets per shift across coated, uncoated, chewable, and specialty tablet formats.

10M / shiftCoated & uncoatedChewable formats

Capsule Filling

Automated capsule filling lines producing up to 11 million capsules per shift. Supports hard-shell gelatin and HPMC vegetarian capsule formats for dietary supplement programs.

11M / shiftGelatin & HPMCPrivate label

Packaging & Labeling

Automated bottle filling at 100 units per minute with inline capping, labeling, and inspection. Supports bottles, blister packs, stick packs, sachets, and custom retail formats.

100 units/minInline inspectionMulti-format
Cleanroom & Environmental Controls

Controlled environments for every production area

Our cleanroom design and environmental controls are built to support consistent, contamination-free production across all supplement formats.

ISO Class 8 Cleanrooms

Production areas planned to meet ISO Class 8 cleanroom standards, maintaining controlled particulate levels throughout manufacturing operations.

Segregated Work Zones

Clearly defined zones for receiving, staging, blending, production, and packaging — each physically separated to prevent cross-contamination and support audit readiness.

Controlled Material Flow

Unidirectional material movement pathways from raw receipt through finished goods. Designed to eliminate backflow and maintain full chain-of-custody traceability.

Air Handling & Pressure

Positive-pressure HVAC in active production rooms with filtered air supply. Differential pressure monitoring between zones reduces contamination risk.

Equipment

Production-grade equipment across every format

The facility is equipped with purpose-built machinery for each supplement format, supported by in-process quality instrumentation and automated packaging lines.

High-speed rotary tablet presses

Automatic capsule filling machines

V-blenders and ribbon blenders

High-speed bottle filling lines

Blister packaging equipment

Temperature-controlled coating pans

Inline checkweighing systems

Metal detection systems

In-process sampling stations

Batch monitoring & data logging

Automated palletizing & shipping prep

Quality & Compliance

Documentation and discipline at every step

ZivaQ is building its quality systems around cGMP principles, thorough documentation, supplier controls, and production practices that give supplement brands the confidence to scale with a dependable partner.

cGMP-Oriented Systems

Operating procedures, batch records, and documentation workflows modeled on current Good Manufacturing Practice expectations for dietary supplement production.

FDA Registration Planning

Facility registration planning in progress with FDA. Operating systems are being structured to meet FDA dietary supplement facility requirements.

Batch Documentation & Traceability

Every production run is tracked with complete batch records including raw material lots, blend data, in-process checks, and finished product disposition.

Supplier Qualification

Incoming raw materials go through supplier qualification and incoming material review before release to production, supporting consistent formulation integrity.

In-Process Quality Checks

Sampling and testing protocols embedded into each production stage — weight checks, hardness, disintegration, capsule fill weight, and visual inspection.

Finished Product Controls

Packaging and labeling operations include inline verification, lot coding, and hold-and-release workflows before product ships to customer.

Location

Centrally located for East Coast operations

Our East Brunswick, New Jersey facility positions ZivaQ at the center of one of the country's most active supplement distribution corridors — with convenient access to major shipping lanes, ports, and regional logistics networks.

East Brunswick, New Jersey
Access to I-95, NJ Turnpike, and Route 1 freight corridors
Proximity to Port Newark and Port of New York/New Jersey
Within one-day delivery reach of major Northeast markets

East Brunswick, NJ

Middlesex County, New Jersey

Facility Size45,000 sq ft
Warehouse Capacity1,600 pallets
Production ShiftsMulti-shift capable
Distribution RegionNortheast & national