Paul Industries LLC is a Virginia-based single-source process-equipment and sanitary-piping contractor serving pharmaceutical, biotech, cosmetic, nutraceutical and food & beverage manufacturers across the state. With 30+ years of cGMP/FDA-compliant work, we design, fabricate, install, validate and maintain high-purity systems in-house. We are headquartered in Kilmarnock, Virginia and work in New Jersey with travelling crews rather than a local branch. Prefabricating spools and skids in the Virginia shop converts field hours, which carry a 15 to 25 percent premium in northern New Jersey, into lower-cost shop hours.
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Who we serveNJ pharma, biotech, cosmetic, nutraceutical, food & beverage manufacturers
ScopeDesign → fabrication → installation → validation → maintenance
StandardscGMP/FDA, ASME BPE, ISO 14644 cleanrooms
Service areaStatewide NJ — Princeton, New Brunswick, Somerset, Cranbury, Bridgewater, Parsippany, Newark regions
Experience30+ years, cGMP/FDA-compliant, single-source
Also availablePreventive maintenance & emergency service for NJ facilities
New Jersey’s manufacturing landscape
New Jersey holds one of the densest life-sciences and pharmaceutical clusters in the United States, and that concentration shapes the way process contractors have to work here. The Route 1 corridor running through Princeton, Plainsboro and New Brunswick anchors a heavy footprint of drug developers and manufacturers, while Middlesex, Somerset, Morris, Bergen and Union counties add generic manufacturing, contract development and manufacturing organizations (CDMOs), and specialty chemical operations. Towns like Cranbury, Somerset, Bridgewater and Parsippany host the kind of GMP production and R&D facilities that depend on validated water, clean steam and sanitary process piping every single day.
Beyond traditional pharma, New Jersey carries a strong biotech pipeline and a long-established cosmetic and personal-care manufacturing base, plus nutraceutical and food & beverage producers that increasingly build to pharmaceutical-grade hygienic standards. These facilities share a common need: process systems that hold up to FDA inspection, deliver repeatable product quality, and can be retrofitted or expanded without shutting down production. Paul Industries builds for exactly that environment. We do not name specific clients, but the systems we install are the ones NJ manufacturers across these sectors rely on to stay compliant and stay running.
The density of that cluster also raises the bar for how work gets executed. Many New Jersey plants run adjacent to occupied production suites, share utilities across multiple product lines, and operate under tight change-control procedures, so tie-ins, welding and validation have to be sequenced carefully rather than forced. A contractor who understands that operating reality — and who can fabricate off-site to shrink the on-site window — protects both your schedule and your compliance posture. That is the environment Paul Industries was built to work in, and it is why our design, fabrication and field teams stay under one roof.
NJ industries served and the systems they need
Typical New Jersey manufacturing sectors and the process systems Paul Industries builds for each
| Sector | NJ regions | Typical systems |
|---|
| Pharmaceutical & generics | Route 1 corridor, Middlesex, Union | USP purified water, WFI, clean steam, sanitary process piping |
|---|
| Biotech & CDMO | Somerset, Morris, Middlesex | High-purity water, ASME BPE piping, cleanroom fit-out |
|---|
| Cosmetic & personal care | Bergen, Passaic, Union | Sanitary process piping, mixing/skid systems, CIP |
|---|
| Nutraceutical | Middlesex, Somerset | Hygienic piping, purified water, blending systems |
|---|
| Food & beverage | Statewide | 3-A sanitary piping, CIP/SIP, process utilities |
|---|
What we build for New Jersey facilities
- High-purity water systems — USP purified water, WFI and clean steam generation and distribution loops sized for NJ pharma and biotech production.
- Sanitary process piping — orbital-welded, ASME BPE-compliant stainless piping with full documentation and passivation for hygienic product contact.
- Cleanroom systems — ISO 14644-classified cleanroom construction and process fit-out for aseptic and controlled-environment manufacturing.
- Process skids & modules — shop-fabricated, pre-tested skids that shorten on-site installation windows at busy NJ plants.
- Turnkey process systems — single-source design through validation so one contractor owns the outcome end to end.
Standards & compliance
- cGMP / FDA
- Current Good Manufacturing Practice governs how regulated product is made. We build and document systems so NJ facilities can defend their processes during FDA inspection, with the material traceability and turnover packages auditors expect.
- ASME BPE
- The Bioprocessing Equipment standard defines hygienic design, surface finish and weld quality for sanitary piping. Our orbital welding and inspection records are built to satisfy it on every high-purity job.
- ISO 14644
- This standard classifies cleanroom air cleanliness. We construct and integrate cleanrooms to the ISO class each process requires, from support spaces to aseptic core areas.
Why a Virginia-based single-source contractor
When your contractor is headquartered in Kilmarnock, Virginia, response and mobilization stop being scheduling problems. We reach facilities in Princeton, New Brunswick, Somerset, Cranbury, Bridgewater, Parsippany and Newark without cross-country travel days or out-of-state mobilization premiums, which matters most when a production line is down or a validation deadline is fixed. Being local also means familiarity with the way NJ facilities operate, the regional trades we work alongside, and the inspection expectations these plants routinely face.
Just as important, everything runs through one accountable team. Paul Industries designs, fabricates, installs, validates and maintains your system in-house rather than handing off between disconnected vendors. That single-source model — backed by 30+ years of cGMP work and complete compliance documentation — means no finger-pointing between a designer, a fabricator and an installer when something needs to be right. One contractor owns the result, from first drawing to final turnover package.
Frequently asked questions
Can Paul Industries support a Kenilworth pharma capacity expansion?
Yes. For Kenilworth expansions we add USP/WFI water,
ASME BPE piping, bioreactors, tanks, and CIP/SIP, On a capacity expansion at an operating site the constraint is rarely the new equipment; it is the tie-in to systems still making product. Each connection to a live compendial loop means proving isolation rather than assuming it, cutting and welding under containment in a cGMP space, cleaning heat tint and re-passivating the affected leg, then assessing requalification scope. That scope is set by risk rather than by how much pipe was touched, so a small tie-in on a WFI loop can require sampling across the whole loop before it releases water again. Establishing that extent before the outage is planned is what keeps the restart date realistic. Call 201-450-8280.
Do you install cleanrooms for a Bridgewater biologics facility?
We do. Bridgewater biologics sites get ISO 14644 cleanrooms, EU GMP Annex 1 support, sanitary process piping, and validated CIP/SIP, Biologics suites raise a specific design question beyond classification: whether the process runs open or closed. Closed or functionally closed processing allows a lower room grade for the same product protection, which is the single largest cost lever available, since a closed operation in a Grade C room is far cheaper to build and to run than an open one in Grade B. Under the revised EU GMP Annex 1 the expectation has moved firmly toward barrier technology and a documented Contamination Control Strategy covering the whole facility. Deciding open versus closed before the room is designed changes both capital cost and annual operating cost substantially.
Can you handle high-purity water for a Cranbury nutraceutical blending plant?
Yes. Cranbury nutraceutical plants get USP-grade high-purity water, sanitary ASME BPE piping, tanks, and filtration, all built and validated IQ/OQ/PQ to cGMP standards. Nutraceutical work differs from pharmaceutical work in ways that should change the specification rather than being treated as a lighter version of it. Dietary supplement manufacture falls under 21 CFR 111 rather than 21 CFR 211, so the water requirement is potable-plus-process rather than compendial unless the company chooses otherwise, and specifying USP Purified Water where it is not required imports a permanent qualification and monitoring obligation for no regulatory benefit. What blending plants do need is dust control at every powder transfer, room finishes that tolerate frequent wet cleaning, and changeover procedures that address allergen and botanical cross-contamination, which is a different risk model from carryover limits.
Do you provide orbital welding and passivation in Branchburg?
We do. Branchburg facilities get orbital welding and ASTM A967/A380
passivation for sanitary and high-purity systems, with full documentation for cGMP and FDA audits. On orbital welding the evidence is what makes the work defensible, and it is worth knowing what to ask for: procedure qualification records covering the exact tube diameter and wall thickness, welder performance qualifications with current continuity records since qualifications lapse through disuse, the coupon frequency actually run, the boroscope rate applied to production welds, and purge verification by oxygen analyser rather than by timing. Heat tint is the visible consequence of a poor purge, and the chromium-depleted layer directly beneath that tint is where corrosion starts, which is why AWS D18.2 provides a visual comparison standard for acceptable discolouration on austenitic tube.
Can Paul Industries do a live-loop tie-in at a Raritan sterile facility?
Yes. We stage tie-ins to live WFI and clean-steam loops at Raritan sterile plants, A live-loop tie-in at a sterile facility is planned backwards from requalification rather than forwards from the weld. The sequence is: prove isolation physically rather than by valve position, drain and make the section safe for hot work, contain grinding debris and weld fume so neither reaches adjacent production, manage argon purge in an enclosed space because it displaces oxygen, weld, clean heat tint, re-passivate the affected leg, boroscope and add the welds to the existing weld map, then sanitise and sample before release. On a compendial system the sampling is governed by laboratory incubation, so the laboratory rather than the crew determines when production restarts. Call 201-450-8280.
Do you serve the pharma cluster along the I-287 Morris and Somerset County corridor?
Yes. Paul Industries serves the I-287 Morris and Somerset pharma corridor, providing single-source design, fabrication, installation, and validation of high-purity water, sanitary ASME BPE piping, What characterises work in that corridor is that almost none of it is greenfield. These are mature plants, many decades old, so the valuable capabilities are proving isolation on live systems, welding in occupied classified space, sequencing into fixed shutdown windows, and re-establishing documentation on a section that was modified. Many of those facilities also have no weld map, material traceability or passivation record for the original installation, which means a retrofit frequently has to create a documented baseline rather than inherit one. That scoping question should be settled before the work is priced, because it materially changes both cost and the requalification that follows.
Can you support biopharma facilities in Summit and Rahway?
Yes. We work with biopharma manufacturers in Summit, Rahway, and surrounding Union County, building bioreactors, WFI water,
clean steam, and process piping to ASME BPE, USP, and EU GMP Annex 1 standards.
Do you install high-purity water systems along the Route 1 Princeton and New Brunswick corridor?
Yes. We design and install USP and WFI water systems throughout the Route 1 life-sciences corridor between Princeton and New Brunswick, On that corridor the recurring technical decision is whether to run the distribution loop hot or ambient, and it has long consequences. A loop circulating at 80 degrees C or above is effectively self-sanitising and removes a recurring manual intervention permanently, at the cost of insulation, heat tracing, expansion provision, a cooling exchanger at points of use and higher energy. An ambient loop is cheaper to build and needs a scheduled sanitisation regime forever, justified by trend data rather than habit. For a plant expecting to run the system for twenty years, the labour and excursion-investigation cost of the ambient option usually exceeds the capital difference.
Do you self-perform in New Jersey or use subcontractors?
We self-perform. Paul Industries’ own crews handle orbital welding, sanitary piping, passivation, and system installation across New Jersey, Self-performing matters most at the seams. When welding, passivation and validation sit with different contractors, the plant frequently discovers during qualification that the weld map does not reconcile with the passivation certificate, or that a section was passivated before the final tie-ins were made so the connecting joints were never treated. Nobody is contractually wrong in that situation and the facility absorbs the cost of resolving it. Holding the scope together also fixes the sequence, which is unforgiving: passivation must follow every weld including the last tie-in, and must precede sanitisation and any qualification sampling.
Can you build cleanrooms for cosmetic manufacturers in New Jersey?
Yes. We build ISO 14644 cleanrooms and hygienic process systems for cosmetic, nutraceutical, and personal-care manufacturers across New Jersey, Cosmetic and personal-care suites are usually specified differently from sterile pharmaceutical rooms, and understanding why avoids overbuilding. The controlling risks are particulate contamination and microbial ingress into water-containing emulsions rather than sterility assurance, so ISO 8 or ISO 7 is generally appropriate rather than the ISO 5 environment an aseptic fill demands. Finishes matter for a different reason: creams, oils, waxes, silicones and pigments are difficult to remove, so wall and floor materials are selected for chemical resistance and washdown tolerance rather than only for particle shedding. Local protection over open product is frequently a far cheaper route to the same result than raising the whole room.
How quickly can you respond to an emergency at a Central Jersey plant?
We provide emergency repair statewide. Call 201-450-8280 for urgent sanitary system, water, or piping failures in Central and Northern New Jersey. What can realistically be done quickly depends on where the failure sits. Pumps, membranes, cartridge filters, ultraviolet lamps, valve diaphragms and controls are replaceable without opening the product-contact surface, so those are typically resolved in a shift or two. A weld failure or a leak in a distribution loop is a different matter: the mechanical repair may take hours, but the affected section then needs heat tint removal, re-passivation and, on a compendial system, re-sanitisation and sampling before water can be released. That is why the useful question in an emergency is not how fast we arrive but how fast the system returns to a qualified state.
Do you serve all of New Jersey?
Yes. Paul Industries serves manufacturing facilities statewide, including the Route 1 corridor around Princeton and New Brunswick, Those counties are not interchangeable as project environments. Northern Bergen and Union county sites tend to be older, denser and more constrained, with limited laydown space and access closer to metropolitan conditions. The Middlesex, Somerset and Morris corridor along Route 1 and Interstate 287 holds the larger pharmaceutical campuses, where access and staging are generally workable and projects look more like conventional industrial work. That difference changes rigging cost, delivery sequencing and how much can be prefabricated as single assemblies, and pricing one environment using experience of the other is where New Jersey estimates most often go wrong. We are based in Kilmarnock, Virginia and work in New Jersey with travelling crews rather than a local branch, which is worth being straightforward about. For planned capital work that makes little difference to price: mobilisation is a fixed cost spread across a job measured in weeks, and the labour rate, weld count and documentation depth drive the number far more than travel does. Where being physically close genuinely matters is unplanned emergency response, and there an honest answer is that response time depends on crew availability at that moment rather than on distance alone. What we do commit to is the same crew and foreman from start to turnover, and returning for warranty and requalification work.
Where is Paul Industries based?
Paul Industries is headquartered in Kilmarnock, Virginia, with New Jersey among our core service areas. We are not a New Jersey firm and do not claim to be. Hygienic spools and skids are prefabricated in the Virginia shop and trucked up, and crews mobilise to site for installation, tie-in, passivation and validation. That arrangement has a real advantage that has nothing to do with proximity: moving welds from the field into a controlled shop removes labour at the northern New Jersey premium, which runs 15 to 25 percent above national, and adds it back at a lower shop rate, while also making boroscope inspection and surface protection easier.
How fast can you respond to an NJ facility?
Kilmarnock, Virginia to most New Jersey plants is a drive of roughly five to six hours, so next-day mobilisation is realistic for an urgent call and same-day is not something we will promise. For a genuine emergency the honest first question is usually not how fast a crew can arrive but whether the affected system can be isolated so production continues while a proper repair is planned, because on hygienic piping a temporary clamp or seal weld is not acceptable on a product-contact line and a real repair means cutting out, re-welding, re-passivating and re-documenting. Call 201-450-8280 to discuss urgent or emergency needs.
What NJ industries do you serve?
We serve pharmaceutical and generic drug manufacturers, biotech and CDMO operations, cosmetic and personal-care producers, nutraceutical companies, and food & beverage manufacturers. The framework governing each of those sectors differs, and matching the specification to the right one avoids both overbuilding and audit failure. Pharmaceutical and generic manufacture falls under 21 CFR 210 and 211 with USP monographs for water. Biotech and CDMO work adds EU GMP Annex 1 where product reaches Europe. Cosmetic manufacture is governed by the Federal Food, Drug, and Cosmetic Act, now with facility registration and product listing obligations under the Modernization of Cosmetics Regulation Act, with ISO 22716 the recognised GMP standard. Nutraceuticals fall under 21 CFR 111. Food and beverage work is typically written to 3-A Sanitary Standards rather than ASME BPE.
Do you handle NJ facility retrofits without stopping production?
Yes. We plan retrofits and expansions around live production using shop-fabricated skids, phased tie-ins and scheduled shutdown windows to minimize disruption. The most effective way to keep a plant running during a retrofit is decided long before the work starts. Installing isolation valves and capped future connections during an earlier planned shutdown allows the eventual tie-in to be made while the system runs, and it is by far the cheapest option if a second phase is even remotely likely. Sectional isolation works where the loop was designed with valving to allow it. Temporary bypass keeps production going on utility systems, though on product-contact lines the bypass must itself be cleanable. Where none of those exist, the outage is the mechanical work plus sanitisation plus sampling, which is frequently longer than production can absorb.
Building or upgrading a process system in New Jersey?
Talk to a Virginia-based single-source contractor who can design, build, validate and maintain it, with one accountable party from mill certificate through to the turnover package.
Request a Project Quote
or call 201-450-8280
Serving New Jersey’s Pharmaceutical Corridor
New Jersey has one of the highest concentrations of pharmaceutical and biotech manufacturing in the United States, and Paul Industries serves process facilities the length of the state. The I-287 corridor through Morris and Somerset Counties, the Route 1 research belt around Princeton and New Brunswick, and established manufacturing centers in Rahway, Summit, and Kenilworth all run demanding high-purity utilities and sterile process systems.
Across this corridor we design, fabricate, install, and validate USP/WFI high-purity water, ASME BPE piping, cleanrooms, bioreactors, process tanks, and CIP/SIP systems. Because we self-perform orbital welding, passivation, and IQ/OQ/PQ commissioning, New Jersey manufacturers hold a single contractor accountable from concept through qualification. Paul Industries is nationwide, and New Jersey’s pharmaceutical corridor is one of our most actively served markets.
- I-287 corridor (Morris & Somerset Counties)
- Route 1 research belt — Princeton & New Brunswick
- Rahway, Summit & Kenilworth pharmaceutical manufacturing
- Northern NJ biotech and nutraceutical plants
Do you serve the Route 1 and I-287 pharma corridor?
Yes. We serve pharmaceutical, biotech, and nutraceutical manufacturers across Princeton, New Brunswick, and the I-287 corridor with high-purity water, sanitary piping, That corridor concentrates a particular kind of work: expansion and modernisation of established plants rather than new construction. In practice that means tie-ins to running systems, retrofitting legacy equipment to current ASME BPE expectations, replacing non-conforming details such as dead legs, unsloped runs, 304 stainless where 316L is now specified and threaded fittings in product contact, and creating documentation where none exists. The technical work is well understood; the difficulty is doing it inside a live facility on a fixed window, which is why sequencing and isolation planning matter more here than welding capability does.
Can you support a sterile or cGMP facility in New Jersey?
We build to ASME BPE, USP, 21 CFR 211, and EU GMP Annex 1 awareness, delivering cleanrooms (ISO 14644), high-purity water, and IQ/OQ/PQ validation. Request a quote.
Can you respond to an emergency at a New Jersey plant?
Yes. Preventive maintenance is what keeps emergencies rare, and for hygienic systems a useful scope is specific rather than general. Boroscope sampling of representative pipe sections against commissioning baseline photographs catches rouge while it is still a wipe-down rather than a derouging campaign. Diaphragm replacement in zero-static valves on a defined interval prevents a failure that is both a leak and a contamination route. Re-checking slope and drainability catches drift as supports settle and modifications accumulate. Calibrating the instruments the monitoring depends on keeps the trend data defensible. Anything found is then scheduled into a planned shutdown rather than forcing an unplanned one. Call 201-450-8280.
What does process equipment work cost in New Jersey, and why is it higher?
New Jersey sits above the national average on installed cost for cGMP process work, and the gap is labour, not material. The table below shows typical New Jersey installed ranges against a national baseline for the same scope, so you can see where the premium actually lands.
| Scope | Typical New Jersey installed cost | Premium over national average | Why |
|---|
| Sanitary process piping, 2 in ASME BPE | $210 to $390 per linear ft | 15 to 25 percent | Pipefitter rates bid against a dense pharmaceutical cluster |
| Industrial process piping, carbon steel 4 in | $70 to $145 per linear ft | 10 to 18 percent | Same labour market, lower skill premium |
| USP Purified Water system, 5,000 gpd | $16 to $34 per gpd | 12 to 20 percent | Skid is priced nationally; loop and tie-in labour is local |
| ISO 7 cleanroom build | $300 to $580 per sq ft | 15 to 22 percent | Mechanical trades and controls labour drive it |
| In-place passivation of a distribution loop | $8 to $20 per linear ft | 10 to 15 percent | NJDEP and local sewer limits raise waste handling cost |
| Emergency call-out, after hours | $180 to $310 per hour | 5 to 12 percent | Offset by short travel times within the corridor |
Two levers move these numbers more than negotiating the rate does. The first is shop fabrication: skids and pipe spools built off site and delivered ready to set convert premium field hours into lower-cost shop hours, which is why the same scope can price very differently depending on how much is prefabricated. The second is timing. Bidding a project outside the summer turnaround window, when every plant in the corridor is competing for the same crews, routinely recovers more than aggressive rate negotiation ever will.
Cost, compliance and contractor questions New Jersey facilities ask before awarding work
How much more does process equipment installation cost in New Jersey than the national average?
Expect a premium in the region of 10 to 25 percent against a national average for the same scope, and the driver is almost entirely labour rather than material. Tube, fittings and valves are commodity items priced nationally. Skilled pipefitting and millwright labour in the northern New Jersey corridor is not, because the same trades are competing for work across a dense concentration of pharmaceutical, biotech and specialty chemical plants. The premium widens during large capital cycles at the major Route 1 and Interstate 287 sites, when crew availability tightens across the whole market. Two things reduce it materially: scheduling outside the summer turnaround season when everyone is competing for the same crews, and shop fabrication of skids and spools off site so that field hours, which carry the premium, are minimised.
How often do New Jersey facilities need to requalify water and clean utility systems?
The interval is set by federal cGMP expectations and by each site’s own validation programme, not by New Jersey. FDA does not publish a fixed requalification frequency, so what matters is the periodic review documented in your validation master plan, commonly annual, combined with change control that triggers requalification whenever the system is modified. Most New Jersey pharmaceutical sites formally requalify compendial water systems on a one to three year cycle. Where the state does enter the picture is on the discharge side rather than the qualification side: regeneration waste from ion exchange, spent passivation acid and cooling tower blowdown all fall under New Jersey Department of Environmental Protection permitting and local sewer authority limits, and those permits carry their own reporting and renewal cycles independent of anything the FDA requires.
What happens if an FDA inspection of a New Jersey facility cites the water system?
A water system observation on a Form 483 starts a clock rather than a shutdown. You have fifteen business days to respond in writing if you want the response considered before the agency decides whether to escalate, and the quality of that response frequently determines whether the matter ends there or becomes a Warning Letter. The response needs three things: an investigation that reaches an actual root cause rather than restating the observation, corrective action with committed dates, and an assessment of whether the same weakness exists on other systems at the site. Physical remediation typically means eliminating dead legs, correcting slope so lines drain, re-passivating, revising the sanitisation regime and requalifying. Because New Jersey has one of the highest concentrations of FDA-registered sites in the country, district investigators here tend to be experienced with water systems specifically, and generic responses do not survive.
What does the New Jersey pharmaceutical corridor mean in practice for a project?
It refers to the concentration of pharmaceutical, biotech and specialty chemical manufacturing running roughly from Bergen and Hudson counties down through Middlesex and Somerset to the Princeton area, with a second cluster along the Delaware River. In practical project terms it means three things. Skilled labour exists in depth but is bid against constantly, so crew commitment matters more than headline rate. Local building departments and inspectors in these municipalities are unusually familiar with cGMP construction, which speeds permitting but raises the standard of documentation expected. And the density of sites means equipment vendors, calibration houses and testing laboratories are close by, so lead times on service work are shorter here than almost anywhere else in the country.
What are the alternatives to a New Jersey based contractor for work in the state?
The real choice is not local versus distant but resident-crew versus travelling-crew, and it turns on project duration. For emergency response and short service calls, a contractor with people already in the state wins on response time, and nothing else compensates. For a multi-week or multi-month capital project, a travelling crew is routinely competitive, because mobilisation and per diem are fixed costs spread across the whole job while the labour rate advantage compounds every hour. What matters more than the contractor’s home address is whether the same crew and the same foreman stay on the job from start to turnover, whether they hold current qualifications for your material and code, and whether they will come back for warranty and requalification work. Paul Industries works throughout New Jersey nationwide from a single contract.
Who are the best process piping and high-purity water contractors in New Jersey?
New Jersey has a deep bench, which makes selection harder rather than easier, so screen on evidence. Ask for welder qualification and continuity records covering your exact material and diameter, a redacted turnover package from a comparable New Jersey site, and named references at facilities of similar regulatory exposure. Ask specifically how they work in an operating plant, because most New Jersey work is a tie-in to a running facility rather than a greenfield build, and ask who carries the passivation and validation scope, since that seam between contractors is where most disputes start. Confirm they hold current New Jersey contractor registration and can meet site-specific insurance and safety prequalification. Paul Industries delivers piping, high-purity water, cleanrooms, passivation, validation and commissioning across New Jersey under one contract.
