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Sample Room Manager Jobs in Chester, NY (NOW HIRING)

Strides Pharma Inc

QA Associate I

Chestnut Ridge, NY · On-site

$22 - $26/hr

... room inspection, and materials. * Collects and appropriately labels packaging retain samples, and ... Responds to and escalates events identified during production to Quality Management * Participates ...

New Jersey Courts

Probation Officer

Sussex, NJ · Hybrid

$55K - $95K/yr

Whether it be in a courtroom, an administrative office, a courthouse training room, an IT office or ... Under the general direction of the Court Executive 2B (Family Division Manager) and the direct ...

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Sample Room Manager information

See Chester, NY salary details

$23.5K

$62.6K

$104.5K

How much do sample room manager jobs pay per year?

As of Aug 31, 2026, the average yearly pay for sample room manager in Chester, NY is $62,554.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,900.00 and $70,400.00 per year, depending on experience, location, and employer.

What is a sample room manager?

A Sample Room Manager is responsible for overseeing the organization, workflow, and staff within a company's sample room, typically in industries like fashion or textiles. They manage the creation, cataloguing, and distribution of product samples, ensuring that prototypes are developed accurately and efficiently according to design specifications. The Sample Room Manager coordinates between design, production, and quality teams to maintain timelines and quality standards. They also ensure that the sample room operates smoothly, maintains inventory, and complies with safety regulations.

How does a sample room manager typically coordinate with design and production teams to ensure timely sample delivery?

A Sample Room Manager plays a key role in bridging the gap between the design and production teams by organizing workflow, setting clear timelines, and monitoring progress. They regularly communicate with designers to clarify specifications and ensure the feasibility of samples, while also collaborating with production staff to allocate resources and resolve technical issues. Effective coordination often involves holding daily or weekly meetings, updating tracking systems, and proactively addressing potential delays to keep sample delivery on schedule.

What are the key skills and qualifications needed to thrive as a sample room manager, and why are they important?

To thrive as a Sample Room Manager, you need expertise in garment construction, fabric knowledge, and production processes, often supported by a degree in fashion or textiles and relevant industry experience. Familiarity with pattern-making software, inventory management systems, and CAD tools is typically required. Strong organizational abilities, attention to detail, and effective communication are vital soft skills for overseeing sample development and coordinating with design and production teams. These skills ensure efficient workflow, high-quality samples, and timely delivery in a fast-paced fashion environment.

What is the difference between Sample Room Manager vs Sample Coordinator?

AspectSample Room ManagerSample Coordinator
CredentialsTypically requires a bachelor's degree in marketing, design, or related field; experience in sample managementOften requires similar education; entry-level roles may need less experience
Work EnvironmentManages sample rooms, oversees staff, coordinates sample logisticsAssists in sample organization, prepares samples for presentations or shipments
Industry UsageCommon in fashion, consumer goods, and design industriesUsed across similar industries for supporting sample management tasks
Search & ComparisonOften compared for roles involving sample oversight and managementCompared as an entry-level or supporting role in sample handling

The Sample Room Manager oversees the entire sample room operations, managing staff and logistics, while the Sample Coordinator typically supports these activities by organizing and preparing samples. Both roles require related skills and experience, but the manager has broader responsibilities and leadership duties.

What job categories do people searching Sample Room Manager jobs in Chester, NY look for?

The top searched job categories for Sample Room Manager jobs in Chester, NY are:

What cities near Chester, NY are hiring for Sample Room Manager jobs?

Cities near Chester, NY with the most Sample Room Manager job openings:

Sample Room Manager jobs near you
Infographic showing various Sample Room Manager job openings in Chester, NY as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $62,554 per year, or $30.1 per hour.

Certified Sterile Compounding Technician

Ramsey, NJ • On-site

Town & Country Compounding and Consultation
Pharmaceutical and Medicine Manufacturing • 11 - 50 employees
Learn more about Town & Country Compounding and Consultationexternal

$22 - $25/hr

Full-time

Re-posted 22 days ago

Job description

Description:

Role Summary


The Sterile Compounding Technician is a registered pharmacy technician responsible for preparing low-, medium-, and high-risk sterile compounded products in a controlled, cleanroom environment. Working under the direct supervision of the Sterile Compounding Pharmacist and Pharmacist-in-Charge, this role demands a precise, detail-oriented professional who is fully committed to patient safety, product quality, and strict regulatory compliance. The Sterile Compounding Technician is responsible not only for accurately preparing sterile formulations but also for maintaining the integrity of the cleanroom environment, upholding USP 797 and 800 standards, and ensuring meticulous management of inventory and batch records.

Requirements:

1.  Sterile Product Compounding 

• Compound low-, medium-, and high-risk sterile preparations in accordance with physician orders and Master Formulation Records, including sterile injections, ophthalmics, inhalation solutions, suspensions, and freeze-dried powders. 

• Consistently meet established standards for strength, quality, purity, integrity, sterility, and endotoxin content for all sterile preparations. 

• Follow all applicable company Standard Operating Procedures (SOPs), NJ Board of Pharmacy regulations, and USP 797 and 800 guidelines without exception. 

• Exercise meticulous attention to detail at every stage of the compounding process to safeguard patient safety and product integrity. 


2.  Batch Records & Quality Control 

• Ensure the accuracy and completeness of all compounding batch records, including documenting lot numbers, manufacturers, and quantities of all components, supplies, and equipment used. 

• Follow all instructions outlined in the Master Formulation Record precisely and without deviation. 

• Perform and document all required Quality Control (QC) checks and results in accordance with applicable SOPs. 

• Report any deviations, discrepancies, or quality-related events to the supervising pharmacist immediately. 


3.  Clean Room Maintenance & Environmental Monitoring 

• Perform daily, weekly, and monthly cleaning of the sterile compounding environment in strict accordance with company SOPs. 

• Conduct environmental monitoring and sampling of the clean room, including surface sampling, air sampling, and viable particle counts, as required by USP 797 and company protocols. 

• Maintain ISO-classified clean room conditions at all times; report any environmental excursions or equipment anomalies to the supervising pharmacist promptly. 

• Ensure proper gowning, garbing, and aseptic technique are maintained throughout all clean room activities. 


4. Inventory Management 

• Notify RPh of inventory levels for all sterile compounding chemicals, APIs, and components; initiate re-ordering for low-inventory or approaching-expiry items in a timely manner.  

• Conduct monthly checks of all inventory for expired or expiring chemicals and components; quarantine and document as appropriate.

• Maintain organized, accurate, and audit-ready controlled-substance inventory records at all times.