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Sample Associate Jobs in Warminster, PA (NOW HIRING)

Wegman

Litigation Associate

Blue Bell, PA

... litigation associate with 3+ years of PA state and federal court experience. Looking for detail ... References and writing samples required. Please email rnutinsky@wegmanpartners.com for more ...

Zeller & Wieliczko, LLP

Associate Attorney

Cherry Hill, NJ · On-site

$65K - $75K/yr

  • Medical

  • Life

  • Retirement

  • PTO

Established Southern New Jersey firm seeks entry level associate to handle matters involving ... References and writing sample requested. Salary commensurate with experience and qualifications.

Burlington Stores

Mail Center Associate I

Burlington, NJ · On-site

$15.75 - $18.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Unpack and hang or re-package all sample merchandise and deliver same day to appropriate sample ... Full-time associates are also eligible for paid time off, paid holidays and a 401(k) plan. We are a ...

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All JobsSample Associate JobsSample Associate Jobs in Warminster, PA

Sample Associate information

See Warminster, PA salary details

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How much do sample associate jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for sample associate in Warminster, PA is $15.71, according to ZipRecruiter salary data. Most workers in this role earn between $13.41 and $17.45 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a sample associate?

To thrive as a Sample Associate, you need attention to detail, organizational skills, and experience with inventory management, typically supported by a high school diploma or equivalent. Familiarity with warehouse management systems, barcode scanners, and spreadsheet software is commonly required. Strong communication, teamwork, and time management skills help you excel in coordinating sample requests and maintaining accurate records. These abilities ensure efficient sample handling, minimize errors, and support seamless operations in product development or retail environments.

What is an example of a sample associate job?

A sample associate job typically involves assisting with product sampling, customer service, or inventory management in retail or promotional environments. The role may require good communication skills, attention to detail, and the ability to follow safety and quality standards. It often involves working flexible hours and may require basic certifications depending on the industry.

What is a sample associate?

Sample Associates are professionals who assist in the preparation, handling, and distribution of product samples, often in retail, laboratory, or promotional settings. Their responsibilities may include setting up sample displays, engaging with customers or clients, collecting feedback, and maintaining inventory records of samples. They play a crucial role in product testing, quality control, and marketing campaigns by ensuring that samples are managed and presented effectively. Sample Associates may work in industries such as food and beverage, cosmetics, pharmaceuticals, or scientific research. Strong communication skills and attention to detail are important qualities for this role.

What is the difference between Sample Associate vs Sample Technician?

AspectSample AssociateSample Technician
Required CredentialsHigh school diploma or equivalent; some roles may require certificationHigh school diploma; technical certification often preferred
Work EnvironmentLaboratory or manufacturing settings, handling samples and dataLaboratory or field settings, performing tests and equipment maintenance
Employer & Industry UsageUsed in healthcare, manufacturing, and research industriesCommon in scientific, healthcare, and industrial labs

The Sample Associate and Sample Technician roles share similar environments and credentials, often working together in labs or manufacturing settings. The main difference lies in their specific responsibilities: Sample Associates typically handle sample collection and data entry, while Sample Technicians focus on testing and equipment operation. Both roles are essential for quality control and research processes.

How does a sample associate typically collaborate with other departments during the product development process?

Sample Associates play a critical role in product development by working closely with design, production, and quality assurance teams. They assist in preparing and organizing product samples, ensuring that designers receive accurate prototypes and that production teams have the correct specifications. Effective communication and attention to detail are essential, as Sample Associates must track sample progress, gather feedback, and coordinate revisions across multiple departments. This collaboration ensures that products meet company standards and are ready for market launch on schedule.
Sample Associate jobs near you
Infographic showing various Sample Associate job openings in Warminster, PA as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $32,671 per year, or $15.7 per hour.

Senior Research Associate or Associate Scientist, Translational Medicine

Cabaletta Bio Inc.

Philadelphia, PA

Full-time

PTO

Posted 9 days ago

Job description

Position Title:  Senior Research Associate/ Associate Scientist, Translational Medicine

Location: On-Site/Philadelphia, PA

Reports to: Senior Scientist Translational Medicine

Department: Research

Cabaletta Bio (Nasdaq: CABA) is a late-stage clinical biotechnology company focused on developing and launching curative targeted cell therapies designed specifically for patients with autoimmune diseases. The CABA platform encompasses two complementary strategies which aim to advance the discovery and development of engineered T cell therapies with the potential to become deep and durable, perhaps curative, treatments for a broad range of autoimmune diseases. The lead CARTA (Chimeric Antigen Receptor T cells for Autoimmunity) strategy is prioritizing the development of rese-cel, a 4-1BB-containing fully human CD19-CAR T cell investigational therapy. Rese-cel is currently being evaluated in the RESET (REstoring SElf-Tolerance) clinical development program spanning multiple therapeutic areas, including rheumatology, neurology and dermatology. Cabaletta Bio's headquarters and labs are located in Philadelphia, PA. For more information, please visit www.cabalettabio.com and connect with us on LinkedIn.

Uniquely Differentiated. Rapid. Elegant.

At Cabaletta, we are driven by the shared mission of developing cures, where a patients' own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew. 

We're proud to be a Great Place to Work-Certified company! #GPTWcertified Check out what our employees say makes working here so great:  Working at Cabaletta Bio Inc | Great Place to Work

About the Position:

Reporting to the Senior Scientist, Translational Medicine we are seeking an experienced, motivated, detail-oriented, and highly skilled Senior Research Associate/Associate Scientist within our Translational Medicine team.

Under scientific and technical supervision, the individual will be primarily responsible for developing and performing autoantibody evaluation assays (MSD, Luminex, ELISA) assays and other molecular based assays such as dPCR. As part of the Translational Medicine team, the individual must be able to perform qualified assays on clinical trial participant materials, adhering to internal compliance standards. 

Responsibilities:

  • With guidance from a Senior Scientist, Translational Medicine, perform assays on clinical samples and potentially pre-clinical samples.
  • Perform qualified or validated molecular based assays (Luminex, dPCR, MSD, ELISA, etc.) on clinical samples to inform on cell product persistence and efficacy in humans.
  • Participate in generating, qualifying, and validating GLP-like assays and contributing to the development of corresponding SOPs.
  • Interfacing heavily with the electronic lab notebook (eLN) system and sample management system; accurately capturing data in a timely manner, ensuring data integrity and protocol compliance using an eLN.
  • Maintain GDP-compliant and detailed records for clinical sample lifecycle (receipt, usage, inventory, etc.).
  • Involvement in clinical sample accessioning with close attention to metadata entry.
  • Opportunities to learn and perform cell based assays such as flow cytometry and cell killing assays.
  • Manage multiple internal projects / workstreams simultaneously.
  • Performing lab associated tasks in accordance with GLP and Cabaletta Bio lab safety policies and SOPs.
  • General maintenance of laboratory space and contribution to weekly activities.

 

Required Qualifications:

 

  • MS degree in Biology, Immunology, Engineering or related field or Bachelor's degree with 2+ years of experience in an academic laboratory or the biotechnology industry is required.
  • Experience with molecular based assays such as ELISA's, MSD, Luminex, and/or dPCR platforms.
  • Significant lab experience including aseptic technique, mammalian cell culture, and DNA extraction.
  • Must be able to follow SOPs and follow good documentation practices.
  • Must be highly organized and efficient, able to work independently. Strong problem-solving skills are preferred.
  • Must be able to communicate clearly verbally and in writing.
  • Must have a desire to be part of a growing organization that uses cutting-edge science.
  • Strong team orientation and passion for continuous self-development.
  • Comfortable in a fast-paced small company environment and able to adjust workload based upon changing priorities.

Preferred Qualifications:

  • Experience in protocol design, qualification, and SOP generation.
  • Experience with qPCR/dPCR platforms.
  • Experience with autoantibody evaluation assays.
  • Experience with clinical sample handling and inventory management is strongly preferred.
  • Experience troubleshooting, qualifying, or validating molecular based assays. 
  • Experience in the biotechnology industry or in a startup industrial setting.
  • Previous experience with GLP/GCP & ICH regulations.
  • Prior use of an electronic laboratory notebook system; involvement in system development is a plus.

 

Our name - Cabaletta - is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression.

For more information, please visit  https://www.cabalettabio.com/join-our-crew

Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans.

Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law.

Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation.

And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm.

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