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Processing Associate Jobs in Doylestown, PA (NOW HIRING)

Labcorp

Specimen Processing Team Lead

Lawrenceville, NJ · On-site

$17.75 - $22/hr

Labcorp is seeking a Specimen Processing Team Lead to join our team in Lawrenceville ,NJ. Work ... Associates degree * 4 years or more experience working in a clinical laboratory * 1 year or more ...

Labcorp

Specimen Processing Team Lead

Lawrenceville, NJ

$17.75 - $22/hr

Labcorp is seeking a Specimen Processing Team Lead to join our team in Lawrenceville ,NJ. Work ... Associates degree * 4 years or more experience working in a clinical laboratory * 1 year or more ...

Labcorp

Specimen Processing Team Lead

Lawrenceville, NJ · On-site

$17.75 - $22/hr

Labcorp is seeking a Specimen Processing Team Lead to join our team in Lawrenceville ,NJ. Work ... Associates degree * 4 years or more experience working in a clinical laboratory * 1 year or more ...

AA2IT

Sample Processing Specialist

Lansdale, PA

$29/hr

Title - Sample Processing Specialist Location - West Point, PA Duration - 12+ months Pay Rate - $29 ... Educational background at a minimum - Associate's Degree in the sciences or related field with 4 ...

AA2IT

Sample Processing Specialist

Lansdale, PA · On-site

$29/hr

Title - Sample Processing Specialist Location - West Point, PA Duration - 12+ months Pay Rate - $29 ... Educational background at a minimum - Associate's Degree in the sciences or related field with 4 ...

AA2IT

Sample Processing Specialist

Lansdale, PA · On-site

$29/hr

Title - Sample Processing Specialist Location - West Point, PA Duration - 12+ months Pay Rate - $29 ... Educational background at a minimum - Associate's Degree in the sciences or related field with 4 ...

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All JobsProcessing Associate JobsProcessing Associate Jobs in Doylestown, PA

Processing Associate information

See Doylestown, PA salary details

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$17

$29

How much do processing associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for processing associate in Doylestown, PA is $17.90, according to ZipRecruiter salary data. Most workers in this role earn between $12.26 and $20.24 per hour, depending on experience, location, and employer.

What is a processing associate?

Processing Associates are professionals responsible for handling, organizing, and processing various types of data, documents, or materials within a company. They often work in administrative, financial, or operational departments to ensure that information is accurately recorded, processed, and transmitted to the appropriate teams or systems. Their duties may include data entry, verifying records, managing workflows, and maintaining documentation standards. Processing Associates play a crucial role in ensuring efficient and accurate operations within their organization.

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

To thrive as a Processing Associate, you need strong attention to detail, organizational skills, and the ability to accurately handle data or materials, often supported by a high school diploma or equivalent. Familiarity with data entry software, inventory management systems, or document processing tools is typically required. Reliability, time management, and effective communication are crucial soft skills for excelling in this role. These skills and qualities ensure accuracy, efficiency, and smooth workflow within processing operations.

What are some common challenges a processing associate may face during peak periods, and how can they be managed?

Processing Associates often encounter increased workloads and tighter deadlines during peak periods, such as end-of-month or holiday seasons. To manage these challenges, effective time management, attention to detail, and strong communication with team members are essential. Many organizations provide additional support or adjust shift schedules to help maintain productivity, while experienced Processing Associates rely on established workflows and prioritize tasks to stay organized and efficient.

What is the difference between Processing Associate vs Data Entry Clerk?

AspectProcessing AssociateData Entry Clerk
Required CredentialsHigh school diploma; some roles may prefer certifications in data managementHigh school diploma; basic computer skills
Work EnvironmentOffice setting, often in finance, healthcare, or logisticsOffice or remote, primarily data input tasks
Employer & Industry UsageFinancial institutions, healthcare providers, logistics companiesAdministrative departments, data management firms
Common Search & ComparisonProcessing Associate vs Data Entry Clerk

Processing Associates typically handle more complex data processing tasks, verifying and managing information, while Data Entry Clerks focus mainly on inputting data accurately. Both roles require attention to detail and basic computer skills, but Processing Associates often work in specialized industries with additional responsibilities.

More about Processing Associate jobs

What cities near Doylestown, PA are hiring for Processing Associate jobs?

Cities near Doylestown, PA with the most Processing Associate job openings:

Processing Associate jobs near you
Infographic showing various Processing Associate job openings in Doylestown, PA as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $37,242 per year, or $17.9 per hour.

(Associate) Director, Viral Downstream Process Development

Dispatch Bio

Philadelphia, PA • On-site

Full-time

Re-posted 24 days ago

Job description

The role:

The (Associate) Director will serve as the downstream processing expert working closely with CDMOs to generate lentivirus and adenovirus products.  Reporting into the Vice President of Process Development, this individual will also be responsible for building out the internal downstream purification capabilities within process development to support scale up and scale down.

Key responsibilities:

  • Oversee planning and execution of tech transfers, development and scale up of viral products being manufactured at CDMOs
  • Serve as the downstream subject matter expert on both internal and external (CDMO, equipment suppliers, etc.) teams
  • Build out internal downstream capabilities by identifying/procuring scale down models for process development
  • Design and execute studies to identify critical process parameters and optimize process setpoints across the clarification, Tangential Flow Filtration (TFF), chromatography and sterile filtration steps
  • Responsibility for execution, data review, analysis, and maintaining accurate and detailed lab notebooks
  • Author and review technical documents, including but not limited batch records, SOPs and development reports and process-specific sections of regulatory documents.
  • Represent the company externally at meetings (professional associations, with regulatory bodies, etc.)
  • Work cross-functionally with analytical development, research and development, program management to advance clinical programs

Required experience & skills: 

  • MS or Ph.D. in Chemical Engineering, Bioengineering or related discipline
  • Minimum of 10 years of experience with downstream purification process development in the biopharma industry
  • Experience directly managing a team
  • Technical experience with downstream unit operations including clarification, TFF, chromatography, sterile filtration and formulation
  • Experience with scale up and scale down of purification processes
  • An understanding of cGMP and regulatory requirements for biopharmaceuticals
  • Strong organizational & problem-solving skills, with the proven ability to collaborate in a dynamic team environment
  • Strong scientific reasoning, problem-solving, and applied statistics skills, including the ability to break down complex problems into manageable hypotheses
  • Proficiency in using Microsoft Word, Excel, Power Point and data analysis/presentation software such as JMP and/or GraphPad
  • Excellent interpersonal, verbal and written communication skills.
  • Excellent organizational and planning skills, strong work ethic and the desire to work in a flexible and fast-paced, entrepreneurial environment

Preferred experience & skills: 

  • Experience with Quality by Design (QbD) approach to drug development including risk assessments, Design of Experiments (DoE) and statistical methods
  • Experience drafting CMC sections for INDs
  • Experience with technology transfers to external manufacturing facilities

 

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