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Process Development Associate Jobs in Raleigh, NC

Orion Group

R&D Associate I

Durham, NC · On-site

$27 - $31/hr

Research & Development Associate I $27 - $31/hr with medical benefits available at a cost 6 month ... Works under immediate supervision, following instructions and established processes. Typically ...

DivIHN

Process Engineer Pharmaceuticals I

NC · On-site

Client is seeking a contract Process Engineer/Research Associate to provide hands-on laboratory and ... Support process development and experimental studies, including process characterization and ...

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All JobsProcess Development Associate JobsProcess Development Associate Jobs in Raleigh, NC

Process Development Associate information

See Raleigh, NC salary details

$18

$32

$48

How much do process development associate jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for process development associate in Raleigh, NC is $32.74, according to ZipRecruiter salary data. Most workers in this role earn between $26.88 and $40.19 per hour, depending on experience, location, and employer.

What is the difference between Process Development Associate vs Process Engineer?

AspectProcess Development AssociateProcess Engineer
Required CredentialsBachelor's in Chemistry, Chemical Engineering, or related field; often some experience in process developmentBachelor's or Master's in Chemical Engineering or related; more emphasis on engineering principles
Work EnvironmentLaboratory and pilot plant settings, focused on process research and developmentManufacturing plants, production lines, and process optimization environments
Employer & Industry UsagePharmaceutical, biotech, and chemical industries; entry to mid-level rolesChemical, manufacturing, and process industries; more senior roles in process optimization

The Process Development Associate primarily focuses on developing and optimizing new processes in lab and pilot settings, often working closely with R&D teams. In contrast, the Process Engineer applies engineering principles to scale up processes, improve manufacturing efficiency, and troubleshoot production issues. While both roles require a background in chemical or process engineering, the Process Development Associate is more research-oriented, whereas the Process Engineer emphasizes process implementation and optimization in production environments.

What are the key skills and qualifications needed to thrive as a Process Development Associate, and why are they important?

To thrive as a Process Development Associate, you need a strong background in biochemistry, chemical engineering, or a related field, often supported by a bachelor’s or master’s degree. Experience with laboratory instrumentation, process optimization tools, and familiarity with regulatory standards such as GMP are typically required. Attention to detail, problem-solving abilities, and effective teamwork are vital soft skills for excelling in this role. These competencies are crucial for ensuring efficient process design, regulatory compliance, and successful scale-up in manufacturing environments.

What is a Process Development Associate?

A Process Development Associate is a professional who assists in designing, optimizing, and scaling up manufacturing processes, typically in industries such as biotechnology, pharmaceuticals, or chemical engineering. They work closely with scientists and engineers to develop efficient, safe, and cost-effective processes for producing products or materials. Their responsibilities often include conducting experiments, collecting and analyzing data, troubleshooting process issues, and supporting technology transfer to manufacturing. This role is essential for ensuring that new or improved products can be produced reliably at larger scales. Process Development Associates help bridge the gap between research and full-scale production.

What are the primary challenges faced by a Process Development Associate when scaling up laboratory processes to manufacturing scale?

A Process Development Associate often encounters challenges in translating small-scale laboratory protocols into large-scale manufacturing processes. Variations in equipment, raw material quality, and environmental conditions can impact reproducibility and efficiency. Addressing these issues requires strong troubleshooting skills, attention to detail, and close collaboration with cross-functional teams such as manufacturing, quality assurance, and engineering to ensure smooth technology transfer and consistent product quality.
What are popular job titles related to Process Development Associate jobs in Raleigh, NC? For Process Development Associate jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Process Development Associate jobs in Raleigh, NC look for? The top searched job categories for Process Development Associate jobs in Raleigh, NC are:
Process Development Associate jobs near you

Process Development Sr Associate - Holly Springs, NC

MSCCN

Holly Springs, NC • On-site

$75K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 24 days ago

Job description

Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
What you will do
Let's do this. Let's change the world. In this vital role you will be part of Amgen's Attribute Sciences (AS) department within the Process Development (PD) organization that defines the favorable quality characteristics of the therapies it produces and optimizes innovative analytical tools to guide that development.
In this vital role, you will work to provide scientific and technical contributions within Process Development Attribute Sciences at Amgen's FleX Batch facility. This laboratory-based role will evaluate attributes of materials based upon multiple analytical techniques, focusing on analytical testing, support, and troubleshooting.
Responsibilities include effectively delivering to the site, process development team, manufacturing and quality control through rapid and robust analytical testing.
Ensure analytical support for small-scale model transfer, method transfers, investigation support, and continuous improvements.
Work closely with functions including but not limited to Drug Substance, Quality, and Manufacturing.
Understand analytical methodologies to detect product quality attributes and process-related impurities testing using a variety of techniques including but not limited to ELISA, qPCR and UV-Vis spectrophotometry.
Execute methods, author reports and ensure safety and compliance for all activities.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The collaborative professional we seek is a motivated, self-starter with these qualifications.
Additional Qualifications/Responsibilities
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The collaborative professional we seek is a motivated, self-starter with these qualifications.
Basic Qualifications:
  • High school diploma / GED and 6 years of related experience OR
  • Associate's degree and 4 years of related experience OR
  • Bachelor's degree and 2 years of related experience OR
  • Master's degree

Preferred Qualifications:
  • Degree in Analytical Chemistry, Biochemistry, or related area.
  • Experience in pharmaceutical process development with related experience in analytical support, execution of methods, and investigational testing.
  • Strong experience in a variety of analytical techniques (i.e., ELISA, qPCR, SoloVPE).
  • Experience in method transfers, method validation, method troubleshooting, and complex investigations.
  • Solid understanding of GMP requirements and familiarity with USP monographs and chapters, as well ICH guidance documents related to analytical method transfer and validation.
  • Knowledgeable in analytical method troubleshooting and analysis of product quality attributes related to biological processing.
  • Strong communication skills and ability to interact effectively with diverse internal and cross-functional teams.
  • Excellent technical writing skills, attention to details and compliance with GDP.
  • Proven ability to work effectively in collaborative, team-based settings.

What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Salary Range
80,044.50USD -108,295.50 USD

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