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Process Development Associate Jobs in Raleigh, NC

ASST-TCHR PRE K

Raleigh, NC · On-site

$15.96/hr

... Development Associate (CDA) credential; or (2) hold or be working toward an Associate Degree or ... Begin CBC application process: * You will need to enter your addresses for the past 5 years. If you ...

ASST-TCHR PRE K

Raleigh, NC · On-site

$15.96/hr

... Development Associate (CDA) credential; or (2) hold or be working toward an Associate Degree or ... Begin CBC application process: * You will need to enter your addresses for the past 5 years. If you ...

... Development Associate (CDA) credential; or (2) hold or be working toward an Associate Degree or ... Begin CBC application process: * You will need to enter your addresses for the past 5 years. If you ...

... Development Associate (CDA) credential; or (2) hold or be working toward an Associate Degree or ... Begin CBC application process: * You will need to enter your addresses for the past 5 years. If you ...

... Development Associate (CDA) credential; or (2) hold or be working toward an Associate Degree or ... Begin CBC application process: * You will need to enter your addresses for the past 5 years. If you ...

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Showing results 1-20

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 20, 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:

Associate Manufacturing- Downstream - Nights (Multiple Positions)

Amgen

Holly Springs, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago


Job description

Career CategoryManufacturingJob Description

HOW MIGHT YOU DEFY IMAGINATION?

You've worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 million patients worldwide. Come do your bestworkalongside other innovative, driven professionals in this meaningful role.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

Associate Manufacturing-Downstream -Nights(Multiple Positions)

Live

What youwill do

Let's do this! Let's change the world! In this dynamic role, you will be an Associate in the manufacturing organization at Amgen North Carolina (ANC).The essential position, which supports our critical 24/7 manufacturing operations,worksa 12-hour 2-2-3 schedule from 5:45pm to 6:15am.Associates will be completing operations on the floor in ourdownstreamareaandwillberesponsible forthe manufacturing of cGMP (Current Good Manufacturing Practices) drug substances.

Withgeneraldirection, the Associate will support all floor operations in accordance with cGMP practices.As Amgen relies upon the regular attendance of staff members to meet legitimate business needs, staff must be able to work assigned 12-hourshift, including during inclement weather, some holidays and requested overtime in support of our 24/7 operations.

Responsibilities will include...

Compliance:

  • Completes work in accordance with establishedcGMPproceduresand policies(Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance

  • Assure proper gowning and aseptic techniques are always followed

Process/Equipment/Facilities:

  • Perform hands-ondownstream bio-tech operations(Column Chromatography, Tangential Flow Filtrationamong others)including set-up, cleaning, sanitization, monitoring of equipment and assigned area

  • Run and monitor critical process tasksperassigned procedures

  • Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records [EBRs])

  • Complete washroom activities: cleaning equipment, small to large scale, used in production activities

  • Initiate and own manufacturing related process deviations

  • Identify and escalateissues and concerns regardingdaily routine functionsrelated to process and tasks; may engage with team on potential solutions

  • Perform documentationfor assigned functions (i.e., equipment logs, EBRs)

  • Collaborate as part of a cross-functional team (i.e., QA/QC, F&E (Facilities & Engineering), PPIC, Mfg., PD (Process Development), Regulatory, etc.) in completing production activities

  • Maintain an organized, clean, and workable space

Win

What we expectofyou

We are all different, yet we all use our unique contributions to serve patients. The hard-working professionalswe seekareteam playerswith these qualifications.

Basic Qualifications:

  • High School/GED + 2 years manufacturingand/or other regulated environmentexperience

Or

  • Associate's Degree+ 6 monthsmanufacturing and/or other regulatedenvironmentexperience

Or

  • Bachelor's Degree

Preferred Qualifications:

  • Completion of NCBioWorksCertification Program

  • Experience inaregulated industry such asbiotechnology or pharmaceutical

  • Basic understanding andprocessexperience in a cGMPmanufacturing facility

  • Excellent verbal and written communication

  • Proficient MicrosoftOffice skills, and knowledge of other electronic systems such as EBR/MES, Delta V,andElectronicQualitySystems

  • An ability to demonstrate desire and drive to learn and grow their understanding of operations and processes

Thrive

What you can expectofus

As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being.

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.

Amgen offers a Total Rewards Plan comprising 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 including:

  • 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 and bi-annual company-wide shutdowns

  • Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities areprovidedreasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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Salary Range

70,985.20USD -96,038.80USD