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Internship Downstream Process Development Scientist Jobs in Raleigh, NC

Valspec

Validation Engineer

Holly Springs, NC

... or life sciences manufacturing * Hands-on experience with downstream processing equipment ... Join a team where your contributions matter, your development is prioritized, and your success is ...

Valspec

Validation Engineer

Raleigh, NC

... or life sciences manufacturing * Hands-on experience with downstream processing equipment ... Join a team where your contributions matter, your development is prioritized, and your success is ...

Amgen

Sr Engineer I

Holly Springs, NC · On-site

$90K - $124K/yr

... PROCESS DEVELOPMENT (DOWNSTREAM) What you will do Let's do this. Let's change the world. In this ... Master's degree in in Engineering or Science discipline * 5+ years of experience in a technical ...

Intellectt INC

CQV Engineer

Holly Springs, NC · On-site

... or life sciences industries * Strong experience supporting greenfield projects * Hands-on ... Experience with upstream and downstream process equipment * Strong knowledge of GMP documentation ...

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How much do internship downstream process development scientist jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for internship downstream process development scientist in Raleigh, NC is $37.58, according to ZipRecruiter salary data. Most workers in this role earn between $27.60 and $44.86 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Internship Downstream Process Development Scientist, and why are they important?

To thrive as an Internship Downstream Process Development Scientist, you need foundational knowledge in biochemistry, molecular biology, or chemical engineering, often supported by ongoing or recent enrollment in a relevant degree program. Familiarity with laboratory techniques such as chromatography, filtration, and analytical instruments, as well as experience with lab management software, is typically expected. Attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this role. These skills and qualifications are crucial for conducting reliable experiments, analyzing data, and contributing to the optimization of bioprocesses in a collaborative research environment.

What does an Internship Downstream Process Development Scientist do?

An Internship Downstream Process Development Scientist works in the biopharmaceutical industry, assisting with the development and optimization of processes that purify biological products such as proteins, antibodies, or vaccines after they are produced by cells. Their role often involves supporting laboratory experiments, analyzing samples, and documenting results to improve the efficiency and scalability of downstream processes like filtration and chromatography. Interns in this position gain hands-on experience with cutting-edge technologies and learn about regulatory requirements and industry standards. This role helps prepare students or recent graduates for a career in process development or biomanufacturing.

What types of projects and responsibilities can an Internship Downstream Process Development Scientist expect to work on?

As an Internship Downstream Process Development Scientist, you can expect to be involved in hands-on laboratory work focusing on the purification and characterization of biopharmaceutical products. Typical responsibilities include preparing buffer solutions, operating chromatography and filtration systems, analyzing samples using various analytical techniques, and documenting experimental results. Interns often collaborate with experienced scientists and engineers, contributing to process optimization and troubleshooting. The role provides valuable exposure to industry-standard procedures and the opportunity to develop technical skills in a team-oriented environment.
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Internship Downstream Process Development Scientist jobs near you
Validation Engineer

Validation Engineer

Valspec

Holly Springs, NC

Full-time

Medical, Retirement

Posted 9 days ago

Job description

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.

Valspec's projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.

Validation Engineer (CQV)

Location: Raleigh-Durham area, NC

Position Overview

We are seeking an experienced Validation Engineer (CQV) to support commissioning, qualification, and startup activities for a large-scale biopharmaceutical manufacturing facility. This role will focus on downstream process systems and requires strong hands-on field execution, system troubleshooting, and automation verification experience in a GMP-regulated environment.

Key Responsibilities

  • Perform field verification of P&IDs, equipment datasheets, vendor drawings, isometrics, and utility connections to confirm system accuracy and readiness ahead of commissioning and startup.
  • Lead and execute mechanical completion walkdowns and turnover package (TOP) reviews, ensuring construction quality, punch list closure, calibration records, weld documentation, and redline updates are complete.
  • Support commissioning readiness by validating system boundaries, flow paths, and equipment installation in alignment with design documentation.
  • Execute commissioning and qualification (CQV) activities for downstream process equipment including:
    • Chromatography skids
    • Ultrafiltration/Diafiltration (UF/DF) systems
    • Viral filtration systems
    • Depth filtration units
    • Buffer preparation vessels
    • Product hold tanks
  • Perform field startup and functional testing of chromatography systems, including:
    • Flow path verification
    • Valve sequencing checks
    • Conductivity and pressure monitoring
    • Automation functionality validation
  • Conduct Operational Qualification (OQ) testing for automated systems using DeltaV, including:
    • Loop checks and I/O verification
    • Interlock and permissive testing
    • Alarm challenge testing
    • Control logic and sequence verification under live conditions
  • Verify process alarms, interlocks, permissives, and emergency shutdown functions through field execution and control system testing.
  • Perform detailed P&ID walkdowns and field verification of valves, instruments, and process flow to support system turnover, TOP approval, and final acceptance.
  • Identify and troubleshoot startup issues related to:
    • Automation logic and control sequences
    • Valve sequencing and flow path discrepancies
    • Equipment integration and skid interfaces
    • Cleaning cycle performance
  • Collaborate cross-functionally with engineering, construction, and operations teams to maintain project timelines and ensure successful system startup.

Required Qualifications

  • Bachelor's degree in Engineering (Chemical, Mechanical, or related discipline) or equivalent industry experience
  • 5+ years of experience in CQV, commissioning, or validation within biopharmaceutical or life sciences manufacturing
  • Hands-on experience with downstream processing equipment, especially chromatography and filtration systems
  • Strong knowledge of cGMP requirements, commissioning processes, and validation lifecycle
  • Experience executing OQ protocols and field testing activities
  • Familiarity with DeltaV or similar DCS platforms (Emerson experience preferred)
  • Proficiency in reading and interpreting P&IDs, isometrics, and technical drawings
  • Demonstrated ability to work in a fast-paced startup environment with significant field presence

Preferred Qualifications

  • Previous experience supporting greenfield or large-scale capital projects
  • Strong troubleshooting and problem-solving skills in live plant environments
  • Experience with automation systems integration and process control verification
  • Ability to manage multiple systems and priorities during commissioning/startup phases

Work Environment

  • Primarily field-based role with significant time in manufacturing and construction areas
  • Requires coordination with multiple stakeholders across CQV, engineering, and operations
  • May involve extended hours during critical commissioning and startup windows

Why Join Valspec?

At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation. We also offer a highly competitive benefits package, including:

  • Premium medical coverage
  • 401(k) with company match
  • Tuition reimbursement
  • Unique performance incentives
  • And more — all designed to support your growth, well-being, and future.

Join a team where your contributions matter, your development is prioritized, and your success is shared.

When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net or @valspec.net. Any other domains are impersonations and should be ignored.

Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time.

Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.

Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.