1

Downstream Process Jobs in Raleigh, NC (NOW HIRING)

Serve as the process equipment engineering lead for a defined subset of upstream and/or downstream systems, which may include: * Large stainless-steel bioreactors (up to 10,000 L) * Tangential flow ...

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 ...

New

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 ...

Experience with upstream and downstream process equipment * Strong knowledge of GMP documentation, IQ/OQ protocol execution, and compliance activities * Ability to support startup, troubleshooting ...

Experience with upstream/downstream process equipment. * Strong GMP documentation and protocol execution skills. * Ability to work independently in fast-paced project environments. Preferred ...

The ideal candidate holds a BS degree and has hands-on expertise within both upstream and downstream processing. Key Responsibilities: * Operate and maintain bioreactors for cell culture and gene ...

This role is execution-focused, supporting upstream and downstream manufacturing operations, routine experiments, and process development studies working in close coordination with manufacturing and ...

next page

Showing results 1-20

Downstream Process information

See Raleigh, NC salary details

$13

$23

$34

How much do downstream process jobs pay per hour?

As of Jul 9, 2026, the average hourly pay for downstream process in Raleigh, NC is $23.98, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $27.36 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals working in downstream process roles within biomanufacturing?

Professionals in downstream process roles often encounter challenges such as optimizing purification steps to maximize yield and product purity while minimizing costs and processing time. They must also troubleshoot issues related to equipment performance, scalability, and regulatory compliance, especially when transitioning from lab-scale to large-scale production. Collaboration with upstream teams, quality assurance, and engineering is critical to address these challenges and ensure a smooth workflow. Staying current with technological advances and regulatory requirements also plays a significant role in day-to-day success.

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

To thrive as a Downstream Process Engineer, you need a solid background in chemical or biochemical engineering, knowledge of purification techniques, and typically a relevant degree. Familiarity with process control systems, chromatography, filtration technologies, and GMP compliance, as well as certifications like Six Sigma, are commonly required. Strong problem-solving, teamwork, and communication skills help you excel in cross-functional teams and address complex production challenges. These skills ensure efficient, high-quality product recovery and compliance with industry standards in biomanufacturing environments.

What is the difference between Downstream Process vs Upstream Process?

AspectDownstream ProcessUpstream Process
PurposePurifies and isolates the target product from the mixtureProduces the initial product, such as cell culture or fermentation
ActivitiesFiltration, chromatography, centrifugation, purificationCell growth, fermentation, media preparation
Work EnvironmentLaboratories, bioprocessing facilitiesBioreactors, fermentation tanks, labs
Required SkillsBioprocessing techniques, chromatography, filtrationMicrobiology, cell culture, fermentation technology

Downstream Process focuses on purifying the product, while Upstream Process involves producing the raw material. Both are essential steps in biopharmaceutical manufacturing, often working sequentially to ensure high-quality product output.

What is a Downstream Process in biotechnology?

A Downstream Process refers to the series of steps involved in the purification and recovery of biological products, such as proteins, enzymes, or antibodies, after they have been produced by microorganisms or cells during fermentation or cell culture. It typically includes cell separation, product isolation, purification, and polishing to achieve the desired product quality and purity. Downstream processing is crucial for ensuring that biopharmaceutical products meet regulatory and safety standards before they reach the market.
What are popular job titles related to Downstream Process jobs in Raleigh, NC? For Downstream Process jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Downstream Process jobs? Cities near Raleigh, NC with the most Downstream Process job openings:
Infographic showing various Downstream Process job openings in Raleigh, NC as of July 2026, with employment types broken down into 18% Locum Tenens, 69% Full Time, 7% Part Time, 1% Temporary, 4% Contract, and 1% Summer. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $49,886 per year, or $24 per hour.
Associate Director, Downstream Process Development, GT-PD

Associate Director, Downstream Process Development, GT-PD

Novartis

Durham, NC

$145K - $270K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 10 days ago


Novartis rating

7.4

Company rating: 7.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

53rd of 73 rated pharmaceutical


Job description

Job Description Summary

Location: Durham, North Carolina #onsite
Novartis will not sponsor visas for this position.
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Role Purpose:
The GT PD Downstream people manager role provides oversight in process and platform development, improvement/optimization, characterization, and tech transfer to support gene therapy programs/products under DQP. This role demonstrates strong scientific and people leadership skills with deep understanding of gene therapy process and development. Shape and develop its strategic direction and drive operational excellence in line with TRD vision and strategy. Leads and manages all project/network activities and apply scientific/technical expertise to address complex development issues and actively support TRD strategies and goals by participating in cross-functional teams. Lead scientific programs, co-ordinate interdisciplinary projects and teams. Develop long term strategies on science and technologies.


Job Description

Major accountabilities:

  • Responsible for building, leading, and advocating for the GT Process Development Downstream team as well as fostering growth and providing development opportunities for

    team members.

  • Technical oversights of GT PD projects.

  • Developing plans and roadmaps for future state of GT Downstream, including improvements to ways of working and product quality.

  • Lead teams and coach technical staff to deliver on objectives in a safe and efficient manner.

  • Interface regularly with cross functional team members and clinical and/or commercial manufacturing units to provide support and input during development of various gene therapy programs.

  • Maintain visibility to both process and analytical development activities and contribute to technical assessments and program decisions.

  • Serve as strategic partner and advisor for cross-functional project teams and committees.

  • Author, review and approve process development and related documents to ensure completeness, accuracy, consistency, and clarity.

  • Delivers high impact, technical findings, and concepts to senior leads within the organization.

  • Provides leadership direction, determining and developing approach to solutions by coordinating multiple resources to solve complex problems.

  • Exhibit an exceptional degree of creativity and resourcefulness.

  • Report and present scientific/technical work at internal/external meetings/conferences and publish in peer reviewed international scientific journals including patents

Key performance indicators:

  • Positive customer/ business partner feedback

  • Contributes to achievement of function objectives and strategy -Accountability for costs, quality, quantity, and timelines for all assigned tasks.

  • Reach budget targets, adhere to agreed efficiency increase and cost effectiveness goals.

  • Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards.

  • Measurable contributions to the success, efficiency and productivity of the department and new programs/initiatives started and implemented.

  • Accountability for costs, quality, quantity, and timelines for all assigned tasks.

  • Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards.

  • Feedback from other team members/leaders.

  • Refer to annual individual and team objective setting.

  • Outcome of risk analyses, process challenge meetings, audits and inspections.

  • Measurable contributions to increasing efficiency and productivity in the work related to assigned projects.

  • Internal and external publications/presentations invited lectures.

The salary for this position is expected to range between $145,600 and $270,400 per year.

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and

disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$145,600.00 - $270,400.00


Skills Desired


What Novartis employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom