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Downstream Purification Jobs (NOW HIRING)

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Downstream Purification information

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How much do downstream purification jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for downstream purification in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What is downstream purification?

Downstream purification is a process in biopharmaceutical manufacturing that involves isolating and refining a target product, such as a protein or antibody, from a mixture of cells, media, and other impurities. It typically includes steps like filtration, chromatography, and concentration to ensure product purity and quality. Downstream purification requires attention to detail, proper use of equipment, and adherence to regulatory standards.

What is the highest paying job in biotechnology?

In biotechnology, senior roles such as Biotech Executive, Director of Research, or Vice President of Biotechnology tend to be the highest paying positions, often earning six-figure salaries. These roles typically require advanced degrees, extensive experience, and leadership skills, with compensation influenced by company size and location.

What are the key skills and qualifications needed to thrive in Downstream Purification, and why are they important?

To excel in Downstream Purification, you need a solid background in biochemistry or chemical engineering, with experience in protein purification techniques and a relevant degree. Familiarity with chromatography systems (e.g., AKTA), filtration technologies, and good manufacturing practice (GMP) certification is highly valuable. Strong analytical thinking, attention to detail, and effective teamwork are important soft skills in this role. These competencies ensure the efficient and reliable production of high-purity biopharmaceutical products, critical for product quality and regulatory compliance.

What are some common challenges faced in a Downstream Purification role, and how can they be addressed?

Professionals in Downstream Purification often encounter challenges such as maintaining product yield and purity, troubleshooting equipment malfunctions, and adapting to process variability. Addressing these requires strong analytical skills, attention to detail, and close collaboration with upstream teams and quality assurance. Continuous training on the latest purification technologies and strict adherence to standard operating procedures also help minimize errors and improve efficiency in the production process.

What is the difference between Downstream Purification vs Downstream Processing?

AspectDownstream PurificationDownstream Processing
FocusPurifying specific products from a mixtureOverall process including purification and initial recovery
CredentialsTypically requires bioprocessing or biotech certificationsSimilar credentials, often overlapping
Work EnvironmentLaboratories, clean rooms, manufacturing facilitiesLabs and production plants
Industry UsageBiotech, pharmaceutical manufacturingBiotech, pharmaceutical, and bioprocessing industries

Downstream Purification is a specialized part of the broader Downstream Processing. While downstream processing includes all steps from initial product recovery to purification, downstream purification specifically focuses on isolating and purifying the target product. Both roles often require similar skills and certifications, and they operate in comparable environments within biotech and pharmaceutical industries.

Is it hard to get a job in biotechnology?

Getting a job in downstream purification within biotechnology can be competitive, often requiring relevant education such as a degree in biochemistry, chemical engineering, or related fields, along with laboratory skills and experience with purification techniques like chromatography. Entry-level positions may be accessible with proper training, but advanced roles typically demand specialized knowledge and certifications. Strong understanding of Good Manufacturing Practices (GMP) and familiarity with bioprocessing tools can improve job prospects.

What biology jobs pay over $100k?

In the field of downstream purification, senior roles such as Process Development Managers, Regulatory Affairs Directors, and Senior Bioprocess Engineers often have salaries exceeding $100,000 annually. These positions typically require advanced degrees, extensive industry experience, and expertise in bioprocessing, quality control, or regulatory compliance.
More about Downstream Purification jobs
What cities are hiring for Downstream Purification jobs? Cities with the most Downstream Purification job openings:
What states have the most Downstream Purification jobs? States with the most job openings for Downstream Purification jobs include:
Infographic showing various Downstream Purification job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

Downstream Manufacturing Associate

Global Life Science Hub

Piscataway, NJ • On-site

Other

Re-posted 6 days ago


Job description

DOWNSTREAM MANUFACTURING ASSOCIATE Piscataway, NJ - Full-Time, Permanent

We are seeking a Downstream Manufacturing Associate to join a well-established biologics manufacturer in Piscataway, NJ. This is a full-time permanent position - not a contract role.


You will be executing cGMP downstream purification processes at scale, working across engineering, clinical, and commercial batches in a regulated manufacturing environment. Hands-on, production floor work with real responsibility from day one.


What you'll be doing:

  • Executing downstream purification processes at 50L to 1000L scale in a cGMP environment
  • Operating and maintaining AKTA purification skids, TFF systems, and chromatography equipment
  • Column packing, process troubleshooting, and data analysis
  • Initiating and completing batch records, deviations, and investigations in line with GMP requirements
  • Supporting environmental health and safety compliance on the manufacturing floor


What you need:

  • 1-2+ years hands-on experience in downstream cGMP manufacturing within biopharma or a CDMO
  • Experience with AKTA or equivalent purification systems and TFF
  • Mammalian cell culture or biologics manufacturing background
  • Comfortable with GMP documentation - batch records, protocols, investigations
  • BS or MS in biochemistry, biotech, chemical or biological sciences


Multiple levels available - MFG I, II, and III - so we are open to candidates across the experience spectrum.

If this sounds like your next move, apply directly or reach out to discuss.