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Thermo Fisher Scientific

Sell Thermo Fisher's Downstream Workflow products to biotech and biopharma accounts for process development and manufacturing. This highly valued individual contributor will model and act in ...

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As of Sep 8, 2026, the average hourly pay for downstream specialist in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $28.85 per hour, depending on experience, location, and employer.

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Infographic showing various Downstream Specialist job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 11% Part Time, and 2% Contract. Highlights an 78% Physical, 2% Hybrid, and 20% Remote job distribution, with an average salary of $51,897 per year, or $25 per hour.

Downstream Manufacturing Specialist

Morrisville, NC • On-site

Astrix Inc.
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Astrix Inc.external

$250/hr

Other

Posted 10 days ago

Job description

We are seeking a Downstream Manufacturing Specialist to support the manufacturing of gene therapy products in a GMP-regulated environment. This role will be responsible for executing and supporting downstream purification and processing activities, ensuring manufacturing operations are performed safely, efficiently, and in accordance with approved procedures and regulatory requirements.

The ideal candidate has hands‑on experience with downstream bioprocessing, strong attention to detail, and a working knowledge of GMP manufacturing practices. This is a contract-to-hire opportunity for an individual who is interested in building a long‑term career within a growing gene therapy organization. Pay rate: $40-42/hr Shift: 1st shift, with occasional 2nd shift

Key Responsibilities
  • Execute downstream manufacturing activities for gene therapy products in accordance with approved batch records, SOPs, protocols, and GMP requirements.
  • Perform and support downstream purification and processing operations, which may include:
    • Clarification and filtration
    • Centrifugation
    • Chromatography
    • Tangential flow filtration (TFF)
    • Buffer and media preparation
    • Ultrafiltration/diafiltration
    • Product concentration and formulation
    • Aseptic processing and final bulk operations
  • Operate, clean, sanitize, and maintain manufacturing equipment and associated systems.
  • Perform in‑process sampling and coordinate with Quality Control for testing as required.
  • Accurately document manufacturing activities in batch records, logbooks, and electronic systems in accordance with Good Documentation Practices (GDP).
  • Identify process deviations, equipment issues, and manufacturing abnormalities and promptly elevate them to appropriate personnel.
  • Support deviation investigations, CAPAs, change controls, and other manufacturing quality initiatives.
  • Follow all applicable GMP, environmental health and safety (EHS), biosafety, and facility procedures.
  • Assist with equipment setup, line clearance, cleaning verification, and manufacturing area preparation.
  • Participate in process optimization, continuous improvement, and manufacturing scale‑up activities.
  • Work closely with Manufacturing, Process Development, Quality Assurance, Quality Control, Engineering, and Facilities teams.
  • Support technology transfer and process validation activities as needed.
  • Maintain a clean, organized, and compliant manufacturing environment.
  • Participate in shift activities, overtime, and occasional weekend work based on manufacturing schedules.
Qualifications Required
  • Bachelor's degree in Biology, Biochemistry, Chemical Engineering, Biotechnology, or a related scientific/engineering discipline, or equivalent relevant experience.
  • 2+ years of experience in biopharmaceutical, biologics, cell therapy, gene therapy, or related GMP manufacturing.
  • Hands‑on experience with downstream bioprocessing and purification operations.
  • Understanding of GMP manufacturing principles and Good Documentation Practices.
  • Ability to follow detailed SOPs and batch records while maintaining a high level of accuracy.
  • Strong communication, organizational, and problem‑solving skills.
  • Ability to work effectively in a cross‑functional, team‑oriented environment.
  • Ability to work on‑site in a manufacturing environment and wear required PPE.
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