Novozen Healthcare LLC
Technology Transfer Engineer – Pharma / Biotech
3 days ago
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Important information
Contract type:
Freelance / Contract
Salary:
$45 – $50 / hour
Location:
Spokane, WA, USA
Work mode:
Onsite
Published on:
22 October 2026
What they need
Job Title: Technology Transfer Engineer – Pharma / Biotech
Company: Novozen Healthcare LLC.
Location: Spokane, WA (100% Onsite)
Employment Type: Contract (6 Months, with Strong Extension Potential)
Job Responsibilities
- Support technology transfer projects from planning through implementation.
- Assist with commissioning, qualification, and validation activities for pharmaceutical manufacturing equipment and supporting systems.
- Author and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols and reports.
- Develop and update validation documentation, protocols, Standard Operating Procedures (SOPs), and User Requirement Specifications (URSs).
- Support equipment installation, startup, and operational readiness activities.
- Collaborate with Engineering, Manufacturing, Quality, Validation, Formulation, and Project teams.
- Troubleshoot qualification-related issues and support investigations and resolutions.
- Execute qualification activities in accordance with Good Manufacturing Practice (GMP) requirements and site procedures.
- Prepare and maintain documentation to support regulatory inspections and audit readiness.
- Support sponsor-driven technology transfer and manufacturing startup initiatives.
Required Qualifications
- Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
- Minimum 5 years of experience in CQV, validation, equipment qualification, manufacturing engineering, technical operations, or a related function.
- Experience in pharmaceutical, biotechnology, biologics, or sterile manufacturing environments.
- Hands-on experience supporting technology transfer, qualification, validation, commissioning, or facility expansion projects.
- Ability to independently author qualification protocols, reports, and technical documentation.
- Working knowledge of IQ/OQ/PQ and commissioning and qualification principles.
- Experience working in GMP-regulated environments.
- Strong technical writing, organizational, problem-solving, and communication skills.
- Ability to collaborate effectively with cross-functional teams.
Preferred Qualifications:
- Experience qualifying process vessels, manufacturing tanks, mixing and formulation equipment, sterility support equipment, manufacturing fixtures, or Clean-in-Place (CIP) systems.
- Experience with ultra-low-temperature freezers, walk-in freezers, cold rooms, refrigerated storage, temperature-controlled warehouses, or temperature mapping studies.
- Experience developing qualification strategies, supporting media fills, and executing manufacturing startup and operational readiness activities.
- Experience developing and revising SOPs, URSs, qualification protocols, and technical reports.
Pay Scale
Anticipated hourly pay range: $45/hr to $50/hr on W2.
Benefits
Employees hired into this position are eligible for the following benefits, subject to applicable plan terms and eligibility requirements:
Health Insurance: Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.
Retirement Benefits: A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.
Paid Time Off (PTO): No PTO is provided other than that required by applicable state and local laws.
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