intellipro

Process Specialist/Research Associate

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At a Glance

Location
Research Triangle Park, North Carolina, United States
Employment
contract
Experience
2+ years

Key Requirements

Required Skills

ExcelPowerPoint

Domain Knowledge

  • Biotech
  • Clinical
  • Education
  • Engineering
  • Manufacturing
  • Regulatory

Benefits & Perks

Health Insurance

telliPro provides a comprehensive benefits package, all subject to eligibility.

Requirements

Minimum 2 years (BS)/0 years (MS) of relevant experience in laboratory research, biologics manufacturing and a desire to continue in a laboratory-focused role, preferably within:

Experience or familiarity with upstream and/or downstream bioprocess operations

Comfort executing experiments under direction, following protocols, and meeting scheduled deliverables

Prior exposure to cGMP manufacturing environments or manufacturing-support laboratories

Hands-on experience executing scale-up, scale-down, or process characterization experiments

Familiarity with DOE concepts and experimental execution (design and analysis support may be provided by others)

Compensation & Benefits

The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.

Responsibilities

Seeking a contract Process Engineer/Research Associate to provide hands-on laboratory and manufacturing support of AAV (rAAV) vector research and late-stage clinical gene therapy programs.

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

The contractor will contribute to the timely completion of manufacturing and laboratory studies, data collection, and manufacturing readiness ensuring alignment with existing protocols to support early-stage gene therapy programs, technology development, and internal research priorities.

This is a laboratory-based contract role intended to support day-to-day manufacturing and experimental execution working closely with pre-clinical manufacturing and MSAT scientists.

Execute routine and defined rAAV manufacturing and laboratory activities for research and GLP-grade studies following established protocols and batch records.

Perform hands-on upstream and downstream operations, including:

About the Company

Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.

IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at

https://intelliprogroup.com/

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