Biotech Jobs in Oregon, IL (NOW HIRING)

Join a dynamic and growing biotechnology team where your work directly supports the quality and integrity of cutting‑edge antibody products. As a QA/QC Inspector, you’ll play a critical role in ensuring products meet the highest standards—supporting research, development, and innovation that matters.

This is an excellent opportunity for a detail-oriented scientific professional looking to grow a career in quality, regulatory, or biotech operations within a collaborative and fast-paced environment.

As a key member of the Quality team, you will:

• Ensure product excellence by inspecting incoming antibody materials and verifying compliance with quality and customer specifications
• Own critical documentation by creating, reviewing, and maintaining product datasheets, specifications, and labeling templates
• Drive accuracy and compliance through thorough data entry, recordkeeping, and adherence to ISO, GMP, and regulatory standards
• Collaborate cross-functionally with vendors and internal teams to resolve discrepancies and clarify technical information
• Support product lifecycle quality by documenting changes, managing material rejections, and updating specifications
• Track and report quality metrics to help improve processes and maintain operational efficiency
• Contribute to continuous improvement in a highly regulated, high-impact production environment

• Bachelor’s degree in Biology or a related scientific discipline
• Foundational knowledge of antibodies, biology, or life sciences
• Experience or exposure to QA/QC, inspection, or quality documentation
• Strong attention to detail with a commitment to accuracy and compliance
• Proficiency with Excel and data systems
• Ability to manage multiple priorities in a fast-paced environment
• Strong communication and collaboration skills
• Familiarity with GMP, ISO standards, or regulated environments (preferred)

• Experience working with antibody products or biotech manufacturing
• Exposure to quality systems, specifications, and material rejection processes
• Comfort working with enterprise systems and electronic documentation tools
• Interest in building a long-term career in biotech quality or regulatory disciplines

• Work in a cutting-edge biotech environment spanning R&D, production, and quality
• Career growth opportunities with potential to transition into a permanent role
• Collaborative culture with exposure to cross-functional teams and end-to-end operations
• Hands-on experience in a GMP/ISO-regulated facility
• Meaningful impact—your work ensures product quality that supports scientific advancement

You’ll be part of a modern, antibody-focused production facility that integrates laboratory, R&D, regulatory, and quality operations. The environment emphasizes safety, compliance, and teamwork, giving you valuable exposure to the full biotech product lifecycle.

If you’re passionate about science, quality, and making a difference in biotech, we'd love to hear from you.

This is a Contract position based out of Loves Park, IL.

The pay range for this position is $20.00 - $20.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Loves Park,IL.

This position is anticipated to close on Aug 14, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.