Quality Assurance Specialist

Job Summary

Primarily responsible for supporting the Company Research and Development quality agreement process with a focus on identifying and implementing process improvements. Assures the quality of manufactured products and processes per standard operating processes (SOP'S) and GMP (Good Manufacturing Practices).

Location:

North Chicago, Illinois
Job type:
Contract
Salary: $39.00 - 43.01 per hour

Work hours:

9 to 5

Education:

Bachelor’s

• Lead or participate in technically complex and strategic cross‑functional projects, demonstrating the ability to work across various teams.
• Drive or support strategic initiatives aimed at improving compliance with regulatory requirements and standards.
• Take a proactive role in process improvements, which includes the review and update of current supporting processes and procedures to enhance efficiency and effectiveness.
• Achieve a difficult balance of involvement, independence, and objectivity.
• Provide support for periodic review of Quality Agreements, ensuring alignment with organizational and regulatory expectations.
• Collect, analyze, and report relevant metrics to inform decision‑making and track the effectiveness of initiatives.
• Consistently demonstrate Company's Ways of Working and Leadership Attributes including a collaborative mindset and leadership. Create a learning environment, embrace the ideas of others, and manage innovation to reality.

• Bachelor's degree preferable in a physical science, life science, pharmacy, business, engineering or equivalent experience required.
• 5‑7 years of experience in Quality Assurance / Regulatory Affairs (Pharmaceutical or Medical Device preferred).
• 3‑5 years of experience in clinical research and development or manufacturing, or analysis of investigational products.
• Minimum of 7 years' total combined experience required (not necessarily the sum of the above).
• Must have experience with quality agreements and knowledge of worldwide regulatory requirements that influence their content.
• Persuasive, effective communication skills are essential with an ability to work effectively across functions, across technical areas, and outside of the company.
• Must have excellent oral/written communication skills, interpersonal skills, leadership, tact, open mindedness, maturity, tenacity, decisiveness, self‑reliance, organizational/administrative skills, and sound judgment.

Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Quality Assurance (QA)

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

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