Contract: Quality Engineer / Specialist

Job Description

Minimum 5 years of pharmaceutical experience and experience in a quality role on the manufacturing / production floor, preferably for sterile liquids. Travel flexibility needed as on-site presence is required in addition to shift flexibility as 24-hour coverage is needed (potential for night shift).

Key Skills:
• Ability to observe, direct, and mentor floor personnel
• Provide decision making choices from the Quality perspective in a timely manner
• Comfortable working in a high energy, fast paced environment
• Excellent oral communication skills to effectively and efficiently convey direction

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About
Protocol Link, Inc.

Headquartered in Chicago metropolitan area, Protocol Link is a leading project management and strategy consulting firm providing comprehensive regulatory affairs, cGMP compliance, quality assurance, and validation services to the FDA-regulated companies worldwide. Protocol Link’s mission is to provide customer-focused services with ethical conduct, mutual trust, and personnel empowerment while striving to offer the best of both quality and efficiency. It's how we've been doing business since 1996. The right way.

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