Nesco Resource is partnering with a top BioTech company in their search to add a Regulatory Document Associate to their ever-growing team!
These are all 12-month temporary roles, with strong potential for permanent hire. Great opportunity for recent graduates in the life sciences!
Role Details:
- 12-month contract (potential for permanent hire)
- $22.00-$24.00 per hour
- M-F 8am-4:30pm
A Typical Day
As a Regulatory Document Associate, you will:
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Review draft regulatory documents for data accuracy, consistency, and clarity
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Cross-check technical content across multiple documents to ensure alignment
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Verify data against source documents and support ongoing document quality initiatives
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Maintain consistent use of terminology, names, and abbreviations
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Recommend improvements in formatting and structure for clarity and readability
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Help develop and maintain internal resources that support high-quality document preparation
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Support broader departmental efforts related to data integrity and continuous improvement
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(Bonus!) Leverage copyediting skills, if you have them, for expanded responsibilities
Skills & Abilities
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A four-year degree in a relevant field
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Previous experience in detailed document review (preferred)
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Exposure to or knowledge of biopharmaceutical development, testing, or manufacturing (a plus)
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Exceptional attention to detail and organizational skills
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Strong communication skills and a collaborative mindset
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Comfort with technical/scientific content and navigating multiple systems
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Ability to manage priorities and thrive under tight deadlines
Nesco Resource and affiliates (Lehigh G.I.T Inc, and Callos Resource, LLC) is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.