Regulatory Affairs Manager

3 weeks ago


Raleigh, United States Randstad USA Full time

Regulatory Affairs Manager- Pharmaceutical Manufacturing -

Resident of Raleigh area, North Carolina, as training is 100% onsite

Schedule: Monday-Friday after training, work remotely.


Establish and govern a regulatory intelligence program for Pharmaceutical Manufacturing Operations & Technology, which consists of researching, analyzing, interpreting, communicating and acting on publicly available regulatory information to drive compliance, shape future regulations, and outline risks and opportunities to GxP operations. GxP oversight related to US, EU, JP and ROW regulations including GMP, GLP, GDP and PV.


Need to have:

Bachelor’s Degree (BS) from a four-year college or university with an emphasis in Science/Engineering; or an equivalent combination of education and experience.


Minimum ten (10) years’ experience in pharmaceutical/biotech industry.


Benefit for you:

Will work @ 6 months temporary before moving on to permanent role. While working temporary with Randstad, we offer insurance benefits including health, dental, vision and 401k plan.

Pay range: $70.00 - 80.00 per hour.


Apply today and let's schedule an introductory phone call to discuss details



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