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Sr. Specialist, Regulatory Affairs



Posting ID: 7306188

Full time
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This role is responsible for coordinating and authoring regulatory submissions for products and processes. Address customer regulatory requests and maintain knowledge of current US and international regulations/guidelines/policies applicable to West's products and services.

Experience in regulatory CMC with technical leadership skills, as well as demonstrated understanding of related pharmaceutical operations (e.g., manufacturing, process development, analytical, quality assurance).
Demonstrated ability to manage multiple tasks/projects/priorities and complex systems simultaneously is required.
Excellent interpersonal, communication and listening skills with a proven record of working with and influencing multi-disciplinary teams and external experts.

About Aerotek:

We know that a company's success starts with its employees. We also know that an individual's success starts with the right career opportunity. As a Best of Staffing® Client and Talent leader, Aerotek's people-focused approach yields competitive advantage for our clients and rewarding careers for our contract employees. Since 1983, Aerotek has grown to become a leader in recruiting and staffing services. With more than 250 non-franchised offices, Aerotek's 8,000 internal employees serve more than 300,000 contract employees and 18,000 clients every year. Aerotek is an Allegis Group company, the global leader in talent solutions. Learn more at

Contact Information

Recruiter: Alexis Henry

Phone: (610) 232-5856


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