The Sr. IT Specialist will be responsible for maximizing engineering and operations tools to provide hands-on support and IT services for the Alvogen/Almatica business. The position will work closely with the US IT team as a lead for various projects and initiatives to further support the business growth.

The Manager, Human Resources is responsible for delivering, coordinating, and managing HR processes for the US Almatica organization.

The Program Manager, Regulatory Affairs is responsible for planning and timely submission of regulatory filings for new and existing marketing authorizations. 

With supervision, helps to author, compile, review and submit high-quality regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. Under supervision, coordinates and writes clear, concise and accurate responses to inquiries from FDA resulting from their review of the submissions.