Diversity is a priority at Alvogen. Diversity drives creativity and innovation – which leads to better value delivered to our customers and enhanced business results. As a global business, we are determined to build a strong team of people around the world, with different backgrounds and views. Without diverse ideas, we simply are not able to remain competitive in the rapidly evolving marketplace. Our commitment to diversity makes us a better company.The Alvogen team is global, diverse and enthusiastic about taking on new challenges. As we continue to grow and expand into new markets, we will look for innovative, street-smart, experienced and ambitious people to join us.
We are an EEO Employer.
If you don´t find what you are looking for, please send us a general Job Application. We review all Job Applications.
Alvogen, Inc. is an affirmative action employer and that age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law, are not taken into account in any employment decision.
If you require further assistance in applying to a position, please contact us at Alvogen-US-HR@alvogen.com
This position will be responsible for managing the Americas finance operations as it relates to actual and forecast reporting.
The Manager, External R&D and Tech. Transfer is responsible to manage R&D and tech. transfer projects utilizing contract development and manufacturing organizations.
The Manager API Sciences is responsible for the management of DMF technical issues related to selected API’s and Suppliers from the adoption of new products through product approval.
The Sr. Scientist II is responsible to independently develops and establishes new analytical methods using advanced analytical techniques that meet the expected FDA standards and can be successfully filed with USFDA.
The Sr. Scientist is responsible to develop products with minimal supervision that meets the expected FDA standards and can be successfully filed with USFDA. The primary focus will be on the development of oral solids for 505(b)(2) and Generics application.
Manager, External R&D (Semisolids) will manage the development and technology transfer of semisolid products at third party sites. The role will also participate in Due Diligence, Portfolio Selection, and CDMO selection.
The Director, Project Management is responsible for supporting department and company initiatives; supervising 1-3 Project Managers; and serving as Project Manager on high profile projects.
The Project Manager will lead cross functional project teams, including internal and third party, to drive development, validation and launch activities for the U.S. Generics solid oral dose portfolio.
Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and submitting highest-quality regulatory submissions to the FDA within company timelines and ...
The Director, R&D Quality provides Quality and Compliance oversight of internal and external development projects in order to ensure that products developed for Alvogen comply with the regulatory and GMP requirements.
Independently prepares reviews and submits high quality regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. Submissions include Annual Reports, amendments, ANDA’s and supplements to ANDAs or NDAs.