Job openings

Strong global team

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.


If you don´t find what you are looking for, please send us a general Job Application. We review all Job Applications.

These are our current job openings


Labeling Associate II, Regulatory Affairs

The Associate, Regulatory Labeling prepares, reviews and submits to his/her manager high-quality regulatory labeling submissions intended for the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws.


Laboratory Technical Associate

The laboratory technical associate performs activities supporting the daily operations of the R&D department.


Director Global Audit & Compliance

This position works with limited supervision primary to lead teams responsible for accomplishing all aspects of assigned internal audits and special projects across functions and participate with the VP of Global Audit in preparing the annual audit plan ...


Senior Associate Complaints US Quality

The Senior Associate ‘Complaints US Quality’ is a member of the US Quality department. The Senior Associate ‘Complaints US Quality’ is primarily responsible for handling and supporting the Quality Management Systems in the area of complaint handling, and for maintaining and adhering to all associated documentation requirements for the Alvogen Inc. and the Almatica Pharma Inc. business units.


Director R&D Quality

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 andGMP requirements for research and development.


Clinical Research Associate Biopharmaceutics

It is the duty of the Clinical Research Associate to attend to his/her work with diligence. The CRA shall ensure that bioequivalence (BE) studies/clinical end point studies sponsored by Alvogen are conducted and data is generated, documented ...


Senior Associate Regulatory Affairs

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. 


Manager Biopharmaceutics

Biopharmaceutics is a department within Alvogen. This position is responsible for management of clinical studies or bioequivalence studies conducted to support ANDAs.