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.

We are an EEO Employer.


CONNECT WITH ALVOGEN

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

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

 

  

5.10.2017

SAP ABAP/EDI Developer

The SAP ABAP/EDI Developer will work with customers and internal business units to support the development, testing, and on-going support of the Gentran Server for Windows EDI system. 


5.10.2017

Sr. Scientist II Analytical R&D

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. 


3.10.2017

Sr. Scientist Formulation Development

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.


15.9.2017

Manager External R&D - Semisolds

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.


29.8.2017

Director Project Management Generic Pharma R&D

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. 


8.8.2017

Project Manager

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. 


31.7.2017

Director, R&D - Injectables

The Director is responsible to provide strategic R&D direction with a special focus on Injectables. This is a key role with a wide responsibility to assist in portfolio selection, due diligence activities, oversee internal and external development, and serve on project teams. Focus of this role is on non Solid Oral dosage forms such as injectables, ointments, creams etc.


20.7.2017

Director Quality - Injectable Products

The Director, Quality- Injectable Products ensures quality and compliance of sterile pharmaceutical products manufactured and tested on behalf of Alvogen.


9.6.2017

Manager Regulatory Affairs

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 ...


7.9.2016

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 and GMP requirements. 


9.5.2016

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.