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.


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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

 

  

16.8.2017

SR Coordinator US R&D

The Senior Coordinator, US R&D is responsible for performing activities to support the operations of US R&D including Project Management and Biopharmaceutics.


8.8.2017

Senior Project Manager

The Project Manager / Senior 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. 


4.8.2017

Manager, External Analytical Development

SUMMARY OF POSITION

Manager, External Analytical Development shall manage the design, development, and methods validation activity to support third party product development and ensure successful implementation of the methods at the CMO manufacturing site. The role shall also be responsible for cGMP compliance and regulatory requirements pertaining to analytical methods.

The candidate must be independently proficient in a variety of analytical techniques, compliance and regulatory areas and effectively manage analytical operations at third party sites.


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

Internal Audit Supervisor

The Internal Audit Supervisor will be responsible for independently completing all aspects of assigned internal audits (e.g., planning, fieldwork, wrap-up) in the US, CEE and APAC regions and special projects across functions as necessary. 


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.


28.6.2017

Contract manager, injectables

Analyze and prepare proposals / compile competitive pricing/ support and coordinate price changes for Injectables portfolio.


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 ...


8.6.2017

Key Accounts Manager – Injectables Austin

The Key Accounts Manager - Injectables is responsible for implementing Alvogen injectables business strategy within their assigned sales territory.


1.6.2017

Key Accounts Manager Injectables - Dallas

The Key Accounts Manager - Injectables is responsible for implementing Alvogen injectables business strategy within their assigned sales territory.


9.5.2017

Regulatory Affairs Associate

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. 


26.4.2017

Manager Biopharmaceutics

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


11.4.2017

Manager, Market Access & Analytics

The Manager, Market Access & Analytics will analyze and prepare proposals, compile competitive pricing, support and coordinate price changes. 


29.3.2017

Pharmaceutical Project Manager

The Pharmaceutical Project Manager / Senior Project will lead cross functional project teams, including internal and third party representatives, to drive development, validation and launch activities for the U.S. Generics portfolio. 


21.3.2017

Key Accounts Manager Injectables - Los Angeles

The Key Accounts Manager - Injectables is responsible for implementing Alvogen injectables business strategy within their assigned sales territory.


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.