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.


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.

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Analyst Corporate Development

Assist projects in support of Corporate Development initiatives, create financial models related to company / product acquisition (income statement, balance sheet, cash flows, DCF, NPV, IRR)


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.


Regulatory Affairs Associate

Multiple openings for Assoc., Reg. Affairs @ Alvogen, Inc.’s Pine Brook, NJ facility. Under supervision of the Manager and or Director Regulatory Affairs, help author, compile, review, & submit high-quality regulatory submissions to the FDA w/in company timelines in accordance w/regulatory guidelines & applicable fed. laws


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. 


IT Support Specialist

The IT Support Specialist position is responsible for the delivery and support of IT services to the end user, including deployment of user computer hardware, software, printing/scanning, telephony, and other workplace technical services.


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.


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. 


Manager, External Analytical Development


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.


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.


Director Quality - Injectable Products

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


Pharmacovigilance Associate

Participate in adverse event case management including intake, triage, and processing of cases. Responsible for intake, documentation and response to unsolicited medical information queries.


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 ...


Manager, Market Access & Analytics

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


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. 


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. 


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.