Operations

Description: The Validation Engineer, Sterile, supports validation and qualification activities for manufacturing and packaging equipment, facilities, utilities, and systems in a sterile GMP environment. Prepares and executes FAT/SAT, IQ/OQ, PQ, and requalification protocols and reports, ensuring do

Description: The Senior Facilities Engineer will lead construction, utilities, and equipment installation for the sterile facility, ensuring all systems meet design and operational requirements. This position will be responsible for overseeing qualification activities and managing project timelines,

Description: The Senior Process Engineer in sterile manufacturing will ensure the compliant, efficient, and safe transfer of new products, implementing manufacturing processes from concept to launch, including scaling up and aseptic process simulation. The position will lead continuous improvement i

The Applied AI Scientist — R&D and Regulatory builds and deploys AI systems that accelerate product development and regulatory submissions. The role applies natural language processing, document intelligence, and generative AI to Amneal's scientific and regulatory content, delivering validated syste

Description: The Packaging Mechanic II will be responsible for the continuous functioning of various types of manufacturing packaging line systems and equipment within the Packaging and Manufacturing departments. The role will perform the setup of packaging equipment, routine maintenance, repair, mi

Description: The Scientist I - QC is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities per

Description: Entry Level Role in the Mixing department. The Mixing operator is responsible for operation of the Mixing and Granulation equipment in accordance with Company Standard Operating Procedures and maintaining 100% cGMP & compliance to ensure the production of quality products. Essential Fun

Description: The Batch Record Reviewer Group Lead is responsible for leading and overseeing batch record review activities across manufacturing, packaging, and related operations in a pharmaceutical manufacturing environment. This role ensures timely, accurate, and compliant review of GMP documentat

Description: The AI Solutions Engineer partners with business functions to identify, design, build, and deploy AI and Generative AI solutions that improve operational efficiency, decision-making, compliance, and business performance. Working within the enterprise AI architecture, governance, and sec

Description: Entry Level Role in the Mixing department. The Mixing operator is responsible for operation of the Mixing and Granulation equipment in accordance with Company Standard Operating Procedures and maintaining 100% cGMP & compliance to ensure the production of quality products. Essential Fun

Description: To monitor and ensure all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. To monitor and ensure all phases of drug manufacturing are in complia

Description: The Research Scientist of R&D is responsible for the designing and development various inhaled dosage forms such as solution, suspension, gel, cream, ointment, sterile products etc. This include literature search, pre-formulation studies, prototype development, process scale up and opti

Description: The NOI Investigations Senior Specialist utilizes deductive reasoning, interviewing skills and technical knowledge when performing investigations to find causes of aberrant events and circumstances impacting the production, sale and/or maintenance of product shelf life of commercialized

Description: The NOI Investigations Specialist utilizes deductive reasoning, interviewing skills and technical knowledge when performing investigations to find causes of aberrant events and circumstances impacting the production, sale and/or maintenance of product shelf life of commercialized produc

Description: The QA Inspector monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector must monitor and ensure all phases o

Description: Project Planning and Execution: Define and manage the scope of post-approval projects. Develop and track project timelines to ensure timely completion. Set and achieve key milestones throughout the project lifecycle. Stakeholder Communication: Coordinate with R&D, manufacturing, marketi

Description: The Medical Science Liaison (MSL) for Amneal's Northeast Territory (MA, CT, ME, NH, VT, RI, NJ) is a field-based professional with scientific, clinical, and therapeutic area expertise. This role is responsible for providing medical and scientific support for Amneal's marketed products,

The Sales Representative plays a crucial role in implementing marketing & sales strategies to promote our products effectively. The incumbent will deliver balanced and informative sales presentations to a defined list of current and prospective customers with a defined frequency. In the assigned ter

Description: The Senior Human Resources Manager serves as a strategic business partner to assigned client groups, consulting with leaders and employees on a broad range of Human Resources matters, including recruiting, employee relations, performance management, immigration, benefits, and compensati

Description: Responsible for leading the strategy and execution of HCP and consumer marketing initiatives across the product lifecycle, with a strong emphasis on launch planning, launch readiness, and post-launch optimization. This role drives impactful brand campaigns, oversees cross-functional and