Operations

Description: This QA Auditing Reviewer role is responsible for thoroughly auditing production records, determining batch disposition (Release, Hold, Reject), and executing those decisions in systems like JDE while ensuring held or rejected batches are properly controlled and stored. It also logs and

Description: Research Scientist III, Analytical Method Development fulfills a critical role in supporting the analytical development and validation of testing methods for the Analytical R&D laboratory. This individual leads analytical development, qualifications, validations for active pharmaceutica

Description: This position will be responsible for the movement of product between facilities, as well as possible deliveries to local customers. This position will also assist in the warehouse, which would include loading and unloading trucks, as well as moving product throughout the facility. Esse

Description: The position of Warehouse Associate III - 2nd Shift is responsible for all aspects of warehouse functions including the receiving, storing, handling, pick/pack operations, preparing and shipping of product for customer delivery, while maintaining the warehouse in a safe and orderly fash

Description: This Warehouse Associate II role handles all core warehouse operations including receiving, storing, picking, packing, and shipping products while keeping the facility safe and organized. It also operates material‑handling equipment, loads/unloads trucks, inspects incoming goods, and su

Description: The Project Engineer supports engineering projects related to sterile/aseptic manufacturing, including facility construction, utility upgrades, modifications, and new equipment installations. This role assists with project activities from planning through execution while following safet

Description: The Continuous Improvement Engineer is responsible for optimizing manufacturing processes, improving operational efficiency, reducing costs, and ensuring compliance with regulatory standards within pharmaceutical production environments. This role focuses on process improvement, capacit

Description: This role will be responsible for maintaining cleanliness and sanitation in our pharmaceutical manufacturing and office facilities. The Janitor will be responsible for ensuring a sterile environment in compliance with industry hygiene standards, including cleaning production areas, offi

Description: The Scientist II - QC is 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, calculating and reporting results on applicable speci

Description: The Scientist, Analytical Chemistry is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. Fulfills a critical role in supporting the analytical development and validation/verification and method transfer of testing meth

Description: The entry level Coating Operator is responsible for the safe and efficient operation of tablet coating equipment in accordance with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role ensures that all coating processes are executed with precis

AMNEAL PHARMACEUTICALS Manager, Analytical QC: Responsible for managing the activities of the quality control technical service to ensure the quality and compliance of Laboratory operation for pharmaceutical products, including managing testing activities, method development, method validation, comp

Description: The packaging mechanic 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, minor

Description: This entry-level role in the Compression Department is responsible for the setup and operation of compression machinery in accordance with company Standard Operating Procedures (SOPs). The Compression Operator ensures full compliance with cGMP standards to support the production of high

Description: This entry-level role in the Compression Department is responsible for the setup and operation of compression machinery in accordance with company Standard Operating Procedures (SOPs). The Compression Operator ensures full compliance with cGMP standards to support the production of high

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

Manager, QC Lab: Responsible for managing the activities of the quality control laboratory to ensure timely delivery of materials for use in production and releases of finished products from the laboratory as committed, ensure testing of stability samples within structure of timelines identified in

Description: The Automation Engineer is responsible for overseeing and optimizing automation systems to improve production efficiency and reduce operational costs. This position involves designing, integrating, and implementing advanced hardware and software solutions within pharmaceutical manufactu

Description: The Packaging Supervisor is responsible for supervising all packaging department activities on a daily basis. This position supervises the production, quality, and warehousing of packed product in a manner that is consistent with company standards, service and cost objectives. The Packa

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