The Scientist is accountable for driving results in a fast paced environment by performing analytical routine and non routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. A Scientist will routinely lead method development/method validation projects. HPLC, dissolution and/or GC based methodologies are commonly employed in the de

As a pharmaceutical intern for FDL at Alcami, you will have the opportunity to gain hands on experience in solid oral formulation and manufacturing principles in addition to various aspects of the pharmaceutical industry. You will assist in the evaluation and optimization of solid oral dosage forms and material evaluations. Under the guidance of experienced professionals,

The Materials Management Coordinator is accountable for driving results in a fast paced environment by generating protocols and facilitating the log in of samples and projects for lab documentation, revenue recognition, and reporting of data for client stability programs. The Materials Management Coordinator provides administrative and organizational support related to st

The Materials & Logistics Technician I is accountable for results in a fast paced environment by following applicable SOPs and cGMPs to perform tasks for the receipt, storage, inventory, and distribution of raw materials, intermediate or finished drugs or drug products and components. The Materials & Logistics Technician I uses the electronic inventory system to track, do

The Manufacturing Manager is accountable for driving results in a fast paced environment by providing leadership to the site's manufacturing function. Focus areas for the Manager, Manufacturing role include operational leadership, parenteral (fill/finish, inspection) manufacturing process, project management, continuous improvement, change management, manufacturing invest

The Associate Scientist III is accountable for driving results in a fast paced environment by performing analytical routine and non routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist III may also be required to work on method development/method validation projects. For this position, ICP methodologies

The Scientist is accountable for driving results in a fast paced environment by performing analytical routine and non routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. A Scientist will routinely lead method development/method validation projects. HPLC, dissolution and/or GC based methodologies are commonly employed in the de

The Laboratory Support Driver is responsible for the safe and reliable transport of customer products and material goods to and between locations of the Alcami Morrisville, North Carolina campus. The Driver will be picking up environmental and utility samples from customer sites within, but not limited to, the Research Triangle Park location. The driver will additionally

The Environmental Monitoring Technician is accountable for driving results in fast paced environment by performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The Environmental Monitoring Technician must be detail oriented and possess organizational skills with a large quantity of data. On Site Expect

The Manufacturing Technician I is accountable for results in a fast paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch reco

The Associate Scientist is accountable for driving results in a fast paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Associate Scientist position, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing. Level II employs other key metholo

The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data,

The Sr. Environmental Monitoring Technician is accountable for driving results in fast paced environment by performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The Sr. Environmental Monitoring Technician must be detail oriented and possess organizational skills with a large quantity of data. On Sit