The Business Process Analyst Intern is responsible for working closely with various departments to understand, document, and optimize business processes across our CDMO operations. This role involves creating detailed process maps, flowcharts, and standard operating procedures (SOPs), identifying areas for improvement, and supporting the implementation of process changes.

The Data Analyst Intern is responsible for turning data into information, information into insight, and insight into business decisions. This role involves conducting a full lifecycle analysis to include requirements, activities, and design. Data Analysts will develop analysis and reporting capabilities, monitor performance and quality control plans to identify improvemen

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 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 methodo

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 Environmental Health and Safety (EH&S) Intern is responsible for assisting the EH&S department in ensuring the routine inspections are conducted in a variety of safety and environmental areas and updating databases evacuation plans and other areas. This position will work closely with other EH&S team members to ensure program alignment across the larger Alcami organiz

The Senior Instrumentation Engineer is accountable for driving results in a fast paced environment by performing diagnostics repair of analytical instrumentation including HPLC, gas chromatography and laboratory equipment; performing instrument calibrations in a pharmaceutical laboratory environment, maintaining calibration of metrology standards, and completing and revie

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

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 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 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 may also be required to work on method development/method validation projects. For this position, ICP methodologies are

The Associate Scientist I/II will perform microbiological routine and non routine testing in support of pharmaceutical product development or pharmaceutical manufacturing and stability bacterial endotoxins, sterility and microbial examination methodologies are commonly employed in the described testing. Other key methodologies applied include liquid particulate matter and

The Senior Manager, Laboratory Operations is accountable for driving results in a fast paced environment by providing leadership for the scientific, regulatory compliance and business functions for the Analytical Testing and Development Services Teams in our St. Louis, Missouri office. These teams focus on providing high quality services for compendial testing, method val

The 2024 Laboratory Intern will complete Company onboarding activities and provide feedback to ensure our onboarding program is efficient and engaging. Interns will develop their laboratory skills and increase their knowledge of cGMP and FDA regulations while working in a world class pharmaceutical laboratory. On Site Expectations 100% on site position in Morrisville, NC.