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 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 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 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 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 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 Wilmington, NC.

The SAP Implementation Project Manager will own and drive the end to end implementation of SAP S/4HANA across the organization, including the Laboratory Services, Drug Product Manufacturing, and Bioservices business units. You will serve as the key liaison between business stakeholders, executive leadership, implementation partners, and internal teams. This leader will le

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.

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.

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 Durham, NC. Resp

The Supervisor, Manufacturing is accountable for driving results in a fast paced environment by leading daily manufacturing operations on second shift, including facility/equipment/component preparation, formulation, and aseptic filling. The Supervisor, Manufacturing works directly with performance and engagement of manufacturing technicians who operate autoclaves, depyro

The Laboratory Support Driver is responsible for the safe and reliable transportation of customer products and material goods to and from the Alcami Wilmington, North Carolina location. The Driver will be delivering and/or picking up customer products primarily in the Petersburg, Virginia area, coordinating deliveries amongst multiple departments and mapping out the most