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 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 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 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 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 Pharma Storage Driver is responsible for safe and reliable transport of customer products and goods to and from Alcami Pharma Storage. The Driver will be delivering and picking up customer products primarily in the New England area, coordinating deliveries amongst multiple departments and mapping out the most efficient route. This position is challenged with a daily r

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 I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch re

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.