We go where others won't, taking on some of the biggest public health challenges to protect and enhance millions of lives, and create a better, more secure world.Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed to protect and enhance life. The Analyst II on the Floor is responsible fo

Reporting to the Director of Client Portfolio & Relationship Management (CPRM), this role is responsible for serving as the primary point of contact for an assigned portfolio of CDMO clients serviced through the Camden site. Clients may include external CDMO customers or internal Emergent product customers. This role collaborates extensively with Quality Leads and Technic

The Analyst II, QC Microbiology position supports the Quality Control group at Emergent BioSolutions Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing,

The Sr Information Security Analyst will be a hands on specialist in our data classification function. The role requires, analytical and data processing skills. This is a results oriented position where accuracy and efficiency are both measured and valued. The Sr. Analyst will contribute to the identification and creation of rules and procedures to classify data, improve

This position is responsible for overseeing the activities of the Global Patient Safety and Epidemiology function and ensuring corporate compliance with all applicable US and foreign legal and regulatory requirements for adverse event reporting & safety management of medicinal products, both approved and in development. The Director, Safety Physician provides medical and/

Lead production and packaging equipment maintenance and reliability program at the Camden campus. Lead team of Equipment Specialists to ensure equipment uptime as well as complete engineering level projects to continuously improve equipment reliability. Heavy focus on personnel/team development as it pertains to repair and troubleshooting current and future manufacturing

The Director, Medical Affairs plays a key role in the Medical Affairs team, serving as the non promotional scientific conduit between the company and healthcare communities through the lifecycle of our product portfolio. The Director, Medical Affairs is a field based scientific expert responsible for developing and maintaining relationships with external advisors, organiz

This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. II Responsibilities Demonstrate competency on assigned qualification blocks Job specific Standard Operating Procedures New Inspector Qualification Execute and document procedural steps in compli

Remote based scientific and medical expert responsible for building and maintaining appropriate scientific and medical interactions with internal cross functional partners, external advisors, organizations, institutions and associated personnel. Serves as the non promotional scientific conduit between the company and the relevant healthcare community across the lifecycle

The Bioprocess Associate position reports to Supervisor Manufacturing. Prior experience in GMP manufacturing, operation of GMP process equipment and aseptic technique are preferred but not required. This role is responsible for filling of parenteral pharmaceuticals in accordance with cGMP regulations, setup and operation of equipment and processes associated with sterile

Accountable for the overall operations of the Warehouse during the shift, including inbound and outbound, inventory control, and material movement throughout the facility, providing leadership to the shift team, overseeing the allocation of job duties as well as performance. This position is 2nd Shift ESSENTIAL FUNCTIONS Reasonable accommodations will be made to enable in

The Operations Specialist is responsible for direct support of process improvement and compliance directives associated with the manufacturing activities at the Emergent Camden facility. Direct performance of process deviation investigations, supporting corrective/preventive action (CAPA) creation and ownership, and change control generation, ownership, and execution in s

The Equipment Specialist is responsible for maintenance and operational support of all equipment and areas needed for the manufacture of parenteral pharmaceuticals at the Baltimore Camden fill/finish facility. Additional duties will include parts and tool management, plant equipment support, parts design, as well as management of moderately sized capital projects. This po

The Equipment Specialist is responsible for maintenance and operational support of all equipment and areas needed for the manufacture of parenteral pharmaceuticals at the Baltimore Camden fill/finish facility. Additional duties will include parts and tool management, plant equipment support, parts design, as well as management of moderately sized capital projects. This po

This position is responsible for the inspection and packaging of product. Will perform all aspects of Inspection and Packaging with the ability to assist in day to day operations. This position is for second shift, Monday through Friday from 2 00PM to 10 30PM. II Responsibilities Demonstrate competency on assigned qualification blocks o Job specific Standard Operating Pro