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34+ Job Results
9 Days Ago
National, MD, USA
1,282 Employees
Senior level
1,282 Employees
Senior level
Biotech
The Supervisor/Sr. Supervisor in Manufacturing leads teams in upstream and downstream processing of biopharmaceutical products, ensuring compliance with safety and quality standards. Responsibilities include planning and monitoring production tasks, reviewing batch documentation, training staff, and driving continuous process improvements.
9 Days Ago
Boulder, CO, USA
1,282 Employees
Entry level
1,282 Employees
Entry level
Biotech
The Process Development Associate I supports laboratory studies, executes lab work, documents and reports results, and authors operational documents. The role requires a basic understanding of Process Development methods, technical writing skills, and the ability to perform experiments from instructions. Responsibilities include evaluating new technologies, maintaining training compliance, and participating in process development meetings.
9 Days Ago
Boulder, CO, USA
1,282 Employees
59K-74K Annually
Junior
1,282 Employees
59K-74K Annually
Junior
Biotech
The MS&T Document Specialist at KBI will manage the creation and revision of batch records, bill of materials, and oversight of change controls within a quality system, ensuring efficient manufacturing processes.
10 Days Ago
National, MD, USA
1,282 Employees
93K-127K Annually
Mid level
1,282 Employees
93K-127K Annually
Mid level
Biotech
The S&OP Master Planner II leads global planning and execution, focusing on Supply Planning and validating purchase requisitions. Responsibilities include collaborating with cross-functional teams, modeling supply risks, reviewing purchase requisitions, and contributing to demand and capacity planning efforts.
10 Days Ago
National, MD, USA
1,282 Employees
Mid level
1,282 Employees
Mid level
Biotech
The EHS&S Specialist III is responsible for implementing environmental, health, safety, and sustainability programs, ensuring compliance, and continuous improvement. Duties include incident response, permit management, risk management, and conducting audits and inspections. The specialist collaborates with KBI staff and management, communicates program activities, and represents KBI during regulatory inspections.
10 Days Ago
National, MD, USA
1,282 Employees
Entry level
1,282 Employees
Entry level
Biotech
The Research Associate I/II/SRA will execute experimental protocols, perform elementary data analysis, and troubleshoot in biopharmaceutical development laboratories while maintaining detailed records and safety protocols.
10 Days Ago
National, MD, USA
1,282 Employees
Senior level
1,282 Employees
Senior level
Biotech
The QA Compliance Auditor will manage the internal audit program for the KBI CMF in Durham, overseeing audits, evaluations of compliance with regulations, and reporting findings. The role includes driving a culture of compliance, supporting quality assurance processes, and leading initiatives to improve operational efficiency in a regulated environment.
16 Days Ago
Boulder, CO, USA
1,282 Employees
50K-70K Annually
Entry level
1,282 Employees
50K-70K Annually
Entry level
Biotech
The Research Associate I/II supports testing for biopharmaceutical manufacturing, conducts laboratory experiments including electrophoresis and HPLC, performs data analysis, and ensures compliance with safety procedures. They maintain knowledge of scientific literature and assist in instrumentation upkeep.
16 Days Ago
Boulder, CO, USA
1,282 Employees
45K-65K Annually
Junior
1,282 Employees
45K-65K Annually
Junior
Biotech
The Research Analyst I/II positions involve supporting in-process testing, conducting laboratory experiments, analyzing data, and maintaining safety protocols within biopharmaceutical development. Analysts are responsible for running tests like electrophoresis and HPLC, managing experiment documentation, and keeping up-to-date with scientific literature.
17 Days Ago
Boulder, CO, USA
1,282 Employees
67K-92K Annually
Junior
1,282 Employees
67K-92K Annually
Junior
Biotech
The QA Specialist I/II is responsible for ensuring products and processes meet quality standards and governmental regulations. Responsibilities include reviewing batch records, authoring SOPs and logs, supporting manufacturing changeovers, resolving compliance issues, and assisting with raw material releases.
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