As a Senior Scientist in QC General Analytics, you will ensure 24/7 QC support, perform analytical method validations, and support regulatory compliance for biopharmaceutical manufacturing.

The job involves maintenance and repair of electrical systems, troubleshooting, coordinating with external technicians, and documenting activities.

The Manager, Engineering oversees engineering activities, project execution, and compliance in a pharmaceutical environment, ensuring successful project outcomes.

The Scientist in the Filling team oversees GMP documentation, deviation management, change control, and supports optimization projects in a cGMP environment.

Support the QC department by managing tasks, collaborating with technicians and scientists, and gaining insight into the biopharmaceutical industry.

Assist in downstream processes by preparing buffers, maintaining lab and equipment, and documenting work in notebooks.

The Quality Control Scientist I conducts microbiological testing, oversees compliance with GMP regulations, leads investigations, and supports cross-functional manufacturing processes and continuous improvement initiatives.

As a QA Principal Scientist, you will support Supply Chain, Process Transfer, and QC for commercial products by overseeing deviations, CAPAs, and material specifications, ensuring compliance with GMP standards.

Assist in internal communications for the organization by creating content, managing social media channels, and supporting communication projects.

As a Student Assistant at AGC Biologics, you'll support pharmaceutical production by sorting supplies and managing disposals, contributing to a dynamic team environment.

The Quality Control Associate I performs QC analysis, documenting activities according to SOPs, focusing on Environmental Monitoring and Microbial assays while learning methods under supervision.

The IT Application Specialist will manage and configure project portfolio management systems according to customer needs, assist in analysis and testing, create reports, and oversee integration with external applications. They will also support users and maintain system documentation, demonstrating strong troubleshooting and communication skills.

Manage client requests and logistics for onsite visits as a Student Assistant in Project Management, gaining insight into biopharmaceuticals.

The role involves managing a QC team for biopharmaceutical products, ensuring compliance with cGMP guidelines and improving laboratory workflows.

The Principal Scientist in QA Microbial ensures compliance and quality in biopharmaceutical production by resolving quality issues, approving technical documents, and supporting audits.

The Process Development Associate III will design and optimize purification processes for monoclonal antibodies, support cGMP manufacturing, and conduct experiment analysis.

Manage QC equipment and software, ensuring compliance with regulations, troubleshooting equipment, and collaborating with teams to optimize processes.

Manage the release lifecycle for business applications in a pharmaceutical environment, coordinating with vendors and stakeholders to ensure timely delivery and compliance with industry standards.

As a QC Bioassay Scientist, you'll review analytical results, validate methods, troubleshoot bioassay techniques, and ensure compliance in a dynamic QC environment.

Responsible for upstream projects in biopharmaceutical development, including planning experiments and working in cross-functional teams for cell line development and bioreactor optimization.