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14 Hours Ago
Madison, WI, USA
13,715 Employees
Senior level
13,715 Employees
Senior level
Biotech • Pharmaceutical
The Specialist in Quality and Compliance is responsible for overseeing customer quality agreements, supporting customer audits, maintaining facility licenses, organizing documentation for regulatory submissions, assessing regulatory changes, enhancing quality systems, authoring SOPs, drafting technical plans, and maintaining statistical tools for process monitoring.
14 Hours Ago
Harmans, MD, USA
13,715 Employees
93K-128K Annually
Senior level
13,715 Employees
93K-128K Annually
Senior level
Biotech • Pharmaceutical
The Senior Specialist, QA Analytical is responsible for providing quality assurance support to analytical development and quality control departments in a pharmaceutical manufacturing facility. Key responsibilities include maintaining quality systems, supporting audits, reviewing documentation, and ensuring compliance with regulatory requirements while implementing continuous improvement initiatives.
14 Hours Ago
Bloomington, MN, USA
13,715 Employees
Senior level
13,715 Employees
Senior level
Biotech • Pharmaceutical
The Principal Scientist will lead technical transfer processes, provide documentation, assess process data, and offer support for manufacturing processes. This role involves collaborating with clients and internal teams to facilitate project progress and improvements in drug substance operations.
14 Hours Ago
Baltimore, MD, USA
13,715 Employees
102K Annually
Mid level
13,715 Employees
102K Annually
Mid level
Biotech • Pharmaceutical
As an Associate Scientist III in Process Development, you will lead downstream processing and purification protocols for macromolecules. You will design and execute experiments, manage data, and participate in technical discussions, contributing to a project team focused on gene and viral vector therapies.
2 Days Ago
Somerset, KY, USA
13,715 Employees
Junior
13,715 Employees
Junior
Biotech • Pharmaceutical
The Scientist will support the Analytical Development team by developing, validating, and transferring analytical methods. Responsibilities include conducting routine analysis, assisting in complex experiments, supporting formulation development, and preparing technical documentation.
2 Days Ago
Field, KY, USA
13,715 Employees
Senior level
13,715 Employees
Senior level
Biotech • Pharmaceutical
The Regional Procurement Manager at Catalent is responsible for developing and executing procurement strategies, managing supplier relationships, optimizing costs, and ensuring compliance across multiple sites. This role includes collaboration with different departments and implementing performance metrics while supporting working capital initiatives and mitigating procurement risks.
2 Days Ago
Somerset, KY, USA
13,715 Employees
Senior level
13,715 Employees
Senior level
Biotech • Pharmaceutical
The Project Manager will oversee project teams, ensuring effective management and delivery of client projects. Responsibilities include coordinating meetings, creating documentation, forecasting program revenue, supporting project introductions, and gathering key performance metrics, while maintaining strong client relationships.
2 Days Ago
San Diego, CA, USA
13,715 Employees
60K-74K Annually
Entry level
13,715 Employees
60K-74K Annually
Entry level
Biotech • Pharmaceutical
The Associate Scientist will conduct formulation development and analytical testing under supervision, preparing reports and maintaining accurate records. Responsibilities include executing formulation procedures, characterizing drug products, and complying with GMP regulations while developing scientific expertise and problem-solving skills.
2 Days Ago
San Diego, CA, USA
13,715 Employees
60K-74K Annually
Entry level
13,715 Employees
60K-74K Annually
Entry level
Biotech • Pharmaceutical
The Associate Scientist in Analytical Development will perform and train others in various analytical techniques, conduct stability studies, develop cleaning methods, and keep accurate records under supervision. The role supports pharmaceutical analysis and compliance with GMP regulations.
2 Days Ago
Madison, WI, USA
13,715 Employees
Mid level
13,715 Employees
Mid level
Biotech • Pharmaceutical
The Scientist I - Quality Control conducts routine testing of process samples, raw materials, and finished products in a cGMP compliant environment. Responsibilities include operating lab equipment, maintaining documentation, entering data into LIMS, and assisting in technical documentation. The role emphasizes adherence to quality standards and laboratory maintenance activities.
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