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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.
18 Days Ago
Boulder, CO, USA
1,282 Employees
95K-130K Annually
Entry level
1,282 Employees
95K-130K Annually
Entry level
Biotech
The Program Manager is responsible for managing client relationships and driving business delivery through exemplary service. They oversee project timelines, coordinate communication with clients and third-party vendors, manage risk, and ensure projects meet quality standards within budget. They also handle financial aspects such as invoicing and budgeting, facilitate strategic discussions, and contribute to departmental initiatives.
19 Days Ago
Boulder, CO, USA
1,282 Employees
Senior level
1,282 Employees
Senior level
Biotech
The Scientist I in Downstream Process Development executes laboratory studies for process development, supports technology transfer, and ensures compliance with cGMP regulations. Responsibilities include optimizing operations, leading development efforts, documenting protocols, and maintaining safety standards. Strong communication skills are essential to produce quality documentation and present findings to clients.
23 Days Ago
Boulder, CO, USA
1,282 Employees
65K-85K Annually
Senior level
1,282 Employees
65K-85K Annually
Senior level
Biotech
The Associate Scientist will perform analytical testing to support the development of microbial protein therapeutics, using various analytical techniques. Responsibilities include method design, documentation, data presentation, and collaboration with teams to ensure compliance with GMP standards.
23 Days Ago
Boulder, CO, USA
1,282 Employees
50K-70K Annually
Junior
1,282 Employees
50K-70K Annually
Junior
Biotech
The Research Associate will perform analytical testing for pharmaceutical clients, develop and support GMP testing, and document results accurately. Responsibilities include method development, data presentation, and compliance with safety and regulatory standards.
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