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64+ Job Results
13 Hours Ago
Armonk, NY, USA
15,000 Employees
130K-212K Annually
Senior level
15,000 Employees
130K-212K Annually
Senior level
Biotech • Pharmaceutical
The Senior Manager of Global Development Quality Management leads quality and compliance in the pharmacovigilance system, supports inspection readiness, collaborates with cross-functional teams, and manages quality issues in post-marketing and clinical trial safety.
13 Hours Ago
Tarrytown, NY, USA
15,000 Employees
106K-173K Annually
Mid level
15,000 Employees
106K-173K Annually
Mid level
Biotech • Pharmaceutical
The Sr Scientist will create antibody production cell lines using mammalian expression technologies, develop new technologies, perform aseptic cell culture and flow cytometry assays, conduct molecular biology and protein biochemistry techniques, and analyze data while contributing to innovative scientific directions.
13 Hours Ago
United States of America
15,000 Employees
58K-124K Annually
Entry level
15,000 Employees
58K-124K Annually
Entry level
Biotech • Pharmaceutical
The Compliance Specialist will support the Process Sciences team by managing compliance activities, preparing documentation, evaluating risks, and coordinating with stakeholders for IPC programs related to manufacturing bioprocesses. This role involves organizing data, reviewing technical documents, presenting compliance topics, and troubleshooting issues.
13 Hours Ago
Sleepy Hollow, NY, USA
15,000 Employees
95K-155K Annually
Mid level
15,000 Employees
95K-155K Annually
Mid level
Biotech • Pharmaceutical
As a Senior Sourcing Specialist at Regeneron, you will manage strategic sourcing initiatives for Commercial teams, conduct supplier performance evaluations using RFIs, RFQs, and RFPs, support category sourcing, ensure compliance with contracts, and assist in contract negotiations. You will also analyze data to help achieve cost savings and monitor spend against budgets.
13 Hours Ago
Sleepy Hollow, NY, USA
15,000 Employees
111K-181K Annually
Mid level
15,000 Employees
111K-181K Annually
Mid level
Biotech • Pharmaceutical
The ESG Reporting Manager will oversee ESG data collection, analysis, and verification to ensure data quality and compliance with sustainability practices. Responsibilities include managing ESG KPIs, collaborating with internal stakeholders for data integrity, and supporting ESG disclosures in line with regulatory frameworks.
13 Hours Ago
Sleepy Hollow, NY, USA
15,000 Employees
145K-237K Annually
Senior level
15,000 Employees
145K-237K Annually
Senior level
Biotech • Pharmaceutical
The Sr Principal Secure SDLC Software Development Engineer will design and govern the Secure Software Development Life Cycle (SSDLC) framework, ensuring alignment with cybersecurity standards. Responsibilities include developing secure solutions, assessing vulnerabilities, collaborating with teams, managing budgets, and providing high-level support for security incidents.
13 Hours Ago
Rensselaer, IN, USA
15,000 Employees
89K-199K Annually
Senior level
15,000 Employees
89K-199K Annually
Senior level
Biotech • Pharmaceutical
The Manager, QA (Supplier Quality) role involves coordinating quality assurance initiatives related to supplier and material quality, supervising a team, tracking quality documentation, defining quality standards, and leading quality events. The role requires problem resolution and compliance monitoring whilst preparing for inspections and improving processes.
13 Hours Ago
Rensselaer, IN, USA
15,000 Employees
58K-124K Annually
Junior
15,000 Employees
58K-124K Annually
Junior
Biotech • Pharmaceutical
The Cleanroom & HEPA Certification Specialist will manage preventive maintenance and certification activities for Cleanroom environments and equipment, coordinate with vendors for certifications, maintain documentation, analyze data, and ensure compliance with SOPs and quality standards.
13 Hours Ago
Rensselaer, IN, USA
15,000 Employees
76K-124K Annually
Senior level
15,000 Employees
76K-124K Annually
Senior level
Biotech • Pharmaceutical
The Supervisor of Quality Assurance is responsible for overseeing product and raw material disposition, ensuring compliance with quality assurance policies, and leading investigations and evaluations related to process deviations. This position requires supervising direct reports and engaging in continuous improvement efforts.
13 Hours Ago
Rensselaer, IN, USA
15,000 Employees
73K-163K Annually
Junior
15,000 Employees
73K-163K Annually
Junior
Biotech • Pharmaceutical
Design, implement, and support Data Acquisition and Analysis Systems. Troubleshoot manufacturing deviations and anomalies. Develop engineering design documents and test plans. Support manufacturing, engineering, and validation projects. Author system specifications and execute acceptance tests. Review cyber security vulnerabilities. Create and maintain automation system documentation.
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