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6 Days Ago
Juncos, PRI
265 Employees
7+ Years of Experience
265 Employees
7+ Years of Experience
Consulting • Pharmaceutical
The Process Development Scientist is responsible for designing and executing scientific experiments, analyzing data, and developing new protocols. They ensure compliance with protocols and guidelines, represent the department in project teams, and may mentor others. The role involves extensive data analysis, literature review, and collaboration within and outside the company.
6 Days Ago
College Station, TX, USA
265 Employees
7+ Years of Experience
265 Employees
7+ Years of Experience
Consulting • Pharmaceutical
The Compliance Specialist will ensure compliance with safety and efficacy guidelines in the FDA-regulated industry by supporting the Facilities Team, managing the Contractor Safety Program, performing audits, monitoring compliance KPIs, and providing compliance training to associates and subcontractors.
6 Days Ago
College Station, TX, USA
265 Employees
3-5 Years of Experience
265 Employees
3-5 Years of Experience
Consulting • Pharmaceutical
The Process Engineer will provide engineering support and expertise for process equipment and utilities, driving improvements and managing installations. Responsibilities include troubleshooting, project execution, and ensuring compliance with safety and quality standards. This role involves collaboration with various teams on new equipment design, project management, and adherence to regulatory guidelines.
6 Days Ago
College Station, TX, USA
265 Employees
7+ Years of Experience
265 Employees
7+ Years of Experience
Consulting • Pharmaceutical
The Process Engineering Manager oversees engineering support for process equipment in the FDA-regulated sector, ensuring compliance with safety regulations. Responsibilities include troubleshooting, managing equipment installations, leading process improvements, and collaborating on project execution and validation activities.
6 Days Ago
Manatí, PRI
265 Employees
3-5 Years of Experience
265 Employees
3-5 Years of Experience
Consulting • Pharmaceutical
The C&Q Specialist will oversee the commissioning and qualification of utilities, develop various protocols, and manage compliance with pharmaceutical safety guidelines. The role requires strong communication skills and the ability to handle multiple tasks independently while ensuring proper management of chemicals and equipment decommissioning.
6 Days Ago
College Station, TX, USA
265 Employees
3-5 Years of Experience
265 Employees
3-5 Years of Experience
Consulting • Pharmaceutical
The Automation Engineer will deliver and maintain automation systems for biopharmaceutical manufacturing. Responsibilities include providing automation support for daily operations and projects in a GMP environment, designing and configuring control systems, and managing technical changes.
6 Days Ago
Vega Baja, PRI
265 Employees
100K Annually
3-5 Years of Experience
265 Employees
100K Annually
3-5 Years of Experience
Consulting • Pharmaceutical
Responsible for the implementation of small Capital/Expense Project
6 Days Ago
Manatí, PRI
265 Employees
5-7 Years of Experience
265 Employees
5-7 Years of Experience
Consulting • Pharmaceutical
The QA Specialist will manage investigations related to pest control, finalize root cause investigations and CAPAs, ensure compliance with FDA and GMP guidelines, provide coaching for colleagues, and analyze CAPA effectiveness to prevent recurrence.
6 Days Ago
Carolina, PRI
265 Employees
7+ Years of Experience
265 Employees
7+ Years of Experience
Consulting • Pharmaceutical
The EHS Specialist is responsible for ensuring compliance with health, safety, and environmental regulations within the pharmaceutical sector. This role involves reviewing contractor documentation, conducting training, performing safety observations, maintaining reporting standards, and leading safety qualification programs for contractors.
6 Days Ago
Gurabo, PRI
265 Employees
3-5 Years of Experience
265 Employees
3-5 Years of Experience
Consulting • Pharmaceutical
The C&Q Specialist is responsible for conducting commissioning and qualification activities, managing chemical substances, performing risk assessments, and ensuring compliance with cGMP requirements. Key tasks include preparing documentation such as protocols and reports in the pharmaceutical, biotech, and medical device sectors.
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