
Commissioning & Qualification Specialist
- Caguas, PR
- Permanente
- Tiempo completo
- Collaborate with C&Q Engineers to develop and maintain commissioning and qualification procedures and documents.
- Write, review, and approve C&Q protocols and reports for various systems (e.g., HVAC, utilities, production equipment, lab equipment).
- Execute commissioning and qualification activities for plants and equipment.
- Coordinate with external consultants and internal resources to ensure timely document generation and execution.
- Manage change controls and deviations related to plants and equipment.
- Support maintenance and calibration functions to improve compliance and quality.
- Provide expertise in troubleshooting and root cause investigations.
- Facilitate the transfer of technical knowledge across units and sites.
- Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Technology, or a related scientific field.
- At least 2 years of experience in GMP manufacturing relevant to the area of expertise.
- Proficiency in English; additional language skills are a plus.
- Strong understanding of regulatory requirements and quality standards.
- Excellent analytical, problem-solving, and communication skills.
- Ability to work collaboratively in a team environment.