
QA Specialist
Flexible & Integrated Technical Services
- Yauco, PR
- Permanente
- Tiempo completo
- Bachelor’s Degree in Engineering or Life Sciences and four (4) years of exposure within the Pharmaceutical or Medical Devices industry.
- Bilingual (Spanish and English)
- Shift: Administrative, and according to business needs.
- Experience in:
- Generation and review procedures
- Preventive maintenance work orders (WO)
- LOTO (Lockout/Tagout)
- SAP or Maximo
- Conducted risk assessments and implemented mitigation strategies for equipment and processes.
- Ensure compliance with industry regulations, quality standards, and Good Manufacturing Practices (GMP).
- Collaborate with cross-functional teams to optimize packaging and manufacturing systems.
- Perform testing and analysis to validate packaging materials and manufacturing equipment.
- Validation engineering support of process and/or equipment upgrades, replacements, and modifications in the manufacturing environment.
- Develops, organizes, analyzes, and presents interpretation of results for operational issues or validation engineering projects of significant scope.
- Complete complex or novel assignments requiring the development of new and/or improved validation engineering techniques and procedures.
- Develop validation engineering policies and procedures.
- Implement tools, techniques, and processes to provide or create information to enable informed decision making within the teams.
- One of these is the excellent, unmatched, never-before-seen customer service of our team (trust us, you’ll be amazed). However, that’s not all we have to offer. Talk with us to find out!