Cleaning Validations Specialist- Añasco

Coordinates cleaning validation activities. prepares and executes protocols and reports. Coordinates sampling activities. Provides input in creation and/or assessment of deviations, including investigations and root cause analyzes. Provides technical support for all start-up activities related to temperature mapping, cleaning and sterilization programs. Development and execution of cleaning and sterilization strategies focused on the validation of production equipment. Lead or provide technical support for root cause investigations related to cleaning, sterilization, and other related activities. Analyze manufacturing data using statistical principles to identify trends, process disruptions, and opportunities for continuous improvements. Experience executing equipment qualification, cleaning validation, and sterilization validation. Ability to analyze complex data and solve problems.
Requisitos:
Bachelor's or Master's Degree in Engineering or Sciences, with at least 3-4 years of professional experiences in cleaning validations, manufacturing and/or Quality experience in medical devices industries. Proficient knowledge of cleaning validation, continuous process improvement and troubleshooting processes. Proficient in Risk Assessment/Management. Proven leadership & teamwork skills, self-starter, results oriented and build and maintain strong relationships with multiple groups. Customer service mindset, decision making & planning, work in cross functional environment. Projects and time management skills. Proficient in understanding, writing and speaking Spanish and English. Professional Services Contract. Experience with Cleaning Validations in Medical Devices manufacturing is required.