Qualification & Validation Engineer for Pharma

We are looking for motivated and dynamic consultants in Santiago with expertise as a Qualification & Validation Engineer. You will play a challenging role and be key players in the success of our clients’ projects.

With Amaris you will:

• Join an international consultancy group in continuous growth and with a strong presence in Europe, America, and Asia.
• Have the opportunity to develop your career as a professional consultant inside a sparkling company.
• Be part of a company, which is able to provide you with rapid career growth and interesting international/local projects.
• Expand your professional network by joining an international employee community across and within our offices.

Technical duties may involve (although not limited to):

• Execute tests (IQ/OQ/PQ).
• Coordinate and review the related GMP documentation needed for change control management.
• Define the validation strategy based on the clients' guidance and benchmarks.
• Ensure the planning of validation and qualification strategies in accordance with all the concerned parties: production, QA, maintenance, among others.
• Develop and implement procedures to comply with corporate and industry standards.
• Participate in project planning, scheduling, and tracking.
• Ensure the operational management & training of the technicians dedicated to the validations.

Our ideal candidate must have:

• At least a Master`s degree in engineering, bioengineering, biology, pharmacy or related fields.
• One year of experience in qualification and validation in GMP environments.
• Knowledge of creation and verification of qualification equipment plans (FAT/SAT/DQ/IQ/OQ/PQ) is a plus.
• Knowledge of FDA and international Pharmaceutical regulations is a plus.
• Familiar with the processes and legal requirements for the pharmaceutical industry.
• Proficient in Spanish. English is a plus.