Validation Engineer Specialist

EQVAL Group Inc. is a company that provides services to the manufacturing industry (Medical Devices Pharmaceuticals Biotechnologies others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers in order to perform and provide a highly effective service.

The Validation Engineer/Specialist is required to support Validation/Qualification activities in a Medical Devices or Pharmaceutical manufacturing environment.

Minimum Requirements:

• Bachelors degree in an Engineering field.
• Experienced in the development and execution of validation documentation and protocols including Validation Assessments Validation Plans Requirements Specifications (URS FRS) IQ OQ PQ and Reports.
• Experience developing and implementing Measurement System Analysis (MSA) including Attribute Analysis GR&R DOEs.
• Project management skills required.
• Experience in Minitab (software statistical tool).
• Good technical writing skills.
• Fully bilingual (English and Spanish) with exceptional communication skills both spoken and written.

Benefits:

• Health insurance (Medical Dental Vision Pharmacy)
• Life Insurance
• Paid time off (PTO)
• Holidays
• Professional Growth (Courses and Certifications by EQVAL Academy)
• Referral program
• Productivity incentive

*This position will be full-time 100% on site in Puerto Rico.

We offer competitive compensation benefits and opportunities for career growth. If you are a motivated individual with passion we would love to hear from you. Apply now!!

EQVAL Group is an EEO. We comply with all federal local and state laws regarding non-discrimination.