Validation Engineer

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.

We are seeking  Validation Engineers or Specialists to support Validation/Qualification activities in a Medical Devices manufacturing environment. 

Key Requirements:

• Bachelor Degree in Engineering  
• Minimum of 4+ years of experience in Pharma, Biotech, or Medical Devices.
• Experienced in development and execution of validation documentation and protocols, including; Validation Assessments, Validation Plans, Requirements Specifications (URS, FRS), IQ, OQ, PQ and Reports . 
• Good technical writing skills . 
• Experience developing and implementing Measurement System Analysis (MSA), Attribute Analysis, GR&R, DOEs. 
• Experience in Minitab (software statistical tool). 
• Fully bilingual (English and Spanish) . 

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 Ponce, 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.