Validation Engineer
EQVAL•Ponce, PR
•Onsite
About The Position
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.
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).
Responsibilities
- Support Validation/Qualification activities in a Medical Devices manufacturing environment.
- Development and execution of validation documentation and protocols, including; Validation Assessments, Validation Plans, Requirements Specifications (URS, FRS), IQ, OQ, PQ and Reports.
- Developing and implementing Measurement System Analysis (MSA), Attribute Analysis, GR&R, DOEs.
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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
