Validation & Engineering Group
MF03-081322 Qualification Engineers / Scientist
Validation & Engineering Group, Guaynabo, Puerto Rico, United States, 00966
Job Opportunity At Validation & Engineering Group, Inc.
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Qualification Engineers / Scientist
Qualifications: Bachelor's Degree in Science or Engineering. Minimum of 2 years of experience in pharmaceutical, parenterals, or biotechnology industries. Dynamic, eager to learn, driving the action, pursuing results Experience in direct process / manufacturing areas, preferably Oral Solid Dosage (OSD) Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Knowledge / Experience developing qualification documents such as User Requirement Specifications (URS), Validation Plans (VP), SOP, Qualification Protocols (Installation Qualification (IQ), Operational Qualification (OQ), Factory Acceptance Test (FAT), Facility Qualification (FQ), Warehouse Mapping, and reports generation. Technical Writing skills. Available to work extended hours, possibility of weekends and holidays.
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Qualification Engineers / Scientist
Qualifications: Bachelor's Degree in Science or Engineering. Minimum of 2 years of experience in pharmaceutical, parenterals, or biotechnology industries. Dynamic, eager to learn, driving the action, pursuing results Experience in direct process / manufacturing areas, preferably Oral Solid Dosage (OSD) Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Knowledge / Experience developing qualification documents such as User Requirement Specifications (URS), Validation Plans (VP), SOP, Qualification Protocols (Installation Qualification (IQ), Operational Qualification (OQ), Factory Acceptance Test (FAT), Facility Qualification (FQ), Warehouse Mapping, and reports generation. Technical Writing skills. Available to work extended hours, possibility of weekends and holidays.