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 for talented, dedicated individuals who are committed to work under the highest standards of ethics to and with expertise in the following area:

•  Process Development Scientist 

Qualifications:

•  Knowledge in 5S, Problem Solving/ Root cause analysis tools (5 Whys, Cause and Effect Diagrams) and Lean Manufacturing Concepts.
• Knowledge in Visual Manual Inspection Techniques.
• Knowledge in GMP Electronic Documentation platforms.
• Knowledge in Smartsheets.
• Advanced Knowledge in Microsoft Excel, Teams.
• Advanced scientific analysis and troubleshooting skills.
• Basic knowledge in formulation and raw materials.
• Advanced work skills on laboratory equipment and instruments such as pipette, micrometer, caliper, microscope and analytical balance.
• Create cosmetic defects on vials and syringes.
• Seed particle in solution on vials and syringes.
• Knowledge in Sample Management.
• Knowledge in aseptic techniques.
• Knowledge or previously certified on manual visual inspection techniques.
• Ability to develop new defective conditions on primary containers.
• Be able to work in fast environment and prioritize multiple tasks.
• Ability to be flexible and handle change.
• Strong knowledge of cGMP’s.
• Fully bilingual (English/Spanish)

Requirements:

• Doctorate degree in Engineering/Sciences or Master degree Engineering/Sciences and 5 years of Scientific experience or Bachelor degree in Engineering/Sciences and 6 years of Scientific experience.

Shift: Non-standard