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:

• Document Control Specialist
  • Procedures (SOPs) design and revision.
  • Write new procedures or perform changes to existing procedures as per schedule.
  • Develop or review procedures according to established requirements, Corporate policies, and regulations.
  • Work SMEs and trainers for crafting new content and updating existing content. (Communication skills.)
  • Able to learn new systems to manage training transactions related to the assigned business area.

Qualifications:

• Bachelor's degree in science or business administration disciplines.
• 2-5 years of experience in the pharmaceutical industry.
• Experience in Learning and Development processes and management of standard operating procedures in a GMP facility.
• Must be fully bilingual (English / Spanish).
• Experience using learning management software, learning request tools and document management systems.
• Proficient in MS Windows formatting.
• Organizational, Communication and Good presentation skills.
• Willing to support operation during weekends, holidays and rotating shifts as needed.
• Available to work extended hours, possibility of weekends and holidays.