Mf01-090924 Document Control Specialist

2 semanas atrás

Paraná, Brasil Validation & Engineering Group Tempo inteiro

**_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.

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