GMP Document Specialist - Downsville, LA, United States - Stellar Enterprises
Description
OUR CLIENT
Our client is a globally operating corporation in the development and production of biologic medicines, with over 20,000 employees worldwide.
For the further expansion of their location in Leverkusen, we are exclusively seeking qualified employees (m/f/d) with experience in the pharmaceutical industry.
This rapidly growing company guarantees excellent working conditions and fair compensation.WE OFFER YOU
- Equal opportunities for all, regardless of age, ethnicity and nationality, gender, religion, worldview, sexual orientation, social background or marital status
- Personal development and growth in a successful and futureoriented company with excellent prospects
- An innovative work environment with flat hierarchies and fast decisionmaking processes
- An attractive salary package and additional benefits
- Comprehensive advice, targeted support and further training opportunities
- A familial, appreciative working atmosphere in a continuously growing pharmaceutical company
- Attractive bonus payment for referring a new employee (m/f/d)
YOUR TASKS
- Coordination and implementation of an efficient documentation workflow
- Consultation and monitoring of the documentation life cycle in paper and EDMS form, compliance with GxP and internal regulations
- Creation, review and processing of documents according to company procedures and templates
- Monitoring of metadata, document references, distribution, paper reconciliation and archiving
- Coordination of activities with department coordinators and providing guidance to them
- Representation as SME for document management during customer audits and regulatory inspections
YOUR PROFILE
- Bachelor's degree
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