Specialist Qualification - Waverly, WV, United States - Emerald Enterprises
Description
Your Responsibilities- Creation of qualification documentation and protocols
- Creation and adaptation of SOPs
- Administration of documents related to quality management
- Support in compliance with GMP regulations
- Coordination of qualification activities (including planning and coordination)
- Close collaboration with project management
- Degree in natural sciences or a comparable education with additional qualifications
- Ideally, first professional experience in the pharmaceutical industry
- Proficient in common MS Office applications
- Independent work style, proactive team player
- Communicative and goaloriented personality
- Exciting challenges in a promising and growing company
- An open working atmosphere in a company culture with short communication channels
- An attractive compensation package and interesting development opportunities
For the sake of readability, the simultaneous use of male, female, and diverse language forms (m/f/d) is omitted.
All personal designations apply equally to all genders.
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