Biotech Quality Assurance: Document Control Specialist
Vyriad Inc.
A leading biotech company in Florida is seeking a Document Control Specialist to manage controlled documents and ensure compliance within a fast-paced environment. This role requires strong organizational and communication skills, with a focus on Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). Ideal candidates will have at least 2 years of experience in a regulated industry and proficiency with Microsoft Office tools. The company offers a supportive environment conducive to career growth. #J-18808-Ljbffr Vyriad Inc.
Vacancy posted 2 days ago
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