Quality Control Analyst
2 weeks ago
Contract Opportunity - Maternity Leave Coverage
Onsite Role - Full-Time
Compensation: $40 - $50 per hour
Key Responsibilities
- Oversee daily functions of Quality Management Systems (Veeva Vault) and Document Control to ensure adherence to regulatory and company standards.
- Assist in initiatives aimed at enhancing quality systems.
- Contribute to the employee training program.
- Maintain and organize documentation for GxP-related projects.
- Ensure proper management and accuracy of controlled documents, including master production records, labels, logbooks, laboratory notebooks, and protocols.
- Facilitate on-site document storage solutions to promote organization and efficient retrieval that supports daily operations.
- Draft, revise, and implement procedures for quality operations.
- Conduct regular audits of Quality Systems logs and records for accuracy and compliance.
- Digitize completed documents to preserve electronic records.
- Assist in the creation of training materials for Quality Systems and periodically educate staff on records management procedures.
- Identify and implement opportunities for continuous improvement within the quality management framework.
- Perform additional tasks or projects as directed by management.
Required Qualifications
- Minimum of 2 years of experience in Quality Systems within the biotech or pharmaceutical sector - REQUIRED
- Experience with Veeva Quality Vault (QualityDocs, Training, QMS) is essential.
- Proven experience as an administrator in the system or familiarity with system configurations.
- Solid understanding of current Good Manufacturing Practices (GMP) related to documentation.
- Strong proficiency in MS Office applications (Word, PowerPoint, Excel, and SharePoint).
- Demonstrated ability to collaborate effectively across various functions.
- Excellent verbal and written communication skills.
- Strong problem-solving, troubleshooting, and time management abilities.
- Proficient in Microsoft and Adobe software applications.
- Ability to work autonomously with minimal supervision.
- Comfortable navigating the dynamic environment of a start-up biotech company.
- Experience in Quality Assurance for both development and commercial products is advantageous.
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