Quality Assurance Specialist
Target PR Range: 27-37/hr
*Depending on experience
• Ensure quality oversight and compliance for MES and PT project activities.
• Support validation and qualification efforts for computerized systems in alignment with GMP requirements.
• Review and approve documentation related to MES workflows, change controls, and deviations.
• Collaborate with cross-functional teams to ensure quality standards are met during system implementation.
• Participate in risk assessments and support mitigation strategies for quality-related issues.
• Ensure that quality processes and procedures are updated and aligned with project deliverables.
• Provide training and guidance on quality practices and regulatory compliance.
• Support audits and inspections by providing documentation and subject matter expertise.
• Monitor and report on quality metrics and continuous improvement initiatives.
• Ensure alignment with global quality standards and local regulatory requirements. Basic Qualifications
• Bachelor's or Master’s degree in Life Sciences, Engineering, or related field.
• Proven experience in quality assurance within a GMP-regulated manufacturing environment.
• Experience supporting MES and process transformation initiatives.
• Strong understanding of validation principles and regulatory compliance.
• Excellent documentation and communication skills.
• Ability to work collaboratively in cross-functional teams.
• Detail-oriented with strong analytical and problem-solving skills.
• At least 5 years of experience in quality assurance or related roles. *CO/NYC candidates might not be considered
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