Pharma Quality Assurance Specialist

Actalent; Cherry Hill Township (NJ); On-site; USD 44,000 - 48,000; Full time

Job summary

Actalent in Cherry Hill, NJ, is seeking a Quality Specialist to ensure accurate, compliant quality documentation and to support investigations, deviations, and customer complaints within a GMP pharmaceutical environment.

The role involves reviewing batch records, assisting in investigations, and collaborating with cross-functional teams to enforce QA processes and regulatory alignment. This onsite contract position emphasizes attention to detail and audit readiness.

Qualifications

• Bachelor's degree in Science or a related discipline is required.
• 5+ years of experience in a pharmaceutical quality role.
• Strong understanding of GMP principles and their application in pharma.
• Hands-on experience with investigations related to quality issues.
• Proven experience managing and documenting deviations.
• Experience handling and documenting customer complaints in a regulated environment.
• Proficiency in batch record review and quality documentation review.
• Solid background in QA practices and processes.
• Ability to perform and document root cause analysis for investigations and deviations.
• Strong attention to detail and accuracy in quality documentation.

Responsibilities

• Complete quality documentation accurately and on time, including investigation reports and deviation records.
• Review batch records to ensure GMP compliance and internal procedures.
• Assist investigations of quality issues and document findings and corrective actions.
• Support management of customer complaints by data gathering, root cause analysis, and documenting outcomes.
• Collaborate with cross-functional teams to apply QA processes consistently.
• Participate in validation activities by reviewing and supporting documentation for regulatory compliance.
• Identify trends to suggest process improvements for investigations, deviations, and complaints.
• Maintain audit-ready quality records in line with regulatory expectations and company policies.

Skills

Bachelor's degree

GMP knowledge

Investigations

Deviations management

Customer complaints

Batch records review

Quality assurance

Root cause analysis

Attention to detail

Documentation

Education

Bachelor's degree in Science or related

Job description

Actalent in Cherry Hill, NJ, is seeking a Quality Specialist to ensure accurate, compliant quality documentation and to support investigations, deviations, and customer complaints within a GMP pharmaceutical environment.

The role involves reviewing batch records, assisting in investigations, and collaborating with cross-functional teams to enforce QA processes and regulatory alignment. This onsite contract position emphasizes attention to detail and audit readiness.