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Job summary
A pharmaceutical solutions company located in Indianapolis is seeking a Quality Manager to develop and maintain a compliant Quality Management System (QMS). The role requires overseeing document control and audits, ensuring compliance across storage and distribution activities, and handling investigations and CAPA. Candidates should have extensive experience in quality or compliance within pharmaceutical manufacturing and strong knowledge of relevant regulations. A bachelor's degree in a related field is required, with an advanced degree preferred.
Qualifications
5+ years of quality or compliance experience within pharmaceutical manufacturing.
Strong knowledge of cGMP, GDP, FDA, and ICH regulations.
Experience managing quality systems, audits, and regulatory inspections.
Responsibilities
Develop and maintain a compliant Quality Management System (QMS).
Oversee document control, change management, and CAPA activities.
Conduct and manage internal audits and coordinate customer audits.
Ensure compliance across all pharmaceutical storage and handling activities.
Monitor temperature-controlled shipments and validate equipment.
Review investigations, deviations, and nonconformances.
Skills
Quality Management Systems
cGMP knowledge
Regulatory compliance
Root cause analysis
Auditing
Education
Bachelor’s degree in Life Sciences or related field
Job description
A pharmaceutical solutions company located in Indianapolis is seeking a Quality Manager to develop and maintain a compliant Quality Management System (QMS). The role requires overseeing document control and audits, ensuring compliance across storage and distribution activities, and handling investigations and CAPA. Candidates should have extensive experience in quality or compliance within pharmaceutical manufacturing and strong knowledge of relevant regulations. A bachelor's degree in a related field is required, with an advanced degree preferred.