QA QMS Manager

Roles and Responsibilities :

• Develop and implement quality management systems (QMS) to ensure compliance with regulatory requirements, industry standards, and company policies.
• Conduct audits, inspections, and investigations to identify areas for improvement and implement corrective actions.
• Collaborate with cross-functional teams to develop and maintain documentation related to QMS, including procedures, protocols, and reports.
• Provide training on QMS principles, regulations, and best practices to employees at all levels within the organization.

Job Requirements :

• 8-12 years of experience in pharmaceutical or life sciences industry with expertise in OSD formulation development.
• Strong understanding of USFDA guidelines and regulations governing pharmaceutical manufacturing processes.
• Experience with CAPA implementation and maintenance of records according to cGMP requirements.
• Proven track record of developing effective documentation strategies for solid oral dosage forms.