Manager - CQA – Quality Assurance | Cohance Lifesciences | Hyderabad, Telangana, India
Cohance Lifesciences is hiring an experienced Manager - CQA for its pharmaceutical operations in Hyderabad, Telangana, India. This full-time opportunity is ideal for professionals with 12 to 18 years of experience in corporate quality assurance, pharmaceutical compliance systems, regulatory documentation, quality audits, and GMP operations. The selected candidate will oversee quality assurance strategies, manage compliance programs, coordinate internal and external audits, and ensure adherence to pharmaceutical regulatory standards across manufacturing and quality systems. Candidates with strong exposure to CAPA management, SOP implementation, validation practices, and global regulatory expectations will be preferred. This role offers an opportunity to work within a professionally managed pharmaceutical organization focused on quality excellence, operational compliance, and continuous improvement initiatives across manufacturing and quality operations.
Location
Hyderabad, Telangana, IndiaEmployment Type
Full-timeExperience Required
12 to 18Compensation & Benefits
Competitive salary package with leadership exposure, compliance management responsibilities, and long-term career growth opportunities in pharmaceutical quality systems.About Cohance Lifesciences
Cohance Lifesciences is a pharmaceutical organization engaged in manufacturing, quality systems management, regulatory compliance, and healthcare product development with a strong focus on operational excellence and quality assurance.Position Overview
The Manager - CQA will lead corporate quality assurance activities, compliance monitoring, audit management, and quality improvement initiatives across pharmaceutical operations.Key Responsibilities
- Manage corporate quality assurance systems and compliance programs.
- Oversee GMP documentation and SOP implementation activities.
- Coordinate internal and external quality audits.
- Monitor CAPA, deviation, and change control systems.
- Support validation and qualification compliance activities.
- Ensure adherence to pharmaceutical regulatory guidelines.
- Coordinate with manufacturing and quality control teams.
- Review quality metrics and operational performance reports.
- Handle regulatory inspection preparation and responses.
- Drive continuous quality improvement initiatives.
Required Skills & Competencies
- Strong pharmaceutical quality assurance expertise.
- Knowledge of GMP and regulatory compliance systems.
- Experience in audit management and CAPA handling.
- Leadership and team coordination abilities.
- Documentation and quality reporting skills.
- Analytical and problem-solving capabilities.
- Communication and stakeholder management skills.
- Understanding of validation and qualification processes.
- Attention to detail and compliance accuracy.
- Ability to manage multiple quality functions.