Manager - QA – Quality Assurance | Hetero | Jadcherla, Telangana, India
Hetero is hiring experienced professionals for the role of Manager - QA at its pharmaceutical operations in Jadcherla, Telangana, India. This full-time opportunity is suitable for candidates with 15 years or more of experience in pharmaceutical quality assurance, regulatory compliance, GMP documentation, audit management, and manufacturing quality systems. The selected candidate will lead QA operations, manage compliance activities, supervise documentation systems, and coordinate with production and regulatory teams to maintain pharmaceutical quality standards. Candidates with expertise in regulatory audits, quality investigations, validation processes, CAPA systems, and compliance monitoring will be preferred. This role offers excellent exposure to regulated pharmaceutical manufacturing environments, quality-driven operational systems, and international compliance standards. Professionals seeking leadership opportunities in pharmaceutical quality assurance and regulatory management are encouraged to apply.
Location
Jadcherla, Telangana, IndiaEmployment Type
Full-timeExperience Required
15+Compensation & Benefits
Competitive compensation package with leadership opportunities, exposure to regulated pharmaceutical operations, and long-term career advancement in quality assurance management.About Hetero
Hetero is a leading pharmaceutical organization engaged in API manufacturing, formulations, research, development, and global pharmaceutical operations.Position Overview
The Manager - QA will oversee pharmaceutical quality assurance systems, regulatory compliance activities, and operational quality management functions.Key Responsibilities
- Manage pharmaceutical quality assurance operations.
- Ensure compliance with GMP and regulatory standards.
- Review quality documentation and batch records.
- Lead internal and external quality audits.
- Coordinate deviation investigations and CAPA implementation.
- Support validation and qualification activities.
- Monitor quality systems and compliance procedures.
- Train teams on QA standards and operational practices.
- Coordinate with production and regulatory departments.
- Prepare reports and compliance documentation.
Required Skills & Competencies
- Strong understanding of pharmaceutical QA systems.
- Knowledge of GMP and regulatory compliance.
- Leadership and team management capabilities.
- Experience in audit handling and quality investigations.
- Problem-solving and analytical thinking abilities.
- Strong documentation and reporting skills.
- Attention to detail and compliance accuracy.
- Ability to manage quality operations independently.
- Communication and cross-functional coordination skills.
- Awareness of pharmaceutical manufacturing standards.