Sr. Manager – Quality Assurance - Audit Compliance | Hetero | Jadcherla, Telangana, India
Hetero is inviting applications for the position of Sr. Manager – Quality Assurance - Audit Compliance at its pharmaceutical facility in Jadcherla, Telangana, India. This full-time opportunity is ideal for highly experienced professionals with 15 to 20 years of expertise in pharmaceutical quality assurance, regulatory compliance management, audit handling, GMP systems, and operational quality governance. The selected candidate will lead audit compliance operations, supervise quality systems, coordinate regulatory inspections, and ensure adherence to international pharmaceutical standards and compliance procedures. Candidates with strong experience in USFDA, MHRA, WHO, and international audit environments along with expertise in CAPA management, deviation investigations, and compliance monitoring will be preferred. This role provides leadership exposure within regulated pharmaceutical manufacturing environments focused on operational excellence, quality assurance systems, and global regulatory compliance.
Location
Jadcherla, Telangana, IndiaEmployment Type
Full-timeExperience Required
15 to 20Compensation & Benefits
Competitive leadership compensation package with opportunities to work in globally regulated pharmaceutical operations and long-term executive career growth.About Hetero
Hetero is a leading pharmaceutical organization engaged in API manufacturing, formulations, research and development, and global healthcare operations.Position Overview
The Sr. Manager – Quality Assurance - Audit Compliance will oversee audit management systems, compliance operations, and pharmaceutical quality governance activities.Key Responsibilities
- Manage audit compliance and quality assurance operations.
- Coordinate regulatory audits and inspection activities.
- Ensure adherence to GMP and pharmaceutical standards.
- Review compliance documentation and quality systems.
- Lead CAPA implementation and deviation investigations.
- Support validation and quality review processes.
- Coordinate with production and regulatory departments.
- Prepare audit reports and compliance documentation.
- Train teams on quality and compliance procedures.
- Monitor operational quality systems and improvements.
Required Skills & Competencies
- Strong knowledge of pharmaceutical QA systems.
- Understanding of international regulatory requirements.
- Leadership and team management capabilities.
- Experience in audit handling and compliance management.
- Problem-solving and analytical thinking abilities.
- Strong communication and reporting skills.
- Awareness of GMP and quality governance systems.
- Attention to detail and compliance accuracy.
- Ability to manage regulated pharmaceutical operations.
- Capability to lead large-scale compliance activities.