Company Overview

Sanmed Healthcare, an Indo-US-German collaboration, manufactures, supplies, and exports disinfectants and antiseptics. Modern manufacturing facilities adhere to WHO GMP standards, focusing on disinfection, hygiene, and skin protection. The company prioritizes innovation and international quality standards in healthcare, committed to high-quality, cost-effective services worldwide. Headquartered in Hyderabad, Sanmed Healthcare belongs to the Pharmaceutical Manufacturing industry, maintaining a global presence.

Job Overview

The Quality Assurance Executive is a mid-level, full-time position located in Hyderabad. The role requires a work experience of 4 to 6 years in the pharmaceutical manufacturing industry. The executive will ensure quality control aligned with WHO GMP standards, aiming to exceed quality benchmarks in disinfection and hygiene solutions. The role involves managing documentation, communication, and coordination with various departments to ensure compliance and efficiency.

EDUCATION: B PHARM / M PHARM

EXPERIENCE: Min 4 yrs. To +7 years, preferably in Healthcare manufacturing unit (liquid formulations / medical devices)

Qualifications and Skills

• Minimum 4 years of experience in quality assurance within the pharmaceutical or healthcare industry.
• Proficiency in documentation processes ensuring accuracy and comprehensibility (Mandatory skill).
• Strong communication skills to effectively liaise with cross-functional teams and external stakeholders (Mandatory skill).
• Experience in Standard Operating Procedures (SOP) preparation and update to align with industry standards.
• In-process Quality Assurance (IPQA) skills to monitor production processes and maintain quality standards.
• Thorough understanding of Good Manufacturing Practice (GMP) regulations and their practical application.
• Experience with the change controls process and ability to manage alterations efficiently.
• Proven record of conducting validations ensuring that processes achieve the intended quality outcomes.
• Ability to perform vendor assessments to ensure suppliers meet quality and regulatory requirements.

Roles and Responsibilities

• Develop, implement, and maintain quality assurance protocols to ensure compliance with WHO GMP standards.
• Conduct regular audits and inspections to identify areas for improvement in production processes and documentation.
• Collaborate with product development teams to ensure quality considerations are integrated into new projects.
• Manage SOP preparation, updates, and training to ensure staff adherence to procedural standards.
• Monitor IPQA activities during production to ensure processes meet predefined quality standards.
• Evaluate and manage change controls to maintain process consistency and product reliability.
• Perform validations to verify and document the efficacy of processes and equipment.
• Conduct vendor assessments to ensure compliance with quality and safety regulations.
• Report to senior management on quality issues, offering solutions for continuous improvement.