Compliance Verification Specialist

We are seeking a skilled Compliance Verification Specialist to join our team. The ideal candidate will have a strong background in quality assurance and a keen eye for detail.

The primary responsibility of this role is to verify compliance with regulatory requirements, ensuring that all activities meet the highest standards of quality and safety. This involves reviewing batch records, conducting line clearances, and overseeing start-up procedures to ensure smooth manufacturing operations.

You will be responsible for executing or assigning tasks related to batch execution, including filling in various formats and creating additional records as needed. Additionally, you will review records maintained by the Production team, create new records as necessary, and conduct documentation with respect to Quality Assurance (QA) activities.

Your responsibilities also include verifying adherence to Quality Management System (QMS) elements, such as change control, incident management, and Corrective and Preventive Actions (CAPA) management on the shop floor. You will provide essential support to supervisors in conducting investigations related to complaints, batch failures, Out-of-Specification (OOS)/Out-of-Trend (OOT) results, incidents, etc.

To excel in this role, you should possess a solid understanding of Quality Systems, an in-depth knowledge of the Bio Pharma and Pharma markets, and awareness of global cGMP/Curent GMP regulatory requirements. Strong communication and influencing skills, analytical thinking abilities, adaptability to the work environment, and a team player attitude are also essential.

This is a fantastic opportunity to grow your career with a reputable organization that prioritizes continuous learning, professional development, and a supportive work culture.

• Assist in the preparation of audit responses and track action item closure
• Support cross-functional teams during investigation processes
• Maintain accurate records and reports

• Bachelor's degree in Pharmacy or Post-Graduation in Life Sciences
• Minimum 4 years of industrial experience in Quality Assurance/IPQA
• Solid understanding of Quality Systems and ability to navigate counter functions
• In-depth knowledge of Bio Pharma and Pharma markets, including product knowledge, market trends, competitors, and customer needs
• Awareness of global cGMP/Curent GMP regulatory requirements

As a Compliance Verification Specialist, you can expect to enjoy a competitive salary, comprehensive benefits package, and opportunities for professional growth and development.

We are a leading pharmaceutical company committed to accelerating access to affordable and innovative medicines. Our mission is to make a positive impact on people's lives, and we believe that our employees are the key to achieving this goal.