Offer summary

Key responsabilities:

Support clients to adhere to regulatory standards and guidelines

Provide expertise in quality management systems and audits

Assist in developing and implementing regulatory strategies

Collaborate for compliance with ISO and FDA regulations

Guide clients through regulatory approval processes and compliance

Job description

About Us:

Excellence Squad is a premier consultancy committed to advancing healthcare through comprehensive consulting services tailored to the diverse needs of the life sciences sector. Our mission is to empower and help companies across pharmaceuticals, biotechnology, and medical devices with expert guidance in regulatory affairs, quality assurance, and clinical solutions. We strive to ensure compliance, innovation, and patient safety throughout the product lifecycle. Our vision is to be the benchmark consulting firm renowned for our commitment to excellence and dedication to inspiring collaboration and growth within the industry.

Role Overview:

As a Consultant in Quality and Regulatory Affairs (QA/RA), you will play a vital role in guiding our clients through the complex regulatory landscape of the healthcare industry. You will lead projects, work on applications, inspections, regulations, clinical evaluation, standards, and contribute to development projects. Your responsibilities will encompass various aspects of quality management, regulatory compliance, and project management within the healthcare sector.

Key Responsibilities:

Support clients in both the private and public sectors, ensuring adherence to regulatory standards and guidelines.

Provide expertise in quality management systems, risk management, process validation, and audits at client sites or third-party audits.

Assist in the development and implementation of regulatory strategies tailored to the specific needs of clients in the medical device and healthcare industry.