Regulatory Affairs Jobs at Convatec | RA/QA Manager | Life Science Jobs
Convatec is offering senior-level regulatory affairs jobs for professionals aiming to advance their careers in global life science jobs. This RA/QA Manager role is central to regulatory compliance, product registrations, labeling approvals, and quality governance across Convatec’s medical device portfolio.
- Job Title: RA/QA Manager
- Location: Gurgaon, Haryana, India
- Job ID: JR00016126
About the Company:
Convatec is a global medical products and technologies company focused on solutions for chronic condition management, including advanced wound care, ostomy care, continence care, and infusion care. With operations in nearly 90 countries and revenues exceeding $2 billion, Convatec delivers meaningful life science jobs through innovation, quality, and patient-centric healthcare solutions.
Job Overview:
Lead regulatory compliance, product registrations, labeling approvals, and lifecycle management for medical devices. Prepare and submit regulatory documents to local authorities and handle post-market activities. Ensure quality system compliance, manage change controls, and support safety reporting. Act as liaison with government agencies for regulatory issues.
Educational Requirements:
- Bachelor’s degree in Science or a relevant Life Science discipline
Key Responsibilities:
- Develop and update regulatory strategies based on regulations and business needs
- Manage regulatory compliance activities as per local authority requirements
- Prepare, review, and submit regulatory submissions
- Liaise with health authorities to ensure timely approvals
- Ensure compliance with post-marketing approval conditions
- Maintain regulatory documentation and secure databases
- Manage product lifecycle activities including renewals and change controls
- Review and approve labeling, promotional, and advertising materials
- Support product safety reporting and field actions
- Participate in quality compliance audits
- Act as focal point for regulatory communication with government agencies
Skills Required:
- Strong knowledge of medical device regulatory affairs
- Experience in regulatory submissions and authority interactions
- Understanding of Quality Management Systems
- Familiarity with ISO 13485 and GDPMDS requirements
- Attention to detail, documentation accuracy, and stakeholder communication
These Regulatory Affairs Jobs at Convatec offer an excellent platform for professionals seeking impactful Life Science Jobs in the medical device sector. Join Convatec to contribute to global healthcare innovation while building a strong, future-ready regulatory career.
