Regulatory Affairs Jobs | ZimVie is Hiring | Apply Now
Looking to grow your career in Regulatory Affairs jobs within the global medical device industry? ZimVie is hiring a QA & RA Specialist – APAC in Mumbai, offering an excellent opportunity for professionals from Biology jobs backgrounds to work across quality systems and regulatory compliance. This role is ideal for candidates aiming to build impactful QA jobs while supporting product registrations across India and the APAC region.
Job Details
- Job Title: QA & RA Specialist – APAC
- Requisition ID: 3390
- Function: Regulatory
- Location: Mumbai, India
- Job Type: Full-time
About the Company
ZimVie is a global life sciences company focused on improving patients’ quality of life through advanced clinical technologies. With a strong foundation of trusted brands and clinical evidence, ZimVie fosters an inclusive, collaborative work culture. The company emphasizes quality, regulatory excellence, and professional growth, making it an ideal destination for long-term Regulatory Affairs jobs in the life sciences sector.
Key Responsibilities
- Responsible for medical device products registration in India, include initial, post-approval and renewal registration.
- Responsible for product registration in APAC region.
- Maintain and update international internal regulatory databases.
- Prepare, review, approve, distribution and training on Quality Management documentation.
- Participate on external and internal audits.
- Training to other departments on quality & regulatory procedures as needed.
- Participate in the assessments of the new or updated regulations and standards applicable to the products, and national laws for any new or updated revisions. Communicate updates to regulatory staff.
- Respond to all market requests (customers, distributors and others) and support CS in providing information to customers.
- This is not an exhaustive list of duties or functions and may not necessarily comprise all of the “essential functions”.
Qualifications
- Bachelor’s or Master’s degree or above in biological or related sciences.
- Above 3-5 years working experience on regulatory and quality in the field for medical device.
Skills
- Good communication skill.
- Good teamwork and actively attitude.
- Professional knowledge on medical device regulatory affairs & quality field.
- Computer skills and be proficient with commonly used software.
- Good at written and oral in English.
- Effectively managing one’s time and resources to ensure that work is completed efficiently.
- Actively participating as a member of a team to move the team toward the completion of goals.
- Attention to detail, initiative, and flexibility, used to work with deadlines, stress Resistant
This role offers an excellent pathway for professionals aiming to advance in Regulatory Affairs jobs while strengthening expertise in QA jobs within a global medical device organization. If you have a background in Biology jobs and regulatory compliance, this position at ZimVie provides both growth and international exposure.
